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Gene: UNK (unk zinc finger) Homo sapiens

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Symbol:

UNK

Name:

unk zinc finger

RGD ID:

1319446

HGNC Page

HGNC:29369

Description:

Enables mRNA CDS binding activity. Involved in cell morphogenesis involved in neuron differentiation and negative regulation of cytoplasmic translation. Located in cytoplasm.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

KIAA1753; RING finger protein unkempt homolog; unk family zinc finger; UNKEMPT; unkempt family zinc finger; unkempt homolog; ZC3H5; ZC3HDC5; zinc finger CCCH domain-containing protein 5; zinc finger CCCH type domain containing 5; zinc finger CCCH-type containing 5; zinc finger CCCH-type domain containing 5

RGD Orthologs

Alliance Orthologs

More Info

more info ...

More Info

Species	Gene symbol and name	Data Source	Assertion derived from	less info ...
Orthologs ¹				less info ...
Mus musculus (house mouse):	Unk (unkempt family zinc finger)	HGNC	Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, Panther, PhylomeDB
Rattus norvegicus (Norway rat):	Unk (unk zinc finger)	HGNC	Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, Panther
Chinchilla lanigera (long-tailed chinchilla):	Unk (unk zinc finger)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	UNK (unk zinc finger)	NCBI	Ortholog
Canis lupus familiaris (dog):	UNK (unk zinc finger)	HGNC	Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, Panther, PhylomeDB
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Unk (unk zinc finger)	NCBI	Ortholog
Sus scrofa (pig):	UNK (unk zinc finger)	HGNC	Ensembl, NCBI, OMA, OrthoDB, Panther
Chlorocebus sabaeus (green monkey):	UNK (unk zinc finger)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Unk (unk zinc finger)	NCBI	Ortholog
Other homologs ²
Mus musculus (house mouse):	Unkl (unkempt family like zinc finger)	HGNC	OrthoDB
Rattus norvegicus (Norway rat):	Unkl (unk like zinc finger)	HGNC	OrthoDB
Sus scrofa (pig):	UNKL (unk like zinc finger)	HGNC	OrthoDB
Rattus norvegicus (Norway rat):	Fam98c (family with sequence similarity 98, member C)	HGNC	OMA
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Unk (unk zinc finger)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Unk (unkempt family zinc finger)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	unk (unk zinc finger)	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid\|ZFIN)
Caenorhabditis elegans (roundworm):	C34D10.2	Alliance	DIOPT (Ensembl Compara\|InParanoid\|OrthoFinder\|OrthoInspector\|PhylomeDB\|SonicParanoid)
Drosophila melanogaster (fruit fly):	unk	Alliance	DIOPT (Ensembl Compara\|InParanoid\|OrthoFinder\|OrthoInspector\|PhylomeDB\|SonicParanoid)
Xenopus tropicalis (tropical clawed frog):	unk	Alliance	DIOPT (Ensembl Compara\|OMA\|OrthoFinder\|PANTHER\|PhylomeDB)
Xenopus laevis (African clawed frog):	unk.L	Alliance	DIOPT (Xenbase)
Xenopus laevis (African clawed frog):	unk.S	Alliance	DIOPT (Xenbase)

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	17	75,784,806 - 75,825,799 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	17	75,784,806 - 75,825,799 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	17	73,780,887 - 73,821,880 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	17	71,292,276 - 71,333,481 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	17	70,370,731 - 70,411,935 (+)	NCBI		Celera
Cytogenetic Map	17	q25.1	NCBI
HuRef	17	69,206,437 - 69,247,636 (+)	NCBI		HuRef
CHM1_1	17	73,845,995 - 73,886,818 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	17	76,678,053 - 76,718,950 (+)	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

peroxisomal acyl-CoA oxidase deficiency (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

17beta-estradiol (EXP)

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

2-methylcholine (EXP)

5-aza-2'-deoxycytidine (EXP)

amphetamine (ISO)

benzo[a]pyrene (EXP)

bisphenol A (ISO)

bisphenol F (ISO)

butanal (EXP)

cadmium dichloride (EXP)

caffeine (EXP)

carbon nanotube (ISO)

CGP 52608 (EXP)

chlorpyrifos (ISO)

cyclosporin A (EXP)

dorsomorphin (EXP)

entinostat (EXP)

enzyme inhibitor (EXP)

FR900359 (EXP)

furan (ISO)

gentamycin (ISO)

methamphetamine (ISO)

methotrexate (ISO)

methyl methanesulfonate (EXP)

paracetamol (EXP,ISO)

pregnenolone 16alpha-carbonitrile (ISO)

SB 431542 (EXP)

sunitinib (EXP)

thioacetamide (ISO)

titanium dioxide (ISO)

triptonide (ISO)

tungsten (ISO)

valproic acid (EXP)

vorinostat (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

cell morphogenesis involved in neuron differentiation (IBA,IMP)

in utero embryonic development (IEA,ISO)

negative regulation of cytoplasmic translation (IMP)

neuron migration (IEA,ISO)

regulation of translation (IEA)

Cellular Component

cytoplasm (IDA,IEA)

Molecular Function

metal ion binding (IEA)

mRNA CDS binding (IBA,IDA,IEA)

ribosome binding (IEA)

RNA binding (HDA,IEA)

zinc ion binding (IEA)

References

References - curated

#	Reference Title	Reference Citation
1.	GOAs Human GO annotations	GOA_HUMAN data from the GO Consortium
2.	ClinVar Automated Import and Annotation Pipeline	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions
4.	Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.	Strausberg RL, etal., Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):16899-903. Epub 2002 Dec 11.

Additional References at PubMed

PMID:11214970	PMID:15302935	PMID:15489334	PMID:16094384	PMID:16713569	PMID:21873635	PMID:22658674	PMID:22681889	PMID:22939629	PMID:24255178	PMID:25737280	PMID:25940091
PMID:26641712	PMID:28718761	PMID:29053956	PMID:29395067	PMID:31091453	PMID:31527615	PMID:32123171	PMID:33060197	PMID:33541421	PMID:33961781	PMID:34079125	PMID:34597346
PMID:34672954	PMID:34709727	PMID:35044719	PMID:35140242	PMID:35563538	PMID:36232890	PMID:36779422	PMID:38580884

Genomics

Comparative Map Data

UNK
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	17	75,784,806 - 75,825,799 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	17	75,784,806 - 75,825,799 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	17	73,780,887 - 73,821,880 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	17	71,292,276 - 71,333,481 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	17	70,370,731 - 70,411,935 (+)	NCBI		Celera
Cytogenetic Map	17	q25.1	NCBI
HuRef	17	69,206,437 - 69,247,636 (+)	NCBI		HuRef
CHM1_1	17	73,845,995 - 73,886,818 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	17	76,678,053 - 76,718,950 (+)	NCBI		T2T-CHM13v2.0

Unk
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	11	115,921,117 - 115,952,040 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	11	115,921,148 - 115,952,040 (+)	Ensembl		GRCm39 Ensembl
GRCm38	11	116,028,616 - 116,061,214 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	11	116,030,322 - 116,061,214 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	11	115,891,636 - 115,922,508 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	11	115,846,412 - 115,877,284 (+)	NCBI		MGSCv36	mm8
Celera	11	127,792,548 - 127,823,396 (+)	NCBI		Celera
Cytogenetic Map	11	E2	NCBI
cM Map	11	80.91	NCBI

Unk
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	10	101,764,732 - 101,794,847 (+)	NCBI		GRCr8
mRatBN7.2	10	101,265,732 - 101,295,950 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	10	101,265,703 - 101,295,967 (+)	Ensembl		mRatBN7.2 Ensembl
Rnor_6.0	10	104,582,531 - 104,613,102 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	10	104,582,955 - 104,612,033 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	10	103,672,269 - 103,702,612 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	10	106,139,489 - 106,169,639 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	10	106,146,657 - 106,184,153 (+)	NCBI
Celera	10	99,839,358 - 99,869,964 (+)	NCBI		Celera
Cytogenetic Map	10	q32.1	NCBI

Unk
(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_004955506	6,424,638 - 6,470,874 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955506	6,424,638 - 6,470,406 (-)	NCBI	ChiLan1.0	ChiLan1.0

UNK
(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	19	91,828,898 - 91,869,727 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	17	96,653,617 - 96,694,449 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	17	69,735,509 - 69,776,345 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	17	75,285,922 - 75,326,427 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	17	75,285,922 - 75,326,427 (+)	Ensembl	panpan1.1		panPan2

UNK
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	9	4,767,696 - 4,801,324 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	9	4,767,743 - 4,801,235 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	9	5,447,885 - 5,481,378 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	9	5,437,874 - 5,471,691 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	9	5,437,874 - 5,471,662 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	9	5,477,644 - 5,511,117 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	9	5,587,735 - 5,621,211 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	9	5,648,419 - 5,682,105 (-)	NCBI		UU_Cfam_GSD_1.0

Unk
(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_024405602	5,406,972 - 5,444,552 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936594	967,448 - 1,004,966 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936594	967,386 - 1,005,085 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

UNK
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	12	5,592,503 - 5,628,247 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	12	5,592,502 - 5,628,249 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	12	5,539,232 - 5,574,622 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

UNK
(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	16	45,858,198 - 45,899,367 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	16	45,857,376 - 45,899,313 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666077	16,613,886 - 16,656,296 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Unk
(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_004624801	5,676,521 - 5,719,128 (+)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624801	5,676,546 - 5,720,483 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in UNK
43 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 17q24.3-25.3(chr17:69209079-83086677)x3	copy number gain	See cases [RCV000052486]	Chr17:69209079..83086677 [GRCh38] Chr17:67205220..81044553 [GRCh37] Chr17:64716815..78637842 [NCBI36] Chr17:17q24.3-25.3	pathogenic
GRCh38/hg38 17q23.2-25.3(chr17:36449220-83086677)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]\|See cases [RCV000052483]	Chr17:36449220..83086677 [GRCh38] Chr17:58617905..81044553 [GRCh37] Chr17:55972687..78637842 [NCBI36] Chr17:17q23.2-25.3	pathogenic
GRCh38/hg38 17q25.1(chr17:75636351-75970744)x1	copy number loss	See cases [RCV000053453]	Chr17:75636351..75970744 [GRCh38] Chr17:73632431..73966825 [GRCh37] Chr17:71144026..71478420 [NCBI36] Chr17:17q25.1	pathogenic
NM_199242.2(UNC13D):c.2956C>T (p.Leu986=)	single nucleotide variant	Malignant melanoma [RCV000071668]	Chr17:75828982 [GRCh38] Chr17:73825063 [GRCh37] Chr17:71336658 [NCBI36] Chr17:17q25.1	not provided
GRCh38/hg38 17q24.3-25.3(chr17:69916435-83102552)x3	copy number gain	See cases [RCV000143342]	Chr17:69916435..83102552 [GRCh38] Chr17:67912576..81048189 [GRCh37] Chr17:65424171..78653717 [NCBI36] Chr17:17q24.3-25.3	pathogenic
GRCh37/hg19 17q24.2-25.3(chr17:64241326-81041938)x3	copy number gain	See cases [RCV000447577]	Chr17:64241326..81041938 [GRCh37] Chr17:17q24.2-25.3	pathogenic
GRCh37/hg19 17q21.31-25.3(chr17:42580684-81085615)x3	copy number gain	See cases [RCV000447823]	Chr17:42580684..81085615 [GRCh37] Chr17:17q21.31-25.3	pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)	copy number gain	See cases [RCV000511439]	Chr17:526..81041938 [GRCh37] Chr17:17p13.3-q25.3	pathogenic
GRCh37/hg19 17q25.1(chr17:73757329-73992584)x3	copy number gain	See cases [RCV000511796]	Chr17:73757329..73992584 [GRCh37] Chr17:17q25.1	uncertain significance
NM_001080419.3(UNK):c.2297C>T (p.Ser766Leu)	single nucleotide variant	not specified [RCV004313564]	Chr17:75824281 [GRCh38] Chr17:73820362 [GRCh37] Chr17:17q25.1	uncertain significance
NM_001080419.3(UNK):c.2083G>A (p.Glu695Lys)	single nucleotide variant	not specified [RCV004318634]	Chr17:75823328 [GRCh38] Chr17:73819409 [GRCh37] Chr17:17q25.1	uncertain significance
NM_001080419.3(UNK):c.132G>T (p.Gln44His)	single nucleotide variant	not specified [RCV004289898]	Chr17:75809787 [GRCh38] Chr17:73805868 [GRCh37] Chr17:17q25.1	uncertain significance
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3	copy number gain	See cases [RCV000512441]	Chr17:526..81041938 [GRCh37] Chr17:17p13.3-q25.3	pathogenic
GRCh37/hg19 17q24.2-25.3(chr17:67002415-81041938)x3	copy number gain	See cases [RCV000512573]	Chr17:67002415..81041938 [GRCh37] Chr17:17q24.2-25.3	pathogenic
GRCh37/hg19 17q25.1(chr17:73414856-74037715)x3	copy number gain	not provided [RCV000683962]	Chr17:73414856..74037715 [GRCh37] Chr17:17q25.1	uncertain significance
GRCh37/hg19 17q24.1-25.3(chr17:63689671-81041938)x3	copy number gain	not provided [RCV000683952]	Chr17:63689671..81041938 [GRCh37] Chr17:17q24.1-25.3	pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:7214-81058310)x3	copy number gain	not provided [RCV000739320]	Chr17:7214..81058310 [GRCh37] Chr17:17p13.3-q25.3	pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:12344-81057996)x3	copy number gain	not provided [RCV000739325]	Chr17:12344..81057996 [GRCh37] Chr17:17p13.3-q25.3	pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:8547-81060040)x3	copy number gain	not provided [RCV000739324]	Chr17:8547..81060040 [GRCh37] Chr17:17p13.3-q25.3	pathogenic
GRCh37/hg19 17q24.1-25.2(chr17:64159738-74891024)x3	copy number gain	not provided [RCV000762750]	Chr17:64159738..74891024 [GRCh37] Chr17:17q24.1-25.2	likely pathogenic
GRCh37/hg19 17q25.1(chr17:73596063-73959466)x3	copy number gain	not provided [RCV000848371]	Chr17:73596063..73959466 [GRCh37] Chr17:17q25.1	uncertain significance
GRCh37/hg19 17q24.1-25.3(chr17:62778720-81041938)x3	copy number gain	not provided [RCV000849900]	Chr17:62778720..81041938 [GRCh37] Chr17:17q24.1-25.3	pathogenic
NM_001080419.3(UNK):c.1105-9T>C	single nucleotide variant	not provided [RCV000955470]	Chr17:75817317 [GRCh38] Chr17:73813398 [GRCh37] Chr17:17q25.1	benign
NM_001080419.3(UNK):c.1485C>T (p.Pro495=)	single nucleotide variant	not provided [RCV000955471]	Chr17:75818755 [GRCh38] Chr17:73814836 [GRCh37] Chr17:17q25.1	benign
GRCh37/hg19 17q25.1(chr17:72718277-74142256)	copy number gain	7q11.23 microduplication syndrome [RCV003325440]	Chr17:72718277..74142256 [GRCh37] Chr17:17q25.1	pathogenic
GRCh37/hg19 17q25.1-25.3(chr17:73261871-78608763)x3	copy number gain	not provided [RCV001006919]	Chr17:73261871..78608763 [GRCh37] Chr17:17q25.1-25.3	pathogenic
NM_001080419.3(UNK):c.1198G>A (p.Val400Ile)	single nucleotide variant	not specified [RCV004685232]	Chr17:75817419 [GRCh38] Chr17:73813500 [GRCh37] Chr17:17q25.1	uncertain significance
NM_001080419.3(UNK):c.1480G>A (p.Val494Ile)	single nucleotide variant	not specified [RCV004685234]	Chr17:75818750 [GRCh38] Chr17:73814831 [GRCh37] Chr17:17q25.1	likely benign
NM_001080419.3(UNK):c.1177C>T (p.Pro393Ser)	single nucleotide variant	not specified [RCV004685236]	Chr17:75817398 [GRCh38] Chr17:73813479 [GRCh37] Chr17:17q25.1	uncertain significance
NM_001080419.3(UNK):c.1568A>G (p.Asp523Gly)	single nucleotide variant	not specified [RCV004685237]	Chr17:75819705 [GRCh38] Chr17:73815786 [GRCh37] Chr17:17q25.1	uncertain significance
NM_001080419.3(UNK):c.961C>T (p.Gln321Ter)	single nucleotide variant	not provided [RCV001806981]	Chr17:75815253 [GRCh38] Chr17:73811334 [GRCh37] Chr17:17q25.1	uncertain significance
GRCh37/hg19 17q25.1-25.3(chr17:73481509-81043199)x3	copy number gain	not provided [RCV002276051]	Chr17:73481509..81043199 [GRCh37] Chr17:17q25.1-25.3	pathogenic
NM_001080419.3(UNK):c.2252G>A (p.Arg751Gln)	single nucleotide variant	not specified [RCV004325725]	Chr17:75823497 [GRCh38] Chr17:73819578 [GRCh37] Chr17:17q25.1	uncertain significance
NM_001080419.3(UNK):c.2078G>A (p.Gly693Asp)	single nucleotide variant	not specified [RCV004143385]	Chr17:75823323 [GRCh38] Chr17:73819404 [GRCh37] Chr17:17q25.1	uncertain significance
NM_001080419.3(UNK):c.2386G>A (p.Glu796Lys)	single nucleotide variant	not specified [RCV004191508]	Chr17:75824370 [GRCh38] Chr17:73820451 [GRCh37] Chr17:17q25.1	uncertain significance
NM_001080419.3(UNK):c.809G>C (p.Gly270Ala)	single nucleotide variant	not specified [RCV004187512]	Chr17:75813811 [GRCh38] Chr17:73809892 [GRCh37] Chr17:17q25.1	uncertain significance
NM_001080419.3(UNK):c.2056G>A (p.Gly686Ser)	single nucleotide variant	not specified [RCV004141681]	Chr17:75823301 [GRCh38] Chr17:73819382 [GRCh37] Chr17:17q25.1	uncertain significance
NM_001080419.3(UNK):c.2182G>A (p.Ala728Thr)	single nucleotide variant	not specified [RCV004113346]	Chr17:75823427 [GRCh38] Chr17:73819508 [GRCh37] Chr17:17q25.1	uncertain significance
NM_001080419.3(UNK):c.1501G>A (p.Ala501Thr)	single nucleotide variant	not specified [RCV004155737]	Chr17:75818771 [GRCh38] Chr17:73814852 [GRCh37] Chr17:17q25.1	uncertain significance
NM_001080419.3(UNK):c.2183C>A (p.Ala728Asp)	single nucleotide variant	not specified [RCV004111357]	Chr17:75823428 [GRCh38] Chr17:73819509 [GRCh37] Chr17:17q25.1	uncertain significance
NM_001080419.3(UNK):c.734G>A (p.Arg245Gln)	single nucleotide variant	not specified [RCV004107993]	Chr17:75813189 [GRCh38] Chr17:73809270 [GRCh37] Chr17:17q25.1	uncertain significance
NM_001080419.3(UNK):c.823G>A (p.Gly275Arg)	single nucleotide variant	not specified [RCV004216450]	Chr17:75813825 [GRCh38] Chr17:73809906 [GRCh37] Chr17:17q25.1	uncertain significance
NM_001080419.3(UNK):c.2098C>T (p.Arg700Trp)	single nucleotide variant	not specified [RCV004142984]	Chr17:75823343 [GRCh38] Chr17:73819424 [GRCh37] Chr17:17q25.1	uncertain significance
NM_001080419.3(UNK):c.2030C>T (p.Ala677Val)	single nucleotide variant	not specified [RCV004111421]	Chr17:75823275 [GRCh38] Chr17:73819356 [GRCh37] Chr17:17q25.1	uncertain significance
NM_001080419.3(UNK):c.2072C>T (p.Ala691Val)	single nucleotide variant	not specified [RCV004096035]	Chr17:75823317 [GRCh38] Chr17:73819398 [GRCh37] Chr17:17q25.1	uncertain significance
NM_001080419.3(UNK):c.1130G>C (p.Gly377Ala)	single nucleotide variant	not specified [RCV004221718]	Chr17:75817351 [GRCh38] Chr17:73813432 [GRCh37] Chr17:17q25.1	uncertain significance
NM_001080419.3(UNK):c.2429C>T (p.Ser810Leu)	single nucleotide variant	not specified [RCV004180588]	Chr17:75824413 [GRCh38] Chr17:73820494 [GRCh37] Chr17:17q25.1	uncertain significance
NM_001080419.3(UNK):c.1585G>A (p.Val529Met)	single nucleotide variant	not specified [RCV004221908]	Chr17:75819722 [GRCh38] Chr17:73815803 [GRCh37] Chr17:17q25.1	uncertain significance
NM_001080419.3(UNK):c.1255G>A (p.Glu419Lys)	single nucleotide variant	not specified [RCV004685235]	Chr17:75817476 [GRCh38] Chr17:73813557 [GRCh37] Chr17:17q25.1	uncertain significance
NM_001080419.3(UNK):c.2309T>G (p.Leu770Arg)	single nucleotide variant	not specified [RCV004339629]	Chr17:75824293 [GRCh38] Chr17:73820374 [GRCh37] Chr17:17q25.1	uncertain significance
NM_001080419.3(UNK):c.1213T>C (p.Ser405Pro)	single nucleotide variant	not specified [RCV004335154]	Chr17:75817434 [GRCh38] Chr17:73813515 [GRCh37] Chr17:17q25.1	uncertain significance
GRCh37/hg19 17q25.1(chr17:73264158-74039659)x3	copy number gain	not provided [RCV003485164]	Chr17:73264158..74039659 [GRCh37] Chr17:17q25.1	uncertain significance
NM_001080419.3(UNK):c.104+23del	deletion	not provided [RCV003663004]	Chr17:75784995 [GRCh38] Chr17:73781076 [GRCh37] Chr17:17q25.1	benign
NM_001080419.3(UNK):c.1831T>C (p.Ser611Pro)	single nucleotide variant	not specified [RCV004482105]	Chr17:75820102 [GRCh38] Chr17:73816183 [GRCh37] Chr17:17q25.1	uncertain significance
NM_001080419.3(UNK):c.209G>A (p.Arg70Gln)	single nucleotide variant	not specified [RCV004482106]	Chr17:75809864 [GRCh38] Chr17:73805945 [GRCh37] Chr17:17q25.1	uncertain significance
NM_001080419.3(UNK):c.2179C>A (p.Gln727Lys)	single nucleotide variant	not specified [RCV004482107]	Chr17:75823424 [GRCh38] Chr17:73819505 [GRCh37] Chr17:17q25.1	uncertain significance
NM_001080419.3(UNK):c.2191G>A (p.Ala731Thr)	single nucleotide variant	not specified [RCV004482108]	Chr17:75823436 [GRCh38] Chr17:73819517 [GRCh37] Chr17:17q25.1	likely benign
NM_001080419.3(UNK):c.103A>C (p.Thr35Pro)	single nucleotide variant	not specified [RCV004482102]	Chr17:75784983 [GRCh38] Chr17:73781064 [GRCh37] Chr17:17q25.1	uncertain significance
NM_001080419.3(UNK):c.1349A>G (p.Gln450Arg)	single nucleotide variant	not specified [RCV004482104]	Chr17:75818146 [GRCh38] Chr17:73814227 [GRCh37] Chr17:17q25.1	uncertain significance
NC_000017.10:g.(?_73720784)_(73975154_?)dup	duplication	Acyl-CoA oxidase deficiency [RCV004581279]	Chr17:73720784..73975154 [GRCh37] Chr17:17q25.1	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	3908
Count of miRNA genes:	1077
Interacting mature miRNAs:	1336
Transcripts:	ENST00000293218, ENST00000586217, ENST00000586527, ENST00000587258, ENST00000587501, ENST00000589666, ENST00000589790, ENST00000592074, ENST00000592629
Prediction methods:	Microtar, Miranda, Pita, Pita,Targetscan, 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
406938593	GWAS587569_H	eosinophil percentage of leukocytes QTL GWAS587569 (human)		2e-10	eosinophil percentage of leukocytes	blood eosinophil count to total leukocyte count ratio (CMO:0000369)	17	75803022	75803023	Human
407114230	GWAS763206_H	total cholesterol measurement QTL GWAS763206 (human)		0.0000007	total cholesterol measurement	blood total cholesterol level (CMO:0000051)	17	75786110	75786111	Human
407114035	GWAS763011_H	low density lipoprotein cholesterol measurement QTL GWAS763011 (human)		2e-11	low density lipoprotein cholesterol measurement	blood low density lipoprotein cholesterol level (CMO:0000053)	17	75786110	75786111	Human
407114435	GWAS763411_H	low density lipoprotein cholesterol measurement QTL GWAS763411 (human)		3e-22	low density lipoprotein cholesterol measurement	blood low density lipoprotein cholesterol level (CMO:0000053)	17	75786110	75786111	Human
407102068	GWAS751044_H	eosinophil count QTL GWAS751044 (human)		5e-15	eosinophil quantity (VT:0002602)	blood eosinophil count (CMO:0000033)	17	75805073	75805074	Human
406967054	GWAS616030_H	basophil count, eosinophil count QTL GWAS616030 (human)		8e-10	eosinophil quantity (VT:0002602)	blood granulocyte count (CMO:0000111)	17	75805073	75805074	Human

Markers in Region

D17S1839

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	17	73,801,863 - 73,802,108	UniSTS	GRCh37
Build 36	17	71,313,458 - 71,313,703	RGD	NCBI36
Celera	17	70,391,913 - 70,392,158	RGD
Cytogenetic Map	17	q25.3	UniSTS
Cytogenetic Map	17	q25.1	UniSTS
HuRef	17	69,227,323 - 69,227,568	UniSTS
Marshfield Genetic Map	17	102.46	RGD
Marshfield Genetic Map	17	102.46	UniSTS
Genethon Genetic Map	17	103.7	UniSTS
TNG Radiation Hybrid Map	17	33729.0	UniSTS
deCODE Assembly Map	17	114.52	UniSTS
Stanford-G3 RH Map	17	3272.0	UniSTS
NCBI RH Map	17	783.3	UniSTS
GeneMap99-G3 RH Map	17	3773.0	UniSTS

RH47803

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	17	73,821,723 - 73,821,850	UniSTS	GRCh37
Build 36	17	71,333,318 - 71,333,445	RGD	NCBI36
Celera	17	70,411,772 - 70,411,899	RGD
Cytogenetic Map	17	q25.1	UniSTS
HuRef	17	69,247,473 - 69,247,600	UniSTS
GeneMap99-GB4 RH Map	17	482.47	UniSTS
NCBI RH Map	17	787.2	UniSTS

RH18221

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	17	73,804,984 - 73,805,113	UniSTS	GRCh37
Build 36	17	71,316,579 - 71,316,708	RGD	NCBI36
Celera	17	70,395,034 - 70,395,163	RGD
Cytogenetic Map	17	q25.1	UniSTS
HuRef	17	69,230,444 - 69,230,573	UniSTS
GeneMap99-GB4 RH Map	17	483.02	UniSTS
NCBI RH Map	17	787.2	UniSTS

RH94321

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	17	73,793,049 - 73,793,187	UniSTS	GRCh37
Build 36	17	71,304,644 - 71,304,782	RGD	NCBI36
Celera	17	70,383,101 - 70,383,239	RGD
Cytogenetic Map	17	q25.1	UniSTS
HuRef	17	69,218,565 - 69,218,703	UniSTS
GeneMap99-GB4 RH Map	17	483.02	UniSTS

SHGC-144594

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	17	73,805,224 - 73,805,573	UniSTS	GRCh37
Build 36	17	71,316,819 - 71,317,168	RGD	NCBI36
Celera	17	70,395,274 - 70,395,623	RGD
Cytogenetic Map	17	q25.1	UniSTS
HuRef	17	69,230,684 - 69,231,033	UniSTS
TNG Radiation Hybrid Map	17	33722.0	UniSTS

SHGC-33699

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	17	73,804,900 - 73,805,026	UniSTS	GRCh37
Build 36	17	71,316,495 - 71,316,621	RGD	NCBI36
Celera	17	70,394,950 - 70,395,076	RGD
Cytogenetic Map	17	q25.1	UniSTS
HuRef	17	69,230,360 - 69,230,486	UniSTS
GeneMap99-G3 RH Map	17	3773.0	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
1204	2432	2788	2245	4942	1723	2345	4	622	1948	464	2268	7281	6454	52	3708	847	1731	1612	171

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001080419	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_038131	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006722145	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006722148	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011525400	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011525401	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017025247	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017025248	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017025249	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017025250	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047436962	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047436963	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047436964	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047436965	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047436966	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317611	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317612	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317613	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317614	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317615	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317616	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317617	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317618	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054317619	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AB051540	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC087289	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AI290733	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK307289	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC033751	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC038802	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC039606	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC046175	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC053362	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC064927	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC080657	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471099	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068261	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000586217 ⟹ ENSP00000466054

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	75,812,148 - 75,815,221 (+)	Ensembl

Ensembl Acc Id:

ENST00000586527 ⟹ ENSP00000467849

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	75,784,855 - 75,794,198 (+)	Ensembl

Ensembl Acc Id:

ENST00000587258 ⟹ ENSP00000467726

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	75,819,739 - 75,824,329 (+)	Ensembl

Ensembl Acc Id:

ENST00000587501 ⟹ ENSP00000464953

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	75,784,849 - 75,794,124 (+)	Ensembl

Ensembl Acc Id:

ENST00000589666 ⟹ ENSP00000464893

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	75,784,806 - 75,825,799 (+)	Ensembl

Ensembl Acc Id:

ENST00000589790

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	75,784,842 - 75,792,165 (+)	Ensembl

Ensembl Acc Id:

ENST00000592074

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	75,791,771 - 75,792,636 (+)	Ensembl

Ensembl Acc Id:

ENST00000592629 ⟹ ENSP00000466431

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	75,784,862 - 75,812,319 (+)	Ensembl

RefSeq Acc Id:

NM_001080419 ⟹ NP_001073888

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	75,784,806 - 75,825,799 (+)	NCBI
GRCh37	17	73,780,920 - 73,821,886 (+)	ENTREZGENE
Build 36	17	71,292,276 - 71,333,481 (+)	NCBI Archive
Celera	17	70,370,731 - 70,411,935 (+)	RGD
HuRef	17	69,206,437 - 69,247,636 (+)	ENTREZGENE
CHM1_1	17	73,845,995 - 73,886,818 (+)	NCBI
T2T-CHM13v2.0	17	76,678,053 - 76,718,950 (+)	NCBI

Sequence:

show sequence

GCACTGGGTCCTCGGCGCGGACCGCGCAGACTGAATAATAAAAGGGGAGCGGCGAAGAGGCAGG
AAGACAAGACCATGTCGAAGGGCCCCGGGCCCGGCGGCTCCGCAGCTTCCTCGGCGCCCCCGGC
CGCTACCGCTCAGGTGCTGCAGGCACAGCCCGAGAAACCGCAGCACTACACGTACCTGAAAGAA
TTCCGCACAGAGCAGTGCCCACTCTTTGTGCAACACAAATGCACGCAGCATCGGCCCTACACCT
GCTTCCACTGGCACTTCGTGAACCAGCGGCGCCGCCGGTCCATCCGCCGTCGGGACGGCACCTT
CAATTACAGCCCTGACGTCTACTGCACCAAGTACGACGAGGCTACAGGCCTCTGCCCGGAGGGC
GACGAGTGCCCATTCCTGCACAGAACCACAGGGGACACTGAGCGCAGGTACCACCTTCGTTACT
ACAAAACTGGAATCTGCATCCACGAGACAGACTCGAAAGGCAACTGCACCAAAAACGGCCTGCA
CTGCGCTTTTGCCCACGGGCCCCATGACCTCCGCTCCCCTGTCTACGACATCAGGGAGCTTCAG
GCCATGGAGGCCTTGCAGAATGGCCAGACCACGGTAGAGGGGAGCATAGAGGGCCAGTCGGCTG
GGGCTGCGAGCCATGCCATGATAGAAAAGATCCTCAGCGAGGAGCCTCGGTGGCAAGAGACTGC
TTATGTGCTGGGGAACTATAAGACGGAGCCTTGCAAGAAGCCCCCGCGGCTGTGCCGCCAAGGC
TATGCCTGTCCCTACTACCACAACAGCAAGGACCGGCGGCGGAGCCCCCGGAAGCACAAATACA
GGTCGTCTCCATGTCCAAACGTCAAGCACGGGGATGAGTGGGGAGACCCTGGCAAGTGTGAGAA
CGGAGACGCCTGCCAGTACTGCCACACCCGCACCGAGCAGCAGTTCCACCCCGAGATCTACAAG
TCCACCAAGTGCAACGACATGCAGCAGTCGGGCAGCTGTCCCCGAGGACCCTTCTGCGCCTTTG
CCCACGTAGAACAGCCACCCCTGAGTGACGACCTGCAGCCTTCCTCAGCTGTGTCCAGCCCCAC
CCAGCCAGGTCCTGTCCTGTACATGCCATCTGCCGCCGGAGACTCGGTGCCTGTGAGCCCCTCC
AGCCCGCATGCCCCTGACCTCAGTGCCCTCCTCTGTAGAAACAGCAGCCTAGGCAGCCCGTCTA
ACCTCTGCGGCTCCCCACCGGGCTCCATCAGGAAGCCCCCAAACCTGGAGGGCATCGTCTTCCC
TGGGGAGTCTGGCCTGGCCCCTGGCAGCTATAAGAAGGCTCCCGGCTTCGAGAGGGAAGACCAG
GTGGGAGCCGAGTACCTGAAAAATTTCAAATGCCAGGCCAAATTAAAACCCCACTCATTAGAGC
CCAGGAGTCAAGAGCAGCCTCTGCTTCAGCCCAAACAGGACATGCTGGGCATCCTCCCCGCAGG
CAGCCCCCTGACCTCAAGCATCTCTTCTAGTATCACCTCCAGCCTGGCAGCTACCCCCCCTAGC
CCAGTGGGCACCAGCAGCGTCCCCGGCATGAATGCAAACGCTCTGCCCTTCTACCCCACCAGCG
ACACGGTAGAGTCAGTCATAGAGTCTGCTTTGGATGACCTGGACCTGAATGAGTTTGGCGTGGC
CGCCCTGGAGAAGACTTTCGATAACAGCACAGTGCCCCACCCAGGAAGCATCACCATCGGCGGC
AGCTTGCTGCAGAGCTCTGCACCCGTGAACATCCCCGGCTCCTTGGGCAGCTCTGCCTCCTTCC
ACTCAGCATCCCCGTCCCCTCCCGTCAGCCTCTCCTCGCATTTCCTGCAGCAGCCCCAGGGCCA
CCTGAGTCAGTCGGAAAACACATTTTTGGGAACCTCAGCATCACATGGATCTTTGGGTCTGAAC
GGGATGAACAGCAGCATCTGGGAGCATTTTGCCTCTGGAAGCTTCTCCCCGGGCACTTCCCCCG
CTTTCCTATCAGGGCCAGGGGCTGCCGAGCTGGCCCGACTTCGGCAAGAGCTGGATGAAGCCAA
CAGCACCATCAAGCAGTGGGAGGAGTCCTGGAAGCAGGCCAAGCAGGCTTGTGATGCCTGGAAG
AAAGAGGCGGAGGAGGCTGGTGAGCGGGCCAGTGCGGCGGGCGCCGAGTGCGAGCTGGCCCGGG
AGCAGCGGGATGCACTGGAGGTGCAGGTGAAGAAGCTCCAGGAGGAGCTGGAGCGGCTACACGC
GGGGCCTGAGCCCCAGGCCCTGCCCGCCTTCTCCGACCTGGAGGCGCTCTCACTCTCCACCCTC
TACTCCCTCCAGAAACAACTGCGGGCCCACCTGGAACAAGTGGACAAGGCCGTGTTCCACATGC
AGTCGGTGAAATGCCTTAAGTGTCAGGAACAGAAGCGGGCAGTGCTGCCGTGCCAACACGCTGC
GCTGTGTGAGCTCTGCGCTGAGGGCAGCGAGTGCCCCATCTGCCAGCCTGGCCGGGCCCACACC
CTCCAGTCGTGACCCTGCAGGCCTGGCCCAGCCTGGCCCAGATCTTCTCACCTAGGACTTTTTA
AAGTATATATATATATATGAATATATATATATATGTGTATGTATGTATGTATATGTATATGATT
ATGTATATGTATACATTTCCGTATGTATGTATATGTATACATTTCCGTATGTGTGCAGGTATGC
GTGGTGGTGTGGACAGTGTCTGTGTGTATATCTGTACATAGATATAGACACACACTTTAAAAGA
CTTACCAAGCACTTTTTAAAAGAAGAAACTATTTTGCAGTCCTCCCCTACCCACTCCCTGCCCT
TCCCACTGCAGAGATGACATCCCCTCTTCTCCCACTGGCCTTTTGGCAGAGAATCTGGTTCTGT
CTCTTTTTTAATGTAGGAACTAACTATTTTTAACTTCTTCCTGGGGCCTGAGCAGGGAAGGGTG
GGACTGGAAGGCACTAAGGGGAAGGGAGAAGCCCTCAGGGCAGGCCCTGCTCCCCCTACCTCCT
TGCCAGGGCAAGGGTGGAGTGTGGAAGACGTGGGTCCCCCAGAGCAGGCCTGGCCCCCAGCTGT
GAGGGCCTCAGGGAGGCCCGAGGGGGAGTGCTGGGGGTCTCAGCTGGCTTAGCTCCTAAGTTTA
CCAAATGTTAATTTAGTCTTGGGGAGAACAGCAAGGGCTGGAGGCCAGTGCTGCAGGGCCAGCC
CCACTCCTGACACCTGGGCCCTTGAAGCTCCTTGAGGGGCAAGGCCCAGGAGTTCCAGCCCTCA
GGTTCCTGAGGGTCCACCCTCAGTCCTTCCCCCCGCCGCCCCTCCCCGGACTCCCCACAAGAGC
CTCCCTGGCCCCAGGGCCGCCTACCAGGCTGGTACTCATTCTATGACCACCGCCCCCAACCAGC
TGCCCCCAGCTCTCCCTGCCCCCTCCCCTCTCTGGCAGCTAGCAGGGCAATTGGCGGGGAGGAG
TGCGGACTGAGGACTGAGGACCAAGGGGGCCCAGGCCCTGCCCTCCTACCCGGAGGGGCTCCGT
TTGCATTCCTTGGTGCTCTCTGAGTGCAGCTGGTGTCCCGCCCTGTTCTGGGCGGACGCCTGTG
TGCGTGTGTGTGTGCCTGTCCAGTGTATATTGTGTCTTAGCTTCCATTTTAAAAATTGTTCTGT
ACAGAGAGAGATGCAGCAGGGGCGGGAGGGCAGAGTGGGCGGAGGGGAGCAGCCGCACCCCCAG
CACCGGGTGTCTGCGGTAGGAACAAGAGGGCTGAGAGGGTCTGGTCCTGGCCCAGGCTCCCCCT
TGGGCTCAGCACGAAAGGGCTTTCAATGAATTAAGTGAAAACTTTTTCCTTTTTTACAAAAATG
CAAAAATCAACAAAGCTCCAAACCTATTGGAAATAAAATATGAACTTGCA

hide sequence

RefSeq Acc Id:

NR_038131

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	75,784,806 - 75,794,193 (+)	NCBI
GRCh37	17	73,780,920 - 73,821,886 (+)	ENTREZGENE
HuRef	17	69,206,437 - 69,247,636 (+)	ENTREZGENE
CHM1_1	17	73,845,995 - 73,855,349 (+)	NCBI
T2T-CHM13v2.0	17	76,678,053 - 76,687,439 (+)	NCBI

Sequence:

show sequence

GCACTGGGTCCTCGGCGCGGACCGCGCAGACTGAATAATAAAAGGGGAGCGGCGAAGAGGCAGG
AAGACAAGACCATGTCGAAGGGCCCCGGGCCCGGCGGCTCCGCAGCTTCCTCGGCGCCCCCGGC
CGCTACCGCTCAGGTGCTGCAGGCACAGCCCGAGAAACCGCAGCACTACACCTATGTTAGATAC
TAAAGAAGGCTTCCCCACAACCCATATGCATCTGCTTTGACTGGTGGTTTCTATCATCCTACAA
AGACTGTGACTTATTGGTGAGGGCAGCTGGACAACTCTGAGAGCAACTTAGAGAAATCCATCTT
GGGCACACTCTATAAAGGAGCTCCTTCTCTGCAAATAGCACCCCAGATAAGTGCACAAAAGCAA
GATACCCTCGTGGACCTACACGTCCTCCCGCTTTTCAACACCCTGATGCCTGAAGCTATGGTTG
ATACTAAAGGAGGTTTTCCCACTATCCGTATGCATCTTCTCTGTTTTGAGATTGCAACTATGGA
CAGTTATGGCTAATCCTAGTAGATTGTCTTCCCTTTTAACATCTTGGATGAATTTGGGTCACAC
TAATTGTTATGTGAAGATGGATGTTGAATTGTGTAGAATTTGACAGCAGTATCAAGAGCTGAGG
AGAAGGAGAAGATGGAAAGGAGTCTAGCAACTTAAAAATCTCACAGCATTCTCTGTGAGGTGAC
CTTTTTTCCTGTTGGTGGCTCAATTTCTTTAGGACATAAAGAAGATACTGAGGCCTGTGACAGC
CTGTGACAGTATCATCAAGTCGTATCTGAACTTATTGAACTGTTTCCTCCCCTTCCTTATTCTT
TATTCACAGTTTGCTTTTCATGTGCATAAGTTGACTCATTTGTTTCCTGTTAGCATTTGAAACA
CCATATAGCCACCATAAGTCCTGACAAAATGACTTTTAATAAGGAGGGGGAAGGTCCATGTCCC
ACCTTCCTATGAAATTTTGGCCTATTCACAAGTCTACCCCCACATAAGAGAAGTAGTTATGTTC
TGTAAAGAAGAGGTTGATAAAAACCTTTAGCATGGTGTTTTGTGACTTAGAAGTTTTAAGTAGT
CGTTCTTATATCTAAGCATTTATTAATTTTGGTAAGAACATTACTATACGTTTCTGATGTCACT
TTTACTGTTAAGAGGTGCCAGGCATCTGGTGACCTGTCACTTCAGGATTTGTGTGAATCAGACC
ATCTAAATATAATATAAATTAGAGACTGGTACTTGTATTTCCTGATTAAAAACAAAGTAACGTC
TGTTTTACTATTGAAGTAAGAGTACTTTATAATGAATACAAAAATGTATATTAAATATCCAGTA
GAGCATGCTAAA

hide sequence

RefSeq Acc Id:

XM_006722148 ⟹ XP_006722211

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	75,812,272 - 75,825,799 (+)	NCBI

Sequence:

show sequence

GAGGCAGGAAGACAAGACCATGTCGAAGGGCCCCGGGCCCGGCGGCTCCGCAGCTTCCTCGGCG
CCCCCGGCCGCTACCGCTCAGGTGCTGCAGGCACAGCCCGAGAAACCGCAGCACTACACGGCAG
AGGAGAGAGACCAGTGAAGGTTGGGAGGAGGCGGCCAAAAGGAGACAGCTTCATGCCCCCAGGA
CATAAATAGCCCGGCTGCTGCAGGTACCTGAAAGAATTCCGCACAGAGCAGTGCCCACTCTTTG
TGCAACACAAATGCACGCAGCATCGGCCCTACACCTGCTTCCACTGGCACTTCGTGAACCAGCG
GCGCCGCCGGTCCATCCGCCGTCGGGACGGCACCTTCAATTACAGCCCTGACGTCTACTGCACC
AAGTACGACGAGGCTACAGGCCTCTGCCCGGAGGGCGACGAGTGCCCATTCCTGCACAGAACCA
CAGGGGACACTGAGCGCAGGTACCACCTTCGTTACTACAAAACTGGAATCTGCATCCACGAGAC
AGACTCGAAAGGCAACTGCACCAAAAACGGCCTGCACTGCGCTTTTGCCCACGGGCCCCATGAC
CTCCGCTCCCCTGTCTACGACATCAGGTGGGCTGGGTGCTGGGCTGGGCTGATGGCAGTAGGCT
GGGGTCCAGGGCAGGGGCCTGGCGGCTAATGATGGGAGCTTCAGGCCATGGAGGCCTTGCAGAA
TGGCCAGACCACGGTAGAGGGGAGCATAGAGGGCCAGTCGGCTGGGGCTGCGAGCCATGCCATG
ATAGAAAAGATCCTCAGCGAGGAGCCTCGGTGGCAAGAGACTGCTTATGTGCTGGGGAACTATA
AGACGGAGCCTTGCAAGAAGCCCCCGCGGCTGTGCCGCCAAGGCTATGCCTGTCCCTACTACCA
CAACAGCAAGGACCGGCGGCGGAGCCCCCGGAAGCACAAATACAGGTCGTCTCCATGTCCAAAC
GTCAAGCACGGGGATGAGTGGGGAGACCCTGGCAAGTGTGAGAACGGAGACGCCTGCCAGTACT
GCCACACCCGCACCGAGCAGCAGTTCCACCCCGAGATCTACAAGTCCACCAAGTGCAACGACAT
GCAGCAGTCGGGCAGCTGTCCCCGAGGACCCTTCTGCGCCTTTGCCCACGTAGAACAGCCACCC
CTGAGTGACGACCTGCAGCCTTCCTCAGCTGTGTCCAGCCCCACCCAGCCAGGTCCTGTCCTGT
ACATGCCATCTGCCGCCGGAGACTCGGTGCCTGTGAGCCCCTCCAGCCCGCATGCCCCTGACCT
CAGTGCCCTCCTCTGTAGAAACAGCAGCCTAGGCAGCCCGTCTAACCTCTGCGGCTCCCCACCG
GGCTCCATCAGGAAGCCCCCAAACCTGGAGGGCATCGTCTTCCCTGGGGAGTCTGGCCTGGCCC
CTGGCAGCTATAAGAAGGCTCCCGGCTTCGAGAGGGAAGACCAGGTGGGAGCCGAGTACCTGAA
AAATTTCAAATGCCAGGCCAAATTAAAACCCCACTCATTAGAGCCCAGGAGTCAAGAGCAGCCT
CTGCTTCAGCCCAAACAGGACATGCTGGGCATCCTCCCCGCAGGCAGCCCCCTGACCTCAAGCA
TCTCTTCTAGTATCACCTCCAGCCTGGCAGCTACCCCCCCTAGCCCAGTGGGCACCAGCAGCGT
CCCCGGCATGAATGCAAACGCTCTGCCCTTCTACCCCACCAGCGACACGGTAGAGTCAGTCATA
GAGTCTGCTTTGGATGACCTGGACCTGAATGAGTTTGGCGTGGCCGCCCTGGAGAAGACTTTCG
ATAACAGCACAGTGCCCCACCCAGGAAGCATCACCATCGGCGGCAGCTTGCTGCAGAGCTCTGC
ACCCGTGAACATCCCCGGCTCCTTGGGCAGCTCTGCCTCCTTCCACTCAGCATCCCCGTCCCCT
CCCGTCAGCCTCTCCTCGCATTTCCTGCAGCAGCCCCAGGGCCACCTGAGTCAGTCGGAAAACA
CATTTTTGGGAACCTCAGCATCACATGGATCTTTGGGTCTGAACGGGATGAACAGCAGCATCTG
GGAGCATTTTGCCTCTGGAAGCTTCTCCCCGGGCACTTCCCCCGCTTTCCTATCAGGGCCAGGG
GCTGCCGAGCTGGCCCGACTTCGGCAAGAGCTGGATGAAGCCAACAGCACCATCAAGCAGTGGG
AGGAGTCCTGGAAGCAGGCCAAGCAGGCTTGTGATGCCTGGAAGAAAGAGGCGGAGGAGGCTGG
TGAGCGGGCCAGTGCGGCGGGCGCCGAGTGCGAGCTGGCCCGGGAGCAGCGGGATGCACTGGAG
GTGCAGGTGAAGAAGCTCCAGGAGGAGCTGGAGCGGCTACACGCGGGGCCTGAGCCCCAGGCCC
TGCCCGCCTTCTCCGACCTGGAGGCGCTCTCACTCTCCACCCTCTACTCCCTCCAGAAACAACT
GCGGGCCCACCTGGAACAAGTGGACAAGGCCGTGTTCCACATGCAGTCGGTGAAATGCCTTAAG
TGTCAGGAACAGAAGCGGGCAGTGCTGCCGTGCCAACACGCTGCGCTGTGTGAGCTCTGCGCTG
AGGGCAGCGAGTGCCCCATCTGCCAGCCTGGCCGGGCCCACACCCTCCAGTCGTGACCCTGCAG
GCCTGGCCCAGCCTGGCCCAGATCTTCTCACCTAGGACTTTTTAAAGTATATATATATATATGA
ATATATATATATATGTGTATGTATGTATGTATATGTATATGATTATGTATATGTATACATTTCC
GTATGTATGTATATGTATACATTTCCGTATGTGTGCAGGTATGCGTGGTGGTGTGGACAGTGTC
TGTGTGTATATCTGTACATAGATATAGACACACACTTTAAAAGACTTACCAAGCACTTTTTAAA
AGAAGAAACTATTTTGCAGTCCTCCCCTACCCACTCCCTGCCCTTCCCACTGCAGAGATGACAT
CCCCTCTTCTCCCACTGGCCTTTTGGCAGAGAATCTGGTTCTGTCTCTTTTTTAATGTAGGAAC
TAACTATTTTTAACTTCTTCCTGGGGCCTGAGCAGGGAAGGGTGGGACTGGAAGGCACTAAGGG
GAAGGGAGAAGCCCTCAGGGCAGGCCCTGCTCCCCCTACCTCCTTGCCAGGGCAAGGGTGGAGT
GTGGAAGACGTGGGTCCCCCAGAGCAGGCCTGGCCCCCAGCTGTGAGGGCCTCAGGGAGGCCCG
AGGGGGAGTGCTGGGGGTCTCAGCTGGCTTAGCTCCTAAGTTTACCAAATGTTAATTTAGTCTT
GGGGAGAACAGCAAGGGCTGGAGGCCAGTGCTGCAGGGCCAGCCCCACTCCTGACACCTGGGCC
CTTGAAGCTCCTTGAGGGGCAAGGCCCAGGAGTTCCAGCCCTCAGGTTCCTGAGGGTCCACCCT
CAGTCCTTCCCCCCGCCGCCCCTCCCCGGACTCCCCACAAGAGCCTCCCTGGCCCCAGGGCCGC
CTACCAGGCTGGTACTCATTCTATGACCACCGCCCCCAACCAGCTGCCCCCAGCTCTCCCTGCC
CCCTCCCCTCTCTGGCAGCTAGCAGGGCAATTGGCGGGGAGGAGTGCGGACTGAGGACTGAGGA
CCAAGGGGGCCCAGGCCCTGCCCTCCTACCCGGAGGGGCTCCGTTTGCATTCCTTGGTGCTCTC
TGAGTGCAGCTGGTGTCCCGCCCTGTTCTGGGCGGACGCCTGTGTGCGTGTGTGTGTGCCTGTC
CAGTGTATATTGTGTCTTAGCTTCCATTTTAAAAATTGTTCTGTACAGAGAGAGATGCAGCAGG
GGCGGGAGGGCAGAGTGGGCGGAGGGGAGCAGCCGCACCCCCAGCACCGGGTGTCTGCGGTAGG
AACAAGAGGGCTGAGAGGGTCTGGTCCTGGCCCAGGCTCCCCCTTGGGCTCAGCACGAAAGGGC
TTTCAATGAATTAAGTGAAAACTTTTTCCTTTTTTACAAAAATGCAAAAATCAACAAAGCTCCA
AACCTATTGGAAATAAAATATGAACTTGCA

hide sequence

RefSeq Acc Id:

XM_011525400 ⟹ XP_011523702

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	75,784,806 - 75,825,799 (+)	NCBI

Sequence:

show sequence

GAGGCAGGAAGACAAGACCATGTCGAAGGGCCCCGGGCCCGGCGGCTCCGCAGCTTCCTCGGCG
CCCCCGGCCGCTACCGCTCAGGTGCTGCAGGCACAGCCCGAGAAACCGCAGCACTACACGGCAG
AGGAGAGAGACCAGTGAAGGTTGGGAGGAGGCGGCCAAAAGGAGACAGCTTCATGCCCCCAGGA
CATAAATAGCCCGGCTGCTGCAGGTACCTGAAAGAATTCCGCACAGAGCAGTGCCCACTCTTTG
TGCAACACAAATGCACGCAGCATCGGCCCTACACCTGCTTCCACTGGCACTTCGTGAACCAGCG
GCGCCGCCGGTCCATCCGCCGTCGGGACGGCACCTTCAATTACAGCCCTGACGTCTACTGCACC
AAGTACGACGAGGCTACAGGCCTCTGCCCGGAGGGCGACGAGTGCCCATTCCTGCACAGAACCA
CAGGGGACACTGAGCGCAGGTACCACCTTCGTTACTACAAAACTGGAATCTGCATCCACGAGAC
AGACTCGAAAGGCAACTGCACCAAAAACGGCCTGCACTGCGCTTTTGCCCACGGGCCCCATGAC
CTCCGCTCCCCTGTCTACGACATCAGGGAGCTTCAGGCCATGGAGGCCTTGCAGAATGGCCAGA
CCACGGTAGAGGGGAGCATAGAGGGCCAGTCGGCTGGGGCTGCGAGCCATGCCATGATAGAAAA
GATCCTCAGCGAGGAGCCTCGGTGGCAAGAGACTGCTTATGTGCTGGGGAACTATAAGACGGAG
CCTTGCAAGAAGCCCCCGCGGCTGTGCCGCCAAGGCTATGCCTGTCCCTACTACCACAACAGCA
AGGACCGGCGGCGGAGCCCCCGGAAGCACAAATACAGGTCGTCTCCATGTCCAAACGTCAAGCA
CGGGGATGAGTGGGGAGACCCTGGCAAGTGTGAGAACGGAGACGCCTGCCAGTACTGCCACACC
CGCACCGAGCAGCAGTTCCACCCCGAGATCTACAAGTCCACCAAGTGCAACGACATGCAGCAGT
CGGGCAGCTGTCCCCGAGGACCCTTCTGCGCCTTTGCCCACGTAGAACAGCCACCCCTGAGTGA
CGACCTGCAGCCTTCCTCAGCTGTGTCCAGCCCCACCCAGCCAGGTCCTGTCCTGTACATGCCA
TCTGCCGCCGGAGACTCGGTGCCTGTGAGCCCCTCCAGCCCGCATGCCCCTGACCTCAGTGCCC
TCCTCTGTAGAAACAGCAGCCTAGGCAGCCCGTCTAACCTCTGCGGCTCCCCACCGGGCTCCAT
CAGGAAGCCCCCAAACCTGGAGGGCATCGTCTTCCCTGGGGAGTCTGGCCTGGCCCCTGGCAGC
TATAAGAAGGCTCCCGGCTTCGAGAGGGAAGACCAGGTGGGAGCCGAGTACCTGAAAAATTTCA
AATGCCAGGCCAAATTAAAACCCCACTCATTAGAGCCCAGGAGTCAAGAGCAGCCTCTGCTTCA
GCCCAAACAGGACATGCTGGGCATCCTCCCCGCAGGCAGCCCCCTGACCTCAAGCATCTCTTCT
AGTATCACCTCCAGCCTGGCAGCTACCCCCCCTAGCCCAGTGGGCACCAGCAGCGTCCCCGGCA
TGAATGCAAACGCTCTGCCCTTCTACCCCACCAGCGACACGGTAGAGTCAGTCATAGAGTCTGC
TTTGGATGACCTGGACCTGAATGAGTTTGGCGTGGCCGCCCTGGAGAAGACTTTCGATAACAGC
ACAGTGCCCCACCCAGGAAGCATCACCATCGGCGGCAGCTTGCTGCAGAGCTCTGCACCCGTGA
ACATCCCCGGCTCCTTGGGCAGCTCTGCCTCCTTCCACTCAGCATCCCCGTCCCCTCCCGTCAG
CCTCTCCTCGCATTTCCTGCAGCAGCCCCAGGGCCACCTGAGTCAGTCGGAAAACACATTTTTG
GGAACCTCAGCATCACATGGATCTTTGGGTCTGAACGGGATGAACAGCAGCATCTGGGAGCATT
TTGCCTCTGGAAGCTTCTCCCCGGGCACTTCCCCCGCTTTCCTATCAGGGCCAGGGGCTGCCGA
GCTGGCCCGACTTCGGCAAGAGCTGGATGAAGCCAACAGCACCATCAAGCAGTGGGAGGAGTCC
TGGAAGCAGGCCAAGCAGGCTTGTGATGCCTGGAAGAAAGAGGCGGAGGAGGCTGGTGAGCGGG
CCAGTGCGGCGGGCGCCGAGTGCGAGCTGGCCCGGGAGCAGCGGGATGCACTGGAGGTGCAGGT
GAAGAAGCTCCAGGAGGAGCTGGAGCGGCTACACGCGGGGCCTGAGCCCCAGGCCCTGCCCGCC
TTCTCCGACCTGGAGGCGCTCTCACTCTCCACCCTCTACTCCCTCCAGAAACAACTGCGGGCCC
ACCTGGAACAAGTGGACAAGGCCGTGTTCCACATGCAGTCGGTGAAATGCCTTAAGTGTCAGGA
ACAGAAGCGGGCAGTGCTGCCGTGCCAACACGCTGCGCTGTGTGAGCTCTGCGCTGAGGGCAGC
GAGTGCCCCATCTGCCAGCCTGGCCGGGCCCACACCCTCCAGTCGTGACCCTGCAGGCCTGGCC
CAGCCTGGCCCAGATCTTCTCACCTAGGACTTTTTAAAGTATATATATATATATGAATATATAT
ATATATGTGTATGTATGTATGTATATGTATATGATTATGTATATGTATACATTTCCGTATGTAT
GTATATGTATACATTTCCGTATGTGTGCAGGTATGCGTGGTGGTGTGGACAGTGTCTGTGTGTA
TATCTGTACATAGATATAGACACACACTTTAAAAGACTTACCAAGCACTTTTTAAAAGAAGAAA
CTATTTTGCAGTCCTCCCCTACCCACTCCCTGCCCTTCCCACTGCAGAGATGACATCCCCTCTT
CTCCCACTGGCCTTTTGGCAGAGAATCTGGTTCTGTCTCTTTTTTAATGTAGGAACTAACTATT
TTTAACTTCTTCCTGGGGCCTGAGCAGGGAAGGGTGGGACTGGAAGGCACTAAGGGGAAGGGAG
AAGCCCTCAGGGCAGGCCCTGCTCCCCCTACCTCCTTGCCAGGGCAAGGGTGGAGTGTGGAAGA
CGTGGGTCCCCCAGAGCAGGCCTGGCCCCCAGCTGTGAGGGCCTCAGGGAGGCCCGAGGGGGAG
TGCTGGGGGTCTCAGCTGGCTTAGCTCCTAAGTTTACCAAATGTTAATTTAGTCTTGGGGAGAA
CAGCAAGGGCTGGAGGCCAGTGCTGCAGGGCCAGCCCCACTCCTGACACCTGGGCCCTTGAAGC
TCCTTGAGGGGCAAGGCCCAGGAGTTCCAGCCCTCAGGTTCCTGAGGGTCCACCCTCAGTCCTT
CCCCCCGCCGCCCCTCCCCGGACTCCCCACAAGAGCCTCCCTGGCCCCAGGGCCGCCTACCAGG
CTGGTACTCATTCTATGACCACCGCCCCCAACCAGCTGCCCCCAGCTCTCCCTGCCCCCTCCCC
TCTCTGGCAGCTAGCAGGGCAATTGGCGGGGAGGAGTGCGGACTGAGGACTGAGGACCAAGGGG
GCCCAGGCCCTGCCCTCCTACCCGGAGGGGCTCCGTTTGCATTCCTTGGTGCTCTCTGAGTGCA
GCTGGTGTCCCGCCCTGTTCTGGGCGGACGCCTGTGTGCGTGTGTGTGTGCCTGTCCAGTGTAT
ATTGTGTCTTAGCTTCCATTTTAAAAATTGTTCTGTACAGAGAGAGATGCAGCAGGGGCGGGAG
GGCAGAGTGGGCGGAGGGGAGCAGCCGCACCCCCAGCACCGGGTGTCTGCGGTAGGAACAAGAG
GGCTGAGAGGGTCTGGTCCTGGCCCAGGCTCCCCCTTGGGCTCAGCACGAAAGGGCTTTCAATG
AATTAAGTGAAAACTTTTTCCTTTTTTACAAAAATGCAAAAATCAACAAAGCTCCAAACCTATT
GGAAATAAAATATGAACTTGCA

hide sequence

RefSeq Acc Id:

XM_011525401 ⟹ XP_011523703

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	75,814,830 - 75,825,799 (+)	NCBI

Sequence:

show sequence

AGGGGTAGTTGCCTGAGATTGTGGCTCCCTTAATGCCCAGGAGGCACGCTTGGAGGCACAGACC
TGGCCATGCCCATCTACAAGTCCACCAAGTGCAACGACATGCAGCAGTCGGGCAGCTGTCCCCG
AGGACCCTTCTGCGCCTTTGCCCACGTAGAACAGCCACCCCTGAGTGACGACCTGCAGCCTTCC
TCAGCTGTGTCCAGCCCCACCCAGCCAGGTCCTGTCCTGTACATGCCATCTGCCGCCGGAGACT
CGGTGCCTGTGAGCCCCTCCAGCCCGCATGCCCCTGACCTCAGTGCCCTCCTCTGTAGAAACAG
CAGCCTAGGCAGCCCGTCTAACCTCTGCGGCTCCCCACCGGGCTCCATCAGGAAGCCCCCAAAC
CTGGAGGGCATCGTCTTCCCTGGGGAGTCTGGCCTGGCCCCTGGCAGCTATAAGAAGGCTCCCG
GCTTCGAGAGGGAAGACCAGGTGGGAGCCGAGTACCTGAAAAATTTCAAATGCCAGGCCAAATT
AAAACCCCACTCATTAGAGCCCAGGAGTCAAGAGCAGCCTCTGCTTCAGCCCAAACAGGACATG
CTGGGCATCCTCCCCGCAGGCAGCCCCCTGACCTCAAGCATCTCTTCTAGTATCACCTCCAGCC
TGGCAGCTACCCCCCCTAGCCCAGTGGGCACCAGCAGCGTCCCCGGCATGAATGCAAACGCTCT
GCCCTTCTACCCCACCAGCGACACGGTAGAGTCAGTCATAGAGTCTGCTTTGGATGACCTGGAC
CTGAATGAGTTTGGCGTGGCCGCCCTGGAGAAGACTTTCGATAACAGCACAGTGCCCCACCCAG
GAAGCATCACCATCGGCGGCAGCTTGCTGCAGAGCTCTGCACCCGTGAACATCCCCGGCTCCTT
GGGCAGCTCTGCCTCCTTCCACTCAGCATCCCCGTCCCCTCCCGTCAGCCTCTCCTCGCATTTC
CTGCAGCAGCCCCAGGGCCACCTGAGTCAGTCGGAAAACACATTTTTGGGAACCTCAGCATCAC
ATGGATCTTTGGGTCTGAACGGGATGAACAGCAGCATCTGGGAGCATTTTGCCTCTGGAAGCTT
CTCCCCGGGCACTTCCCCCGCTTTCCTATCAGGGCCAGGGGCTGCCGAGCTGGCCCGACTTCGG
CAAGAGCTGGATGAAGCCAACAGCACCATCAAGCAGTGGGAGGAGTCCTGGAAGCAGGCCAAGC
AGGCTTGTGATGCCTGGAAGAAAGAGGCGGAGGAGGCTGGTGAGCGGGCCAGTGCGGCGGGCGC
CGAGTGCGAGCTGGCCCGGGAGCAGCGGGATGCACTGGAGGTGCAGGTGAAGAAGCTCCAGGAG
GAGCTGGAGCGGCTACACGCGGGGCCTGAGCCCCAGGCCCTGCCCGCCTTCTCCGACCTGGAGG
CGCTCTCACTCTCCACCCTCTACTCCCTCCAGAAACAACTGCGGGCCCACCTGGAACAAGTGGA
CAAGGCCGTGTTCCACATGCAGTCGGTGAAATGCCTTAAGTGTCAGGAACAGAAGCGGGCAGTG
CTGCCGTGCCAACACGCTGCGCTGTGTGAGCTCTGCGCTGAGGGCAGCGAGTGCCCCATCTGCC
AGCCTGGCCGGGCCCACACCCTCCAGTCGTGACCCTGCAGGCCTGGCCCAGCCTGGCCCAGATC
TTCTCACCTAGGACTTTTTAAAGTATATATATATATATGAATATATATATATATGTGTATGTAT
GTATGTATATGTATATGATTATGTATATGTATACATTTCCGTATGTATGTATATGTATACATTT
CCGTATGTGTGCAGGTATGCGTGGTGGTGTGGACAGTGTCTGTGTGTATATCTGTACATAGATA
TAGACACACACTTTAAAAGACTTACCAAGCACTTTTTAAAAGAAGAAACTATTTTGCAGTCCTC
CCCTACCCACTCCCTGCCCTTCCCACTGCAGAGATGACATCCCCTCTTCTCCCACTGGCCTTTT
GGCAGAGAATCTGGTTCTGTCTCTTTTTTAATGTAGGAACTAACTATTTTTAACTTCTTCCTGG
GGCCTGAGCAGGGAAGGGTGGGACTGGAAGGCACTAAGGGGAAGGGAGAAGCCCTCAGGGCAGG
CCCTGCTCCCCCTACCTCCTTGCCAGGGCAAGGGTGGAGTGTGGAAGACGTGGGTCCCCCAGAG
CAGGCCTGGCCCCCAGCTGTGAGGGCCTCAGGGAGGCCCGAGGGGGAGTGCTGGGGGTCTCAGC
TGGCTTAGCTCCTAAGTTTACCAAATGTTAATTTAGTCTTGGGGAGAACAGCAAGGGCTGGAGG
CCAGTGCTGCAGGGCCAGCCCCACTCCTGACACCTGGGCCCTTGAAGCTCCTTGAGGGGCAAGG
CCCAGGAGTTCCAGCCCTCAGGTTCCTGAGGGTCCACCCTCAGTCCTTCCCCCCGCCGCCCCTC
CCCGGACTCCCCACAAGAGCCTCCCTGGCCCCAGGGCCGCCTACCAGGCTGGTACTCATTCTAT
GACCACCGCCCCCAACCAGCTGCCCCCAGCTCTCCCTGCCCCCTCCCCTCTCTGGCAGCTAGCA
GGGCAATTGGCGGGGAGGAGTGCGGACTGAGGACTGAGGACCAAGGGGGCCCAGGCCCTGCCCT
CCTACCCGGAGGGGCTCCGTTTGCATTCCTTGGTGCTCTCTGAGTGCAGCTGGTGTCCCGCCCT
GTTCTGGGCGGACGCCTGTGTGCGTGTGTGTGTGCCTGTCCAGTGTATATTGTGTCTTAGCTTC
CATTTTAAAAATTGTTCTGTACAGAGAGAGATGCAGCAGGGGCGGGAGGGCAGAGTGGGCGGAG
GGGAGCAGCCGCACCCCCAGCACCGGGTGTCTGCGGTAGGAACAAGAGGGCTGAGAGGGTCTGG
TCCTGGCCCAGGCTCCCCCTTGGGCTCAGCACGAAAGGGCTTTCAATGAATTAAGTGAAAACTT
TTTCCTTTTTTACAAAAATGCAAAAATCAACAAAGCTCCAAACCTATTGGAAATAAAATATGAA
CTTGCA

hide sequence

RefSeq Acc Id:

XM_017025248 ⟹ XP_016880737

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	75,790,787 - 75,825,799 (+)	NCBI

Sequence:

show sequence

GGGGGGTCTTCACGTTCTCGTGGCGCGGCGCAGGCGCACTGGGTCCTCGGCGCGGACCGCGCAG
ACTGAATAATAAAAGGGGAGCGGCGAAGAGGCAGGAAGACAAGACCATGTCGAAGGGCCCCGGG
CCCGGCGGCTCCGCAGCTTCCTCGGCGCCCCCGGCCGCTACCGCTCAGGTGCTGCAGGCACAGC
CCGAGAAACCGCAGCACTACACCTATGTTAGATACTAAAGAAGGCTTCCCCACAACCCATATGC
ATCTGCTTTGACTGGTGGTTTCTATCATCCTACAAAGACTGTGACTTATTGGTGAGGGCAGCTG
GACAACTCTGAGAGCAACTTAGAGAAATCCATCTTGGGCACACTCTATAAAGGAGCTCCTTCTC
TGCAAATAGCACCCCAGATAAGTGCACAAAAGCAAGATACCCTCGTGGACCTACACGTCCTCCC
GCTTTTCAACACCCTGATGCCTGAAGTGTGTAGAATTTGACAGCAGTATCAAGAGCTGAGGAGA
AGGAGAAGATGGAAAGGAGTCTAGCAACTTAAAAATCTCACAGCATTCTCTGTGAGGTGACCTT
TTTTCCTGTTGGTGGCTCAATTTCTTTAGGACATAAAGAAGATACTGAGGCCTGTGACAGCCTG
TGACAGTATCATCAAGTCGTATCTGAACTTATTGAACTGTTTCCTCCCCTTCCTTATTCTTTAT
TCACAGTTTGCTTTTCATGTGCATAAGTTGACTCATTTGTTTCCTGTTAGCATTTGAAACACCA
TATAGCCACCATAAGTCCTGACAAAATGACTTTTAATAAGGAGGGGGAAGGTCCATGTCCCACC
TTCCTATGAAATTTTGGCCTATTCACAAGTCTACCCCCACATAAGAGAAGTAGTTATGTTCTGT
AAAGAAGAGGTTGATAAAAACCTTTAGCATGGTGTTTTGTGACTTAGAAGTTTTAAGTAGTCGT
TCTTATATCTAAGCATTTATTAATTTTGGTAAGAACATTACTATACGTTTCTGATGTCACTTTT
ACTGTTAAGAGGTGCCAGGCATCTGGTGACCTGTCACTTCAGGATTTGTGTGAATCAGACCATC
TAAATATAATATAAATTAGAGACTGGTACTTGTATTTCCTGATTAAAAACAAAGTAACGTCTGT
TTTACTATTGAAGTAAGAGTACTTTATAATGAATACAAAAATGTATATTAAATATCCAGTAGAG
CATGCTAAAGTGAACATTTCTGTTTTTATTTCAGCAACTTATTTTATGGTATTGTAGTTATGGC
CTGTCCGAAACTCTCTGACATATTCTAAACAGCTTTCAGAGAGTCACTGAGGCTTATTTGCTAC
TACTGTTGTTTTTCCTTTAGCTCAGTTAAGAAATGTTTAGTTAGCCGGGCATGGTGGCTCACGC
CTGTAATCCCAGCATTTTGGGAGGCTGAGGCGGGTGGATTGCCTGAGGTCAGGAGCTCGAGACC
AGCCTGGCCAACATAGTGAAACCCCGTCTCTACTAAAAATACAAAAAACTAGCTGGGTGTGGTG
GCGGGCACCTGTAATCCCAGCTACTAGGGAGGCTGAGGCAGGAGAATCACTAGGACCCAGGAGG
CGCAGGTTGCGGTGAGCCGAGATCACGCCATTGCACTCCAACCTGGGCAACAAGAGTGAAACTC
CGTCTCAAAAAAAAAAAAAAATGCTTAGTTAATAGTCAGCATGGTAGTTAAGAGTACTGACTCC
AGGGTCACACCACCTGGGTTTGAGGCCCAGCTCTGTCAGTTACTAGCTGTGAGATCTTGGGCAA
GTGACTTACCTCTTTGTGTATCAGTTTCCTGAGAATAGGAATATTACCTGTCTCATGGGGTTGT
TATAAGGGTGAAATAAATGAGTTCATACATGTAAAGCGCTTAAAACAGTGCTTGGCACTTAGCA
CAGCGTAGGTACTGTTCTCCGCCATTATTTGAACAGGGCCCTAGTCACTGCTTTCAGTTGCATT
GCTCCTTGCTTCAACAGCCCTGATTGAATGCCTTCTTTAGTTGCATCCACACTAAAATAGATCC
TTCAGTTCCTAGGGCACGCACGGGGCAGCAGCATCTTCAGAGAACAGTTCTCTCTTCCACGTCC
ACTTGAATTCTTATTTCATTCTCCAGTCTTTGTAGCGCCTCCATCATACTGCTTGTATCTTACA
TGATGGATGTGTGTTCTAAACTGACCCATGCAGTTTAGGGCCAAATACGTTGTTGTACAGAAAA
CAATGTACAAAGAACATGTTAGTTTAAACATATTACTAAAGGGTCATAAAACTGGAGGTTTTCC
AGGCTAGCTTTTTCAGGTTAGCTATGTACAGAAAAACTTTGTGGGCTTTTTGTTGTTGTTGTTG
TTGTTGTTGTTTTTGGTTTTTGAGACAGGGTCTCGCTCTGTTGTCCAGGCTGGAGTGCAGTGGT
GTGATCTCCGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGTGATTGTAGTGCCTCAGCCTCCT
GAGTAGCTGAGATTACAGGCACGCGCCACCACACCTGGCTAATTTTTGTATTTTTAGTAGAGAC
GGGGTTTCGCTATGTTGGCCAGGCTGGTCTCATACTCCTGACCTCGAGTGATCTGCCCGTCTTG
ACCTCTCAAAAGTGCTGAGATTACAGGTGTGAGCCACCATGCCTGGCCAGAAAAACTTTGGATA
AAGTCAAGGTATTATATAATTTGGGGGAGGATGAACGGGGGTTTGTAGTACTCTCGAATATTCT
CTAACATCAGTGACGTGAGTGACCCTTATATGAATCTTCCTCAGTTTCACCAGCTCTAGGCCCC
ACAGGGCAAGGGGACAGTTATAGAAAGAAGGGACCATGGACACACAGGACTAATTGCACACCCT
TCCTGGCTCTTGTTAGTTCTTGGGGCCAGGACAGCTCACAGGTGTCAGAAAGTTCCAGTGAGCC
CCAGTGAAAAGTGGGCTGAAATAATTGCCAGTGATTGGCTCCCCCACTGTAAAACACTGACTTG
CTTGAGTGCCCGTAGCACTTGAACTGTGGGTTGCTGTGTGTGTGTGCACGGGCGTGTGTGCCCA
GGTGCGGTAGGGAGTTTCATCGCATCTAGGAGCTTCATAGTAGCCATAAGATCATATTGTATTT
ACTCTGACTAAAGGCCAGTGTGGGATCAAAGACTCCCTTAAAGGTTCAGACACACTTACAAATT
CACCAGACACTTATTTTATTTGCCTGAATAATACTCCCTGAGCTTGCTTTTTCTGCCAGAGAGA
ATATTCTAAATCAGGATCACTTTAGAAGATTTGGAAGCCACATCTCTATAGCTGTGTAGTGTGT
CAGATCCATCCAAATATTTAAAGCTTTTTTTTTTTTTTTTGAGATATGGTCTTACTGTGTCACC
CAGGCTAGAGTGCAGTGACGTAATCATAGCTCACTGCAGCCTTGAACTCCTGGGCTCAAATGAT
CCTCTCACTTCAGCCTCCTGAGTAGCTGGGACTGCAGGTGTTTACCACCATACCCGACTAATTT
TTTATTTTTAAATTTGTTTTGTGAAGTCAGGTTCTTACTGTGTTGCCAGGCTGGTCTGGAACTT
CTGGCCTCAAGCAGTCGTCCTGCCTCTGCTCCCCAAAGTGCTGGGCCTGAGACACCACACCCAG
CCTAAACTAAAAGCCATTTTTAGTAACTCCCACCAATGTGGTTACTGTTACAAAGTTGTATGGT
TTCTGGGTCATGTTTGGTATCAGAATGTGTATGTATATCCTTATAAATATGGAATGTAGAACTG
ATAATAGTTTACCTATCAGATTTGCAAAAATAAGGAAAGATTTTTAGCAGCTTGTAACAAACAT
ATACATACTTGGATAAATAATTTAGAATTTTAACCCATGGCTCATATGCTCTTACAATATTCTC
TTTGAGGGTAAAACATACTTTATTCTTAAACTTAAAGAACCTTTGATAAGCCGTGAATTATGAT
CTCAGTGACTACATTTCTTTTTAGGAGTTATATGTGGGGGAAGGAAAGAAGTAGCTAGCAGGGT
TAACATGGAAAGCAGGAGATTATAGACAAGCATCATTTGAGCCTTTGGATACTACAAATAATCT
TCAAAAATGACAGGTTTTTTGGCTTTTTGTTTTTCCTTTCCTTTAGTGCTAGTTGCAGAATCCT
ATCATATTGTGGTTAGATTTCAATAAAGAATGTTTAAGATTAGGACTATGTCTTGCTTTTTAAA
AAGATCCTATATTCATGTTAAAGCTTGTATATATTTGTTTTTTGTTTTTGTTTTTGTTTTTGAG
ATGGAGTTTCACTCTGTCCCCCAGGCTGGAGTGCGGTGGCGCAATCTCGGCTCACTACAACCTC
TGCCTCCCAGGCTCAAGCAGTTGTCTGCCTCAGCCTCCCAAGCAGCTGGGACTACAGGCATGTG
CCACCATACCCAGGTACCTGAAAGAATTCCGCACAGAGCAGTGCCCACTCTTTGTGCAACACAA
ATGCACGCAGCATCGGCCCTACACCTGCTTCCACTGGCACTTCGTGAACCAGCGGCGCCGCCGG
TCCATCCGCCGTCGGGACGGCACCTTCAATTACAGCCCTGACGTCTACTGCACCAAGTACGACG
AGGCTACAGGCCTCTGCCCGGAGGGCGACGAGTGCCCATTCCTGCACAGAACCACAGGGGACAC
TGAGCGCAGGTACCACCTTCGTTACTACAAAACTGGAATCTGCATCCACGAGACAGACTCGAAA
GGCAACTGCACCAAAAACGGCCTGCACTGCGCTTTTGCCCACGGGCCCCATGACCTCCGCTCCC
CTGTCTACGACATCAGGGAGCTTCAGGCCATGGAGGCCTTGCAGAATGGCCAGACCACGGTAGA
GGGGAGCATAGAGGGCCAGTCGGCTGGGGCTGCGAGCCATGCCATGATAGAAAAGATCCTCAGC
GAGGAGCCTCGGTGGCAAGAGACTGCTTATGTGCTGGGGAACTATAAGACGGAGCCTTGCAAGA
AGCCCCCGCGGCTGTGCCGCCAAGGCTATGCCTGTCCCTACTACCACAACAGCAAGGACCGGCG
GCGGAGCCCCCGGAAGCACAAATACAGGTCGTCTCCATGTCCAAACGTCAAGCACGGGGATGAG
TGGGGAGACCCTGGCAAGTGTGAGAACGGAGACGCCTGCCAGTACTGCCACACCCGCACCGAGC
AGCAGTTCCACCCCGAGATCTACAAGTCCACCAAGTGCAACGACATGCAGCAGTCGGGCAGCTG
TCCCCGAGGACCCTTCTGCGCCTTTGCCCACGTAGAACAGCCACCCCTGAGTGACGACCTGCAG
CCTTCCTCAGCTGTGTCCAGCCCCACCCAGCCAGGTCCTGTCCTGTACATGCCATCTGCCGCCG
GAGACTCGGTGCCTGTGAGCCCCTCCAGCCCGCATGCCCCTGACCTCAGTGCCCTCCTCTGTAG
AAACAGCAGCCTAGGCAGCCCGTCTAACCTCTGCGGCTCCCCACCGGGCTCCATCAGGAAGCCC
CCAAACCTGGAGGGCATCGTCTTCCCTGGGGAGTCTGGCCTGGCCCCTGGCAGCTATAAGAAGG
CTCCCGGCTTCGAGAGGGAAGACCAGGTGGGAGCCGAGTACCTGAAAAATTTCAAATGCCAGGC
CAAATTAAAACCCCACTCATTAGAGCCCAGGAGTCAAGAGCAGCCTCTGCTTCAGCCCAAACAG
GACATGCTGGGCATCCTCCCCGCAGGCAGCCCCCTGACCTCAAGCATCTCTTCTAGTATCACCT
CCAGCCTGGCAGCTACCCCCCCTAGCCCAGTGGGCACCAGCAGCGTCCCCGGCATGAATGCAAA
CGCTCTGCCCTTCTACCCCACCAGCGACACGGTAGAGTCAGTCATAGAGTCTGCTTTGGATGAC
CTGGACCTGAATGAGTTTGGCGTGGCCGCCCTGGAGAAGACTTTCGATAACAGCACAGTGCCCC
ACCCAGGAAGCATCACCATCGGCGGCAGCTTGCTGCAGAGCTCTGCACCCGTGAACATCCCCGG
CTCCTTGGGCAGCTCTGCCTCCTTCCACTCAGCATCCCCGTCCCCTCCCGTCAGCCTCTCCTCG
CATTTCCTGCAGCAGCCCCAGGGCCACCTGAGTCAGTCGGAAAACACATTTTTGGGAACCTCAG
CATCACATGGATCTTTGGGTCTGAACGGGATGAACAGCAGCATCTGGGAGCATTTTGCCTCTGG
AAGCTTCTCCCCGGGCACTTCCCCCGCTTTCCTATCAGGGCCAGGGGCTGCCGAGCTGGCCCGA
CTTCGGCAAGAGCTGGATGAAGCCAACAGCACCATCAAGCAGTGGGAGGAGTCCTGGAAGCAGG
CCAAGCAGGCTTGTGATGCCTGGAAGAAAGAGGCGGAGGAGGCTGGTGAGCGGGCCAGTGCGGC
GGGCGCCGAGTGCGAGCTGGCCCGGGAGCAGCGGGATGCACTGGAGGTGCAGGTGAAGAAGCTC
CAGGAGGAGCTGGAGCGGCTACACGCGGGGCCTGAGCCCCAGGCCCTGCCCGCCTTCTCCGACC
TGGAGGCGCTCTCACTCTCCACCCTCTACTCCCTCCAGAAACAACTGCGGGCCCACCTGGAACA
AGTGGACAAGGCCGTGTTCCACATGCAGTCGGTGAAATGCCTTAAGTGTCAGGAACAGAAGCGG
GCAGTGCTGCCGTGCCAACACGCTGCGCTGTGTGAGCTCTGCGCTGAGGGCAGCGAGTGCCCCA
TCTGCCAGCCTGGCCGGGCCCACACCCTCCAGTCGTGACCCTGCAGGCCTGGCCCAGCCTGGCC
CAGATCTTCTCACCTAGGACTTTTTAAAGTATATATATATATATGAATATATATATATATGTGT
ATGTATGTATGTATATGTATATGATTATGTATATGTATACATTTCCGTATGTATGTATATGTAT
ACATTTCCGTATGTGTGCAGGTATGCGTGGTGGTGTGGACAGTGTCTGTGTGTATATCTGTACA
TAGATATAGACACACACTTTAAAAGACTTACCAAGCACTTTTTAAAAGAAGAAACTATTTTGCA
GTCCTCCCCTACCCACTCCCTGCCCTTCCCACTGCAGAGATGACATCCCCTCTTCTCCCACTGG
CCTTTTGGCAGAGAATCTGGTTCTGTCTCTTTTTTAATGTAGGAACTAACTATTTTTAACTTCT
TCCTGGGGCCTGAGCAGGGAAGGGTGGGACTGGAAGGCACTAAGGGGAAGGGAGAAGCCCTCAG
GGCAGGCCCTGCTCCCCCTACCTCCTTGCCAGGGCAAGGGTGGAGTGTGGAAGACGTGGGTCCC
CCAGAGCAGGCCTGGCCCCCAGCTGTGAGGGCCTCAGGGAGGCCCGAGGGGGAGTGCTGGGGGT
CTCAGCTGGCTTAGCTCCTAAGTTTACCAAATGTTAATTTAGTCTTGGGGAGAACAGCAAGGGC
TGGAGGCCAGTGCTGCAGGGCCAGCCCCACTCCTGACACCTGGGCCCTTGAAGCTCCTTGAGGG
GCAAGGCCCAGGAGTTCCAGCCCTCAGGTTCCTGAGGGTCCACCCTCAGTCCTTCCCCCCGCCG
CCCCTCCCCGGACTCCCCACAAGAGCCTCCCTGGCCCCAGGGCCGCCTACCAGGCTGGTACTCA
TTCTATGACCACCGCCCCCAACCAGCTGCCCCCAGCTCTCCCTGCCCCCTCCCCTCTCTGGCAG
CTAGCAGGGCAATTGGCGGGGAGGAGTGCGGACTGAGGACTGAGGACCAAGGGGGCCCAGGCCC
TGCCCTCCTACCCGGAGGGGCTCCGTTTGCATTCCTTGGTGCTCTCTGAGTGCAGCTGGTGTCC
CGCCCTGTTCTGGGCGGACGCCTGTGTGCGTGTGTGTGTGCCTGTCCAGTGTATATTGTGTCTT
AGCTTCCATTTTAAAAATTGTTCTGTACAGAGAGAGATGCAGCAGGGGCGGGAGGGCAGAGTGG
GCGGAGGGGAGCAGCCGCACCCCCAGCACCGGGTGTCTGCGGTAGGAACAAGAGGGCTGAGAGG
GTCTGGTCCTGGCCCAGGCTCCCCCTTGGGCTCAGCACGAAAGGGCTTTCAATGAATTAAGTGA
AAACTTTTTCCTTTTTTACAAAAATGCAAAAATCAACAAAGCTCCAAACCTATTGGAAATAAAA
TATGAACTTGCA

hide sequence

RefSeq Acc Id:

XM_017025249 ⟹ XP_016880738

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	75,790,906 - 75,825,799 (+)	NCBI

Sequence:

show sequence

AATAATAAAAGGGGAGCGGCGAAGAGGCAGGAAGACAAGACCATGTCGAAGGGCCCCGGGCCCG
GCGGCTCCGCAGCTTCCTCGGCGCCCCCGGCCGCTACCGCTCAGGTGCTGCAGGCACAGCCCGA
GAAACCGCAGCACTACACCTATGTTAGATACTAAAGAAGGCTTCCCCACAACCCATATGCATCT
GCTTTGACTGGTGGTTTCTATCATCCTACAAAGACTGTGACTTATTGGTGAGGGCAGCTGGACA
ACTCTGAGAGCAACTTAGAGAAATCCATCTTGGGCACACTCTATAAAGGAGCTCCTTCTCTGCA
AATAGCACCCCAGATAAGTGCACAAAAGCAAGATACCCTCGTGGACCTACACGTCCTCCCGCTT
TTCAACACCCTGATGCCTGAAGCTATGGTTGATACTAAAGGAGGTTTTCCCACTATCCGTATGC
ATCTTCTCTGTTTTGAGATTGCAACTATGGACAGTTATGGCTAATCCTAGTAGATTGTCTTCCC
TTTTAACATCTTGGATGAATTTGGGTCACACTAATTGTTATGTGAAGATGGATGTTGAATGTAC
CTGAAAGAATTCCGCACAGAGCAGTGCCCACTCTTTGTGCAACACAAATGCACGCAGCATCGGC
CCTACACCTGCTTCCACTGGCACTTCGTGAACCAGCGGCGCCGCCGGTCCATCCGCCGTCGGGA
CGGCACCTTCAATTACAGCCCTGACGTCTACTGCACCAAGTACGACGAGGCTACAGGCCTCTGC
CCGGAGGGCGACGAGTGCCCATTCCTGCACAGAACCACAGGGGACACTGAGCGCAGGTACCACC
TTCGTTACTACAAAACTGGAATCTGCATCCACGAGACAGACTCGAAAGGCAACTGCACCAAAAA
CGGCCTGCACTGCGCTTTTGCCCACGGGCCCCATGACCTCCGCTCCCCTGTCTACGACATCAGG
GAGCTTCAGGCCATGGAGGCCTTGCAGAATGGCCAGACCACGGTAGAGGGGAGCATAGAGGGCC
AGTCGGCTGGGGCTGCGAGCCATGCCATGATAGAAAAGATCCTCAGCGAGGAGCCTCGGTGGCA
AGAGACTGCTTATGTGCTGGGGAACTATAAGACGGAGCCTTGCAAGAAGCCCCCGCGGCTGTGC
CGCCAAGGCTATGCCTGTCCCTACTACCACAACAGCAAGGACCGGCGGCGGAGCCCCCGGAAGC
ACAAATACAGGTCGTCTCCATGTCCAAACGTCAAGCACGGGGATGAGTGGGGAGACCCTGGCAA
GTGTGAGAACGGAGACGCCTGCCAGTACTGCCACACCCGCACCGAGCAGCAGTTCCACCCCGAG
ATCTACAAGTCCACCAAGTGCAACGACATGCAGCAGTCGGGCAGCTGTCCCCGAGGACCCTTCT
GCGCCTTTGCCCACGTAGAACAGCCACCCCTGAGTGACGACCTGCAGCCTTCCTCAGCTGTGTC
CAGCCCCACCCAGCCAGGTCCTGTCCTGTACATGCCATCTGCCGCCGGAGACTCGGTGCCTGTG
AGCCCCTCCAGCCCGCATGCCCCTGACCTCAGTGCCCTCCTCTGTAGAAACAGCAGCCTAGGCA
GCCCGTCTAACCTCTGCGGCTCCCCACCGGGCTCCATCAGGAAGCCCCCAAACCTGGAGGGCAT
CGTCTTCCCTGGGGAGTCTGGCCTGGCCCCTGGCAGCTATAAGAAGGCTCCCGGCTTCGAGAGG
GAAGACCAGGTGGGAGCCGAGTACCTGAAAAATTTCAAATGCCAGGCCAAATTAAAACCCCACT
CATTAGAGCCCAGGAGTCAAGAGCAGCCTCTGCTTCAGCCCAAACAGGACATGCTGGGCATCCT
CCCCGCAGGCAGCCCCCTGACCTCAAGCATCTCTTCTAGTATCACCTCCAGCCTGGCAGCTACC
CCCCCTAGCCCAGTGGGCACCAGCAGCGTCCCCGGCATGAATGCAAACGCTCTGCCCTTCTACC
CCACCAGCGACACGGTAGAGTCAGTCATAGAGTCTGCTTTGGATGACCTGGACCTGAATGAGTT
TGGCGTGGCCGCCCTGGAGAAGACTTTCGATAACAGCACAGTGCCCCACCCAGGAAGCATCACC
ATCGGCGGCAGCTTGCTGCAGAGCTCTGCACCCGTGAACATCCCCGGCTCCTTGGGCAGCTCTG
CCTCCTTCCACTCAGCATCCCCGTCCCCTCCCGTCAGCCTCTCCTCGCATTTCCTGCAGCAGCC
CCAGGGCCACCTGAGTCAGTCGGAAAACACATTTTTGGGAACCTCAGCATCACATGGATCTTTG
GGTCTGAACGGGATGAACAGCAGCATCTGGGAGCATTTTGCCTCTGGAAGCTTCTCCCCGGGCA
CTTCCCCCGCTTTCCTATCAGGGCCAGGGGCTGCCGAGCTGGCCCGACTTCGGCAAGAGCTGGA
TGAAGCCAACAGCACCATCAAGCAGTGGGAGGAGTCCTGGAAGCAGGCCAAGCAGGCTTGTGAT
GCCTGGAAGAAAGAGGCGGAGGAGGCTGGTGAGCGGGCCAGTGCGGCGGGCGCCGAGTGCGAGC
TGGCCCGGGAGCAGCGGGATGCACTGGAGGTGCAGGTGAAGAAGCTCCAGGAGGAGCTGGAGCG
GCTACACGCGGGGCCTGAGCCCCAGGCCCTGCCCGCCTTCTCCGACCTGGAGGCGCTCTCACTC
TCCACCCTCTACTCCCTCCAGAAACAACTGCGGGCCCACCTGGAACAAGTGGACAAGGCCGTGT
TCCACATGCAGTCGGTGAAATGCCTTAAGTGTCAGGAACAGAAGCGGGCAGTGCTGCCGTGCCA
ACACGCTGCGCTGTGTGAGCTCTGCGCTGAGGGCAGCGAGTGCCCCATCTGCCAGCCTGGCCGG
GCCCACACCCTCCAGTCGTGACCCTGCAGGCCTGGCCCAGCCTGGCCCAGATCTTCTCACCTAG
GACTTTTTAAAGTATATATATATATATGAATATATATATATATGTGTATGTATGTATGTATATG
TATATGATTATGTATATGTATACATTTCCGTATGTATGTATATGTATACATTTCCGTATGTGTG
CAGGTATGCGTGGTGGTGTGGACAGTGTCTGTGTGTATATCTGTACATAGATATAGACACACAC
TTTAAAAGACTTACCAAGCACTTTTTAAAAGAAGAAACTATTTTGCAGTCCTCCCCTACCCACT
CCCTGCCCTTCCCACTGCAGAGATGACATCCCCTCTTCTCCCACTGGCCTTTTGGCAGAGAATC
TGGTTCTGTCTCTTTTTTAATGTAGGAACTAACTATTTTTAACTTCTTCCTGGGGCCTGAGCAG
GGAAGGGTGGGACTGGAAGGCACTAAGGGGAAGGGAGAAGCCCTCAGGGCAGGCCCTGCTCCCC
CTACCTCCTTGCCAGGGCAAGGGTGGAGTGTGGAAGACGTGGGTCCCCCAGAGCAGGCCTGGCC
CCCAGCTGTGAGGGCCTCAGGGAGGCCCGAGGGGGAGTGCTGGGGGTCTCAGCTGGCTTAGCTC
CTAAGTTTACCAAATGTTAATTTAGTCTTGGGGAGAACAGCAAGGGCTGGAGGCCAGTGCTGCA
GGGCCAGCCCCACTCCTGACACCTGGGCCCTTGAAGCTCCTTGAGGGGCAAGGCCCAGGAGTTC
CAGCCCTCAGGTTCCTGAGGGTCCACCCTCAGTCCTTCCCCCCGCCGCCCCTCCCCGGACTCCC
CACAAGAGCCTCCCTGGCCCCAGGGCCGCCTACCAGGCTGGTACTCATTCTATGACCACCGCCC
CCAACCAGCTGCCCCCAGCTCTCCCTGCCCCCTCCCCTCTCTGGCAGCTAGCAGGGCAATTGGC
GGGGAGGAGTGCGGACTGAGGACTGAGGACCAAGGGGGCCCAGGCCCTGCCCTCCTACCCGGAG
GGGCTCCGTTTGCATTCCTTGGTGCTCTCTGAGTGCAGCTGGTGTCCCGCCCTGTTCTGGGCGG
ACGCCTGTGTGCGTGTGTGTGTGCCTGTCCAGTGTATATTGTGTCTTAGCTTCCATTTTAAAAA
TTGTTCTGTACAGAGAGAGATGCAGCAGGGGCGGGAGGGCAGAGTGGGCGGAGGGGAGCAGCCG
CACCCCCAGCACCGGGTGTCTGCGGTAGGAACAAGAGGGCTGAGAGGGTCTGGTCCTGGCCCAG
GCTCCCCCTTGGGCTCAGCACGAAAGGGCTTTCAATGAATTAAGTGAAAACTTTTTCCTTTTTT
ACAAAAATGCAAAAATCAACAAAGCTCCAAACCTATTGGAAATAAAATATGAACTTGCA

hide sequence

RefSeq Acc Id:

XM_047436962 ⟹ XP_047292918

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	75,785,048 - 75,825,799 (+)	NCBI

RefSeq Acc Id:

XM_047436963 ⟹ XP_047292919

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	75,790,906 - 75,825,799 (+)	NCBI

RefSeq Acc Id:

XM_047436964 ⟹ XP_047292920

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	75,784,806 - 75,825,799 (+)	NCBI

RefSeq Acc Id:

XM_047436965 ⟹ XP_047292921

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	75,784,806 - 75,825,799 (+)	NCBI

RefSeq Acc Id:

XM_047436966 ⟹ XP_047292922

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	75,790,906 - 75,825,799 (+)	NCBI

RefSeq Acc Id:

XM_054317611 ⟹ XP_054173586

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	76,680,072 - 76,718,950 (+)	NCBI

RefSeq Acc Id:

XM_054317612 ⟹ XP_054173587

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	76,684,152 - 76,718,950 (+)	NCBI

RefSeq Acc Id:

XM_054317613 ⟹ XP_054173588

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	76,678,053 - 76,718,950 (+)	NCBI

RefSeq Acc Id:

XM_054317614 ⟹ XP_054173589

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	76,684,152 - 76,718,950 (+)	NCBI

RefSeq Acc Id:

XM_054317615 ⟹ XP_054173590

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	76,680,072 - 76,718,950 (+)	NCBI

RefSeq Acc Id:

XM_054317616 ⟹ XP_054173591

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	76,684,152 - 76,718,950 (+)	NCBI

RefSeq Acc Id:

XM_054317617 ⟹ XP_054173592

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	76,678,053 - 76,718,950 (+)	NCBI

RefSeq Acc Id:

XM_054317618 ⟹ XP_054173593

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	76,705,424 - 76,718,950 (+)	NCBI

RefSeq Acc Id:

XM_054317619 ⟹ XP_054173594

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	76,707,982 - 76,718,950 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_001073888	(Get FASTA)	NCBI Sequence Viewer
	XP_006722211	(Get FASTA)	NCBI Sequence Viewer
	XP_011523702	(Get FASTA)	NCBI Sequence Viewer
	XP_011523703	(Get FASTA)	NCBI Sequence Viewer
	XP_016880737	(Get FASTA)	NCBI Sequence Viewer
	XP_016880738	(Get FASTA)	NCBI Sequence Viewer
	XP_047292918	(Get FASTA)	NCBI Sequence Viewer
	XP_047292919	(Get FASTA)	NCBI Sequence Viewer
	XP_047292920	(Get FASTA)	NCBI Sequence Viewer
	XP_047292921	(Get FASTA)	NCBI Sequence Viewer
	XP_047292922	(Get FASTA)	NCBI Sequence Viewer
	XP_054173586	(Get FASTA)	NCBI Sequence Viewer
	XP_054173587	(Get FASTA)	NCBI Sequence Viewer
	XP_054173588	(Get FASTA)	NCBI Sequence Viewer
	XP_054173589	(Get FASTA)	NCBI Sequence Viewer
	XP_054173590	(Get FASTA)	NCBI Sequence Viewer
	XP_054173591	(Get FASTA)	NCBI Sequence Viewer
	XP_054173592	(Get FASTA)	NCBI Sequence Viewer
	XP_054173593	(Get FASTA)	NCBI Sequence Viewer
	XP_054173594	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH53362	(Get FASTA)	NCBI Sequence Viewer
	BAB21844	(Get FASTA)	NCBI Sequence Viewer
	EAW89320	(Get FASTA)	NCBI Sequence Viewer
	EAW89321	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000464893
	ENSP00000464893.1
	ENSP00000464953.1
	ENSP00000466054.1
	ENSP00000466431.1
	ENSP00000467726.1
	ENSP00000467849.1
GenBank Protein	Q9C0B0	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:

NP_001073888 ⟸ NM_001080419

- UniProtKB:

Q9C0B0 (UniProtKB/Swiss-Prot)

- Sequence:

show sequence

MSKGPGPGGSAASSAPPAATAQVLQAQPEKPQHYTYLKEFRTEQCPLFVQHKCTQHRPYTCFHW
HFVNQRRRRSIRRRDGTFNYSPDVYCTKYDEATGLCPEGDECPFLHRTTGDTERRYHLRYYKTG
ICIHETDSKGNCTKNGLHCAFAHGPHDLRSPVYDIRELQAMEALQNGQTTVEGSIEGQSAGAAS
HAMIEKILSEEPRWQETAYVLGNYKTEPCKKPPRLCRQGYACPYYHNSKDRRRSPRKHKYRSSP
CPNVKHGDEWGDPGKCENGDACQYCHTRTEQQFHPEIYKSTKCNDMQQSGSCPRGPFCAFAHVE
QPPLSDDLQPSSAVSSPTQPGPVLYMPSAAGDSVPVSPSSPHAPDLSALLCRNSSLGSPSNLCG
SPPGSIRKPPNLEGIVFPGESGLAPGSYKKAPGFEREDQVGAEYLKNFKCQAKLKPHSLEPRSQ
EQPLLQPKQDMLGILPAGSPLTSSISSSITSSLAATPPSPVGTSSVPGMNANALPFYPTSDTVE
SVIESALDDLDLNEFGVAALEKTFDNSTVPHPGSITIGGSLLQSSAPVNIPGSLGSSASFHSAS
PSPPVSLSSHFLQQPQGHLSQSENTFLGTSASHGSLGLNGMNSSIWEHFASGSFSPGTSPAFLS
GPGAAELARLRQELDEANSTIKQWEESWKQAKQACDAWKKEAEEAGERASAAGAECELAREQRD
ALEVQVKKLQEELERLHAGPEPQALPAFSDLEALSLSTLYSLQKQLRAHLEQVDKAVFHMQSVK
CLKCQEQKRAVLPCQHAALCELCAEGSECPICQPGRAHTLQS

hide sequence

RefSeq Acc Id:

XP_006722211 ⟸ XM_006722148

- Peptide Label:

isoform X5

- Sequence:

show sequence

MEALQNGQTTVEGSIEGQSAGAASHAMIEKILSEEPRWQETAYVLGNYKTEPCKKPPRLCRQGY
ACPYYHNSKDRRRSPRKHKYRSSPCPNVKHGDEWGDPGKCENGDACQYCHTRTEQQFHPEIYKS
TKCNDMQQSGSCPRGPFCAFAHVEQPPLSDDLQPSSAVSSPTQPGPVLYMPSAAGDSVPVSPSS
PHAPDLSALLCRNSSLGSPSNLCGSPPGSIRKPPNLEGIVFPGESGLAPGSYKKAPGFEREDQV
GAEYLKNFKCQAKLKPHSLEPRSQEQPLLQPKQDMLGILPAGSPLTSSISSSITSSLAATPPSP
VGTSSVPGMNANALPFYPTSDTVESVIESALDDLDLNEFGVAALEKTFDNSTVPHPGSITIGGS
LLQSSAPVNIPGSLGSSASFHSASPSPPVSLSSHFLQQPQGHLSQSENTFLGTSASHGSLGLNG
MNSSIWEHFASGSFSPGTSPAFLSGPGAAELARLRQELDEANSTIKQWEESWKQAKQACDAWKK
EAEEAGERASAAGAECELAREQRDALEVQVKKLQEELERLHAGPEPQALPAFSDLEALSLSTLY
SLQKQLRAHLEQVDKAVFHMQSVKCLKCQEQKRAVLPCQHAALCELCAEGSECPICQPGRAHTL
QS

hide sequence

RefSeq Acc Id:

XP_011523702 ⟸ XM_011525400

- Peptide Label:

isoform X5

- Sequence:

show sequence

MEALQNGQTTVEGSIEGQSAGAASHAMIEKILSEEPRWQETAYVLGNYKTEPCKKPPRLCRQGY
ACPYYHNSKDRRRSPRKHKYRSSPCPNVKHGDEWGDPGKCENGDACQYCHTRTEQQFHPEIYKS
TKCNDMQQSGSCPRGPFCAFAHVEQPPLSDDLQPSSAVSSPTQPGPVLYMPSAAGDSVPVSPSS
PHAPDLSALLCRNSSLGSPSNLCGSPPGSIRKPPNLEGIVFPGESGLAPGSYKKAPGFEREDQV
GAEYLKNFKCQAKLKPHSLEPRSQEQPLLQPKQDMLGILPAGSPLTSSISSSITSSLAATPPSP
VGTSSVPGMNANALPFYPTSDTVESVIESALDDLDLNEFGVAALEKTFDNSTVPHPGSITIGGS
LLQSSAPVNIPGSLGSSASFHSASPSPPVSLSSHFLQQPQGHLSQSENTFLGTSASHGSLGLNG
MNSSIWEHFASGSFSPGTSPAFLSGPGAAELARLRQELDEANSTIKQWEESWKQAKQACDAWKK
EAEEAGERASAAGAECELAREQRDALEVQVKKLQEELERLHAGPEPQALPAFSDLEALSLSTLY
SLQKQLRAHLEQVDKAVFHMQSVKCLKCQEQKRAVLPCQHAALCELCAEGSECPICQPGRAHTL
QS

hide sequence

RefSeq Acc Id:

XP_011523703 ⟸ XM_011525401

- Peptide Label:

isoform X6

- Sequence:

show sequence

MPIYKSTKCNDMQQSGSCPRGPFCAFAHVEQPPLSDDLQPSSAVSSPTQPGPVLYMPSAAGDSV
PVSPSSPHAPDLSALLCRNSSLGSPSNLCGSPPGSIRKPPNLEGIVFPGESGLAPGSYKKAPGF
EREDQVGAEYLKNFKCQAKLKPHSLEPRSQEQPLLQPKQDMLGILPAGSPLTSSISSSITSSLA
ATPPSPVGTSSVPGMNANALPFYPTSDTVESVIESALDDLDLNEFGVAALEKTFDNSTVPHPGS
ITIGGSLLQSSAPVNIPGSLGSSASFHSASPSPPVSLSSHFLQQPQGHLSQSENTFLGTSASHG
SLGLNGMNSSIWEHFASGSFSPGTSPAFLSGPGAAELARLRQELDEANSTIKQWEESWKQAKQA
CDAWKKEAEEAGERASAAGAECELAREQRDALEVQVKKLQEELERLHAGPEPQALPAFSDLEAL
SLSTLYSLQKQLRAHLEQVDKAVFHMQSVKCLKCQEQKRAVLPCQHAALCELCAEGSECPICQP
GRAHTLQS

hide sequence

RefSeq Acc Id:

XP_016880737 ⟸ XM_017025248

- Peptide Label:

isoform X1

- Sequence:

show sequence

MLKLVYICFLFLFLFLRWSFTLSPRLECGGAISAHYNLCLPGSSSCLPQPPKQLGLQACATIPR
YLKEFRTEQCPLFVQHKCTQHRPYTCFHWHFVNQRRRRSIRRRDGTFNYSPDVYCTKYDEATGL
CPEGDECPFLHRTTGDTERRYHLRYYKTGICIHETDSKGNCTKNGLHCAFAHGPHDLRSPVYDI
RELQAMEALQNGQTTVEGSIEGQSAGAASHAMIEKILSEEPRWQETAYVLGNYKTEPCKKPPRL
CRQGYACPYYHNSKDRRRSPRKHKYRSSPCPNVKHGDEWGDPGKCENGDACQYCHTRTEQQFHP
EIYKSTKCNDMQQSGSCPRGPFCAFAHVEQPPLSDDLQPSSAVSSPTQPGPVLYMPSAAGDSVP
VSPSSPHAPDLSALLCRNSSLGSPSNLCGSPPGSIRKPPNLEGIVFPGESGLAPGSYKKAPGFE
REDQVGAEYLKNFKCQAKLKPHSLEPRSQEQPLLQPKQDMLGILPAGSPLTSSISSSITSSLAA
TPPSPVGTSSVPGMNANALPFYPTSDTVESVIESALDDLDLNEFGVAALEKTFDNSTVPHPGSI
TIGGSLLQSSAPVNIPGSLGSSASFHSASPSPPVSLSSHFLQQPQGHLSQSENTFLGTSASHGS
LGLNGMNSSIWEHFASGSFSPGTSPAFLSGPGAAELARLRQELDEANSTIKQWEESWKQAKQAC
DAWKKEAEEAGERASAAGAECELAREQRDALEVQVKKLQEELERLHAGPEPQALPAFSDLEALS
LSTLYSLQKQLRAHLEQVDKAVFHMQSVKCLKCQEQKRAVLPCQHAALCELCAEGSECPICQPG
RAHTLQS

hide sequence

RefSeq Acc Id:

XP_016880738 ⟸ XM_017025249

- Peptide Label:

isoform X4

- Sequence:

show sequence

MYLKEFRTEQCPLFVQHKCTQHRPYTCFHWHFVNQRRRRSIRRRDGTFNYSPDVYCTKYDEATG
LCPEGDECPFLHRTTGDTERRYHLRYYKTGICIHETDSKGNCTKNGLHCAFAHGPHDLRSPVYD
IRELQAMEALQNGQTTVEGSIEGQSAGAASHAMIEKILSEEPRWQETAYVLGNYKTEPCKKPPR
LCRQGYACPYYHNSKDRRRSPRKHKYRSSPCPNVKHGDEWGDPGKCENGDACQYCHTRTEQQFH
PEIYKSTKCNDMQQSGSCPRGPFCAFAHVEQPPLSDDLQPSSAVSSPTQPGPVLYMPSAAGDSV
PVSPSSPHAPDLSALLCRNSSLGSPSNLCGSPPGSIRKPPNLEGIVFPGESGLAPGSYKKAPGF
EREDQVGAEYLKNFKCQAKLKPHSLEPRSQEQPLLQPKQDMLGILPAGSPLTSSISSSITSSLA
ATPPSPVGTSSVPGMNANALPFYPTSDTVESVIESALDDLDLNEFGVAALEKTFDNSTVPHPGS
ITIGGSLLQSSAPVNIPGSLGSSASFHSASPSPPVSLSSHFLQQPQGHLSQSENTFLGTSASHG
SLGLNGMNSSIWEHFASGSFSPGTSPAFLSGPGAAELARLRQELDEANSTIKQWEESWKQAKQA
CDAWKKEAEEAGERASAAGAECELAREQRDALEVQVKKLQEELERLHAGPEPQALPAFSDLEAL
SLSTLYSLQKQLRAHLEQVDKAVFHMQSVKCLKCQEQKRAVLPCQHAALCELCAEGSECPICQP
GRAHTLQS

hide sequence

Ensembl Acc Id:

ENSP00000466054 ⟸ ENST00000586217

Ensembl Acc Id:

ENSP00000467849 ⟸ ENST00000586527

Ensembl Acc Id:

ENSP00000464953 ⟸ ENST00000587501

Ensembl Acc Id:

ENSP00000467726 ⟸ ENST00000587258

Ensembl Acc Id:

ENSP00000464893 ⟸ ENST00000589666

Ensembl Acc Id:

ENSP00000466431 ⟸ ENST00000592629

RefSeq Acc Id:	XP_047292921 ⟸ XM_047436965
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_047292920 ⟸ XM_047436964
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_047292918 ⟸ XM_047436962
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_047292919 ⟸ XM_047436963
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_047292922 ⟸ XM_047436966
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054173592 ⟸ XM_054317617
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054173588 ⟸ XM_054317613
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054173590 ⟸ XM_054317615
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054173586 ⟸ XM_054317611
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054173589 ⟸ XM_054317614
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054173587 ⟸ XM_054317612
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054173591 ⟸ XM_054317616
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054173593 ⟸ XM_054317618
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054173594 ⟸ XM_054317619
- Peptide Label:	isoform X6

Protein Domains

C3H1-type

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q9C0B0-F1-model_v2	AlphaFold	Q9C0B0	1-810	view protein structure

Promoters

RGD ID:

6794725

Promoter ID:

HG_KWN:27126

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, CD4+TCell_12Hour, CD4+TCell_2Hour, Jurkat

Transcripts:

ENST00000293218, NM_001080419, UC002JPN.2, UC002JPO.2

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	17	71,292,056 - 71,292,722 (+)	MPROMDB

RGD ID:

7236337

Promoter ID:

EPDNEW_H23913

Type:

initiation region

Name:

UNK_1

Description:

unkempt family zinc finger

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	17	75,784,833 - 75,784,893	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:29369	AgrOrtholog
COSMIC	UNK	COSMIC
Ensembl Genes	ENSG00000132478	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000586217.1	UniProtKB/TrEMBL
	ENST00000586527	ENTREZGENE
	ENST00000586527.1	UniProtKB/TrEMBL
	ENST00000587258.1	UniProtKB/TrEMBL
	ENST00000587501.1	UniProtKB/TrEMBL
	ENST00000589666	ENTREZGENE
	ENST00000589666.6	UniProtKB/Swiss-Prot
	ENST00000592629.1	UniProtKB/TrEMBL
Gene3D-CATH	Zinc finger, CCCH-type	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000132478	GTEx
HGNC ID	HGNC:29369	ENTREZGENE
Human Proteome Map	UNK	Human Proteome Map
InterPro	Unkempt-like	UniProtKB/Swiss-Prot
	Unkempt_Znf	UniProtKB/Swiss-Prot
	Znf_CCCH	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Znf_CCCH_sf	UniProtKB/Swiss-Prot
KEGG Report	hsa:85451	UniProtKB/Swiss-Prot
NCBI Gene	85451	ENTREZGENE
OMIM	616375	OMIM
PANTHER	PTHR14493	UniProtKB/Swiss-Prot
	RING FINGER PROTEIN UNKEMPT	UniProtKB/Swiss-Prot
Pfam	zf-CCCH	UniProtKB/Swiss-Prot
	zf_CCCH_5	UniProtKB/Swiss-Prot
PharmGKB	PA162408651	PharmGKB
PROSITE	ZF_C3H1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART	ZnF_C3H1	UniProtKB/Swiss-Prot
Superfamily-SCOP	SSF90229	UniProtKB/Swiss-Prot
UniProt	K7EIZ1_HUMAN	UniProtKB/TrEMBL
	K7ELF5_HUMAN	UniProtKB/TrEMBL
	K7EMB1_HUMAN	UniProtKB/TrEMBL
	K7EQ93_HUMAN	UniProtKB/TrEMBL
	K7EQJ1_HUMAN	UniProtKB/TrEMBL
	Q9C0B0	ENTREZGENE, UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2018-11-29	UNK	unk zinc finger		unkempt family zinc finger	Symbol and/or name change	5135510	APPROVED
2013-10-22	UNK	unkempt family zinc finger		unkempt homolog (Drosophila)	Symbol and/or name change	5135510	APPROVED

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)

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Imported Disease Annotations - ClinVar