HVCN1 (hydrogen voltage gated channel 1)

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Gene: HVCN1 (hydrogen voltage gated channel 1) Homo sapiens

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Symbol:

HVCN1

Name:

hydrogen voltage gated channel 1

RGD ID:

1603943

HGNC Page

HGNC:28240

Description:

Enables protein homodimerization activity and voltage-gated proton channel activity. Involved in several processes, including cellular response to zinc ion; proton transmembrane transport; and regulation of reactive oxygen species biosynthetic process. Located in phagocytic vesicle membrane; plasma membrane; and sperm flagellum.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

HV1; hydrogen voltage-gated channel 1; MGC15619; voltage sensor domain-only protein; voltage-gated hydrogen channel 1; VSOP

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):	Hvcn1 (hydrogen voltage-gated channel 1)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):	Hvcn1 (hydrogen voltage-gated channel 1)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Chinchilla lanigera (long-tailed chinchilla):	Hvcn1 (hydrogen voltage gated channel 1)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	HVCN1 (hydrogen voltage gated channel 1)	NCBI	Ortholog
Canis lupus familiaris (dog):	HVCN1 (hydrogen voltage gated channel 1)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Hvcn1 (hydrogen voltage gated channel 1)	NCBI	Ortholog
Sus scrofa (pig):	HVCN1 (hydrogen voltage gated channel 1)	HGNC	EggNOG, Ensembl, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	HVCN1 (hydrogen voltage gated channel 1)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Hvcn1 (hydrogen voltage gated channel 1)	NCBI	Ortholog
Other homologs ²
Rattus norvegicus (Norway rat):	Vps26c (VPS26 endosomal protein sorting factor C)	HGNC	OMA
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Hvcn1 (hydrogen voltage-gated channel 1)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Hvcn1 (hydrogen voltage-gated channel 1)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	hvcn1 (hydrogen voltage-gated channel 1)	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid\|ZFIN)
Xenopus laevis (African clawed frog):	hvcn1.L	Alliance	DIOPT (Xenbase)
Xenopus tropicalis (tropical clawed frog):	hvcn1	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Xenopus laevis (African clawed frog):	hvcn1.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	12	110,648,686 - 110,704,952 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	12	110,627,841 - 110,704,950 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	12	111,086,491 - 111,127,582 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	12	109,570,874 - 109,612,000 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	12	110,713,319 - 110,754,445 (-)	NCBI		Celera
Cytogenetic Map	12	q24.11	NCBI
HuRef	12	108,104,197 - 108,145,322 (-)	NCBI		HuRef
CHM1_1	12	111,054,153 - 111,095,269 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	12	110,626,380 - 110,682,642 (-)	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

COVID-19 (HEP)

middle cerebral artery infarction (ISO)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

1,1-dichloroethene (ISO)

1,2-dimethylhydrazine (ISO)

17beta-estradiol (ISO)

17beta-estradiol 3-benzoate (ISO)

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

4,4'-sulfonyldiphenol (ISO)

4-hydroxyphenyl retinamide (ISO)

5-aza-2'-deoxycytidine (EXP)

all-trans-retinoic acid (EXP)

alpha-Zearalanol (ISO)

amphetamine (ISO)

benzo[a]pyrene (EXP,ISO)

bis(2-ethylhexyl) phthalate (EXP)

bisphenol A (ISO)

carbon nanotube (ISO)

CGP 52608 (EXP)

chlordecone (ISO)

choline (ISO)

chromium(6+) (ISO)

cisplatin (EXP)

cocaine (ISO)

crocidolite asbestos (ISO)

Cuprizon (ISO)

dimethylarsinic acid (ISO)

dioxygen (ISO)

endosulfan (ISO)

ethyl methanesulfonate (EXP)

folic acid (ISO)

formaldehyde (EXP)

genistein (ISO)

gentamycin (ISO)

L-methionine (ISO)

lidocaine (ISO)

methyl methanesulfonate (EXP)

methylarsonic acid (ISO)

nickel atom (EXP)

niclosamide (EXP)

ozone (ISO)

paracetamol (EXP,ISO)

silicon dioxide (ISO)

sodium arsenate (ISO)

sodium arsenite (EXP,ISO)

testosterone (EXP,ISO)

thioacetamide (ISO)

titanium dioxide (ISO)

trichloroethene (ISO)

triclosan (EXP)

triphenyl phosphate (EXP)

valproic acid (EXP,ISO)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

cell redox homeostasis (TAS)

cellular response to pH (IDA)

cellular response to zinc ion (IDA)

innate immune response (IEA)

monoatomic ion transport (IEA)

positive regulation of superoxide anion generation (IEA,ISO)

proton transmembrane transport (IBA,IDA,IEA,ISO,ISS)

regulation of acrosome reaction (IDA)

regulation of intracellular pH (IEA,IMP,ISO,ISS)

regulation of reactive oxygen species biosynthetic process (IDA,IEA)

response to pH (IEA,ISS)

response to zinc ion (IDA,IEA,ISS)

single fertilization (IEA)

Cellular Component

apical plasma membrane (IEA,ISO)

cytoplasmic vesicle (IEA)

membrane (IDA,IEA)

monoatomic ion channel complex (IEA)

motile cilium (IEA)

phagocytic vesicle membrane (IDA,IEA,TAS)

plasma membrane (IBA,IDA,IEA,TAS)

secretory granule membrane (TAS)

specific granule membrane (TAS)

sperm flagellum (IDA)

Molecular Function

identical protein binding (IEA,IPI)

protein binding (IPI)

protein homodimerization activity (IDA,IEA)

voltage-gated monoatomic cation channel activity (EXP)

voltage-gated proton channel activity (IBA,IDA,IEA,IMP,ISS)

References

References - curated

#	Reference Title	Reference Citation
1.	Neurovascular protection in voltage-gated proton channel Hv1 knock-out rats after ischemic stroke: interaction with Na+ /H+ exchanger-1 antagonism.	Li W, etal., Physiol Rep. 2019 Aug;7(13):e14142. doi: 10.14814/phy2.14142.
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.	Transcriptomic characteristics of bronchoalveolar lavage fluid and peripheral blood mononuclear cells in COVID-19 patients.	Xiong Y, etal., Emerg Microbes Infect. 2020 Dec;9(1):761-770. doi: 10.1080/22221751.2020.1747363.

Additional References at PubMed

PMID:12477932	PMID:12975309	PMID:15342556	PMID:16344560	PMID:16554753	PMID:16556803	PMID:17948262	PMID:18356202	PMID:18509058	PMID:19233200	PMID:19255483	PMID:19805063
PMID:20018719	PMID:20037153	PMID:20139987	PMID:20144758	PMID:20147290	PMID:20543828	PMID:20548053	PMID:20676047	PMID:20693294	PMID:20961760	PMID:21124855	PMID:21516116
PMID:21821008	PMID:21843503	PMID:21873635	PMID:22020278	PMID:22056415	PMID:22367212	PMID:22388960	PMID:23352164	PMID:23352165	PMID:23891691	PMID:23940591	PMID:24379371
PMID:24415791	PMID:24867409	PMID:25296308	PMID:25425665	PMID:25446125	PMID:25964989	PMID:26186194	PMID:26458876	PMID:26559003	PMID:27572256	PMID:27859356	PMID:28013412
PMID:28064239	PMID:28514442	PMID:29743300	PMID:29925021	PMID:30021884	PMID:30196744	PMID:30478045	PMID:31462498	PMID:31633762	PMID:32346069	PMID:32374759	PMID:32788354
PMID:32788614	PMID:32814053	PMID:33807711	PMID:33875847	PMID:33961781	PMID:34158477	PMID:36788452	PMID:37315791	PMID:38272234	PMID:39259593

Genomics

Comparative Map Data

HVCN1
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	12	110,648,686 - 110,704,952 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	12	110,627,841 - 110,704,950 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	12	111,086,491 - 111,127,582 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	12	109,570,874 - 109,612,000 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	12	110,713,319 - 110,754,445 (-)	NCBI		Celera
Cytogenetic Map	12	q24.11	NCBI
HuRef	12	108,104,197 - 108,145,322 (-)	NCBI		HuRef
CHM1_1	12	111,054,153 - 111,095,269 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	12	110,626,380 - 110,682,642 (-)	NCBI		T2T-CHM13v2.0

Hvcn1
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	5	122,344,872 - 122,380,360 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	5	122,344,867 - 122,380,360 (+)	Ensembl		GRCm39 Ensembl
GRCm38	5	122,206,805 - 122,242,297 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	5	122,206,804 - 122,242,297 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	5	122,659,746 - 122,692,306 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	5	122,470,904 - 122,502,890 (+)	NCBI		MGSCv36	mm8
Celera	5	119,292,209 - 119,324,695 (+)	NCBI		Celera
Cytogenetic Map	5	F	NCBI
cM Map	5	62.23	NCBI

Hvcn1
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	12	40,001,205 - 40,030,671 (-)	NCBI		GRCr8
mRatBN7.2	12	34,341,673 - 34,370,010 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	12	34,335,190 - 34,370,141 (-)	Ensembl		mRatBN7.2 Ensembl
Rnor_6.0	12	39,822,814 - 39,851,093 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	12	39,822,637 - 39,850,567 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	12	41,702,567 - 41,731,349 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	12	35,536,954 - 35,556,666 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	12	35,401,133 - 35,431,692 (-)	NCBI
Celera	12	36,012,998 - 36,041,213 (-)	NCBI		Celera
Cytogenetic Map	12	q16	NCBI

Hvcn1
(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_004955482	7,529,277 - 7,538,363 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955482	7,529,009 - 7,563,273 (-)	NCBI	ChiLan1.0	ChiLan1.0

HVCN1
(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	10	118,708,433 - 118,749,147 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	12	118,704,838 - 118,745,536 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	12	108,217,516 - 108,258,210 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	12	111,611,645 - 111,652,240 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	12	111,591,050 - 111,645,632 (-)	Ensembl	panpan1.1		panPan2

HVCN1
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	26	8,437,032 - 8,474,831 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	26	8,419,269 - 8,466,523 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	26	8,600,377 - 8,638,008 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	26	8,695,233 - 8,733,429 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	26	8,693,835 - 8,730,452 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	26	8,653,672 - 8,691,298 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	26	8,715,797 - 8,753,482 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	26	8,668,380 - 8,703,287 (-)	NCBI		UU_Cfam_GSD_1.0

Hvcn1
(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_024405118	155,869,670 - 155,899,754 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936558	3,579,341 - 3,609,789 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936558	3,581,409 - 3,609,714 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

HVCN1
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	14	31,989,170 - 32,043,744 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	14	32,006,837 - 32,044,165 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	14	33,930,483 - 33,965,967 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

HVCN1
(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	11	105,892,024 - 105,932,671 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
Vero_WHO_p1.0	NW_023666037	139,183,839 - 139,225,073 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Hvcn1
(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_004624747	21,256,918 - 21,264,984 (+)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624747	21,237,736 - 21,266,531 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in HVCN1
9 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 12q23.3-24.13(chr12:105234677-112194686)x1	copy number loss	See cases [RCV000050807]	Chr12:105234677..112194686 [GRCh38] Chr12:105628455..112632490 [GRCh37] Chr12:104152585..111116873 [NCBI36] Chr12:12q23.3-24.13	pathogenic
NM_001040107.1(HVCN1):c.95G>A (p.Gly32Glu)	single nucleotide variant	Malignant melanoma [RCV000062397]	Chr12:110661375 [GRCh38] Chr12:111099180 [GRCh37] Chr12:109583563 [NCBI36] Chr12:12q24.11	not provided
NM_024549.5(TCTN1):c.1457C>T (p.Ser486Phe)	single nucleotide variant	Malignant melanoma [RCV000069812]	Chr12:110647215 [GRCh38] Chr12:111085020 [GRCh37] Chr12:109569403 [NCBI36] Chr12:12q24.11	not provided
GRCh38/hg38 12p13.33-q24.33(chr12:121271-133196807)x3	copy number gain	See cases [RCV000139555]	Chr12:121271..133196807 [GRCh38] Chr12:282465..133773393 [GRCh37] Chr12:100698..132283466 [NCBI36] Chr12:12p13.33-q24.33	pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:1-133851895)x3	copy number gain	See cases [RCV000258805]	Chr12:1..133851895 [GRCh37] Chr12:12p13.33-q24.33	pathogenic\|likely pathogenic
GRCh37/hg19 12q23.2-24.11(chr12:103044333-111639805)x1	copy number loss	See cases [RCV000445832]	Chr12:103044333..111639805 [GRCh37] Chr12:12q23.2-24.11	likely pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)x3	copy number gain	See cases [RCV000510482]	Chr12:173787..133777902 [GRCh37] Chr12:12p13.33-q24.33	pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)	copy number gain	See cases [RCV000511643]	Chr12:173787..133777902 [GRCh37] Chr12:12p13.33-q24.33	pathogenic
NM_032369.4(HVCN1):c.535G>A (p.Val179Met)	single nucleotide variant	not specified [RCV004324674]	Chr12:110651325 [GRCh38] Chr12:111089130 [GRCh37] Chr12:12q24.11	uncertain significance
GRCh37/hg19 12p13.33-q24.33(chr12:191619-133777645)x3	copy number gain	not provided [RCV000750246]	Chr12:191619..133777645 [GRCh37] Chr12:12p13.33-q24.33	pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:621220-133779118)x3	copy number gain	not provided [RCV000750253]	Chr12:621220..133779118 [GRCh37] Chr12:12p13.33-q24.33	pathogenic
GRCh37/hg19 12q23.3-24.12(chr12:106498814-112252906)x1	copy number loss	not provided [RCV001259630]	Chr12:106498814..112252906 [GRCh37] Chr12:12q23.3-24.12	pathogenic
GRCh37/hg19 12q23.3-24.12(chr12:104230462-111984801)x1	copy number loss	not provided [RCV001834231]	Chr12:104230462..111984801 [GRCh37] Chr12:12q23.3-24.12	pathogenic
GRCh37/hg19 12q23.2-24.11(chr12:103044333-111639805)	copy number loss	not specified [RCV002053016]	Chr12:103044333..111639805 [GRCh37] Chr12:12q23.2-24.11	likely pathogenic
NM_032369.4(HVCN1):c.704A>G (p.Asn235Ser)	single nucleotide variant	not specified [RCV004107596]	Chr12:110650220 [GRCh38] Chr12:111088025 [GRCh37] Chr12:12q24.11	uncertain significance
NM_032369.4(HVCN1):c.797A>G (p.His266Arg)	single nucleotide variant	not specified [RCV004242064]	Chr12:110649435 [GRCh38] Chr12:111087240 [GRCh37] Chr12:12q24.11	uncertain significance
NM_032369.4(HVCN1):c.713T>C (p.Leu238Ser)	single nucleotide variant	not specified [RCV004273438]	Chr12:110650211 [GRCh38] Chr12:111088016 [GRCh37] Chr12:12q24.11	uncertain significance
NM_032369.4(HVCN1):c.667C>A (p.Arg223Ser)	single nucleotide variant	not specified [RCV004635371]	Chr12:110650257 [GRCh38] Chr12:111088062 [GRCh37] Chr12:12q24.11	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	2193
Count of miRNA genes:	838
Interacting mature miRNAs:	969
Transcripts:	ENST00000242607, ENST00000356742, ENST00000439744, ENST00000546425, ENST00000546713, ENST00000547887, ENST00000548312, ENST00000549442
Prediction methods:	Microtar, 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
407151620	GWAS800596_H	platelet count QTL GWAS800596 (human)		2e-08	platelet quantity (VT:0003179)	platelet count (CMO:0000029)	12	110672222	110672223	Human
407120133	GWAS769109_H	eosinophil count QTL GWAS769109 (human)		3e-10	eosinophil quantity (VT:0002602)	blood eosinophil count (CMO:0000033)	12	110695283	110695284	Human
1559125	SPSL2_H	Serum P-selectin level QTL 2 (human)	2.59		Serum P-selectin level		12	89897665	115897665	Human
1298449	UAE2_H	Urinary albumin excretion QTL 2 (human)	2	0.005	Urinary albumin excretion	urine albumin:creatinine ratio (ACR)	12	102836889	128836889	Human
1643258	BW205_H	Body weight QTL 205 (human)	4.08	0.00001	Body fat amount	percent body fat	12	96630114	122630114	Human
1643452	BW104_H	Body weight QTL 104 (human)	1.89	0.005	Body fat amount	abdominal visceral	12	102395874	128395874	Human
1357361	BW37_H	Body weight QTL 37 (human)	4.08	0.00001	Body fat amount		12	102836889	116423339	Human
407332396	GWAS981372_H	diastolic blood pressure QTL GWAS981372 (human)		1e-13	diastolic blood pressure	diastolic blood pressure (CMO:0000005)	12	110687004	110687005	Human
407284759	GWAS933735_H	body height QTL GWAS933735 (human)		3e-10	body height (VT:0001253)	body height (CMO:0000106)	12	110672222	110672223	Human
407330806	GWAS979782_H	vital capacity QTL GWAS979782 (human)		0.000003	vital capacity		12	110672222	110672223	Human
407106260	GWAS755236_H	erythrocyte count QTL GWAS755236 (human)		2e-11	erythrocyte count	red blood cell count (CMO:0000025)	12	110672958	110672959	Human
1643264	BW195_H	Body weight QTL 195 (human)		0.0151	Body weight	BMI	12	89897665	115897665	Human
406992411	GWAS641387_H	immunoglobulin isotype switching measurement QTL GWAS641387 (human)		1e-09	immunoglobulin isotype switching measurement		12	110688804	110688805	Human
1357387	BW58_H	Body weight QTL 58 (human)	2.3	0.0001	Body weight	fat free mass after exercise training	12	89438856	115438856	Human
1358827	MULTSCL22_H	Multiple sclerosis susceptibility QTL 22 (human)			Multiple sclerosis susceptibility		12	89897665	115897665	Human
407148507	GWAS797483_H	platelet count QTL GWAS797483 (human)		4e-14	platelet quantity (VT:0003179)	platelet count (CMO:0000029)	12	110672222	110672223	Human

Markers in Region

RH68803

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	12	111,087,059 - 111,087,170	UniSTS	GRCh37
Build 36	12	109,571,442 - 109,571,553	RGD	NCBI36
Celera	12	110,713,887 - 110,713,998	RGD
Cytogenetic Map	12	q24.11	UniSTS
HuRef	12	108,104,765 - 108,104,876	UniSTS
GeneMap99-GB4 RH Map	12	427.17	UniSTS
NCBI RH Map	12	711.2	UniSTS

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001040107	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001256413	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_032369	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005253948	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011538838	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011538839	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011538840	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011538841	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011538842	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011538844	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011538845	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011538846	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011538847	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017020026	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017020027	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024449225	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047429669	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047429670	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054373470	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054373471	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054373472	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054373473	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054373474	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054373475	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054373476	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054373477	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054373478	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054373479	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054373480	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054373481	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054373482	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054373483	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC144522	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK293543	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY359054	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC007277	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC009731	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC032672	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BP369986	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BP375483	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471054	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068266	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB310328	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	GU211002	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000242607 ⟹ ENSP00000242607

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	110,648,686 - 110,689,115 (-)	Ensembl

Ensembl Acc Id:

ENST00000356742 ⟹ ENSP00000349181

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	110,648,797 - 110,688,709 (-)	Ensembl

Ensembl Acc Id:

ENST00000439744 ⟹ ENSP00000412052

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	110,649,133 - 110,689,778 (-)	Ensembl

Ensembl Acc Id:

ENST00000546425

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	110,682,655 - 110,689,819 (-)	Ensembl

Ensembl Acc Id:

ENST00000546713 ⟹ ENSP00000447227

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	110,661,235 - 110,704,950 (-)	Ensembl

Ensembl Acc Id:

ENST00000547887 ⟹ ENSP00000448379

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	110,651,325 - 110,683,267 (-)	Ensembl

Ensembl Acc Id:

ENST00000548312 ⟹ ENSP00000449601

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	110,627,841 - 110,689,417 (-)	Ensembl

Ensembl Acc Id:

ENST00000549442 ⟹ ENSP00000450106

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	110,651,218 - 110,689,809 (-)	Ensembl

Ensembl Acc Id:

ENST00000620084 ⟹ ENSP00000479812

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	110,648,686 - 110,683,267 (-)	Ensembl

RefSeq Acc Id:

NM_001040107 ⟹ NP_001035196

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	110,648,686 - 110,689,777 (-)	NCBI
GRCh37	12	111,086,491 - 111,130,276 (-)	NCBI
Build 36	12	109,570,874 - 109,612,000 (-)	NCBI Archive
HuRef	12	108,104,197 - 108,145,322 (-)	ENTREZGENE
CHM1_1	12	111,054,153 - 111,095,269 (-)	NCBI
T2T-CHM13v2.0	12	110,626,380 - 110,667,470 (-)	NCBI

Sequence:

show sequence

GTACGAGTTGGCCCGGAGCAAGGCGGCCCAGGACAGGCAGGGGCTGCACGCGGTGAAGAAACCA
AGACGCAGAGAGGCCAAGCCCCTTGCCTTGGGTCACACAGCCAAAGGAGGCAGAGCCAGAACTC
ACAACCAGATCCAGAGGCAACAGGGACATGGCCACCTGGGACGAAAAGGCAGTCACCCGCAGGG
CCAAGGTGGCTCCCGCTGAGAGGATGAGCAAGTTCTTAAGGCACTTCACGGTCGTGGGAGACGA
CTACCATGCCTGGAACATCAACTACAAGAAATGGGAGAATGAAGAGGAGGAGGAGGAGGAGGAG
CAGCCACCACCCACACCAGTCTCAGGCGAGGAAGGCAGAGCTGCAGCCCCTGACGTTGCCCCTG
CCCCTGGCCCCGCACCCAGGGCCCCCCTTGACTTCAGGGGCATGTTGAGGAAACTGTTCAGCTC
CCACAGGTTTCAGGTCATCATCATCTGCTTGGTGGTTCTGGATGCCCTCCTGGTGCTTGCTGAG
CTCATCCTGGACCTGAAGATCATCCAGCCCGACAAGAATAACTATGCTGCCATGGTATTCCACT
ACATGAGCATCACCATCTTGGTCTTTTTTATGATGGAGATCATCTTTAAATTATTTGTCTTCCG
CCTGGAGTTCTTTCACCACAAGTTTGAGATCCTGGATGCCGTCGTGGTGGTGGTCTCATTCATC
CTCGACATTGTCCTCCTGTTCCAGGAGCACCAGTTTGAGGCTCTGGGCCTGCTGATTCTGCTCC
GGCTGTGGCGGGTGGCCCGGATCATCAATGGGATTATCATCTCAGTTAAGACACGTTCAGAACG
GCAACTCTTAAGGTTAAAACAGATGAATGTACAATTGGCCGCCAAGATTCAACACCTTGAGTTC
AGCTGCTCTGAGAAGGAACAAGAAATTGAAAGACTTAACAAACTATTGCGACAGCATGGACTTC
TTGGTGAAGTGAACTAGACCCGGACCAGCTCCCCTCAAAAAGAAGACACTGTCTCATGGGCCTG
TGCTGTCACGAGAGGAACAGCTGCCCCTCCTGGGCCGCTTGGTGAGAGGTTTGGTTTGATACCT
CTGCCTCCCTCCTGCCAGCATGGATTCTGGGTGGACACAGCCTTGTGGAAGGTCCAGTACCACC
AAGAGCTGCCCATCCACTCCCACCCCACACTGTATCAAATGTATCACATTTTCTCATGTTGAAC
ACTTTAGCCTTAATTGAAAATGAGCAACAAAGCTGGACAATTGCTAGTTGTATATAAAATTTAA
TCTCACCGAATGTACAGTTTTCAAATTTCACGTGTATATTAAGGAACTGATGCATCTGAGCATT
CTGAAAGAAAGAAAAAGAAGCTACTTTAGCTGCCACCCCATTCTAGAAAAGTCTCTTATTTTCA
AGCTGTTCTAAATAGCTTCGTCTCAGTTTCCCCAAAAGGGGTACCCAGGCCCCTCCTCTGTGTG
CCCCAGCTGCATCAGCCAGCTTCTAGGTGGCTCCATTGTTTTCTGCCACCTGACAACATTTTTC
CTCAATTACTGTACAACTACTGTATAAAATAAAACAACTACTGTATAAAATAAACTCTCTCTTT
TCCCTGGACCCTCCTACTGTATTCTTTCCTCTGTGGCACCCATACCAGCCTGCCAGTCGGAGAG
CAAGCTAGCTACAGTGCCTGGTGCAGAAATGGCAATT

hide sequence

RefSeq Acc Id:

NM_001256413 ⟹ NP_001243342

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	110,648,686 - 110,689,777 (-)	NCBI
GRCh37	12	111,086,491 - 111,130,276 (-)	NCBI
HuRef	12	108,104,197 - 108,145,322 (-)	NCBI
CHM1_1	12	111,054,153 - 111,095,269 (-)	NCBI
T2T-CHM13v2.0	12	110,626,380 - 110,667,470 (-)	NCBI

Sequence:

show sequence

GTACGAGTTGGCCCGGAGCAAGGCGGCCCAGGACAGGCAGGGGCTGCACGCGGTGAAGAAACCA
AGACGCAGAGAGGCCAAGCCCCTTGCCTTGGGTCACACAGCCAAAGGAGGCAGAGCCAGAACTC
ACAACCAGGCAGTCACCCGCAGGGCCAAGGTGGCTCCCGCTGAGAGGATGAGCAAGTTCTTAAG
GCACTTCACGGTCGTGGGAGACGACTACCATGCCTGGAACATCAACTACAAGAAATGGGAGAAT
GAAGAGGAGGAGGAGGAGGAGGAGCAGCCACCACCCACACCAGTCTCAGGCGAGGAAGGCAGAG
CTGCAGCCCCTGACGTTGCCCCTGCCCCTGGCCCCGCACCCAGGGCCCCCCTTGACTTCAGGGG
CATGTTGAGGAAACTGTTCAGCTCCCACAGGTTTCAGGTCATCATCATCTGCTTGGTGGTTCTG
GATGCCCTCCTGGTGCTTGCTGAGCTCATCCTGGACCTGAAGATCATCCAGCCCGACAAGAATA
ACTATGCTGCCATGGTATTCCACTACATGAGCATCACCATCTTGGTCTTTTTTATGATGGAGAT
CATCTTTAAATTATTTGTCTTCCGCCTGGAGTTCTTTCACCACAAGTTTGAGATCCTGGATGCC
GTCGTGGTGGTGGTCTCATTCATCCTCGACATTGTCCTCCTGTTCCAGGAGCACCAGTTTGAGG
CTCTGGGCCTGCTGATTCTGCTCCGGCTGTGGCGGGTGGCCCGGATCATCAATGGGATTATCAT
CTCAGTTAAGACACGTTCAGAACGGCAACTCTTAAGGTTAAAACAGATGAATGTACAATTGGCC
GCCAAGATTCAACACCTTGAGTTCAGCTGCTCTGAGAAGGAACAAGAAATTGAAAGACTTAACA
AACTATTGCGACAGCATGGACTTCTTGGTGAAGTGAACTAGACCCGGACCAGCTCCCCTCAAAA
AGAAGACACTGTCTCATGGGCCTGTGCTGTCACGAGAGGAACAGCTGCCCCTCCTGGGCCGCTT
GGTGAGAGGTTTGGTTTGATACCTCTGCCTCCCTCCTGCCAGCATGGATTCTGGGTGGACACAG
CCTTGTGGAAGGTCCAGTACCACCAAGAGCTGCCCATCCACTCCCACCCCACACTGTATCAAAT
GTATCACATTTTCTCATGTTGAACACTTTAGCCTTAATTGAAAATGAGCAACAAAGCTGGACAA
TTGCTAGTTGTATATAAAATTTAATCTCACCGAATGTACAGTTTTCAAATTTCACGTGTATATT
AAGGAACTGATGCATCTGAGCATTCTGAAAGAAAGAAAAAGAAGCTACTTTAGCTGCCACCCCA
TTCTAGAAAAGTCTCTTATTTTCAAGCTGTTCTAAATAGCTTCGTCTCAGTTTCCCCAAAAGGG
GTACCCAGGCCCCTCCTCTGTGTGCCCCAGCTGCATCAGCCAGCTTCTAGGTGGCTCCATTGTT
TTCTGCCACCTGACAACATTTTTCCTCAATTACTGTACAACTACTGTATAAAATAAAACAACTA
CTGTATAAAATAAACTCTCTCTTTTCCCTGGACCCTCCTACTGTATTCTTTCCTCTGTGGCACC
CATACCAGCCTGCCAGTCGGAGAGCAAGCTAGCTACAGTGCCTGGTGCAGAAATGGCAATT

hide sequence

RefSeq Acc Id:

NM_032369 ⟹ NP_115745

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	110,648,686 - 110,689,115 (-)	NCBI
GRCh37	12	111,086,491 - 111,130,276 (-)	NCBI
Build 36	12	109,570,874 - 109,611,329 (-)	NCBI Archive
HuRef	12	108,104,197 - 108,145,322 (-)	ENTREZGENE
CHM1_1	12	111,054,153 - 111,094,614 (-)	NCBI
T2T-CHM13v2.0	12	110,626,380 - 110,666,808 (-)	NCBI

Sequence:

show sequence

AGTCGCAGCGGTGACCGCGGGCGGGTGGGGCGCCGGGTGAAGAAACCAAGACGCAGAGAGGCCA
AGCCCCTTGCCTTGGGTCACACAGCCAAAGGAGGCAGAGCCAGAACTCACAACCAGATCCAGAG
GCAACAGGGACATGGCCACCTGGGACGAAAAGGCAGTCACCCGCAGGGCCAAGGTGGCTCCCGC
TGAGAGGATGAGCAAGTTCTTAAGGCACTTCACGGTCGTGGGAGACGACTACCATGCCTGGAAC
ATCAACTACAAGAAATGGGAGAATGAAGAGGAGGAGGAGGAGGAGGAGCAGCCACCACCCACAC
CAGTCTCAGGCGAGGAAGGCAGAGCTGCAGCCCCTGACGTTGCCCCTGCCCCTGGCCCCGCACC
CAGGGCCCCCCTTGACTTCAGGGGCATGTTGAGGAAACTGTTCAGCTCCCACAGGTTTCAGGTC
ATCATCATCTGCTTGGTGGTTCTGGATGCCCTCCTGGTGCTTGCTGAGCTCATCCTGGACCTGA
AGATCATCCAGCCCGACAAGAATAACTATGCTGCCATGGTATTCCACTACATGAGCATCACCAT
CTTGGTCTTTTTTATGATGGAGATCATCTTTAAATTATTTGTCTTCCGCCTGGAGTTCTTTCAC
CACAAGTTTGAGATCCTGGATGCCGTCGTGGTGGTGGTCTCATTCATCCTCGACATTGTCCTCC
TGTTCCAGGAGCACCAGTTTGAGGCTCTGGGCCTGCTGATTCTGCTCCGGCTGTGGCGGGTGGC
CCGGATCATCAATGGGATTATCATCTCAGTTAAGACACGTTCAGAACGGCAACTCTTAAGGTTA
AAACAGATGAATGTACAATTGGCCGCCAAGATTCAACACCTTGAGTTCAGCTGCTCTGAGAAGG
AACAAGAAATTGAAAGACTTAACAAACTATTGCGACAGCATGGACTTCTTGGTGAAGTGAACTA
GACCCGGACCAGCTCCCCTCAAAAAGAAGACACTGTCTCATGGGCCTGTGCTGTCACGAGAGGA
ACAGCTGCCCCTCCTGGGCCGCTTGGTGAGAGGTTTGGTTTGATACCTCTGCCTCCCTCCTGCC
AGCATGGATTCTGGGTGGACACAGCCTTGTGGAAGGTCCAGTACCACCAAGAGCTGCCCATCCA
CTCCCACCCCACACTGTATCAAATGTATCACATTTTCTCATGTTGAACACTTTAGCCTTAATTG
AAAATGAGCAACAAAGCTGGACAATTGCTAGTTGTATATAAAATTTAATCTCACCGAATGTACA
GTTTTCAAATTTCACGTGTATATTAAGGAACTGATGCATCTGAGCATTCTGAAAGAAAGAAAAA
GAAGCTACTTTAGCTGCCACCCCATTCTAGAAAAGTCTCTTATTTTCAAGCTGTTCTAAATAGC
TTCGTCTCAGTTTCCCCAAAAGGGGTACCCAGGCCCCTCCTCTGTGTGCCCCAGCTGCATCAGC
CAGCTTCTAGGTGGCTCCATTGTTTTCTGCCACCTGACAACATTTTTCCTCAATTACTGTACAA
CTACTGTATAAAATAAAACAACTACTGTATAAAATAAACTCTCTCTTTTCCCTGGACCCTCCTA
CTGTATTCTTTCCTCTGTGGCACCCATACCAGCCTGCCAGTCGGAGAGCAAGCTAGCTACAGTG
CCTGGTGCAGAAATGGCAATT

hide sequence

RefSeq Acc Id:

XM_005253948 ⟹ XP_005254005

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	110,648,686 - 110,689,777 (-)	NCBI
GRCh37	12	111,086,491 - 111,130,276 (-)	NCBI

Sequence:

show sequence

CCCATGAGCAGCCTCAGAGCCCTCGACCAAGGGAAGTTCTGAGGGCTGAGAGGTTGCTCATTCG
TCAGAGCGTGCTGCCCACCCTCCACCCCTGCATGGCAGAAACTGTGCAGGGGACGAGGCCAAGG
AATCAGGAGACCCAGAGGCAGGGGTGGCCCGGAGACGGTGAAGAAACCAAGACGCAGAGAGGCC
AAGCCCCTTGCCTTGGGTCACACAGCCAAAGGAGGCAGAGCCAGAACTCACAACCAGATCCAGA
GGCAACAGGGACATGGCCACCTGGGACGAAAAGGCAGTCACCCGCAGGGCCAAGGTGGCTCCCG
CTGAGAGGATGAGCAAGTTCTTAAGGCACTTCACGGTCGTGGGAGACGACTACCATGCCTGGAA
CATCAACTACAAGAAATGGGAGAATGAAGAGGAGGAGGAGGAGGAGGAGCAGCCACCACCCACA
CCAGTCTCAGGCGAGGAAGGCAGAGCTGCAGCCCCTGACGTTGCCCCTGCCCCTGGCCCCGCAC
CCAGGGCCCCCCTTGACTTCAGGGGCATGTTGAGGAAACTGTTCAGCTCCCACAGGTTTCAGGT
CATCATCATCTGCTTGGTGGTTCTGGATGCCCTCCTGGTGCTTGCTGAGCTCATCCTGGACCTG
AAGATCATCCAGCCCGACAAGAATAACTATGCTGCCATGGTATTCCACTACATGAGCATCACCA
TCTTGGTCTTTTTTATGATGGAGATCATCTTTAAATTATTTGTCTTCCGCCTGGAGTTCTTTCA
CCACAAGTTTGAGATCCTGGATGCCGTCGTGGTGGTGGTCTCATTCATCCTCGACATTGTCCTC
CTGTTCCAGGAGCACCAGTTTGAGGCTCTGGGCCTGCTGATTCTGCTCCGGCTGTGGCGGGTGG
CCCGGATCATCAATGGGATTATCATCTCAGTTAAGACACGTTCAGAACGGCAACTCTTAAGGTT
AAAACAGATGAATGTACAATTGGCCGCCAAGATTCAACACCTTGAGTTCAGCTGCTCTGAGAAG
GAACAAGAAATTGAAAGACTTAACAAACTATTGCGACAGCATGGACTTCTTGGTGAAGTGAACT
AGACCCGGACCAGCTCCCCTCAAAAAGAAGACACTGTCTCATGGGCCTGTGCTGTCACGAGAGG
AACAGCTGCCCCTCCTGGGCCGCTTGGTGAGAGGTTTGGTTTGATACCTCTGCCTCCCTCCTGC
CAGCATGGATTCTGGGTGGACACAGCCTTGTGGAAGGTCCAGTACCACCAAGAGCTGCCCATCC
ACTCCCACCCCACACTGTATCAAATGTATCACATTTTCTCATGTTGAACACTTTAGCCTTAATT
GAAAATGAGCAACAAAGCTGGACAATTGCTAGTTGTATATAAAATTTAATCTCACCGAATGTAC
AGTTTTCAAATTTCACGTGTATATTAAGGAACTGATGCATCTGAGCATTCTGAAAGAAAGAAAA
AGAAGCTACTTTAGCTGCCACCCCATTCTAGAAAAGTCTCTTATTTTCAAGCTGTTCTAAATAG
CTTCGTCTCAGTTTCCCCAAAAGGGGTACCCAGGCCCCTCCTCTGTGTGCCCCAGCTGCATCAG
CCAGCTTCTAGGTGGCTCCATTGTTTTCTGCCACCTGACAACATTTTTCCTCAATTACTGTACA
ACTACTGTATAAAATAAAACAACTACTGTATAAAATAAACTCTCTCTTTTCCCTGGA

hide sequence

RefSeq Acc Id:

XM_011538838 ⟹ XP_011537140

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	110,648,686 - 110,689,115 (-)	NCBI

Sequence:

show sequence

GCGGGACGGGCTGGGCCGGACCTGCTCTGAGGCTCCCAGTCGCAGCGGTGACCGCGGGCGGGTG
GGGCGCCGGGTGAAGAAACCAAGACGCAGAGAGGCCAAGCCCCTTGCCTTGGGTCACACAGCCA
AAGGAGGCAGAGCCAGAACTCACAACCAGATCCAGAGGCAACAGGGACATGGCCACCTGGGACG
AAAAGGCCTTCCTCAGAACACGGATCCCCTGGGGCAGGAAGGGAGAAGTGCTGGGGGCAGCTGA
GCCTGCTGCTTGGAGTCCTCTTGCCTCCCCACAGAGAAGAGATTTGCTCAGGGGTTTCATTCCA
CCTTCCACCATCCAGGAGGCAGTCACCCGCAGGGCCAAGGTGGCTCCCGCTGAGAGGATGAGCA
AGTTCTTAAGGCACTTCACGGTCGTGGGAGACGACTACCATGCCTGGAACATCAACTACAAGAA
ATGGGAGAATGAAGAGGAGGAGGAGGAGGAGGAGCAGCCACCACCCACACCAGTCTCAGGCGAG
GAAGGCAGAGCTGCAGCCCCTGACGTTGCCCCTGCCCCTGGCCCCGCACCCAGGGCCCCCCTTG
ACTTCAGGGGCATGTTGAGGAAACTGTTCAGCTCCCACAGGTTTCAGGTCATCATCATCTGCTT
GGTGGTTCTGGATGCCCTCCTGGTGCTTGCTGAGCTCATCCTGGACCTGAAGATCATCCAGCCC
GACAAGAATAACTATGCTGCCATGGTATTCCACTACATGAGCATCACCATCTTGGTCTTTTTTA
TGATGGAGATCATCTTTAAATTATTTGTCTTCCGCCTGGAGTTCTTTCACCACAAGTTTGAGAT
CCTGGATGCCGTCGTGGTGGTGGTCTCATTCATCCTCGACATTGTCCTCCTGTTCCAGGAGCAC
CAGTTTGAGGCTCTGGGCCTGCTGATTCTGCTCCGGCTGTGGCGGGTGGCCCGGATCATCAATG
GGATTATCATCTCAGTTAAGACACGTTCAGAACGGCAACTCTTAAGGTTAAAACAGATGAATGT
ACAATTGGCCGCCAAGATTCAACACCTTGAGTTCAGCTGCTCTGAGAAGGAACAAGAAATTGAA
AGACTTAACAAACTATTGCGACAGCATGGACTTCTTGGTGAAGTGAACTAGACCCGGACCAGCT
CCCCTCAAAAAGAAGACACTGTCTCATGGGCCTGTGCTGTCACGAGAGGAACAGCTGCCCCTCC
TGGGCCGCTTGGTGAGAGGTTTGGTTTGATACCTCTGCCTCCCTCCTGCCAGCATGGATTCTGG
GTGGACACAGCCTTGTGGAAGGTCCAGTACCACCAAGAGCTGCCCATCCACTCCCACCCCACAC
TGTATCAAATGTATCACATTTTCTCATGTTGAACACTTTAGCCTTAATTGAAAATGAGCAACAA
AGCTGGACAATTGCTAGTTGTATATAAAATTTAATCTCACCGAATGTACAGTTTTCAAATTTCA
CGTGTATATTAAGGAACTGATGCATCTGAGCATTCTGAAAGAAAGAAAAAGAAGCTACTTTAGC
TGCCACCCCATTCTAGAAAAGTCTCTTATTTTCAAGCTGTTCTAAATAGCTTCGTCTCAGTTTC
CCCAAAAGGGGTACCCAGGCCCCTCCTCTGTGTGCCCCAGCTGCATCAGCCAGCTTCTAGGTGG
CTCCATTGTTTTCTGCCACCTGACAACATTTTTCCTCAATTACTGTACAACTACTGTATAAAAT
AAAACAACTACTGTATAAAATAAACTCTCTCTTTTCCCTGGA

hide sequence

RefSeq Acc Id:

XM_011538839 ⟹ XP_011537141

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	110,648,686 - 110,689,777 (-)	NCBI

Sequence:

show sequence

CCACAGGGGAGGGACTTCAGAGCTGGGCCTGCGCCTGCGGGGCCGTACGAGTTGGCCCGGAGCA
AGGCGGCCCAGGACAGGCAGGGGCTGCACGCGGTGAAGAAACCAAGACGCAGAGAGGCCAAGCC
CCTTGCCTTGGGTCACACAGCCAAAGGAGGCAGAGCCAGAACTCACAACCAGATCCAGAGGCAA
CAGGGACATGGCCACCTGGGACGAAAAGGCCTTCCTCAGAACACGGATCCCCTGGGGCAGGAAG
GGAGAAGTGCTGGGGGCAGCTGAGCCTGCTGCTTGGAGTCCTCTTGCCTCCCCACAGAGAAGAG
ATTTGCTCAGGGGTTTCATTCCACCTTCCACCATCCAGGAGGCAGTCACCCGCAGGGCCAAGGT
GGCTCCCGCTGAGAGGATGAGCAAGTTCTTAAGGCACTTCACGGTCGTGGGAGACGACTACCAT
GCCTGGAACATCAACTACAAGAAATGGGAGAATGAAGAGGAGGAGGAGGAGGAGGAGCAGCCAC
CACCCACACCAGTCTCAGGCGAGGAAGGCAGAGCTGCAGCCCCTGACGTTGCCCCTGCCCCTGG
CCCCGCACCCAGGGCCCCCCTTGACTTCAGGGGCATGTTGAGGAAACTGTTCAGCTCCCACAGG
TTTCAGGTCATCATCATCTGCTTGGTGGTTCTGGATGCCCTCCTGGTGCTTGCTGAGCTCATCC
TGGACCTGAAGATCATCCAGCCCGACAAGAATAACTATGCTGCCATGGTATTCCACTACATGAG
CATCACCATCTTGGTCTTTTTTATGATGGAGATCATCTTTAAATTATTTGTCTTCCGCCTGGAG
TTCTTTCACCACAAGTTTGAGATCCTGGATGCCGTCGTGGTGGTGGTCTCATTCATCCTCGACA
TTGTCCTCCTGTTCCAGGAGCACCAGTTTGAGGCTCTGGGCCTGCTGATTCTGCTCCGGCTGTG
GCGGGTGGCCCGGATCATCAATGGGATTATCATCTCAGTTAAGACACGTTCAGAACGGCAACTC
TTAAGGTTAAAACAGATGAATGTACAATTGGCCGCCAAGATTCAACACCTTGAGTTCAGCTGCT
CTGAGAAGGAACAAGAAATTGAAAGACTTAACAAACTATTGCGACAGCATGGACTTCTTGGTGA
AGTGAACTAGACCCGGACCAGCTCCCCTCAAAAAGAAGACACTGTCTCATGGGCCTGTGCTGTC
ACGAGAGGAACAGCTGCCCCTCCTGGGCCGCTTGGTGAGAGGTTTGGTTTGATACCTCTGCCTC
CCTCCTGCCAGCATGGATTCTGGGTGGACACAGCCTTGTGGAAGGTCCAGTACCACCAAGAGCT
GCCCATCCACTCCCACCCCACACTGTATCAAATGTATCACATTTTCTCATGTTGAACACTTTAG
CCTTAATTGAAAATGAGCAACAAAGCTGGACAATTGCTAGTTGTATATAAAATTTAATCTCACC
GAATGTACAGTTTTCAAATTTCACGTGTATATTAAGGAACTGATGCATCTGAGCATTCTGAAAG
AAAGAAAAAGAAGCTACTTTAGCTGCCACCCCATTCTAGAAAAGTCTCTTATTTTCAAGCTGTT
CTAAATAGCTTCGTCTCAGTTTCCCCAAAAGGGGTACCCAGGCCCCTCCTCTGTGTGCCCCAGC
TGCATCAGCCAGCTTCTAGGTGGCTCCATTGTTTTCTGCCACCTGACAACATTTTTCCTCAATT
ACTGTACAACTACTGTATAAAATAAAACAACTACTGTATAAAATAAACTCTCTCTTTTCCCTGG
A

hide sequence

RefSeq Acc Id:

XM_011538840 ⟹ XP_011537142

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	110,648,686 - 110,689,777 (-)	NCBI

Sequence:

show sequence

TTCTGAGGGCTGAGAGGTTGCTCATTCGTCAGAGCGTGCTGCCCACCCTCCACCCCTGCATGGC
AGAAACTGTGCAGGGGACGAGGCCAAGGAATCAGGAGACCCAGAGGCAGGGGTGGCCCGGAGAC
GGTGAAGAAACCAAGACGCAGAGAGGCCAAGCCCCTTGCCTTGGGTCACACAGCCAAAGGAGGC
AGAGCCAGAACTCACAACCAGATCCAGAGGCAACAGGGACATGGCCACCTGGGACGAAAAGGCC
TTCCTCAGAACACGGATCCCCTGGGGCAGGAAGGGAGAAGTGCTGGGGGCAGCTGAGCCTGCTG
CTTGGAGTCCTCTTGCCTCCCCACAGAGAAGAGATTTGCTCAGGGGTTTCATTCCACCTTCCAC
CATCCAGGAGGCAGTCACCCGCAGGGCCAAGGTGGCTCCCGCTGAGAGGATGAGCAAGTTCTTA
AGGCACTTCACGGTCGTGGGAGACGACTACCATGCCTGGAACATCAACTACAAGAAATGGGAGA
ATGAAGAGGAGGAGGAGGAGGAGGAGCAGCCACCACCCACACCAGTCTCAGGCGAGGAAGGCAG
AGCTGCAGCCCCTGACGTTGCCCCTGCCCCTGGCCCCGCACCCAGGGCCCCCCTTGACTTCAGG
GGCATGTTGAGGAAACTGTTCAGCTCCCACAGGTTTCAGGTCATCATCATCTGCTTGGTGGTTC
TGGATGCCCTCCTGGTGCTTGCTGAGCTCATCCTGGACCTGAAGATCATCCAGCCCGACAAGAA
TAACTATGCTGCCATGGTATTCCACTACATGAGCATCACCATCTTGGTCTTTTTTATGATGGAG
ATCATCTTTAAATTATTTGTCTTCCGCCTGGAGTTCTTTCACCACAAGTTTGAGATCCTGGATG
CCGTCGTGGTGGTGGTCTCATTCATCCTCGACATTGTCCTCCTGTTCCAGGAGCACCAGTTTGA
GGCTCTGGGCCTGCTGATTCTGCTCCGGCTGTGGCGGGTGGCCCGGATCATCAATGGGATTATC
ATCTCAGTTAAGACACGTTCAGAACGGCAACTCTTAAGGTTAAAACAGATGAATGTACAATTGG
CCGCCAAGATTCAACACCTTGAGTTCAGCTGCTCTGAGAAGGAACAAGAAATTGAAAGACTTAA
CAAACTATTGCGACAGCATGGACTTCTTGGTGAAGTGAACTAGACCCGGACCAGCTCCCCTCAA
AAAGAAGACACTGTCTCATGGGCCTGTGCTGTCACGAGAGGAACAGCTGCCCCTCCTGGGCCGC
TTGGTGAGAGGTTTGGTTTGATACCTCTGCCTCCCTCCTGCCAGCATGGATTCTGGGTGGACAC
AGCCTTGTGGAAGGTCCAGTACCACCAAGAGCTGCCCATCCACTCCCACCCCACACTGTATCAA
ATGTATCACATTTTCTCATGTTGAACACTTTAGCCTTAATTGAAAATGAGCAACAAAGCTGGAC
AATTGCTAGTTGTATATAAAATTTAATCTCACCGAATGTACAGTTTTCAAATTTCACGTGTATA
TTAAGGAACTGATGCATCTGAGCATTCTGAAAGAAAGAAAAAGAAGCTACTTTAGCTGCCACCC
CATTCTAGAAAAGTCTCTTATTTTCAAGCTGTTCTAAATAGCTTCGTCTCAGTTTCCCCAAAAG
GGGTACCCAGGCCCCTCCTCTGTGTGCCCCAGCTGCATCAGCCAGCTTCTAGGTGGCTCCATTG
TTTTCTGCCACCTGACAACATTTTTCCTCAATTACTGTACAACTACTGTATAAAATAAAACAAC
TACTGTATAAAATAAACTCTCTCTTTTCCCTGGA

hide sequence

RefSeq Acc Id:

XM_011538841 ⟹ XP_011537143

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	110,648,686 - 110,689,409 (-)	NCBI

Sequence:

show sequence

GGATTTTTGTGATCCGCGATTCGCTCCCACGGGCGGGACCTTTGTAACTGCGGGAGGCCCAGGA
CAGGCCCACCCTGCGGGGCGGGAGGCAGCCGGGGTGAGGGAGGTGAAGAAACCAAGACGCAGAG
AGGCCAAGCCCCTTGCCTTGGGTCACACAGCCAAAGGAGGCAGAGCCAGAACTCACAACCAGAT
CCAGAGGCAACAGGGACATGGCCACCTGGGACGAAAAGGCCTTCCTCAGAACACGGATCCCCTG
GGGCAGGAAGGGAGAAGTGCTGGGGGCAGCTGAGCCTGCTGCTTGGAGTCCTCTTGCCTCCCCA
CAGAGAAGAGATTTGCTCAGGGGTTTCATTCCACCTTCCACCATCCAGGAGGCAGTCACCCGCA
GGGCCAAGGTGGCTCCCGCTGAGAGGATGAGCAAGTTCTTAAGGCACTTCACGGTCGTGGGAGA
CGACTACCATGCCTGGAACATCAACTACAAGAAATGGGAGAATGAAGAGGAGGAGGAGGAGGAG
GAGCAGCCACCACCCACACCAGTCTCAGGCGAGGAAGGCAGAGCTGCAGCCCCTGACGTTGCCC
CTGCCCCTGGCCCCGCACCCAGGGCCCCCCTTGACTTCAGGGGCATGTTGAGGAAACTGTTCAG
CTCCCACAGGTTTCAGGTCATCATCATCTGCTTGGTGGTTCTGGATGCCCTCCTGGTGCTTGCT
GAGCTCATCCTGGACCTGAAGATCATCCAGCCCGACAAGAATAACTATGCTGCCATGGTATTCC
ACTACATGAGCATCACCATCTTGGTCTTTTTTATGATGGAGATCATCTTTAAATTATTTGTCTT
CCGCCTGGAGTTCTTTCACCACAAGTTTGAGATCCTGGATGCCGTCGTGGTGGTGGTCTCATTC
ATCCTCGACATTGTCCTCCTGTTCCAGGAGCACCAGTTTGAGGCTCTGGGCCTGCTGATTCTGC
TCCGGCTGTGGCGGGTGGCCCGGATCATCAATGGGATTATCATCTCAGTTAAGACACGTTCAGA
ACGGCAACTCTTAAGGTTAAAACAGATGAATGTACAATTGGCCGCCAAGATTCAACACCTTGAG
TTCAGCTGCTCTGAGAAGGAACAAGAAATTGAAAGACTTAACAAACTATTGCGACAGCATGGAC
TTCTTGGTGAAGTGAACTAGACCCGGACCAGCTCCCCTCAAAAAGAAGACACTGTCTCATGGGC
CTGTGCTGTCACGAGAGGAACAGCTGCCCCTCCTGGGCCGCTTGGTGAGAGGTTTGGTTTGATA
CCTCTGCCTCCCTCCTGCCAGCATGGATTCTGGGTGGACACAGCCTTGTGGAAGGTCCAGTACC
ACCAAGAGCTGCCCATCCACTCCCACCCCACACTGTATCAAATGTATCACATTTTCTCATGTTG
AACACTTTAGCCTTAATTGAAAATGAGCAACAAAGCTGGACAATTGCTAGTTGTATATAAAATT
TAATCTCACCGAATGTACAGTTTTCAAATTTCACGTGTATATTAAGGAACTGATGCATCTGAGC
ATTCTGAAAGAAAGAAAAAGAAGCTACTTTAGCTGCCACCCCATTCTAGAAAAGTCTCTTATTT
TCAAGCTGTTCTAAATAGCTTCGTCTCAGTTTCCCCAAAAGGGGTACCCAGGCCCCTCCTCTGT
GTGCCCCAGCTGCATCAGCCAGCTTCTAGGTGGCTCCATTGTTTTCTGCCACCTGACAACATTT
TTCCTCAATTACTGTACAACTACTGTATAAAATAAAACAACTACTGTATAAAATAAACTCTCTC
TTTTCCCTGGA

hide sequence

RefSeq Acc Id:

XM_011538842 ⟹ XP_011537144

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	110,648,686 - 110,698,718 (-)	NCBI

Sequence:

show sequence

GAGGAAACTCCTGGAAGTCCCTGCAGACAGTGCTCGGGTCCCCCTGGCCAGAGCATTTGATGAT
CACATGACCTCTGCTGCAACAGGTGAAGAAACCAAGACGCAGAGAGGCCAAGCCCCTTGCCTTG
GGTCACACAGCCAAAGGAGGCAGAGCCAGAACTCACAACCAGATCCAGAGGCAACAGGGACATG
GCCACCTGGGACGAAAAGGCCTTCCTCAGAACACGGATCCCCTGGGGCAGGAAGGGAGAAGTGC
TGGGGGCAGCTGAGCCTGCTGCTTGGAGTCCTCTTGCCTCCCCACAGAGAAGAGATTTGCTCAG
GGGTTTCATTCCACCTTCCACCATCCAGGAGGCAGTCACCCGCAGGGCCAAGGTGGCTCCCGCT
GAGAGGATGAGCAAGTTCTTAAGGCACTTCACGGTCGTGGGAGACGACTACCATGCCTGGAACA
TCAACTACAAGAAATGGGAGAATGAAGAGGAGGAGGAGGAGGAGGAGCAGCCACCACCCACACC
AGTCTCAGGCGAGGAAGGCAGAGCTGCAGCCCCTGACGTTGCCCCTGCCCCTGGCCCCGCACCC
AGGGCCCCCCTTGACTTCAGGGGCATGTTGAGGAAACTGTTCAGCTCCCACAGGTTTCAGGTCA
TCATCATCTGCTTGGTGGTTCTGGATGCCCTCCTGGTGCTTGCTGAGCTCATCCTGGACCTGAA
GATCATCCAGCCCGACAAGAATAACTATGCTGCCATGGTATTCCACTACATGAGCATCACCATC
TTGGTCTTTTTTATGATGGAGATCATCTTTAAATTATTTGTCTTCCGCCTGGAGTTCTTTCACC
ACAAGTTTGAGATCCTGGATGCCGTCGTGGTGGTGGTCTCATTCATCCTCGACATTGTCCTCCT
GTTCCAGGAGCACCAGTTTGAGGCTCTGGGCCTGCTGATTCTGCTCCGGCTGTGGCGGGTGGCC
CGGATCATCAATGGGATTATCATCTCAGTTAAGACACGTTCAGAACGGCAACTCTTAAGGTTAA
AACAGATGAATGTACAATTGGCCGCCAAGATTCAACACCTTGAGTTCAGCTGCTCTGAGAAGGA
ACAAGAAATTGAAAGACTTAACAAACTATTGCGACAGCATGGACTTCTTGGTGAAGTGAACTAG
ACCCGGACCAGCTCCCCTCAAAAAGAAGACACTGTCTCATGGGCCTGTGCTGTCACGAGAGGAA
CAGCTGCCCCTCCTGGGCCGCTTGGTGAGAGGTTTGGTTTGATACCTCTGCCTCCCTCCTGCCA
GCATGGATTCTGGGTGGACACAGCCTTGTGGAAGGTCCAGTACCACCAAGAGCTGCCCATCCAC
TCCCACCCCACACTGTATCAAATGTATCACATTTTCTCATGTTGAACACTTTAGCCTTAATTGA
AAATGAGCAACAAAGCTGGACAATTGCTAGTTGTATATAAAATTTAATCTCACCGAATGTACAG
TTTTCAAATTTCACGTGTATATTAAGGAACTGATGCATCTGAGCATTCTGAAAGAAAGAAAAAG
AAGCTACTTTAGCTGCCACCCCATTCTAGAAAAGTCTCTTATTTTCAAGCTGTTCTAAATAGCT
TCGTCTCAGTTTCCCCAAAAGGGGTACCCAGGCCCCTCCTCTGTGTGCCCCAGCTGCATCAGCC
AGCTTCTAGGTGGCTCCATTGTTTTCTGCCACCTGACAACATTTTTCCTCAATTACTGTACAAC
TACTGTATAAAATAAAACAACTACTGTATAAAATAAACTCTCTCTTTTCCCTGGA

hide sequence

RefSeq Acc Id:

XM_011538844 ⟹ XP_011537146

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	110,648,686 - 110,689,409 (-)	NCBI

Sequence:

show sequence

GGCAGGATTTTTGTGATCCGCGATTCGCTCCCACGGGCGGGACCTTTGTAACTGCGGGAGGCCC
AGGACAGGCCCACCCTGCGGGGCGGGAGGCAGCCGGGGTGAAGAAACCAAGACGCAGAGAGGCC
AAGCCCCTTGCCTTGGGTCACACAGCCAAAGGAGGCAGAGCCAGAACTCACAACCAGATCCAGA
GGCAACAGGGACATGGCCACCTGGGACGAAAAGGCCTTCCTCAGAACACGGATCCCCTGGGGCA
GGAAGGGAGAAGTGCTGGGGGCAGCTGAGCCTGCTGCTTGGAGTCCTCTTGCCTCCCCACAGAG
AAGAGATTTGCTCAGGGGTTTCATTCCACCTTCCACCATCCAGGAGGCAGTCACCCGCAGGGCC
AAGGTGGCTCCCGCTGAGAGGATGAGCAAGTTCTTAAGGCACTTCACGGTCGTGGGAGACGACT
ACCATGCCTGGAACATCAACTACAAGAAATGGGAGAATGAAGAGGAGGAGGAGGAGGAGGAGCA
GCCACCACCCACACCAGTCTCAGGCGAGGAAGGCAGAGCTGCAGCCCCTGACGTTGCCCCTGCC
CCTGGCCCCGCACCCAGGGCCCCCCTTGACTTCAGGGGCATGTTGAGGAAACTGTTCAGCTCCC
ACAGGTTTCAGGTCATCATCATCTGCTTGGTGGTTCTGGATGCCCTCCTGGTGCTTGCTGAGCT
CATCCTGGACCTGAAGATCATCCAGCCCGACAAGAATAACTATGCTGCCATGGTATTCCACTAC
ATGAGCATCACCATCTTGGTCTTTTTTATGATGGAGATCATCTTTAAATTATTTGTCTTCCGCC
TGGAGTTCTTTCACCACAAGTTTGAGATCCTGGATGCCGTCGTGGTGGTGGTCTCATTCATCCT
CGACATTGTCCTCCTGTTCCAGGAGCACCAGTTTGAGGCTCTGGGCCTGCTGATTCTGCTCCGG
CTGTGGCGGGTGGCCCGGATCATCAATGGGATTATCATCTCAGTTAAGACACGTTCAGAACGGC
AACTCTTAAGGTTAAAACAGATGAATGTACAATTGGCCGCCAAGATTCAACACCTTGAGTTCAG
CTGCTCTGAGAAGGAACAAGAAATTGAAAGACTTAACAAACTATTGCGACAGCATGGACTTCTT
GGTGAAGTGAACTAGACCCGGACCAGCTCCCCTCAAAAAGAAGACACTGTCTCATGGGCCTGTG
CTGTCACGAGAGGAACAGCTGCCCCTCCTGGGCCGCTTGGTGAGAGGTTTGGTTTGATACCTCT
GCCTCCCTCCTGCCAGCATGGATTCTGGGTGGACACAGCCTTGTGGAAGGTCCAGTACCACCAA
GAGCTGCCCATCCACTCCCACCCCACACTGTATCAAATGTATCACATTTTCTCATGTTGAACAC
TTTAGCCTTAATTGAAAATGAGCAACAAAGCTGGACAATTGCTAGTTGTATATAAAATTTAATC
TCACCGAATGTACAGTTTTCAAATTTCACGTGTATATTAAGGAACTGATGCATCTGAGCATTCT
GAAAGAAAGAAAAAGAAGCTACTTTAGCTGCCACCCCATTCTAGAAAAGTCTCTTATTTTCAAG
CTGTTCTAAATAGCTTCGTCTCAGTTTCCCCAAAAGGGGTACCCAGGCCCCTCCTCTGTGTGCC
CCAGCTGCATCAGCCAGCTTCTAGGTGGCTCCATTGTTTTCTGCCACCTGACAACATTTTTCCT
CAATTACTGTACAACTACTGTATAAAATAAAACAACTACTGTATAAAATAAACTCTCTCTTTTC
CCTGGA

hide sequence

RefSeq Acc Id:

XM_011538845 ⟹ XP_011537147

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	110,648,686 - 110,689,409 (-)	NCBI

Sequence:

show sequence

TTTTGTGATCCGCGATTCGCTCCCACGGGCGGGACCTTTGTAACTGCGGGAGGCCCAGGACAGG
CCCACCCTGCGGGGCGGGAGGCAGCCGGGGTGAGGGAGGTGAAGAAACCAAGACGCAGAGAGGC
CAAGCCCCTTGCCTTGGGTCACACAGCCAAAGGAGGCAGAGCCAGAACTCACAACCAGATCCAG
AGGCAACAGGGACATGGCCACCTGGGACGAAAAGGCAGTCACCCGCAGGGCCAAGGTGGCTCCC
GCTGAGAGGATGAGCAAGTTCTTAAGGCACTTCACGGTCGTGGGAGACGACTACCATGCCTGGA
ACATCAACTACAAGAAATGGGAGAATGAAGAGGAGGAGGAGGAGGAGGAGCAGCCACCACCCAC
ACCAGTCTCAGGCGAGGAAGGCAGAGCTGCAGCCCCTGACGTTGCCCCTGCCCCTGGCCCCGCA
CCCAGGGCCCCCCTTGACTTCAGGGGCATGTTGAGGAAACTGTTCAGCTCCCACAGGTTTCAGG
TCATCATCATCTGCTTGGTGGTTCTGGATGCCCTCCTGGTGCTTGCTGAGCTCATCCTGGACCT
GAAGATCATCCAGCCCGACAAGAATAACTATGCTGCCATGGTATTCCACTACATGAGCATCACC
ATCTTGGTCTTTTTTATGATGGAGATCATCTTTAAATTATTTGTCTTCCGCCTGGAGTTCTTTC
ACCACAAGTTTGAGATCCTGGATGCCGTCGTGGTGGTGGTCTCATTCATCCTCGACATTGTCCT
CCTGTTCCAGGAGCACCAGTTTGAGGCTCTGGGCCTGCTGATTCTGCTCCGGCTGTGGCGGGTG
GCCCGGATCATCAATGGGATTATCATCTCAGTTAAGACACGTTCAGAACGGCAACTCTTAAGGT
TAAAACAGATGAATGTACAATTGGCCGCCAAGATTCAACACCTTGAGTTCAGCTGCTCTGAGAA
GGAACAAGAAATTGAAAGACTTAACAAACTATTGCGACAGCATGGACTTCTTGGTGAAGTGAAC
TAGACCCGGACCAGCTCCCCTCAAAAAGAAGACACTGTCTCATGGGCCTGTGCTGTCACGAGAG
GAACAGCTGCCCCTCCTGGGCCGCTTGGTGAGAGGTTTGGTTTGATACCTCTGCCTCCCTCCTG
CCAGCATGGATTCTGGGTGGACACAGCCTTGTGGAAGGTCCAGTACCACCAAGAGCTGCCCATC
CACTCCCACCCCACACTGTATCAAATGTATCACATTTTCTCATGTTGAACACTTTAGCCTTAAT
TGAAAATGAGCAACAAAGCTGGACAATTGCTAGTTGTATATAAAATTTAATCTCACCGAATGTA
CAGTTTTCAAATTTCACGTGTATATTAAGGAACTGATGCATCTGAGCATTCTGAAAGAAAGAAA
AAGAAGCTACTTTAGCTGCCACCCCATTCTAGAAAAGTCTCTTATTTTCAAGCTGTTCTAAATA
GCTTCGTCTCAGTTTCCCCAAAAGGGGTACCCAGGCCCCTCCTCTGTGTGCCCCAGCTGCATCA
GCCAGCTTCTAGGTGGCTCCATTGTTTTCTGCCACCTGACAACATTTTTCCTCAATTACTGTAC
AACTACTGTATAAAATAAAACAACTACTGTATAAAATAAACTCTCTCTTTTCCCTGGA

hide sequence

RefSeq Acc Id:

XM_011538846 ⟹ XP_011537148

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	110,648,686 - 110,704,952 (-)	NCBI

Sequence:

show sequence

TTTCCCAGCCTGCCTCCTGGAGGTGAACATGTGCAGGTGGAGAAGTGCCCACTGCATCGGGGCC
AAAAGAGAGAACGCTGCCTACCTCACCCCAACGGCATTTGAAAGTAGACTGGCTCATCTGAAAT
GCTTATTTGCAAGCATCTAACTTCCTGACCCTGTGTCACAGATGGCCCCACTTGGCCCCAAGCC
CCTGGTGAAGAAACCAAGACGCAGAGAGGCCAAGCCCCTTGCCTTGGGTCACACAGCCAAAGGA
GGCAGAGCCAGAACTCACAACCAGATCCAGAGGCAACAGGGACATGGCCACCTGGGACGAAAAG
GCAGTCACCCGCAGGGCCAAGGTGGCTCCCGCTGAGAGGATGAGCAAGTTCTTAAGGCACTTCA
CGGTCGTGGGAGACGACTACCATGCCTGGAACATCAACTACAAGAAATGGGAGAATGAAGAGGA
GGAGGAGGAGGAGGAGCAGCCACCACCCACACCAGTCTCAGGCGAGGAAGGCAGAGCTGCAGCC
CCTGACGTTGCCCCTGCCCCTGGCCCCGCACCCAGGGCCCCCCTTGACTTCAGGGGCATGTTGA
GGAAACTGTTCAGCTCCCACAGGTTTCAGGTCATCATCATCTGCTTGGTGGTTCTGGATGCCCT
CCTGGTGCTTGCTGAGCTCATCCTGGACCTGAAGATCATCCAGCCCGACAAGAATAACTATGCT
GCCATGGTATTCCACTACATGAGCATCACCATCTTGGTCTTTTTTATGATGGAGATCATCTTTA
AATTATTTGTCTTCCGCCTGGAGTTCTTTCACCACAAGTTTGAGATCCTGGATGCCGTCGTGGT
GGTGGTCTCATTCATCCTCGACATTGTCCTCCTGTTCCAGGAGCACCAGTTTGAGGCTCTGGGC
CTGCTGATTCTGCTCCGGCTGTGGCGGGTGGCCCGGATCATCAATGGGATTATCATCTCAGTTA
AGACACGTTCAGAACGGCAACTCTTAAGGTTAAAACAGATGAATGTACAATTGGCCGCCAAGAT
TCAACACCTTGAGTTCAGCTGCTCTGAGAAGGAACAAGAAATTGAAAGACTTAACAAACTATTG
CGACAGCATGGACTTCTTGGTGAAGTGAACTAGACCCGGACCAGCTCCCCTCAAAAAGAAGACA
CTGTCTCATGGGCCTGTGCTGTCACGAGAGGAACAGCTGCCCCTCCTGGGCCGCTTGGTGAGAG
GTTTGGTTTGATACCTCTGCCTCCCTCCTGCCAGCATGGATTCTGGGTGGACACAGCCTTGTGG
AAGGTCCAGTACCACCAAGAGCTGCCCATCCACTCCCACCCCACACTGTATCAAATGTATCACA
TTTTCTCATGTTGAACACTTTAGCCTTAATTGAAAATGAGCAACAAAGCTGGACAATTGCTAGT
TGTATATAAAATTTAATCTCACCGAATGTACAGTTTTCAAATTTCACGTGTATATTAAGGAACT
GATGCATCTGAGCATTCTGAAAGAAAGAAAAAGAAGCTACTTTAGCTGCCACCCCATTCTAGAA
AAGTCTCTTATTTTCAAGCTGTTCTAAATAGCTTCGTCTCAGTTTCCCCAAAAGGGGTACCCAG
GCCCCTCCTCTGTGTGCCCCAGCTGCATCAGCCAGCTTCTAGGTGGCTCCATTGTTTTCTGCCA
CCTGACAACATTTTTCCTCAATTACTGTACAACTACTGTATAAAATAAAACAACTACTGTATAA
AATAAACTCTCTCTTTTCCCTGGA

hide sequence

RefSeq Acc Id:

XM_011538847 ⟹ XP_011537149

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	110,648,686 - 110,699,299 (-)	NCBI

Sequence:

show sequence

GCCGAGAACACGAAATGTGCCCTGGGCTGCAGCCAAGACCCAGCAAAGCCCAGCAAAGCCCAGC
AAATCCCAGCAAAGGTCAAGTCTGGCCAAGTCTGTGAAGAAACCAAGACGCAGAGAGGCCAAGC
CCCTTGCCTTGGGTCACACAGCCAAAGGAGGCAGAGCCAGAACTCACAACCAGATCCAGAGGCA
ACAGGGACATGGCCACCTGGGACGAAAAGGCAGTCACCCGCAGGGCCAAGGTGGCTCCCGCTGA
GAGGATGAGCAAGTTCTTAAGGCACTTCACGGTCGTGGGAGACGACTACCATGCCTGGAACATC
AACTACAAGAAATGGGAGAATGAAGAGGAGGAGGAGGAGGAGGAGCAGCCACCACCCACACCAG
TCTCAGGCGAGGAAGGCAGAGCTGCAGCCCCTGACGTTGCCCCTGCCCCTGGCCCCGCACCCAG
GGCCCCCCTTGACTTCAGGGGCATGTTGAGGAAACTGTTCAGCTCCCACAGGTTTCAGGTCATC
ATCATCTGCTTGGTGGTTCTGGATGCCCTCCTGGTGCTTGCTGAGCTCATCCTGGACCTGAAGA
TCATCCAGCCCGACAAGAATAACTATGCTGCCATGGTATTCCACTACATGAGCATCACCATCTT
GGTCTTTTTTATGATGGAGATCATCTTTAAATTATTTGTCTTCCGCCTGGAGTTCTTTCACCAC
AAGTTTGAGATCCTGGATGCCGTCGTGGTGGTGGTCTCATTCATCCTCGACATTGTCCTCCTGT
TCCAGGAGCACCAGTTTGAGGCTCTGGGCCTGCTGATTCTGCTCCGGCTGTGGCGGGTGGCCCG
GATCATCAATGGGATTATCATCTCAGTTAAGACACGTTCAGAACGGCAACTCTTAAGGTTAAAA
CAGATGAATGTACAATTGGCCGCCAAGATTCAACACCTTGAGTTCAGCTGCTCTGAGAAGGAAC
AAGAAATTGAAAGACTTAACAAACTATTGCGACAGCATGGACTTCTTGGTGAAGTGAACTAGAC
CCGGACCAGCTCCCCTCAAAAAGAAGACACTGTCTCATGGGCCTGTGCTGTCACGAGAGGAACA
GCTGCCCCTCCTGGGCCGCTTGGTGAGAGGTTTGGTTTGATACCTCTGCCTCCCTCCTGCCAGC
ATGGATTCTGGGTGGACACAGCCTTGTGGAAGGTCCAGTACCACCAAGAGCTGCCCATCCACTC
CCACCCCACACTGTATCAAATGTATCACATTTTCTCATGTTGAACACTTTAGCCTTAATTGAAA
ATGAGCAACAAAGCTGGACAATTGCTAGTTGTATATAAAATTTAATCTCACCGAATGTACAGTT
TTCAAATTTCACGTGTATATTAAGGAACTGATGCATCTGAGCATTCTGAAAGAAAGAAAAAGAA
GCTACTTTAGCTGCCACCCCATTCTAGAAAAGTCTCTTATTTTCAAGCTGTTCTAAATAGCTTC
GTCTCAGTTTCCCCAAAAGGGGTACCCAGGCCCCTCCTCTGTGTGCCCCAGCTGCATCAGCCAG
CTTCTAGGTGGCTCCATTGTTTTCTGCCACCTGACAACATTTTTCCTCAATTACTGTACAACTA
CTGTATAAAATAAAACAACTACTGTATAAAATAAACTCTCTCTTTTCCCTGGA

hide sequence

RefSeq Acc Id:

XM_017020026 ⟹ XP_016875515

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	110,648,686 - 110,702,395 (-)	NCBI

Sequence:

show sequence

TGCTTATTTGCAAGCATCTAACTTCCTGACCCTGTGTCACAGATGGCCCCACTTGGCCCCAAGC
CCCTGGTGAAGAAACCAAGACGCAGAGAGGCCAAGCCCCTTGCCTTGGGTCACACAGCCAAAGG
AGGCAGAGCCAGAACTCACAACCAGATCCAGAGGCAACAGGGACATGGCCACCTGGGACGAAAA
GGCCTTCCTCAGAACACGGATCCCCTGGGGCAGGAAGGGAGAAGTGCTGGGGGCAGCTGAGCCT
GCTGCTTGGAGTCCTCTTGCCTCCCCACAGAGAAGAGATTTGCTCAGGGGTTTCATTCCACCTT
CCACCATCCAGGAGGCAGTCACCCGCAGGGCCAAGGTGGCTCCCGCTGAGAGGATGAGCAAGTT
CTTAAGGCACTTCACGGTCGTGGGAGACGACTACCATGCCTGGAACATCAACTACAAGAAATGG
GAGAATGAAGAGGAGGAGGAGGAGGAGGAGCAGCCACCACCCACACCAGTCTCAGGCGAGGAAG
GCAGAGCTGCAGCCCCTGACGTTGCCCCTGCCCCTGGCCCCGCACCCAGGGCCCCCCTTGACTT
CAGGGGCATGTTGAGGAAACTGTTCAGCTCCCACAGGTTTCAGGTCATCATCATCTGCTTGGTG
GTTCTGGATGCCCTCCTGGTGCTTGCTGAGCTCATCCTGGACCTGAAGATCATCCAGCCCGACA
AGAATAACTATGCTGCCATGGTATTCCACTACATGAGCATCACCATCTTGGTCTTTTTTATGAT
GGAGATCATCTTTAAATTATTTGTCTTCCGCCTGGAGTTCTTTCACCACAAGTTTGAGATCCTG
GATGCCGTCGTGGTGGTGGTCTCATTCATCCTCGACATTGTCCTCCTGTTCCAGGAGCACCAGT
TTGAGGCTCTGGGCCTGCTGATTCTGCTCCGGCTGTGGCGGGTGGCCCGGATCATCAATGGGAT
TATCATCTCAGTTAAGACACGTTCAGAACGGCAACTCTTAAGGTTAAAACAGATGAATGTACAA
TTGGCCGCCAAGATTCAACACCTTGAGTTCAGCTGCTCTGAGAAGGAACAAGAAATTGAAAGAC
TTAACAAACTATTGCGACAGCATGGACTTCTTGGTGAAGTGAACTAGACCCGGACCAGCTCCCC
TCAAAAAGAAGACACTGTCTCATGGGCCTGTGCTGTCACGAGAGGAACAGCTGCCCCTCCTGGG
CCGCTTGGTGAGAGGTTTGGTTTGATACCTCTGCCTCCCTCCTGCCAGCATGGATTCTGGGTGG
ACACAGCCTTGTGGAAGGTCCAGTACCACCAAGAGCTGCCCATCCACTCCCACCCCACACTGTA
TCAAATGTATCACATTTTCTCATGTTGAACACTTTAGCCTTAATTGAAAATGAGCAACAAAGCT
GGACAATTGCTAGTTGTATATAAAATTTAATCTCACCGAATGTACAGTTTTCAAATTTCACGTG
TATATTAAGGAACTGATGCATCTGAGCATTCTGAAAGAAAGAAAAAGAAGCTACTTTAGCTGCC
ACCCCATTCTAGAAAAGTCTCTTATTTTCAAGCTGTTCTAAATAGCTTCGTCTCAGTTTCCCCA
AAAGGGGTACCCAGGCCCCTCCTCTGTGTGCCCCAGCTGCATCAGCCAGCTTCTAGGTGGCTCC
ATTGTTTTCTGCCACCTGACAACATTTTTCCTCAATTACTGTACAACTACTGTATAAAATAAAA
CAACTACTGTATAAAATAAACTCTCTCTTTTCCCTGGA

hide sequence

RefSeq Acc Id:

XM_017020027 ⟹ XP_016875516

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	110,648,686 - 110,689,409 (-)	NCBI

Sequence:

show sequence

GATTTTTGTGATCCGCGATTCGCTCCCACGGGCGGGACCTTTGTAACTGCGGGAGGCCCAGGAC
AGGCCCACCCTGCGGGGCGGGAGGCAGCCGGGGTGAAGAAACCAAGACGCAGAGAGGCCAAGCC
CCTTGCCTTGGGTCACACAGCCAAAGGAGGCAGAGCCAGAACTCACAACCAGATCCAGAGGCAA
CAGGGACATGGCCACCTGGGACGAAAAGGCAGTCACCCGCAGGGCCAAGGTGGCTCCCGCTGAG
AGGATGAGCAAGTTCTTAAGGCACTTCACGGTCGTGGGAGACGACTACCATGCCTGGAACATCA
ACTACAAGAAATGGGAGAATGAAGAGGAGGAGGAGGAGGAGGAGCAGCCACCACCCACACCAGT
CTCAGGCGAGGAAGGCAGAGCTGCAGCCCCTGACGTTGCCCCTGCCCCTGGCCCCGCACCCAGG
GCCCCCCTTGACTTCAGGGGCATGTTGAGGAAACTGTTCAGCTCCCACAGGTTTCAGGTCATCA
TCATCTGCTTGGTGGTTCTGGATGCCCTCCTGGTGCTTGCTGAGCTCATCCTGGACCTGAAGAT
CATCCAGCCCGACAAGAATAACTATGCTGCCATGGTATTCCACTACATGAGCATCACCATCTTG
GTCTTTTTTATGATGGAGATCATCTTTAAATTATTTGTCTTCCGCCTGGAGTTCTTTCACCACA
AGTTTGAGATCCTGGATGCCGTCGTGGTGGTGGTCTCATTCATCCTCGACATTGTCCTCCTGTT
CCAGGAGCACCAGTTTGAGGCTCTGGGCCTGCTGATTCTGCTCCGGCTGTGGCGGGTGGCCCGG
ATCATCAATGGGATTATCATCTCAGTTAAGACACGTTCAGAACGGCAACTCTTAAGGTTAAAAC
AGATGAATGTACAATTGGCCGCCAAGATTCAACACCTTGAGTTCAGCTGCTCTGAGAAGGAACA
AGAAATTGAAAGACTTAACAAACTATTGCGACAGCATGGACTTCTTGGTGAAGTGAACTAGACC
CGGACCAGCTCCCCTCAAAAAGAAGACACTGTCTCATGGGCCTGTGCTGTCACGAGAGGAACAG
CTGCCCCTCCTGGGCCGCTTGGTGAGAGGTTTGGTTTGATACCTCTGCCTCCCTCCTGCCAGCA
TGGATTCTGGGTGGACACAGCCTTGTGGAAGGTCCAGTACCACCAAGAGCTGCCCATCCACTCC
CACCCCACACTGTATCAAATGTATCACATTTTCTCATGTTGAACACTTTAGCCTTAATTGAAAA
TGAGCAACAAAGCTGGACAATTGCTAGTTGTATATAAAATTTAATCTCACCGAATGTACAGTTT
TCAAATTTCACGTGTATATTAAGGAACTGATGCATCTGAGCATTCTGAAAGAAAGAAAAAGAAG
CTACTTTAGCTGCCACCCCATTCTAGAAAAGTCTCTTATTTTCAAGCTGTTCTAAATAGCTTCG
TCTCAGTTTCCCCAAAAGGGGTACCCAGGCCCCTCCTCTGTGTGCCCCAGCTGCATCAGCCAGC
TTCTAGGTGGCTCCATTGTTTTCTGCCACCTGACAACATTTTTCCTCAATTACTGTACAACTAC
TGTATAAAATAAAACAACTACTGTATAAAATAAACTCTCTCTTTTCCCTGGA

hide sequence

RefSeq Acc Id:

XM_024449225 ⟹ XP_024304993

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	110,648,686 - 110,698,718 (-)	NCBI

Sequence:

show sequence

TTGTCCAGAGGAAGGAGACGCAGGAGGAGGAAACTCCTGGAAGTCCCTGCAGACAGTGCTCGGG
TCCCCCTGGCCAGAGCATTTGATGATCACATGACCTCTGCTGCAACAGGTGAAGAAACCAAGAC
GCAGAGAGGCCAAGCCCCTTGCCTTGGGTCACACAGCCAAAGGAGGCAGAGCCAGAACTCACAA
CCAGATCCAGAGGCAACAGGGACATGGCCACCTGGGACGAAAAGGCAGTCACCCGCAGGGCCAA
GGTGGCTCCCGCTGAGAGGATGAGCAAGTTCTTAAGGCACTTCACGGTCGTGGGAGACGACTAC
CATGCCTGGAACATCAACTACAAGAAATGGGAGAATGAAGAGGAGGAGGAGGAGGAGGAGCAGC
CACCACCCACACCAGTCTCAGGCGAGGAAGGCAGAGCTGCAGCCCCTGACGTTGCCCCTGCCCC
TGGCCCCGCACCCAGGGCCCCCCTTGACTTCAGGGGCATGTTGAGGAAACTGTTCAGCTCCCAC
AGGTTTCAGGTCATCATCATCTGCTTGGTGGTTCTGGATGCCCTCCTGGTGCTTGCTGAGCTCA
TCCTGGACCTGAAGATCATCCAGCCCGACAAGAATAACTATGCTGCCATGGTATTCCACTACAT
GAGCATCACCATCTTGGTCTTTTTTATGATGGAGATCATCTTTAAATTATTTGTCTTCCGCCTG
GAGTTCTTTCACCACAAGTTTGAGATCCTGGATGCCGTCGTGGTGGTGGTCTCATTCATCCTCG
ACATTGTCCTCCTGTTCCAGGAGCACCAGTTTGAGGCTCTGGGCCTGCTGATTCTGCTCCGGCT
GTGGCGGGTGGCCCGGATCATCAATGGGATTATCATCTCAGTTAAGACACGTTCAGAACGGCAA
CTCTTAAGGTTAAAACAGATGAATGTACAATTGGCCGCCAAGATTCAACACCTTGAGTTCAGCT
GCTCTGAGAAGGAACAAGAAATTGAAAGACTTAACAAACTATTGCGACAGCATGGACTTCTTGG
TGAAGTGAACTAGACCCGGACCAGCTCCCCTCAAAAAGAAGACACTGTCTCATGGGCCTGTGCT
GTCACGAGAGGAACAGCTGCCCCTCCTGGGCCGCTTGGTGAGAGGTTTGGTTTGATACCTCTGC
CTCCCTCCTGCCAGCATGGATTCTGGGTGGACACAGCCTTGTGGAAGGTCCAGTACCACCAAGA
GCTGCCCATCCACTCCCACCCCACACTGTATCAAATGTATCACATTTTCTCATGTTGAACACTT
TAGCCTTAATTGAAAATGAGCAACAAAGCTGGACAATTGCTAGTTGTATATAAAATTTAATCTC
ACCGAATGTACAGTTTTCAAATTTCACGTGTATATTAAGGAACTGATGCATCTGAGCATTCTGA
AAGAAAGAAAAAGAAGCTACTTTAGCTGCCACCCCATTCTAGAAAAGTCTCTTATTTTCAAGCT
GTTCTAAATAGCTTCGTCTCAGTTTCCCCAAAAGGGGTACCCAGGCCCCTCCTCTGTGTGCCCC
AGCTGCATCAGCCAGCTTCTAGGTGGCTCCATTGTTTTCTGCCACCTGACAACATTTTTCCTCA
ATTACTGTACAACTACTGTATAAAATAAAACAACTACTGTATAAAATAAACTCTCTCTTTTCCC
TGGA

hide sequence

RefSeq Acc Id:

XM_047429669 ⟹ XP_047285625

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	110,648,686 - 110,689,115 (-)	NCBI

RefSeq Acc Id:

XM_047429670 ⟹ XP_047285626

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	110,648,686 - 110,689,115 (-)	NCBI

RefSeq Acc Id:

XM_054373470 ⟹ XP_054229445

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	110,626,380 - 110,666,808 (-)	NCBI

RefSeq Acc Id:

XM_054373471 ⟹ XP_054229446

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	110,626,380 - 110,667,470 (-)	NCBI

RefSeq Acc Id:

XM_054373472 ⟹ XP_054229447

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	110,626,380 - 110,667,135 (-)	NCBI

RefSeq Acc Id:

XM_054373473 ⟹ XP_054229448

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	110,626,380 - 110,667,117 (-)	NCBI

RefSeq Acc Id:

XM_054373474 ⟹ XP_054229449

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	110,626,380 - 110,667,369 (-)	NCBI

RefSeq Acc Id:

XM_054373475 ⟹ XP_054229450

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	110,626,380 - 110,676,383 (-)	NCBI

RefSeq Acc Id:

XM_054373476 ⟹ XP_054229451

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	110,626,380 - 110,680,089 (-)	NCBI

RefSeq Acc Id:

XM_054373477 ⟹ XP_054229452

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	110,626,380 - 110,667,135 (-)	NCBI

RefSeq Acc Id:

XM_054373478 ⟹ XP_054229453

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	110,626,380 - 110,667,129 (-)	NCBI

RefSeq Acc Id:

XM_054373479 ⟹ XP_054229454

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	110,626,380 - 110,676,994 (-)	NCBI

RefSeq Acc Id:

XM_054373480 ⟹ XP_054229455

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	110,626,380 - 110,666,752 (-)	NCBI

RefSeq Acc Id:

XM_054373481 ⟹ XP_054229456

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	110,626,380 - 110,667,392 (-)	NCBI

RefSeq Acc Id:

XM_054373482 ⟹ XP_054229457

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	110,626,380 - 110,676,433 (-)	NCBI

RefSeq Acc Id:

XM_054373483 ⟹ XP_054229458

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	110,626,380 - 110,682,642 (-)	NCBI

Protein Sequences


Protein RefSeqs	NP_001035196	(Get FASTA)	NCBI Sequence Viewer
	NP_001243342	(Get FASTA)	NCBI Sequence Viewer
	NP_115745	(Get FASTA)	NCBI Sequence Viewer
	XP_005254005	(Get FASTA)	NCBI Sequence Viewer
	XP_011537140	(Get FASTA)	NCBI Sequence Viewer
	XP_011537141	(Get FASTA)	NCBI Sequence Viewer
	XP_011537142	(Get FASTA)	NCBI Sequence Viewer
	XP_011537143	(Get FASTA)	NCBI Sequence Viewer
	XP_011537144	(Get FASTA)	NCBI Sequence Viewer
	XP_011537146	(Get FASTA)	NCBI Sequence Viewer
	XP_011537147	(Get FASTA)	NCBI Sequence Viewer
	XP_011537148	(Get FASTA)	NCBI Sequence Viewer
	XP_011537149	(Get FASTA)	NCBI Sequence Viewer
	XP_016875515	(Get FASTA)	NCBI Sequence Viewer
	XP_016875516	(Get FASTA)	NCBI Sequence Viewer
	XP_024304993	(Get FASTA)	NCBI Sequence Viewer
	XP_047285625	(Get FASTA)	NCBI Sequence Viewer
	XP_047285626	(Get FASTA)	NCBI Sequence Viewer
	XP_054229445	(Get FASTA)	NCBI Sequence Viewer
	XP_054229446	(Get FASTA)	NCBI Sequence Viewer
	XP_054229447	(Get FASTA)	NCBI Sequence Viewer
	XP_054229448	(Get FASTA)	NCBI Sequence Viewer
	XP_054229449	(Get FASTA)	NCBI Sequence Viewer
	XP_054229450	(Get FASTA)	NCBI Sequence Viewer
	XP_054229451	(Get FASTA)	NCBI Sequence Viewer
	XP_054229452	(Get FASTA)	NCBI Sequence Viewer
	XP_054229453	(Get FASTA)	NCBI Sequence Viewer
	XP_054229454	(Get FASTA)	NCBI Sequence Viewer
	XP_054229455	(Get FASTA)	NCBI Sequence Viewer
	XP_054229456	(Get FASTA)	NCBI Sequence Viewer
	XP_054229457	(Get FASTA)	NCBI Sequence Viewer
	XP_054229458	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH07277	(Get FASTA)	NCBI Sequence Viewer
	AAH09731	(Get FASTA)	NCBI Sequence Viewer
	AAH32672	(Get FASTA)	NCBI Sequence Viewer
	AAQ89413	(Get FASTA)	NCBI Sequence Viewer
	ADA61023	(Get FASTA)	NCBI Sequence Viewer
	BAG57024	(Get FASTA)	NCBI Sequence Viewer
	EAW97933	(Get FASTA)	NCBI Sequence Viewer
	EAW97934	(Get FASTA)	NCBI Sequence Viewer
	EAW97935	(Get FASTA)	NCBI Sequence Viewer
	EAW97936	(Get FASTA)	NCBI Sequence Viewer
	EAW97937	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000242607
	ENSP00000242607.8
	ENSP00000349181.5
	ENSP00000412052
	ENSP00000412052.2
	ENSP00000447227.1
	ENSP00000448379.1
	ENSP00000449601
	ENSP00000449601.1
	ENSP00000450106.2
	ENSP00000479812.1
GenBank Protein	Q96D96	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_001035196 ⟸ NM_001040107
- Peptide Label:	isoform 1
- UniProtKB:	Q6UW11 (UniProtKB/Swiss-Prot), F8WCH5 (UniProtKB/Swiss-Prot), B4DEB3 (UniProtKB/Swiss-Prot), A8MQ37 (UniProtKB/Swiss-Prot), Q96IS5 (UniProtKB/Swiss-Prot), Q96D96 (UniProtKB/Swiss-Prot), D2KFF9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MATWDEKAVTRRAKVAPAERMSKFLRHFTVVGDDYHAWNINYKKWENEEEEEEEEQPPPTPVSG EEGRAAAPDVAPAPGPAPRAPLDFRGMLRKLFSSHRFQVIIICLVVLDALLVLAELILDLKIIQ PDKNNYAAMVFHYMSITILVFFMMEIIFKLFVFRLEFFHHKFEILDAVVVVVSFILDIVLLFQE HQFEALGLLILLRLWRVARIINGIIISVKTRSERQLLRLKQMNVQLAAKIQHLEFSCSEKEQEI ERLNKLLRQHGLLGEVN hide sequence

RefSeq Acc Id:	NP_115745 ⟸ NM_032369
- Peptide Label:	isoform 1
- UniProtKB:	Q6UW11 (UniProtKB/Swiss-Prot), F8WCH5 (UniProtKB/Swiss-Prot), B4DEB3 (UniProtKB/Swiss-Prot), A8MQ37 (UniProtKB/Swiss-Prot), Q96IS5 (UniProtKB/Swiss-Prot), Q96D96 (UniProtKB/Swiss-Prot), D2KFF9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MATWDEKAVTRRAKVAPAERMSKFLRHFTVVGDDYHAWNINYKKWENEEEEEEEEQPPPTPVSG EEGRAAAPDVAPAPGPAPRAPLDFRGMLRKLFSSHRFQVIIICLVVLDALLVLAELILDLKIIQ PDKNNYAAMVFHYMSITILVFFMMEIIFKLFVFRLEFFHHKFEILDAVVVVVSFILDIVLLFQE HQFEALGLLILLRLWRVARIINGIIISVKTRSERQLLRLKQMNVQLAAKIQHLEFSCSEKEQEI ERLNKLLRQHGLLGEVN hide sequence

RefSeq Acc Id:	NP_001243342 ⟸ NM_001256413
- Peptide Label:	isoform 2
- UniProtKB:	D2KFF9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MSKFLRHFTVVGDDYHAWNINYKKWENEEEEEEEEQPPPTPVSGEEGRAAAPDVAPAPGPAPRA PLDFRGMLRKLFSSHRFQVIIICLVVLDALLVLAELILDLKIIQPDKNNYAAMVFHYMSITILV FFMMEIIFKLFVFRLEFFHHKFEILDAVVVVVSFILDIVLLFQEHQFEALGLLILLRLWRVARI INGIIISVKTRSERQLLRLKQMNVQLAAKIQHLEFSCSEKEQEIERLNKLLRQHGLLGEVN hide sequence

RefSeq Acc Id:	XP_005254005 ⟸ XM_005253948
- Peptide Label:	isoform X2
- UniProtKB:	Q6UW11 (UniProtKB/Swiss-Prot), F8WCH5 (UniProtKB/Swiss-Prot), B4DEB3 (UniProtKB/Swiss-Prot), A8MQ37 (UniProtKB/Swiss-Prot), Q96IS5 (UniProtKB/Swiss-Prot), Q96D96 (UniProtKB/Swiss-Prot), D2KFF9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MATWDEKAVTRRAKVAPAERMSKFLRHFTVVGDDYHAWNINYKKWENEEEEEEEEQPPPTPVSG EEGRAAAPDVAPAPGPAPRAPLDFRGMLRKLFSSHRFQVIIICLVVLDALLVLAELILDLKIIQ PDKNNYAAMVFHYMSITILVFFMMEIIFKLFVFRLEFFHHKFEILDAVVVVVSFILDIVLLFQE HQFEALGLLILLRLWRVARIINGIIISVKTRSERQLLRLKQMNVQLAAKIQHLEFSCSEKEQEI ERLNKLLRQHGLLGEVN hide sequence

RefSeq Acc Id:	XP_011537148 ⟸ XM_011538846
- Peptide Label:	isoform X2
- UniProtKB:	Q6UW11 (UniProtKB/Swiss-Prot), F8WCH5 (UniProtKB/Swiss-Prot), B4DEB3 (UniProtKB/Swiss-Prot), A8MQ37 (UniProtKB/Swiss-Prot), Q96IS5 (UniProtKB/Swiss-Prot), Q96D96 (UniProtKB/Swiss-Prot), D2KFF9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MATWDEKAVTRRAKVAPAERMSKFLRHFTVVGDDYHAWNINYKKWENEEEEEEEEQPPPTPVSG EEGRAAAPDVAPAPGPAPRAPLDFRGMLRKLFSSHRFQVIIICLVVLDALLVLAELILDLKIIQ PDKNNYAAMVFHYMSITILVFFMMEIIFKLFVFRLEFFHHKFEILDAVVVVVSFILDIVLLFQE HQFEALGLLILLRLWRVARIINGIIISVKTRSERQLLRLKQMNVQLAAKIQHLEFSCSEKEQEI ERLNKLLRQHGLLGEVN hide sequence

RefSeq Acc Id:	XP_011537149 ⟸ XM_011538847
- Peptide Label:	isoform X2
- UniProtKB:	Q6UW11 (UniProtKB/Swiss-Prot), F8WCH5 (UniProtKB/Swiss-Prot), B4DEB3 (UniProtKB/Swiss-Prot), A8MQ37 (UniProtKB/Swiss-Prot), Q96IS5 (UniProtKB/Swiss-Prot), Q96D96 (UniProtKB/Swiss-Prot), D2KFF9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MATWDEKAVTRRAKVAPAERMSKFLRHFTVVGDDYHAWNINYKKWENEEEEEEEEQPPPTPVSG EEGRAAAPDVAPAPGPAPRAPLDFRGMLRKLFSSHRFQVIIICLVVLDALLVLAELILDLKIIQ PDKNNYAAMVFHYMSITILVFFMMEIIFKLFVFRLEFFHHKFEILDAVVVVVSFILDIVLLFQE HQFEALGLLILLRLWRVARIINGIIISVKTRSERQLLRLKQMNVQLAAKIQHLEFSCSEKEQEI ERLNKLLRQHGLLGEVN hide sequence

RefSeq Acc Id:	XP_011537144 ⟸ XM_011538842
- Peptide Label:	isoform X1
- UniProtKB:	D2KFF9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MATWDEKAFLRTRIPWGRKGEVLGAAEPAAWSPLASPQRRDLLRGFIPPSTIQEAVTRRAKVAP AERMSKFLRHFTVVGDDYHAWNINYKKWENEEEEEEEEQPPPTPVSGEEGRAAAPDVAPAPGPA PRAPLDFRGMLRKLFSSHRFQVIIICLVVLDALLVLAELILDLKIIQPDKNNYAAMVFHYMSIT ILVFFMMEIIFKLFVFRLEFFHHKFEILDAVVVVVSFILDIVLLFQEHQFEALGLLILLRLWRV ARIINGIIISVKTRSERQLLRLKQMNVQLAAKIQHLEFSCSEKEQEIERLNKLLRQHGLLGEVN hide sequence

RefSeq Acc Id:	XP_011537141 ⟸ XM_011538839
- Peptide Label:	isoform X1
- UniProtKB:	D2KFF9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MATWDEKAFLRTRIPWGRKGEVLGAAEPAAWSPLASPQRRDLLRGFIPPSTIQEAVTRRAKVAP AERMSKFLRHFTVVGDDYHAWNINYKKWENEEEEEEEEQPPPTPVSGEEGRAAAPDVAPAPGPA PRAPLDFRGMLRKLFSSHRFQVIIICLVVLDALLVLAELILDLKIIQPDKNNYAAMVFHYMSIT ILVFFMMEIIFKLFVFRLEFFHHKFEILDAVVVVVSFILDIVLLFQEHQFEALGLLILLRLWRV ARIINGIIISVKTRSERQLLRLKQMNVQLAAKIQHLEFSCSEKEQEIERLNKLLRQHGLLGEVN hide sequence

RefSeq Acc Id:	XP_011537142 ⟸ XM_011538840
- Peptide Label:	isoform X1
- UniProtKB:	D2KFF9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MATWDEKAFLRTRIPWGRKGEVLGAAEPAAWSPLASPQRRDLLRGFIPPSTIQEAVTRRAKVAP AERMSKFLRHFTVVGDDYHAWNINYKKWENEEEEEEEEQPPPTPVSGEEGRAAAPDVAPAPGPA PRAPLDFRGMLRKLFSSHRFQVIIICLVVLDALLVLAELILDLKIIQPDKNNYAAMVFHYMSIT ILVFFMMEIIFKLFVFRLEFFHHKFEILDAVVVVVSFILDIVLLFQEHQFEALGLLILLRLWRV ARIINGIIISVKTRSERQLLRLKQMNVQLAAKIQHLEFSCSEKEQEIERLNKLLRQHGLLGEVN hide sequence

RefSeq Acc Id:	XP_011537140 ⟸ XM_011538838
- Peptide Label:	isoform X1
- UniProtKB:	D2KFF9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MATWDEKAFLRTRIPWGRKGEVLGAAEPAAWSPLASPQRRDLLRGFIPPSTIQEAVTRRAKVAP AERMSKFLRHFTVVGDDYHAWNINYKKWENEEEEEEEEQPPPTPVSGEEGRAAAPDVAPAPGPA PRAPLDFRGMLRKLFSSHRFQVIIICLVVLDALLVLAELILDLKIIQPDKNNYAAMVFHYMSIT ILVFFMMEIIFKLFVFRLEFFHHKFEILDAVVVVVSFILDIVLLFQEHQFEALGLLILLRLWRV ARIINGIIISVKTRSERQLLRLKQMNVQLAAKIQHLEFSCSEKEQEIERLNKLLRQHGLLGEVN hide sequence

RefSeq Acc Id:	XP_011537147 ⟸ XM_011538845
- Peptide Label:	isoform X2
- UniProtKB:	Q6UW11 (UniProtKB/Swiss-Prot), F8WCH5 (UniProtKB/Swiss-Prot), B4DEB3 (UniProtKB/Swiss-Prot), A8MQ37 (UniProtKB/Swiss-Prot), Q96IS5 (UniProtKB/Swiss-Prot), Q96D96 (UniProtKB/Swiss-Prot), D2KFF9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MATWDEKAVTRRAKVAPAERMSKFLRHFTVVGDDYHAWNINYKKWENEEEEEEEEQPPPTPVSG EEGRAAAPDVAPAPGPAPRAPLDFRGMLRKLFSSHRFQVIIICLVVLDALLVLAELILDLKIIQ PDKNNYAAMVFHYMSITILVFFMMEIIFKLFVFRLEFFHHKFEILDAVVVVVSFILDIVLLFQE HQFEALGLLILLRLWRVARIINGIIISVKTRSERQLLRLKQMNVQLAAKIQHLEFSCSEKEQEI ERLNKLLRQHGLLGEVN hide sequence

RefSeq Acc Id:	XP_011537146 ⟸ XM_011538844
- Peptide Label:	isoform X1
- UniProtKB:	D2KFF9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MATWDEKAFLRTRIPWGRKGEVLGAAEPAAWSPLASPQRRDLLRGFIPPSTIQEAVTRRAKVAP AERMSKFLRHFTVVGDDYHAWNINYKKWENEEEEEEEEQPPPTPVSGEEGRAAAPDVAPAPGPA PRAPLDFRGMLRKLFSSHRFQVIIICLVVLDALLVLAELILDLKIIQPDKNNYAAMVFHYMSIT ILVFFMMEIIFKLFVFRLEFFHHKFEILDAVVVVVSFILDIVLLFQEHQFEALGLLILLRLWRV ARIINGIIISVKTRSERQLLRLKQMNVQLAAKIQHLEFSCSEKEQEIERLNKLLRQHGLLGEVN hide sequence

RefSeq Acc Id:	XP_011537143 ⟸ XM_011538841
- Peptide Label:	isoform X1
- UniProtKB:	D2KFF9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MATWDEKAFLRTRIPWGRKGEVLGAAEPAAWSPLASPQRRDLLRGFIPPSTIQEAVTRRAKVAP AERMSKFLRHFTVVGDDYHAWNINYKKWENEEEEEEEEQPPPTPVSGEEGRAAAPDVAPAPGPA PRAPLDFRGMLRKLFSSHRFQVIIICLVVLDALLVLAELILDLKIIQPDKNNYAAMVFHYMSIT ILVFFMMEIIFKLFVFRLEFFHHKFEILDAVVVVVSFILDIVLLFQEHQFEALGLLILLRLWRV ARIINGIIISVKTRSERQLLRLKQMNVQLAAKIQHLEFSCSEKEQEIERLNKLLRQHGLLGEVN hide sequence

RefSeq Acc Id:	XP_016875515 ⟸ XM_017020026
- Peptide Label:	isoform X1
- UniProtKB:	D2KFF9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MATWDEKAFLRTRIPWGRKGEVLGAAEPAAWSPLASPQRRDLLRGFIPPSTIQEAVTRRAKVAP AERMSKFLRHFTVVGDDYHAWNINYKKWENEEEEEEEEQPPPTPVSGEEGRAAAPDVAPAPGPA PRAPLDFRGMLRKLFSSHRFQVIIICLVVLDALLVLAELILDLKIIQPDKNNYAAMVFHYMSIT ILVFFMMEIIFKLFVFRLEFFHHKFEILDAVVVVVSFILDIVLLFQEHQFEALGLLILLRLWRV ARIINGIIISVKTRSERQLLRLKQMNVQLAAKIQHLEFSCSEKEQEIERLNKLLRQHGLLGEVN hide sequence

RefSeq Acc Id:	XP_016875516 ⟸ XM_017020027
- Peptide Label:	isoform X2
- UniProtKB:	Q6UW11 (UniProtKB/Swiss-Prot), F8WCH5 (UniProtKB/Swiss-Prot), B4DEB3 (UniProtKB/Swiss-Prot), A8MQ37 (UniProtKB/Swiss-Prot), Q96IS5 (UniProtKB/Swiss-Prot), Q96D96 (UniProtKB/Swiss-Prot), D2KFF9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MATWDEKAVTRRAKVAPAERMSKFLRHFTVVGDDYHAWNINYKKWENEEEEEEEEQPPPTPVSG EEGRAAAPDVAPAPGPAPRAPLDFRGMLRKLFSSHRFQVIIICLVVLDALLVLAELILDLKIIQ PDKNNYAAMVFHYMSITILVFFMMEIIFKLFVFRLEFFHHKFEILDAVVVVVSFILDIVLLFQE HQFEALGLLILLRLWRVARIINGIIISVKTRSERQLLRLKQMNVQLAAKIQHLEFSCSEKEQEI ERLNKLLRQHGLLGEVN hide sequence

RefSeq Acc Id:	XP_024304993 ⟸ XM_024449225
- Peptide Label:	isoform X2
- UniProtKB:	Q96D96 (UniProtKB/Swiss-Prot), Q6UW11 (UniProtKB/Swiss-Prot), F8WCH5 (UniProtKB/Swiss-Prot), B4DEB3 (UniProtKB/Swiss-Prot), A8MQ37 (UniProtKB/Swiss-Prot), Q96IS5 (UniProtKB/Swiss-Prot), D2KFF9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MATWDEKAVTRRAKVAPAERMSKFLRHFTVVGDDYHAWNINYKKWENEEEEEEEEQPPPTPVSG EEGRAAAPDVAPAPGPAPRAPLDFRGMLRKLFSSHRFQVIIICLVVLDALLVLAELILDLKIIQ PDKNNYAAMVFHYMSITILVFFMMEIIFKLFVFRLEFFHHKFEILDAVVVVVSFILDIVLLFQE HQFEALGLLILLRLWRVARIINGIIISVKTRSERQLLRLKQMNVQLAAKIQHLEFSCSEKEQEI ERLNKLLRQHGLLGEVN hide sequence

Ensembl Acc Id:

ENSP00000479812 ⟸ ENST00000620084

Ensembl Acc Id:

ENSP00000412052 ⟸ ENST00000439744

Ensembl Acc Id:

ENSP00000242607 ⟸ ENST00000242607

Ensembl Acc Id:

ENSP00000447227 ⟸ ENST00000546713

Ensembl Acc Id:

ENSP00000448379 ⟸ ENST00000547887

Ensembl Acc Id:

ENSP00000449601 ⟸ ENST00000548312

Ensembl Acc Id:

ENSP00000450106 ⟸ ENST00000549442

Ensembl Acc Id:

ENSP00000349181 ⟸ ENST00000356742

RefSeq Acc Id:	XP_047285626 ⟸ XM_047429670
- Peptide Label:	isoform X2
- UniProtKB:	Q96D96 (UniProtKB/Swiss-Prot), Q6UW11 (UniProtKB/Swiss-Prot), F8WCH5 (UniProtKB/Swiss-Prot), B4DEB3 (UniProtKB/Swiss-Prot), A8MQ37 (UniProtKB/Swiss-Prot), Q96IS5 (UniProtKB/Swiss-Prot), D2KFF9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047285625 ⟸ XM_047429669
- Peptide Label:	isoform X1
- UniProtKB:	D2KFF9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054229458 ⟸ XM_054373483
- Peptide Label:	isoform X2
- UniProtKB:	Q96D96 (UniProtKB/Swiss-Prot), Q6UW11 (UniProtKB/Swiss-Prot), F8WCH5 (UniProtKB/Swiss-Prot), B4DEB3 (UniProtKB/Swiss-Prot), A8MQ37 (UniProtKB/Swiss-Prot), Q96IS5 (UniProtKB/Swiss-Prot), D2KFF9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054229451 ⟸ XM_054373476
- Peptide Label:	isoform X1
- UniProtKB:	D2KFF9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054229454 ⟸ XM_054373479
- Peptide Label:	isoform X2
- UniProtKB:	Q96D96 (UniProtKB/Swiss-Prot), Q6UW11 (UniProtKB/Swiss-Prot), F8WCH5 (UniProtKB/Swiss-Prot), B4DEB3 (UniProtKB/Swiss-Prot), A8MQ37 (UniProtKB/Swiss-Prot), Q96IS5 (UniProtKB/Swiss-Prot), D2KFF9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054229457 ⟸ XM_054373482
- Peptide Label:	isoform X2
- UniProtKB:	Q96D96 (UniProtKB/Swiss-Prot), Q6UW11 (UniProtKB/Swiss-Prot), F8WCH5 (UniProtKB/Swiss-Prot), B4DEB3 (UniProtKB/Swiss-Prot), A8MQ37 (UniProtKB/Swiss-Prot), Q96IS5 (UniProtKB/Swiss-Prot), D2KFF9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054229450 ⟸ XM_054373475
- Peptide Label:	isoform X1
- UniProtKB:	D2KFF9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054229446 ⟸ XM_054373471
- Peptide Label:	isoform X1
- UniProtKB:	D2KFF9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054229456 ⟸ XM_054373481
- Peptide Label:	isoform X2
- UniProtKB:	Q96D96 (UniProtKB/Swiss-Prot), Q6UW11 (UniProtKB/Swiss-Prot), F8WCH5 (UniProtKB/Swiss-Prot), B4DEB3 (UniProtKB/Swiss-Prot), A8MQ37 (UniProtKB/Swiss-Prot), Q96IS5 (UniProtKB/Swiss-Prot), D2KFF9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054229449 ⟸ XM_054373474
- Peptide Label:	isoform X1
- UniProtKB:	D2KFF9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054229452 ⟸ XM_054373477
- Peptide Label:	isoform X2
- UniProtKB:	Q96D96 (UniProtKB/Swiss-Prot), Q6UW11 (UniProtKB/Swiss-Prot), F8WCH5 (UniProtKB/Swiss-Prot), B4DEB3 (UniProtKB/Swiss-Prot), A8MQ37 (UniProtKB/Swiss-Prot), Q96IS5 (UniProtKB/Swiss-Prot), D2KFF9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054229447 ⟸ XM_054373472
- Peptide Label:	isoform X1
- UniProtKB:	D2KFF9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054229453 ⟸ XM_054373478
- Peptide Label:	isoform X2
- UniProtKB:	Q96D96 (UniProtKB/Swiss-Prot), Q6UW11 (UniProtKB/Swiss-Prot), F8WCH5 (UniProtKB/Swiss-Prot), B4DEB3 (UniProtKB/Swiss-Prot), A8MQ37 (UniProtKB/Swiss-Prot), Q96IS5 (UniProtKB/Swiss-Prot), D2KFF9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054229448 ⟸ XM_054373473
- Peptide Label:	isoform X1
- UniProtKB:	D2KFF9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054229445 ⟸ XM_054373470
- Peptide Label:	isoform X1
- UniProtKB:	D2KFF9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054229455 ⟸ XM_054373480
- Peptide Label:	isoform X2
- UniProtKB:	Q96D96 (UniProtKB/Swiss-Prot), Q6UW11 (UniProtKB/Swiss-Prot), F8WCH5 (UniProtKB/Swiss-Prot), B4DEB3 (UniProtKB/Swiss-Prot), A8MQ37 (UniProtKB/Swiss-Prot), Q96IS5 (UniProtKB/Swiss-Prot), D2KFF9 (UniProtKB/TrEMBL)

Protein Domains

Ion transport Voltage-gated hydrogen channel 1 C-terminal

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q96D96-F1-model_v2	AlphaFold	Q96D96	1-273	view protein structure

Promoters

RGD ID:

6810299

Promoter ID:

HG_ACW:18851

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

Lymphoblastoid, NB4

Transcripts:

HVCN1.FAPR07

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	12	109,583,476 - 109,583,976 (-)	MPROMDB

RGD ID:

6789932

Promoter ID:

HG_KWN:16666

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

Lymphoblastoid

Transcripts:

ENST00000242607

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	12	109,584,636 - 109,585,352 (-)	MPROMDB

RGD ID:

6810297

Promoter ID:

HG_ACW:18853

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

K562

Transcripts:

HVCN1.DAPR07

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	12	109,599,321 - 109,599,821 (-)	MPROMDB

RGD ID:

6789934

Promoter ID:

HG_KWN:16667

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

Lymphoblastoid

Transcripts:

ENST00000377649

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	12	109,602,376 - 109,603,327 (-)	MPROMDB

RGD ID:

6790121

Promoter ID:

HG_KWN:16668

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

Lymphoblastoid

Transcripts:

ENST00000356742

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	12	109,605,026 - 109,605,526 (-)	MPROMDB

RGD ID:

6790122

Promoter ID:

HG_KWN:16669

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell_12Hour, Jurkat, K562, Lymphoblastoid, NB4

Transcripts:

NM_001040107, NM_032369, UC001TRQ.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	12	109,611,326 - 109,611,997 (-)	MPROMDB

RGD ID:

7225411

Promoter ID:

EPDNEW_H18451

Type:

initiation region

Name:

HVCN1_1

Description:

hydrogen voltage gated channel 1

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	12	110,689,115 - 110,689,175	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:28240	AgrOrtholog
COSMIC	HVCN1	COSMIC
Ensembl Genes	ENSG00000122986	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000242607	ENTREZGENE
	ENST00000242607.13	UniProtKB/Swiss-Prot
	ENST00000356742.9	UniProtKB/Swiss-Prot
	ENST00000439744	ENTREZGENE
	ENST00000439744.6	UniProtKB/Swiss-Prot
	ENST00000546713.5	UniProtKB/TrEMBL
	ENST00000547887.1	UniProtKB/TrEMBL
	ENST00000548312	ENTREZGENE
	ENST00000548312.5	UniProtKB/Swiss-Prot
	ENST00000549442.5	UniProtKB/TrEMBL
	ENST00000620084.4	UniProtKB/Swiss-Prot
Gene3D-CATH	1.20.120.350	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	1.20.5.170	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000122986	GTEx
HGNC ID	HGNC:28240	ENTREZGENE
Human Proteome Map	HVCN1	Human Proteome Map
InterPro	Hvcn1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Ion_trans_dom	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	VGPC1_C	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Volt_channel_dom_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:84329	UniProtKB/Swiss-Prot
NCBI Gene	84329	ENTREZGENE
OMIM	611227	OMIM
PANTHER	PTHR46480	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	VOLTAGE-GATED HYDROGEN CHANNEL 1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	Ion_trans	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	VGPC1_C	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA144596422	PharmGKB
Superfamily-SCOP	Voltage-gated potassium channels	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	A8MQ37	ENTREZGENE
	B4DEB3	ENTREZGENE
	D2KFF9	ENTREZGENE, UniProtKB/TrEMBL
	F8VPF7_HUMAN	UniProtKB/TrEMBL
	F8VS40_HUMAN	UniProtKB/TrEMBL
	F8W0B3_HUMAN	UniProtKB/TrEMBL
	F8WCH5	ENTREZGENE
	HVCN1_HUMAN	UniProtKB/Swiss-Prot
	Q6UW11	ENTREZGENE
	Q96D96	ENTREZGENE
	Q96IS5	ENTREZGENE
UniProt Secondary	A8MQ37	UniProtKB/Swiss-Prot
	B4DEB3	UniProtKB/Swiss-Prot
	F8WCH5	UniProtKB/Swiss-Prot
	Q6UW11	UniProtKB/Swiss-Prot
	Q96IS5	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2015-01-20	HVCN1	hydrogen voltage gated channel 1		hydrogen voltage-gated channel 1	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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