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Gene: WWP2 (WW domain containing E3 ubiquitin protein ligase 2) Homo sapiens

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Symbol:

WWP2

Name:

WW domain containing E3 ubiquitin protein ligase 2

RGD ID:

1320797

HGNC Page

HGNC:16804

Description:

Enables RNA polymerase II-specific DNA-binding transcription factor binding activity and ubiquitin-protein transferase activity. Involved in several processes, including negative regulation of macromolecule biosynthetic process; negative regulation of transport; and protein autoubiquitination. Acts upstream of or within protein ubiquitination. Located in nucleus.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

AIP2; atrophin-1 interacting protein 2; atrophin-1-interacting protein 2; HECT-type E3 ubiquitin transferase WWP2; Nedd-4-like ubiquitin-protein ligase; NEDD4-like E3 ubiquitin-protein ligase WWP2; WW domain-containing protein 2; WWp2-like

RGD Orthologs

Alliance Orthologs

More Info

more info ...

Related Pseudogenes:

AL513321.1

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	16	69,762,332 - 69,941,739 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	16	69,762,328 - 69,941,741 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	16	69,796,235 - 69,975,642 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	16	68,353,775 - 68,533,144 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	16	54,311,024 - 54,490,955 (+)	NCBI		Celera
Cytogenetic Map	16	q22.1	NCBI
HuRef	16	55,674,737 - 55,853,946 (+)	NCBI		HuRef
CHM1_1	16	71,204,171 - 71,383,517 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	16	75,564,847 - 75,744,318 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

autosomal dominant dyskeratosis congenita 6 (IAGP)

Chromosome 16q12 Duplication Syndrome (IAGP)

Knee Osteoarthritis (EXP)

spondyloepiphyseal dysplasia Nishimura type (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

1,2-dimethylhydrazine (ISO)

2,3,7,8-tetrachlorodibenzodioxine (ISO)

2,4-dinitrotoluene (ISO)

4,4'-sulfonyldiphenol (ISO)

4-hydroxyphenyl retinamide (ISO)

acrolein (EXP)

aflatoxin B1 (EXP)

Aflatoxin B2 alpha (EXP)

all-trans-retinoic acid (EXP)

alpha-pinene (EXP)

aristolochic acid A (EXP)

arsane (EXP)

arsenic atom (EXP)

atrazine (EXP)

benzo[a]pyrene (EXP,ISO)

benzo[e]pyrene (EXP)

beta-lapachone (EXP)

bis(2-ethylhexyl) phthalate (ISO)

bisphenol A (ISO)

cadmium atom (ISO)

CGP 52608 (EXP)

chlorpyrifos (ISO)

coumarin (EXP)

cypermethrin (ISO)

diazinon (ISO)

Dibutyl phosphate (EXP)

dibutyl phthalate (ISO)

dicrotophos (EXP)

dieldrin (ISO)

dioxygen (EXP,ISO)

folic acid (EXP)

FR900359 (EXP)

methapyrilene (EXP)

N-nitrosodiethylamine (ISO)

nickel dichloride (ISO)

ozone (EXP)

paracetamol (EXP,ISO)

resveratrol (EXP)

selenomethionine (EXP)

sodium arsenite (EXP)

testosterone (ISO)

testosterone enanthate (EXP)

thiram (EXP)

triphenyl phosphate (EXP)

valproic acid (EXP)

zearalenone (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

extracellular transport (IMP)

negative regulation of DNA-binding transcription factor activity (ISO)

negative regulation of DNA-templated transcription (IEA,ISS)

negative regulation of gene expression (IMP)

negative regulation of Notch signaling pathway (TAS)

negative regulation of potassium ion export across plasma membrane (IDA)

negative regulation of protein transport (IMP)

negative regulation of transcription by RNA polymerase II (IBA,IEA,IMP,ISS)

negative regulation of transporter activity (IDA)

positive regulation of transcription by RNA polymerase II (IEA)

proteasome-mediated ubiquitin-dependent protein catabolic process (IBA,IEA,IMP)

protein autoubiquitination (IDA)

protein K63-linked ubiquitination (IEA,ISS)

protein modification process (TAS)

protein ubiquitination (IDA,IEA,IMP)

regulation of membrane potential (IDA)

regulation of monoatomic ion transmembrane transport (IBA)

symbiont entry into host cell (TAS)

transcription by RNA polymerase II (IEA)

ubiquitin-dependent protein catabolic process (IEA)

Cellular Component

cytoplasm (IBA,IEA,ISS)

cytosol (TAS)

extracellular exosome (HDA)

membrane (HDA)

nucleus (IDA,IEA)

ubiquitin ligase complex (TAS)

Molecular Function

potassium channel inhibitor activity (IDA)

protein binding (IPI)

RNA polymerase II-specific DNA-binding transcription factor binding (IBA,IEA,IPI,ISS)

transcription regulator inhibitor activity (IEA,ISS)

transferase activity (IEA)

transmembrane transporter binding (IPI)

ubiquitin protein ligase activity (IBA,IEA,TAS)

ubiquitin-protein transferase activity (IDA,IEA,IMP,TAS)

Molecular Pathway Annotations Click to see Annotation Detail View

ubiquitin/proteasome degradation pathway (IEA)

Phenotype Annotations Click to see Annotation Detail View

Human Phenotype

Immunodeficiency (IAGP)

References

References - curated

#	Reference Title	Reference Citation
1.	KEGG Annotation Import Pipeline	Pipeline to import KEGG annotations from KEGG into RGD
2.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:9169421	PMID:9595660	PMID:9647693	PMID:11046148	PMID:11244092	PMID:11748237	PMID:12167593	PMID:12450395	PMID:12477932	PMID:15047715	PMID:15231748	PMID:15252135
PMID:15489334	PMID:15548568	PMID:15717329	PMID:16189514	PMID:16344560	PMID:16713569	PMID:16964243	PMID:17289006	PMID:17719543	PMID:17996703	PMID:18570872	PMID:18729074
PMID:18776082	PMID:19144635	PMID:19158374	PMID:19274063	PMID:19307600	PMID:19366705	PMID:19651900	PMID:19946888	PMID:19997087	PMID:20379614	PMID:20522958	PMID:20858735
PMID:21145461	PMID:21191027	PMID:21258410	PMID:21516116	PMID:21532586	PMID:21555855	PMID:21572392	PMID:21750408	PMID:21847096	PMID:21873635	PMID:21956701	PMID:22315426
PMID:22387393	PMID:22427670	PMID:22496338	PMID:22658674	PMID:22761572	PMID:22773947	PMID:22939629	PMID:22948661	PMID:23146381	PMID:23236378	PMID:23479606	PMID:23533145
PMID:23644597	PMID:23651516	PMID:23938591	PMID:24063548	PMID:24105792	PMID:24365151	PMID:24457600	PMID:24850914	PMID:24981174	PMID:25071155	PMID:25092867	PMID:25231870
PMID:25266661	PMID:25356737	PMID:25416956	PMID:25544563	PMID:25723849	PMID:25910212	PMID:25921289	PMID:25963657	PMID:26186194	PMID:26280536	PMID:26490116	PMID:26496610
PMID:26662306	PMID:26701932	PMID:26783238	PMID:26871637	PMID:26894970	PMID:26949039	PMID:27107012	PMID:27107014	PMID:27182664	PMID:27295432	PMID:27462019	PMID:27578003
PMID:27609421	PMID:27684187	PMID:27852060	PMID:28292929	PMID:28388416	PMID:28431233	PMID:28475870	PMID:28500134	PMID:28514442	PMID:28611215	PMID:29237971	PMID:29378950
PMID:29393344	PMID:29416926	PMID:29507755	PMID:29534260	PMID:29742433	PMID:29892012	PMID:30016585	PMID:30207403	PMID:30415470	PMID:30849479	PMID:31015455	PMID:31048545
PMID:31091453	PMID:31160553	PMID:31340145	PMID:31353912	PMID:31399586	PMID:31430374	PMID:31515488	PMID:31546607	PMID:31578285	PMID:31592114	PMID:31677789	PMID:31845480
PMID:31871319	PMID:31924572	PMID:31985874	PMID:32139900	PMID:32248569	PMID:32296183	PMID:32513696	PMID:32526160	PMID:32614325	PMID:32627301	PMID:32807901	PMID:32814053
PMID:33039560	PMID:33107021	PMID:33484499	PMID:33762578	PMID:33845483	PMID:33957083	PMID:33961781	PMID:34546340	PMID:34709727	PMID:34732716	PMID:34927784	PMID:35156780
PMID:35258167	PMID:35271311	PMID:35331737	PMID:35780838	PMID:35842443	PMID:35880837	PMID:35983977	PMID:36208715	PMID:36211818	PMID:36244648	PMID:36257929	PMID:36398662
PMID:36450710	PMID:36773333	PMID:36795754	PMID:36803368	PMID:36897111	PMID:36931259	PMID:37005481	PMID:37010382	PMID:37149668	PMID:37156795	PMID:37223976	PMID:37921219
PMID:38117590	PMID:38270169

Genomics

Comparative Map Data

WWP2
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	16	69,762,332 - 69,941,739 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	16	69,762,328 - 69,941,741 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	16	69,796,235 - 69,975,642 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	16	68,353,775 - 68,533,144 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	16	54,311,024 - 54,490,955 (+)	NCBI		Celera
Cytogenetic Map	16	q22.1	NCBI
HuRef	16	55,674,737 - 55,853,946 (+)	NCBI		HuRef
CHM1_1	16	71,204,171 - 71,383,517 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	16	75,564,847 - 75,744,318 (+)	NCBI		T2T-CHM13v2.0

Wwp2
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	8	108,162,966 - 108,285,922 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	8	108,162,997 - 108,285,227 (+)	Ensembl		GRCm39 Ensembl
GRCm38	8	107,436,334 - 107,559,290 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	8	107,436,365 - 107,558,595 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	8	109,960,298 - 110,082,495 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	8	110,325,527 - 110,447,724 (+)	NCBI		MGSCv36	mm8
Celera	8	111,667,038 - 111,789,943 (+)	NCBI		Celera
Cytogenetic Map	8	D3	NCBI
cM Map	8	54.15	NCBI

Wwp2
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	19	52,256,563 - 52,380,967 (+)	NCBI		GRCr8
mRatBN7.2	19	35,346,826 - 35,471,251 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	19	35,346,814 - 35,472,699 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	19	42,162,280 - 42,286,677 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	19	42,815,647 - 42,940,037 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	19	45,124,358 - 45,244,666 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	19	39,543,246 - 39,614,624 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	19	39,543,242 - 39,614,625 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	19	50,405,611 - 50,476,926 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
Rnor_5.0	19	49,207,226 - 49,255,597 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	19	37,302,346 - 37,428,377 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	19	37,307,245 - 37,433,162 (+)	NCBI
Celera	19	34,768,243 - 34,893,337 (+)	NCBI		Celera
Cytogenetic Map	19	q12	NCBI

Wwp2
(Chinchilla lanigera - long-tailed chinchilla)

Chinchilla Assembly	Chr	Position (strand)	Source	Genome Browsers
Chinchilla Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChiLan1.0 Ensembl	NW_004955484	6,851,307 - 6,967,261 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955484	6,853,820 - 6,967,261 (-)	NCBI	ChiLan1.0	ChiLan1.0

WWP2
(Pan paniscus - bonobo/pygmy chimpanzee)

Bonobo Assembly	Chr	Position (strand)	Source	Genome Browsers
Bonobo Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
NHGRI_mPanPan1-v2	18	79,311,991 - 79,492,082 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	16	85,224,164 - 85,404,265 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	16	50,142,402 - 50,322,052 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	16	69,525,246 - 69,703,831 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	16	69,525,246 - 69,703,831 (+)	Ensembl	panpan1.1		panPan2

WWP2
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	5	79,806,424 - 79,926,846 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	5	79,806,425 - 79,957,830 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	5	79,795,391 - 79,915,753 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	5	80,236,686 - 80,381,748 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	5	80,236,697 - 80,381,709 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	5	80,064,823 - 80,185,270 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	5	79,753,925 - 79,874,160 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	5	80,386,601 - 80,507,100 (-)	NCBI		UU_Cfam_GSD_1.0

Wwp2
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)

Squirrel Assembly	Chr	Position (strand)	Source	Genome Browsers
Squirrel Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HiC_Itri_2	NW_024409349	39,644,689 - 39,753,240 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936475	19,828,763 - 19,942,632 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936475	19,835,909 - 19,944,426 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

WWP2
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	6	17,066,799 - 17,227,926 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	6	17,068,780 - 17,227,982 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1

WWP2
(Chlorocebus sabaeus - green monkey)

Green Monkey Assembly	Chr	Position (strand)	Source	Genome Browsers
Green Monkey Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChlSab1.1	5	57,465,559 - 57,676,224 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	5	57,465,441 - 57,644,461 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666047	20,195,261 - 20,373,652 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Wwp2
(Heterocephalus glaber - naked mole-rat)

Naked Mole-Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Naked Mole-Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HetGla_female_1.0 Ensembl	NW_004624746	16,501,324 - 16,654,691 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624746	16,501,320 - 16,661,423 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in WWP2
97 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 16q13-22.2(chr16:56883592-71279975)x3	copy number gain	See cases [RCV000052405]	Chr16:56883592..71279975 [GRCh38] Chr16:56917504..71313878 [GRCh37] Chr16:55475005..69871379 [NCBI36] Chr16:16q13-22.2	pathogenic
GRCh38/hg38 16q21-23.1(chr16:58456122-74708723)x3	copy number gain	See cases [RCV000052408]	Chr16:58456122..74708723 [GRCh38] Chr16:58490026..74742621 [GRCh37] Chr16:57047527..73300122 [NCBI36] Chr16:16q21-23.1	pathogenic
GRCh38/hg38 16q21-24.3(chr16:65313395-90081985)x3	copy number gain	See cases [RCV000052421]	Chr16:65313395..90081985 [GRCh38] Chr16:65347298..90148393 [GRCh37] Chr16:63904799..88675894 [NCBI36] Chr16:16q21-24.3	pathogenic
GRCh38/hg38 16q22.1-23.1(chr16:69918076-76723348)x1	copy number loss	See cases [RCV000053356]	Chr16:69918076..76723348 [GRCh38] Chr16:69951979..76757245 [GRCh37] Chr16:68509480..75314746 [NCBI36] Chr16:16q22.1-23.1	pathogenic
GRCh38/hg38 16q21-22.1(chr16:63318997-70555249)x1	copy number loss	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053334]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053334]\|See cases [RCV000053334]	Chr16:63318997..70555249 [GRCh38] Chr16:63352901..70589152 [GRCh37] Chr16:61910402..69146653 [NCBI36] Chr16:16q21-22.1	pathogenic
GRCh38/hg38 16q22.1-23.1(chr16:68698941-74353205)x1	copy number loss	See cases [RCV000053337]	Chr16:68698941..74353205 [GRCh38] Chr16:68732844..74387103 [GRCh37] Chr16:67290345..72944604 [NCBI36] Chr16:16q22.1-23.1	pathogenic
GRCh38/hg38 16q21-24.1(chr16:62925929-84585795)x3	copy number gain	See cases [RCV000135863]	Chr16:62925929..84585795 [GRCh38] Chr16:62959833..84619401 [GRCh37] Chr16:61517334..83176902 [NCBI36] Chr16:16q21-24.1	pathogenic
GRCh38/hg38 16q22.1(chr16:69144650-70257882)x1	copy number loss	See cases [RCV000136580]	Chr16:69144650..70257882 [GRCh38] Chr16:69178553..70291785 [GRCh37] Chr16:67736054..68849286 [NCBI36] Chr16:16q22.1	uncertain significance
GRCh38/hg38 16q22.1-22.2(chr16:69918076-71541872)x3	copy number gain	See cases [RCV000137875]	Chr16:69918076..71541872 [GRCh38] Chr16:69951979..71575775 [GRCh37] Chr16:68509480..70133276 [NCBI36] Chr16:16q22.1-22.2	uncertain significance
GRCh38/hg38 16q21-24.3(chr16:65511483-90096995)x3	copy number gain	See cases [RCV000139426]	Chr16:65511483..90096995 [GRCh38] Chr16:65545386..90163403 [GRCh37] Chr16:64102887..88690904 [NCBI36] Chr16:16q21-24.3	pathogenic
GRCh38/hg38 16q22.1-23.3(chr16:69053457-83274681)x3	copy number gain	See cases [RCV000142038]	Chr16:69053457..83274681 [GRCh38] Chr16:69087360..83308286 [GRCh37] Chr16:67644861..81865787 [NCBI36] Chr16:16q22.1-23.3	pathogenic
GRCh38/hg38 16q21-24.3(chr16:64389378-90081985)x3	copy number gain	See cases [RCV000142578]	Chr16:64389378..90081985 [GRCh38] Chr16:64423281..90148393 [GRCh37] Chr16:62980782..88675894 [NCBI36] Chr16:16q21-24.3	pathogenic\|likely pathogenic
GRCh38/hg38 16q12.2-24.3(chr16:52899183-90088654)x3	copy number gain	See cases [RCV000143425]	Chr16:52899183..90088654 [GRCh38] Chr16:52933095..90155062 [GRCh37] Chr16:51490596..88682563 [NCBI36] Chr16:16q12.2-24.3	pathogenic
GRCh38/hg38 16q21-23.3(chr16:65957829-83611443)x3	copy number gain	See cases [RCV000143742]	Chr16:65957829..83611443 [GRCh38] Chr16:65991732..83645048 [GRCh37] Chr16:64549233..82202549 [NCBI36] Chr16:16q21-23.3	pathogenic
GRCh37/hg19 16q11.2-24.3(chr16:46615804-90142285)x1	copy number loss	Breast ductal adenocarcinoma [RCV000207138]	Chr16:46615804..90142285 [GRCh37] Chr16:16q11.2-24.3	uncertain significance
GRCh37/hg19 16q12.2-22.2(chr16:55359026-70884455)x1	copy number loss	Breast ductal adenocarcinoma [RCV000207067]	Chr16:55359026..70884455 [GRCh37] Chr16:16q12.2-22.2	likely pathogenic\|uncertain significance
Single allele	complex	Breast ductal adenocarcinoma [RCV000207314]	Chr16:56368689..90141355 [GRCh37] Chr16:16q12.2-24.3	uncertain significance
NR_029681.1(MIR140):n.24A>G	single nucleotide variant	Spondyloepiphyseal dysplasia MIR140 type Nishimura [RCV000735792]\|Spondyloepiphyseal dysplasia, nishimura type [RCV000853066]	Chr16:69933104 [GRCh38] Chr16:69967007 [GRCh37] Chr16:16q22.1	pathogenic
GRCh37/hg19 16q11.2-24.3(chr16:46464488-90155062)x3	copy number gain	See cases [RCV000446110]	Chr16:46464488..90155062 [GRCh37] Chr16:16q11.2-24.3	pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:69193-90274381)x3	copy number gain	See cases [RCV000446684]	Chr16:69193..90274381 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16q22.1(chr16:69385913-70336760)x1	copy number loss	See cases [RCV000510349]	Chr16:69385913..70336760 [GRCh37] Chr16:16q22.1	uncertain significance
GRCh37/hg19 16p13.2-q24.3(chr16:9273328-89548493)x3	copy number gain	See cases [RCV000511622]	Chr16:9273328..89548493 [GRCh37] Chr16:16p13.2-q24.3	uncertain significance
GRCh37/hg19 16q22.1(chr16:69369131-69941373)x3	copy number gain	See cases [RCV000511639]	Chr16:69369131..69941373 [GRCh37] Chr16:16q22.1	uncertain significance
GRCh37/hg19 16q22.1(chr16:69771851-69988373)x1	copy number loss	See cases [RCV000510787]	Chr16:69771851..69988373 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.1860G>T (p.Lys620Asn)	single nucleotide variant	not specified [RCV004324153]	Chr16:69935870 [GRCh38] Chr16:69969773 [GRCh37] Chr16:16q22.1	uncertain significance
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062)	copy number gain	See cases [RCV000511296]	Chr16:85881..90155062 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16q11.2-24.3(chr16:46455960-90354753)x1	copy number loss	Poly (ADP-Ribose) polymerase inhibitor response [RCV000626435]	Chr16:46455960..90354753 [GRCh37] Chr16:16q11.2-24.3	drug response
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062)x3	copy number gain	See cases [RCV000512138]	Chr16:85881..90155062 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16q11.2-24.3(chr16:46497599-90354753)x1	copy number loss	Poly (ADP-Ribose) polymerase inhibitor response [RCV000626429]	Chr16:46497599..90354753 [GRCh37] Chr16:16q11.2-24.3	drug response
NM_001270454.2(WWP2):c.1621C>T (p.Arg541Cys)	single nucleotide variant	not specified [RCV004317406]	Chr16:69931829 [GRCh38] Chr16:69965732 [GRCh37] Chr16:16q22.1	uncertain significance
GRCh37/hg19 16q13-24.3(chr16:57051473-89797669)x3	copy number gain	See cases [RCV000512511]	Chr16:57051473..89797669 [GRCh37] Chr16:16q13-24.3	pathogenic
GRCh37/hg19 16q22.1(chr16:69865323-69976962)x3	copy number gain	not provided [RCV000659226]	Chr16:69865323..69976962 [GRCh37] Chr16:16q22.1	likely benign
GRCh37/hg19 16q12.2-22.2(chr16:54416050-72453266)x3	copy number gain	not provided [RCV000683820]	Chr16:54416050..72453266 [GRCh37] Chr16:16q12.2-22.2	pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90274695)x3	copy number gain	not provided [RCV000738918]	Chr16:88165..90274695 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:61451-90294632)x3	copy number gain	not provided [RCV000738915]	Chr16:61451..90294632 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90163275)x3	copy number gain	not provided [RCV000738917]	Chr16:88165..90163275 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
NM_001270454.2(WWP2):c.590C>T (p.Ser197Leu)	single nucleotide variant	not provided [RCV000896577]	Chr16:69871818 [GRCh38] Chr16:69905721 [GRCh37] Chr16:16q22.1	benign
NM_001270454.2(WWP2):c.767C>T (p.Pro256Leu)	single nucleotide variant	not specified [RCV004296298]	Chr16:69888102 [GRCh38] Chr16:69922005 [GRCh37] Chr16:16q22.1	uncertain significance
GRCh37/hg19 16q22.1(chr16:69666939-69945532)x3	copy number gain	not provided [RCV000751723]	Chr16:69666939..69945532 [GRCh37] Chr16:16q22.1	benign
GRCh37/hg19 16q22.1(chr16:69814610-69941373)x1	copy number loss	not provided [RCV000846515]	Chr16:69814610..69941373 [GRCh37] Chr16:16q22.1	uncertain significance
GRCh37/hg19 16q22.1(chr16:69701301-69988373)x1	copy number loss	not provided [RCV000848865]	Chr16:69701301..69988373 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.708T>A (p.Asn236Lys)	single nucleotide variant	not specified [RCV004305582]	Chr16:69888043 [GRCh38] Chr16:69921946 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.543C>T (p.Pro181=)	single nucleotide variant	not provided [RCV000971807]	Chr16:69842088 [GRCh38] Chr16:69875991 [GRCh37] Chr16:16q22.1	benign
NM_001270454.2(WWP2):c.1449G>A (p.Thr483=)	single nucleotide variant	not provided [RCV004810220]	Chr16:69931155 [GRCh38] Chr16:69965058 [GRCh37] Chr16:16q22.1	likely benign
GRCh37/hg19 16q21-24.3(chr16:61524229-90155062)x3	copy number gain	not provided [RCV001249359]	Chr16:61524229..90155062 [GRCh37] Chr16:16q21-24.3	not provided
GRCh37/hg19 16q21-22.1(chr16:65669673-70180183)x1	copy number loss	not provided [RCV001006797]	Chr16:65669673..70180183 [GRCh37] Chr16:16q21-22.1	pathogenic
GRCh37/hg19 16q22.1(chr16:69638086-70040372)x3	copy number gain	not provided [RCV001259862]	Chr16:69638086..70040372 [GRCh37] Chr16:16q22.1	uncertain significance
GRCh37/hg19 16q22.1(chr16:69369131-69942990)x3	copy number gain	not provided [RCV001259864]	Chr16:69369131..69942990 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.390C>A (p.Ser130Arg)	single nucleotide variant	not specified [RCV004685652]	Chr16:69840175 [GRCh38] Chr16:69874078 [GRCh37] Chr16:16q22.1	uncertain significance
GRCh37/hg19 16q22.1-23.1(chr16:68971067-74823560)x1	copy number loss	See cases [RCV002285074]	Chr16:68971067..74823560 [GRCh37] Chr16:16q22.1-23.1	pathogenic
NC_000016.9:g.(?_69680960)_(72146396_?)dup	duplication	Immunodeficiency [RCV001950695]	Chr16:69680960..72146396 [GRCh37] Chr16:16q22.1-22.2	uncertain significance
NC_000016.9:g.(?_66545871)_(72146396_?)dup	duplication	Dyskeratosis congenita, autosomal dominant 6 [RCV001900384]\|Immunodeficiency [RCV001900385]\|not provided [RCV001900386]	Chr16:66545871..72146396 [GRCh37] Chr16:16q21-22.2	uncertain significance
GRCh37/hg19 16q11.2-24.3(chr16:46503968-90155062)x3	copy number gain	not provided [RCV002221458]	Chr16:46503968..90155062 [GRCh37] Chr16:16q11.2-24.3	pathogenic
NC_000016.9:g.(?_65821800)_(72146396_?)del	deletion	Dyskeratosis congenita, autosomal dominant 6 [RCV003122496]	Chr16:65821800..72146396 [GRCh37] Chr16:16q21-22.2	uncertain significance
NM_001270454.2(WWP2):c.178A>T (p.Ile60Phe)	single nucleotide variant	not specified [RCV004308795]	Chr16:69798789 [GRCh38] Chr16:69832692 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.748G>A (p.Val250Ile)	single nucleotide variant	not provided [RCV004695710]\|not specified [RCV004216206]	Chr16:69888083 [GRCh38] Chr16:69921986 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.2331G>C (p.Gln777His)	single nucleotide variant	not specified [RCV004182382]	Chr16:69937640 [GRCh38] Chr16:69971543 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.1199A>G (p.Asp400Gly)	single nucleotide variant	not specified [RCV004136751]	Chr16:69925449 [GRCh38] Chr16:69959352 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.2216A>G (p.Tyr739Cys)	single nucleotide variant	not specified [RCV004139715]	Chr16:69937216 [GRCh38] Chr16:69971119 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.1000C>G (p.Pro334Ala)	single nucleotide variant	not specified [RCV004159702]	Chr16:69908846 [GRCh38] Chr16:69942749 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.476A>C (p.Asp159Ala)	single nucleotide variant	not specified [RCV004190761]	Chr16:69840261 [GRCh38] Chr16:69874164 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.2483A>G (p.Lys828Arg)	single nucleotide variant	not specified [RCV004069689]	Chr16:69939383 [GRCh38] Chr16:69973286 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.167C>A (p.Thr56Asn)	single nucleotide variant	not specified [RCV004120401]	Chr16:69798778 [GRCh38] Chr16:69832681 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.514G>C (p.Ala172Pro)	single nucleotide variant	not specified [RCV004189435]	Chr16:69842059 [GRCh38] Chr16:69875962 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.2195C>T (p.Ala732Val)	single nucleotide variant	not specified [RCV004187588]	Chr16:69937195 [GRCh38] Chr16:69971098 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.383A>C (p.Lys128Thr)	single nucleotide variant	not specified [RCV004114467]	Chr16:69840168 [GRCh38] Chr16:69874071 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.335G>A (p.Gly112Asp)	single nucleotide variant	not specified [RCV004082939]	Chr16:69799290 [GRCh38] Chr16:69833193 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.806C>T (p.Thr269Met)	single nucleotide variant	not specified [RCV004099885]	Chr16:69888141 [GRCh38] Chr16:69922044 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.944G>A (p.Arg315His)	single nucleotide variant	not specified [RCV004086382]	Chr16:69908790 [GRCh38] Chr16:69942693 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.1055A>G (p.Asn352Ser)	single nucleotide variant	not specified [RCV004134425]	Chr16:69917759 [GRCh38] Chr16:69951662 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.1567A>G (p.Thr523Ala)	single nucleotide variant	not specified [RCV004140287]	Chr16:69931554 [GRCh38] Chr16:69965457 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.1237A>G (p.Lys413Glu)	single nucleotide variant	not specified [RCV004155641]	Chr16:69929450 [GRCh38] Chr16:69963353 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.590C>G (p.Ser197Trp)	single nucleotide variant	not specified [RCV004166177]	Chr16:69871818 [GRCh38] Chr16:69905721 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.2331G>T (p.Gln777His)	single nucleotide variant	not specified [RCV004150126]	Chr16:69937640 [GRCh38] Chr16:69971543 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.2438T>C (p.Ile813Thr)	single nucleotide variant	not specified [RCV004307638]	Chr16:69939121 [GRCh38] Chr16:69973024 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.865A>G (p.Thr289Ala)	single nucleotide variant	not specified [RCV004273425]	Chr16:69888200 [GRCh38] Chr16:69922103 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.440A>G (p.Asp147Gly)	single nucleotide variant	not specified [RCV004258592]	Chr16:69840225 [GRCh38] Chr16:69874128 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.415A>G (p.Ile139Val)	single nucleotide variant	not specified [RCV004274600]	Chr16:69840200 [GRCh38] Chr16:69874103 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.22C>T (p.Arg8Trp)	single nucleotide variant	not specified [RCV004294233]	Chr16:69787032 [GRCh38] Chr16:69820935 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.1430C>T (p.Pro477Leu)	single nucleotide variant	not specified [RCV004251332]	Chr16:69930243 [GRCh38] Chr16:69964146 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.2273G>A (p.Ser758Asn)	single nucleotide variant	not specified [RCV004685650]	Chr16:69937582 [GRCh38] Chr16:69971485 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.835G>A (p.Ala279Thr)	single nucleotide variant	not specified [RCV004685651]	Chr16:69888170 [GRCh38] Chr16:69922073 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.1723A>G (p.Met575Val)	single nucleotide variant	not specified [RCV004685654]	Chr16:69934010 [GRCh38] Chr16:69967913 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.185G>A (p.Ser62Asn)	single nucleotide variant	not specified [RCV004355882]	Chr16:69798796 [GRCh38] Chr16:69832699 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.1273C>G (p.His425Asp)	single nucleotide variant	not specified [RCV004365655]	Chr16:69929486 [GRCh38] Chr16:69963389 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.560T>A (p.Phe187Tyr)	single nucleotide variant	not specified [RCV004346346]	Chr16:69842105 [GRCh38] Chr16:69876008 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.2309C>G (p.Thr770Ser)	single nucleotide variant	not specified [RCV004365572]	Chr16:69937618 [GRCh38] Chr16:69971521 [GRCh37] Chr16:16q22.1	uncertain significance
GRCh37/hg19 16q22.1-22.3(chr16:69709450-73535741)x1	copy number loss	not provided [RCV003483292]	Chr16:69709450..73535741 [GRCh37] Chr16:16q22.1-22.3	pathogenic
NM_001270454.2(WWP2):c.402C>T (p.Gly134=)	single nucleotide variant	not provided [RCV004810033]	Chr16:69840187 [GRCh38] Chr16:69874090 [GRCh37] Chr16:16q22.1	likely benign
GRCh37/hg19 16q22.1(chr16:67583728-69977397)x3	copy number gain	not specified [RCV003987175]	Chr16:67583728..69977397 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.725C>A (p.Ala242Asp)	single nucleotide variant	not specified [RCV004483325]	Chr16:69888060 [GRCh38] Chr16:69921963 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.1015C>T (p.Arg339Cys)	single nucleotide variant	not specified [RCV004483321]	Chr16:69917719 [GRCh38] Chr16:69951622 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.1393C>T (p.His465Tyr)	single nucleotide variant	not specified [RCV004483323]	Chr16:69930206 [GRCh38] Chr16:69964109 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.574C>T (p.Arg192Trp)	single nucleotide variant	not specified [RCV004483324]	Chr16:69842119 [GRCh38] Chr16:69876022 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.755G>A (p.Gly252Asp)	single nucleotide variant	not specified [RCV004483326]	Chr16:69888090 [GRCh38] Chr16:69921993 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.938A>G (p.Asn313Ser)	single nucleotide variant	not specified [RCV004483327]	Chr16:69908784 [GRCh38] Chr16:69942687 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.107C>T (p.Pro36Leu)	single nucleotide variant	not specified [RCV004685653]	Chr16:69798718 [GRCh38] Chr16:69832621 [GRCh37] Chr16:16q22.1	uncertain significance
NC_000016.9:g.(?_68679283)_(72146396_?)del	deletion	Immunodeficiency [RCV004581539]	Chr16:68679283..72146396 [GRCh37] Chr16:16q22.1-22.2	uncertain significance
NC_000016.9:g.(?_48799549)_(70756330_?)dup	duplication	Chromosome 16q12 duplication syndrome [RCV004595820]	Chr16:48799549..70756330 [GRCh37] Chr16:16q12.1-22.1	likely pathogenic
NM_001270454.2(WWP2):c.108T>G (p.Pro36=)	single nucleotide variant	not provided [RCV004810974]	Chr16:69798719 [GRCh38] Chr16:69832622 [GRCh37] Chr16:16q22.1	likely benign
GRCh37/hg19 16q21-24.1(chr16:62746020-84485022)x3	copy number gain	not provided [RCV004819314]	Chr16:62746020..84485022 [GRCh37] Chr16:16q21-24.1	pathogenic
NM_001270454.2(WWP2):c.479G>A (p.Gly160Glu)	single nucleotide variant	not specified [RCV004880132]	Chr16:69842024 [GRCh38] Chr16:69875927 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.1604T>C (p.Met535Thr)	single nucleotide variant	not specified [RCV004880131]	Chr16:69931812 [GRCh38] Chr16:69965715 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.2200C>A (p.Leu734Met)	single nucleotide variant	not specified [RCV004880129]	Chr16:69937200 [GRCh38] Chr16:69971103 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.1907A>G (p.Asn636Ser)	single nucleotide variant	not specified [RCV004880133]	Chr16:69935917 [GRCh38] Chr16:69969820 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.926G>A (p.Arg309Gln)	single nucleotide variant	not specified [RCV004880134]	Chr16:69908772 [GRCh38] Chr16:69942675 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.424G>C (p.Asp142His)	single nucleotide variant	not specified [RCV004880135]	Chr16:69840209 [GRCh38] Chr16:69874112 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.535C>T (p.His179Tyr)	single nucleotide variant	not specified [RCV004880136]	Chr16:69842080 [GRCh38] Chr16:69875983 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.551C>G (p.Thr184Arg)	single nucleotide variant	not specified [RCV004880137]	Chr16:69842096 [GRCh38] Chr16:69875999 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.2084G>A (p.Arg695Gln)	single nucleotide variant	not specified [RCV004892706]	Chr16:69936419 [GRCh38] Chr16:69970322 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.175C>T (p.Arg59Cys)	single nucleotide variant	not specified [RCV004880130]	Chr16:69798786 [GRCh38] Chr16:69832689 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.2358G>A (p.Met786Ile)	single nucleotide variant	not specified [RCV004892711]	Chr16:69939041 [GRCh38] Chr16:69972944 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.1780G>A (p.Ala594Thr)	single nucleotide variant	not specified [RCV004892707]	Chr16:69934067 [GRCh38] Chr16:69967970 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.841G>A (p.Gly281Arg)	single nucleotide variant	not specified [RCV004892709]	Chr16:69888176 [GRCh38] Chr16:69922079 [GRCh37] Chr16:16q22.1	uncertain significance
NM_001270454.2(WWP2):c.1258G>A (p.Val420Met)	single nucleotide variant	not specified [RCV004892710]	Chr16:69929471 [GRCh38] Chr16:69963374 [GRCh37] Chr16:16q22.1	uncertain significance

miRNA Target Status (No longer updated)

Predicted Target Of

	Summary Value
Count of predictions:	8633
Count of miRNA genes:	1336
Interacting mature miRNAs:	1786
Transcripts:	ENST00000356003, ENST00000359154, ENST00000448661, ENST00000542271, ENST00000544162, ENST00000561780, ENST00000563618, ENST00000563659, ENST00000566463, ENST00000567161, ENST00000567303, ENST00000567579, ENST00000567986, ENST00000568185, ENST00000568684, ENST00000568818, ENST00000568845, ENST00000569174, ENST00000569297, ENST00000569620, ENST00000569658, ENST00000570104
Prediction methods:	Miranda, Rnahybrid, Targetscan
Result types:	miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

QTLs in Region (GRCh38)

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
597205913	GWAS1301987_H	smoking status measurement, Cannabis use, schizophrenia QTL GWAS1301987 (human)		6e-09	smoking status measurement, Cannabis use, schizophrenia		16	69940756	69940757	Human
597061265	GWAS1157339_H	vital capacity QTL GWAS1157339 (human)		2e-25	vital capacity		16	69873542	69873543	Human
597253022	GWAS1349096_H	alkaline phosphatase measurement QTL GWAS1349096 (human)		3e-12	alkaline phosphatase measurement	blood alkaline phosphatase activity level (CMO:0000576)	16	69910432	69910433	Human
597109919	GWAS1205993_H	protein measurement QTL GWAS1205993 (human)		5e-09	protein measurement		16	69796206	69796207	Human
597239955	GWAS1336029_H	appendicular lean mass QTL GWAS1336029 (human)		3e-20	appendicular lean mass		16	69833932	69833933	Human
597618325	GWAS1675185_H	diverticular disease QTL GWAS1675185 (human)		2e-11	diverticular disease		16	69849074	69849075	Human
597057946	GWAS1154020_H	intelligence QTL GWAS1154020 (human)		0.000001	intelligence		16	69844631	69844632	Human
597101211	GWAS1197285_H	diverticular disease QTL GWAS1197285 (human)		0.000004	diverticular disease		16	69853611	69853612	Human
406959949	GWAS608925_H	pulse pressure measurement QTL GWAS608925 (human)		2e-08	aortic measurement	aorta measurement (CMO:0001474)	16	69869262	69869263	Human
596953497	GWAS1073016_H	size QTL GWAS1073016 (human)		5e-34	size		16	69833932	69833933	Human
597620627	GWAS1677487_H	coronary artery disease QTL GWAS1677487 (human)		5e-11	hypertension		16	69931118	69931119	Human
597298325	GWAS1394399_H	NAD(P)H dehydrogenase [quinone] 1 measurement QTL GWAS1394399 (human)		6e-79	NAD(P)H dehydrogenase [quinone] 1 measurement		16	69795259	69795262	Human
597268620	GWAS1364694_H	aortic measurement QTL GWAS1364694 (human)		1e-13	aortic measurement	aorta measurement (CMO:0001474)	16	69931118	69931119	Human
406942301	GWAS591277_H	forced expiratory volume QTL GWAS591277 (human)		7e-19	forced expiratory volume	forced expiratory volume (CMO:0000254)	16	69857607	69857608	Human
597103240	GWAS1199314_H	myocardial infarction QTL GWAS1199314 (human)		2e-08	myocardial infarction		16	69931118	69931119	Human
597268614	GWAS1364688_H	aortic measurement QTL GWAS1364688 (human)		4e-14	aortic measurement	aorta measurement (CMO:0001474)	16	69935396	69935397	Human
597125559	GWAS1221633_H	osteoarthritis, knee QTL GWAS1221633 (human)		3e-13	osteoarthritis, knee		16	69921787	69921788	Human
596962741	GWAS1082260_H	irritable bowel syndrome, forced expiratory volume QTL GWAS1082260 (human)		8e-09	irritable bowel syndrome, forced expiratory volume		16	69900769	69900770	Human
597078195	GWAS1174269_H	Plantar Fasciitis, Plantar Fibromatosis QTL GWAS1174269 (human)		2e-08	Plantar Fasciitis, Plantar Fibromatosis		16	69825279	69825280	Human
597220528	GWAS1316602_H	cataract QTL GWAS1316602 (human)		4e-14	cataract		16	69850403	69850404	Human
597268403	GWAS1364477_H	aortic measurement QTL GWAS1364477 (human)		8e-12	aortic measurement	aorta measurement (CMO:0001474)	16	69931118	69931119	Human
597197225	GWAS1293299_H	blood urea nitrogen measurement QTL GWAS1293299 (human)		7e-13	blood urea nitrogen measurement	blood urea nitrogen level (CMO:0000049)	16	69890930	69890931	Human
597268140	GWAS1364214_H	aortic measurement QTL GWAS1364214 (human)		6e-22	aortic measurement	aorta measurement (CMO:0001474)	16	69931118	69931119	Human
597596075	GWAS1652935_H	diastolic blood pressure change measurement QTL GWAS1652935 (human)		3e-14	diastolic blood pressure change measurement	change in diastolic blood pressure (CMO:0001016)	16	69935396	69935397	Human
597299363	GWAS1395437_H	lymphocyte count QTL GWAS1395437 (human)		3e-09	lymphocyte count	blood lymphocyte count (CMO:0000031)	16	69778092	69778093	Human
597115310	GWAS1211384_H	mathematical ability QTL GWAS1211384 (human)		4e-08	mathematical ability		16	69878064	69878065	Human
597207202	GWAS1303276_H	insulin measurement QTL GWAS1303276 (human)		1e-08	insulin measurement	pancreatic islet insulin release measurement (CMO:0001216)	16	69790120	69790121	Human
407080569	GWAS729545_H	diastolic blood pressure QTL GWAS729545 (human)		4e-16	diastolic blood pressure	diastolic blood pressure (CMO:0000005)	16	69931118	69931119	Human
597061546	GWAS1157620_H	age at menarche QTL GWAS1157620 (human)		1e-36	age at menarche		16	69815643	69815644	Human
596962472	GWAS1081991_H	irritable bowel syndrome, vital capacity QTL GWAS1081991 (human)		6e-09	irritable bowel syndrome, vital capacity		16	69900769	69900770	Human
597268132	GWAS1364206_H	aortic measurement QTL GWAS1364206 (human)		6e-17	aortic measurement	aorta measurement (CMO:0001474)	16	69931118	69931119	Human
597202598	GWAS1298672_H	diastolic blood pressure QTL GWAS1298672 (human)		0.000003	diastolic blood pressure	diastolic blood pressure (CMO:0000005)	16	69931118	69931119	Human
597591514	GWAS1648374_H	coronary atherosclerosis QTL GWAS1648374 (human)		2e-17	coronary atherosclerosis		16	69931118	69931119	Human
596978896	GWAS1098415_H	body height QTL GWAS1098415 (human)		2e-40	body height		16	69833932	69833933	Human
597120986	GWAS1217060_H	verbal-numerical reasoning measurement QTL GWAS1217060 (human)		2e-08	cognitive behavior trait (VT:0010450)		16	69844631	69844632	Human
597052377	GWAS1148451_H	smoking status measurement QTL GWAS1148451 (human)		4e-11	smoking status measurement		16	69940643	69940644	Human
597592015	GWAS1648875_H	coronary artery disease QTL GWAS1648875 (human)		9e-19	coronary artery disease		16	69931118	69931119	Human
597607631	GWAS1664491_H	systolic blood pressure QTL GWAS1664491 (human)		8e-37	systolic blood pressure	systolic blood pressure (CMO:0000004)	16	69935396	69935397	Human
597030337	GWAS1126411_H	waist-hip ratio QTL GWAS1126411 (human)		7e-19	waist-hip ratio	waist to hip ratio (WHR) (CMO:0000020)	16	69889660	69889661	Human
597332942	GWAS1429016_H	body mass index QTL GWAS1429016 (human)		3e-18	body mass index	body mass index (BMI) (CMO:0000105)	16	69936426	69936427	Human
597170382	GWAS1266456_H	osteoarthritis, knee QTL GWAS1266456 (human)		7e-09	osteoarthritis, knee		16	69923322	69923331	Human
597332941	GWAS1429015_H	body mass index QTL GWAS1429015 (human)		3e-18	body mass index	body mass index (BMI) (CMO:0000105)	16	69789875	69789876	Human
596976322	GWAS1095841_H	hypertension QTL GWAS1095841 (human)		5e-11	hypertension		16	69931118	69931119	Human
597045455	GWAS1141529_H	triglyceride measurement QTL GWAS1141529 (human)		0.000007	triglyceride measurement	blood triglyceride level (CMO:0000118)	16	69801198	69801199	Human
597170373	GWAS1266447_H	osteoarthritis, knee QTL GWAS1266447 (human)		1e-15	osteoarthritis, knee		16	69923322	69923331	Human
597043657	GWAS1139731_H	body fat distribution QTL GWAS1139731 (human)		0.000005	body fat distribution	body fat morphological measurement (CMO:0000089)	16	69850716	69850717	Human
597609153	GWAS1666013_H	heart disease QTL GWAS1666013 (human)		4e-17	heart disease		16	69931118	69931119	Human
597343482	GWAS1439556_H	diverticular disease QTL GWAS1439556 (human)		6e-18	diverticular disease		16	69853369	69853370	Human
597124086	GWAS1220160_H	self reported educational attainment QTL GWAS1220160 (human)		2e-09	self reported educational attainment		16	69832824	69832825	Human
597043959	GWAS1140033_H	body fat distribution QTL GWAS1140033 (human)		2e-17	body fat distribution	body fat morphological measurement (CMO:0000089)	16	69850716	69850717	Human
597581821	GWAS1638681_H	pulse pressure measurement QTL GWAS1638681 (human)		2e-58	pulse pressure measurement	pulse pressure (CMO:0000292)	16	69931118	69931119	Human
597291005	GWAS1387079_H	irritable bowel syndrome, vital capacity QTL GWAS1387079 (human)		6e-09	irritable bowel syndrome, vital capacity		16	69900769	69900770	Human
597271037	GWAS1367111_H	aortic measurement QTL GWAS1367111 (human)		2e-13	aortic measurement	aorta measurement (CMO:0001474)	16	69931118	69931119	Human
597244669	GWAS1340743_H	aortic measurement QTL GWAS1340743 (human)		1e-23	aortic measurement	aorta measurement (CMO:0001474)	16	69935396	69935397	Human
597199603	GWAS1295677_H	systolic blood pressure QTL GWAS1295677 (human)		4e-28	systolic blood pressure	systolic blood pressure (CMO:0000004)	16	69931118	69931119	Human
597164776	GWAS1260850_H	myocardial infarction QTL GWAS1260850 (human)		1e-09	myocardial infarction		16	69931118	69931119	Human
596966884	GWAS1086403_H	systolic blood pressure QTL GWAS1086403 (human)		3e-31	systolic blood pressure		16	69935396	69935397	Human
597029860	GWAS1125934_H	osteoarthritis, knee QTL GWAS1125934 (human)		3e-11	osteoarthritis, knee		16	69921787	69921788	Human
597111013	GWAS1207087_H	mathematical ability QTL GWAS1207087 (human)		1e-09	mathematical ability		16	69878064	69878065	Human
597143008	GWAS1239082_H	educational attainment QTL GWAS1239082 (human)		4e-08	educational attainment		16	69910432	69910433	Human
597321954	GWAS1418028_H	systolic blood pressure QTL GWAS1418028 (human)		3e-31	systolic blood pressure	systolic blood pressure (CMO:0000004)	16	69935396	69935397	Human
407109694	GWAS758670_H	eosinophil count QTL GWAS758670 (human)		2e-10	eosinophil quantity (VT:0002602)	blood eosinophil count (CMO:0000033)	16	69844631	69844632	Human
597607139	GWAS1663999_H	systolic blood pressure QTL GWAS1663999 (human)		4e-12	systolic blood pressure	systolic blood pressure (CMO:0000004)	16	69931118	69931119	Human
597579036	GWAS1635896_H	cataract QTL GWAS1635896 (human)		1e-12	cataract		16	69789875	69789876	Human
597306392	GWAS1402466_H	pulse pressure measurement QTL GWAS1402466 (human)		9e-66	pulse pressure measurement	pulse pressure (CMO:0000292)	16	69931118	69931119	Human
597043989	GWAS1140063_H	smoking initiation QTL GWAS1140063 (human)		5e-09	smoking initiation		16	69796425	69796426	Human
597206032	GWAS1302106_H	grip strength measurement QTL GWAS1302106 (human)		7e-16	grip strength measurement		16	69862345	69862346	Human
597189136	GWAS1285210_H	forced expiratory volume QTL GWAS1285210 (human)		8e-29	forced expiratory volume	forced expiratory volume (CMO:0000254)	16	69883837	69883838	Human
597043484	GWAS1139558_H	body fat distribution QTL GWAS1139558 (human)		0.000003	body fat distribution	body fat morphological measurement (CMO:0000089)	16	69850716	69850717	Human
597275670	GWAS1371744_H	stenosing tenosynovitis QTL GWAS1371744 (human)		1e-10	digit morphology trait (VT:0002110)		16	69853804	69853805	Human
406940884	GWAS589860_H	vital capacity QTL GWAS589860 (human)		1e-18	vital capacity		16	69857607	69857608	Human
597131522	GWAS1227596_H	pulse pressure measurement QTL GWAS1227596 (human)		2e-85	pulse pressure measurement	pulse pressure (CMO:0000292)	16	69931118	69931119	Human
597150209	GWAS1246283_H	chronic musculoskeletal pain QTL GWAS1246283 (human)		2e-09	chronic musculoskeletal pain		16	69833932	69833933	Human
597268026	GWAS1364100_H	aortic measurement QTL GWAS1364100 (human)		5e-38	aortic measurement	aorta measurement (CMO:0001474)	16	69935396	69935397	Human
597223740	GWAS1319814_H	cataract QTL GWAS1319814 (human)		9e-09	cataract		16	69850403	69850404	Human
597039166	GWAS1135240_H	pulse pressure measurement QTL GWAS1135240 (human)		1e-33	pulse pressure measurement	pulse pressure (CMO:0000292)	16	69935396	69935397	Human
597620019	GWAS1676879_H	triglyceride measurement QTL GWAS1676879 (human)		1e-16	triglyceride measurement	blood triglyceride level (CMO:0000118)	16	69828206	69828207	Human
597259572	GWAS1355646_H	aortic measurement QTL GWAS1355646 (human)		8e-33	aortic measurement	aorta measurement (CMO:0001474)	16	69935396	69935397	Human
597044007	GWAS1140081_H	forced expiratory volume QTL GWAS1140081 (human)		0.0000003	forced expiratory volume	forced expiratory volume (CMO:0000254)	16	69851026	69851027	Human
597269027	GWAS1365101_H	aortic measurement QTL GWAS1365101 (human)		7e-22	aortic measurement	aorta measurement (CMO:0001474)	16	69935396	69935397	Human
597620261	GWAS1677121_H	triglyceride measurement QTL GWAS1677121 (human)		7e-17	triglyceride measurement	blood triglyceride level (CMO:0000118)	16	69828206	69828207	Human
597618469	GWAS1675329_H	coronary atherosclerosis QTL GWAS1675329 (human)		2e-12	coronary atherosclerosis		16	69931118	69931119	Human
597608994	GWAS1665854_H	synovial bursa disorder QTL GWAS1665854 (human)		1e-18	synovial bursa disorder		16	69850716	69850717	Human
597589793	GWAS1646653_H	atherosclerosis QTL GWAS1646653 (human)		5e-13	atherosclerosis		16	69935396	69935397	Human
597325403	GWAS1421477_H	vital capacity QTL GWAS1421477 (human)		2e-31	vital capacity		16	69889430	69889431	Human
597617244	GWAS1674104_H	tenosynovitis QTL GWAS1674104 (human)		9e-22	tenosynovitis		16	69853804	69853805	Human
597185370	GWAS1281444_H	vital capacity QTL GWAS1281444 (human)		5e-37	vital capacity		16	69883837	69883838	Human
597040479	GWAS1136553_H	low density lipoprotein cholesterol measurement QTL GWAS1136553 (human)		5e-09	low density lipoprotein cholesterol measurement	blood low density lipoprotein cholesterol level (CMO:0000053)	16	69839928	69839929	Human
597268819	GWAS1364893_H	aortic measurement QTL GWAS1364893 (human)		2e-10	aortic measurement	aorta measurement (CMO:0001474)	16	69931118	69931119	Human
597259339	GWAS1355413_H	aortic measurement QTL GWAS1355413 (human)		3e-34	aortic measurement	aorta measurement (CMO:0001474)	16	69935396	69935397	Human
597288781	GWAS1384855_H	hypertension QTL GWAS1384855 (human)		5e-11	hypertension		16	69931118	69931119	Human
597615691	GWAS1672551_H	systolic blood pressure QTL GWAS1672551 (human)		3e-22	systolic blood pressure	systolic blood pressure (CMO:0000004)	16	69935396	69935397	Human
597061710	GWAS1157784_H	systolic blood pressure QTL GWAS1157784 (human)		9e-31	systolic blood pressure	systolic blood pressure (CMO:0000004)	16	69931118	69931119	Human
597051471	GWAS1147545_H	smoking status measurement QTL GWAS1147545 (human)		8e-09	smoking status measurement		16	69919605	69919606	Human
597030732	GWAS1126806_H	tobacco smoke exposure measurement QTL GWAS1126806 (human)		6e-09	tobacco smoke exposure measurement		16	69938583	69938584	Human
597046600	GWAS1142674_H	body fat distribution QTL GWAS1142674 (human)		3e-12	body fat distribution	body fat morphological measurement (CMO:0000089)	16	69850716	69850717	Human
597314373	GWAS1410447_H	systolic blood pressure QTL GWAS1410447 (human)		7e-23	systolic blood pressure	systolic blood pressure (CMO:0000004)	16	69931118	69931119	Human
597322619	GWAS1418693_H	high density lipoprotein cholesterol measurement QTL GWAS1418693 (human)		5e-23	high density lipoprotein cholesterol measurement	blood high density lipoprotein cholesterol level (CMO:0000052)	16	69892673	69892674	Human
597291121	GWAS1387195_H	size QTL GWAS1387195 (human)		5e-34	size		16	69833932	69833933	Human
597213559	GWAS1309633_H	triglyceride measurement QTL GWAS1309633 (human)		7e-11	triglyceride measurement	blood triglyceride level (CMO:0000118)	16	69828206	69828207	Human
597164138	GWAS1260212_H	cataract QTL GWAS1260212 (human)		2e-12	cataract		16	69863566	69863567	Human
597248877	GWAS1344951_H	serum alanine aminotransferase measurement QTL GWAS1344951 (human)		2e-09	serum alanine aminotransferase measurement	serum alanine aminotransferase activity level (CMO:0000575)	16	69931118	69931119	Human
597159521	GWAS1255595_H	amino acid measurement QTL GWAS1255595 (human)		0.000009	amino acid measurement		16	69830772	69830773	Human
597041262	GWAS1137336_H	cataract QTL GWAS1137336 (human)		8e-11	cataract		16	69851263	69851264	Human
597268833	GWAS1364907_H	aortic measurement QTL GWAS1364907 (human)		1e-37	aortic measurement	aorta measurement (CMO:0001474)	16	69935396	69935397	Human
597292128	GWAS1388202_H	irritable bowel syndrome, forced expiratory volume QTL GWAS1388202 (human)		8e-09	irritable bowel syndrome, forced expiratory volume	forced expiratory volume (CMO:0000254)	16	69900769	69900770	Human
597617252	GWAS1674112_H	synovial bursa disorder QTL GWAS1674112 (human)		4e-17	synovial bursa disorder		16	69850716	69850717	Human

Markers in Region

D16S3095

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	16	69,946,230 - 69,946,387	UniSTS	GRCh37
Build 36	16	68,503,731 - 68,503,888	RGD	NCBI36
Celera	16	54,461,436 - 54,461,587	RGD
Cytogenetic Map	16	q22.1	UniSTS
HuRef	16	55,824,442 - 55,824,599	UniSTS
Marshfield Genetic Map	16	87.06	RGD
Marshfield Genetic Map	16	87.06	UniSTS
Genethon Genetic Map	16	85.5	UniSTS
TNG Radiation Hybrid Map	16	30379.0	UniSTS
deCODE Assembly Map	16	86.16	UniSTS
GeneMap99-GB4 RH Map	16	420.48	UniSTS

SHGC-153661

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	16	69,905,353 - 69,905,633	UniSTS	GRCh37
Build 36	16	68,462,854 - 68,463,134	RGD	NCBI36
Celera	16	54,420,556 - 54,420,836	RGD
Cytogenetic Map	16	q22.1	UniSTS
HuRef	16	55,784,225 - 55,784,505	UniSTS

RH68624

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	16	69,943,903 - 69,944,082	UniSTS	GRCh37
Build 36	16	68,501,404 - 68,501,583	RGD	NCBI36
Celera	16	54,459,109 - 54,459,288	RGD
Cytogenetic Map	16	q22.1	UniSTS
HuRef	16	55,822,115 - 55,822,294	UniSTS
GeneMap99-GB4 RH Map	16	423.52	UniSTS

RH69974

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	16	69,975,470 - 69,975,624	UniSTS	GRCh37
Build 36	16	68,532,971 - 68,533,125	RGD	NCBI36
Celera	16	54,490,782 - 54,490,936	RGD
Cytogenetic Map	16	q22.1	UniSTS
HuRef	16	55,853,772 - 55,853,926	UniSTS
GeneMap99-GB4 RH Map	16	420.28	UniSTS

G69462

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	16	69,916,598 - 69,917,591	UniSTS	GRCh37
Build 36	16	68,474,099 - 68,475,092	RGD	NCBI36
Celera	16	54,431,801 - 54,432,794	RGD
Cytogenetic Map	16	q22.1	UniSTS
HuRef	16	55,795,470 - 55,796,463	UniSTS

Expression

RNA-SEQ Expression

Click on a value in the shaded box below the category label to view a detailed expression data table for that system.

Download All Expressed Objects for this Gene

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	entire extraembryonic component	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	renal system	reproductive system	respiratory system	sensory system	visual system
1204	2436	2788	2248	4971	1725	2347	4	622	1950	464	2268	7290	6460	53	3734	848	1737	1614	175	1

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001270453	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001270454	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001270455	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_007014	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_199424	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011522823	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011522825	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011522826	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017022879	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017022880	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017022881	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047433520	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047433521	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047433522	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047433523	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047433524	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054379421	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054379422	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054379423	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054379424	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054379425	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054379426	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054379427	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054379428	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054379429	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054379430	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054379431	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC026468	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC092115	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AI494370	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AI635734	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AJ001982	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK126332	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK295070	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK295701	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK300266	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK312792	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK316097	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL527115	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL583085	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC000108	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC013645	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC064531	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BQ183829	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BU167468	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX372347	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471092	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068262	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB288556	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DC402912	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	JN712744	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	U96114	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000356003 ⟹ ENSP00000348283

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	69,838,737 - 69,941,741 (+)	Ensembl

Ensembl Acc Id:

ENST00000359154 ⟹ ENSP00000352069

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	69,762,332 - 69,941,739 (+)	Ensembl

Ensembl Acc Id:

ENST00000544162

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	69,798,865 - 69,940,178 (+)	Ensembl

Ensembl Acc Id:

ENST00000561780 ⟹ ENSP00000456451

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	69,762,328 - 69,799,276 (+)	Ensembl

Ensembl Acc Id:

ENST00000563618

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	69,838,737 - 69,888,158 (+)	Ensembl

Ensembl Acc Id:

ENST00000563659 ⟹ ENSP00000455347

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	69,762,362 - 69,798,796 (+)	Ensembl

Ensembl Acc Id:

ENST00000566463

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	69,917,583 - 69,940,176 (+)	Ensembl

Ensembl Acc Id:

ENST00000567161

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	69,934,051 - 69,936,796 (+)	Ensembl

Ensembl Acc Id:

ENST00000567303

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	69,936,920 - 69,939,397 (+)	Ensembl

Ensembl Acc Id:

ENST00000567579

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	69,894,962 - 69,929,466 (+)	Ensembl

Ensembl Acc Id:

ENST00000567986

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	69,799,046 - 69,871,865 (+)	Ensembl

Ensembl Acc Id:

ENST00000568185

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	69,925,012 - 69,926,096 (+)	Ensembl

Ensembl Acc Id:

ENST00000568684 ⟹ ENSP00000456216

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	69,924,990 - 69,941,738 (+)	Ensembl

Ensembl Acc Id:

ENST00000568818

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	69,930,166 - 69,933,981 (+)	Ensembl

Ensembl Acc Id:

ENST00000568845

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	69,762,332 - 69,788,202 (+)	Ensembl

Ensembl Acc Id:

ENST00000569174 ⟹ ENSP00000455311

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	69,776,187 - 69,910,250 (+)	Ensembl

Ensembl Acc Id:

ENST00000569297

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	69,890,798 - 69,940,621 (+)	Ensembl

Ensembl Acc Id:

ENST00000569620 ⟹ ENSP00000456582

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	69,762,328 - 69,840,144 (+)	Ensembl

Ensembl Acc Id:

ENST00000569658

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	69,762,362 - 69,799,493 (+)	Ensembl

Ensembl Acc Id:

ENST00000570104

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	69,871,713 - 69,908,882 (+)	Ensembl

RefSeq Acc Id:

NM_001270453 ⟹ NP_001257382

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	69,838,737 - 69,941,739 (+)	NCBI
GRCh37	16	69,796,187 - 69,975,644 (+)	NCBI
HuRef	16	55,674,737 - 55,853,946 (+)	NCBI
CHM1_1	16	71,280,620 - 71,383,517 (+)	NCBI
T2T-CHM13v2.0	16	75,641,261 - 75,744,318 (+)	NCBI

Sequence:

show sequence

ATTTTATAGAAACGTTTAGTACTCACCAAGGCCCTCAGTGGAACTGGCTGAAAATAGCAGCAGA
CTCACTCAGAAAAGAATTGGAGAGATCCATGGCAGGGAAGAGAGATTAAGGGAAGGTAGAGCGC
TTAGGAGAGCTTGAAAACCCAAAGGTGGAGAACATGCAGCTGACCCTGAACCTGCAGACGGAGA
ACAAAGGCAGCGTTGTCTCAGGCGGAGAGCTGACAATTTTCCTGGACGGGCCAACTGTTGATCT
GGGAAATGTGCCTAATGGCAGTGCCCTGACAGATGGATCACAGCTGCCTTCGAGAGACTCCAGT
GGAACAGCAGTAGCTCCAGAGAACCGGCACCAGCCCCCCAGCACAAACTGCTTTGGTGGAAGAT
CCCGGACGCACAGACATTCGGGTGCTTCAGCCAGAACAACCCCAGCAACCGGCGAGCAAAGCCC
CGGTGCTCGGAGCCGGCACCGCCAGCCCGTCAAGAACTCAGGCCACAGTGGCTTGGCCAATGGC
ACAGTGAATGATGAACCCACAACAGCCACTGATCCCGAAGAACCTTCCGTTGTTGGTGTGACGT
CCCCACCTGCTGCACCCTTGAGTGTGACCCCGAATCCCAACACGACTTCTCTCCCTGCCCCAGC
CACACCGGCTGAAGGAGAGGAACCCAGCACTTCGGGTACACAGCAGCTCCCAGCGGCTGCCCAG
GCCCCCGACGCTCTGCCTGCTGGATGGGAACAGCGAGAGCTGCCCAACGGACGTGTCTATTATG
TTGACCACAATACCAAGACCACCACCTGGGAGCGGCCCCTTCCTCCAGGCTGGGAAAAACGCAC
AGATCCCCGAGGCAGGTTTTACTATGTGGATCACAATACTCGGACCACCACCTGGCAGCGTCCG
ACCGCGGAGTACGTGCGCAACTATGAGCAGTGGCAGTCGCAGCGGAATCAGCTCCAGGGGGCCA
TGCAGCACTTCAGCCAAAGATTCCTCTACCAGTCTTCGAGTGCTTCGACTGACCATGATCCCCT
GGGCCCCCTCCCTCCTGGCTGGGAGAAGAGACAGGACAATGGACGGGTGTATTACGTGAACCAT
AACACTCGCACGACCCAGTGGGAGGATCCCCGGACCCAGGGGATGATCCAGGAACCAGCTCTGC
CCCCAGGATGGGAGATGAAATACACCAGCGAGGGGGTGCGATACTTTGTGGACCACAATACCCG
CACCACCACCTTTAAGGATCCTCGCCCGGGGTTTGAGTCGGGGACGAAGCAAGGTTCCCCTGGT
GCTTATGACCGCAGTTTTCGGTGGAAGTATCACCAGTTCCGTTTCCTCTGCCATTCAAATGCCC
TACCTAGCCACGTGAAGATCAGCGTTTCCAGGCAGACGCTTTTCGAAGATTCCTTCCAACAGAT
CATGAACATGAAACCCTATGACCTGCGCCGCCGGCTCTACATCATCATGCGTGGCGAGGAGGGC
CTGGACTATGGGGGCATCGCCAGAGAGTGGTTTTTCCTCCTGTCTCATGAGGTGCTCAACCCTA
TGTATTGTTTATTTGAATATGCCGGAAAGAACAATTACTGCCTGCAGATCAACCCCGCCTCCTC
CATCAACCCGGACCACCTCACCTACTTTCGCTTTATAGGCAGATTCATCGCCATGGCGCTGTAC
CATGGAAAGTTCATCGACACGGGCTTCACCCTCCCTTTCTACAAGCGGATGCTCAATAAGAGAC
CAACCCTGAAAGACCTGGAGTCCATTGACCCTGAGTTCTACAACTCCATTGTCTGGATCAAAGA
GAACAACCTGGAAGAATGTGGCCTGGAGCTGTACTTCATCCAGGACATGGAGATACTGGGCAAG
GTGACGACCCACGAGCTGAAGGAGGGCGGCGAGAGCATCCGGGTCACAGAGGAGAACAAGGAAG
AGTACATCATGCTGCTGACTGACTGGCGTTTCACCCGAGGCGTGGAAGAGCAGACCAAAGCCTT
CCTGGATGGCTTCAACGAGGTGGCCCCGCTGGAGTGGCTGCGCTACTTTGACGAGAAAGAGCTG
GAGCTGATGCTGTGCGGCATGCAGGAGATAGACATGAGCGACTGGCAGAAGAGCACCATCTACC
GGCACTACACCAAGAACAGCAAGCAGATCCAGTGGTTCTGGCAGGTGGTGAAGGAGATGGACAA
CGAGAAGAGGATCCGGCTGCTGCAGTTTGTCACCGGTACCTGCCGCCTGCCCGTCGGGGGATTT
GCCGAACTCATCGGTAGCAACGGACCACAGAAGTTTTGCATTGACAAAGTTGGCAAGGAAACCT
GGCTGCCCAGAAGCCACACCTGCTTCAACCGTCTGGATCTTCCACCCTACAAGAGCTACGAACA
GCTGAGAGAGAAGCTGCTGTATGCCATTGAGGAGACCGAGGGCTTTGGACAGGAGTAACCGAGG
CCGCCCCTCCCACGCCCCCCAGCGCACATGTAGTCCTGAGTCCTCCCTGCCTGAGAGGCCACTG
GCCCCGCAGCCCTTGGGAGGCCCCCGTGGATGTGGCCCTGTGTGGGACCACACTGTCATCTCGC
TGCTGGCAGAAAAGCCTGATCCCAGGAGGCCCTGCAGTTCCCCCGACCCGCGGATGGCAGTCTG
GAATAAAGCCCCCTAGTTGCCTTTGGCCCCACCTTTGCAAAGTTCCAGAGGGCTGACCCTCTCT
GCAAAACTCTCCCCTGTCCTCTAGACCCCACCCTGGGTGTATGTGAGTGTGCAAGGGAAGGTGT
TGCATCCCCAGGGGCTGCCGCAGAGGCCGGAGACCTCCTGGACTAGTTCGGCGAGGAGACTGGC
CACTGGGGGTGGCTGTTCGGGACTGAGAGCGCCAAGGGTCTTTGCCAGCAAAGGAGGTTCTGCC
TGTAATTGAGCCTCTCTGATGATGGAGATGAAGTGAAGGTCTGAGGGAGCGGGCCCTGGGGCGA
GGCCATCTCTGCCTGCCTCCCTAGCAGGCGCCAGCGGTGGAGGCTGAGTCGCAGGACACATGCC
GGCCAGTTAATTCATTCTCAGCCAATGAAGGTTTGTCTAAGCTGCCTGGGTATCCACGGGACAA
AAACAGCAAACTCCCTCAGACTTTGTCCATGTATAAACTTGAAGTGGTTGTGTTGTAGGGTTGC
AGGTTTTTTGTTACGCTGCTGTCACTTTCTGTCCAGGAGCTGGCACCCCAGGTGTTCTGAGACC
TTGAGGGACCCAGACCTTTGGGTCCAAGAGTTTCCCAAACAGCCACGCCTCTCAGGAACCCACC
TGGCGGTTCCGTGAGCTCAGGCAGGCCTGACCCGGCGGCACAGCCTGGCAGGGACCTCGTCCCC
AAGCCTGGCAGAATGAGAGGGGTTGAGGTCCCGAGCGCCACTCCTAGCCTTGCCGCCTTCAATA
GAGAAGAAATCCCTTTGCTAGATAGGGTCCCCCAGGCAGTCCCCAGTGGCGGGACACAGGGGTC
CGGCTGTGGAGCTCCCCTGCCAGCCCCTGGAGCTCCAGGAGGGCCTGTTGGTCCCCTGTTCAGA
ATGGAGTGCAGCCCGCCAGCGGAAAGTGTTCATTCTGCATAGGTGTGAGGCTTTATCTGCACAC
AGGACATGAAAACCAGCAGAAAGGCCCTGAGCTGCTGCATAGCCCCATCTGATTTCTGCAGTTC
CCGCCAGCCTCCAACACGGGGACTCTGCCGTAACTGGAATCTTCATAGGTCATATTGAAATCTT
CAAGGTGACCATGCCCCACCGGGGTGCTGGGGCAGTAGTCATGGCAGACTCCCGGCCTGGGCCC
CCAGGATTCTAGGACCCCCAGGCAGCCCCTTGGACTGGTCCCGGGTGCCTTCCAAGCACAGTCT
CCATGCTCCCAGATTCTCGACCTTCCCCCGGCCCGGGAGGTGCAGCCTGCGTCTGCCTCTGTCG
TGTGTGCTGATTTGAGTGGCTTAGCTTGCCACAGCGCAGCCTCTTCTGTCCCTTTCAGTCATTT
GCTGTACTTCCCTGTGGCACGTTACCATGGAAGCCGCTCCAGGGTGGGTCAGGGTGCAAGCTGC
TGGTGAGGTTTGGAAGCATCAGGCTCACGGGTGTTCATGTGTGTTCGTGCGTGTGTGTGCGTAC
GTGTATATAACTGAAGTGTCTGTACGGAATGCCCTTTGCTAGCCATGGGCTGGTCACCAGATTG
TTTTGTAATGCCCGCCCCTTGCCTCGATATTGCCAGTTTCTTGTGCAATAAACAATCAGCAGCT
G

hide sequence

RefSeq Acc Id:

NM_001270454 ⟹ NP_001257383

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	69,762,332 - 69,941,739 (+)	NCBI
GRCh37	16	69,796,187 - 69,975,644 (+)	NCBI
HuRef	16	55,674,737 - 55,853,946 (+)	NCBI
CHM1_1	16	71,204,171 - 71,383,517 (+)	NCBI
T2T-CHM13v2.0	16	75,564,863 - 75,744,318 (+)	NCBI

Sequence:

show sequence

GCGGGCGGTGGAAGGCGGAAGTAGGAGAGGAGTTCGGCGCCGCTTCTGTGGCCACGGCAGCTTC
ACGGTGATGATATGGCATCTGCCAGCTCTAGCCGGGCAGGAGTGGCCCTGCCTTTTGAGAAGTC
TCAGCTCACTTTGAAAGTGGTGTCCGCAAAGCCCAAGGTGCATAATCGTCAACCTCGAATTAAC
TCCTACGTGGAGGTGGCGGTGGATGGACTCCCCAGTGAGACCAAGAAGACTGGGAAGCGCATTG
GGAGCTCTGAGCTTCTCTGGAATGAGATCATCATTTTGAATGTCACGGCACAGAGTCATTTAGA
TTTAAAGGTCTGGAGCTGCCATACCTTGAGAAATGAACTGCTAGGCACCGCATCTGTCAACCTC
TCCAACGTCTTGAAGAACAATGGGGGCAAAATGGAGAACATGCAGCTGACCCTGAACCTGCAGA
CGGAGAACAAAGGCAGCGTTGTCTCAGGCGGAGAGCTGACAATTTTCCTGGACGGGCCAACTGT
TGATCTGGGAAATGTGCCTAATGGCAGTGCCCTGACAGATGGATCACAGCTGCCTTCGAGAGAC
TCCAGTGGAACAGCAGTAGCTCCAGAGAACCGGCACCAGCCCCCCAGCACAAACTGCTTTGGTG
GAAGATCCCGGACGCACAGACATTCGGGTGCTTCAGCCAGAACAACCCCAGCAACCGGCGAGCA
AAGCCCCGGTGCTCGGAGCCGGCACCGCCAGCCCGTCAAGAACTCAGGCCACAGTGGCTTGGCC
AATGGCACAGTGAATGATGAACCCACAACAGCCACTGATCCCGAAGAACCTTCCGTTGTTGGTG
TGACGTCCCCACCTGCTGCACCCTTGAGTGTGACCCCGAATCCCAACACGACTTCTCTCCCTGC
CCCAGCCACACCGGCTGAAGGAGAGGAACCCAGCACTTCGGGTACACAGCAGCTCCCAGCGGCT
GCCCAGGCCCCCGACGCTCTGCCTGCTGGATGGGAACAGCGAGAGCTGCCCAACGGACGTGTCT
ATTATGTTGACCACAATACCAAGACCACCACCTGGGAGCGGCCCCTTCCTCCAGGCTGGGAAAA
ACGCACAGATCCCCGAGGCAGGTTTTACTATGTGGATCACAATACTCGGACCACCACCTGGCAG
CGTCCGACCGCGGAGTACGTGCGCAACTATGAGCAGTGGCAGTCGCAGCGGAATCAGCTCCAGG
GGGCCATGCAGCACTTCAGCCAAAGATTCCTCTACCAGTCTTCGAGTGCTTCGACTGACCATGA
TCCCCTGGGCCCCCTCCCTCCTGGCTGGGAGAAGAGACAGGACAATGGACGGGTGTATTACGTG
AACCATAACACTCGCACGACCCAGTGGGAGGATCCCCGGACCCAGGGGATGATCCAGGAACCAG
CTCTGCCCCCAGGATGGGAGATGAAATACACCAGCGAGGGGGTGCGATACTTTGTGGACCACAA
TACCCGCACCACCACCTTTAAGGATCCTCGCCCGGGGTTTGAGTCGGGGACGAAGCAAGGTTCC
CCTGGTGCTTATGACCGCAGTTTTCGGTGGAAGTATCACCAGTTCCGTTTCCTCTGCCATTCAA
ATGCCCTACCTAGCCACGTGAAGATCAGCGTTTCCAGGCAGACGCTTTTCGAAGATTCCTTCCA
ACAGATCATGAACATGAAACCCTATGACCTGCGCCGCCGGCTCTACATCATCATGCGTGGCGAG
GAGGGCCTGGACTATGGGGGCATCGCCAGAGAGTGGTTTTTCCTCCTGTCTCATGAGGTGCTCA
ACCCTATGTATTGTTTATTTGAATATGCCGGAAAGAACAATTACTGCCTGCAGATCAACCCCGC
CTCCTCCATCAACCCGGACCACCTCACCTACTTTCGCTTTATAGGCAGATTCATCGCCATGGCG
CTGTACCATGGAAAGTTCATCGACACGGGCTTCACCCTCCCTTTCTACAAGCGGATGCTCAATA
AGAGACCAACCCTGAAAGACCTGGAGTCCATTGACCCTGAGTTCTACAACTCCATTGTCTGGAT
CAAAGAGAACAACCTGGAAGAATGTGGCCTGGAGCTGTACTTCATCCAGGACATGGAGATACTG
GGCAAGGTGACGACCCACGAGCTGAAGGAGGGCGGCGAGAGCATCCGGGTCACAGAGGAGAACA
AGGAAGAGTACATCATGCTGCTGACTGACTGGCGTTTCACCCGAGGCGTGGAAGAGCAGACCAA
AGCCTTCCTGGATGGCTTCAACGAGGTGGCCCCGCTGGAGTGGCTGCGCTACTTTGACGAGAAA
GAGCTGGAGCTGATGCTGTGCGGCATGCAGGAGATAGACATGAGCGACTGGCAGAAGAGCACCA
TCTACCGGCACTACACCAAGAACAGCAAGCAGATCCAGTGGTTCTGGCAGGTGGTGAAGGAGAT
GGACAACGAGAAGAGGATCCGGCTGCTGCAGTTTGTCACCGGTACCTGCCGCCTGCCCGTCGGG
GGATTTGCCGAACTCATCGGTAGCAACGGACCACAGAAGTTTTGCATTGACAAAGTTGGCAAGG
AAACCTGGCTGCCCAGAAGCCACACCTGCTTCAACCGTCTGGATCTTCCACCCTACAAGAGCTA
CGAACAGCTGAGAGAGAAGCTGCTGTATGCCATTGAGGAGACCGAGGGCTTTGGACAGGAGTAA
CCGAGGCCGCCCCTCCCACGCCCCCCAGCGCACATGTAGTCCTGAGTCCTCCCTGCCTGAGAGG
CCACTGGCCCCGCAGCCCTTGGGAGGCCCCCGTGGATGTGGCCCTGTGTGGGACCACACTGTCA
TCTCGCTGCTGGCAGAAAAGCCTGATCCCAGGAGGCCCTGCAGTTCCCCCGACCCGCGGATGGC
AGTCTGGAATAAAGCCCCCTAGTTGCCTTTGGCCCCACCTTTGCAAAGTTCCAGAGGGCTGACC
CTCTCTGCAAAACTCTCCCCTGTCCTCTAGACCCCACCCTGGGTGTATGTGAGTGTGCAAGGGA
AGGTGTTGCATCCCCAGGGGCTGCCGCAGAGGCCGGAGACCTCCTGGACTAGTTCGGCGAGGAG
ACTGGCCACTGGGGGTGGCTGTTCGGGACTGAGAGCGCCAAGGGTCTTTGCCAGCAAAGGAGGT
TCTGCCTGTAATTGAGCCTCTCTGATGATGGAGATGAAGTGAAGGTCTGAGGGAGCGGGCCCTG
GGGCGAGGCCATCTCTGCCTGCCTCCCTAGCAGGCGCCAGCGGTGGAGGCTGAGTCGCAGGACA
CATGCCGGCCAGTTAATTCATTCTCAGCCAATGAAGGTTTGTCTAAGCTGCCTGGGTATCCACG
GGACAAAAACAGCAAACTCCCTCAGACTTTGTCCATGTATAAACTTGAAGTGGTTGTGTTGTAG
GGTTGCAGGTTTTTTGTTACGCTGCTGTCACTTTCTGTCCAGGAGCTGGCACCCCAGGTGTTCT
GAGACCTTGAGGGACCCAGACCTTTGGGTCCAAGAGTTTCCCAAACAGCCACGCCTCTCAGGAA
CCCACCTGGCGGTTCCGTGAGCTCAGGCAGGCCTGACCCGGCGGCACAGCCTGGCAGGGACCTC
GTCCCCAAGCCTGGCAGAATGAGAGGGGTTGAGGTCCCGAGCGCCACTCCTAGCCTTGCCGCCT
TCAATAGAGAAGAAATCCCTTTGCTAGATAGGGTCCCCCAGGCAGTCCCCAGTGGCGGGACACA
GGGGTCCGGCTGTGGAGCTCCCCTGCCAGCCCCTGGAGCTCCAGGAGGGCCTGTTGGTCCCCTG
TTCAGAATGGAGTGCAGCCCGCCAGCGGAAAGTGTTCATTCTGCATAGGTGTGAGGCTTTATCT
GCACACAGGACATGAAAACCAGCAGAAAGGCCCTGAGCTGCTGCATAGCCCCATCTGATTTCTG
CAGTTCCCGCCAGCCTCCAACACGGGGACTCTGCCGTAACTGGAATCTTCATAGGTCATATTGA
AATCTTCAAGGTGACCATGCCCCACCGGGGTGCTGGGGCAGTAGTCATGGCAGACTCCCGGCCT
GGGCCCCCAGGATTCTAGGACCCCCAGGCAGCCCCTTGGACTGGTCCCGGGTGCCTTCCAAGCA
CAGTCTCCATGCTCCCAGATTCTCGACCTTCCCCCGGCCCGGGAGGTGCAGCCTGCGTCTGCCT
CTGTCGTGTGTGCTGATTTGAGTGGCTTAGCTTGCCACAGCGCAGCCTCTTCTGTCCCTTTCAG
TCATTTGCTGTACTTCCCTGTGGCACGTTACCATGGAAGCCGCTCCAGGGTGGGTCAGGGTGCA
AGCTGCTGGTGAGGTTTGGAAGCATCAGGCTCACGGGTGTTCATGTGTGTTCGTGCGTGTGTGT
GCGTACGTGTATATAACTGAAGTGTCTGTACGGAATGCCCTTTGCTAGCCATGGGCTGGTCACC
AGATTGTTTTGTAATGCCCGCCCCTTGCCTCGATATTGCCAGTTTCTTGTGCAATAAACAATCA
GCAGCTG

hide sequence

RefSeq Acc Id:

NM_001270455 ⟹ NP_001257384

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	69,762,332 - 69,910,405 (+)	NCBI
GRCh37	16	69,796,187 - 69,975,644 (+)	NCBI
HuRef	16	55,674,737 - 55,853,946 (+)	NCBI
CHM1_1	16	71,204,171 - 71,352,254 (+)	NCBI
T2T-CHM13v2.0	16	75,564,863 - 75,712,948 (+)	NCBI

Sequence:

show sequence

GCGGGCGGTGGAAGGCGGAAGTAGGAGAGGAGTTCGGCGCCGCTTCTGTGGCCACGGCAGCTTC
ACGGTGATGATATGGCATCTGCCAGCTCTAGCCGGGCAGGAGTGGCCCTGCCTTTTGAGAAGTC
TCAGCTCACTTTGAAAGTGGTGTCCGCAAAGCCCAAGGTGCATAATCGTCAACCTCGAATTAAC
TCCTACGTGGAGGTGGCGGTGGATGGACTCCCCAGTGAGACCAAGAAGACTGGGAAGCGCATTG
GGAGCTCTGAGCTTCTCTGGAATGAGATCATCATTTTGAATGTCACGGCACAGAGTCATTTAGA
TTTAAAGGTCTGGAGCTGCCATACCTTGAGAAATGAACTGCTAGGCACCGCATCTGTCAACCTC
TCCAACGTCTTGAAGAACAATGGGGGCAAAATGGAGAACATGCAGCTGACCCTGAACCTGCAGA
CGGAGAACAAAGGCAGCGTTGTCTCAGGCGGAGAGCTGACAATTTTCCTGGACGGGCCAACTGT
TGATCTGGGAAATGTGCCTAATGGCAGTGCCCTGACAGATGGATCACAGCTGCCTTCGAGAGAC
TCCAGTGGAACAGCAGTAGCTCCAGAGAACCGGCACCAGCCCCCCAGCACAAACTGCTTTGGTG
GAAGATCCCGGACGCACAGACATTCGGGTGCTTCAGCCAGAACAACCCCAGCAACCGGCGAGCA
AAGCCCCGGTGCTCGGAGCCGGCACCGCCAGCCCGTCAAGAACTCAGGCCACAGTGGCTTGGCC
AATGGCACAGTGAATGATGAACCCACAACAGCCACTGATCCCGAAGAACCTTCCGTTGTTGGTG
TGACGTCCCCACCTGCTGCACCCTTGAGTGTGACCCCGAATCCCAACACGACTTCTCTCCCTGC
CCCAGCCACACCGGCTGAAGGAGAGGAACCCAGCACTTCGGGTACACAGCAGCTCCCAGCGGCT
GCCCAGGCCCCCGACGCTCTGCCTGCTGGATGGGAACAGCGAGAGCTGCCCAACGGACGTGTCT
ATTATGTTGACCACAATACCAAGACCACCACCTGGGAGCGGCCCCTTCCTCCAGGGTAGGTCAT
CAACTGAGAAGACCTGAGACTCTGGAACTGACACCATGAGTCACCCAATGGCTTCTTGAAACGG
TCCCTTTCTGCGGAGGTAGCATAGCACAGTGACGTTTATTCCGGGTCACTTGATTGCTTTTCCT
ATCCACTTACCTTAATATTGCTCCCATGTCTTAGGACATATTAGAATTATTAGAAGATCTCTGG
GAAACAAAAGGCGCATGGGAGGCCAAGATTTAGAGTGTTGATGCATTCCGCCGTACCCTATGCC
CAGCCTGTCCCTAAAGGCAGAGTGCTTCTTATTCGGCAGGGCTTCGTGAGAATGCCGCCAAGTT
ATCCAAAACCAAAGGATGAGAGAGGCTTCCAAGAGAGGGAAGACTGTCCAAGTTCAAGGAGAAG
GGGTTTGGTTCCCTGTCTGCCAGGGACAGAAAGTTCTTTCCACATGTGTCTCCTGGTCCCGAGA
GCTTTCAAAAGGGGATGTATTCTGCTCCAAGAAAGAATCACCTCCCAGTAAAGTAGCCATGAAG
GGCTCCTGTATAAAATATGCACACTTCCCCTGCCCTGAGTTTGTGGAGGGAAAGGCTGTCGGAA
GTAGGGACTCTTAGGAGAGCCCGTGTGCCCTGTTTGGTTCAGCTGTCAGGCGTGTGCCACACAC
ATCCCACCTCATCTTCTGGTCCCATAATTCTCCATGGATGGGCTGCTTTTAGCTCCAGTTTTCC
AGTAGAATGCTTGAGTTTTCCTTTTTTCCGTACCTCCTGGAGGATGAAACTCATAACCTGTCAT
CATCAGTACTCACTGTGTTTTCCACTTTGACTTGAAGTCAAATGAAGTTACCAAAGTTAAACAT
GGACTTCTCAAATTAGAAAAAAACAAACAACAAAAAAACAGGTTAAGTGTTTTGTTATGAAAAT
TATGAAAATGTTCTTATTATTATGGAAAATTTCAAATAGATATAGAGAGAATAATGTTACAAAC
CCCCACATACTCAACATTTAGCTTCAAAAATTATCAACTCATGGCGGGTTTTGTTTCATCTGTA
CAAACTAGTCGGCACACTATGATGGCCTGTGGACAAAATCCGGCCCTCTGACTGTTTTTGTAAA
TAAGGTTTTATTGGAACACAGCCACACATATTTGTTGACTTATTGTTTTTGGCTGTTTTTGTAC
TTCATTGGCAGAGTTGAGTAATTGCAGCAGACTCTATGGCTTGCAAAACCTAAAATAATTACTT
TGTGTAGCGCTTTATAGAAAAAATTTGCTAACTCCCGATCTGTAACCCCCAACCTATCCGCCGC
ACCCTGATCTAGGTAATTTTGAAGCAAATCCCAAATGTCACATCATCTATCCATATTTCACTAT
GTATTTCTAAAACATATTCTTTTATTCAAAATAAAACTCTAATATCATTAACAGTATTTTGTTT
ATATTATCAAATACCCAGTCAATATTTGACTTTCTATAATTGTGTCACAAATTAAACATTGACT
TTAACAGTATGTATTACACACTTGTACTTTGTGTACTTTATAACATGTGCACTTTAAAACAGCA
GGAGCTCTGT

hide sequence

RefSeq Acc Id:

NM_007014 ⟹ NP_008945

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	69,762,332 - 69,941,739 (+)	NCBI
GRCh37	16	69,796,187 - 69,975,644 (+)	NCBI
Build 36	16	68,353,775 - 68,533,144 (+)	NCBI Archive
HuRef	16	55,674,737 - 55,853,946 (+)	NCBI
CHM1_1	16	71,204,171 - 71,383,517 (+)	NCBI
T2T-CHM13v2.0	16	75,564,863 - 75,744,318 (+)	NCBI

Sequence:

show sequence

GCGGGCGGTGGAAGGCGGAAGTAGGAGAGGAGTTCGGCGCCGCTTCTGTGGCCACGGCAGATGA
AACAGAAAGGCTAAAGAGGGCTGGAGTCAGGGGACTTCTCTTCCACCAGCTTCACGGTGATGAT
ATGGCATCTGCCAGCTCTAGCCGGGCAGGAGTGGCCCTGCCTTTTGAGAAGTCTCAGCTCACTT
TGAAAGTGGTGTCCGCAAAGCCCAAGGTGCATAATCGTCAACCTCGAATTAACTCCTACGTGGA
GGTGGCGGTGGATGGACTCCCCAGTGAGACCAAGAAGACTGGGAAGCGCATTGGGAGCTCTGAG
CTTCTCTGGAATGAGATCATCATTTTGAATGTCACGGCACAGAGTCATTTAGATTTAAAGGTCT
GGAGCTGCCATACCTTGAGAAATGAACTGCTAGGCACCGCATCTGTCAACCTCTCCAACGTCTT
GAAGAACAATGGGGGCAAAATGGAGAACATGCAGCTGACCCTGAACCTGCAGACGGAGAACAAA
GGCAGCGTTGTCTCAGGCGGAGAGCTGACAATTTTCCTGGACGGGCCAACTGTTGATCTGGGAA
ATGTGCCTAATGGCAGTGCCCTGACAGATGGATCACAGCTGCCTTCGAGAGACTCCAGTGGAAC
AGCAGTAGCTCCAGAGAACCGGCACCAGCCCCCCAGCACAAACTGCTTTGGTGGAAGATCCCGG
ACGCACAGACATTCGGGTGCTTCAGCCAGAACAACCCCAGCAACCGGCGAGCAAAGCCCCGGTG
CTCGGAGCCGGCACCGCCAGCCCGTCAAGAACTCAGGCCACAGTGGCTTGGCCAATGGCACAGT
GAATGATGAACCCACAACAGCCACTGATCCCGAAGAACCTTCCGTTGTTGGTGTGACGTCCCCA
CCTGCTGCACCCTTGAGTGTGACCCCGAATCCCAACACGACTTCTCTCCCTGCCCCAGCCACAC
CGGCTGAAGGAGAGGAACCCAGCACTTCGGGTACACAGCAGCTCCCAGCGGCTGCCCAGGCCCC
CGACGCTCTGCCTGCTGGATGGGAACAGCGAGAGCTGCCCAACGGACGTGTCTATTATGTTGAC
CACAATACCAAGACCACCACCTGGGAGCGGCCCCTTCCTCCAGGCTGGGAAAAACGCACAGATC
CCCGAGGCAGGTTTTACTATGTGGATCACAATACTCGGACCACCACCTGGCAGCGTCCGACCGC
GGAGTACGTGCGCAACTATGAGCAGTGGCAGTCGCAGCGGAATCAGCTCCAGGGGGCCATGCAG
CACTTCAGCCAAAGATTCCTCTACCAGTCTTCGAGTGCTTCGACTGACCATGATCCCCTGGGCC
CCCTCCCTCCTGGCTGGGAGAAGAGACAGGACAATGGACGGGTGTATTACGTGAACCATAACAC
TCGCACGACCCAGTGGGAGGATCCCCGGACCCAGGGGATGATCCAGGAACCAGCTCTGCCCCCA
GGATGGGAGATGAAATACACCAGCGAGGGGGTGCGATACTTTGTGGACCACAATACCCGCACCA
CCACCTTTAAGGATCCTCGCCCGGGGTTTGAGTCGGGGACGAAGCAAGGTTCCCCTGGTGCTTA
TGACCGCAGTTTTCGGTGGAAGTATCACCAGTTCCGTTTCCTCTGCCATTCAAATGCCCTACCT
AGCCACGTGAAGATCAGCGTTTCCAGGCAGACGCTTTTCGAAGATTCCTTCCAACAGATCATGA
ACATGAAACCCTATGACCTGCGCCGCCGGCTCTACATCATCATGCGTGGCGAGGAGGGCCTGGA
CTATGGGGGCATCGCCAGAGAGTGGTTTTTCCTCCTGTCTCATGAGGTGCTCAACCCTATGTAT
TGTTTATTTGAATATGCCGGAAAGAACAATTACTGCCTGCAGATCAACCCCGCCTCCTCCATCA
ACCCGGACCACCTCACCTACTTTCGCTTTATAGGCAGATTCATCGCCATGGCGCTGTACCATGG
AAAGTTCATCGACACGGGCTTCACCCTCCCTTTCTACAAGCGGATGCTCAATAAGAGACCAACC
CTGAAAGACCTGGAGTCCATTGACCCTGAGTTCTACAACTCCATTGTCTGGATCAAAGAGAACA
ACCTGGAAGAATGTGGCCTGGAGCTGTACTTCATCCAGGACATGGAGATACTGGGCAAGGTGAC
GACCCACGAGCTGAAGGAGGGCGGCGAGAGCATCCGGGTCACAGAGGAGAACAAGGAAGAGTAC
ATCATGCTGCTGACTGACTGGCGTTTCACCCGAGGCGTGGAAGAGCAGACCAAAGCCTTCCTGG
ATGGCTTCAACGAGGTGGCCCCGCTGGAGTGGCTGCGCTACTTTGACGAGAAAGAGCTGGAGCT
GATGCTGTGCGGCATGCAGGAGATAGACATGAGCGACTGGCAGAAGAGCACCATCTACCGGCAC
TACACCAAGAACAGCAAGCAGATCCAGTGGTTCTGGCAGGTGGTGAAGGAGATGGACAACGAGA
AGAGGATCCGGCTGCTGCAGTTTGTCACCGGTACCTGCCGCCTGCCCGTCGGGGGATTTGCCGA
ACTCATCGGTAGCAACGGACCACAGAAGTTTTGCATTGACAAAGTTGGCAAGGAAACCTGGCTG
CCCAGAAGCCACACCTGCTTCAACCGTCTGGATCTTCCACCCTACAAGAGCTACGAACAGCTGA
GAGAGAAGCTGCTGTATGCCATTGAGGAGACCGAGGGCTTTGGACAGGAGTAACCGAGGCCGCC
CCTCCCACGCCCCCCAGCGCACATGTAGTCCTGAGTCCTCCCTGCCTGAGAGGCCACTGGCCCC
GCAGCCCTTGGGAGGCCCCCGTGGATGTGGCCCTGTGTGGGACCACACTGTCATCTCGCTGCTG
GCAGAAAAGCCTGATCCCAGGAGGCCCTGCAGTTCCCCCGACCCGCGGATGGCAGTCTGGAATA
AAGCCCCCTAGTTGCCTTTGGCCCCACCTTTGCAAAGTTCCAGAGGGCTGACCCTCTCTGCAAA
ACTCTCCCCTGTCCTCTAGACCCCACCCTGGGTGTATGTGAGTGTGCAAGGGAAGGTGTTGCAT
CCCCAGGGGCTGCCGCAGAGGCCGGAGACCTCCTGGACTAGTTCGGCGAGGAGACTGGCCACTG
GGGGTGGCTGTTCGGGACTGAGAGCGCCAAGGGTCTTTGCCAGCAAAGGAGGTTCTGCCTGTAA
TTGAGCCTCTCTGATGATGGAGATGAAGTGAAGGTCTGAGGGAGCGGGCCCTGGGGCGAGGCCA
TCTCTGCCTGCCTCCCTAGCAGGCGCCAGCGGTGGAGGCTGAGTCGCAGGACACATGCCGGCCA
GTTAATTCATTCTCAGCCAATGAAGGTTTGTCTAAGCTGCCTGGGTATCCACGGGACAAAAACA
GCAAACTCCCTCAGACTTTGTCCATGTATAAACTTGAAGTGGTTGTGTTGTAGGGTTGCAGGTT
TTTTGTTACGCTGCTGTCACTTTCTGTCCAGGAGCTGGCACCCCAGGTGTTCTGAGACCTTGAG
GGACCCAGACCTTTGGGTCCAAGAGTTTCCCAAACAGCCACGCCTCTCAGGAACCCACCTGGCG
GTTCCGTGAGCTCAGGCAGGCCTGACCCGGCGGCACAGCCTGGCAGGGACCTCGTCCCCAAGCC
TGGCAGAATGAGAGGGGTTGAGGTCCCGAGCGCCACTCCTAGCCTTGCCGCCTTCAATAGAGAA
GAAATCCCTTTGCTAGATAGGGTCCCCCAGGCAGTCCCCAGTGGCGGGACACAGGGGTCCGGCT
GTGGAGCTCCCCTGCCAGCCCCTGGAGCTCCAGGAGGGCCTGTTGGTCCCCTGTTCAGAATGGA
GTGCAGCCCGCCAGCGGAAAGTGTTCATTCTGCATAGGTGTGAGGCTTTATCTGCACACAGGAC
ATGAAAACCAGCAGAAAGGCCCTGAGCTGCTGCATAGCCCCATCTGATTTCTGCAGTTCCCGCC
AGCCTCCAACACGGGGACTCTGCCGTAACTGGAATCTTCATAGGTCATATTGAAATCTTCAAGG
TGACCATGCCCCACCGGGGTGCTGGGGCAGTAGTCATGGCAGACTCCCGGCCTGGGCCCCCAGG
ATTCTAGGACCCCCAGGCAGCCCCTTGGACTGGTCCCGGGTGCCTTCCAAGCACAGTCTCCATG
CTCCCAGATTCTCGACCTTCCCCCGGCCCGGGAGGTGCAGCCTGCGTCTGCCTCTGTCGTGTGT
GCTGATTTGAGTGGCTTAGCTTGCCACAGCGCAGCCTCTTCTGTCCCTTTCAGTCATTTGCTGT
ACTTCCCTGTGGCACGTTACCATGGAAGCCGCTCCAGGGTGGGTCAGGGTGCAAGCTGCTGGTG
AGGTTTGGAAGCATCAGGCTCACGGGTGTTCATGTGTGTTCGTGCGTGTGTGTGCGTACGTGTA
TATAACTGAAGTGTCTGTACGGAATGCCCTTTGCTAGCCATGGGCTGGTCACCAGATTGTTTTG
TAATGCCCGCCCCTTGCCTCGATATTGCCAGTTTCTTGTGCAATAAACAATCAGCAGCTG

hide sequence

RefSeq Acc Id:

NM_199424 ⟹ NP_955456

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	69,925,039 - 69,941,739 (+)	NCBI
GRCh37	16	69,796,187 - 69,975,644 (+)	NCBI
Build 36	16	68,516,402 - 68,533,144 (+)	NCBI Archive
HuRef	16	55,674,737 - 55,853,946 (+)	NCBI
CHM1_1	16	71,366,760 - 71,383,517 (+)	NCBI
T2T-CHM13v2.0	16	75,727,619 - 75,744,318 (+)	NCBI

Sequence:

show sequence

AGTCGCCTTGGCCGCCTTGAGCCGGAGCTGAGCGGAGGCACTGGGCCGAGCCTGCTTCCCGGGC
CTTCCTACCATGCCAGGGCTGCTCCCTGCCTCCGCCACCCTGGCACACCTTCACCCGCGTACCG
CCTCCTCCCCGTCGCTCTGCCTTTTCCAAAACTCACTTGGGCCCTCCGTGCGCAGGGTTCTTTT
TTGGTTTTTCTGTAAAAATCAAAACAAAAAACAGAGACTTTTGAGAGGAGCAGATGCCACCTAA
AGTCCCACTGCATTCCCTGCAAAGCGCTCAAATGTGGAAGCCAGTCATTGGCATTTTTATTTTT
TATTGATTGATTGATTTTTTCACCAGTGGCTTTTTGTAACCTCTGTGTTCTGCTGTGTTTCTTG
TGTTTAGTCTTCGAGTGCTTCGACTGACCATGATCCCCTGGGCCCCCTCCCTCCTGGCTGGGAG
AAGAGACAGGACAATGGACGGGTGTATTACGTGAACCATAACACTCGCACGACCCAGTGGGAGG
ATCCCCGGACCCAGGGGATGATCCAGGAACCAGCTCTGCCCCCAGGATGGGAGATGAAATACAC
CAGCGAGGGGGTGCGATACTTTGTGGACCACAATACCCGCACCACCACCTTTAAGGATCCTCGC
CCGGGGTTTGAGTCGGGGACGAAGCAAGGTTCCCCTGGTGCTTATGACCGCAGTTTTCGGTGGA
AGTATCACCAGTTCCGTTTCCTCTGCCATTCAAATGCCCTACCTAGCCACGTGAAGATCAGCGT
TTCCAGGCAGACGCTTTTCGAAGATTCCTTCCAACAGATCATGAACATGAAACCCTATGACCTG
CGCCGCCGGCTCTACATCATCATGCGTGGCGAGGAGGGCCTGGACTATGGGGGCATCGCCAGAG
AGTGGTTTTTCCTCCTGTCTCATGAGGTGCTCAACCCTATGTATTGTTTATTTGAATATGCCGG
AAAGAACAATTACTGCCTGCAGATCAACCCCGCCTCCTCCATCAACCCGGACCACCTCACCTAC
TTTCGCTTTATAGGCAGATTCATCGCCATGGCGCTGTACCATGGAAAGTTCATCGACACGGGCT
TCACCCTCCCTTTCTACAAGCGGATGCTCAATAAGAGACCAACCCTGAAAGACCTGGAGTCCAT
TGACCCTGAGTTCTACAACTCCATTGTCTGGATCAAAGAGAACAACCTGGAAGAATGTGGCCTG
GAGCTGTACTTCATCCAGGACATGGAGATACTGGGCAAGGTGACGACCCACGAGCTGAAGGAGG
GCGGCGAGAGCATCCGGGTCACAGAGGAGAACAAGGAAGAGTACATCATGCTGCTGACTGACTG
GCGTTTCACCCGAGGCGTGGAAGAGCAGACCAAAGCCTTCCTGGATGGCTTCAACGAGGTGGCC
CCGCTGGAGTGGCTGCGCTACTTTGACGAGAAAGAGCTGGAGCTGATGCTGTGCGGCATGCAGG
AGATAGACATGAGCGACTGGCAGAAGAGCACCATCTACCGGCACTACACCAAGAACAGCAAGCA
GATCCAGTGGTTCTGGCAGGTGGTGAAGGAGATGGACAACGAGAAGAGGATCCGGCTGCTGCAG
TTTGTCACCGGTACCTGCCGCCTGCCCGTCGGGGGATTTGCCGAACTCATCGGTAGCAACGGAC
CACAGAAGTTTTGCATTGACAAAGTTGGCAAGGAAACCTGGCTGCCCAGAAGCCACACCTGCTT
CAACCGTCTGGATCTTCCACCCTACAAGAGCTACGAACAGCTGAGAGAGAAGCTGCTGTATGCC
ATTGAGGAGACCGAGGGCTTTGGACAGGAGTAACCGAGGCCGCCCCTCCCACGCCCCCCAGCGC
ACATGTAGTCCTGAGTCCTCCCTGCCTGAGAGGCCACTGGCCCCGCAGCCCTTGGGAGGCCCCC
GTGGATGTGGCCCTGTGTGGGACCACACTGTCATCTCGCTGCTGGCAGAAAAGCCTGATCCCAG
GAGGCCCTGCAGTTCCCCCGACCCGCGGATGGCAGTCTGGAATAAAGCCCCCTAGTTGCCTTTG
GCCCCACCTTTGCAAAGTTCCAGAGGGCTGACCCTCTCTGCAAAACTCTCCCCTGTCCTCTAGA
CCCCACCCTGGGTGTATGTGAGTGTGCAAGGGAAGGTGTTGCATCCCCAGGGGCTGCCGCAGAG
GCCGGAGACCTCCTGGACTAGTTCGGCGAGGAGACTGGCCACTGGGGGTGGCTGTTCGGGACTG
AGAGCGCCAAGGGTCTTTGCCAGCAAAGGAGGTTCTGCCTGTAATTGAGCCTCTCTGATGATGG
AGATGAAGTGAAGGTCTGAGGGAGCGGGCCCTGGGGCGAGGCCATCTCTGCCTGCCTCCCTAGC
AGGCGCCAGCGGTGGAGGCTGAGTCGCAGGACACATGCCGGCCAGTTAATTCATTCTCAGCCAA
TGAAGGTTTGTCTAAGCTGCCTGGGTATCCACGGGACAAAAACAGCAAACTCCCTCAGACTTTG
TCCATGTATAAACTTGAAGTGGTTGTGTTGTAGGGTTGCAGGTTTTTTGTTACGCTGCTGTCAC
TTTCTGTCCAGGAGCTGGCACCCCAGGTGTTCTGAGACCTTGAGGGACCCAGACCTTTGGGTCC
AAGAGTTTCCCAAACAGCCACGCCTCTCAGGAACCCACCTGGCGGTTCCGTGAGCTCAGGCAGG
CCTGACCCGGCGGCACAGCCTGGCAGGGACCTCGTCCCCAAGCCTGGCAGAATGAGAGGGGTTG
AGGTCCCGAGCGCCACTCCTAGCCTTGCCGCCTTCAATAGAGAAGAAATCCCTTTGCTAGATAG
GGTCCCCCAGGCAGTCCCCAGTGGCGGGACACAGGGGTCCGGCTGTGGAGCTCCCCTGCCAGCC
CCTGGAGCTCCAGGAGGGCCTGTTGGTCCCCTGTTCAGAATGGAGTGCAGCCCGCCAGCGGAAA
GTGTTCATTCTGCATAGGTGTGAGGCTTTATCTGCACACAGGACATGAAAACCAGCAGAAAGGC
CCTGAGCTGCTGCATAGCCCCATCTGATTTCTGCAGTTCCCGCCAGCCTCCAACACGGGGACTC
TGCCGTAACTGGAATCTTCATAGGTCATATTGAAATCTTCAAGGTGACCATGCCCCACCGGGGT
GCTGGGGCAGTAGTCATGGCAGACTCCCGGCCTGGGCCCCCAGGATTCTAGGACCCCCAGGCAG
CCCCTTGGACTGGTCCCGGGTGCCTTCCAAGCACAGTCTCCATGCTCCCAGATTCTCGACCTTC
CCCCGGCCCGGGAGGTGCAGCCTGCGTCTGCCTCTGTCGTGTGTGCTGATTTGAGTGGCTTAGC
TTGCCACAGCGCAGCCTCTTCTGTCCCTTTCAGTCATTTGCTGTACTTCCCTGTGGCACGTTAC
CATGGAAGCCGCTCCAGGGTGGGTCAGGGTGCAAGCTGCTGGTGAGGTTTGGAAGCATCAGGCT
CACGGGTGTTCATGTGTGTTCGTGCGTGTGTGTGCGTACGTGTATATAACTGAAGTGTCTGTAC
GGAATGCCCTTTGCTAGCCATGGGCTGGTCACCAGATTGTTTTGTAATGCCCGCCCCTTGCCTC
GATATTGCCAGTTTCTTGTGCAATAAACAATCAGCAGCTG

hide sequence

RefSeq Acc Id:

XM_011522823 ⟹ XP_011521125

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	69,762,332 - 69,941,739 (+)	NCBI

Sequence:

show sequence

ACCGCGCGCGGTCACGTGACCCGGCCCGAGTGCGGGCGGTGGAAGGCGGAAGTAGGAGAGGAGT
TCGGCGCCGCTTCTGTGGCCACGGCAGATGAAACAGAAAGGCTAAAGAGGGCTGGAGTCAGGGG
ACTTCTCTTCCACCAGGTTCAAGCGATTCTTCTGCCTCAGCCTCCGGATACCTGGGATTACAGC
TTCACGGTGATGATATGGCATCTGCCAGCTCTAGCCGGGCAGGAGTGGCCCTGCCTTTTGAGAA
GTCTCAGCTCACTTTGAAAGTGGTGTCCGCAAAGCCCAAGGTGCATAATCGTCAACCTCGAATT
AACTCCTACGTGGAGGTGGCGGTGGATGGACTCCCCAGTGAGACCAAGAAGACTGGGAAGCGCA
TTGGGAGCTCTGAGCTTCTCTGGAATGAGATCATCATTTTGAATGTCACGGCACAGAGTCATTT
AGATTTAAAGGTCTGGAGCTGCCATACCTTGAGAAATGAACTGCTAGGCACCGCATCTGTCAAC
CTCTCCAACGTCTTGAAGAACAATGGGGGCAAAATGGAGAACATGCAGCTGACCCTGAACCTGC
AGACGGAGAACAAAGGCAGCGTTGTCTCAGGCGGAGAGCTGACAATTTTCCTGGACGGGCCAAC
TGTTGATCTGGGAAATGTGCCTAATGGCAGTGCCCTGACAGATGGATCACAGCTGCCTTCGAGA
GACTCCAGTGGAACAGCAGTAGCTCCAGAGAACCGGCACCAGCCCCCCAGCACAAACTGCTTTG
GTGGAAGATCCCGGACGCACAGACATTCGGGTGCTTCAGCCAGAACAACCCCAGCAACCGGCGA
GCAAAGCCCCGGTGCTCGGAGCCGGCACCGCCAGCCCGTCAAGAACTCAGGCCACAGTGGCTTG
GCCAATGGCACAGTGAATGATGAACCCACAACAGCCACTGATCCCGAAGAACCTTCCGTTGTTG
GTGTGACGTCCCCACCTGCTGCACCCTTGAGTGTGACCCCGAATCCCAACACGACTTCTCTCCC
TGCCCCAGCCACACCGGCTGAAGGAGAGGAACCCAGCACTTCGGGTACACAGCAGCTCCCAGCG
GCTGCCCAGGCCCCCGACGCTCTGCCTGCTGGATGGGAACAGCGAGAGCTGCCCAACGGACGTG
TCTATTATGTTGACCACAATACCAAGACCACCACCTGGGAGCGGCCCCTTCCTCCAGGCTGGGA
AAAACGCACAGATCCCCGAGGCAGGTTTTACTATGTGGATCACAATACTCGGACCACCACCTGG
CAGCGTCCGACCGCGGAGTACGTGCGCAACTATGAGCAGTGGCAGTCGCAGCGGAATCAGCTCC
AGGGGGCCATGCAGCACTTCAGCCAAAGATTCCTCTACCAGTCTTCGAGTGCTTCGACTGACCA
TGATCCCCTGGGCCCCCTCCCTCCTGGCTGGGAGAAGAGACAGGACAATGGACGGGTGTATTAC
GTGAACCATAACACTCGCACGACCCAGTGGGAGGATCCCCGGACCCAGGGGATGATCCAGGAAC
CAGCTCTGCCCCCAGGATGGGAGATGAAATACACCAGCGAGGGGGTGCGATACTTTGTGGACCA
CAATACCCGCACCACCACCTTTAAGGATCCTCGCCCGGGGTTTGAGTCGGGGACGAAGCAAGGT
TCCCCTGGTGCTTATGACCGCAGTTTTCGGTGGAAGTATCACCAGTTCCGTTTCCTCTGCCATT
CAAATGCCCTACCTAGCCACGTGAAGATCAGCGTTTCCAGGCAGACGCTTTTCGAAGATTCCTT
CCAACAGATCATGAACATGAAACCCTATGACCTGCGCCGCCGGCTCTACATCATCATGCGTGGC
GAGGAGGGCCTGGACTATGGGGGCATCGCCAGAGAGTGGTTTTTCCTCCTGTCTCATGAGGTGC
TCAACCCTATGTATTGTTTATTTGAATATGCCGGAAAGAACAATTACTGCCTGCAGATCAACCC
CGCCTCCTCCATCAACCCGGACCACCTCACCTACTTTCGCTTTATAGGCAGATTCATCGCCATG
GCGCTGTACCATGGAAAGTTCATCGACACGGGCTTCACCCTCCCTTTCTACAAGCGGATGCTCA
ATAAGAGACCAACCCTGAAAGACCTGGAGTCCATTGACCCTGAGTTCTACAACTCCATTGTCTG
GATCAAAGAGAACAACCTGGAAGAATGTGGCCTGGAGCTGTACTTCATCCAGGACATGGAGATA
CTGGGCAAGGTGACGACCCACGAGCTGAAGGAGGGCGGCGAGAGCATCCGGGTCACAGAGGAGA
ACAAGGAAGAGTACATCATGCTGCTGACTGACTGGCGTTTCACCCGAGGCGTGGAAGAGCAGAC
CAAAGCCTTCCTGGATGGCTTCAACGAGGTGGCCCCGCTGGAGTGGCTGCGCTACTTTGACGAG
AAAGAGCTGGAGCTGATGCTGTGCGGCATGCAGGAGATAGACATGAGCGACTGGCAGAAGAGCA
CCATCTACCGGCACTACACCAAGAACAGCAAGCAGATCCAGTGGTTCTGGCAGGTGGTGAAGGA
GATGGACAACGAGAAGAGGATCCGGCTGCTGCAGTTTGTCACCGGTACCTGCCGCCTGCCCGTC
GGGGGATTTGCCGAACTCATCGGTAGCAACGGACCACAGAAGTTTTGCATTGACAAAGTTGGCA
AGGAAACCTGGCTGCCCAGAAGCCACACCTGCTTCAACCGTCTGGATCTTCCACCCTACAAGAG
CTACGAACAGCTGAGAGAGAAGCTGCTGTATGCCATTGAGGAGACCGAGGGCTTTGGACAGGAG
TAACCGAGGCCGCCCCTCCCACGCCCCCCAGCGCACATGTAGTCCTGAGTCCTCCCTGCCTGAG
AGGCCACTGGCCCCGCAGCCCTTGGGAGGCCCCCGTGGATGTGGCCCTGTGTGGGACCACACTG
TCATCTCGCTGCTGGCAGAAAAGCCTGATCCCAGGAGGCCCTGCAGTTCCCCCGACCCGCGGAT
GGCAGTCTGGAATAAAGCCCCCTAGTTGCCTTTGGCCCCACCTTTGCAAAGTTCCAGAGGGCTG
ACCCTCTCTGCAAAACTCTCCCCTGTCCTCTAGACCCCACCCTGGGTGTATGTGAGTGTGCAAG
GGAAGGTGTTGCATCCCCAGGGGCTGCCGCAGAGGCCGGAGACCTCCTGGACTAGTTCGGCGAG
GAGACTGGCCACTGGGGGTGGCTGTTCGGGACTGAGAGCGCCAAGGGTCTTTGCCAGCAAAGGA
GGTTCTGCCTGTAATTGAGCCTCTCTGATGATGGAGATGAAGTGAAGGTCTGAGGGAGCGGGCC
CTGGGGCGAGGCCATCTCTGCCTGCCTCCCTAGCAGGCGCCAGCGGTGGAGGCTGAGTCGCAGG
ACACATGCCGGCCAGTTAATTCATTCTCAGCCAATGAAGGTTTGTCTAAGCTGCCTGGGTATCC
ACGGGACAAAAACAGCAAACTCCCTCAGACTTTGTCCATGTATAAACTTGAAGTGGTTGTGTTG
TAGGGTTGCAGGTTTTTTGTTACGCTGCTGTCACTTTCTGTCCAGGAGCTGGCACCCCAGGTGT
TCTGAGACCTTGAGGGACCCAGACCTTTGGGTCCAAGAGTTTCCCAAACAGCCACGCCTCTCAG
GAACCCACCTGGCGGTTCCGTGAGCTCAGGCAGGCCTGACCCGGCGGCACAGCCTGGCAGGGAC
CTCGTCCCCAAGCCTGGCAGAATGAGAGGGGTTGAGGTCCCGAGCGCCACTCCTAGCCTTGCCG
CCTTCAATAGAGAAGAAATCCCTTTGCTAGATAGGGTCCCCCAGGCAGTCCCCAGTGGCGGGAC
ACAGGGGTCCGGCTGTGGAGCTCCCCTGCCAGCCCCTGGAGCTCCAGGAGGGCCTGTTGGTCCC
CTGTTCAGAATGGAGTGCAGCCCGCCAGCGGAAAGTGTTCATTCTGCATAGGTGTGAGGCTTTA
TCTGCACACAGGACATGAAAACCAGCAGAAAGGCCCTGAGCTGCTGCATAGCCCCATCTGATTT
CTGCAGTTCCCGCCAGCCTCCAACACGGGGACTCTGCCGTAACTGGAATCTTCATAGGTCATAT
TGAAATCTTCAAGGTGACCATGCCCCACCGGGGTGCTGGGGCAGTAGTCATGGCAGACTCCCGG
CCTGGGCCCCCAGGATTCTAGGACCCCCAGGCAGCCCCTTGGACTGGTCCCGGGTGCCTTCCAA
GCACAGTCTCCATGCTCCCAGATTCTCGACCTTCCCCCGGCCCGGGAGGTGCAGCCTGCGTCTG
CCTCTGTCGTGTGTGCTGATTTGAGTGGCTTAGCTTGCCACAGCGCAGCCTCTTCTGTCCCTTT
CAGTCATTTGCTGTACTTCCCTGTGGCACGTTACCATGGAAGCCGCTCCAGGGTGGGTCAGGGT
GCAAGCTGCTGGTGAGGTTTGGAAGCATCAGGCTCACGGGTGTTCATGTGTGTTCGTGCGTGTG
TGTGCGTACGTGTATATAACTGAAGTGTCTGTACGGAATGCCCTTTGCTAGCCATGGGCTGGTC
ACCAGATTGTTTTGTAATGCCCGCCCCTTGCCTCGATATTGCCAGTTTCTTGTGCAATAAACAA
TCAGCAGCTGTG

hide sequence

RefSeq Acc Id:

XM_011522825 ⟹ XP_011521127

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	69,762,332 - 69,941,739 (+)	NCBI

Sequence:

show sequence

GTGACCCGGCCCGAGTGCGGGCGGTGGAAGGCGGAAGTAGGAGAGGAGTTCGGCGCCGCTTCTG
TGGCCACGCTTCACGGTGATGATATGGCATCTGCCAGCTCTAGCCGGGCAGGAGTGGCCCTGCC
TTTTGAGAAGTCTCAGCTCACTTTGAAAGTGGTGTCCGCAAAGCCCAAGGTGCATAATCGTCAA
CCTCGAATTAACTCCTACGTGGAGGTGGCGGTGGATGGACTCCCCAGTGAGACCAAGAAGACTG
GGAAGCGCATTGGGAGCTCTGAGCTTCTCTGGAATGAGATCATCATTTTGAATGTCACGGCACA
GAGTCATTTAGATTTAAAGGTCTGGAGCTGCCATACCTTGAGAAATGAACTGCTAGGCACCGCA
TCTGTCAACCTCTCCAACGTCTTGAAGAACAATGGGGGCAAAATGGAGAACATGCAGCTGACCC
TGAACCTGCAGACGGAGAACAAAGGCAGCGTTGTCTCAGGCGGAGAGCTGACAATTTTCCTGGA
CGGGCCAACTGTTGATCTGGGAAATGTGCCTAATGGCAGTGCCCTGACAGATGGATCACAGCTG
CCTTCGAGAGACTCCAGTGGAACAGCAGTAGCTCCAGAGAACCGGCACCAGCCCCCCAGCACAA
ACTGCTTTGGTGGAAGATCCCGGACGCACAGACATTCGGGTGCTTCAGCCAGAACAACCCCAGC
AACCGGCGAGCAAAGCCCCGGTGCTCGGAGCCGGCACCGCCAGCCCGTCAAGAACTCAGGCCAC
AGTGGCTTGGCCAATGGCACAGTGAATGATGAACCCACAACAGCCACTGATCCCGAAGAACCTT
CCGTTGTTGGTGTGACGTCCCCACCTGCTGCACCCTTGAGTGTGACCCCGAATCCCAACACGAC
TTCTCTCCCTGCCCCAGCCACACCGGCTGAAGGAGAGGAACCCAGCACTTCGGGTACACAGCAG
CTCCCAGCGGCTGCCCAGGCCCCCGACGCTCTGCCTGCTGGATGGGAACAGCGAGAGCTGCCCA
ACGGACGTGTCTATTATGTTGACCACAATACCAAGACCACCACCTGGGAGCGGCCCCTTCCTCC
AGGCTGGGAAAAACGCACAGATCCCCGAGGCAGGTTTTACTATGTGGATCACAATACTCGGACC
ACCACCTGGCAGCGTCCGACCGCGGAGTACGTGCGCAACTATGAGCAGTGGCAGTCGCAGCGGA
ATCAGCTCCAGGGGGCCATGCAGCACTTCAGCCAAAGATTCCTCTACCAGTCTTCGAGTGCTTC
GACTGACCATGATCCCCTGGGCCCCCTCCCTCCTGGCTGGGAGAAGAGACAGGACAATGGACGG
GTGTATTACGTGAACCATAACACTCGCACGACCCAGTGGGAGGATCCCCGGACCCAGGGGATGA
TCCAGGAACCAGCTCTGCCCCCAGGATGGGAGATGAAATACACCAGCGAGGGGGTGCGATACTT
TGTGGACCACAATACCCGCACCACCACCTTTAAGGATCCTCGCCCGGGGTTTGAGTCGGGGACG
AAGCAAGGTTCCCCTGGTGCTTATGACCGCAGTTTTCGGTGGAAGTATCACCAGTTCCGTTTCC
TCTGCCATTCAAATGCCCTACCTAGCCACGTGAAGATCAGCGTTTCCAGGCAGACGCTTTTCGA
AGATTCCTTCCAACAGATCATGAACATGAAACCCTATGACCTGCGCCGCCGGCTCTACATCATC
ATGCGTGGCGAGGAGGGCCTGGACTATGGGGGCATCGCCAGAGAGTGGTTTTTCCTCCTGTCTC
ATGAGGTGCTCAACCCTATGTATTGTTTATTTGAATATGCCGGAAAGAACAATTACTGCCTGCA
GATCAACCCCGCCTCCTCCATCAACCCGGACCACCTCACCTACTTTCGCTTTATAGGCAGATTC
ATCGCCATGGCGCTGTACCATGGAAAGTTCATCGACACGGGCTTCACCCTCCCTTTCTACAAGC
GGATGCTCAATAAGAGACCAACCCTGAAAGACCTGGAGTCCATTGACCCTGAGTTCTACAACTC
CATTGTCTGGATCAAAGAGAACAACCTGGAAGAATGTGGCCTGGAGCTGTACTTCATCCAGGAC
ATGGAGATACTGGGCAAGGTGACGACCCACGAGCTGAAGGAGGGCGGCGAGAGCATCCGGGTCA
CAGAGGAGAACAAGGAAGAGTACATCATGCTGCTGACTGACTGGCGTTTCACCCGAGGCGTGGA
AGAGCAGACCAAAGCCTTCCTGGATGGCTTCAACGAGGTGGCCCCGCTGGAGTGGCTGCGCTAC
TTTGACGAGAAAGAGCTGGAGCTGATGCTGTGCGGCATGCAGGAGATAGACATGAGCGACTGGC
AGAAGAGCACCATCTACCGGCACTACACCAAGAACAGCAAGCAGATCCAGTGGTTCTGGCAGGT
GGTGAAGGAGATGGACAACGAGAAGAGGATCCGGCTGCTGCAGTTTGTCACCGGTACCTGCCGC
CTGCCCGTCGGGGGATTTGCCGAACTCATCGGTAGCAACGGACCACAGAAGTTTTGCATTGACA
AAGTTGGCAAGGAAACCTGGCTGCCCAGAAGCCACACCTGCTTCAACCGTCTGGATCTTCCACC
CTACAAGAGCTACGAACAGCTGAGAGAGAAGCTGCTGTATGCCATTGAGGAGACCGAGGGCTTT
GGACAGGAGTAACCGAGGCCGCCCCTCCCACGCCCCCCAGCGCACATGTAGTCCTGAGTCCTCC
CTGCCTGAGAGGCCACTGGCCCCGCAGCCCTTGGGAGGCCCCCGTGGATGTGGCCCTGTGTGGG
ACCACACTGTCATCTCGCTGCTGGCAGAAAAGCCTGATCCCAGGAGGCCCTGCAGTTCCCCCGA
CCCGCGGATGGCAGTCTGGAATAAAGCCCCCTAGTTGCCTTTGGCCCCACCTTTGCAAAGTTCC
AGAGGGCTGACCCTCTCTGCAAAACTCTCCCCTGTCCTCTAGACCCCACCCTGGGTGTATGTGA
GTGTGCAAGGGAAGGTGTTGCATCCCCAGGGGCTGCCGCAGAGGCCGGAGACCTCCTGGACTAG
TTCGGCGAGGAGACTGGCCACTGGGGGTGGCTGTTCGGGACTGAGAGCGCCAAGGGTCTTTGCC
AGCAAAGGAGGTTCTGCCTGTAATTGAGCCTCTCTGATGATGGAGATGAAGTGAAGGTCTGAGG
GAGCGGGCCCTGGGGCGAGGCCATCTCTGCCTGCCTCCCTAGCAGGCGCCAGCGGTGGAGGCTG
AGTCGCAGGACACATGCCGGCCAGTTAATTCATTCTCAGCCAATGAAGGTTTGTCTAAGCTGCC
TGGGTATCCACGGGACAAAAACAGCAAACTCCCTCAGACTTTGTCCATGTATAAACTTGAAGTG
GTTGTGTTGTAGGGTTGCAGGTTTTTTGTTACGCTGCTGTCACTTTCTGTCCAGGAGCTGGCAC
CCCAGGTGTTCTGAGACCTTGAGGGACCCAGACCTTTGGGTCCAAGAGTTTCCCAAACAGCCAC
GCCTCTCAGGAACCCACCTGGCGGTTCCGTGAGCTCAGGCAGGCCTGACCCGGCGGCACAGCCT
GGCAGGGACCTCGTCCCCAAGCCTGGCAGAATGAGAGGGGTTGAGGTCCCGAGCGCCACTCCTA
GCCTTGCCGCCTTCAATAGAGAAGAAATCCCTTTGCTAGATAGGGTCCCCCAGGCAGTCCCCAG
TGGCGGGACACAGGGGTCCGGCTGTGGAGCTCCCCTGCCAGCCCCTGGAGCTCCAGGAGGGCCT
GTTGGTCCCCTGTTCAGAATGGAGTGCAGCCCGCCAGCGGAAAGTGTTCATTCTGCATAGGTGT
GAGGCTTTATCTGCACACAGGACATGAAAACCAGCAGAAAGGCCCTGAGCTGCTGCATAGCCCC
ATCTGATTTCTGCAGTTCCCGCCAGCCTCCAACACGGGGACTCTGCCGTAACTGGAATCTTCAT
AGGTCATATTGAAATCTTCAAGGTGACCATGCCCCACCGGGGTGCTGGGGCAGTAGTCATGGCA
GACTCCCGGCCTGGGCCCCCAGGATTCTAGGACCCCCAGGCAGCCCCTTGGACTGGTCCCGGGT
GCCTTCCAAGCACAGTCTCCATGCTCCCAGATTCTCGACCTTCCCCCGGCCCGGGAGGTGCAGC
CTGCGTCTGCCTCTGTCGTGTGTGCTGATTTGAGTGGCTTAGCTTGCCACAGCGCAGCCTCTTC
TGTCCCTTTCAGTCATTTGCTGTACTTCCCTGTGGCACGTTACCATGGAAGCCGCTCCAGGGTG
GGTCAGGGTGCAAGCTGCTGGTGAGGTTTGGAAGCATCAGGCTCACGGGTGTTCATGTGTGTTC
GTGCGTGTGTGTGCGTACGTGTATATAACTGAAGTGTCTGTACGGAATGCCCTTTGCTAGCCAT
GGGCTGGTCACCAGATTGTTTTGTAATGCCCGCCCCTTGCCTCGATATTGCCAGTTTCTTGTGC
AATAAACAATCAGCAGCTGTG

hide sequence

RefSeq Acc Id:

XM_011522826 ⟹ XP_011521128

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	69,839,705 - 69,941,739 (+)	NCBI

Sequence:

show sequence

TCCTGTTGACAGTTCCTTAGGGTCTCCTCGGTTTCTATGGGCAGGGGGATATTACTTGCAACTA
ATTTCTTCGTCTGTACGCCATCAATATCCCTATGCTTTTCTCACAGTCCTGCAAGTATAAACAA
ACTAATACATCAGTAATGTGGAAATTATGGTGCTGACCCAGTGATATGAAATGTTTAGAAAGAG
TGCAGCTTCCCCTCCAGCCTGATACAACAGTGATTTCATTAGACATATTCCTTCCCACTCTTTT
TTCCATGCCACGAGGCAAAATGTGAAGATGTGGAGAAAGCATTCCCAGAGAAGCCAGCAAAGTG
GAGAACATGCAGCTGACCCTGAACCTGCAGACGGAGAACAAAGGCAGCGTTGTCTCAGGCGGAG
AGCTGACAATTTTCCTGGACGGGCCAACTGTTGATCTGGGAAATGTGCCTAATGGCAGTGCCCT
GACAGATGGATCACAGCTGCCTTCGAGAGACTCCAGTGGAACAGCAGTAGCTCCAGAGAACCGG
CACCAGCCCCCCAGCACAAACTGCTTTGGTGGAAGATCCCGGACGCACAGACATTCGGGTGCTT
CAGCCAGAACAACCCCAGCAACCGGCGAGCAAAGCCCCGGTGCTCGGAGCCGGCACCGCCAGCC
CGTCAAGAACTCAGGCCACAGTGGCTTGGCCAATGGCACAGTGAATGATGAACCCACAACAGCC
ACTGATCCCGAAGAACCTTCCGTTGTTGGTGTGACGTCCCCACCTGCTGCACCCTTGAGTGTGA
CCCCGAATCCCAACACGACTTCTCTCCCTGCCCCAGCCACACCGGCTGAAGGAGAGGAACCCAG
CACTTCGGGTACACAGCAGCTCCCAGCGGCTGCCCAGGCCCCCGACGCTCTGCCTGCTGGATGG
GAACAGCGAGAGCTGCCCAACGGACGTGTCTATTATGTTGACCACAATACCAAGACCACCACCT
GGGAGCGGCCCCTTCCTCCAGGCTGGGAAAAACGCACAGATCCCCGAGGCAGGTTTTACTATGT
GGATCACAATACTCGGACCACCACCTGGCAGCGTCCGACCGCGGAGTACGTGCGCAACTATGAG
CAGTGGCAGTCGCAGCGGAATCAGCTCCAGGGGGCCATGCAGCACTTCAGCCAAAGATTCCTCT
ACCAGTCTTCGAGTGCTTCGACTGACCATGATCCCCTGGGCCCCCTCCCTCCTGGCTGGGAGAA
GAGACAGGACAATGGACGGGTGTATTACGTGAACCATAACACTCGCACGACCCAGTGGGAGGAT
CCCCGGACCCAGGGGATGATCCAGGAACCAGCTCTGCCCCCAGGATGGGAGATGAAATACACCA
GCGAGGGGGTGCGATACTTTGTGGACCACAATACCCGCACCACCACCTTTAAGGATCCTCGCCC
GGGGTTTGAGTCGGGGACGAAGCAAGGTTCCCCTGGTGCTTATGACCGCAGTTTTCGGTGGAAG
TATCACCAGTTCCGTTTCCTCTGCCATTCAAATGCCCTACCTAGCCACGTGAAGATCAGCGTTT
CCAGGCAGACGCTTTTCGAAGATTCCTTCCAACAGATCATGAACATGAAACCCTATGACCTGCG
CCGCCGGCTCTACATCATCATGCGTGGCGAGGAGGGCCTGGACTATGGGGGCATCGCCAGAGAG
TGGTTTTTCCTCCTGTCTCATGAGGTGCTCAACCCTATGTATTGTTTATTTGAATATGCCGGAA
AGAACAATTACTGCCTGCAGATCAACCCCGCCTCCTCCATCAACCCGGACCACCTCACCTACTT
TCGCTTTATAGGCAGATTCATCGCCATGGCGCTGTACCATGGAAAGTTCATCGACACGGGCTTC
ACCCTCCCTTTCTACAAGCGGATGCTCAATAAGAGACCAACCCTGAAAGACCTGGAGTCCATTG
ACCCTGAGTTCTACAACTCCATTGTCTGGATCAAAGAGAACAACCTGGAAGAATGTGGCCTGGA
GCTGTACTTCATCCAGGACATGGAGATACTGGGCAAGGTGACGACCCACGAGCTGAAGGAGGGC
GGCGAGAGCATCCGGGTCACAGAGGAGAACAAGGAAGAGTACATCATGCTGCTGACTGACTGGC
GTTTCACCCGAGGCGTGGAAGAGCAGACCAAAGCCTTCCTGGATGGCTTCAACGAGGTGGCCCC
GCTGGAGTGGCTGCGCTACTTTGACGAGAAAGAGCTGGAGCTGATGCTGTGCGGCATGCAGGAG
ATAGACATGAGCGACTGGCAGAAGAGCACCATCTACCGGCACTACACCAAGAACAGCAAGCAGA
TCCAGTGGTTCTGGCAGGTGGTGAAGGAGATGGACAACGAGAAGAGGATCCGGCTGCTGCAGTT
TGTCACCGGTACCTGCCGCCTGCCCGTCGGGGGATTTGCCGAACTCATCGGTAGCAACGGACCA
CAGAAGTTTTGCATTGACAAAGTTGGCAAGGAAACCTGGCTGCCCAGAAGCCACACCTGCTTCA
ACCGTCTGGATCTTCCACCCTACAAGAGCTACGAACAGCTGAGAGAGAAGCTGCTGTATGCCAT
TGAGGAGACCGAGGGCTTTGGACAGGAGTAACCGAGGCCGCCCCTCCCACGCCCCCCAGCGCAC
ATGTAGTCCTGAGTCCTCCCTGCCTGAGAGGCCACTGGCCCCGCAGCCCTTGGGAGGCCCCCGT
GGATGTGGCCCTGTGTGGGACCACACTGTCATCTCGCTGCTGGCAGAAAAGCCTGATCCCAGGA
GGCCCTGCAGTTCCCCCGACCCGCGGATGGCAGTCTGGAATAAAGCCCCCTAGTTGCCTTTGGC
CCCACCTTTGCAAAGTTCCAGAGGGCTGACCCTCTCTGCAAAACTCTCCCCTGTCCTCTAGACC
CCACCCTGGGTGTATGTGAGTGTGCAAGGGAAGGTGTTGCATCCCCAGGGGCTGCCGCAGAGGC
CGGAGACCTCCTGGACTAGTTCGGCGAGGAGACTGGCCACTGGGGGTGGCTGTTCGGGACTGAG
AGCGCCAAGGGTCTTTGCCAGCAAAGGAGGTTCTGCCTGTAATTGAGCCTCTCTGATGATGGAG
ATGAAGTGAAGGTCTGAGGGAGCGGGCCCTGGGGCGAGGCCATCTCTGCCTGCCTCCCTAGCAG
GCGCCAGCGGTGGAGGCTGAGTCGCAGGACACATGCCGGCCAGTTAATTCATTCTCAGCCAATG
AAGGTTTGTCTAAGCTGCCTGGGTATCCACGGGACAAAAACAGCAAACTCCCTCAGACTTTGTC
CATGTATAAACTTGAAGTGGTTGTGTTGTAGGGTTGCAGGTTTTTTGTTACGCTGCTGTCACTT
TCTGTCCAGGAGCTGGCACCCCAGGTGTTCTGAGACCTTGAGGGACCCAGACCTTTGGGTCCAA
GAGTTTCCCAAACAGCCACGCCTCTCAGGAACCCACCTGGCGGTTCCGTGAGCTCAGGCAGGCC
TGACCCGGCGGCACAGCCTGGCAGGGACCTCGTCCCCAAGCCTGGCAGAATGAGAGGGGTTGAG
GTCCCGAGCGCCACTCCTAGCCTTGCCGCCTTCAATAGAGAAGAAATCCCTTTGCTAGATAGGG
TCCCCCAGGCAGTCCCCAGTGGCGGGACACAGGGGTCCGGCTGTGGAGCTCCCCTGCCAGCCCC
TGGAGCTCCAGGAGGGCCTGTTGGTCCCCTGTTCAGAATGGAGTGCAGCCCGCCAGCGGAAAGT
GTTCATTCTGCATAGGTGTGAGGCTTTATCTGCACACAGGACATGAAAACCAGCAGAAAGGCCC
TGAGCTGCTGCATAGCCCCATCTGATTTCTGCAGTTCCCGCCAGCCTCCAACACGGGGACTCTG
CCGTAACTGGAATCTTCATAGGTCATATTGAAATCTTCAAGGTGACCATGCCCCACCGGGGTGC
TGGGGCAGTAGTCATGGCAGACTCCCGGCCTGGGCCCCCAGGATTCTAGGACCCCCAGGCAGCC
CCTTGGACTGGTCCCGGGTGCCTTCCAAGCACAGTCTCCATGCTCCCAGATTCTCGACCTTCCC
CCGGCCCGGGAGGTGCAGCCTGCGTCTGCCTCTGTCGTGTGTGCTGATTTGAGTGGCTTAGCTT
GCCACAGCGCAGCCTCTTCTGTCCCTTTCAGTCATTTGCTGTACTTCCCTGTGGCACGTTACCA
TGGAAGCCGCTCCAGGGTGGGTCAGGGTGCAAGCTGCTGGTGAGGTTTGGAAGCATCAGGCTCA
CGGGTGTTCATGTGTGTTCGTGCGTGTGTGTGCGTACGTGTATATAACTGAAGTGTCTGTACGG
AATGCCCTTTGCTAGCCATGGGCTGGTCACCAGATTGTTTTGTAATGCCCGCCCCTTGCCTCGA
TATTGCCAGTTTCTTGTGCAATAAACAATCAGCAGCTGTG

hide sequence

RefSeq Acc Id:

XM_017022879 ⟹ XP_016878368

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	69,762,332 - 69,941,739 (+)	NCBI

Sequence:

show sequence

ACCGCGCGCGGTCACGTGACCCGGCCCGAGTGCGGGCGGTGGAAGGCGGAAGTAGGAGAGGAGT
TCGGCGCCGCTTCTGTGGCCACGGCAGATGAAACAGAAAGGCTAAAGAGGGCTGGAGTCAGGGG
ACTTCTCTTCCACCAGATGGAGTCTCACTCTCTCCCCCAGGCTGGGGTGCAGCGGCGTGATCTC
AGCTCACTCCAACCTCTGCTTCCCAGGTTCAAGCGATTCTTCTGCCTCAGCCTCCGGATACCTG
GGATTACAGCTTCACGGTGATGATATGGCATCTGCCAGCTCTAGCCGGGCAGGAGTGGCCCTGC
CTTTTGAGAAGTCTCAGCTCACTTTGAAAGTGGTGTCCGCAAAGCCCAAGGTGCATAATCGTCA
ACCTCGAATTAACTCCTACGTGGAGGTGGCGGTGGATGGACTCCCCAGTGAGACCAAGAAGACT
GGGAAGCGCATTGGGAGCTCTGAGCTTCTCTGGAATGAGATCATCATTTTGAATGTCACGGCAC
AGAGTCATTTAGATTTAAAGGTCTGGAGCTGCCATACCTTGAGAAATGAACTGCTAGGCACCGC
ATCTGTCAACCTCTCCAACGTCTTGAAGAACAATGGGGGCAAAATGGAGAACATGCAGCTGACC
CTGAACCTGCAGACGGAGAACAAAGGCAGCGTTGTCTCAGGCGGAGAGCTGACAATTTTCCTGG
ACGGGCCAACTGTTGATCTGGGAAATGTGCCTAATGGCAGTGCCCTGACAGATGGATCACAGCT
GCCTTCGAGAGACTCCAGTGGAACAGCAGTAGCTCCAGAGAACCGGCACCAGCCCCCCAGCACA
AACTGCTTTGGTGGAAGATCCCGGACGCACAGACATTCGGGTGCTTCAGCCAGAACAACCCCAG
CAACCGGCGAGCAAAGCCCCGGTGCTCGGAGCCGGCACCGCCAGCCCGTCAAGAACTCAGGCCA
CAGTGGCTTGGCCAATGGCACAGTGAATGATGAACCCACAACAGCCACTGATCCCGAAGAACCT
TCCGTTGTTGGTGTGACGTCCCCACCTGCTGCACCCTTGAGTGTGACCCCGAATCCCAACACGA
CTTCTCTCCCTGCCCCAGCCACACCGGCTGAAGGAGAGGAACCCAGCACTTCGGGTACACAGCA
GCTCCCAGCGGCTGCCCAGGCCCCCGACGCTCTGCCTGCTGGATGGGAACAGCGAGAGCTGCCC
AACGGACGTGTCTATTATGTTGACCACAATACCAAGACCACCACCTGGGAGCGGCCCCTTCCTC
CAGGCTGGGAAAAACGCACAGATCCCCGAGGCAGGTTTTACTATGTGGATCACAATACTCGGAC
CACCACCTGGCAGCGTCCGACCGCGGAGTACGTGCGCAACTATGAGCAGTGGCAGTCGCAGCGG
AATCAGCTCCAGGGGGCCATGCAGCACTTCAGCCAAAGATTCCTCTACCAGTCTTCGAGTGCTT
CGACTGACCATGATCCCCTGGGCCCCCTCCCTCCTGGCTGGGAGAAGAGACAGGACAATGGACG
GGTGTATTACGTGAACCATAACACTCGCACGACCCAGTGGGAGGATCCCCGGACCCAGGGGATG
ATCCAGGAACCAGCTCTGCCCCCAGGATGGGAGATGAAATACACCAGCGAGGGGGTGCGATACT
TTGTGGACCACAATACCCGCACCACCACCTTTAAGGATCCTCGCCCGGGGTTTGAGTCGGGGAC
GAAGCAAGGTTCCCCTGGTGCTTATGACCGCAGTTTTCGGTGGAAGTATCACCAGTTCCGTTTC
CTCTGCCATTCAAATGCCCTACCTAGCCACGTGAAGATCAGCGTTTCCAGGCAGACGCTTTTCG
AAGATTCCTTCCAACAGATCATGAACATGAAACCCTATGACCTGCGCCGCCGGCTCTACATCAT
CATGCGTGGCGAGGAGGGCCTGGACTATGGGGGCATCGCCAGAGAGTGGTTTTTCCTCCTGTCT
CATGAGGTGCTCAACCCTATGTATTGTTTATTTGAATATGCCGGAAAGAACAATTACTGCCTGC
AGATCAACCCCGCCTCCTCCATCAACCCGGACCACCTCACCTACTTTCGCTTTATAGGCAGATT
CATCGCCATGGCGCTGTACCATGGAAAGTTCATCGACACGGGCTTCACCCTCCCTTTCTACAAG
CGGATGCTCAATAAGAGACCAACCCTGAAAGACCTGGAGTCCATTGACCCTGAGTTCTACAACT
CCATTGTCTGGATCAAAGAGAACAACCTGGAAGAATGTGGCCTGGAGCTGTACTTCATCCAGGA
CATGGAGATACTGGGCAAGGTGACGACCCACGAGCTGAAGGAGGGCGGCGAGAGCATCCGGGTC
ACAGAGGAGAACAAGGAAGAGTACATCATGCTGCTGACTGACTGGCGTTTCACCCGAGGCGTGG
AAGAGCAGACCAAAGCCTTCCTGGATGGCTTCAACGAGGTGGCCCCGCTGGAGTGGCTGCGCTA
CTTTGACGAGAAAGAGCTGGAGCTGATGCTGTGCGGCATGCAGGAGATAGACATGAGCGACTGG
CAGAAGAGCACCATCTACCGGCACTACACCAAGAACAGCAAGCAGATCCAGTGGTTCTGGCAGG
TGGTGAAGGAGATGGACAACGAGAAGAGGATCCGGCTGCTGCAGTTTGTCACCGGTACCTGCCG
CCTGCCCGTCGGGGGATTTGCCGAACTCATCGGTAGCAACGGACCACAGAAGTTTTGCATTGAC
AAAGTTGGCAAGGAAACCTGGCTGCCCAGAAGCCACACCTGCTTCAACCGTCTGGATCTTCCAC
CCTACAAGAGCTACGAACAGCTGAGAGAGAAGCTGCTGTATGCCATTGAGGAGACCGAGGGCTT
TGGACAGGAGTAACCGAGGCCGCCCCTCCCACGCCCCCCAGCGCACATGTAGTCCTGAGTCCTC
CCTGCCTGAGAGGCCACTGGCCCCGCAGCCCTTGGGAGGCCCCCGTGGATGTGGCCCTGTGTGG
GACCACACTGTCATCTCGCTGCTGGCAGAAAAGCCTGATCCCAGGAGGCCCTGCAGTTCCCCCG
ACCCGCGGATGGCAGTCTGGAATAAAGCCCCCTAGTTGCCTTTGGCCCCACCTTTGCAAAGTTC
CAGAGGGCTGACCCTCTCTGCAAAACTCTCCCCTGTCCTCTAGACCCCACCCTGGGTGTATGTG
AGTGTGCAAGGGAAGGTGTTGCATCCCCAGGGGCTGCCGCAGAGGCCGGAGACCTCCTGGACTA
GTTCGGCGAGGAGACTGGCCACTGGGGGTGGCTGTTCGGGACTGAGAGCGCCAAGGGTCTTTGC
CAGCAAAGGAGGTTCTGCCTGTAATTGAGCCTCTCTGATGATGGAGATGAAGTGAAGGTCTGAG
GGAGCGGGCCCTGGGGCGAGGCCATCTCTGCCTGCCTCCCTAGCAGGCGCCAGCGGTGGAGGCT
GAGTCGCAGGACACATGCCGGCCAGTTAATTCATTCTCAGCCAATGAAGGTTTGTCTAAGCTGC
CTGGGTATCCACGGGACAAAAACAGCAAACTCCCTCAGACTTTGTCCATGTATAAACTTGAAGT
GGTTGTGTTGTAGGGTTGCAGGTTTTTTGTTACGCTGCTGTCACTTTCTGTCCAGGAGCTGGCA
CCCCAGGTGTTCTGAGACCTTGAGGGACCCAGACCTTTGGGTCCAAGAGTTTCCCAAACAGCCA
CGCCTCTCAGGAACCCACCTGGCGGTTCCGTGAGCTCAGGCAGGCCTGACCCGGCGGCACAGCC
TGGCAGGGACCTCGTCCCCAAGCCTGGCAGAATGAGAGGGGTTGAGGTCCCGAGCGCCACTCCT
AGCCTTGCCGCCTTCAATAGAGAAGAAATCCCTTTGCTAGATAGGGTCCCCCAGGCAGTCCCCA
GTGGCGGGACACAGGGGTCCGGCTGTGGAGCTCCCCTGCCAGCCCCTGGAGCTCCAGGAGGGCC
TGTTGGTCCCCTGTTCAGAATGGAGTGCAGCCCGCCAGCGGAAAGTGTTCATTCTGCATAGGTG
TGAGGCTTTATCTGCACACAGGACATGAAAACCAGCAGAAAGGCCCTGAGCTGCTGCATAGCCC
CATCTGATTTCTGCAGTTCCCGCCAGCCTCCAACACGGGGACTCTGCCGTAACTGGAATCTTCA
TAGGTCATATTGAAATCTTCAAGGTGACCATGCCCCACCGGGGTGCTGGGGCAGTAGTCATGGC
AGACTCCCGGCCTGGGCCCCCAGGATTCTAGGACCCCCAGGCAGCCCCTTGGACTGGTCCCGGG
TGCCTTCCAAGCACAGTCTCCATGCTCCCAGATTCTCGACCTTCCCCCGGCCCGGGAGGTGCAG
CCTGCGTCTGCCTCTGTCGTGTGTGCTGATTTGAGTGGCTTAGCTTGCCACAGCGCAGCCTCTT
CTGTCCCTTTCAGTCATTTGCTGTACTTCCCTGTGGCACGTTACCATGGAAGCCGCTCCAGGGT
GGGTCAGGGTGCAAGCTGCTGGTGAGGTTTGGAAGCATCAGGCTCACGGGTGTTCATGTGTGTT
CGTGCGTGTGTGTGCGTACGTGTATATAACTGAAGTGTCTGTACGGAATGCCCTTTGCTAGCCA
TGGGCTGGTCACCAGATTGTTTTGTAATGCCCGCCCCTTGCCTCGATATTGCCAGTTTCTTGTG
CAATAAACAATCAGCAGCTGTG

hide sequence

RefSeq Acc Id:

XM_017022880 ⟹ XP_016878369

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	69,774,694 - 69,941,739 (+)	NCBI

Sequence:

show sequence

GTGCTGTGGCTTACGTTTATAATCCCATCACTTTGGGAGGCCAAGGCAGGAGGATGGCTTGAGC
CTAGGAGTTCAAGACCAGTCTGGACAACTTGGTTTGATGAAGAGTGGACAATCGTGGAGAAATA
CGATTGGACAAAAGGGATGAAACAGAAAGGCTAAAGAGGGCTGGAGTCAGGGGACTTCTCTTCC
ACCAGCTTCACGGTGATGATATGGCATCTGCCAGCTCTAGCCGGGCAGGAGTGGCCCTGCCTTT
TGAGAAGTCTCAGCTCACTTTGAAAGTGGTGTCCGCAAAGCCCAAGGTGCATAATCGTCAACCT
CGAATTAACTCCTACGTGGAGGTGGCGGTGGATGGACTCCCCAGTGAGACCAAGAAGACTGGGA
AGCGCATTGGGAGCTCTGAGCTTCTCTGGAATGAGATCATCATTTTGAATGTCACGGCACAGAG
TCATTTAGATTTAAAGGTCTGGAGCTGCCATACCTTGAGAAATGAACTGCTAGGCACCGCATCT
GTCAACCTCTCCAACGTCTTGAAGAACAATGGGGGCAAAATGGAGAACATGCAGCTGACCCTGA
ACCTGCAGACGGAGAACAAAGGCAGCGTTGTCTCAGGCGGAGAGCTGACAATTTTCCTGGACGG
GCCAACTGTTGATCTGGGAAATGTGCCTAATGGCAGTGCCCTGACAGATGGATCACAGCTGCCT
TCGAGAGACTCCAGTGGAACAGCAGTAGCTCCAGAGAACCGGCACCAGCCCCCCAGCACAAACT
GCTTTGGTGGAAGATCCCGGACGCACAGACATTCGGGTGCTTCAGCCAGAACAACCCCAGCAAC
CGGCGAGCAAAGCCCCGGTGCTCGGAGCCGGCACCGCCAGCCCGTCAAGAACTCAGGCCACAGT
GGCTTGGCCAATGGCACAGTGAATGATGAACCCACAACAGCCACTGATCCCGAAGAACCTTCCG
TTGTTGGTGTGACGTCCCCACCTGCTGCACCCTTGAGTGTGACCCCGAATCCCAACACGACTTC
TCTCCCTGCCCCAGCCACACCGGCTGAAGGAGAGGAACCCAGCACTTCGGGTACACAGCAGCTC
CCAGCGGCTGCCCAGGCCCCCGACGCTCTGCCTGCTGGATGGGAACAGCGAGAGCTGCCCAACG
GACGTGTCTATTATGTTGACCACAATACCAAGACCACCACCTGGGAGCGGCCCCTTCCTCCAGG
CTGGGAAAAACGCACAGATCCCCGAGGCAGGTTTTACTATGTGGATCACAATACTCGGACCACC
ACCTGGCAGCGTCCGACCGCGGAGTACGTGCGCAACTATGAGCAGTGGCAGTCGCAGCGGAATC
AGCTCCAGGGGGCCATGCAGCACTTCAGCCAAAGATTCCTCTACCAGTCTTCGAGTGCTTCGAC
TGACCATGATCCCCTGGGCCCCCTCCCTCCTGGCTGGGAGAAGAGACAGGACAATGGACGGGTG
TATTACGTGAACCATAACACTCGCACGACCCAGTGGGAGGATCCCCGGACCCAGGGGATGATCC
AGGAACCAGCTCTGCCCCCAGGATGGGAGATGAAATACACCAGCGAGGGGGTGCGATACTTTGT
GGACCACAATACCCGCACCACCACCTTTAAGGATCCTCGCCCGGGGTTTGAGTCGGGGACGAAG
CAAGGTTCCCCTGGTGCTTATGACCGCAGTTTTCGGTGGAAGTATCACCAGTTCCGTTTCCTCT
GCCATTCAAATGCCCTACCTAGCCACGTGAAGATCAGCGTTTCCAGGCAGACGCTTTTCGAAGA
TTCCTTCCAACAGATCATGAACATGAAACCCTATGACCTGCGCCGCCGGCTCTACATCATCATG
CGTGGCGAGGAGGGCCTGGACTATGGGGGCATCGCCAGAGAGTGGTTTTTCCTCCTGTCTCATG
AGGTGCTCAACCCTATGTATTGTTTATTTGAATATGCCGGAAAGAACAATTACTGCCTGCAGAT
CAACCCCGCCTCCTCCATCAACCCGGACCACCTCACCTACTTTCGCTTTATAGGCAGATTCATC
GCCATGGCGCTGTACCATGGAAAGTTCATCGACACGGGCTTCACCCTCCCTTTCTACAAGCGGA
TGCTCAATAAGAGACCAACCCTGAAAGACCTGGAGTCCATTGACCCTGAGTTCTACAACTCCAT
TGTCTGGATCAAAGAGAACAACCTGGAAGAATGTGGCCTGGAGCTGTACTTCATCCAGGACATG
GAGATACTGGGCAAGGTGACGACCCACGAGCTGAAGGAGGGCGGCGAGAGCATCCGGGTCACAG
AGGAGAACAAGGAAGAGTACATCATGCTGCTGACTGACTGGCGTTTCACCCGAGGCGTGGAAGA
GCAGACCAAAGCCTTCCTGGATGGCTTCAACGAGGTGGCCCCGCTGGAGTGGCTGCGCTACTTT
GACGAGAAAGAGCTGGAGCTGATGCTGTGCGGCATGCAGGAGATAGACATGAGCGACTGGCAGA
AGAGCACCATCTACCGGCACTACACCAAGAACAGCAAGCAGATCCAGTGGTTCTGGCAGGTGGT
GAAGGAGATGGACAACGAGAAGAGGATCCGGCTGCTGCAGTTTGTCACCGGTACCTGCCGCCTG
CCCGTCGGGGGATTTGCCGAACTCATCGGTAGCAACGGACCACAGAAGTTTTGCATTGACAAAG
TTGGCAAGGAAACCTGGCTGCCCAGAAGCCACACCTGCTTCAACCGTCTGGATCTTCCACCCTA
CAAGAGCTACGAACAGCTGAGAGAGAAGCTGCTGTATGCCATTGAGGAGACCGAGGGCTTTGGA
CAGGAGTAACCGAGGCCGCCCCTCCCACGCCCCCCAGCGCACATGTAGTCCTGAGTCCTCCCTG
CCTGAGAGGCCACTGGCCCCGCAGCCCTTGGGAGGCCCCCGTGGATGTGGCCCTGTGTGGGACC
ACACTGTCATCTCGCTGCTGGCAGAAAAGCCTGATCCCAGGAGGCCCTGCAGTTCCCCCGACCC
GCGGATGGCAGTCTGGAATAAAGCCCCCTAGTTGCCTTTGGCCCCACCTTTGCAAAGTTCCAGA
GGGCTGACCCTCTCTGCAAAACTCTCCCCTGTCCTCTAGACCCCACCCTGGGTGTATGTGAGTG
TGCAAGGGAAGGTGTTGCATCCCCAGGGGCTGCCGCAGAGGCCGGAGACCTCCTGGACTAGTTC
GGCGAGGAGACTGGCCACTGGGGGTGGCTGTTCGGGACTGAGAGCGCCAAGGGTCTTTGCCAGC
AAAGGAGGTTCTGCCTGTAATTGAGCCTCTCTGATGATGGAGATGAAGTGAAGGTCTGAGGGAG
CGGGCCCTGGGGCGAGGCCATCTCTGCCTGCCTCCCTAGCAGGCGCCAGCGGTGGAGGCTGAGT
CGCAGGACACATGCCGGCCAGTTAATTCATTCTCAGCCAATGAAGGTTTGTCTAAGCTGCCTGG
GTATCCACGGGACAAAAACAGCAAACTCCCTCAGACTTTGTCCATGTATAAACTTGAAGTGGTT
GTGTTGTAGGGTTGCAGGTTTTTTGTTACGCTGCTGTCACTTTCTGTCCAGGAGCTGGCACCCC
AGGTGTTCTGAGACCTTGAGGGACCCAGACCTTTGGGTCCAAGAGTTTCCCAAACAGCCACGCC
TCTCAGGAACCCACCTGGCGGTTCCGTGAGCTCAGGCAGGCCTGACCCGGCGGCACAGCCTGGC
AGGGACCTCGTCCCCAAGCCTGGCAGAATGAGAGGGGTTGAGGTCCCGAGCGCCACTCCTAGCC
TTGCCGCCTTCAATAGAGAAGAAATCCCTTTGCTAGATAGGGTCCCCCAGGCAGTCCCCAGTGG
CGGGACACAGGGGTCCGGCTGTGGAGCTCCCCTGCCAGCCCCTGGAGCTCCAGGAGGGCCTGTT
GGTCCCCTGTTCAGAATGGAGTGCAGCCCGCCAGCGGAAAGTGTTCATTCTGCATAGGTGTGAG
GCTTTATCTGCACACAGGACATGAAAACCAGCAGAAAGGCCCTGAGCTGCTGCATAGCCCCATC
TGATTTCTGCAGTTCCCGCCAGCCTCCAACACGGGGACTCTGCCGTAACTGGAATCTTCATAGG
TCATATTGAAATCTTCAAGGTGACCATGCCCCACCGGGGTGCTGGGGCAGTAGTCATGGCAGAC
TCCCGGCCTGGGCCCCCAGGATTCTAGGACCCCCAGGCAGCCCCTTGGACTGGTCCCGGGTGCC
TTCCAAGCACAGTCTCCATGCTCCCAGATTCTCGACCTTCCCCCGGCCCGGGAGGTGCAGCCTG
CGTCTGCCTCTGTCGTGTGTGCTGATTTGAGTGGCTTAGCTTGCCACAGCGCAGCCTCTTCTGT
CCCTTTCAGTCATTTGCTGTACTTCCCTGTGGCACGTTACCATGGAAGCCGCTCCAGGGTGGGT
CAGGGTGCAAGCTGCTGGTGAGGTTTGGAAGCATCAGGCTCACGGGTGTTCATGTGTGTTCGTG
CGTGTGTGTGCGTACGTGTATATAACTGAAGTGTCTGTACGGAATGCCCTTTGCTAGCCATGGG
CTGGTCACCAGATTGTTTTGTAATGCCCGCCCCTTGCCTCGATATTGCCAGTTTCTTGTGCAAT
AAACAATCAGCAGCTGTG

hide sequence

RefSeq Acc Id:

XM_017022881 ⟹ XP_016878370

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	69,762,332 - 69,941,739 (+)	NCBI

Sequence:

show sequence

ACCGCGCGCGGTCACGTGACCCGGCCCGAGTGCGGGCGGTGGAAGGCGGAAGTAGGAGAGGAGT
TCGGCGCCGCTTCTGTGGCCACGGCAGATGAAACAGAAAGGCTAAAGAGGGCTGGAGTCAGGGG
ACTTCTCTTCCACCAGGCTGGGGTGCAGCGGCGTGATCTCAGCTCACTCCAACCTCTGCTTCCC
AGGTTCAAGCGATTCTTCTGCCTCAGCCTCCGGATACCTGGGATTACAGCTTCACGGTGATGAT
ATGGCATCTGCCAGCTCTAGCCGGGCAGGAGTGGCCCTGCCTTTTGAGAAGTCTCAGCTCACTT
TGAAAGTGGTGTCCGCAAAGCCCAAGGTGCATAATCGTCAACCTCGAATTAACTCCTACGTGGA
GGTGGCGGTGGATGGACTCCCCAGTGAGACCAAGAAGACTGGGAAGCGCATTGGGAGCTCTGAG
CTTCTCTGGAATGAGATCATCATTTTGAATGTCACGGCACAGAGTCATTTAGATTTAAAGGTCT
GGAGCTGCCATACCTTGAGAAATGAACTGCTAGGCACCGCATCTGTCAACCTCTCCAACGTCTT
GAAGAACAATGGGGGCAAAATGGAGAACATGCAGCTGACCCTGAACCTGCAGACGGAGAACAAA
GGCAGCGTTGTCTCAGGCGGAGAGCTGACAATTTTCCTGGACGGGCCAACTGTTGATCTGGGAA
ATGTGCCTAATGGCAGTGCCCTGACAGATGGATCACAGCTGCCTTCGAGAGACTCCAGTGGAAC
AGCAGTAGCTCCAGAGAACCGGCACCAGCCCCCCAGCACAAACTGCTTTGGTGGAAGATCCCGG
ACGCACAGACATTCGGGTGCTTCAGCCAGAACAACCCCAGCAACCGGCGAGCAAAGCCCCGGTG
CTCGGAGCCGGCACCGCCAGCCCGTCAAGAACTCAGGCCACAGTGGCTTGGCCAATGGCACAGT
GAATGATGAACCCACAACAGCCACTGATCCCGAAGAACCTTCCGTTGTTGGTGTGACGTCCCCA
CCTGCTGCACCCTTGAGTGTGACCCCGAATCCCAACACGACTTCTCTCCCTGCCCCAGCCACAC
CGGCTGAAGGAGAGGAACCCAGCACTTCGGGTACACAGCAGCTCCCAGCGGCTGCCCAGGCCCC
CGACGCTCTGCCTGCTGGATGGGAACAGCGAGAGCTGCCCAACGGACGTGTCTATTATGTTGAC
CACAATACCAAGACCACCACCTGGGAGCGGCCCCTTCCTCCAGGCTGGGAAAAACGCACAGATC
CCCGAGGCAGGTTTTACTATGTGGATCACAATACTCGGACCACCACCTGGCAGCGTCCGACCGC
GGAGTACGTGCGCAACTATGAGCAGTGGCAGTCGCAGCGGAATCAGCTCCAGGGGGCCATGCAG
CACTTCAGCCAAAGATTCCTCTACCAGTCTTCGAGTGCTTCGACTGACCATGATCCCCTGGGCC
CCCTCCCTCCTGGCTGGGAGAAGAGACAGGACAATGGACGGGTGTATTACGTGAACCATAACAC
TCGCACGACCCAGTGGGAGGATCCCCGGACCCAGGGGATGATCCAGGAACCAGCTCTGCCCCCA
GGATGGGAGATGAAATACACCAGCGAGGGGGTGCGATACTTTGTGGACCACAATACCCGCACCA
CCACCTTTAAGGATCCTCGCCCGGGGTTTGAGTCGGGGACGAAGCAAGGTTCCCCTGGTGCTTA
TGACCGCAGTTTTCGGTGGAAGTATCACCAGTTCCGTTTCCTCTGCCATTCAAATGCCCTACCT
AGCCACGTGAAGATCAGCGTTTCCAGGCAGACGCTTTTCGAAGATTCCTTCCAACAGATCATGA
ACATGAAACCCTATGACCTGCGCCGCCGGCTCTACATCATCATGCGTGGCGAGGAGGGCCTGGA
CTATGGGGGCATCGCCAGAGAGTGGTTTTTCCTCCTGTCTCATGAGGTGCTCAACCCTATGTAT
TGTTTATTTGAATATGCCGGAAAGAACAATTACTGCCTGCAGATCAACCCCGCCTCCTCCATCA
ACCCGGACCACCTCACCTACTTTCGCTTTATAGGCAGATTCATCGCCATGGCGCTGTACCATGG
AAAGTTCATCGACACGGGCTTCACCCTCCCTTTCTACAAGCGGATGCTCAATAAGAGACCAACC
CTGAAAGACCTGGAGTCCATTGACCCTGAGTTCTACAACTCCATTGTCTGGATCAAAGAGAACA
ACCTGGAAGAATGTGGCCTGGAGCTGTACTTCATCCAGGACATGGAGATACTGGGCAAGGTGAC
GACCCACGAGCTGAAGGAGGGCGGCGAGAGCATCCGGGTCACAGAGGAGAACAAGGAAGAGTAC
ATCATGCTGCTGACTGACTGGCGTTTCACCCGAGGCGTGGAAGAGCAGACCAAAGCCTTCCTGG
ATGGCTTCAACGAGGTGGCCCCGCTGGAGTGGCTGCGCTACTTTGACGAGAAAGAGCTGGAGCT
GATGCTGTGCGGCATGCAGGAGATAGACATGAGCGACTGGCAGAAGAGCACCATCTACCGGCAC
TACACCAAGAACAGCAAGCAGATCCAGTGGTTCTGGCAGGTGGTGAAGGAGATGGACAACGAGA
AGAGGATCCGGCTGCTGCAGTTTGTCACCGGTACCTGCCGCCTGCCCGTCGGGGGATTTGCCGA
ACTCATCGGTAGCAACGGACCACAGAAGTTTTGCATTGACAAAGTTGGCAAGGAAACCTGGCTG
CCCAGAAGCCACACCTGCTTCAACCGTCTGGATCTTCCACCCTACAAGAGCTACGAACAGCTGA
GAGAGAAGCTGCTGTATGCCATTGAGGAGACCGAGGGCTTTGGACAGGAGTAACCGAGGCCGCC
CCTCCCACGCCCCCCAGCGCACATGTAGTCCTGAGTCCTCCCTGCCTGAGAGGCCACTGGCCCC
GCAGCCCTTGGGAGGCCCCCGTGGATGTGGCCCTGTGTGGGACCACACTGTCATCTCGCTGCTG
GCAGAAAAGCCTGATCCCAGGAGGCCCTGCAGTTCCCCCGACCCGCGGATGGCAGTCTGGAATA
AAGCCCCCTAGTTGCCTTTGGCCCCACCTTTGCAAAGTTCCAGAGGGCTGACCCTCTCTGCAAA
ACTCTCCCCTGTCCTCTAGACCCCACCCTGGGTGTATGTGAGTGTGCAAGGGAAGGTGTTGCAT
CCCCAGGGGCTGCCGCAGAGGCCGGAGACCTCCTGGACTAGTTCGGCGAGGAGACTGGCCACTG
GGGGTGGCTGTTCGGGACTGAGAGCGCCAAGGGTCTTTGCCAGCAAAGGAGGTTCTGCCTGTAA
TTGAGCCTCTCTGATGATGGAGATGAAGTGAAGGTCTGAGGGAGCGGGCCCTGGGGCGAGGCCA
TCTCTGCCTGCCTCCCTAGCAGGCGCCAGCGGTGGAGGCTGAGTCGCAGGACACATGCCGGCCA
GTTAATTCATTCTCAGCCAATGAAGGTTTGTCTAAGCTGCCTGGGTATCCACGGGACAAAAACA
GCAAACTCCCTCAGACTTTGTCCATGTATAAACTTGAAGTGGTTGTGTTGTAGGGTTGCAGGTT
TTTTGTTACGCTGCTGTCACTTTCTGTCCAGGAGCTGGCACCCCAGGTGTTCTGAGACCTTGAG
GGACCCAGACCTTTGGGTCCAAGAGTTTCCCAAACAGCCACGCCTCTCAGGAACCCACCTGGCG
GTTCCGTGAGCTCAGGCAGGCCTGACCCGGCGGCACAGCCTGGCAGGGACCTCGTCCCCAAGCC
TGGCAGAATGAGAGGGGTTGAGGTCCCGAGCGCCACTCCTAGCCTTGCCGCCTTCAATAGAGAA
GAAATCCCTTTGCTAGATAGGGTCCCCCAGGCAGTCCCCAGTGGCGGGACACAGGGGTCCGGCT
GTGGAGCTCCCCTGCCAGCCCCTGGAGCTCCAGGAGGGCCTGTTGGTCCCCTGTTCAGAATGGA
GTGCAGCCCGCCAGCGGAAAGTGTTCATTCTGCATAGGTGTGAGGCTTTATCTGCACACAGGAC
ATGAAAACCAGCAGAAAGGCCCTGAGCTGCTGCATAGCCCCATCTGATTTCTGCAGTTCCCGCC
AGCCTCCAACACGGGGACTCTGCCGTAACTGGAATCTTCATAGGTCATATTGAAATCTTCAAGG
TGACCATGCCCCACCGGGGTGCTGGGGCAGTAGTCATGGCAGACTCCCGGCCTGGGCCCCCAGG
ATTCTAGGACCCCCAGGCAGCCCCTTGGACTGGTCCCGGGTGCCTTCCAAGCACAGTCTCCATG
CTCCCAGATTCTCGACCTTCCCCCGGCCCGGGAGGTGCAGCCTGCGTCTGCCTCTGTCGTGTGT
GCTGATTTGAGTGGCTTAGCTTGCCACAGCGCAGCCTCTTCTGTCCCTTTCAGTCATTTGCTGT
ACTTCCCTGTGGCACGTTACCATGGAAGCCGCTCCAGGGTGGGTCAGGGTGCAAGCTGCTGGTG
AGGTTTGGAAGCATCAGGCTCACGGGTGTTCATGTGTGTTCGTGCGTGTGTGTGCGTACGTGTA
TATAACTGAAGTGTCTGTACGGAATGCCCTTTGCTAGCCATGGGCTGGTCACCAGATTGTTTTG
TAATGCCCGCCCCTTGCCTCGATATTGCCAGTTTCTTGTGCAATAAACAATCAGCAGCTGTG

hide sequence

RefSeq Acc Id:

XM_047433520 ⟹ XP_047289476

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	69,773,025 - 69,941,739 (+)	NCBI

RefSeq Acc Id:

XM_047433521 ⟹ XP_047289477

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	69,775,084 - 69,941,739 (+)	NCBI

RefSeq Acc Id:

XM_047433522 ⟹ XP_047289478

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	69,773,025 - 69,941,739 (+)	NCBI

RefSeq Acc Id:

XM_047433523 ⟹ XP_047289479

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	69,774,694 - 69,941,739 (+)	NCBI

RefSeq Acc Id:

XM_047433524 ⟹ XP_047289480

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	69,838,737 - 69,941,739 (+)	NCBI

RefSeq Acc Id:

XM_054379421 ⟹ XP_054235396

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	75,564,863 - 75,744,318 (+)	NCBI

RefSeq Acc Id:

XM_054379422 ⟹ XP_054235397

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	75,564,863 - 75,744,318 (+)	NCBI

RefSeq Acc Id:

XM_054379423 ⟹ XP_054235398

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	75,564,863 - 75,744,318 (+)	NCBI

RefSeq Acc Id:

XM_054379424 ⟹ XP_054235399

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	75,574,477 - 75,744,318 (+)	NCBI

RefSeq Acc Id:

XM_054379425 ⟹ XP_054235400

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	75,577,613 - 75,744,318 (+)	NCBI

RefSeq Acc Id:

XM_054379426 ⟹ XP_054235401

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	75,574,477 - 75,744,318 (+)	NCBI

RefSeq Acc Id:

XM_054379427 ⟹ XP_054235402

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	75,564,847 - 75,744,318 (+)	NCBI

RefSeq Acc Id:

XM_054379428 ⟹ XP_054235403

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	75,577,223 - 75,744,318 (+)	NCBI

RefSeq Acc Id:

XM_054379429 ⟹ XP_054235404

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	75,577,223 - 75,744,318 (+)	NCBI

RefSeq Acc Id:

XM_054379430 ⟹ XP_054235405

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	75,642,229 - 75,744,318 (+)	NCBI

RefSeq Acc Id:

XM_054379431 ⟹ XP_054235406

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	75,641,261 - 75,744,318 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_001257382	(Get FASTA)	NCBI Sequence Viewer
	NP_001257383	(Get FASTA)	NCBI Sequence Viewer
	NP_001257384	(Get FASTA)	NCBI Sequence Viewer
	NP_008945	(Get FASTA)	NCBI Sequence Viewer
	NP_955456	(Get FASTA)	NCBI Sequence Viewer
	XP_011521125	(Get FASTA)	NCBI Sequence Viewer
	XP_011521127	(Get FASTA)	NCBI Sequence Viewer
	XP_011521128	(Get FASTA)	NCBI Sequence Viewer
	XP_016878368	(Get FASTA)	NCBI Sequence Viewer
	XP_016878369	(Get FASTA)	NCBI Sequence Viewer
	XP_016878370	(Get FASTA)	NCBI Sequence Viewer
	XP_047289476	(Get FASTA)	NCBI Sequence Viewer
	XP_047289477	(Get FASTA)	NCBI Sequence Viewer
	XP_047289478	(Get FASTA)	NCBI Sequence Viewer
	XP_047289479	(Get FASTA)	NCBI Sequence Viewer
	XP_047289480	(Get FASTA)	NCBI Sequence Viewer
	XP_054235396	(Get FASTA)	NCBI Sequence Viewer
	XP_054235397	(Get FASTA)	NCBI Sequence Viewer
	XP_054235398	(Get FASTA)	NCBI Sequence Viewer
	XP_054235399	(Get FASTA)	NCBI Sequence Viewer
	XP_054235400	(Get FASTA)	NCBI Sequence Viewer
	XP_054235401	(Get FASTA)	NCBI Sequence Viewer
	XP_054235402	(Get FASTA)	NCBI Sequence Viewer
	XP_054235403	(Get FASTA)	NCBI Sequence Viewer
	XP_054235404	(Get FASTA)	NCBI Sequence Viewer
	XP_054235405	(Get FASTA)	NCBI Sequence Viewer
	XP_054235406	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAC51325	(Get FASTA)	NCBI Sequence Viewer
	AAH00108	(Get FASTA)	NCBI Sequence Viewer
	AAH13645	(Get FASTA)	NCBI Sequence Viewer
	AAH64531	(Get FASTA)	NCBI Sequence Viewer
	AFK29253	(Get FASTA)	NCBI Sequence Viewer
	BAC86528	(Get FASTA)	NCBI Sequence Viewer
	BAG35653	(Get FASTA)	NCBI Sequence Viewer
	BAG58117	(Get FASTA)	NCBI Sequence Viewer
	BAG58549	(Get FASTA)	NCBI Sequence Viewer
	BAG62027	(Get FASTA)	NCBI Sequence Viewer
	BAH14468	(Get FASTA)	NCBI Sequence Viewer
	EAW83287	(Get FASTA)	NCBI Sequence Viewer
	EAW83288	(Get FASTA)	NCBI Sequence Viewer
	EAW83289	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000348283
	ENSP00000348283.3
	ENSP00000352069
	ENSP00000352069.2
	ENSP00000455311
	ENSP00000455311.1
	ENSP00000455347.1
	ENSP00000456216
	ENSP00000456216.1
	ENSP00000456451.1
	ENSP00000456582.1
GenBank Protein	O00308	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_008945 ⟸ NM_007014
- Peptide Label:	isoform WWP2-FL
- UniProtKB:	Q96CZ2 (UniProtKB/Swiss-Prot), Q6ZTQ5 (UniProtKB/Swiss-Prot), I3RSG8 (UniProtKB/Swiss-Prot), H3BRF3 (UniProtKB/Swiss-Prot), F5H213 (UniProtKB/Swiss-Prot), B4DTL5 (UniProtKB/Swiss-Prot), B2R706 (UniProtKB/Swiss-Prot), A6NEP1 (UniProtKB/Swiss-Prot), Q9BWN6 (UniProtKB/Swiss-Prot), O00308 (UniProtKB/Swiss-Prot), B4DIN7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MASASSSRAGVALPFEKSQLTLKVVSAKPKVHNRQPRINSYVEVAVDGLPSETKKTGKRIGSSE LLWNEIIILNVTAQSHLDLKVWSCHTLRNELLGTASVNLSNVLKNNGGKMENMQLTLNLQTENK GSVVSGGELTIFLDGPTVDLGNVPNGSALTDGSQLPSRDSSGTAVAPENRHQPPSTNCFGGRSR THRHSGASARTTPATGEQSPGARSRHRQPVKNSGHSGLANGTVNDEPTTATDPEEPSVVGVTSP PAAPLSVTPNPNTTSLPAPATPAEGEEPSTSGTQQLPAAAQAPDALPAGWEQRELPNGRVYYVD HNTKTTTWERPLPPGWEKRTDPRGRFYYVDHNTRTTTWQRPTAEYVRNYEQWQSQRNQLQGAMQ HFSQRFLYQSSSASTDHDPLGPLPPGWEKRQDNGRVYYVNHNTRTTQWEDPRTQGMIQEPALPP GWEMKYTSEGVRYFVDHNTRTTTFKDPRPGFESGTKQGSPGAYDRSFRWKYHQFRFLCHSNALP SHVKISVSRQTLFEDSFQQIMNMKPYDLRRRLYIIMRGEEGLDYGGIAREWFFLLSHEVLNPMY CLFEYAGKNNYCLQINPASSINPDHLTYFRFIGRFIAMALYHGKFIDTGFTLPFYKRMLNKRPT LKDLESIDPEFYNSIVWIKENNLEECGLELYFIQDMEILGKVTTHELKEGGESIRVTEENKEEY IMLLTDWRFTRGVEEQTKAFLDGFNEVAPLEWLRYFDEKELELMLCGMQEIDMSDWQKSTIYRH YTKNSKQIQWFWQVVKEMDNEKRIRLLQFVTGTCRLPVGGFAELIGSNGPQKFCIDKVGKETWL PRSHTCFNRLDLPPYKSYEQLREKLLYAIEETEGFGQE hide sequence

RefSeq Acc Id:	NP_955456 ⟸ NM_199424
- Peptide Label:	isoform WWP2-C
- UniProtKB:	B4DHF6 (UniProtKB/TrEMBL)
- Sequence:	show sequence MIQEPALPPGWEMKYTSEGVRYFVDHNTRTTTFKDPRPGFESGTKQGSPGAYDRSFRWKYHQFR FLCHSNALPSHVKISVSRQTLFEDSFQQIMNMKPYDLRRRLYIIMRGEEGLDYGGIAREWFFLL SHEVLNPMYCLFEYAGKNNYCLQINPASSINPDHLTYFRFIGRFIAMALYHGKFIDTGFTLPFY KRMLNKRPTLKDLESIDPEFYNSIVWIKENNLEECGLELYFIQDMEILGKVTTHELKEGGESIR VTEENKEEYIMLLTDWRFTRGVEEQTKAFLDGFNEVAPLEWLRYFDEKELELMLCGMQEIDMSD WQKSTIYRHYTKNSKQIQWFWQVVKEMDNEKRIRLLQFVTGTCRLPVGGFAELIGSNGPQKFCI DKVGKETWLPRSHTCFNRLDLPPYKSYEQLREKLLYAIEETEGFGQE hide sequence

RefSeq Acc Id:	NP_001257383 ⟸ NM_001270454
- Peptide Label:	isoform WWP2-FL
- UniProtKB:	Q96CZ2 (UniProtKB/Swiss-Prot), Q6ZTQ5 (UniProtKB/Swiss-Prot), I3RSG8 (UniProtKB/Swiss-Prot), H3BRF3 (UniProtKB/Swiss-Prot), F5H213 (UniProtKB/Swiss-Prot), B4DTL5 (UniProtKB/Swiss-Prot), B2R706 (UniProtKB/Swiss-Prot), A6NEP1 (UniProtKB/Swiss-Prot), Q9BWN6 (UniProtKB/Swiss-Prot), O00308 (UniProtKB/Swiss-Prot), B4DIN7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MASASSSRAGVALPFEKSQLTLKVVSAKPKVHNRQPRINSYVEVAVDGLPSETKKTGKRIGSSE LLWNEIIILNVTAQSHLDLKVWSCHTLRNELLGTASVNLSNVLKNNGGKMENMQLTLNLQTENK GSVVSGGELTIFLDGPTVDLGNVPNGSALTDGSQLPSRDSSGTAVAPENRHQPPSTNCFGGRSR THRHSGASARTTPATGEQSPGARSRHRQPVKNSGHSGLANGTVNDEPTTATDPEEPSVVGVTSP PAAPLSVTPNPNTTSLPAPATPAEGEEPSTSGTQQLPAAAQAPDALPAGWEQRELPNGRVYYVD HNTKTTTWERPLPPGWEKRTDPRGRFYYVDHNTRTTTWQRPTAEYVRNYEQWQSQRNQLQGAMQ HFSQRFLYQSSSASTDHDPLGPLPPGWEKRQDNGRVYYVNHNTRTTQWEDPRTQGMIQEPALPP GWEMKYTSEGVRYFVDHNTRTTTFKDPRPGFESGTKQGSPGAYDRSFRWKYHQFRFLCHSNALP SHVKISVSRQTLFEDSFQQIMNMKPYDLRRRLYIIMRGEEGLDYGGIAREWFFLLSHEVLNPMY CLFEYAGKNNYCLQINPASSINPDHLTYFRFIGRFIAMALYHGKFIDTGFTLPFYKRMLNKRPT LKDLESIDPEFYNSIVWIKENNLEECGLELYFIQDMEILGKVTTHELKEGGESIRVTEENKEEY IMLLTDWRFTRGVEEQTKAFLDGFNEVAPLEWLRYFDEKELELMLCGMQEIDMSDWQKSTIYRH YTKNSKQIQWFWQVVKEMDNEKRIRLLQFVTGTCRLPVGGFAELIGSNGPQKFCIDKVGKETWL PRSHTCFNRLDLPPYKSYEQLREKLLYAIEETEGFGQE hide sequence

RefSeq Acc Id:	NP_001257384 ⟸ NM_001270455
- Peptide Label:	isoform WWP2-N
- UniProtKB:	O00308 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MASASSSRAGVALPFEKSQLTLKVVSAKPKVHNRQPRINSYVEVAVDGLPSETKKTGKRIGSSE LLWNEIIILNVTAQSHLDLKVWSCHTLRNELLGTASVNLSNVLKNNGGKMENMQLTLNLQTENK GSVVSGGELTIFLDGPTVDLGNVPNGSALTDGSQLPSRDSSGTAVAPENRHQPPSTNCFGGRSR THRHSGASARTTPATGEQSPGARSRHRQPVKNSGHSGLANGTVNDEPTTATDPEEPSVVGVTSP PAAPLSVTPNPNTTSLPAPATPAEGEEPSTSGTQQLPAAAQAPDALPAGWEQRELPNGRVYYVD HNTKTTTWERPLPPG hide sequence

RefSeq Acc Id:	NP_001257382 ⟸ NM_001270453
- Peptide Label:	isoform 4
- UniProtKB:	B4DIN7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MQLTLNLQTENKGSVVSGGELTIFLDGPTVDLGNVPNGSALTDGSQLPSRDSSGTAVAPENRHQ PPSTNCFGGRSRTHRHSGASARTTPATGEQSPGARSRHRQPVKNSGHSGLANGTVNDEPTTATD PEEPSVVGVTSPPAAPLSVTPNPNTTSLPAPATPAEGEEPSTSGTQQLPAAAQAPDALPAGWEQ RELPNGRVYYVDHNTKTTTWERPLPPGWEKRTDPRGRFYYVDHNTRTTTWQRPTAEYVRNYEQW QSQRNQLQGAMQHFSQRFLYQSSSASTDHDPLGPLPPGWEKRQDNGRVYYVNHNTRTTQWEDPR TQGMIQEPALPPGWEMKYTSEGVRYFVDHNTRTTTFKDPRPGFESGTKQGSPGAYDRSFRWKYH QFRFLCHSNALPSHVKISVSRQTLFEDSFQQIMNMKPYDLRRRLYIIMRGEEGLDYGGIAREWF FLLSHEVLNPMYCLFEYAGKNNYCLQINPASSINPDHLTYFRFIGRFIAMALYHGKFIDTGFTL PFYKRMLNKRPTLKDLESIDPEFYNSIVWIKENNLEECGLELYFIQDMEILGKVTTHELKEGGE SIRVTEENKEEYIMLLTDWRFTRGVEEQTKAFLDGFNEVAPLEWLRYFDEKELELMLCGMQEID MSDWQKSTIYRHYTKNSKQIQWFWQVVKEMDNEKRIRLLQFVTGTCRLPVGGFAELIGSNGPQK FCIDKVGKETWLPRSHTCFNRLDLPPYKSYEQLREKLLYAIEETEGFGQE hide sequence

RefSeq Acc Id:	XP_011521125 ⟸ XM_011522823
- Peptide Label:	isoform X1
- UniProtKB:	Q96CZ2 (UniProtKB/Swiss-Prot), Q6ZTQ5 (UniProtKB/Swiss-Prot), I3RSG8 (UniProtKB/Swiss-Prot), H3BRF3 (UniProtKB/Swiss-Prot), F5H213 (UniProtKB/Swiss-Prot), B4DTL5 (UniProtKB/Swiss-Prot), B2R706 (UniProtKB/Swiss-Prot), A6NEP1 (UniProtKB/Swiss-Prot), Q9BWN6 (UniProtKB/Swiss-Prot), O00308 (UniProtKB/Swiss-Prot), B4DIN7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MASASSSRAGVALPFEKSQLTLKVVSAKPKVHNRQPRINSYVEVAVDGLPSETKKTGKRIGSSE LLWNEIIILNVTAQSHLDLKVWSCHTLRNELLGTASVNLSNVLKNNGGKMENMQLTLNLQTENK GSVVSGGELTIFLDGPTVDLGNVPNGSALTDGSQLPSRDSSGTAVAPENRHQPPSTNCFGGRSR THRHSGASARTTPATGEQSPGARSRHRQPVKNSGHSGLANGTVNDEPTTATDPEEPSVVGVTSP PAAPLSVTPNPNTTSLPAPATPAEGEEPSTSGTQQLPAAAQAPDALPAGWEQRELPNGRVYYVD HNTKTTTWERPLPPGWEKRTDPRGRFYYVDHNTRTTTWQRPTAEYVRNYEQWQSQRNQLQGAMQ HFSQRFLYQSSSASTDHDPLGPLPPGWEKRQDNGRVYYVNHNTRTTQWEDPRTQGMIQEPALPP GWEMKYTSEGVRYFVDHNTRTTTFKDPRPGFESGTKQGSPGAYDRSFRWKYHQFRFLCHSNALP SHVKISVSRQTLFEDSFQQIMNMKPYDLRRRLYIIMRGEEGLDYGGIAREWFFLLSHEVLNPMY CLFEYAGKNNYCLQINPASSINPDHLTYFRFIGRFIAMALYHGKFIDTGFTLPFYKRMLNKRPT LKDLESIDPEFYNSIVWIKENNLEECGLELYFIQDMEILGKVTTHELKEGGESIRVTEENKEEY IMLLTDWRFTRGVEEQTKAFLDGFNEVAPLEWLRYFDEKELELMLCGMQEIDMSDWQKSTIYRH YTKNSKQIQWFWQVVKEMDNEKRIRLLQFVTGTCRLPVGGFAELIGSNGPQKFCIDKVGKETWL PRSHTCFNRLDLPPYKSYEQLREKLLYAIEETEGFGQE hide sequence

RefSeq Acc Id:	XP_011521127 ⟸ XM_011522825
- Peptide Label:	isoform X1
- UniProtKB:	Q96CZ2 (UniProtKB/Swiss-Prot), Q6ZTQ5 (UniProtKB/Swiss-Prot), I3RSG8 (UniProtKB/Swiss-Prot), H3BRF3 (UniProtKB/Swiss-Prot), F5H213 (UniProtKB/Swiss-Prot), B4DTL5 (UniProtKB/Swiss-Prot), B2R706 (UniProtKB/Swiss-Prot), A6NEP1 (UniProtKB/Swiss-Prot), Q9BWN6 (UniProtKB/Swiss-Prot), O00308 (UniProtKB/Swiss-Prot), B4DIN7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MASASSSRAGVALPFEKSQLTLKVVSAKPKVHNRQPRINSYVEVAVDGLPSETKKTGKRIGSSE LLWNEIIILNVTAQSHLDLKVWSCHTLRNELLGTASVNLSNVLKNNGGKMENMQLTLNLQTENK GSVVSGGELTIFLDGPTVDLGNVPNGSALTDGSQLPSRDSSGTAVAPENRHQPPSTNCFGGRSR THRHSGASARTTPATGEQSPGARSRHRQPVKNSGHSGLANGTVNDEPTTATDPEEPSVVGVTSP PAAPLSVTPNPNTTSLPAPATPAEGEEPSTSGTQQLPAAAQAPDALPAGWEQRELPNGRVYYVD HNTKTTTWERPLPPGWEKRTDPRGRFYYVDHNTRTTTWQRPTAEYVRNYEQWQSQRNQLQGAMQ HFSQRFLYQSSSASTDHDPLGPLPPGWEKRQDNGRVYYVNHNTRTTQWEDPRTQGMIQEPALPP GWEMKYTSEGVRYFVDHNTRTTTFKDPRPGFESGTKQGSPGAYDRSFRWKYHQFRFLCHSNALP SHVKISVSRQTLFEDSFQQIMNMKPYDLRRRLYIIMRGEEGLDYGGIAREWFFLLSHEVLNPMY CLFEYAGKNNYCLQINPASSINPDHLTYFRFIGRFIAMALYHGKFIDTGFTLPFYKRMLNKRPT LKDLESIDPEFYNSIVWIKENNLEECGLELYFIQDMEILGKVTTHELKEGGESIRVTEENKEEY IMLLTDWRFTRGVEEQTKAFLDGFNEVAPLEWLRYFDEKELELMLCGMQEIDMSDWQKSTIYRH YTKNSKQIQWFWQVVKEMDNEKRIRLLQFVTGTCRLPVGGFAELIGSNGPQKFCIDKVGKETWL PRSHTCFNRLDLPPYKSYEQLREKLLYAIEETEGFGQE hide sequence

RefSeq Acc Id:	XP_011521128 ⟸ XM_011522826
- Peptide Label:	isoform X2
- UniProtKB:	B4DIN7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MQLTLNLQTENKGSVVSGGELTIFLDGPTVDLGNVPNGSALTDGSQLPSRDSSGTAVAPENRHQ PPSTNCFGGRSRTHRHSGASARTTPATGEQSPGARSRHRQPVKNSGHSGLANGTVNDEPTTATD PEEPSVVGVTSPPAAPLSVTPNPNTTSLPAPATPAEGEEPSTSGTQQLPAAAQAPDALPAGWEQ RELPNGRVYYVDHNTKTTTWERPLPPGWEKRTDPRGRFYYVDHNTRTTTWQRPTAEYVRNYEQW QSQRNQLQGAMQHFSQRFLYQSSSASTDHDPLGPLPPGWEKRQDNGRVYYVNHNTRTTQWEDPR TQGMIQEPALPPGWEMKYTSEGVRYFVDHNTRTTTFKDPRPGFESGTKQGSPGAYDRSFRWKYH QFRFLCHSNALPSHVKISVSRQTLFEDSFQQIMNMKPYDLRRRLYIIMRGEEGLDYGGIAREWF FLLSHEVLNPMYCLFEYAGKNNYCLQINPASSINPDHLTYFRFIGRFIAMALYHGKFIDTGFTL PFYKRMLNKRPTLKDLESIDPEFYNSIVWIKENNLEECGLELYFIQDMEILGKVTTHELKEGGE SIRVTEENKEEYIMLLTDWRFTRGVEEQTKAFLDGFNEVAPLEWLRYFDEKELELMLCGMQEID MSDWQKSTIYRHYTKNSKQIQWFWQVVKEMDNEKRIRLLQFVTGTCRLPVGGFAELIGSNGPQK FCIDKVGKETWLPRSHTCFNRLDLPPYKSYEQLREKLLYAIEETEGFGQE hide sequence

RefSeq Acc Id:	XP_016878368 ⟸ XM_017022879
- Peptide Label:	isoform X1
- UniProtKB:	Q96CZ2 (UniProtKB/Swiss-Prot), Q6ZTQ5 (UniProtKB/Swiss-Prot), I3RSG8 (UniProtKB/Swiss-Prot), H3BRF3 (UniProtKB/Swiss-Prot), F5H213 (UniProtKB/Swiss-Prot), B4DTL5 (UniProtKB/Swiss-Prot), B2R706 (UniProtKB/Swiss-Prot), A6NEP1 (UniProtKB/Swiss-Prot), Q9BWN6 (UniProtKB/Swiss-Prot), O00308 (UniProtKB/Swiss-Prot), B4DIN7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MASASSSRAGVALPFEKSQLTLKVVSAKPKVHNRQPRINSYVEVAVDGLPSETKKTGKRIGSSE LLWNEIIILNVTAQSHLDLKVWSCHTLRNELLGTASVNLSNVLKNNGGKMENMQLTLNLQTENK GSVVSGGELTIFLDGPTVDLGNVPNGSALTDGSQLPSRDSSGTAVAPENRHQPPSTNCFGGRSR THRHSGASARTTPATGEQSPGARSRHRQPVKNSGHSGLANGTVNDEPTTATDPEEPSVVGVTSP PAAPLSVTPNPNTTSLPAPATPAEGEEPSTSGTQQLPAAAQAPDALPAGWEQRELPNGRVYYVD HNTKTTTWERPLPPGWEKRTDPRGRFYYVDHNTRTTTWQRPTAEYVRNYEQWQSQRNQLQGAMQ HFSQRFLYQSSSASTDHDPLGPLPPGWEKRQDNGRVYYVNHNTRTTQWEDPRTQGMIQEPALPP GWEMKYTSEGVRYFVDHNTRTTTFKDPRPGFESGTKQGSPGAYDRSFRWKYHQFRFLCHSNALP SHVKISVSRQTLFEDSFQQIMNMKPYDLRRRLYIIMRGEEGLDYGGIAREWFFLLSHEVLNPMY CLFEYAGKNNYCLQINPASSINPDHLTYFRFIGRFIAMALYHGKFIDTGFTLPFYKRMLNKRPT LKDLESIDPEFYNSIVWIKENNLEECGLELYFIQDMEILGKVTTHELKEGGESIRVTEENKEEY IMLLTDWRFTRGVEEQTKAFLDGFNEVAPLEWLRYFDEKELELMLCGMQEIDMSDWQKSTIYRH YTKNSKQIQWFWQVVKEMDNEKRIRLLQFVTGTCRLPVGGFAELIGSNGPQKFCIDKVGKETWL PRSHTCFNRLDLPPYKSYEQLREKLLYAIEETEGFGQE hide sequence

RefSeq Acc Id:	XP_016878370 ⟸ XM_017022881
- Peptide Label:	isoform X1
- UniProtKB:	Q96CZ2 (UniProtKB/Swiss-Prot), Q6ZTQ5 (UniProtKB/Swiss-Prot), I3RSG8 (UniProtKB/Swiss-Prot), H3BRF3 (UniProtKB/Swiss-Prot), F5H213 (UniProtKB/Swiss-Prot), B4DTL5 (UniProtKB/Swiss-Prot), B2R706 (UniProtKB/Swiss-Prot), A6NEP1 (UniProtKB/Swiss-Prot), Q9BWN6 (UniProtKB/Swiss-Prot), O00308 (UniProtKB/Swiss-Prot), B4DIN7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MASASSSRAGVALPFEKSQLTLKVVSAKPKVHNRQPRINSYVEVAVDGLPSETKKTGKRIGSSE LLWNEIIILNVTAQSHLDLKVWSCHTLRNELLGTASVNLSNVLKNNGGKMENMQLTLNLQTENK GSVVSGGELTIFLDGPTVDLGNVPNGSALTDGSQLPSRDSSGTAVAPENRHQPPSTNCFGGRSR THRHSGASARTTPATGEQSPGARSRHRQPVKNSGHSGLANGTVNDEPTTATDPEEPSVVGVTSP PAAPLSVTPNPNTTSLPAPATPAEGEEPSTSGTQQLPAAAQAPDALPAGWEQRELPNGRVYYVD HNTKTTTWERPLPPGWEKRTDPRGRFYYVDHNTRTTTWQRPTAEYVRNYEQWQSQRNQLQGAMQ HFSQRFLYQSSSASTDHDPLGPLPPGWEKRQDNGRVYYVNHNTRTTQWEDPRTQGMIQEPALPP GWEMKYTSEGVRYFVDHNTRTTTFKDPRPGFESGTKQGSPGAYDRSFRWKYHQFRFLCHSNALP SHVKISVSRQTLFEDSFQQIMNMKPYDLRRRLYIIMRGEEGLDYGGIAREWFFLLSHEVLNPMY CLFEYAGKNNYCLQINPASSINPDHLTYFRFIGRFIAMALYHGKFIDTGFTLPFYKRMLNKRPT LKDLESIDPEFYNSIVWIKENNLEECGLELYFIQDMEILGKVTTHELKEGGESIRVTEENKEEY IMLLTDWRFTRGVEEQTKAFLDGFNEVAPLEWLRYFDEKELELMLCGMQEIDMSDWQKSTIYRH YTKNSKQIQWFWQVVKEMDNEKRIRLLQFVTGTCRLPVGGFAELIGSNGPQKFCIDKVGKETWL PRSHTCFNRLDLPPYKSYEQLREKLLYAIEETEGFGQE hide sequence

RefSeq Acc Id:	XP_016878369 ⟸ XM_017022880
- Peptide Label:	isoform X1
- UniProtKB:	Q96CZ2 (UniProtKB/Swiss-Prot), Q6ZTQ5 (UniProtKB/Swiss-Prot), I3RSG8 (UniProtKB/Swiss-Prot), H3BRF3 (UniProtKB/Swiss-Prot), F5H213 (UniProtKB/Swiss-Prot), B4DTL5 (UniProtKB/Swiss-Prot), B2R706 (UniProtKB/Swiss-Prot), A6NEP1 (UniProtKB/Swiss-Prot), Q9BWN6 (UniProtKB/Swiss-Prot), O00308 (UniProtKB/Swiss-Prot), B4DIN7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MASASSSRAGVALPFEKSQLTLKVVSAKPKVHNRQPRINSYVEVAVDGLPSETKKTGKRIGSSE LLWNEIIILNVTAQSHLDLKVWSCHTLRNELLGTASVNLSNVLKNNGGKMENMQLTLNLQTENK GSVVSGGELTIFLDGPTVDLGNVPNGSALTDGSQLPSRDSSGTAVAPENRHQPPSTNCFGGRSR THRHSGASARTTPATGEQSPGARSRHRQPVKNSGHSGLANGTVNDEPTTATDPEEPSVVGVTSP PAAPLSVTPNPNTTSLPAPATPAEGEEPSTSGTQQLPAAAQAPDALPAGWEQRELPNGRVYYVD HNTKTTTWERPLPPGWEKRTDPRGRFYYVDHNTRTTTWQRPTAEYVRNYEQWQSQRNQLQGAMQ HFSQRFLYQSSSASTDHDPLGPLPPGWEKRQDNGRVYYVNHNTRTTQWEDPRTQGMIQEPALPP GWEMKYTSEGVRYFVDHNTRTTTFKDPRPGFESGTKQGSPGAYDRSFRWKYHQFRFLCHSNALP SHVKISVSRQTLFEDSFQQIMNMKPYDLRRRLYIIMRGEEGLDYGGIAREWFFLLSHEVLNPMY CLFEYAGKNNYCLQINPASSINPDHLTYFRFIGRFIAMALYHGKFIDTGFTLPFYKRMLNKRPT LKDLESIDPEFYNSIVWIKENNLEECGLELYFIQDMEILGKVTTHELKEGGESIRVTEENKEEY IMLLTDWRFTRGVEEQTKAFLDGFNEVAPLEWLRYFDEKELELMLCGMQEIDMSDWQKSTIYRH YTKNSKQIQWFWQVVKEMDNEKRIRLLQFVTGTCRLPVGGFAELIGSNGPQKFCIDKVGKETWL PRSHTCFNRLDLPPYKSYEQLREKLLYAIEETEGFGQE hide sequence

Ensembl Acc Id:

ENSP00000352069 ⟸ ENST00000359154

Ensembl Acc Id:

ENSP00000456582 ⟸ ENST00000569620

Ensembl Acc Id:

ENSP00000456451 ⟸ ENST00000561780

Ensembl Acc Id:

ENSP00000455347 ⟸ ENST00000563659

Ensembl Acc Id:

ENSP00000348283 ⟸ ENST00000356003

Ensembl Acc Id:

ENSP00000456216 ⟸ ENST00000568684

Ensembl Acc Id:

ENSP00000455311 ⟸ ENST00000569174

RefSeq Acc Id:	XP_047289476 ⟸ XM_047433520
- Peptide Label:	isoform X1
- UniProtKB:	Q96CZ2 (UniProtKB/Swiss-Prot), Q6ZTQ5 (UniProtKB/Swiss-Prot), O00308 (UniProtKB/Swiss-Prot), I3RSG8 (UniProtKB/Swiss-Prot), H3BRF3 (UniProtKB/Swiss-Prot), F5H213 (UniProtKB/Swiss-Prot), B4DTL5 (UniProtKB/Swiss-Prot), B2R706 (UniProtKB/Swiss-Prot), A6NEP1 (UniProtKB/Swiss-Prot), Q9BWN6 (UniProtKB/Swiss-Prot), B4DIN7 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047289478 ⟸ XM_047433522
- Peptide Label:	isoform X1
- UniProtKB:	Q96CZ2 (UniProtKB/Swiss-Prot), Q6ZTQ5 (UniProtKB/Swiss-Prot), O00308 (UniProtKB/Swiss-Prot), I3RSG8 (UniProtKB/Swiss-Prot), H3BRF3 (UniProtKB/Swiss-Prot), F5H213 (UniProtKB/Swiss-Prot), B4DTL5 (UniProtKB/Swiss-Prot), B2R706 (UniProtKB/Swiss-Prot), A6NEP1 (UniProtKB/Swiss-Prot), Q9BWN6 (UniProtKB/Swiss-Prot), B4DIN7 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047289479 ⟸ XM_047433523
- Peptide Label:	isoform X1
- UniProtKB:	Q96CZ2 (UniProtKB/Swiss-Prot), Q6ZTQ5 (UniProtKB/Swiss-Prot), O00308 (UniProtKB/Swiss-Prot), I3RSG8 (UniProtKB/Swiss-Prot), H3BRF3 (UniProtKB/Swiss-Prot), F5H213 (UniProtKB/Swiss-Prot), B4DTL5 (UniProtKB/Swiss-Prot), B2R706 (UniProtKB/Swiss-Prot), A6NEP1 (UniProtKB/Swiss-Prot), Q9BWN6 (UniProtKB/Swiss-Prot), B4DIN7 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047289477 ⟸ XM_047433521
- Peptide Label:	isoform X1
- UniProtKB:	Q96CZ2 (UniProtKB/Swiss-Prot), Q6ZTQ5 (UniProtKB/Swiss-Prot), O00308 (UniProtKB/Swiss-Prot), I3RSG8 (UniProtKB/Swiss-Prot), H3BRF3 (UniProtKB/Swiss-Prot), F5H213 (UniProtKB/Swiss-Prot), B4DTL5 (UniProtKB/Swiss-Prot), B2R706 (UniProtKB/Swiss-Prot), A6NEP1 (UniProtKB/Swiss-Prot), Q9BWN6 (UniProtKB/Swiss-Prot), B4DIN7 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047289480 ⟸ XM_047433524
- Peptide Label:	isoform X2
- UniProtKB:	B4DIN7 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054235402 ⟸ XM_054379427
- Peptide Label:	isoform X1
- UniProtKB:	F5H213 (UniProtKB/Swiss-Prot), B4DTL5 (UniProtKB/Swiss-Prot), B2R706 (UniProtKB/Swiss-Prot), A6NEP1 (UniProtKB/Swiss-Prot), Q96CZ2 (UniProtKB/Swiss-Prot), Q6ZTQ5 (UniProtKB/Swiss-Prot), O00308 (UniProtKB/Swiss-Prot), I3RSG8 (UniProtKB/Swiss-Prot), H3BRF3 (UniProtKB/Swiss-Prot), Q9BWN6 (UniProtKB/Swiss-Prot), B4DIN7 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054235396 ⟸ XM_054379421
- Peptide Label:	isoform X1
- UniProtKB:	Q96CZ2 (UniProtKB/Swiss-Prot), Q6ZTQ5 (UniProtKB/Swiss-Prot), O00308 (UniProtKB/Swiss-Prot), I3RSG8 (UniProtKB/Swiss-Prot), H3BRF3 (UniProtKB/Swiss-Prot), F5H213 (UniProtKB/Swiss-Prot), B4DTL5 (UniProtKB/Swiss-Prot), B2R706 (UniProtKB/Swiss-Prot), A6NEP1 (UniProtKB/Swiss-Prot), Q9BWN6 (UniProtKB/Swiss-Prot), B4DIN7 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054235397 ⟸ XM_054379422
- Peptide Label:	isoform X1
- UniProtKB:	Q96CZ2 (UniProtKB/Swiss-Prot), Q6ZTQ5 (UniProtKB/Swiss-Prot), O00308 (UniProtKB/Swiss-Prot), I3RSG8 (UniProtKB/Swiss-Prot), H3BRF3 (UniProtKB/Swiss-Prot), F5H213 (UniProtKB/Swiss-Prot), B4DTL5 (UniProtKB/Swiss-Prot), B2R706 (UniProtKB/Swiss-Prot), A6NEP1 (UniProtKB/Swiss-Prot), Q9BWN6 (UniProtKB/Swiss-Prot), B4DIN7 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054235398 ⟸ XM_054379423
- Peptide Label:	isoform X1
- UniProtKB:	Q96CZ2 (UniProtKB/Swiss-Prot), Q6ZTQ5 (UniProtKB/Swiss-Prot), O00308 (UniProtKB/Swiss-Prot), I3RSG8 (UniProtKB/Swiss-Prot), H3BRF3 (UniProtKB/Swiss-Prot), F5H213 (UniProtKB/Swiss-Prot), B4DTL5 (UniProtKB/Swiss-Prot), B2R706 (UniProtKB/Swiss-Prot), A6NEP1 (UniProtKB/Swiss-Prot), Q9BWN6 (UniProtKB/Swiss-Prot), B4DIN7 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054235399 ⟸ XM_054379424
- Peptide Label:	isoform X1
- UniProtKB:	Q96CZ2 (UniProtKB/Swiss-Prot), Q6ZTQ5 (UniProtKB/Swiss-Prot), O00308 (UniProtKB/Swiss-Prot), I3RSG8 (UniProtKB/Swiss-Prot), H3BRF3 (UniProtKB/Swiss-Prot), F5H213 (UniProtKB/Swiss-Prot), B4DTL5 (UniProtKB/Swiss-Prot), B2R706 (UniProtKB/Swiss-Prot), A6NEP1 (UniProtKB/Swiss-Prot), Q9BWN6 (UniProtKB/Swiss-Prot), B4DIN7 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054235401 ⟸ XM_054379426
- Peptide Label:	isoform X1
- UniProtKB:	Q96CZ2 (UniProtKB/Swiss-Prot), Q6ZTQ5 (UniProtKB/Swiss-Prot), O00308 (UniProtKB/Swiss-Prot), I3RSG8 (UniProtKB/Swiss-Prot), H3BRF3 (UniProtKB/Swiss-Prot), F5H213 (UniProtKB/Swiss-Prot), B4DTL5 (UniProtKB/Swiss-Prot), B2R706 (UniProtKB/Swiss-Prot), A6NEP1 (UniProtKB/Swiss-Prot), Q9BWN6 (UniProtKB/Swiss-Prot), B4DIN7 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054235403 ⟸ XM_054379428
- Peptide Label:	isoform X1
- UniProtKB:	Q96CZ2 (UniProtKB/Swiss-Prot), Q6ZTQ5 (UniProtKB/Swiss-Prot), O00308 (UniProtKB/Swiss-Prot), I3RSG8 (UniProtKB/Swiss-Prot), H3BRF3 (UniProtKB/Swiss-Prot), F5H213 (UniProtKB/Swiss-Prot), B4DTL5 (UniProtKB/Swiss-Prot), B2R706 (UniProtKB/Swiss-Prot), A6NEP1 (UniProtKB/Swiss-Prot), Q9BWN6 (UniProtKB/Swiss-Prot), B4DIN7 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054235404 ⟸ XM_054379429
- Peptide Label:	isoform X1
- UniProtKB:	Q96CZ2 (UniProtKB/Swiss-Prot), Q6ZTQ5 (UniProtKB/Swiss-Prot), O00308 (UniProtKB/Swiss-Prot), I3RSG8 (UniProtKB/Swiss-Prot), H3BRF3 (UniProtKB/Swiss-Prot), F5H213 (UniProtKB/Swiss-Prot), B4DTL5 (UniProtKB/Swiss-Prot), B2R706 (UniProtKB/Swiss-Prot), A6NEP1 (UniProtKB/Swiss-Prot), Q9BWN6 (UniProtKB/Swiss-Prot), B4DIN7 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054235400 ⟸ XM_054379425
- Peptide Label:	isoform X1
- UniProtKB:	Q96CZ2 (UniProtKB/Swiss-Prot), Q6ZTQ5 (UniProtKB/Swiss-Prot), O00308 (UniProtKB/Swiss-Prot), I3RSG8 (UniProtKB/Swiss-Prot), H3BRF3 (UniProtKB/Swiss-Prot), F5H213 (UniProtKB/Swiss-Prot), B4DTL5 (UniProtKB/Swiss-Prot), B2R706 (UniProtKB/Swiss-Prot), A6NEP1 (UniProtKB/Swiss-Prot), Q9BWN6 (UniProtKB/Swiss-Prot), B4DIN7 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054235406 ⟸ XM_054379431
- Peptide Label:	isoform X2
- UniProtKB:	B4DIN7 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054235405 ⟸ XM_054379430
- Peptide Label:	isoform X2
- UniProtKB:	B4DIN7 (UniProtKB/TrEMBL)

Protein Domains

C2 HECT WW

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-O00308-F1-model_v2	AlphaFold	O00308	1-870	view protein structure

Promoters

RGD ID:

6793605

Promoter ID:

HG_KWN:24134

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, CD4+TCell_12Hour, CD4+TCell_2Hour, HeLa_S3, Jurkat, K562, Lymphoblastoid, NB4

Transcripts:

ENST00000359154, NM_007014, NM_199423

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	16	68,353,476 - 68,353,976 (+)	MPROMDB

RGD ID:

7232721

Promoter ID:

EPDNEW_H22106

Type:

initiation region

Name:

WWP2_1

Description:

WW domain containing E3 ubiquitin protein ligase 2

SO ACC ID:

SO:0000170

Source:

EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	69,762,332 - 69,762,392	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:16804	AgrOrtholog
COSMIC	WWP2	COSMIC
Ensembl Genes	ENSG00000198373	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000356003	ENTREZGENE
	ENST00000356003.6	UniProtKB/Swiss-Prot
	ENST00000359154	ENTREZGENE
	ENST00000359154.7	UniProtKB/Swiss-Prot
	ENST00000561780.5	UniProtKB/TrEMBL
	ENST00000563659.5	UniProtKB/TrEMBL
	ENST00000568684	ENTREZGENE
	ENST00000568684.1	UniProtKB/Swiss-Prot
	ENST00000569174	ENTREZGENE
	ENST00000569174.5	UniProtKB/Swiss-Prot
	ENST00000569620.5	UniProtKB/TrEMBL
Gene3D-CATH	2.20.70.10	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	2.60.40.150	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Hect, E3 ligase catalytic domain	UniProtKB/Swiss-Prot
	Hect, E3 ligase catalytic domain	UniProtKB/Swiss-Prot
	Hect, E3 ligase catalytic domain	UniProtKB/TrEMBL
	Hect, E3 ligase catalytic domain	UniProtKB/TrEMBL
	Hect, E3 ligase catalytic domains	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000198373	GTEx
HGNC ID	HGNC:16804	ENTREZGENE
Human Proteome Map	WWP2	Human Proteome Map
InterPro	C2_dom	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	C2_domain_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	E3_ub_ligase_SMURF1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	E3_ubiq-protein_ligase	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	HECT_dom	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Hect_E3_ubiquitin_ligase	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	WW_dom	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	WW_dom_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:11060	UniProtKB/Swiss-Prot
NCBI Gene	11060	ENTREZGENE
OMIM	602308	OMIM
PANTHER	HECT DOMAIN UBIQUITIN-PROTEIN LIGASE	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	NEDD4-LIKE E3 UBIQUITIN-PROTEIN LIGASE WWP2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	HECT	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	PF00168	UniProtKB/TrEMBL
	PF00397	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA134946925	PharmGKB
PIRSF	E3_ub_ligase_SMURF1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE	HECT	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	PS50004	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	WW_DOMAIN_1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	WW_DOMAIN_2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART	HECTc	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SM00239	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SM00456	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP	SSF49562	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SSF51045	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SSF56204	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	A6NEP1	ENTREZGENE
	B2R706	ENTREZGENE
	B4DHF6	ENTREZGENE, UniProtKB/TrEMBL
	B4DIN7	ENTREZGENE, UniProtKB/TrEMBL
	B4DTL5	ENTREZGENE
	F5H213	ENTREZGENE
	H3BPJ8_HUMAN	UniProtKB/TrEMBL
	H3BRF3	ENTREZGENE
	H3BRX8_HUMAN	UniProtKB/TrEMBL
	H3BS79_HUMAN	UniProtKB/TrEMBL
	I3RSG8	ENTREZGENE
	O00308	ENTREZGENE
	Q6ZTQ5	ENTREZGENE
	Q96CZ2	ENTREZGENE
	Q9BWN6	ENTREZGENE
	WWP2_HUMAN	UniProtKB/Swiss-Prot
UniProt Secondary	A6NEP1	UniProtKB/Swiss-Prot
	B2R706	UniProtKB/Swiss-Prot
	B4DTL5	UniProtKB/Swiss-Prot
	F5H213	UniProtKB/Swiss-Prot
	H3BRF3	UniProtKB/Swiss-Prot
	I3RSG8	UniProtKB/Swiss-Prot
	Q6ZTQ5	UniProtKB/Swiss-Prot
	Q96CZ2	UniProtKB/Swiss-Prot
	Q9BWN6	UniProtKB/Swiss-Prot

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Imported Disease Annotations - ClinVar

Imported Disease Annotations - CTD

Imported Annotations - KEGG (archival)

Imported Human Phenotype Annotations - ClinVar

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Imported Disease Annotations - ClinVar

Imported Disease Annotations - CTD

Imported Annotations - KEGG (archival)

Imported Human Phenotype Annotations - ClinVar