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Gene: DNAI7 (dynein axonemal intermediate chain 7) Homo sapiens

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Symbol:

DNAI7

Name:

dynein axonemal intermediate chain 7

RGD ID:

1322554

HGNC Page

HGNC:29599

Description:

Predicted to enable beta-tubulin binding activity and microtubule binding activity. Predicted to be located in cilium and microtubule cytoskeleton. Predicted to be part of axonemal dynein complex. Predicted to be active in axoneme and cytoplasmic microtubule.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

cancer susceptibility 1; cancer susceptibility candidate 1; cancer susceptibility candidate gene 1 protein; cancer susceptibility candidate protein 1; CASC1; CFAP94; cilia and flagella associated protein 94; dynein intermediate chain CFAP94, axonemal; FLJ10921; LAS1; lung adenoma susceptibility 1-like protein; PPP1R54; protein phosphatase 1, regulatory subunit 54

RGD Orthologs

Alliance Orthologs

More Info

more info ...

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	25,107,047 - 25,195,160 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	12	25,108,289 - 25,195,162 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	12	25,261,223 - 25,348,094 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	12	25,152,490 - 25,239,361 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	12	25,152,489 - 25,239,361	NCBI
Celera	12	30,408,204 - 30,495,049 (-)	NCBI		Celera
Cytogenetic Map	12	p12.1	NCBI
HuRef	12	25,031,916 - 25,118,815 (-)	NCBI		HuRef
CHM1_1	12	25,226,353 - 25,313,239 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	12	24,977,958 - 25,066,403 (-)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
DNAI7	Human	lung cancer	ameliorates	ISO	Dnai7 (Mus musculus)	152998907	DNA:missense mutation:CDS:p.N60S (mouse)	RGD
DNAI7	Human	Lung Neoplasms	susceptibility	ISO	Dnai7 (Mus musculus)	11340955		RGD
DNAI7	Human	lung non-small cell carcinoma	ameliorates	ISO	Dnai7 (Mus musculus)	152998908		RGD

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
DNAI7	Human	Lung Neoplasms		EXP		11554173	CTD Direct Evidence: marker/mechanism	CTD	PMID:15064703

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
DNAI7	Human	2,2',4,4'-Tetrabromodiphenyl ether	decreases expression	ISO	Dnai7 (Rattus norvegicus)	6480464	2 more ...	CTD	PMID:27291303
DNAI7	Human	2,3,7,8-tetrachlorodibenzodioxine	increases expression	ISO	Dnai7 (Rattus norvegicus)	6480464	Tetrachlorodibenzodioxin results in increased expression of DNAI7 mRNA	CTD	PMID:33387578
DNAI7	Human	6-propyl-2-thiouracil	decreases expression	ISO	Dnai7 (Rattus norvegicus)	6480464	Propylthiouracil results in decreased expression of CASC1 mRNA and Propylthiouracil results in decreased expression of DNAI7 mRNA	CTD	PMID:24780913 and PMID:30047161
DNAI7	Human	acetamide	increases expression	ISO	Dnai7 (Rattus norvegicus)	6480464	acetamide results in increased expression of DNAI7 mRNA	CTD	PMID:31881176
DNAI7	Human	aflatoxin B1	decreases methylation	EXP		6480464	Aflatoxin B1 results in decreased methylation of DNAI7 gene and Aflatoxin B1 results in decreased methylation of DNAI7 intron	CTD	PMID:27153756 and PMID:30157460
DNAI7	Human	amitrole	decreases expression	ISO	Dnai7 (Rattus norvegicus)	6480464	Amitrole results in decreased expression of CASC1 mRNA	CTD	PMID:30047161
DNAI7	Human	amphetamine	increases expression	ISO	Dnai7 (Rattus norvegicus)	6480464	Amphetamine results in increased expression of DNAI7 mRNA	CTD	PMID:30779732
DNAI7	Human	benzo[a]pyrene	decreases expression	ISO	Dnai7 (Mus musculus)	6480464	Benzo(a)pyrene results in decreased expression of DNAI7 mRNA	CTD	PMID:22228805
DNAI7	Human	benzo[a]pyrene	decreases expression	EXP		6480464	Benzo(a)pyrene results in decreased expression of DNAI7 mRNA	CTD	PMID:32234424
DNAI7	Human	benzo[e]pyrene	increases methylation	EXP		6480464	benzo(e)pyrene results in increased methylation of DNAI7 intron	CTD	PMID:30157460
DNAI7	Human	bisphenol A	decreases expression	ISO	Dnai7 (Rattus norvegicus)	6480464	bisphenol A results in decreased expression of DNAI7 mRNA	CTD	PMID:25181051 and PMID:34947998
DNAI7	Human	bisphenol A	multiple interactions	EXP		6480464	[bisphenol A co-treated with Fulvestrant] results in increased methylation of DNAI7 gene	CTD	PMID:31601247
DNAI7	Human	bisphenol A	increases methylation	EXP		6480464	bisphenol A results in increased methylation of DNAI7 gene	CTD	PMID:31601247
DNAI7	Human	bisphenol A	decreases expression	ISO	Dnai7 (Mus musculus)	6480464	bisphenol A results in decreased expression of DNAI7 mRNA	CTD	PMID:29161229
DNAI7	Human	bisphenol A	increases methylation	ISO	Dnai7 (Rattus norvegicus)	6480464	bisphenol A results in increased methylation of DNAI7 gene	CTD	PMID:28505145
DNAI7	Human	butanal	decreases expression	EXP		6480464	butyraldehyde results in decreased expression of DNAI7 mRNA	CTD	PMID:26079696
DNAI7	Human	carbon nanotube	decreases expression	ISO	Dnai7 (Mus musculus)	6480464	Nanotubes more ...	CTD	PMID:25554681
DNAI7	Human	clothianidin	decreases expression	EXP		6480464	clothianidin results in decreased expression of DNAI7 mRNA	CTD	PMID:31626844
DNAI7	Human	Cuprizon	increases expression	ISO	Dnai7 (Rattus norvegicus)	6480464	Cuprizone results in increased expression of DNAI7 mRNA	CTD	PMID:26577399
DNAI7	Human	diethylstilbestrol	decreases expression	EXP		6480464	Diethylstilbestrol results in decreased expression of DNAI7 mRNA	CTD	PMID:19371625
DNAI7	Human	endosulfan	decreases expression	ISO	Dnai7 (Rattus norvegicus)	6480464	Endosulfan results in decreased expression of DNAI7 mRNA	CTD	PMID:29391264
DNAI7	Human	fenvalerate	increases expression	ISO	Dnai7 (Rattus norvegicus)	6480464	fenvalerate results in increased expression of DNAI7 mRNA	CTD	PMID:30307764
DNAI7	Human	fulvestrant	multiple interactions	EXP		6480464	[bisphenol A co-treated with Fulvestrant] results in increased methylation of DNAI7 gene	CTD	PMID:31601247
DNAI7	Human	furan	increases expression	ISO	Dnai7 (Rattus norvegicus)	6480464	furan results in increased expression of DNAI7 mRNA	CTD	PMID:25539665
DNAI7	Human	lipopolysaccharide	multiple interactions	EXP		6480464	[S-(1 more ...	CTD	PMID:35811015
DNAI7	Human	methapyrilene	increases methylation	EXP		6480464	Methapyrilene results in increased methylation of DNAI7 intron	CTD	PMID:30157460
DNAI7	Human	methimazole	decreases expression	ISO	Dnai7 (Rattus norvegicus)	6480464	Methimazole results in decreased expression of CASC1 mRNA	CTD	PMID:30047161
DNAI7	Human	methyl methanesulfonate	increases expression	EXP		6480464	Methyl Methanesulfonate results in increased expression of DNAI7 mRNA	CTD	PMID:23649840
DNAI7	Human	perfluorononanoic acid	increases expression	EXP		6480464	perfluoro-n-nonanoic acid results in increased expression of DNAI7 mRNA	CTD	PMID:25812627
DNAI7	Human	perfluorooctane-1-sulfonic acid	increases expression	EXP		6480464	perfluorooctane sulfonic acid results in increased expression of DNAI7 mRNA	CTD	PMID:25812627
DNAI7	Human	pregnenolone 16alpha-carbonitrile	decreases expression	ISO	Dnai7 (Rattus norvegicus)	6480464	Pregnenolone Carbonitrile results in decreased expression of CASC1 mRNA	CTD	PMID:30047161
DNAI7	Human	propanal	increases expression	EXP		6480464	propionaldehyde results in increased expression of DNAI7 mRNA	CTD	PMID:26079696
DNAI7	Human	S-(1,2-dichlorovinyl)-L-cysteine	increases expression	EXP		6480464	S-(1 and 2-dichlorovinyl)cysteine results in increased expression of DNAI7 mRNA	CTD	PMID:35811015
DNAI7	Human	S-(1,2-dichlorovinyl)-L-cysteine	multiple interactions	EXP		6480464	[S-(1 more ...	CTD	PMID:35811015
DNAI7	Human	silicon dioxide	decreases expression	EXP		6480464	Silicon Dioxide analog results in decreased expression of DNAI7 mRNA	CTD	PMID:25895662
DNAI7	Human	sodium arsenite	affects methylation	EXP		6480464	sodium arsenite affects the methylation of DNAI7 gene	CTD	PMID:28589171
DNAI7	Human	sodium arsenite	affects expression	EXP		6480464	sodium arsenite affects the expression of DNAI7 mRNA	CTD	PMID:29319823
DNAI7	Human	sodium dichromate	increases expression	ISO	Dnai7 (Rattus norvegicus)	6480464	sodium bichromate results in increased expression of DNAI7 mRNA	CTD	PMID:22561333
DNAI7	Human	sulfadimethoxine	decreases expression	ISO	Dnai7 (Rattus norvegicus)	6480464	Sulfadimethoxine results in decreased expression of CASC1 mRNA	CTD	PMID:30047161
DNAI7	Human	titanium dioxide	decreases methylation	ISO	Dnai7 (Mus musculus)	6480464	titanium dioxide results in decreased methylation of CASC1 gene	CTD	PMID:35295148
DNAI7	Human	trichloroethene	increases expression	ISO	Dnai7 (Rattus norvegicus)	6480464	Trichloroethylene results in increased expression of DNAI7 mRNA	CTD	PMID:33387578
DNAI7	Human	Triptolide	increases expression	ISO	Dnai7 (Mus musculus)	6480464	triptolide results in increased expression of DNAI7 mRNA	CTD	PMID:32835833
DNAI7	Human	triptonide	increases expression	ISO	Dnai7 (Mus musculus)	6480464	triptonide results in increased expression of DNAI7 mRNA	CTD	PMID:33045310
DNAI7	Human	valproic acid	decreases methylation	EXP		6480464	Valproic Acid results in decreased methylation of DNAI7 gene	CTD	PMID:29154799
DNAI7	Human	valproic acid	affects expression	ISO	Dnai7 (Mus musculus)	6480464	Valproic Acid affects the expression of DNAI7 mRNA	CTD	PMID:17292431
DNAI7	Human	vorinostat	increases expression	EXP		6480464	Vorinostat results in increased expression of DNAI7 mRNA	CTD	PMID:27188386

Cellular Component

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
DNAI7	Human	axonemal dynein complex	part_of	ISS	UniProtKB:Q6TDU8	150520179		UniProt	GO_REF:0000024
DNAI7	Human	axoneme	is_active_in	IBA	MGI:2444480 more ...	150520179		GO_Central	GO_REF:0000033
DNAI7	Human	cell projection	located_in	IEA	UniProtKB-KW:KW-0966	150520179		UniProt	GO_REF:0000043
DNAI7	Human	cilium	located_in	IEA	UniProtKB-SubCell:SL-0066	150520179		UniProt	GO_REF:0000044
DNAI7	Human	cilium	located_in	ISS	UniProtKB:Q6TDU8	150520179		UniProt	GO_REF:0000024
DNAI7	Human	cytoplasm	located_in	IEA	UniProtKB-SubCell:SL-0086	150520179		UniProt	GO_REF:0000044
DNAI7	Human	cytoplasm	located_in	IEA	UniProtKB-KW:KW-0963	150520179		UniProt	GO_REF:0000043
DNAI7	Human	cytoplasmic microtubule	is_active_in	ISO	Dnai7 (Mus musculus)	9068941	PMID:17974961	MGI	PMID:17974961
DNAI7	Human	cytoplasmic microtubule	located_in	ISO	Dnai7 (Mus musculus)	9068941	PMID:17974961	MGI	PMID:17974961
DNAI7	Human	microtubule cytoskeleton	located_in	ISO	Dnai7 (Mus musculus)	9068941	PMID:17974961	MGI	PMID:17974961

Molecular Function

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
DNAI7	Human	beta-tubulin binding	enables	ISS	UniProtKB:Q6TDU8	150520179		UniProt	GO_REF:0000024
DNAI7	Human	beta-tubulin binding	enables	IBA	MGI:2444480 and PANTHER:PTN000467967	150520179		GO_Central	GO_REF:0000033
DNAI7	Human	microtubule binding	enables	ISS	UniProtKB:Q6TDU8	150520179		UniProt	GO_REF:0000024
DNAI7	Human	microtubule binding	enables	IBA	MGI:2444480 and PANTHER:PTN000467967	150520179		GO_Central	GO_REF:0000033
DNAI7	Human	protein binding	enables	IPI	UniProtKB:Q9NYB9-2 and UniProtKB:Q9Y5B8	150520179	PMID:32296183	IntAct	PMID:32296183

#	Reference Title	Reference Citation
1.	Candidate lung tumor susceptibility genes identified through whole-genome association analyses in inbred mice.	Liu P, etal., Nat Genet. 2006 Aug;38(8):888-95. Epub 2006 Jul 23.
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.	Mechanisms promoting escape from mitotic stress-induced tumor cell death.	Sinnott R, etal., Cancer Res. 2014 Jul 15;74(14):3857-69. doi: 10.1158/0008-5472.CAN-13-3398. Epub 2014 May 23.
5.	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.
6.	Positional cloning of the major quantitative trait locus underlying lung tumor susceptibility in mice.	Zhang Z, etal., Proc Natl Acad Sci U S A. 2003 Oct 28;100(22):12642-7. doi: 10.1073/pnas.2133947100.

PMID:8889548	PMID:14702039	PMID:16344560	PMID:16410263	PMID:18299280	PMID:19389623	PMID:20639392	PMID:20734064	PMID:21873635	PMID:22990118	PMID:28514442	PMID:30021884
PMID:32296183	PMID:35914814	PMID:36774506

DNAI7
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	12	25,107,047 - 25,195,160 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	12	25,108,289 - 25,195,162 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	12	25,261,223 - 25,348,094 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	12	25,152,490 - 25,239,361 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	12	25,152,489 - 25,239,361	NCBI
Celera	12	30,408,204 - 30,495,049 (-)	NCBI		Celera
Cytogenetic Map	12	p12.1	NCBI
HuRef	12	25,031,916 - 25,118,815 (-)	NCBI		HuRef
CHM1_1	12	25,226,353 - 25,313,239 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	12	24,977,958 - 25,066,403 (-)	NCBI		T2T-CHM13v2.0

Dnai7
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	6	145,120,556 - 145,156,866 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	6	145,120,560 - 145,156,731 (-)	Ensembl		GRCm39 Ensembl
GRCm38	6	145,174,833 - 145,211,017 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	6	145,174,834 - 145,211,005 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	6	145,123,392 - 145,159,490 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	6	145,132,084 - 145,168,060 (-)	NCBI		MGSCv36	mm8
Celera	6	148,249,078 - 148,285,257 (-)	NCBI		Celera
Cytogenetic Map	6	G3	NCBI
cM Map	6	77.37	NCBI

Dnai7
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	4	179,874,338 - 179,910,716 (-)	NCBI		GRCr8
mRatBN7.2	4	178,143,499 - 178,179,871 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	4	178,143,500 - 178,179,980 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	4	184,444,178 - 184,480,647 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	4	180,228,678 - 180,265,147 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	4	178,849,095 - 178,885,568 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	4	179,440,984 - 179,476,965 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	4	179,440,953 - 179,477,070 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	4	243,622,214 - 243,658,236 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	4	182,823,026 - 182,859,566 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	4	183,068,145 - 183,104,849 (-)	NCBI
Celera	4	166,662,914 - 166,699,171 (-)	NCBI		Celera
Cytogenetic Map	4	q44	NCBI

Dnai7
(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_004955413	20,227,903 - 20,287,131 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955413	20,227,807 - 20,287,211 (-)	NCBI	ChiLan1.0	ChiLan1.0

DNAI7
(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	71,620,868 - 71,707,847 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	12	71,617,264 - 71,704,233 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	12	61,117,886 - 61,204,888 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	12	63,733,801 - 63,819,991 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	12	63,733,785 - 63,819,991 (+)	Ensembl	panpan1.1		panPan2

DNAI7
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	27	22,309,705 - 22,369,052 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	27	22,303,849 - 22,369,051 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	27	23,999,487 - 24,071,297 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	27	22,502,481 - 22,568,288 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	27	22,502,580 - 22,568,282 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	27	22,317,692 - 22,384,301 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	27	22,336,520 - 22,403,282 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	27	24,171,481 - 24,238,226 (-)	NCBI		UU_Cfam_GSD_1.0

Dnai7
(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_024404945	84,200,357 - 84,274,388 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936548	2,123,360 - 2,202,032 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936548	2,123,248 - 2,197,245 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

DNAI7
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	5	48,555,688 - 48,651,365 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	5	48,555,637 - 48,651,370 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1

DNAI7
(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	24,871,767 - 24,953,586 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	11	24,875,416 - 24,953,375 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666069	10,173,735 - 10,255,300 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Dnai7
(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_004624752	13,855,426 - 13,936,764 (+)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624752	13,855,328 - 13,932,210 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants in DNAI7
60 total Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 1p31.1-13.3(chr1:72661709-107456880)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051825]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051825]\|See cases [RCV000051825]	Chr1:72661709..107456880 [GRCh38] Chr1:73127392..107999502 [GRCh37] Chr1:72899980..107801025 [NCBI36] Chr1:1p31.1-13.3	pathogenic
NM_012093.3(AK5):c.1069+12565A>T	single nucleotide variant	Lung cancer [RCV000090988]	Chr1:77498917 [GRCh38] Chr1:77964602 [GRCh37] Chr1:1p31.1	uncertain significance
GRCh38/hg38 1p32.1-22.3(chr1:58819605-86098611)x1	copy number loss	See cases [RCV000136913]	Chr1:58819605..86098611 [GRCh38] Chr1:59285277..86564294 [GRCh37] Chr1:59057865..86336882 [NCBI36] Chr1:1p32.1-22.3	pathogenic
GRCh38/hg38 1p31.1-22.2(chr1:76419302-88628464)x1	copy number loss	See cases [RCV000138957]	Chr1:76419302..88628464 [GRCh38] Chr1:76884987..89094147 [GRCh37] Chr1:76657575..88866735 [NCBI36] Chr1:1p31.1-22.2	pathogenic
GRCh38/hg38 1p31.1(chr1:77256993-77510214)x1	copy number loss	See cases [RCV000142131]	Chr1:77256993..77510214 [GRCh38] Chr1:77722678..77975899 [GRCh37] Chr1:77495266..77748487 [NCBI36] Chr1:1p31.1	uncertain significance
GRCh38/hg38 1p31.1(chr1:77264562-77493002)x1	copy number loss	See cases [RCV000143317]	Chr1:77264562..77493002 [GRCh38] Chr1:77730247..77958687 [GRCh37] Chr1:77502835..77731275 [NCBI36] Chr1:1p31.1	likely benign\|uncertain significance
GRCh37/hg19 1p36.12-12(chr1:20608823-120546301)x3	copy number loss	not provided [RCV000762767]	Chr1:20608823..120546301 [GRCh37] Chr1:1p36.12-12	likely benign
GRCh37/hg19 1p31.1(chr1:77722678-77970795)x1	copy number loss	See cases [RCV000448416]	Chr1:77722678..77970795 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.609= (p.Lys203=)	single nucleotide variant	not provided [RCV004713972]\|not specified [RCV000454614]	Chr1:77297857 [GRCh38] Chr1:77763542 [GRCh37] Chr1:1p31.1	benign
NM_174858.3(AK5):c.1681_1683dup (p.Ile561dup)	duplication	not specified [RCV000454873]	Chr1:77558660..77558661 [GRCh38] Chr1:78024345..78024346 [GRCh37] Chr1:1p31.1	benign
NM_174858.3(AK5):c.1059+12C>T	single nucleotide variant	not provided [RCV004715175]\|not specified [RCV000455276]	Chr1:77417727 [GRCh38] Chr1:77883412 [GRCh37] Chr1:1p31.1	benign
NM_174858.3(AK5):c.1621-3T>C	single nucleotide variant	not provided [RCV004715176]\|not specified [RCV000456016]	Chr1:77558599 [GRCh38] Chr1:78024284 [GRCh37] Chr1:1p31.1	benign
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3	copy number gain	See cases [RCV000510383]	Chr1:849467..249224684 [GRCh37] Chr1:1p36.33-q44	pathogenic
GRCh37/hg19 1p31.1-22.1(chr1:72044544-92505091)x1	copy number loss	See cases [RCV000510161]	Chr1:72044544..92505091 [GRCh37] Chr1:1p31.1-22.1	pathogenic
GRCh37/hg19 1p31.3-22.3(chr1:64321264-88153669)x1	copy number loss	See cases [RCV000511392]	Chr1:64321264..88153669 [GRCh37] Chr1:1p31.3-22.3	pathogenic\|uncertain significance
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)	copy number gain	See cases [RCV000510926]	Chr1:849467..249224684 [GRCh37] Chr1:1p36.33-q44	pathogenic
GRCh37/hg19 1p31.1(chr1:74848936-80324850)x3	copy number gain	See cases [RCV000510973]	Chr1:74848936..80324850 [GRCh37] Chr1:1p31.1	uncertain significance
GRCh37/hg19 1p31.1(chr1:75648797-77770044)x1	copy number loss	See cases [RCV000510871]	Chr1:75648797..77770044 [GRCh37] Chr1:1p31.1	likely pathogenic
GRCh37/hg19 1p31.1(chr1:77823556-78281638)x1	copy number loss	See cases [RCV000511213]	Chr1:77823556..78281638 [GRCh37] Chr1:1p31.1	uncertain significance
GRCh37/hg19 1p31.3-31.1(chr1:61351024-79583933)x1	copy number loss	See cases [RCV000512152]	Chr1:61351024..79583933 [GRCh37] Chr1:1p31.3-31.1	pathogenic
GRCh37/hg19 1p31.1(chr1:77717646-77970795)x1	copy number loss	not provided [RCV000684592]	Chr1:77717646..77970795 [GRCh37] Chr1:1p31.1	uncertain significance
GRCh37/hg19 1p36.33-q44(chr1:47851-249228449)x3	copy number gain	not provided [RCV000736295]	Chr1:47851..249228449 [GRCh37] Chr1:1p36.33-q44	pathogenic
GRCh37/hg19 1p36.33-q44(chr1:82154-249218992)x3	copy number gain	not provided [RCV000736305]	Chr1:82154..249218992 [GRCh37] Chr1:1p36.33-q44	pathogenic
GRCh37/hg19 1p31.1(chr1:77768016-77781567)x1	copy number loss	not provided [RCV000736543]	Chr1:77768016..77781567 [GRCh37] Chr1:1p31.1	benign
GRCh37/hg19 1p31.1(chr1:77955577-78040287)x3	copy number gain	not provided [RCV000736544]	Chr1:77955577..78040287 [GRCh37] Chr1:1p31.1	benign
GRCh37/hg19 1p31.1(chr1:71410579-78131158)	copy number gain	not provided [RCV000767771]	Chr1:71410579..78131158 [GRCh37] Chr1:1p31.1	pathogenic
GRCh37/hg19 1p36.22-21.1(chr1:103343285-103455144)x3	copy number gain	Global developmental delay [RCV000787285]	Chr1:103343285..103455144 [GRCh37] Chr1:1p36.22-21.1	uncertain significance
GRCh37/hg19 1p31.1(chr1:77954138-78053851)x3	copy number gain	not provided [RCV000847497]	Chr1:77954138..78053851 [GRCh37] Chr1:1p31.1	uncertain significance
Single allele	deletion	not provided [RCV000844927]	Chr1:66085524..88429789 [GRCh37] Chr1:1p31.3-22.2	not provided
GRCh37/hg19 1p31.1(chr1:77153809-78015058)x3	copy number gain	not provided [RCV000847465]	Chr1:77153809..78015058 [GRCh37] Chr1:1p31.1	uncertain significance
GRCh37/hg19 1p31.3-22.3(chr1:67851233-86101340)x1	copy number loss	not provided [RCV000846441]	Chr1:67851233..86101340 [GRCh37] Chr1:1p31.3-22.3	pathogenic
GRCh37/hg19 1p31.3-22.1(chr1:68180293-92731957)	copy number loss	not specified [RCV002053392]	Chr1:68180293..92731957 [GRCh37] Chr1:1p31.3-22.1	pathogenic
GRCh37/hg19 1p31.1(chr1:77722678-77970795)x1	copy number loss	not specified [RCV002053447]	Chr1:77722678..77970795 [GRCh37] Chr1:1p31.1	uncertain significance
Single allele	duplication	not specified [RCV002286371]	Chr1:66885559..77949895 [GRCh38] Chr1:1p31.3-31.1	uncertain significance
NM_174858.3(AK5):c.280C>T (p.Arg94Trp)	single nucleotide variant	not specified [RCV004108567]	Chr1:77293825 [GRCh38] Chr1:77759510 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.1420G>A (p.Gly474Arg)	single nucleotide variant	not specified [RCV004207491]	Chr1:77521935 [GRCh38] Chr1:77987620 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.195G>T (p.Lys65Asn)	single nucleotide variant	not specified [RCV004119458]	Chr1:77287075 [GRCh38] Chr1:77752760 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.47C>T (p.Pro16Leu)	single nucleotide variant	not specified [RCV004082392]	Chr1:77282360 [GRCh38] Chr1:77748045 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.1393C>T (p.Arg465Trp)	single nucleotide variant	not specified [RCV004114865]	Chr1:77521908 [GRCh38] Chr1:77987593 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.1642G>A (p.Glu548Lys)	single nucleotide variant	not specified [RCV004153590]	Chr1:77558623 [GRCh38] Chr1:78024308 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.1070A>G (p.Gln357Arg)	single nucleotide variant	not specified [RCV004105866]	Chr1:77483327 [GRCh38] Chr1:77949012 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.886A>G (p.Met296Val)	single nucleotide variant	not specified [RCV004082684]	Chr1:77340563 [GRCh38] Chr1:77806248 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.1420G>C (p.Gly474Arg)	single nucleotide variant	not specified [RCV004166622]	Chr1:77521935 [GRCh38] Chr1:77987620 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.1344G>A (p.Met448Ile)	single nucleotide variant	not specified [RCV004177212]	Chr1:77521859 [GRCh38] Chr1:77987544 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.487G>A (p.Val163Met)	single nucleotide variant	not specified [RCV004146678]	Chr1:77297630 [GRCh38] Chr1:77763315 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.1010T>C (p.Ile337Thr)	single nucleotide variant	not specified [RCV004110183]	Chr1:77417666 [GRCh38] Chr1:77883351 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.518G>A (p.Ser173Asn)	single nucleotide variant	not specified [RCV004124961]	Chr1:77297661 [GRCh38] Chr1:77763346 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.957A>T (p.Leu319Phe)	single nucleotide variant	not specified [RCV004197894]	Chr1:77411046 [GRCh38] Chr1:77876731 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.796G>A (p.Asp266Asn)	single nucleotide variant	not specified [RCV004122178]	Chr1:77340473 [GRCh38] Chr1:77806158 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.1225G>C (p.Glu409Gln)	single nucleotide variant	not specified [RCV004168989]	Chr1:77518641 [GRCh38] Chr1:77984326 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.290G>A (p.Arg97Gln)	single nucleotide variant	not specified [RCV004177573]	Chr1:77293835 [GRCh38] Chr1:77759520 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.751A>G (p.Lys251Glu)	single nucleotide variant	not specified [RCV004267923]	Chr1:77340428 [GRCh38] Chr1:77806113 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.172A>G (p.Thr58Ala)	single nucleotide variant	not specified [RCV004327430]	Chr1:77287052 [GRCh38] Chr1:77752737 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.1595A>T (p.Tyr532Phe)	single nucleotide variant	not specified [RCV004323861]	Chr1:77536013 [GRCh38] Chr1:78001698 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.1291C>T (p.Arg431Cys)	single nucleotide variant	not specified [RCV004363369]	Chr1:77518707 [GRCh38] Chr1:77984392 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.1318G>A (p.Val440Ile)	single nucleotide variant	not specified [RCV004349734]	Chr1:77521833 [GRCh38] Chr1:77987518 [GRCh37] Chr1:1p31.1	likely benign
NM_174858.3(AK5):c.360G>A (p.Glu120=)	single nucleotide variant	not provided [RCV003406565]	Chr1:77293905 [GRCh38] Chr1:77759590 [GRCh37] Chr1:1p31.1	likely benign
NM_174858.3(AK5):c.1314C>T (p.Gly438=)	single nucleotide variant	not provided [RCV003406566]	Chr1:77521829 [GRCh38] Chr1:77987514 [GRCh37] Chr1:1p31.1	likely benign
GRCh37/hg19 1p31.1-22.3(chr1:73616197-87012961)x1	copy number loss	not provided [RCV003885448]	Chr1:73616197..87012961 [GRCh37] Chr1:1p31.1-22.3	likely pathogenic
NM_174858.3(AK5):c.1061G>T (p.Gly354Val)	single nucleotide variant	not specified [RCV004388827]	Chr1:77483318 [GRCh38] Chr1:77949003 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.1357G>A (p.Gly453Arg)	single nucleotide variant	not specified [RCV004391347]	Chr1:77521872 [GRCh38] Chr1:77987557 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.1531A>G (p.Thr511Ala)	single nucleotide variant	not specified [RCV004391394]	Chr1:77535949 [GRCh38] Chr1:78001634 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.382A>G (p.Thr128Ala)	single nucleotide variant	not specified [RCV004396406]	Chr1:77293927 [GRCh38] Chr1:77759612 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.893T>G (p.Phe298Cys)	single nucleotide variant	not specified [RCV004396456]	Chr1:77410982 [GRCh38] Chr1:77876667 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.1384G>A (p.Gly462Ser)	single nucleotide variant	not specified [RCV004391357]	Chr1:77521899 [GRCh38] Chr1:77987584 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.1504C>T (p.Arg502Trp)	single nucleotide variant	not specified [RCV004391384]	Chr1:77535922 [GRCh38] Chr1:78001607 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.227G>A (p.Arg76Gln)	single nucleotide variant	not specified [RCV004396385]	Chr1:77287107 [GRCh38] Chr1:77752792 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.289C>T (p.Arg97Trp)	single nucleotide variant	not specified [RCV004621532]	Chr1:77293834 [GRCh38] Chr1:77759519 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.271C>T (p.Pro91Ser)	single nucleotide variant	not specified [RCV004915950]	Chr1:77293816 [GRCh38] Chr1:77759501 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.1403A>T (p.Lys468Met)	single nucleotide variant	not specified [RCV004915959]	Chr1:77521918 [GRCh38] Chr1:77987603 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.1634G>C (p.Gly545Ala)	single nucleotide variant	not specified [RCV004915968]	Chr1:77558615 [GRCh38] Chr1:78024300 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.1582G>A (p.Val528Met)	single nucleotide variant	not specified [RCV004915948]	Chr1:77536000 [GRCh38] Chr1:78001685 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.1286T>C (p.Met429Thr)	single nucleotide variant	not specified [RCV004915946]	Chr1:77518702 [GRCh38] Chr1:77984387 [GRCh37] Chr1:1p31.1	uncertain significance
NM_174858.3(AK5):c.94G>A (p.Glu32Lys)	single nucleotide variant	not specified [RCV004915947]	Chr1:77286974 [GRCh38] Chr1:77752659 [GRCh37] Chr1:1p31.1	uncertain significance
GRCh37/hg19 1p31.1-22.2(chr1:76492334-91166951)x1	copy number loss	not provided [RCV004819327]	Chr1:76492334..91166951 [GRCh37] Chr1:1p31.1-22.2	pathogenic
NM_174858.3(AK5):c.1235G>A (p.Arg412His)	single nucleotide variant	not specified [RCV004915945]	Chr1:77518651 [GRCh38] Chr1:77984336 [GRCh37] Chr1:1p31.1	uncertain significance
GRCh37/hg19 1p34.1-22.2(chr1:44475302-89585894)x3	copy number gain	not provided [RCV004819297]	Chr1:44475302..89585894 [GRCh37] Chr1:1p34.1-22.2	pathogenic

Predicted Target Of

	Summary Value
Count of predictions:	1459
Count of miRNA genes:	594
Interacting mature miRNAs:	652
Transcripts:	ENST00000320267, ENST00000354189, ENST00000395987, ENST00000395990, ENST00000537577, ENST00000545133, ENST00000554347, ENST00000554533, ENST00000555240, ENST00000555554, ENST00000556006, ENST00000556467, ENST00000556547, ENST00000557684
Prediction methods:	Microtar, Miranda, Rnahybrid
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.

RH92803

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	12	25,261,476 - 25,261,595	UniSTS	GRCh37
Build 36	12	25,152,743 - 25,152,862	RGD	NCBI36
Celera	12	30,408,457 - 30,408,576	RGD
Cytogenetic Map	12	p12.1	UniSTS
HuRef	12	25,032,169 - 25,032,288	UniSTS
GeneMap99-GB4 RH Map	12	92.63	UniSTS

SHGC-83826

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	12	25,265,038 - 25,265,314	UniSTS	GRCh37
Build 36	12	25,156,305 - 25,156,581	RGD	NCBI36
Celera	12	30,412,040 - 30,412,316	RGD
Cytogenetic Map	12	p12.1	UniSTS
HuRef	12	25,035,752 - 25,036,028	UniSTS
TNG Radiation Hybrid Map	12	11299.0	UniSTS

SHGC-132095

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	12	25,261,069 - 25,261,169	UniSTS	GRCh37
Build 36	12	25,152,336 - 25,152,436	RGD	NCBI36
Celera	12	30,408,050 - 30,408,150	RGD
Cytogenetic Map	12	p12.1	UniSTS
HuRef	12	25,031,762 - 25,031,862	UniSTS
TNG Radiation Hybrid Map	12	11291.0	UniSTS

LRMP_7815

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	12	25,260,821 - 25,261,289	UniSTS	GRCh37
Build 36	12	25,152,088 - 25,152,556	RGD	NCBI36
Celera	12	30,407,802 - 30,408,270	RGD
HuRef	12	25,031,514 - 25,031,982	UniSTS

CASC1_9888

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	12	25,261,055 - 25,261,643	UniSTS	GRCh37
Build 36	12	25,152,322 - 25,152,910	RGD	NCBI36
Celera	12	30,408,036 - 30,408,624	RGD
HuRef	12	25,031,748 - 25,032,336	UniSTS

D12S1350E

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	12	25,260,995 - 25,261,169	UniSTS	GRCh37
Build 36	12	25,152,262 - 25,152,436	RGD	NCBI36
Celera	12	30,407,976 - 30,408,150	RGD
Cytogenetic Map	12	p12.1	UniSTS
HuRef	12	25,031,688 - 25,031,862	UniSTS
Stanford-G3 RH Map	12	1228.0	UniSTS
Whitehead-YAC Contig Map	12		UniSTS
NCBI RH Map	12	278.3	UniSTS
GeneMap99-G3 RH Map	12	1228.0	UniSTS

RH17991

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	12	25,260,768 - 25,261,005	UniSTS	GRCh37
Build 36	12	25,152,035 - 25,152,272	RGD	NCBI36
Celera	12	30,407,749 - 30,407,986	RGD
Cytogenetic Map	12	p12.1	UniSTS
HuRef	12	25,031,461 - 25,031,698	UniSTS
GeneMap99-GB4 RH Map	12	92.63	UniSTS

STS-AA005176

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	12	25,297,363 - 25,297,582	UniSTS	GRCh37
Build 36	12	25,188,630 - 25,188,849	RGD	NCBI36
Celera	12	30,444,336 - 30,444,555	RGD
Cytogenetic Map	12	p12.1	UniSTS
HuRef	12	25,068,098 - 25,068,317	UniSTS
GeneMap99-GB4 RH Map	12	93.32	UniSTS

RH45039

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	12	25,261,081 - 25,261,200	UniSTS	GRCh37
Build 36	12	25,152,348 - 25,152,467	RGD	NCBI36
Celera	12	30,408,062 - 30,408,181	RGD
Cytogenetic Map	12	p12.1	UniSTS
HuRef	12	25,031,774 - 25,031,893	UniSTS
GeneMap99-GB4 RH Map	12	92.63	UniSTS

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

Download All Expressed Objects for this Gene

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	entire extraembryonic component	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	renal system	reproductive system	respiratory system	sensory system	visual system
1183	2385	2706	2209	4947	1640	2257	6	538	1790	380	2240	6893	6239	52	3731	843	1735	1608	172	1


RefSeq Transcripts	NM_001082972	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001082973	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001204101	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001204102	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001319977	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001319978	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352061	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352062	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352063	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352064	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352065	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352066	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352067	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001352068	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_018272	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_147909	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_147910	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_147911	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005253406	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005253408	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006719101	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011520723	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011520726	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011520727	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017019560	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017019565	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024449031	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047429074	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047429075	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047429076	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047429077	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047429078	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372411	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372412	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372413	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372414	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372415	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372416	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372417	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372418	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372419	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372420	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372421	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372422	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001748797	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC023510	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC092794	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK001783	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK093102	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK297998	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK301763	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK302235	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK304602	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY423543	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC028415	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC031047	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC047415	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC057795	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC117281	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC117283	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BM979714	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471094	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068266	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA753279	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000320267 ⟹ ENSP00000313141

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	25,108,420 - 25,195,160 (-)	Ensembl

Ensembl Acc Id:

ENST00000354189 ⟹ ENSP00000346126

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	25,108,420 - 25,195,098 (-)	Ensembl

Ensembl Acc Id:

ENST00000395987 ⟹ ENSP00000379310

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	25,108,289 - 25,195,160 (-)	Ensembl

Ensembl Acc Id:

ENST00000395990 ⟹ ENSP00000379313

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	25,108,420 - 25,195,160 (-)	Ensembl

Ensembl Acc Id:

ENST00000545133 ⟹ ENSP00000437373

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	25,108,424 - 25,195,126 (-)	Ensembl

Ensembl Acc Id:

ENST00000554347 ⟹ ENSP00000451232

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	25,154,341 - 25,195,130 (-)	Ensembl

Ensembl Acc Id:

ENST00000554533 ⟹ ENSP00000450703

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	25,108,421 - 25,195,162 (-)	Ensembl

Ensembl Acc Id:

ENST00000555240

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	25,154,375 - 25,195,127 (-)	Ensembl

Ensembl Acc Id:

ENST00000555554

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	25,111,817 - 25,149,692 (-)	Ensembl

Ensembl Acc Id:

ENST00000556006 ⟹ ENSP00000451813

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	25,108,420 - 25,158,563 (-)	Ensembl

Ensembl Acc Id:

ENST00000556467 ⟹ ENSP00000451011

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	25,149,762 - 25,195,160 (-)	Ensembl

Ensembl Acc Id:

ENST00000556547

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	25,149,628 - 25,195,157 (-)	Ensembl

Ensembl Acc Id:

ENST00000557684

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	25,111,772 - 25,195,126 (-)	Ensembl

Ensembl Acc Id:

ENST00000674567 ⟹ ENSP00000502075

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	25,108,436 - 25,195,144 (-)	Ensembl

Ensembl Acc Id:

ENST00000676236 ⟹ ENSP00000501714

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	25,108,477 - 25,195,108 (-)	Ensembl

RefSeq Acc Id:

NM_001082972 ⟹ NP_001076441

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	25,108,289 - 25,195,160 (-)	NCBI
GRCh37	12	25,261,223 - 25,348,096 (-)	NCBI
Build 36	12	25,152,490 - 25,239,361 (-)	NCBI Archive
Celera	12	30,408,204 - 30,495,049 (-)	RGD
HuRef	12	25,031,916 - 25,118,815 (-)	RGD
CHM1_1	12	25,226,353 - 25,313,241 (-)	NCBI
T2T-CHM13v2.0	12	24,979,200 - 25,066,403 (-)	NCBI

Sequence:

show sequence

GTCGTCCGGGCAACCCGGGAGCGTTTGTCCACACAATTTCTGCTCCGACTCTGCGGACTACTGCAGTGGAGCTTGACTCTTAATGGTGAGCAAGGCAAATGAGGCAGACAGGTGGAGGGGCGACCACT
GATTCTGCTTCACCAGTGTTAAATAATGTAATCAAGAGCCAGTCATATTTTACAGCGAAGCGGGTCGGTTTGGGAAATAACTCATACCTTGGGGTGGGTCGGCCCTCTTCTCAGCAATGGCTTTCCTT
ACCTGGACCAGGCGGACAGGGTCCCAAAGCAAAAAAGTCTGGCAGTAAGAAAAAGAAAGTCACCAAAGCTGAACGATTGAAGCTGCTACAAGAGGAGGAGGAGAGACGACTGAAAGAGGAAGAGGAAG
CCCGTTTGAAATATGAGAAAGAAGAAATGGAAAGGCTTGAAATACAGCGAATTGAGAAAGAAAAATGGCATCGACTTGAAGCAAAAGATCTAGAAAGGAGAAATGAAGAACTTGAAGAACTTTATTTA
TTAGAGAGGTGTTTTCCTGAAGCAGAGAAATTGAAACAGGAAACTAAATTGCTTTCTCAGTGGAAGCACTACATTCAATGTGATGGGAGTCCTGATCCTTCAGTAGCCCAAGAAATGAACACGTTTAT
TAGTTTGTGGAAAGAGAAAACAAATGAGACTTTTGAGGAAGTGATTGAGAAGAGTAAAGTAGTGCTAAATTTAATTGAGAAATTGAAATTTATTTTACTGGAAACTCCACCATGTGATTTGCAAGATA
AAAATATAATACAGTACCAAGAATCAATACTACAACTGCAGGAGCTCCTTCATCTTAAATTCGGTGTAGCCACAGAAATACTTCTCAAACAAGCTAGTACTTTGGCAGATCTGGACAGTGGAAATATG
GAAAAAGTCATTAAAGATGAAAATGTTACTCTGTATGTGTGGGCAAACCTCAAGAAGAATCCAAGGCACAGAAGTGTTAGATTCTCTGAAACACAAATTGGATTTGAGATTCCAAGGATATTAGCAAC
AAGTGACATTGCTGTACGACTCCTGCATACCCACTATGATCATGTTTCTGCACTGCACCCTGTTTCAACACCATCAAAAGAATACACTTCTGCAGTAACTGAGCTTGTCAAAGATGATGTTAAGAATG
TAGAAAAAGCAATCAGCAAGGAGGTCGAAGAAGAGTCCAAACAACAAGAAAGAGGGTCTCACTTAATTCAGGAGGAAGAAATAAAAGTTGAGGAGGAACAAGGTGATATTGAAGTGAAAATGAGTTCT
GCTGAGGAAGAATCTGAAGCCATAAAATGTGAACGAGAGATGAAAGTATTAAGTGAAACTGTTTCAGCAGCACAGTTGTTGCTGGTAGAGAATTCTTCTGAAAAGCCAGATTTCTTTGAAGACAATGT
GGTGGATTTATGCCAGTTCACAACTCTGGGTGGAGTATACCACTTGGATATTTTGGAGCTTCCTCCACAGTGTAAACCAGTGAAGGGATGGATGATTGTGGAAATACTCAAAGAAGGATTACAGAAAT
ACACATATCCTCCGGAAACTACAGAAGAGTTTGAGACAGAAAATGCTTTCCCACCTATAGAGGTCACACTTGAGGTTCATGAGAATGTAATCTTTTTTGAGGATCCTGTGGTTGTAAGGTGGGATGCT
GAAGGTAAACATTGGAGAACTGATGGCATCAGCAATGTATCCTACAAACCAAAAGAAAGACTTGTAACATTCAGCCTGGACACCTTTGGCCCTGTTACCTTGATTCAAGATGCTCATATTAACATGCC
GTACCAGTCATGGGAACTAAGACCACTTGATGTAAATAAAGTACTTTTAACTGTGACTACAGTATTTACTGAGATTCAAATACAAATTAAGGAAAACCTCTGCATGTTATCTTCAATCAAACTAAAAG
ACAAGAAACACATCTCTATTTTGGAAGGAACCTGGATGACTCCTATTCCTTTCATTATTGCTTTGAAAGAAGCTGGACTGAATATCTTTCCTACTAGACACTCTCATTTTTATGTTATTATAAACAAT
AAGGTTCCTTTGGTAGAAGTGAAAGCTTATCGACAGATGGCCCTACTAAGTTCTGCTTTTGCATTTGGTTGGAGCAAGTGGAACCTACTATGTAATTCTACAAAAGTCGTATTTAAGTGGTGACAGAG
CACAAAGACTGAAGATCAAGGAAGAGAGTGAGGCATTTTCTGAAGCACTTAAAGAAGAAACTGAGTTTCATTCTACTTTATATCACATGGTGAAGGATTTTGCTTCTGAGGAAGCAATGGAGAAAGTC
AGGAGTTCCAACTGTCAGTTTGTCAACTCTGTGTGCCACATGCTGCTCTCTACCAGATTGCTCAGCTACTCCTAACCTCCACTTACAAACTGTATTGTAAGTATGAAGAACCAAGCATGGTGAAAGAC
AGGTATTTCTGCAACACAATGTAATGAGTGAATGAATACATTTCAAATCAACTATTAAAAATTTTCTAATCTGCATTTTCTACTCAAGTTTTATTTTAAAAACAGTATTTTTTTTTCCTTTGAATACT
TGGCCTGTTAAGAATTTCAGCTTTCACTCTATGAAGATTTAAATGATTCTTTATTTCAATAAACTTTAACAAACAATA

hide sequence

RefSeq Acc Id:

NM_001082973 ⟹ NP_001076442

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	25,108,289 - 25,195,160 (-)	NCBI
GRCh37	12	25,261,223 - 25,348,096 (-)	NCBI
Build 36	12	25,152,490 - 25,239,361 (-)	NCBI Archive
Celera	12	30,408,204 - 30,495,049 (-)	RGD
HuRef	12	25,031,916 - 25,118,815 (-)	RGD
CHM1_1	12	25,226,353 - 25,313,241 (-)	NCBI
T2T-CHM13v2.0	12	24,979,200 - 25,066,403 (-)	NCBI

Sequence:

show sequence

GTCGTCCGGGCAACCCGGGAGCGTTTGTCCACACAATTTCTGCTCCGACTCTGCGGACTACTGCAGTGGAGCTTGACTCTTAATGTCTGGCAGTAAGAAAAAGAAAGTCACCAAAGCTGAACGATTGA
AGCTGCTACAAGAGGAGGAGGAGAGACGACTGAAAGAGGAAGAGGAAGCCCGTTTGAAATATGAGAAAGAAGAAATGGAAAGGCTTGAAATACAGCGAATTGAGAAAGAAAAATGGCATCGACTTGAA
GCAAAAGATCTAGAAAGGAGAAATGAAGAACTTGAAGAACTTTATTTATTAGAGAGGTGTTTTCCTGAAGCAGAGAAATTGAAACAGGAAACTAAATTGCTTTCTCAGTGGAAGCACTACATTCAATG
TGATGGGAGTCCTGATCCTTCAGTAGCCCAAGAAATGAACACGTTTATTAGTTTGTGGAAAGAGAAAACAAATGAGACTTTTGAGGAAGTGATTGAGAAGAGTAAAGTAGTGCTAAATTTAATTGAGA
AATTGAAATTTATTTTACTGGAAACTCCACCATGTGATTTGCAAGATAAAAATATAATACAGTACCAAGAATCAATACTACAACTGCAGGAGCTCCTTCATCTTAAATTCGGTGTAGCCACAGAAATA
CTTCTCAAACAAGCTAGTACTTTGGCAGATCTGGACAGTGGAAATATGGAAAAAGTCATTAAAGATGAAAATGTTACTCTGTATGTGTGGGCAAACCTCAAGAAGAATCCAAGGCACAGAAGTGTTAG
ATTCTCTGAAACACAAATTGGATTTGAGATTCCAAGGATATTAGCAACAAGTGACATTGCTGTACGACTCCTGCATACCCACTATGATCATGTTTCTGCACTGCACCCTGTTTCAACACCATCAAAAG
AATACACTTCTGCAGTAACTGAGCTTGTCAAAGATGATGTTAAGAATGTAGAAAAAGCAATCAGCAAGGAGGTCGAAGAAGAGTCCAAACAACAAGAAAGAGGGTCTCACTTAATTCAGGAGGAAGAA
ATAAAAGTTGAGGAGGAACAAGGTGATATTGAAGTGAAAATGAGTTCTGCTGAGGAAGAATCTGAAGCCATAAAATGTGAACGAGAGATGAAAGTATTAAGTGAAACTGTTTCAGCAGCACAGTTGTT
GCTGGTAGAGAATTCTTCTGAAAAGCCAGATTTCTTTGAAGACAATGTGGTGGATTTATGCCAGTTCACAACTCTGGGTGGAGTATACCACTTGGATATTTTGGAGCTTCCTCCACAGTGTAAACCAG
TGAAGGGATGGATGATTGTGGAAATACTCAAAGAAGGATTACAGAAATACACATATCCTCCGGAAACTACAGAAGAGTTTGAGACAGAAAATGCTTTCCCACCTATAGAGGTCACACTTGAGGTTCAT
GAGAATGTAATCTTTTTTGAGGATCCTGTGGTTGTAAGGTGGGATGCTGAAGGTAAACATTGGAGAACTGATGGCATCAGCAATGTATCCTACAAACCAAAAGAAAGACTTGTAACATTCAGCCTGGA
CACCTTTGGCCCTGTTACCTTGATTCAAGATGCTCATATTAACATGCCGTACCAGTCATGGGAACTAAGACCACTTGATGTAAATAAAGTACTTTTAACTGTGACTACAGTATTTACTGAGATTCAAA
TACAAATTAAGGAAAACCTCTGCATGTTATCTTCAATCAAACTAAAAGACAAGAAACACATCTCTATTTTGGAAGGAACCTGGATGACTCCTATTCCTTTCATTATTGCTTTGAAAGAAGCTGGACTG
AATATCTTTCCTACTAGACACTCTCATTTTTATGTTATTATAAACAATAAGGTTCCTTTGGTAGAAGTGAAAGCTTATCGACAGATGGCCCTACTAAGTTCTGCTTTTGCATTTGGTTGGAGCAAGTG
GAACCTACTATGTAATTCTACAAAAGTCGTATTTAAGGTGAGGGAACACCTTACTGAAGCATGTACTGAGAATCCTAATTGGGCCCTTTTAATGTTTAGTGGTGACAGAGCACAAAGACTGAAGATCA
AGGAAGAGAGTGAGGCATTTTCTGAAGCACTTAAAGAAGAAACTGAGTTTCATTCTACTTTATATCACATGGTGAAGGATTTTGCTTCTGAGGAAGCAATGGAGAAAGTCAGGAGTTCCAACTGTCAG
TTTGTCAACTCTGTGTGCCACATGCTGCTCTCTACCAGATTGCTCAGCTACTCCTAACCTCCACTTACAAACTGTATTGTAAGTATGAAGAACCAAGCATGGTGAAAGACAGGTATTTCTGCAACACA
ATGTAATGAGTGAATGAATACATTTCAAATCAACTATTAAAAATTTTCTAATCTGCATTTTCTACTCAAGTTTTATTTTAAAAACAGTATTTTTTTTTCCTTTGAATACTTGGCCTGTTAAGAATTTC
AGCTTTCACTCTATGAAGATTTAAATGATTCTTTATTTCAATAAACTTTAACAAACAATA

hide sequence

RefSeq Acc Id:

NM_001204101 ⟹ NP_001191030

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	25,108,289 - 25,195,160 (-)	NCBI
GRCh37	12	25,261,223 - 25,348,096 (-)	NCBI
HuRef	12	25,031,916 - 25,118,815 (-)	RGD
CHM1_1	12	25,226,353 - 25,313,241 (-)	NCBI
T2T-CHM13v2.0	12	24,979,200 - 25,066,403 (-)	NCBI

Sequence:

show sequence

GTCGTCCGGGCAACCCGGGAGCGTTTGTCCACACAATTTCTGCTCCGACTCTGCGGACTACTGC
AGTGGAGCTTGACTCTTAATGGATCTAGAAAGGAGAAATGAAGAACTTGAAGAACTTTATTTATTAGAGAGGTGTTTTCCTGAAGCAGAGAAATTGAAACAGGAAACTAAATTGCTTTCTCAGTGGAA
GCACTACATTCAATGTGATGGGAGTCCTGATCCTTCAGTAGCCCAAGAAATGAACACGTTTATTAGTTTGTGGAAAGAGAAAACAAATGAGACTTTTGAGGAAGTGATTGAGAAGAGTAAAGTAGTGC
TAAATTTAATTGAGAAATTGAAATTTATTTTACTGGAAACTCCACCATGTGATTTGCAAGATAAAAATATAATACAGTACCAAGAATCAATACTACAACTGCAGGAGCTCCTTCATCTTAAATTCGGT
GTAGCCACAGAAATACTTCTCAAACAAGCTAGTACTTTGGCAGATCTGGACAGTGGAAATATGGAAAAAGTCATTAAAGATGAAAATGTTACTCTGTATGTGTGGGCAAACCTCAAGAAGAATCCAAG
GCACAGAAGTGTTAGATTCTCTGAAACACAAATTGGATTTGAGATTCCAAGGATATTAGCAACAAGTGACATTGCTGTACGACTCCTGCATACCCACTATGATCATGTTTCTGCACTGCACCCTGTTT
CAACACCATCAAAAGAATACACTTCTGCAGTAACTGAGCTTGTCAAAGATGATGTTAAGAATGTAGAAAAAGCAATCAGCAAGGAGGTCGAAGAAGAGTCCAAACAACAAGAAAGAGGGTCTCACTTA
ATTCAGGAGGAAGAAATAAAAGTTGAGGAGGAACAAGGTGATATTGAAGTGAAAATGAGTTCTGCTGAGGAAGAATCTGAAGCCATAAAATGTGAACGAGAGATGAAAGTATTAAGTGAAACTGTTTC
AGCAGCACAGTTGTTGCTGGTAGAGAATTCTTCTGAAAAGCCAGATTTCTTTGAAGACAATGTGGTGGATTTATGCCAGTTCACAACTCTGGGTGGAGTATACCACTTGGATATTTTGGAGCTTCCTC
CACAGTGTAAACCAGTGAAGGGATGGATGATTGTGGAAATACTCAAAGAAGGATTACAGAAATACACATATCCTCCGGAAACTACAGAAGAGTTTGAGACAGAAAATGCTTTCCCACCTATAGAGGTC
ACACTTGAGGTTCATGAGAATGTAATCTTTTTTGAGGATCCTGTGGTTGTAAGGTGGGATGCTGAAGGTAAACATTGGAGAACTGATGGCATCAGCAATGTATCCTACAAACCAAAAGAAAGACTTGT
AACATTCAGCCTGGACACCTTTGGCCCTGTTACCTTGATTCAAGATGCTCATATTAACATGCCGTACCAGTCATGGGAACTAAGACCACTTGATGTAAATAAAGTACTTTTAACTGTGACTACAGTAT
TTACTGAGATTCAAATACAAATTAAGGAAAACCTCTGCATGTTATCTTCAATCAAACTAAAAGACAAGAAACACATCTCTATTTTGGAAGGAACCTGGATGACTCCTATTCCTTTCATTATTGCTTTG
AAAGAAGCTGGACTGAATATCTTTCCTACTAGACACTCTCATTTTTATGTTATTATAAACAATAAGGTTCCTTTGGTAGAAGTGAAAGCTTATCGACAGATGGCCCTACTAAGTTCTGCTTTTGCATT
TGGTTGGAGCAAGTGGAACCTACTATGTAATTCTACAAAAGTCGTATTTAAGGTGAGGGAACACCTTACTGAAGCATGTACTGAGAATCCTAATTGGGCCCTTTTAATGTTTAGTGGTGACAGAGCAC
AAAGACTGAAGATCAAGGAAGAGAGTGAGGCATTTTCTGAAGCACTTAAAGAAGAAACTGAGTTTCATTCTACTTTATATCACATGGTGAAGGATTTTGCTTCTGAGGAAGCAATGGAGAAAGTCAGG
AGTTCCAACTGTCAGTTTGTCAACTCTGTGTGCCACATGCTGCTCTCTACCAGATTGCTCAGCTACTCCTAACCTCCACTTACAAACTGTATTGTAAGTATGAAGAACCAAGCATGGTGAAAGACAGG
TATTTCTGCAACACAATGTAATGAGTGAATGAATACATTTCAAATCAACTATTAAAAATTTTCTAATCTGCATTTTCTACTCAAGTTTTATTTTAAAAACAGTATTTTTTTTTCCTTTGAATACTTGG
CCTGTTAAGAATTTCAGCTTTCACTCTATGAAGATTTAAATGATTCTTTATTTCAATAAACTTTAACAAACAATA

hide sequence

RefSeq Acc Id:

NM_001204102 ⟹ NP_001191031

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	25,108,289 - 25,195,160 (-)	NCBI
GRCh37	12	25,261,223 - 25,348,096 (-)	NCBI
HuRef	12	25,031,916 - 25,118,815 (-)	RGD
CHM1_1	12	25,226,353 - 25,313,241 (-)	NCBI
T2T-CHM13v2.0	12	24,979,200 - 25,066,403 (-)	NCBI

Sequence:

show sequence

GTCGTCCGGGCAACCCGGGAGCGTTTGTCCACACAATTTCTGCTCCGACTCTGCGGACTACTGCAGTGGAGCTTGACTCTTAATGGGTCCCAAAGCAAAAAAGGAACACTGTCATCACAAACAGGCTT
CAGTGGCCAAAGATCTGGCAGTAAGAAAAAGAAAGTCACCAAAGCTGAACGATTGAAGCTGCTACAAGAGGAGGAGGAGAGACGACTGAAAGAGGAAGAGGAAGCCCGTTTGAAATATGAGAAAGAAG
AAATGGAAAGGCTTGAAATACAGCGAATTGAGAAAGAAAAATGGCATCGACTTGAAGCAAAAGATCTAGAAAGGAGAAATGAAGAACTTGAAGAACTTTATTTATTAGAGAGGTGTTTTCCTGAAGCA
GAGAAATTGAAACAGGAAACTAAATTGCTTTCTCAGTGGAAGCACTACATTCAATGTGATGGGAGTCCTGATCCTTCAGTAGCCCAAGAAATGAACACGTTTATTAGTTTGTGGAAAGAGAAAACAAA
TGAGACTTTTGAGGAAGTGATTGAGAAGAGTAAAGTAGTGCTAAATTTAATTGAGAAATTGAAATTTATTTTACTGGAAACTCCACCATGTGATTTGCAAGATAAAAATATAATACAGTACCAAGAAT
CAATACTACAACTGCAGGAGCTCCTTCATCTTAAATTCGGTGTAGCCACAGAAATACTTCTCAAACAAGCTAGTACTTTGGCAGATCTGGACAGTGGAAATATGGAAAAAGTCATTAAAGATGAAAAT
GTTACTCTGTATGTGTGGGCAAACCTCAAGAAGAATCCAAGGCACAGAAGTGTTAGATTCTCTGAAACACAAATTGGATTTGAGATTCCAAGGATATTAGCAACAAGTGACATTGCTGTACGACTCCT
GCATACCCACTATGATCATGTTTCTGCACTGCACCCTGTTTCAACACCATCAAAAGAATACACTTCTGCAGTAACTGAGCTTGTCAAAGATGATGTTAAGAATGTAGAAAAAGCAATCAGCAAGGAGG
TCGAAGAAGAGTCCAAACAACAAGAAAGAGGGTCTCACTTAATTCAGGAGGAAGAAATAAAAGTTGAGGAGGAACAAGGTGATATTGAAGTGAAAATGAGTTCTGCTGAGGAAGAATCTGAAGCCATA
AAATGTGAACGAGAGATGAAAGTATTAAGTGAAACTGTTTCAGCAGCACAGTTGTTGCTGGTAGAGAATTCTTCTGAAAAGCCAGATTTCTTTGAAGACAATGTGGTGGATTTATGCCAGTTCACAAC
TCTGGGTGGAGTATACCACTTGGATATTTTGGAGCTTCCTCCACAGTGTAAACCAGTGAAGGGATGGATGATTGTGGAAATACTCAAAGAAGGATTACAGAAATACACATATCCTCCGGAAACTACAG
AAGAGTTTGAGACAGAAAATGCTTTCCCACCTATAGAGGTCACACTTGAGGTTCATGAGAATGTAATCTTTTTTGAGGATCCTGTGGTTGTAAGGTGGGATGCTGAAGGTAAACATTGGAGAACTGAT
GGCATCAGCAATGTATCCTACAAACCAAAAGAAAGACTTGTAACATTCAGCCTGGACACCTTTGGCCCTGTTACCTTGATTCAAGATGCTCATATTAACATGCCGTACCAGTCATGGGAACTAAGACC
ACTTGATGTAAATAAAGTACTTTTAACTGTGACTACAGTATTTACTGAGATTCAAATACAAATTAAGGAAAACCTCTGCATGTTATCTTCAATCAAACTAAAAGACAAGAAACACATCTCTATTTTGG
AAGGAACCTGGATGACTCCTATTCCTTTCATTATTGCTTTGAAAGAAGCTGGACTGAATATCTTTCCTACTAGACACTCTCATTTTTATGTTATTATAAACAATAAGGTTCCTTTGGTAGAAGTGAAA
GCTTATCGACAGATGGCCCTACTAAGTTCTGCTTTTGCATTTGGTTGGAGCAAGTGGAACCTACTATGTAATTCTACAAAAGTCGTATTTAAGGTGAGGGAACACCTTACTGAAGCATGTACTGAGAA
TCCTAATTGGGCCCTTTTAATGTTTAGTGGTGACAGAGCACAAAGACTGAAGATCAAGGAAGAGAGTGAGGCATTTTCTGAAGCACTTAAAGAAGAAACTGAGTTTCATTCTACTTTATATCACATGG
TGAAGGATTTTGCTTCTGAGGAAGCAATGGAGAAAGTCAGGAGTTCCAACTGTCAGTTTGTCAACTCTGTGTGCCACATGCTGCTCTCTACCAGATTGCTCAGCTACTCCTAACCTCCACTTACAAAC
TGTATTGTAAGTATGAAGAACCAAGCATGGTGAAAGACAGGTATTTCTGCAACACAATGTAATGAGTGAATGAATACATTTCAAATCAACTATTAAAAATTTTCTAATCTGCATTTTCTACTCAAGTT
TTATTTTAAAAACAGTATTTTTTTTTCCTTTGAATACTTGGCCTGTTAAGAATTTCAGCTTTCACTCTATGAAGATTTAAATGATTCTTTATTTCAATAAACTTTAACAAACAATA

hide sequence

RefSeq Acc Id:

NM_001319977 ⟹ NP_001306906

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	25,108,289 - 25,195,160 (-)	NCBI
CHM1_1	12	25,226,353 - 25,313,241 (-)	NCBI
T2T-CHM13v2.0	12	24,979,200 - 25,066,403 (-)	NCBI

Sequence:

show sequence

GTCGTCCGGGCAACCCGGGAGCGTTTGTCCACACAATTTCTGCTCCGACTCTGCGGACTACTGCAGTGGAGCTTGACTCTTAATGTCTGGCAGTAAGAAAAAGAAAGTCACCAAAGCTGAACGATTGA
AGCTGCTACAAGAGGAGGAGGAGAGACGACTGAAAGAGGAAGGATCTAGAAAGGAGAAATGAAGAACTTGAAGAACTTTATTTATTAGAGAGGTGTTTTCCTGAAGCAGAGAAATTGAAACAGGAAAC
TAAATTGCTTTCTCAGTGGAAGCACTACATTCAATGTGATGGGAGTCCTGATCCTTCAGTAGCCCAAGAAATGAACACGTTTATTAGTTTGTGGAAAGAGAAAACAAATGAGACTTTTGAGGAAGTGA
TTGAGAAGAGTAAAGTAGTGCTAAATTTAATTGAGAAATTGAAATTTATTTTACTGGAAACTCCACCATGTGATTTGCAAGATAAAAATATAATACAGTACCAAGAATCAATACTACAACTGCAGGAG
CTCCTTCATCTTAAATTCGGTGTAGCCACAGAAATACTTCTCAAACAAGCTAGTACTTTGGCAGATCTGGACAGTGGAAATATGGAAAAAGTCATTAAAGATGAAAATGTTACTCTGTATGTGTGGGC
AAACCTCAAGAAGAATCCAAGGCACAGAAGTGTTAGATTCTCTGAAACACAAATTGGATTTGAGATTCCAAGGATATTAGCAACAAGTGACATTGCTGTACGACTCCTGCATACCCACTATGATCATG
TTTCTGCACTGCACCCTGTTTCAACACCATCAAAAGAATACACTTCTGCAGTAACTGAGCTTGTCAAAGATGATGTTAAGAATGTAGAAAAAGCAATCAGCAAGGAGGTCGAAGAAGAGTCCAAACAA
CAAGAAAGAGGGTCTCACTTAATTCAGGAGGAAGAAATAAAAGTTGAGGAGGAACAAGGTGATATTGAAGTGAAAATGAGTTCTGCTGAGGAAGAATCTGAAGCCATAAAATGTGAACGAGAGATGAA
AGTATTAAGTGAAACTGTTTCAGCAGCACAGTTGTTGCTGGTAGAGAATTCTTCTGAAAAGCCAGATTTCTTTGAAGACAATGTGGTGGATTTATGCCAGTTCACAACTCTGGGTGGAGTATACCACT
TGGATATTTTGGAGCTTCCTCCACAGTGTAAACCAGTGAAGGGATGGATGATTGTGGAAATACTCAAAGAAGGATTACAGAAATACACATATCCTCCGGAAACTACAGAAGAGTTTGAGACAGAAAAT
GCTTTCCCACCTATAGAGGTCACACTTGAGGTTCATGAGAATGTAATCTTTTTTGAGGATCCTGTGGTTGTAAGGTGGGATGCTGAAGGTAAACATTGGAGAACTGATGGCATCAGCAATGTATCCTA
CAAACCAAAAGAAAGACTTGTAACATTCAGCCTGGACACCTTTGGCCCTGTTACCTTGATTCAAGATGCTCATATTAACATGCCGTACCAGTCATGGGAACTAAGACCACTTGATGTAAATAAAGTAC
TTTTAACTGTGACTACAGTATTTACTGAGATTCAAATACAAATTAAGGAAAACCTCTGCATGTTATCTTCAATCAAACTAAAAGACAAGAAACACATCTCTATTTTGGAAGGAACCTGGATGACTCCT
ATTCCTTTCATTATTGCTTTGAAAGAAGCTGGACTGAATATCTTTCCTACTAGACACTCTCATTTTTATGTTATTATAAACAATAAGGTTCCTTTGGTAGAAGTGAAAGCTTATCGACAGATGGCCCT
ACTAAGTTCTGCTTTTGCATTTGGTTGGAGCAAGTGGAACCTACTATGTAATTCTACAAAAGTCGTATTTAAGTGGTGACAGAGCACAAAGACTGAAGATCAAGGAAGAGAGTGAGGCATTTTCTGAA
GCACTTAAAGAAGAAACTGAGTTTCATTCTACTTTATATCACATGGTGAAGGATTTTGCTTCTGAGGAAGCAATGGAGAAAGTCAGGAGTTCCAACTGTCAGTTTGTCAACTCTGTGTGCCACATGCT
GCTCTCTACCAGATTGCTCAGCTACTCCTAACCTCCACTTACAAACTGTATTGTAAGTATGAAGAACCAAGCATGGTGAAAGACAGGTATTTCTGCAACACAATGTAATGAGTGAATGAATACATTTC
AAATCAACTATTAAAAATTTTCTAATCTGCATTTTCTACTCAAGTTTTATTTTAAAAACAGTATTTTTTTTTCCTTTGAATACTTGGCCTGTTAAGAATTTCAGCTTTCACTCTATGAAGATTTAAAT
GATTCTTTATTTCAATAAACTTTAACAAACAATA

hide sequence

RefSeq Acc Id:

NM_001319978 ⟹ NP_001306907

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	25,108,289 - 25,195,160 (-)	NCBI
CHM1_1	12	25,226,353 - 25,313,241 (-)	NCBI
T2T-CHM13v2.0	12	24,979,200 - 25,066,403 (-)	NCBI

Sequence:

show sequence

GTCGTCCGGGCAACCCGGGAGCGTTTGTCCACACAATTTCTGCTCCGACTCTGCGGACTACTGC
AGTGGAGCTTGACTCTTAATGTCTGGCAGTAAGAAAAAGAAAGTCACCAAAGCTGAACGATTGAAGCTGCTACAAGAGGAGGAGGAGAGACGACTGAAAGAGGAAGTTACTGTCTTGAAGAAAGGAGA
ACTGACACTTTTCTCATATCTACCATGTAATAAAGACTGTGACTTCTATAAAAGATTCCACCACTACATCTTGAAAATATTAGGAGTAATTTTAAGGGCTTAAAAATACAGTGATCTATTCACTGAGA
AAAAAATTATTTTTGGTTCTTTAGAGGAAGCCCGTTTGAAATATGAGAAAGAAGAAATGGAAAGGCTTGAAATACAGCGAATTGAGAAAGAAAAATGGCATCGACTTGAAGCAAAAGATCTAGAAAGG
AGAAATGAAGAACTTGAAGAACTTTATTTATTAGAGAGGTGTTTTCCTGAAGCAGAGAAATTGAAACAGGAAACTAAATTGCTTTCTCAGTGGAAGCACTACATTCAATGTGATGGGAGTCCTGATCC
TTCAGTAGCCCAAGAAATGAACACGTTTATTAGTTTGTGGAAAGAGAAAACAAATGAGACTTTTGAGGAAGTGATTGAGAAGAGTAAAGTAGTGCTAAATTTAATTGAGAAATTGAAATTTATTTTAC
TGGAAACTCCACCATGTGATTTGCAAGATAAAAATATAATACAGTACCAAGAATCAATACTACAACTGCAGGAGCTCCTTCATCTTAAATTCGGTGTAGCCACAGAAATACTTCTCAAACAAGCTAGT
ACTTTGGCAGATCTGGACAGTGGAAATATGGAAAAAGTCATTAAAGATGAAAATGTTACTCTGTATGTGTGGGCAAACCTCAAGAAGAATCCAAGGCACAGAAGTGTTAGATTCTCTGAAACACAAAT
TGGATTTGAGATTCCAAGGATATTAGCAACAAGTGACATTGCTGTACGACTCCTGCATACCCACTATGATCATGTTTCTGCACTGCACCCTGTTTCAACACCATCAAAAGAATACACTTCTGCAGTAA
CTGAGCTTGTCAAAGATGATGTTAAGAATGTAGAAAAAGCAATCAGCAAGGAGGTCGAAGAAGAGTCCAAACAACAAGAAAGAGGGTCTCACTTAATTCAGGAGGAAGAAATAAAAGTTGAGGAGGAA
CAAGGTGATATTGAAGTGAAAATGAGTTCTGCTGAGGAAGAATCTGAAGCCATAAAATGTGAACGAGAGATGAAAGTATTAAGTGAAACTGTTTCAGCAGCACAGTTGTTGCTGGTAGAGAATTCTTC
TGAAAAGCCAGATTTCTTTGAAGACAATGTGGTGGATTTATGCCAGTTCACAACTCTGGGTGGAGTATACCACTTGGATATTTTGGAGCTTCCTCCACAGTGTAAACCAGTGAAGGGATGGATGATTG
TGGAAATACTCAAAGAAGGATTACAGAAATACACATATCCTCCGGAAACTACAGAAGAGTTTGAGACAGAAAATGCTTTCCCACCTATAGAGGTCACACTTGAGGTTCATGAGAATGTAATCTTTTTT
GAGGATCCTGTGGTTGTAAGGTGGGATGCTGAAGGTAAACATTGGAGAACTGATGGCATCAGCAATGTATCCTACAAACCAAAAGAAAGACTTGTAACATTCAGCCTGGACACCTTTGGCCCTGTTAC
CTTGATTCAAGATGCTCATATTAACATGCCGTACCAGTCATGGGAACTAAGACCACTTGATGTAAATAAAGTACTTTTAACTGTGACTACAGTATTTACTGAGATTCAAATACAAATTAAGGAAAACC
TCTGCATGTTATCTTCAATCAAACTAAAAGACAAGAAACACATCTCTATTTTGGAAGGAACCTGGATGACTCCTATTCCTTTCATTATTGCTTTGAAAGAAGCTGGACTGAATATCTTTCCTACTAGA
CACTCTCATTTTTATGTTATTATAAACAATAAGGTTCCTTTGGTAGAAGTGAAAGCTTATCGACAGATGGCCCTACTAAGTTCTGCTTTTGCATTTGGTTGGAGCAAGTGGAACCTACTATGTAATTC
TACAAAAGTCGTATTTAAGGTGAGGGAACACCTTACTGAAGCATGTACTGAGAATCCTAATTGGGCCCTTTTAATGTTTAGTGGTGACAGAGCACAAAGACTGAAGATCAAGGAAGAGAGTGAGGCAT
TTTCTGAAGCACTTAAAGAAGAAACTGAGTTTCATTCTACTTTATATCACATGGTGAAGGATTTTGCTTCTGAGGAAGCAATGGAGAAAGTCAGGAGTTCCAACTGTCAGTTTGTCAACTCTGTGTGC
CACATGCTGCTCTCTACCAGATTGCTCAGCTACTCCTAACCTCCACTTACAAACTGTATTGTAAGTATGAAGAACCAAGCATGGTGAAAGACAGGTATTTCTGCAACACAATGTAATGAGTGAATGAA
TACATTTCAAATCAACTATTAAAAATTTTCTAATCTGCATTTTCTACTCAAGTTTTATTTTAAAAACAGTATTTTTTTTTCCTTTGAATACTTGGCCTGTTAAGAATTTCAGCTTTCACTCTATGAAG
ATTTAAATGATTCTTTATTTCAATAAACTTTAACAAACAATA

hide sequence

RefSeq Acc Id:

NM_001352061 ⟹ NP_001338990

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	25,108,289 - 25,195,160 (-)	NCBI
T2T-CHM13v2.0	12	24,979,200 - 25,066,403 (-)	NCBI

Sequence:

show sequence

GTCGTCCGGGCAACCCGGGAGCGTTTGTCCACACAATTTCTGCTCCGACTCTGCGGACTACTGC
AGTGGAGCTTGACTCTTAATGTTACTGTCTTGAAGAAAGGAGAACTGACACTTTTCTCATATCTACCATGTAATAAAGACTGTGACTTCTATAAAAGATTCCACCACTACATCTTGAAAATATTAGGA
GTAATTTTAAGGGCTTAAAAATACAGTGATCTATTCACTGAGAAAAAAATTATTTTTGGTTCTTTAGAGGAAGCCCGTTTGAAATATGAGAAAGAAGAAATGGAAAGGCTTGAAATACAGCGAATTGA
GAAAGAAAAATGGCATCGACTTGAAGCAAAAGATCTAGAAAGGAGAAATGAAGAACTTGAAGAACTTTATTTATTAGAGAGGTGTTTTCCTGAAGCAGAGAAATTGAAACAGGAAACTAAATTGCTTT
CTCAGTGGAAGCACTACATTCAATGTGATGGGAGTCCTGATCCTTCAGTAGCCCAAGAAATGAACACGTTTATTAGTTTGTGGAAAGAGAAAACAAATGAGACTTTTGAGGAAGTGATTGAGAAGAGT
AAAGTAGTGCTAAATTTAATTGAGAAATTGAAATTTATTTTACTGGAAACTCCACCATGTGATTTGCAAGATAAAAATATAATACAGTACCAAGAATCAATACTACAACTGCAGGAGCTCCTTCATCT
TAAATTCGGTGTAGCCACAGAAATACTTCTCAAACAAGCTAGTACTTTGGCAGATCTGGACAGTGGAAATATGGAAAAAGTCATTAAAGATGAAAATGTTACTCTGTATGTGTGGGCAAACCTCAAGA
AGAATCCAAGGCACAGAAGTGTTAGATTCTCTGAAACACAAATTGGATTTGAGATTCCAAGGATATTAGCAACAAGTGACATTGCTGTACGACTCCTGCATACCCACTATGATCATGTTTCTGCACTG
CACCCTGTTTCAACACCATCAAAAGAATACACTTCTGCAGTAACTGAGCTTGTCAAAGATGATGTTAAGAATGTAGAAAAAGCAATCAGCAAGGAGGTCGAAGAAGAGTCCAAACAACAAGAAAGAGG
GTCTCACTTAATTCAGGAGGAAGAAATAAAAGTTGAGGAGGAACAAGGTGATATTGAAGTGAAAATGAGTTCTGCTGAGGAAGAATCTGAAGCCATAAAATGTGAACGAGAGATGAAAGTATTAAGTG
AAACTGTTTCAGCAGCACAGTTGTTGCTGGTAGAGAATTCTTCTGAAAAGCCAGATTTCTTTGAAGACAATGTGGTGGATTTATGCCAGTTCACAACTCTGGGTGGAGTATACCACTTGGATATTTTG
GAGCTTCCTCCACAGTGTAAACCAGTGAAGGGATGGATGATTGTGGAAATACTCAAAGAAGGATTACAGAAATACACATATCCTCCGGAAACTACAGAAGAGTTTGAGACAGAAAATGCTTTCCCACC
TATAGAGGTCACACTTGAGGTTCATGAGAATGTAATCTTTTTTGAGGATCCTGTGGTTGTAAGGTGGGATGCTGAAGGTAAACATTGGAGAACTGATGGCATCAGCAATGTATCCTACAAACCAAAAG
AAAGACTTGTAACATTCAGCCTGGACACCTTTGGCCCTGTTACCTTGATTCAAGATGCTCATATTAACATGCCGTACCAGTCATGGGAACTAAGACCACTTGATGTAAATAAAGTACTTTTAACTGTG
ACTACAGTATTTACTGAGATTCAAATACAAATTAAGGAAAACCTCTGCATGTTATCTTCAATCAAACTAAAAGACAAGAAACACATCTCTATTTTGGAAGGAACCTGGATGACTCCTATTCCTTTCAT
TATTGCTTTGAAAGAAGCTGGACTGAATATCTTTCCTACTAGACACTCTCATTTTTATGTTATTATAAACAATAAGGTTCCTTTGGTAGAAGTGAAAGCTTATCGACAGATGGCCCTACTAAGTTCTG
CTTTTGCATTTGGTTGGAGCAAGTGGAACCTACTATGTAATTCTACAAAAGTCGTATTTAAGGTGAGGGAACACCTTACTGAAGCATGTACTGAGAATCCTAATTGGGCCCTTTTAATGTTTAGTGGT
GACAGAGCACAAAGACTGAAGATCAAGGAAGAGAGTGAGGCATTTTCTGAAGCACTTAAAGAAGAAACTGAGTTTCATTCTACTTTATATCACATGGTGAAGGATTTTGCTTCTGAGGAAGCAATGGA
GAAAGTCAGGAGTTCCAACTGTCAGTTTGTCAACTCTGTGTGCCACATGCTGCTCTCTACCAGATTGCTCAGCTACTCCTAACCTCCACTTACAAACTGTATTGTAAGTATGAAGAACCAAGCATGGT
GAAAGACAGGTATTTCTGCAACACAATGTAATGAGTGAATGAATACATTTCAAATCAACTATTAAAAATTTTCTAATCTGCATTTTCTACTCAAGTTTTATTTTAAAAACAGTATTTTTTTTTCCTTT
GAATACTTGGCCTGTTAAGAATTTCAGCTTTCACTCTATGAAGATTTAAATGATTCTTTATTTCAATAAACTTTAACAAACAATA

hide sequence

RefSeq Acc Id:

NM_001352062 ⟹ NP_001338991

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	25,108,289 - 25,195,160 (-)	NCBI
T2T-CHM13v2.0	12	24,979,200 - 25,066,403 (-)	NCBI

Sequence:

show sequence

GTCGTCCGGGCAACCCGGGAGCGTTTGTCCACACAATTTCTGCTCCGACTCTGCGGACTACTGCAGTGGAGCTTGACTCTTAATGTCTGGCAGTAAGAAAAAGAAAGTCACCAAAGCTGAACGATTGA
AGCTGCTACAAGAGGAGGAGGAGAGACGACTGAAAGAGGAAGAGGAAGCCCGTTTGAAATATGAGAAAGAAGAAATGGAAAGGCTTGAAATACAGCGAATTGAGAAAGAAAAATGGCATCGACTTGAA
GCAAAAGATCTAGAAAGGAGAAATGAAGAACTTGAAGAACTTTATTTATTAGAGAGGTGTTTTCCTGAAGCAGAGAAATTGAAACAGGAAACTAAATTGCTTTCTCAGTGGAAGCACTACATTCAATG
TGATGGGAGTCCTGATCCTTCAGTAGCCCAAGAAATGAACACGTTTATTAGTTTGTGGAAAGAGAAAACAAATGAGACTTTTGAGGAAGTGATTGAGAAGAGTAAAGTAGTGCTAAATTTAATTGAGA
AATTGAAATTTATTTTACTGGAAACTCCACCATGTGATTTGCAAGATAAAAATATAATACAGTACCAAGAATCAATACTACAACTGCAGGAGCTCCTTCATCTTAAATTCGGTGTAGCCACAGAAATA
CTTCTCAAACAAGCTAGTACTTTGGCAGATCTGGACAGTGGAAATATGGAAAAAGTCATTAAAGATGAAAATGTTACTCTGTATGTGTGGGCAAACCTCAAGAAGAATCCAAGGCACAGAAGTGTTAG
ATTCTCTGAAACACAAATTGGATTTGAGATTCCAAGGATATTAGCAACAAGTGACATTGCTGTACGACTCCTGCATACCCACTATGATCATGTTTCTGCACTGCACCCTGTTTCAACACCATCAAAAG
AATACACTTCTGCAGTAACTGAGCTTGTCAAAGATGATGTTAAGAATGTAGAAAAAGCAATCAGCAAGGAGGTCGAAGAAGAGTCCAAACAACAAGAAAGAGGGTCTCACTTAATTCAGGAGGAAGAA
ATAAAAGTTGAGGAGGAACAAGGTGATATTGAAGTGAAAATGAGTTCTGCTGAGGAAGAATCTGAAGCCATAAAATGTGAACGAGAGATGAAAGTATTAAGTGAAACTGTTTCAGCAGCACAGTTGTT
GCTGGTAGAGAATTCTTCTGAAAAGCCAGATTTCTTTGAAGACAATGTGGTGGATTTATGCCAGTTCACAACTCTGGGTGGAGTATACCACTTGGATATTTTGGAGCTTCCTCCACAGTGTAAACCAG
TGAAGGGATGGATGATTGTGGAAATACTCAAAGAAGGATTACAGAAATACACATATCCTCCGGAAACTACAGAAGAGTTTGAGACAGAAAATGCTTTCCCACCTATAGAGGTCACACTTGAGGTTCAT
GAGAATGTAATCTTTTTTGAGGATCCTGTGGTTGTAAGGTGGGATGCTGAAGGTAAACATTGGAGAACTGATGGCATCAGCAATGTATCCTACAAACCAAAAGAAAGACTTGTAACATTCAGCCTGGA
CACCTTTGGCCCTGTTACCTTGATTCAAGATGCTCATATTAACATGCCGTACCAGTCATGGGAACTAAGACCACTTGATGTAAATAAAGTACTTTTAACTGTGACTACAGTATTTACTGAGATTCAAA
TACAAATTAAGGAAAACCTCTGCATGTTATCTTCAATCAAACTAAAAGACAAGAAACACATCTCTATTTTGGAAGGAACCTGGATGACTCCTATTCCTTTCATTATTGCTTTGAAAGAAGCTGGACTG
AATATCTTTCCTACTAGACACTCTCATTTTTATGTTATTATAAACAATAAGGTTCCTTTGGTAGAAGTGAAAGCTTATCGACAGATGGCCCTACTAAGTTCTGCTTTTGCATTTGGTTGGAGCAAGTG
GAACCTACTATGTAATTCTACAAAAGTCGTATTTAAGTGGTGACAGAGCACAAAGACTGAAGATCAAGGAAGAGAGTGAGGCATTTTCTGAAGCACTTAAAGAAGAAACTGAGTTTCATTCTACTTTA
TATCACATGGTGAAGGATTTTGCTTCTGAGGAAGCAATGGAGAAAGTCAGGAGTTCCAACTGTCAGTTTGTCAACTCTGTGTGCCACATGCTGCTCTCTACCAGATTGCTCAGCTACTCCTAACCTCC
ACTTACAAACTGTATTGTAAGTATGAAGAACCAAGCATGGTGAAAGACAGGTATTTCTGCAACACAATGTAATGAGTGAATGAATACATTTCAAATCAACTATTAAAAATTTTCTAATCTGCATTTTC
TACTCAAGTTTTATTTTAAAAACAGTATTTTTTTTTCCTTTGAATACTTGGCCTGTTAAGAATTTCAGCTTTCACTCTATGAAGATTTAAATGATTCTTTATTTCAATAAACTTTAACAAACAATA

hide sequence

RefSeq Acc Id:

NM_001352063 ⟹ NP_001338992

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	25,108,289 - 25,195,160 (-)	NCBI
T2T-CHM13v2.0	12	24,979,200 - 25,066,403 (-)	NCBI

Sequence:

show sequence

GTCGTCCGGGCAACCCGGGAGCGTTTGTCCACACAATTTCTGCTCCGACTCTGCGGACTACTGCAGTGGAGCTTGACTCTTAATGGGTCCCAAAGCAAAAAAGTCTGGCAGTAAGAAAAAGAAAGTCA
CCAAAGCTGAACGATTGAAGCTGCTACAAGAGGAGGAGGAGAGACGACTGAAAGAGGAAGAGGAAGCCCGTTTGAAATATGAGAAAGAAGAAATGGAAAGGCTTGAAATACAGCGAATTGAGAAAGAA
AAATGGCATCGACTTGAAGCAAAAGATCTAGAAAGGAGAAATGAAGAACTTGAAGAACTTTATTTATTAGAGAGGTGTTTTCCTGAAGCAGAGAAATTGAAACAGGAAACTAAATTGCTTTCTCAGTG
GAAGCACTACATTCAATGTGATGGGAGTCCTGATCCTTCAGTAGCCCAAGAAATGAACACGTTTATTAGTTTGTGGAAAGAGAAAACAAATGAGACTTTTGAGGAAGTGATTGAGAAGAGTAAAGTAG
TGCTAAATTTAATTGAGAAATTGAAATTTATTTTACTGGAAACTCCACCATGTGATTTGCAAGATAAAAATATAATACAGTACCAAGAATCAATACTACAACTGCAGGAGCTCCTTCATCTTAAATTC
GGTGTAGCCACAGAAATACTTCTCAAACAAGCTAGTACTTTGGCAGATCTGGACAGTGGAAATATGGAAAAAGTCATTAAAGATGAAAATGTTACTCTGTATGTGTGGGCAAACCTCAAGAAGAATCC
AAGGCACAGAAGTGTTAGATTCTCTGAAACACAAATTGGATTTGAGATTCCAAGGATATTAGCAACAAGTGACATTGCTGTACGACTCCTGCATACCCACTATGATCATGTTTCTGCACTGCACCCTG
TTTCAACACCATCAAAAGAATACACTTCTGCAGTAACTGAGCTTGTCAAAGATGATGTTAAGAATGTAGAAAAAGCAATCAGCAAGGAGGTCGAAGAAGAGTCCAAACAACAAGAAAGAGGGTCTCAC
TTAATTCAGGAGGAAGAAATAAAAGTTGAGGAGGAACAAGGTGATATTGAAGTGAAAATGAGTTCTGCTGAGGAAGAATCTGAAGCCATAAAATGTGAACGAGAGATGAAAGTATTAAGTGAAACTGT
TTCAGCAGGTAAACATTGGAGAACTGATGGCATCAGCAATGTATCCTACAAACCAAAAGAAAGACTTGTAACATTCAGCCTGGACACCTTTGGCCCTGTTACCTTGATTCAAGATGCTCATATTAACA
TGCCGTACCAGTCATGGGAACTAAGACCACTTGATGTAAATAAAGTACTTTTAACTGTGACTACAGTATTTACTGAGATTCAAATACAAATTAAGGAAAACCTCTGCATGTTATCTTCAATCAAACTA
AAAGACAAGAAACACATCTCTATTTTGGAAGGAACCTGGATGACTCCTATTCCTTTCATTATTGCTTTGAAAGAAGCTGGACTGAATATCTTTCCTACTAGACACTCTCATTTTTATGTTATTATAAA
CAATAAGGTTCCTTTGGTAGAAGTGAAAGCTTATCGACAGATGGCCCTACTAAGTTCTGCTTTTGCATTTGGTTGGAGCAAGTGGAACCTACTATGTAATTCTACAAAAGTCGTATTTAAGGTGAGGG
AACACCTTACTGAAGCATGTACTGAGAATCCTAATTGGGCCCTTTTAATGTTTAGTGGTGACAGAGCACAAAGACTGAAGATCAAGGAAGAGAGTGAGGCATTTTCTGAAGCACTTAAAGAAGAAACT
GAGTTTCATTCTACTTTATATCACATGGTGAAGGATTTTGCTTCTGAGGAAGCAATGGAGAAAGTCAGGAGTTCCAACTGTCAGTTTGTCAACTCTGTGTGCCACATGCTGCTCTCTACCAGATTGCT
CAGCTACTCCTAACCTCCACTTACAAACTGTATTGTAAGTATGAAGAACCAAGCATGGTGAAAGACAGGTATTTCTGCAACACAATGTAATGAGTGAATGAATACATTTCAAATCAACTATTAAAAAT
TTTCTAATCTGCATTTTCTACTCAAGTTTTATTTTAAAAACAGTATTTTTTTTTCCTTTGAATACTTGGCCTGTTAAGAATTTCAGCTTTCACTCTATGAAGATTTAAATGATTCTTTATTTCAATAA
ACTTTAACAAACAATA

hide sequence

RefSeq Acc Id:

NM_001352064 ⟹ NP_001338993

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	25,108,289 - 25,195,160 (-)	NCBI
T2T-CHM13v2.0	12	24,979,200 - 25,066,403 (-)	NCBI

Sequence:

show sequence

GTCGTCCGGGCAACCCGGGAGCGTTTGTCCACACAATTTCTGCTCCGACTCTGCGGACTACTGC
AGTGGAGCTTGACTCTTAATGTCTGGCAGTAAGAAAAAGAAAGTCACCAAAGCTGAACGATTGAAGCTGCTACAAGAGGAGGAGGAGAGACGACTGAAAGAGGAAGAGGAAGCCCGTTTGAAATATGA
GAAAGAAGAAATGGAAAGGCTTGAAATACAGCGAATTGAGAAAGAAAAATGGCATCGACTTGAAGCAAAAGATCTAGAAAGGAGAAATGAAGAACTTGAAGAACTTTATTTATTAGAGAGGTGTTTTC
CTGAAGCAGAGAAATTGAAACAGGAAACTAAATTGCTTTCTCAGTGGAAGCACTACATTCAATGTGATGGGAGTCCTGATCCTTCAGTAGCCCAAGAAATGAACACGTTTATTAGTTTGTGGAAAGAG
AAAACAAATGAGACTTTTGAGGAAGTGATTGAGAAGAGTAAAGTAGTGCTAAATTTAATTGAGAAATTGAAATTTATTTTACTGGAAACTCCACCATGTGATTTGCAAGATAAAAATATAATACAGTA
CCAAGAATCAATACTACAACTGCAGGAGCTCCTTCATCTTAAATTCGGTGTAGCCACAGAAATACTTCTCAAACAAGCTAGTACTTTGGCAGATCTGGACAGTGGAAATATGGAAAAAGTCATTAAAG
ATGAAAATGTTACTCTGTATGTGTGGGCAAACCTCAAGAAGAATCCAAGGCACAGAAGTGTTAGATTCTCTGAAACACAAATTGGATTTGAGATTCCAAGGATATTAGCAACAAGTGACATTGCTGTA
CGACTCCTGCATACCCACTATGATCATGTTTCTGCACTGCACCCTGTTTCAACACCATCAAAAGAATACACTTCTGCAGTAACTGAGCTTGTCAAAGATGATGTTAAGAATGTAGAAAAAGCAATCAG
CAAGGAGGTCGAAGAAGAGTCCAAACAACAAGAAAGAGGGTCTCACTTAATTCAGGAGGAAGAAATAAAAGTTGAGGAGGAACAAGGTGATATTGAAGTGAAAATGAGTTCTGCTGAGGAAGAATCTG
AAGCCATAAAATGTGAACGAGAGATGAAAGTATTAAGTGAAACTGTTTCAGCAGGTAAACATTGGAGAACTGATGGCATCAGCAATGTATCCTACAAACCAAAAGAAAGACTTGTAACATTCAGCCTG
GACACCTTTGGCCCTGTTACCTTGATTCAAGATGCTCATATTAACATGCCGTACCAGTCATGGGAACTAAGACCACTTGATGTAAATAAAGTACTTTTAACTGTGACTACAGTATTTACTGAGATTCA
AATACAAATTAAGGAAAACCTCTGCATGTTATCTTCAATCAAACTAAAAGACAAGAAACACATCTCTATTTTGGAAGGAACCTGGATGACTCCTATTCCTTTCATTATTGCTTTGAAAGAAGCTGGAC
TGAATATCTTTCCTACTAGACACTCTCATTTTTATGTTATTATAAACAATAAGGTTCCTTTGGTAGAAGTGAAAGCTTATCGACAGATGGCCCTACTAAGTTCTGCTTTTGCATTTGGTTGGAGCAAG
TGGAACCTACTATGTAATTCTACAAAAGTCGTATTTAAGGTGAGGGAACACCTTACTGAAGCATGTACTGAGAATCCTAATTGGGCCCTTTTAATGTTTAGTGGTGACAGAGCACAAAGACTGAAGAT
CAAGGAAGAGAGTGAGGCATTTTCTGAAGCACTTAAAGAAGAAACTGAGTTTCATTCTACTTTATATCACATGGTGAAGGATTTTGCTTCTGAGGAAGCAATGGAGAAAGTCAGGAGTTCCAACTGTC
AGTTTGTCAACTCTGTGTGCCACATGCTGCTCTCTACCAGATTGCTCAGCTACTCCTAACCTCCACTTACAAACTGTATTGTAAGTATGAAGAACCAAGCATGGTGAAAGACAGGTATTTCTGCAACA
CAATGTAATGAGTGAATGAATACATTTCAAATCAACTATTAAAAATTTTCTAATCTGCATTTTCTACTCAAGTTTTATTTTAAAAACAGTATTTTTTTTTCCTTTGAATACTTGGCCTGTTAAGAATT
TCAGCTTTCACTCTATGAAGATTTAAATGATTCTTTATTTCAATAAACTTTAACAAACAATA

hide sequence

RefSeq Acc Id:

NM_001352065 ⟹ NP_001338994

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	25,108,289 - 25,195,160 (-)	NCBI
T2T-CHM13v2.0	12	24,979,200 - 25,066,403 (-)	NCBI

Sequence:

show sequence

GTCGTCCGGGCAACCCGGGAGCGTTTGTCCACACAATTTCTGCTCCGACTCTGCGGACTACTGC
AGTGGAGCTTGACTCTTAATGTCTGGCAGTAAGAAAAAGAAAGTCACCAAAGCTGAACGATTGAAGCTGCTACAAGAGGAGGAGGAGAGACGACTGAAAGAGGAAGGATCTAGAAAGGAGAAATGAAG
AACTTGAAGAACTTTATTTATTAGAGAGGTGTTTTCCTGAAGCAGAGAAATTGAAACAGGAAACTAAATTGCTTTCTCAGTGGAAGCACTACATTCAATGTGATGGGAGTCCTGATCCTTCAGTAGCC
CAAGAAATGAACACGTTTATTAGTTTGTGGAAAGAGAAAACAAATGAGACTTTTGAGGAAGTGATTGAGAAGAGTAAAGTAGTGCTAAATTTAATTGAGAAATTGAAATTTATTTTACTGGAAACTCC
ACCATGTGATTTGCAAGATAAAAATATAATACAGTACCAAGAATCAATACTACAACTGCAGGAGCTCCTTCATCTTAAATTCGGTGTAGCCACAGAAATACTTCTCAAACAAGCTAGTACTTTGGCAG
ATCTGGACAGTGGAAATATGGAAAAAGTCATTAAAGATGAAAATGTTACTCTGTATGTGTGGGCAAACCTCAAGAAGAATCCAAGGCACAGAAGTGTTAGATTCTCTGAAACACAAATTGGATTTGAG
ATTCCAAGGATATTAGCAACAAGTGACATTGCTGTACGACTCCTGCATACCCACTATGATCATGTTTCTGCACTGCACCCTGTTTCAACACCATCAAAAGAATACACTTCTGCAGTAACTGAGCTTGT
CAAAGATGATGTTAAGAATGTAGAAAAAGCAATCAGCAAGGAGGTCGAAGAAGAGTCCAAACAACAAGAAAGAGGGTCTCACTTAATTCAGGAGGAAGAAATAAAAGTTGAGGAGGAACAAGGTGATA
TTGAAGTGAAAATGAGTTCTGCTGAGGAAGAATCTGAAGCCATAAAATGTGAACGAGAGATGAAAGTATTAAGTGAAACTGTTTCAGCAGCACAGTTGTTGCTGGTAGAGAATTCTTCTGAAAAGCCA
GATTTCTTTGAAGACAATGTGGTGGATTTATGCCAGTTCACAACTCTGGGTGGAGTATACCACTTGGATATTTTGGAGCTTCCTCCACAGTGTAAACCAGTGAAGGGATGGATGATTGTGGAAATACT
CAAAGAAGGATTACAGAAATACACATATCCTCCGGAAACTACAGAAGAGTTTGAGACAGAAAATGCTTTCCCACCTATAGAGGTCACACTTGAGGTTCATGAGAATGTAATCTTTTTTGAGGATCCTG
TGGTTGTAAGGTGGGATGCTGAAGGTAAACATTGGAGAACTGATGGCATCAGCAATGTATCCTACAAACCAAAAGAAAGACTTGTAACATTCAGCCTGGACACCTTTGGCCCTGTTACCTTGATTCAA
GATGCTCATATTAACATGCCGTACCAGTCATGGGAACTAAGACCACTTGATGTAAATAAAGTACTTTTAACTGTGACTACAGTATTTACTGAGATTCAAATACAAATTAAGGAAAACCTCTGCATGTT
ATCTTCAATCAAACTAAAAGACAAGAAACACATCTCTATTTTGGAAGGAACCTGGATGACTCCTATTCCTTTCATTATTGCTTTGAAAGAAGCTGGACTGAATATCTTTCCTACTAGACACTCTCATT
TTTATGTTATTATAAACAATAAGGTTCCTTTGGTAGAAGTGAAAGCTTATCGACAGATGGCCCTACTAAGTTCTGCTTTTGCATTTGGTTGGAGCAAGTGGAACCTACTATGTAATTCTACAAAAGTC
GTATTTAAGGTGAGGGAACACCTTACTGAAGCATGTACTGAGAATCCTAATTGGGCCCTTTTAATGTTTAGTGGTGACAGAGCACAAAGACTGAAGATCAAGGAAGAGAGTGAGGCATTTTCTGAAGC
ACTTAAAGAAGAAACTGAGTTTCATTCTACTTTATATCACATGGTGAAGGATTTTGCTTCTGAGGAAGCAATGGAGAAAGTCAGGAGTTCCAACTGTCAGTTTGTCAACTCTGTGTGCCACATGCTGC
TCTCTACCAGATTGCTCAGCTACTCCTAACCTCCACTTACAAACTGTATTGTAAGTATGAAGAACCAAGCATGGTGAAAGACAGGTATTTCTGCAACACAATGTAATGAGTGAATGAATACATTTCAA
ATCAACTATTAAAAATTTTCTAATCTGCATTTTCTACTCAAGTTTTATTTTAAAAACAGTATTTTTTTTTCCTTTGAATACTTGGCCTGTTAAGAATTTCAGCTTTCACTCTATGAAGATTTAAATGA
TTCTTTATTTCAATAAACTTTAACAAACAATA

hide sequence

RefSeq Acc Id:

NM_001352066 ⟹ NP_001338995

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	25,108,289 - 25,195,160 (-)	NCBI
T2T-CHM13v2.0	12	24,979,200 - 25,066,403 (-)	NCBI

Sequence:

show sequence

GTCGTCCGGGCAACCCGGGAGCGTTTGTCCACACAATTTCTGCTCCGACTCTGCGGACTACTGC
AGTGGAGCTTGACTCTTAATGGTGAGCAAGGCAAATGAGGCAGACAGGTGGAGGGGCGACCACTGATTCTGCTTCACCAGTGTTAAATAATGTAATCAAGAGCCAGTCATATTTTACAGCGAAGCGGG
TCGGTTTGGGAAATAACTCATACCTTGGGGTGGGTCGGCCCTCTTCTCAGCAATGGCTTTCCTTACCTGGACCAGGCGGACAGGGTCCCAAAGCAAAAAAGTCTGGCAGTAAGAAAAAGAAAGTCACC
AAAGCTGAACGATTGAAGCTGCTACAAGAGGAGGAGGAGAGACGACTGAAAGAGGAAGTTACTGTCTTGAAGAAAGGAGAACTGACACTTTTCTCATATCTACCATGTAATAAAGACTGTGACTTCTA
TAAAAGATTCCACCACTACATCTTGAAAATATTAGGAGTAATTTTAAGGGCTTAAAAATACAGTGATCTATTCACTGAGAAAAAAATTATTTTTGGTTCTTTAGAGGAAGCCCGTTTGAAATATGAGA
AAGAAGAAATGGAAAGGCTTGAAATACAGCGAATTGAGAAAGAAAAATGGCATCGACTTGAAGCAAAAGATCTAGAAAGGAGAAATGAAGAACTTGAAGAACTTTATTTATTAGAGAGGTGTTTTCCT
GAAGCAGAGAAATTGAAACAGGAAACTAAATTGCTTTCTCAGTGGAAGCACTACATTCAATGTGATGGGAGTCCTGATCCTTCAGTAGCCCAAGAAATGAACACGTTTATTAGTTTGTGGAAAGAGAA
AACAAATGAGACTTTTGAGGAAGTGATTGAGAAGAGTAAAGTAGTGCTAAATTTAATTGAGAAATTGAAATTTATTTTACTGGAAACTCCACCATGTGATTTGCAAGATAAAAATATAATACAGTACC
AAGAATCAATACTACAACTGCAGGAGCTCCTTCATCTTAAATTCGGTGTAGCCACAGAAATACTTCTCAAACAAGCTAGTACTTTGGCAGATCTGGACAGTGGAAATATGGAAAAAGTCATTAAAGAT
GAAAATGTTACTCTGTATGTGTGGGCAAACCTCAAGAAGAATCCAAGGCACAGAAGTGTTAGATTCTCTGAAACACAAATTGGATTTGAGATTCCAAGGATATTAGCAACAAGTGACATTGCTGTACG
ACTCCTGCATACCCACTATGATCATGTTTCTGCACTGCACCCTGTTTCAACACCATCAAAAGAATACACTTCTGCAGTAACTGAGCTTGTCAAAGATGATGTTAAGAATGTAGAAAAAGCAATCAGCA
AGGAGGTCGAAGAAGAGTCCAAACAACAAGAAAGAGGGTCTCACTTAATTCAGGAGGAAGAAATAAAAGTTGAGGAGGAACAAGGTGATATTGAAGTGAAAATGAGTTCTGCTGAGGAAGAATCTGAA
GCCATAAAATGTGAACGAGAGATGAAAGTATTAAGTGAAACTGTTTCAGCAGGTAAACATTGGAGAACTGATGGCATCAGCAATGTATCCTACAAACCAAAAGAAAGACTTGTAACATTCAGCCTGGA
CACCTTTGGCCCTGTTACCTTGATTCAAGATGCTCATATTAACATGCCGTACCAGTCATGGGAACTAAGACCACTTGATGTAAATAAAGTACTTTTAACTGTGACTACAGTATTTACTGAGATTCAAA
TACAAATTAAGGAAAACCTCTGCATGTTATCTTCAATCAAACTAAAAGACAAGAAACACATCTCTATTTTGGAAGGAACCTGGATGACTCCTATTCCTTTCATTATTGCTTTGAAAGAAGCTGGACTG
AATATCTTTCCTACTAGACACTCTCATTTTTATGTTATTATAAACAATAAGGTTCCTTTGGTAGAAGTGAAAGCTTATCGACAGATGGCCCTACTAAGTTCTGCTTTTGCATTTGGTTGGAGCAAGTG
GAACCTACTATGTAATTCTACAAAAGTCGTATTTAAGGTGAGGGAACACCTTACTGAAGCATGTACTGAGAATCCTAATTGGGCCCTTTTAATGTTTAGTGGTGACAGAGCACAAAGACTGAAGATCA
AGGAAGAGAGTGAGGCATTTTCTGAAGCACTTAAAGAAGAAACTGAGTTTCATTCTACTTTATATCACATGGTGAAGGATTTTGCTTCTGAGGAAGCAATGGAGAAAGTCAGGAGTTCCAACTGTCAG
TTTGTCAACTCTGTGTGCCACATGCTGCTCTCTACCAGATTGCTCAGCTACTCCTAACCTCCACTTACAAACTGTATTGTAAGTATGAAGAACCAAGCATGGTGAAAGACAGGTATTTCTGCAACACA
ATGTAATGAGTGAATGAATACATTTCAAATCAACTATTAAAAATTTTCTAATCTGCATTTTCTACTCAAGTTTTATTTTAAAAACAGTATTTTTTTTTCCTTTGAATACTTGGCCTGTTAAGAATTTC
AGCTTTCACTCTATGAAGATTTAAATGATTCTTTATTTCAATAAACTTTAACAAACAATA

hide sequence

RefSeq Acc Id:

NM_001352067 ⟹ NP_001338996

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	25,108,289 - 25,195,160 (-)	NCBI
T2T-CHM13v2.0	12	24,979,200 - 25,066,403 (-)	NCBI

Sequence:

show sequence

GTCGTCCGGGCAACCCGGGAGCGTTTGTCCACACAATTTCTGCTCCGACTCTGCGGACTACTGC
AGTGGAGCTTGACTCTTAATGGATCTAGAAAGGAGAAATGAAGAACTTGAAGAACTTTATTTATTAGAGAGGTGTTTTCCTGAAGCAGAGAAATTGAAACAGGAAACTAAATTGCTTTCTCAGTGGAA
GCACTACATTCAATGTGATGGGAGTCCTGATCCTTCAGTAGCCCAAGAAATGAACACGTTTATTAGTTTGTGGAAAGAGAAAACAAATGAGACTTTTGAGGAAGTGATTGAGAAGAGTAAAGTAGTGC
TAAATTTAATTGAGAAATTGAAATTTATTTTACTGGAAACTCCACCATGTGATTTGCAAGATAAAAATATAATACAGTACCAAGAATCAATACTACAACTGCAGGAGCTCCTTCATCTTAAATTCGGT
GTAGCCACAGAAATACTTCTCAAACAAGCTAGTACTTTGGCAGATCTGGACAGTGGAAATATGGAAAAAGTCATTAAAGATGAAAATGTTACTCTGTATGTGTGGGCAAACCTCAAGAAGAATCCAAG
GCACAGAAGTGTTAGATTCTCTGAAACACAAATTGGATTTGAGATTCCAAGGATATTAGCAACAAGTGACATTGCTGTACGACTCCTGCATACCCACTATGATCATGTTTCTGCACTGCACCCTGTTT
CAACACCATCAAAAGAATACACTTCTGCAGTAACTGAGCTTGTCAAAGATGATGTTAAGAATGTAGAAAAAGCAATCAGCAAGGAGGTCGAAGAAGAGTCCAAACAACAAGAAAGAGGGTCTCACTTA
ATTCAGGAGGAAGAAATAAAAGTTGAGGAGGAACAAGGTGATATTGAAGTGAAAATGAGTTCTGCTGAGGAAGAATCTGAAGCCATAAAATGTGAACGAGAGATGAAAGTATTAAGTGAAACTGTTTC
AGCAGGTAAACATTGGAGAACTGATGGCATCAGCAATGTATCCTACAAACCAAAAGAAAGACTTGTAACATTCAGCCTGGACACCTTTGGCCCTGTTACCTTGATTCAAGATGCTCATATTAACATGC
CGTACCAGTCATGGGAACTAAGACCACTTGATGTAAATAAAGTACTTTTAACTGTGACTACAGTATTTACTGAGATTCAAATACAAATTAAGGAAAACCTCTGCATGTTATCTTCAATCAAACTAAAA
GACAAGAAACACATCTCTATTTTGGAAGGAACCTGGATGACTCCTATTCCTTTCATTATTGCTTTGAAAGAAGCTGGACTGAATATCTTTCCTACTAGACACTCTCATTTTTATGTTATTATAAACAA
TAAGGTTCCTTTGGTAGAAGTGAAAGCTTATCGACAGATGGCCCTACTAAGTTCTGCTTTTGCATTTGGTTGGAGCAAGTGGAACCTACTATGTAATTCTACAAAAGTCGTATTTAAGGTGAGGGAAC
ACCTTACTGAAGCATGTACTGAGAATCCTAATTGGGCCCTTTTAATGTTTAGTGGTGACAGAGCACAAAGACTGAAGATCAAGGAAGAGAGTGAGGCATTTTCTGAAGCACTTAAAGAAGAAACTGAG
TTTCATTCTACTTTATATCACATGGTGAAGGATTTTGCTTCTGAGGAAGCAATGGAGAAAGTCAGGAGTTCCAACTGTCAGTTTGTCAACTCTGTGTGCCACATGCTGCTCTCTACCAGATTGCTCAG
CTACTCCTAACCTCCACTTACAAACTGTATTGTAAGTATGAAGAACCAAGCATGGTGAAAGACAGGTATTTCTGCAACACAATGTAATGAGTGAATGAATACATTTCAAATCAACTATTAAAAATTTT
CTAATCTGCATTTTCTACTCAAGTTTTATTTTAAAAACAGTATTTTTTTTTCCTTTGAATACTTGGCCTGTTAAGAATTTCAGCTTTCACTCTATGAAGATTTAAATGATTCTTTATTTCAATAAACT
TTAACAAACAATA

hide sequence

RefSeq Acc Id:

NM_001352068 ⟹ NP_001338997

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	25,108,289 - 25,195,160 (-)	NCBI
T2T-CHM13v2.0	12	24,979,200 - 25,066,403 (-)	NCBI

Sequence:

show sequence

GTCGTCCGGGCAACCCGGGAGCGTTTGTCCACACAATTTCTGCTCCGACTCTGCGGACTACTGC
AGTGGAGCTTGACTCTTAATGAGGAAGCCCGTTTGAAATATGAGAAAGAAGAAATGGAAAGGCTTGAAATACAGCGAATTGAGAAAGAAAAATGGCATCGACTTGAAGCAAAAGATCTAGAAAGGAGA
AATGAAGAACTTGAAGAACTTTATTTATTAGAGAGGTGTTTTCCTGAAGCAGAGAAATTGAAACAGGAAACTAAATTGCTTTCTCAGTGGAAGCACTACATTCAATGTGATGGGAGTCCTGATCCTTC
AGTAGCCCAAGAAATGAACACGTTTATTAGTTTGTGGAAAGAGAAAACAAATGAGACTTTTGAGGAAGTGATTGAGAAGAGTAAAGTAGTGCTAAATTTAATTGAGAAATTGAAATTTATTTTACTGG
AAACTCCACCATGTGATTTGCAAGATAAAAATATAATACAGTACCAAGAATCAATACTACAACTGCAGGAGCTCCTTCATCTTAAATTCGGTGTAGCCACAGAAATACTTCTCAAACAAGCTAGTACT
TTGGCAGATCTGGACAGTGGAAATATGGAAAAAGTCATTAAAGATGAAAATGTTACTCTGTATGTGTGGGCAAACCTCAAGAAGAATCCAAGGCACAGAAGTGTTAGATTCTCTGAAACACAAATTGG
ATTTGAGATTCCAAGGATATTAGCAACAAGTGACATTGCTGTACGACTCCTGCATACCCACTATGATCATGTTTCTGCACTGCACCCTGTTTCAACACCATCAAAAGAATACACTTCTGCAGTAACTG
AGCTTGTCAAAGATGATGTTAAGAATGTAGAAAAAGCAATCAGCAAGGAGGTCGAAGAAGAGTCCAAACAACAAGAAAGAGGGTCTCACTTAATTCAGGAGGAAGAAATAAAAGTTGAGGAGGAACAA
GGTGATATTGAAGTGAAAATGAGTTCTGCTGAGGAAGAATCTGAAGCCATAAAATGTGAACGAGAGATGAAAGTATTAAGTGAAACTGTTTCAGCAGGTAAACATTGGAGAACTGATGGCATCAGCAA
TGTATCCTACAAACCAAAAGAAAGACTTGTAACATTCAGCCTGGACACCTTTGGCCCTGTTACCTTGATTCAAGATGCTCATATTAACATGCCGTACCAGTCATGGGAACTAAGACCACTTGATGTAA
ATAAAGTACTTTTAACTGTGACTACAGTATTTACTGAGATTCAAATACAAATTAAGGAAAACCTCTGCATGTTATCTTCAATCAAACTAAAAGACAAGAAACACATCTCTATTTTGGAAGGAACCTGG
ATGACTCCTATTCCTTTCATTATTGCTTTGAAAGAAGCTGGACTGAATATCTTTCCTACTAGACACTCTCATTTTTATGTTATTATAAACAATAAGGTTCCTTTGGTAGAAGTGAAAGCTTATCGACA
GATGGCCCTACTAAGTTCTGCTTTTGCATTTGGTTGGAGCAAGTGGAACCTACTATGTAATTCTACAAAAGTCGTATTTAAGTGGTGACAGAGCACAAAGACTGAAGATCAAGGAAGAGAGTGAGGCA
TTTTCTGAAGCACTTAAAGAAGAAACTGAGTTTCATTCTACTTTATATCACATGGTGAAGGATTTTGCTTCTGAGGAAGCAATGGAGAAAGTCAGGAGTTCCAACTGTCAGTTTGTCAACTCTGTGTG
CCACATGCTGCTCTCTACCAGATTGCTCAGCTACTCCTAACCTCCACTTACAAACTGTATTGTAAGTATGAAGAACCAAGCATGGTGAAAGACAGGTATTTCTGCAACACAATGTAATGAGTGAATGA
ATACATTTCAAATCAACTATTAAAAATTTTCTAATCTGCATTTTCTACTCAAGTTTTATTTTAAAAACAGTATTTTTTTTTCCTTTGAATACTTGGCCTGTTAAGAATTTCAGCTTTCACTCTATGAA
GATTTAAATGATTCTTTATTTCAATAAACTTTAACAAACAATA

hide sequence

RefSeq Acc Id:

NM_018272 ⟹ NP_060742

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	25,108,289 - 25,195,160 (-)	NCBI
GRCh37	12	25,261,223 - 25,348,096 (-)	NCBI
Build 36	12	25,152,490 - 25,239,361 (-)	NCBI Archive
Celera	12	30,408,204 - 30,495,049 (-)	RGD
HuRef	12	25,031,916 - 25,118,815 (-)	RGD
CHM1_1	12	25,226,353 - 25,313,241 (-)	NCBI
T2T-CHM13v2.0	12	24,979,200 - 25,066,403 (-)	NCBI

Sequence:

show sequence

GTCGTCCGGGCAACCCGGGAGCGTTTGTCCACACAATTTCTGCTCCGACTCTGCGGACTACTGC
AGTGGAGCTTGACTCTTAATGGGTCCCAAAGCAAAAAAGTCTGGCAGTAAGAAAAAGAAAGTCACCAAAGCTGAACGATTGAAGCTGCTACAAGAGGAGGAGGAGAGACGACTGAAAGAGGAAGAGGA
AGCCCGTTTGAAATATGAGAAAGAAGAAATGGAAAGGCTTGAAATACAGCGAATTGAGAAAGAAAAATGGCATCGACTTGAAGCAAAAGATCTAGAAAGGAGAAATGAAGAACTTGAAGAACTTTATT
TATTAGAGAGGTGTTTTCCTGAAGCAGAGAAATTGAAACAGGAAACTAAATTGCTTTCTCAGTGGAAGCACTACATTCAATGTGATGGGAGTCCTGATCCTTCAGTAGCCCAAGAAATGAACACGTTT
ATTAGTTTGTGGAAAGAGAAAACAAATGAGACTTTTGAGGAAGTGATTGAGAAGAGTAAAGTAGTGCTAAATTTAATTGAGAAATTGAAATTTATTTTACTGGAAACTCCACCATGTGATTTGCAAGA
TAAAAATATAATACAGTACCAAGAATCAATACTACAACTGCAGGAGCTCCTTCATCTTAAATTCGGTGTAGCCACAGAAATACTTCTCAAACAAGCTAGTACTTTGGCAGATCTGGACAGTGGAAATA
TGGAAAAAGTCATTAAAGATGAAAATGTTACTCTGTATGTGTGGGCAAACCTCAAGAAGAATCCAAGGCACAGAAGTGTTAGATTCTCTGAAACACAAATTGGATTTGAGATTCCAAGGATATTAGCA
ACAAGTGACATTGCTGTACGACTCCTGCATACCCACTATGATCATGTTTCTGCACTGCACCCTGTTTCAACACCATCAAAAGAATACACTTCTGCAGTAACTGAGCTTGTCAAAGATGATGTTAAGAA
TGTAGAAAAAGCAATCAGCAAGGAGGTCGAAGAAGAGTCCAAACAACAAGAAAGAGGGTCTCACTTAATTCAGGAGGAAGAAATAAAAGTTGAGGAGGAACAAGGTGATATTGAAGTGAAAATGAGTT
CTGCTGAGGAAGAATCTGAAGCCATAAAATGTGAACGAGAGATGAAAGTATTAAGTGAAACTGTTTCAGCAGCACAGTTGTTGCTGGTAGAGAATTCTTCTGAAAAGCCAGATTTCTTTGAAGACAAT
GTGGTGGATTTATGCCAGTTCACAACTCTGGGTGGAGTATACCACTTGGATATTTTGGAGCTTCCTCCACAGTGTAAACCAGTGAAGGGATGGATGATTGTGGAAATACTCAAAGAAGGATTACAGAA
ATACACATATCCTCCGGAAACTACAGAAGAGTTTGAGACAGAAAATGCTTTCCCACCTATAGAGGTCACACTTGAGGTTCATGAGAATGTAATCTTTTTTGAGGATCCTGTGGTTGTAAGGTGGGATG
CTGAAGGTAAACATTGGAGAACTGATGGCATCAGCAATGTATCCTACAAACCAAAAGAAAGACTTGTAACATTCAGCCTGGACACCTTTGGCCCTGTTACCTTGATTCAAGATGCTCATATTAACATG
CCGTACCAGTCATGGGAACTAAGACCACTTGATGTAAATAAAGTACTTTTAACTGTGACTACAGTATTTACTGAGATTCAAATACAAATTAAGGAAAACCTCTGCATGTTATCTTCAATCAAACTAAA
AGACAAGAAACACATCTCTATTTTGGAAGGAACCTGGATGACTCCTATTCCTTTCATTATTGCTTTGAAAGAAGCTGGACTGAATATCTTTCCTACTAGACACTCTCATTTTTATGTTATTATAAACA
ATAAGGTTCCTTTGGTAGAAGTGAAAGCTTATCGACAGATGGCCCTACTAAGTTCTGCTTTTGCATTTGGTTGGAGCAAGTGGAACCTACTATGTAATTCTACAAAAGTCGTATTTAAGGTGAGGGAA
CACCTTACTGAAGCATGTACTGAGAATCCTAATTGGGCCCTTTTAATGTTTAGTGGTGACAGAGCACAAAGACTGAAGATCAAGGAAGAGAGTGAGGCATTTTCTGAAGCACTTAAAGAAGAAACTGA
GTTTCATTCTACTTTATATCACATGGTGAAGGATTTTGCTTCTGAGGAAGCAATGGAGAAAGTCAGGAGTTCCAACTGTCAGTTTGTCAACTCTGTGTGCCACATGCTGCTCTCTACCAGATTGCTCA
GCTACTCCTAACCTCCACTTACAAACTGTATTGTAAGTATGAAGAACCAAGCATGGTGAAAGACAGGTATTTCTGCAACACAATGTAATGAGTGAATGAATACATTTCAAATCAACTATTAAAAATTT
TCTAATCTGCATTTTCTACTCAAGTTTTATTTTAAAAACAGTATTTTTTTTTCCTTTGAATACTTGGCCTGTTAAGAATTTCAGCTTTCACTCTATGAAGATTTAAATGATTCTTTATTTCAATAAAC
TTTAACAAACAATA

hide sequence

RefSeq Acc Id:

NR_147909

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	25,108,289 - 25,195,160 (-)	NCBI
T2T-CHM13v2.0	12	24,979,200 - 25,066,403 (-)	NCBI

Sequence:

show sequence

GTCGTCCGGGCAACCCGGGAGCGTTTGTCCACACAATTTCTGCTCCGACTCTGCGGACTACTGC
AGTGGAGCTTGACTCTTAATGTCTGGCAGTAAGAAAAAGAAAGTCACCAAAGCTGAACGATTGAAGCTGCTACAAGAGGAGGAGGAGAGACGACTGAAAGAGGAAGAGGAAGCCCGTTTGAAATATGA
GAAAGAAGAAATGGAAAGGCTTGAAATACAGCGAATTGAGAAAGAAAAATGGCATCGACTTGAAGCAAAAGATCTAGAAAGGAGAAATGAAGAACTTGAAGAACTTTATTTATTAGAGAGGTGTTTTC
CTGAAGCAGAGAAATTGAAACAGGAAACTAAATTGCTTTCTCAGTGGAAGCACTACATTCAATGTGATGGGAGTCCTGATCCTTCAGTAGCCCAAGAAATGAACACGTTTATTAGTTTGTGGAAAGAG
AAAACAAATGAGACTTTTGAGGAAGTGATTGAGAAGAGTAAAGTAGTGCTAAATTTAATTGAGAAATTGAAATTTATTTTACTGGAAACTCCACCATGTGATTTGCAAGATAAAAATATAATACAGTA
CCAAGAATCAATACTACAACTGCAGGAGCTCCTTCATCTTAAATTCGGTGTAGCCACAGAAATACTTCTCAAACAAGCTAGTACTTTGGCAGATCTGGACAGTGGAAATATGGAAAAAGTCATTAAAG
ATGAAAATGTTACTCTGTATGTGTGGGCAAACCTCAAGAAGAATCCAAGGCACAGAAGTGTTAGATTCTCTGAAACACAAATTGGATTTGAGATTCCAAGGATATTAGCAACAAGTGACATTGCTGTA
CGACTCCTGCATACCCACTATGATCATGTTTCTGCACTGCACCCTGTTTCAACACCATCAAAAGAATACACTTCTGCAGTAACTGAGCTTGTCAAAGATGATGTTAAGAATGTAGAAAAAGCAATCAG
CAAGGAGGTCGAAGAAGAGTCCAAACAACAAGAAAGAGGGTCTCACTTAATTCAGGAGGAAGAAATAAAAGTTGAGGAGGAACAAGGTGATATTGAAGTGAAAATGAGTTCTGCTGAGGAAGAATCTG
AAGCCATAAAATGTGAACGAGAGATGAAAGTATTAAGTGAAACTGTTTCAGCAGCACAGTTGTTGCTGGTAGAGAATTCTTCTGAAAAGCCAGATTTCTTTGAAGACAATGTGGTGGATTTATGCCAG
TTCACAACTCTGGGTGGAGTATACCACTTGGATATTTTGGAGCTTCCTCCACAGTGTAAACCAGTGAAGGGATGGATGATTGTGGAAATACTCAAAGAAGGATTACAGAAATACACATATCCTCCGGA
AACTACAGAAGAGTTTGAGACAGAAAATGCTTTCCCACCTATAGAGGTCACACTTGAGGTTCATGAGAATGTAATCTTTTTTGAGGATCCTGTGGTTGTAAGGTAAACATTGGAGAACTGATGGCATC
AGCAATGTATCCTACAAACCAAAAGAAAGACTTGTAACATTCAGCCTGGACACCTTTGGCCCTGTTACCTTGATTCAAGATGCTCATATTAACATGCCGTACCAGTCATGGGAACTAAGACCACTTGA
TGTAAATAAAGTACTTTTAACTGTGACTACAGTATTTACTGAGATTCAAATACAAATTAAGGAAAACCTCTGCATGTTATCTTCAATCAAACTAAAAGACAAGAAACACATCTCTATTTTGGAAGGAA
CCTGGATGACTCCTATTCCTTTCATTATTGCTTTGAAAGAAGCTGGACTGAATATCTTTCCTACTAGACACTCTCATTTTTATGTTATTATAAACAATAAGGTTCCTTTGGTAGAAGTGAAAGCTTAT
CGACAGATGGCCCTACTAAGTTCTGCTTTTGCATTTGGTTGGAGCAAGTGGAACCTACTATGTAATTCTACAAAAGTCGTATTTAAGGTGAGGGAACACCTTACTGAAGCATGTACTGAGAATCCTAA
TTGGGCCCTTTTAATGTTTAGTGGTGACAGAGCACAAAGACTGAAGATCAAGGAAGAGAGTGAGGCATTTTCTGAAGCACTTAAAGAAGAAACTGAGTTTCATTCTACTTTATATCACATGGTGAAGG
ATTTTGCTTCTGAGGAAGCAATGGAGAAAGTCAGGAGTTCCAACTGTCAGTTTGTCAACTCTGTGTGCCACATGCTGCTCTCTACCAGATTGCTCAGCTACTCCTAACCTCCACTTACAAACTGTATT
GTAAGTATGAAGAACCAAGCATGGTGAAAGACAGGTATTTCTGCAACACAATGTAATGAGTGAATGAATACATTTCAAATCAACTATTAAAAATTTTCTAATCTGCATTTTCTACTCAAGTTTTATTT
TAAAAACAGTATTTTTTTTTCCTTTGAATACTTGGCCTGTTAAGAATTTCAGCTTTCACTCTATGAAGATTTAAATGATTCTTTATTTCAATAAACTTTAACAAACAATA

hide sequence

RefSeq Acc Id:

NR_147910

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	25,108,289 - 25,195,160 (-)	NCBI
T2T-CHM13v2.0	12	24,979,200 - 25,066,403 (-)	NCBI

Sequence:

show sequence

GTCGTCCGGGCAACCCGGGAGCGTTTGTCCACACAATTTCTGCTCCGACTCTGCGGACTACTGCAGTGGAGCTTGACTCTTAATGTCTGGCAGTAAGAAAAAGAAAGTCACCAAAGCTGAACGATTGA
AGCTGCTACAAGAGGAGGAGGAGAGACGACTGAAAGAGGAAGAGGAAGCCCGTTTGAAATATGAGAAAGAAGAAATGGAAAGGCTTGAAATACAGCGAATTGAGAAAGAAAAATGGCATCGACTTGAA
GCAAAAGATCTAGAAAGGAGAAATGAAGAACTTGAAGAACTTTATTTATTAGAGAGGTGTTTTCCTGAAGCAGAGAAATTGAAACAGGAAACTAAATTGCTTTCTCAGTGGAAGCACTACATTCAATG
TGATGGGAGTCCTGATCCTTCAGTAGCCCAAGAAATGAACACGTTTATTAGTTTGTGGAAAGAGAAAACAAATGAGACTTTTGAGGAAGTGATTGAGAAGAGTAAAGTAGTGCTAAATTTAATTGAGA
AATTGAAATTTATTTTACTGGAAACTCCACCATGTGATTTGCAAGATAAAAATATAATACAGTACCAAGAATCAATACTACAACTGCAGGAGCTCCTTCATCTTAAATTCGGTGTAGCCACAGAAATA
CTTCTCAAACAAGCTAGTACTTTGGCAGATCTGGACAGTGGAAATATGGAAAAAGTCATTAAAGATGAAAATGTTACTCTGTATGTGTGGGCAAACCTCAAGAAGAATCCAAGAGTTCTGCTGAGGAA
GAATCTGAAGCCATAAAATGTGAACGAGAGATGAAAGTATTAAGTGAAACTGTTTCAGCAGGTAAACATTGGAGAACTGATGGCATCAGCAATGTATCCTACAAACCAAAAGAAAGACTTGTAACATT
CAGCCTGGACACCTTTGGCCCTGTTACCTTGATTCAAGATGCTCATATTAACATGCCGTACCAGTCATGGGAACTAAGACCACTTGATGTAAATAAAGTACTTTTAACTGTGACTACAGTATTTACTG
AGATTCAAATACAAATTAAGGAAAACCTCTGCATGTTATCTTCAATCAAACTAAAAGACAAGAAACACATCTCTATTTTGGAAGGAACCTGGATGACTCCTATTCCTTTCATTATTGCTTTGAAAGAA
GCTGGACTGAATATCTTTCCTACTAGACACTCTCATTTTTATGTTATTATAAACAATAAGGTTCCTTTGGTAGAAGTGAAAGCTTATCGACAGATGGCCCTACTAAGTTCTGCTTTTGCATTTGGTTG
GAGCAAGTGGAACCTACTATGTAATTCTACAAAAGTCGTATTTAAGGTGAGGGAACACCTTACTGAAGCATGTACTGAGAATCCTAATTGGGCCCTTTTAATGTTTAGTGGTGACAGAGCACAAAGAC
TGAAGATCAAGGAAGAGAGTGAGGCATTTTCTGAAGCACTTAAAGAAGAAACTGAGTTTCATTCTACTTTATATCACATGGTGAAGGATTTTGCTTCTGAGGAAGCAATGGAGAAAGTCAGGAGTTCC
AACTGTCAGTTTGTCAACTCTGTGTGCCACATGCTGCTCTCTACCAGATTGCTCAGCTACTCCTAACCTCCACTTACAAACTGTATTGTAAGTATGAAGAACCAAGCATGGTGAAAGACAGGTATTTC
TGCAACACAATGTAATGAGTGAATGAATACATTTCAAATCAACTATTAAAAATTTTCTAATCTGCATTTTCTACTCAAGTTTTATTTTAAAAACAGTATTTTTTTTTCCTTTGAATACTTGGCCTGTT
AAGAATTTCAGCTTTCACTCTATGAAGATTTAAATGATTCTTTATTTCAATAAACTTTAACAAACAATA

hide sequence

RefSeq Acc Id:

NR_147911

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	25,108,289 - 25,195,160 (-)	NCBI
T2T-CHM13v2.0	12	24,979,200 - 25,066,403 (-)	NCBI

Sequence:

show sequence

GTCGTCCGGGCAACCCGGGAGCGTTTGTCCACACAATTTCTGCTCCGACTCTGCGGACTACTGCAGTGGAGCTTGACTCTTAATGTAAGAAAAAGAAAGTCACCAAAGCTGAACGATTGAAGCTGCTA
CAAGAGGAGGAGGAGAGACGACTGAAAGAGGAAGGATCTAGAAAGGAGAAATGAAGAACTTGAAGAACTTTATTTATTAGAGAGGTGTTTTCCTGAAGCAGAGAAATTGAAACAGGAAACTAAATTGC
TTTCTCAGTGGAAGCACTACATTCAATGTGATGGGAGTCCTGATCCTTCAGTAGCCCAAGAAATGAACACGTTTATTAGTTTGTGGAAAGAGAAAACAAATGAGACTTTTGAGGAAGTGATTGAGAAG
AGTAAAGTAGTGCTAAATTTAATTGAGAAATTGAAATTTATTTTACTGGAAACTCCACCATGTGATTTGCAAGATAAAAATATAATACAGTACCAAGAATCAATACTACAACTGCAGGAGCTCCTTCA
TCTTAAATTCGGTGTAGCCACAGAAATACTTCTCAAACAAGCTAGTACTTTGGCAGATCTGGACAGTGGAAATATGGAAAAAGTCATTAAAGATGAAAATGTTACTCTGTATGTGTGGGCAAACCTCA
AGAAGAATCCAAGGCACAGAAGTGTTAGATTCTCTGAAACACAAATTGGATTTGAGATTCCAAGGATATTAGCAACAAGTGACATTGCTGTACGACTCCTGCATACCCACTATGATCATGTTTCTGCA
CTGCACCCTGTTTCAACACCATCAAAAGAATACACTTCTGCAGTAACTGAGCTTGTCAAAGATGATGTTAAGAATGTAGAAAAAGCAATCAGCAAGGAGGTCGAAGAAGAGTCCAAACAACAAGAAAG
AGGGTCTCACTTAATTCAGGAGGAAGAAATAAAAGTTGAGGAGGAACAAGGTGATATTGAAGTGAAAATGAGTTCTGCTGAGGAAGAATCTGAAGCCATAAAATGTGAACGAGAGATGAAAGTATTAA
GTGAAACTGTTTCAGCAGCACAGTTGTTGCTGGTAGAGAATTCTTCTGAAAAGCCAGATTTCTTTGAAGACAATGTGGTGGATTTATGCCAGTTCACAACTCTGGGTGGAGTATACCACTTGGATATT
TTGGAGCTTCCTCCACAGTGTAAACCAGTGAAGGGATGGATGATTGTGGAAATACTCAAAGAAGGATTACAGAAATACACATATCCTCCGGAAACTACAGAAGAGTTTGAGACAGAAAATGCTTTCCC
ACCTATAGAGGTCACACTTGAGGTTCATGAGAATGTAATCTTTTTTGAGGATCCTGTGGTTGTAAGGTAAACATTGGAGAACTGATGGCATCAGCAATGTATCCTACAAACCAAAAGAAAGACTTGTA
ACATTCAGCCTGGACACCTTTGGCCCTGTTACCTTGATTCAAGATGCTCATATTAACATGCCGTACCAGTCATGGGAACTAAGACCACTTGATGTAAATAAAGTACTTTTAACTGTGACTACAGTATT
TACTGAGATTCAAATACAAATTAAGGAAAACCTCTGCATGTTATCTTCAATCAAACTAAAAGACAAGAAACACATCTCTATTTTGGAAGGAACCTGGATGACTCCTATTCCTTTCATTATTGCTTTGA
AAGAAGCTGGACTGAATATCTTTCCTACTAGACACTCTCATTTTTATGTTATTATAAACAATAAGGTTCCTTTGGTAGAAGTGAAAGCTTATCGACAGATGGCCCTACTAAGTTCTGCTTTTGCATTT
GGTTGGAGCAAGTGGAACCTACTATGTAATTCTACAAAAGTCGTATTTAAGGTGAGGGAACACCTTACTGAAGCATGTACTGAGAATCCTAATTGGGCCCTTTTAATGTTTAGTGGTGACAGAGCACA
AAGACTGAAGATCAAGGAAGAGAGTGAGGCATTTTCTGAAGCACTTAAAGAAGAAACTGAGTTTCATTCTACTTTATATCACATGGTGAAGGATTTTGCTTCTGAGGAAGCAATGGAGAAAGTCAGGA
GTTCCAACTGTCAGTTTGTCAACTCTGTGTGCCACATGCTGCTCTCTACCAGATTGCTCAGCTACTCCTAACCTCCACTTACAAACTGTATTGTAAGTATGAAGAACCAAGCATGGTGAAAGACAGGT
ATTTCTGCAACACAATGTAATGAGTGAATGAATACATTTCAAATCAACTATTAAAAATTTTCTAATCTGCATTTTCTACTCAAGTTTTATTTTAAAAACAGTATTTTTTTTTCCTTTGAATACTTGGC
CTGTTAAGAATTTCAGCTTTCACTCTATGAAGATTTAAATGATTCTTTATTTCAATAAACTTTAACAAACAATA

hide sequence

RefSeq Acc Id:

XM_005253406 ⟹ XP_005253463

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	25,108,289 - 25,195,160 (-)	NCBI
GRCh37	12	25,261,223 - 25,348,096 (-)	NCBI

Sequence:

show sequence

GACTCTTAATGGTGAGCAAGGCAAATGAGGCAGACAGGTGGAGGGGCGACCACTGATTCTGCTTCACCAGTGTTAAATAATGTAATCAAGAGCCAGTCATATTTTACAGCGAAGCGGGTCGGTTTGGG
AAATAACTCATACCTTGGGGTGGGTCGGCCCTCTTCTCAGCAATGGCTTTCCTTACCTGGACCAGGCGGACAGGGTCCCAAAGCAAAAAAGTCTGGCAGTAAGAAAAAGAAAGTCACCAAAGCTGAAC
GATTGAAGCTGCTACAAGAGGAGGAGGAGAGACGACTGAAAGAGGAAGAGGAAGCCCGTTTGAAATATGAGAAAGAAGAAATGGAAAGGCTTGAAATACAGCGAATTGAGAAAGAAAAATGGCATCGA
CTTGAAGCAAAAGATCTAGAAAGGAGAAATGAAGAACTTGAAGAACTTTATTTATTAGAGAGGTGTTTTCCTGAAGCAGAGAAATTGAAACAGGAAACTAAATTGCTTTCTCAGTGGAAGCACTACAT
TCAATGTGATGGGAGTCCTGATCCTTCAGTAGCCCAAGAAATGAACACGTTTATTAGTTTGTGGAAAGAGAAAACAAATGAGACTTTTGAGGAAGTGATTGAGAAGAGTAAAGTAGTGCTAAATTTAA
TTGAGAAATTGAAATTTATTTTACTGGAAACTCCACCATGTGATTTGCAAGATAAAAATATAATACAGTACCAAGAATCAATACTACAACTGCAGGAGCTCCTTCATCTTAAATTCGGTGTAGCCACA
GAAATACTTCTCAAACAAGCTAGTACTTTGGCAGATCTGGACAGTGGAAATATGGAAAAAGTCATTAAAGATGAAAATGTTACTCTGTATGTGTGGGCAAACCTCAAGAAGAATCCAAGGCACAGAAG
TGTTAGATTCTCTGAAACACAAATTGGATTTGAGATTCCAAGGATATTAGCAACAAGTGACATTGCTGTACGACTCCTGCATACCCACTATGATCATGTTTCTGCACTGCACCCTGTTTCAACACCAT
CAAAAGAATACACTTCTGCAGTAACTGAGCTTGTCAAAGATGATGTTAAGAATGTAGAAAAAGCAATCAGCAAGGAGGTCGAAGAAGAGTCCAAACAACAAGAAAGAGGGTCTCACTTAATTCAGGAG
GAAGAAATAAAAGTTGAGGAGGAACAAGGTGATATTGAAGTGAAAATGAGTTCTGCTGAGGAAGAATCTGAAGCCATAAAATGTGAACGAGAGATGAAAGTATTAAGTGAAACTGTTTCAGCAGCACA
GTTGTTGCTGGTAGAGAATTCTTCTGAAAAGCCAGATTTCTTTGAAGACAATGTGGTGGATTTATGCCAGTTCACAACTCTGGGTGGAGTATACCACTTGGATATTTTGGAGCTTCCTCCACAGTGTA
AACCAGTGAAGGGATGGATGATTGTGGAAATACTCAAAGAAGGATTACAGAAATACACATATCCTCCGGAAACTACAGAAGAGTTTGAGACAGAAAATGCTTTCCCACCTATAGAGGTCACACTTGAG
GTTCATGAGAATGTAATCTTTTTTGAGGATCCTGTGGTTGTAAGGTGGGATGCTGAAGGTAAACATTGGAGAACTGATGGCATCAGCAATGTATCCTACAAACCAAAAGAAAGACTTGTAACATTCAG
CCTGGACACCTTTGGCCCTGTTACCTTGATTCAAGATGCTCATATTAACATGCCGTACCAGTCATGGGAACTAAGACCACTTGATGTAAATAAAGTACTTTTAACTGTGACTACAGTATTTACTGAGA
TTCAAATACAAATTAAGGAAAACCTCTGCATGTTATCTTCAATCAAACTAAAAGACAAGAAACACATCTCTATTTTGGAAGGAACCTGGATGACTCCTATTCCTTTCATTATTGCTTTGAAAGAAGCT
GGACTGAATATCTTTCCTACTAGACACTCTCATTTTTATGTTATTATAAACAATAAGGTTCCTTTGGTAGAAGTGAAAGCTTATCGACAGATGGCCCTACTAAGTTCTGCTTTTGCATTTGGTTGGAG
CAAGTGGAACCTACTATGTAATTCTACAAAAGTCGTATTTAAGGTGAGGGAACACCTTACTGAAGCATGTACTGAGAATCCTAATTGGGCCCTTTTAATGTTTAGTGGTGACAGAGCACAAAGACTGA
AGATCAAGGAAGAGAGTGAGGCATTTTCTGAAGCACTTAAAGAAGAAACTGAGTTTCATTCTACTTTATATCACATGGTGAAGGATTTTGCTTCTGAGGAAGCAATGGAGAAAGTCAGGAGTTCCAAC
TGTCAGTTTGTCAACTCTGTGTGCCACATGCTGCTCTCTACCAGATTGCTCAGCTACTCCTAACCTCCACTTACAAACTGTATTGTAAGTATGAAGAACCAAGCATGGTGAAAGACAGGTATTTCTGC
AACACAATGTAATGAGTGAATGAATACATTTCAAATCAACTATTAAAAATTTTCTAATCTGCA

hide sequence

RefSeq Acc Id:

XM_006719101 ⟹ XP_006719164

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	25,108,289 - 25,195,160 (-)	NCBI

Sequence:

show sequence

GACTCTTAATGGTGAGCAAGGCAAATGAGGCAGACAGGTGGAGGGGCGACCACTGATTCTGCTT
CACCAGTGTTAAATAATGTAATCAAGAGCCAGTCATATTTTACAGCGAAGCGGGTCGGTTTGGGAAATAACTCATACCTTGGGGTGGGTCGGCCCTCTTCTCAGCAATGGCTTTCCTTACCTGGACCA
GGCGGACAGGGTCCCAAAGCAAAAAAGTCTGGCAGTAAGAAAAAGAAAGTCACCAAAGCTGAACGATTGAAGCTGCTACAAGAGGAGGAGGAGAGACGACTGAAAGAGGAAGAGGAAGCCCGTTTGAA
ATATGAGAAAGAAGAAATGGAAAGGCTTGAAATACAGCGAATTGAGAAAGAAAAATGGCATCGACTTGAAGCAAAAGATCTAGAAAGGAGAAATGAAGAACTTGAAGAACTTTATTTATTAGAGAGGT
GTTTTCCTGAAGCAGAGAAATTGAAACAGGAAACTAAATTGCTTTCTCAGTGGAAGCACTACATTCAATGTGATGGGAGTCCTGATCCTTCAGTAGCCCAAGAAATGAACACGTTTATTAGTTTGTGG
AAAGAGAAAACAAATGAGACTTTTGAGGAAGTGATTGAGAAGAGTAAAGTAGTGCTAAATTTAATTGAGAAATTGAAATTTATTTTACTGGAAACTCCACCATGTGATTTGCAAGATAAAAATATAAT
ACAGTACCAAGAATCAATACTACAACTGCAGGAGCTCCTTCATCTTAAATTCGGTGTAGCCACAGAAATACTTCTCAAACAAGCTAGTACTTTGGCAGATCTGGACAGTGGAAATATGGAAAAAGTCA
TTAAAGATGAAAATGTTACTCTGTATGTGTGGGCAAACCTCAAGAAGAATCCAAGGCACAGAAGTGTTAGATTCTCTGAAACACAAATTGGATTTGAGATTCCAAGGATATTAGCAACAAGTGACATT
GCTGTACGACTCCTGCATACCCACTATGATCATGTTTCTGCACTGCACCCTGTTTCAACACCATCAAAAGAATACACTTCTGCAGTAACTGAGCTTGTCAAAGATGATGTTAAGAATGTAGAAAAAGC
AATCAGCAAGGAGGTCGAAGAAGAGTCCAAACAACAAGAAAGAGGGTCTCACTTAATTCAGGAGGAAGAAATAAAAGTTGAGGAGGAACAAGGTGATATTGAAGTGAAAATGAGTTCTGCTGAGGAAG
AATCTGAAGCCATAAAATGTGAACGAGAGATGAAAGTATTAAGTGAAACTGTTTCAGCAGGTAAACATTGGAGAACTGATGGCATCAGCAATGTATCCTACAAACCAAAAGAAAGACTTGTAACATTC
AGCCTGGACACCTTTGGCCCTGTTACCTTGATTCAAGATGCTCATATTAACATGCCGTACCAGTCATGGGAACTAAGACCACTTGATGTAAATAAAGTACTTTTAACTGTGACTACAGTATTTACTGA
GATTCAAATACAAATTAAGGAAAACCTCTGCATGTTATCTTCAATCAAACTAAAAGACAAGAAACACATCTCTATTTTGGAAGGAACCTGGATGACTCCTATTCCTTTCATTATTGCTTTGAAAGAAG
CTGGACTGAATATCTTTCCTACTAGACACTCTCATTTTTATGTTATTATAAACAATAAGGTTCCTTTGGTAGAAGTGAAAGCTTATCGACAGATGGCCCTACTAAGTTCTGCTTTTGCATTTGGTTGG
AGCAAGTGGAACCTACTATGTAATTCTACAAAAGTCGTATTTAAGGTGAGGGAACACCTTACTGAAGCATGTACTGAGAATCCTAATTGGGCCCTTTTAATGTTTAGTGGTGACAGAGCACAAAGACT
GAAGATCAAGGAAGAGAGTGAGGCATTTTCTGAAGCACTTAAAGAAGAAACTGAGTTTCATTCTACTTTATATCACATGGTGAAGGATTTTGCTTCTGAGGAAGCAATGGAGAAAGTCAGGAGTTCCA
ACTGTCAGTTTGTCAACTCTGTGTGCCACATGCTGCTCTCTACCAGATTGCTCAGCTACTCCTAACCTCCACTTACAAACTGTATTGTAAGTATGAAGAACCAAGCATGGTGAAAGACAGGTATTTCT
GCAACACAATGTAATGAGTGAATGAATACATTTCAAATCAACTATTAAAAATTTTCTAATCTGCA

hide sequence

RefSeq Acc Id:

XM_011520723 ⟹ XP_011519025

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	25,107,047 - 25,195,160 (-)	NCBI

Sequence:

show sequence

GACTCTTAATGGTGAGCAAGGCAAATGAGGCAGACAGGTGGAGGGGCGACCACTGATTCTGCTTCACCAGTGTTAAATAATGTAATCAAGAGCCAGTCATATTTTACAGCGAAGCGGGTCGGTTTGGG
AAATAACTCATACCTTGGGGTGGGTCGGCCCTCTTCTCAGCAATGGCTTTCCTTACCTGGACCAGGCGGACAGGGTCCCAAAGCAAAAAAGTCTGGCAGTAAGAAAAAGAAAGTCACCAAAGCTGAAC
GATTGAAGCTGCTACAAGAGGAGGAGGAGAGACGACTGAAAGAGGAAGAGGAAGCCCGTTTGAAATATGAGAAAGAAGAAATGGAAAGGCTTGAAATACAGCGAATTGAGAAAGAAAAATGGCATCGA
CTTGAAGCAAAAGATCTAGAAAGGAGAAATGAAGAACTTGAAGAACTTTATTTATTAGAGAGGTGTTTTCCTGAAGCAGAGAAATTGAAACAGGAAACTAAATTGCTTTCTCAGTGGAAGCACTACAT
TCAATGTGATGGGAGTCCTGATCCTTCAGTAGCCCAAGAAATGAACACGTTTATTAGTTTGTGGAAAGAGAAAACAAATGAGACTTTTGAGGAAGTGATTGAGAAGAGTAAAGTAGTGCTAAATTTAA
TTGAGAAATTGAAATTTATTTTACTGGAAACTCCACCATGTGATTTGCAAGATAAAAATATAATACAGTACCAAGAATCAATACTACAACTGCAGGAGCTCCTTCATCTTAAATTCGGTGTAGCCACA
GAAATACTTCTCAAACAAGCTAGTACTTTGGCAGATCTGGACAGTGGAAATATGGAAAAAGTCATTAAAGATGAAAATGTTACTCTGTATGTGTGGGCAAACCTCAAGAAGAATCCAAGGCACAGAAG
TGTTAGATTCTCTGAAACACAAATTGGATTTGAGATTCCAAGGATATTAGCAACAAGTGACATTGCTGTACGACTCCTGCATACCCACTATGATCATGTTTCTGCACTGCACCCTGTTTCAACACCAT
CAAAAGAATACACTTCTGCAGTAACTGAGCTTGTCAAAGATGATGTTAAGAATGTAGAAAAAGCAATCAGCAAGGAGGTCGAAGAAGAGTCCAAACAACAAGAAAGAGGGTCTCACTTAATTCAGGAG
GAAGAAATAAAAGTTGAGGAGGAACAAGGTGATATTGAAGTGAAAATGAGTTCTGCTGAGGAAGAATCTGAAGCCATAAAATGTGAACGAGAGATGAAAGTATTAAGTGAAACTGTTTCAGCAGCACA
GTTGTTGCTGGTAGAGAATTCTTCTGAAAAGCCAGATTTCTTTGAAGACAATGTGGTGGATTTATGCCAGTTCACAACTCTGGGTGGAGTATACCACTTGGATATTTTGGAGCTTCCTCCACAGTGTA
AACCAGTGAAGGGATGGATGATTGTGGAAATACTCAAAGAAGGATTACAGAAATACACATATCCTCCGGAAACTACAGAAGAGTTTGAGACAGAAAATGCTTTCCCACCTATAGAGGTCACACTTGAG
GTTCATGAGAATGTAATCTTTTTTGAGGATCCTGTGGTTGTAAGGTGGGATGCTGAAGGTAAACATTGGAGAACTGATGGCATCAGCAATGTATCCTACAAACCAAAAGAAAGACTTGTAACATTCAG
CCTGGACACCTTTGGCCCTGTTACCTTGATTCAAGATGCTCATATTAACATGCCGTACCAGTCATGGGAACTAAGACCACTTGATGTAAATAAAGTACTTTTAACTGTGACTACAGTATTTACTGAGA
TTCAAATACAAATTAAGGAAAACCTCTGCATGTTATCTTCAATCAAACTAAAAGACAAGAAACACATCTCTATTTTGGAAGGAACCTGGATGACTCCTATTCCTTTCATTATTGCTTTGAAAGAAGCT
GGACTGAATATCTTTCCTACTAGACACTCTCATTTTTATGTTATTATAAACAATAAGGTTCCTTTGGTAGAAGTGAAAGCTTATCGACAGATGGCCCTACTAAGTTCTGCTTTTGCATTTGGTTGGAG
CAAGTGGAACCTACTATGTAATTCTACAAAAGTCGTATTTAAGGTGAGGGAACACCTTACTGAAGCATGTACTGAGAATCCTAATTGGGCCCTTTTAATGTTTAGTGGTGACAGAGCACAAAGACTGA
AGATCAAGGAAGAGAGTGAGGCATTTTCTGAAGCACTTAAAGAAGAAACTGAGTTTCATTCTACTTTATATCACATGGTGAAGGATTTTGCTTCTGAGGAAGCAATGGAGAAAGTCAGGAGTTCCAAC
TGTCAGTTTGTCAACTCTGTGTGCCACATGCTGCTCTCTACCAGATTGCTCAGCTACTCCTAACCTCCACTTACAAACTGTATTGATTAAAGAAATGATGTGCTACGATGAGAATCTGAAAATTACGT
GATGTAGGCAGTATCTTCTAATAAGTACATACAAGTATCTCATTCTTTCAGTAAGGTAAGGCAACATATTCCTACAGTGGAAACAAAAATGTTATTTGCTGGGTAGAGTGGATGTCTGTGTATGTACT
TATGTGTGTGTACAGTAGTCCCCCTTTATTCTTGTGGGATATGCTCCAAGACCTCCAGTGGATGCCTGAAGCTGAAAATAGTACTAAACCCAGTATATACTGTTTTTTTCCTATGGATACATGCCTAT
AACAAAATTGAATTTATAAATTAGGCATAGTAAAAGATGAACAATAACTAACATAAAATAGAATATAACATATATTACAGTAAAAGTTATGTGAATGTAGTCTGTCTCTCAAAATAGATAACATAGGT
TCAAGGATAACCTGACATACAAAGTTTGTTATTCATCTTAAATACAACAATTTGGCATGTCTTTTAGTAATTTGATTAGGATTAATACTGTCAGCCCTGCCTCACCCTTTCCCATTCCACTAAAATGG
TAGAATTTATCAAGTAGATA

hide sequence

RefSeq Acc Id:

XM_011520726 ⟹ XP_011519028

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	25,114,655 - 25,195,160 (-)	NCBI

Sequence:

show sequence

GACTCTTAATGGTGAGCAAGGCAAATGAGGCAGACAGGTGGAGGGGCGACCACTGATTCTGCTT
CACCAGTGTTAAATAATGTAATCAAGAGCCAGTCATATTTTACAGCGAAGCGGGTCGGTTTGGGAAATAACTCATACCTTGGGGTGGGTCGGCCCTCTTCTCAGCAATGGCTTTCCTTACCTGGACCA
GGCGGACAGGGTCCCAAAGCAAAAAAGTCTGGCAGTAAGAAAAAGAAAGTCACCAAAGCTGAACGATTGAAGCTGCTACAAGAGGAGGAGGAGAGACGACTGAAAGAGGAAGAGGAAGCCCGTTTGAA
ATATGAGAAAGAAGAAATGGAAAGGCTTGAAATACAGCGAATTGAGAAAGAAAAATGGCATCGACTTGAAGCAAAAGATCTAGAAAGGAGAAATGAAGAACTTGAAGAACTTTATTTATTAGAGAGGT
GTTTTCCTGAAGCAGAGAAATTGAAACAGGAAACTAAATTGCTTTCTCAGTGGAAGCACTACATTCAATGTGATGGGAGTCCTGATCCTTCAGTAGCCCAAGAAATGAACACGTTTATTAGTTTGTGG
AAAGAGAAAACAAATGAGACTTTTGAGGAAGTGATTGAGAAGAGTAAAGTAGTGCTAAATTTAATTGAGAAATTGAAATTTATTTTACTGGAAACTCCACCATGTGATTTGCAAGATAAAAATATAAT
ACAGTACCAAGAATCAATACTACAACTGCAGGAGCTCCTTCATCTTAAATTCGGTGTAGCCACAGAAATACTTCTCAAACAAGCTAGTACTTTGGCAGATCTGGACAGTGGAAATATGGAAAAAGTCA
TTAAAGATGAAAATGTTACTCTGTATGTGTGGGCAAACCTCAAGAAGAATCCAAGGCACAGAAGTGTTAGATTCTCTGAAACACAAATTGGATTTGAGATTCCAAGGATATTAGCAACAAGTGACATT
GCTGTACGACTCCTGCATACCCACTATGATCATGTTTCTGCACTGCACCCTGTTTCAACACCATCAAAAGAATACACTTCTGCAGTAACTGAGCTTGTCAAAGATGATGTTAAGAATGTAGAAAAAGC
AATCAGCAAGGAGGTCGAAGAAGAGTCCAAACAACAAGAAAGAGGGTCTCACTTAATTCAGGAGGAAGAAATAAAAGTTGAGGAGGAACAAGGTGATATTGAAGTGAAAATGAGTTCTGCTGAGGAAG
AATCTGAAGCCATAAAATGTGAACGAGAGATGAAAGTATTAAGTGAAACTGTTTCAGCAGCACAGTTGTTGCTGGTAGAGAATTCTTCTGAAAAGCCAGATTTCTTTGAAGACAATGTGGTGGATTTA
TGCCAGTTCACAACTCTGGGTGGAGTATACCACTTGGATATTTTGGAGCTTCCTCCACAGTGTAAACCAGTGAAGGGATGGATGATTGTGGAAATACTCAAAGAAGGATTACAGAAATACACATATCC
TCCGGAAACTACAGAAGAGTTTGAGACAGAAAATGCTTTCCCACCTATAGAGGTCACACTTGAGGTTCATGAGAATGTAATCTTTTTTGAGGATCCTGTGGTTGTAAGGGAAAAAATGAAACTAGTGT
CACTTTCTTCATCAATTATAAAGGTAAACATTGGAGAACTGATGGCATCAGCAATGTATCCTACAAACCAAAAGAAAGACTTGTAACATTCAGCCTGGACACCTTTGGCCCTGTTACCTTGATTCAAG
ATGCTCATATTAACATGCCGTACCAGTCATGGGAACTAAGACCACTTGATGTAAATAAAGTACTTTTAACTGTGACTACAGTATTTACTGAGATTCAAATACAAA

hide sequence

RefSeq Acc Id:

XM_011520727 ⟹ XP_011519029

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	25,114,787 - 25,195,160 (-)	NCBI

Sequence:

show sequence

GACTCTTAATGGTGAGCAAGGCAAATGAGGCAGACAGGTGGAGGGGCGACCACTGATTCTGCTTCACCAGTGTTAAATAATGTAATCAAGAGCCAGTCATATTTTACAGCGAAGCGGGTCGGTTTGGG
AAATAACTCATACCTTGGGGTGGGTCGGCCCTCTTCTCAGCAATGGCTTTCCTTACCTGGACCAGGCGGACAGGGTCCCAAAGCAAAAAAGTCTGGCAGTAAGAAAAAGAAAGTCACCAAAGCTGAAC
GATTGAAGCTGCTACAAGAGGAGGAGGAGAGACGACTGAAAGAGGAAGAGGAAGCCCGTTTGAAATATGAGAAAGAAGAAATGGAAAGGCTTGAAATACAGCGAATTGAGAAAGAAAAATGGCATCGA
CTTGAAGCAAAAGATCTAGAAAGGAGAAATGAAGAACTTGAAGAACTTTATTTATTAGAGAGGTGTTTTCCTGAAGCAGAGAAATTGAAACAGGAAACTAAATTGCTTTCTCAGTGGAAGCACTACAT
TCAATGTGATGGGAGTCCTGATCCTTCAGTAGCCCAAGAAATGAACACGTTTATTAGTTTGTGGAAAGAGAAAACAAATGAGACTTTTGAGGAAGTGATTGAGAAGAGTAAAGTAGTGCTAAATTTAA
TTGAGAAATTGAAATTTATTTTACTGGAAACTCCACCATGTGATTTGCAAGATAAAAATATAATACAGTACCAAGAATCAATACTACAACTGCAGGAGCTCCTTCATCTTAAATTCGGTGTAGCCACA
GAAATACTTCTCAAACAAGCTAGTACTTTGGCAGATCTGGACAGTGGAAATATGGAAAAAGTCATTAAAGATGAAAATGTTACTCTGTATGTGTGGGCAAACCTCAAGAAGAATCCAAGGCACAGAAG
TGTTAGATTCTCTGAAACACAAATTGGATTTGAGATTCCAAGGATATTAGCAACAAGTGACATTGCTGTACGACTCCTGCATACCCACTATGATCATGTTTCTGCACTGCACCCTGTTTCAACACCAT
CAAAAGAATACACTTCTGCAGTAACTGAGCTTGTCAAAGATGATGTTAAGAATGTAGAAAAAGCAATCAGCAAGGAGGTCGAAGAAGAGTCCAAACAACAAGAAAGAGGGTCTCACTTAATTCAGGAG
GAAGAAATAAAAGTTGAGGAGGAACAAGGTGATATTGAAGTGAAAATGAGTTCTGCTGAGGAAGAATCTGAAGCCATAAAATGTGAACGAGAGATGAAAGTATTAAGTGAAACTGTTTCAGCAGCACA
GTTGTTGCTGGTAGAGAATTCTTCTGAAAAGCCAGATTTCTTTGAAGACAATGTGGTGGATTTATGCCAGTTCACAACTCTGGGTGGAGTATACCACTTGGATATTTTGGAGCTTCCTCCACAGTGTA
AACCAGTGAAGGGATGGATGATTGTGGAAATACTCAAAGAAGGATTACAGAAATACACATATCCTCCGGAAACTACAGAAGAGTTTGAGACAGAAAATGCTTTCCCACCTATAGAGGTCACACTTGAG
GTTCATGAGAATGTAATCTTTTTTGAGGATCCTGTGGTTGTAAGGTAAACATTGGAGAACTGATGGCATCAGCAATGTATCCTACAAACCAAAAGAAAGACTTGTAACATTCAGCCTGGACACCTTTG

hide sequence

RefSeq Acc Id:

XM_017019560 ⟹ XP_016875049

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	25,108,289 - 25,195,160 (-)	NCBI

Sequence:

show sequence

AAGGCAAATGAGGCAGACAGGTGGAGGGGCGACCACTGATTCTGCTTCACCAGTGTTAAATAATGTAATCAAGAGCCAGTCATATTTTACAGCGAAGCGGGTCGGTTTGGGAAATAACTCATACCTTG
GGGTGGGTCGGCCCTCTTCTCAGCAATGGCTTTCCTTACCTGGACCAGGCGGACAGTCTGGCAGTAAGAAAAAGAAAGTCACCAAAGCTGAACGATTGAAGCTGCTACAAGAGGAGGAGGAGAGACGA
CTGAAAGAGGAAGAGGAAGCCCGTTTGAAATATGAGAAAGAAGAAATGGAAAGGCTTGAAATACAGCGAATTGAGAAAGAAAAATGGCATCGACTTGAAGCAAAAGATCTAGAAAGGAGAAATGAAGA
ACTTGAAGAACTTTATTTATTAGAGAGGTGTTTTCCTGAAGCAGAGAAATTGAAACAGGAAACTAAATTGCTTTCTCAGTGGAAGCACTACATTCAATGTGATGGGAGTCCTGATCCTTCAGTAGCCC
AAGAAATGAACACGTTTATTAGTTTGTGGAAAGAGAAAACAAATGAGACTTTTGAGGAAGTGATTGAGAAGAGTAAAGTAGTGCTAAATTTAATTGAGAAATTGAAATTTATTTTACTGGAAACTCCA
CCATGTGATTTGCAAGATAAAAATATAATACAGTACCAAGAATCAATACTACAACTGCAGGAGCTCCTTCATCTTAAATTCGGTGTAGCCACAGAAATACTTCTCAAACAAGCTAGTACTTTGGCAGA
TCTGGACAGTGGAAATATGGAAAAAGTCATTAAAGATGAAAATGTTACTCTGTATGTGTGGGCAAACCTCAAGAAGAATCCAAGGCACAGAAGTGTTAGATTCTCTGAAACACAAATTGGATTTGAGA
TTCCAAGGATATTAGCAACAAGTGACATTGCTGTACGACTCCTGCATACCCACTATGATCATGTTTCTGCACTGCACCCTGTTTCAACACCATCAAAAGAATACACTTCTGCAGTAACTGAGCTTGTC
AAAGATGATGTTAAGAATGTAGAAAAAGCAATCAGCAAGGAGGTCGAAGAAGAGTCCAAACAACAAGAAAGAGGGTCTCACTTAATTCAGGAGGAAGAAATAAAAGTTGAGGAGGAACAAGGTGATAT
TGAAGTGAAAATGAGTTCTGCTGAGGAAGAATCTGAAGCCATAAAATGTGAACGAGAGATGAAAGTATTAAGTGAAACTGTTTCAGCAGCACAGTTGTTGCTGGTAGAGAATTCTTCTGAAAAGCCAG
ATTTCTTTGAAGACAATGTGGTGGATTTATGCCAGTTCACAACTCTGGGTGGAGTATACCACTTGGATATTTTGGAGCTTCCTCCACAGTGTAAACCAGTGAAGGGATGGATGATTGTGGAAATACTC
AAAGAAGGATTACAGAAATACACATATCCTCCGGAAACTACAGAAGAGTTTGAGACAGAAAATGCTTTCCCACCTATAGAGGTCACACTTGAGGTTCATGAGAATGTAATCTTTTTTGAGGATCCTGT
GGTTGTAAGGTGGGATGCTGAAGGTAAACATTGGAGAACTGATGGCATCAGCAATGTATCCTACAAACCAAAAGAAAGACTTGTAACATTCAGCCTGGACACCTTTGGCCCTGTTACCTTGATTCAAG
ATGCTCATATTAACATGCCGTACCAGTCATGGGAACTAAGACCACTTGATGTAAATAAAGTACTTTTAACTGTGACTACAGTATTTACTGAGATTCAAATACAAATTAAGGAAAACCTCTGCATGTTA
TCTTCAATCAAACTAAAAGACAAGAAACACATCTCTATTTTGGAAGGAACCTGGATGACTCCTATTCCTTTCATTATTGCTTTGAAAGAAGCTGGACTGAATATCTTTCCTACTAGACACTCTCATTT
TTATGTTATTATAAACAATAAGGTTCCTTTGGTAGAAGTGAAAGCTTATCGACAGATGGCCCTACTAAGTTCTGCTTTTGCATTTGGTTGGAGCAAGTGGAACCTACTATGTAATTCTACAAAAGTCG
TATTTAAGGTGAGGGAACACCTTACTGAAGCATGTACTGAGAATCCTAATTGGGCCCTTTTAATGTTTAGTGGTGACAGAGCACAAAGACTGAAGATCAAGGAAGAGAGTGAGGCATTTTCTGAAGCA
CTTAAAGAAGAAACTGAGTTTCATTCTACTTTATATCACATGGTGAAGGATTTTGCTTCTGAGGAAGCAATGGAGAAAGTCAGGAGTTCCAACTGTCAGTTTGTCAACTCTGTGTGCCACATGCTGCT
CTCTACCAGATTGCTCAGCTACTCCTAACCTCCACTTACAAACTGTATTGTAAGTATGAAGAACCAAGCATGGTGAAAGACAGGTATTTCTGCAACACAATGTAATGAGTGAATGAATACATTTCAAA
TCAACTATTAAAAATTTTCTAATCTGCA

hide sequence

RefSeq Acc Id:

XM_017019565 ⟹ XP_016875054

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	25,108,289 - 25,195,160 (-)	NCBI

Sequence:

show sequence

GACTCTTAATGGTGAGCAAGGCAAATGAGGCAGACAGGTGGAGGGGCGACCACTGATTCTGCTT
CACCAGTGTTAAATAATGTAATCAAGAGCCAGTCATATTTTACAGCGAAGCGGGTCGGTTTGGGAAATAACTCATACCTTGGGGTGGGTCGGCCCTCTTCTCAGCAATGGCTTTCCTTACCTGGACCA
GGCGGACAGGGTCCCAAAGCAAAAAAGTCTGGCAGTAAGAAAAAGAAAGTCACCAAAGCTGAACGATTGAAGCTGCTACAAGAGGAGGAGGAGAGACGACTGAAAGAGGAAGAGGAAGCCCGTTTGAA
ATATGAGAAAGAAGAAATGGAAAGGCTTGAAATACAGCGAATTGAGAAAGAAAAATGGCATCGACTTGAAGCAAAAGATCTAGAAAGGAGAAATGAAGAACTTGAAGAACTTTATTTATTAGAGAGGT
GTTTTCCTGAAGCAGAGAAATTGAAACAGGAAACTAAATTGCTTTCTCAGTGGAAGCACTACATTCAATGTGATGGGAGTCCTGATCCTTCAGTAGCCCAAGAAATGAACACGTTTATTAGTTTGTGG
AAAGAGAAAACAAATGAGACTTTTGAGGAAGTGATTGAGAAGAGTAAAGTAGTGCTAAATTTAATTGAGAAATTGAAATTTATTTTACTGGAAACTCCACCATGTGATTTGCAAGATAAAAATATAAT
ACAGTACCAAGAATCAATACTACAACTGCAGGAGCTCCTTCATCTTAAATTCGGTGTAGCCACAGAAATACTTCTCAAACAAGCTAGTACTTTGGCAGATCTGGACAGTGGAAATATGGAAAAAGTCA
TTAAAGATGAAAATGTTACTCTGTATGTGTGGGCAAACCTCAAGAAGAATCCAAGGCACAGAAGTGTTAGATTCTCTGAAACACAAATTGGATTTGAGATTCCAAGGATATTAGCAACAAGTGACATT
GCTGTACGACTCCTGCATACCCACTATGATCATGTTTCTGCACTGCACCCTGTTTCAACACCATCAAAAGAATACACTTCTGCAGTAACTGAGCTTGTCAAAGATGATGTTAAGAATGTAGAAAAAGC
AATCAGCAAGGAGGTCGAAGAAGAGTCCAAACAACAAGAAAGAGGGTCTCACTTAATTCAGGAGGAAGAAATAAAAGTTGAGGAGGAACAAGGTGATATTGAAGTGAAAATGAGTTCTGCTGAGGAAG
AATCTGAAGCCATAAAATGTGAACGAGAGATGAAAGTATTAAGTGAAACTGTTTCAGCAGGTAAACATTGGAGAACTGATGGCATCAGCAATGTATCCTACAAACCAAAAGAAAGACTTGTAACATTC
AGCCTGGACACCTTTGGCCCTGTTACCTTGATTCAAGATGCTCATATTAACATGCCGTACCAGTCATGGGAACTAAGACCACTTGATGTAAATAAAGTACTTTTAACTGTGACTACAGTATTTACTGA
GATTCAAATACAAATTAAGGAAAACCTCTGCATGTTATCTTCAATCAAACTAAAAGACAAGAAACACATCTCTATTTTGGAAGGAACCTGGATGACTCCTATTCCTTTCATTATTGCTTTGAAAGAAG
CTGGACTGAATATCTTTCCTACTAGACACTCTCATTTTTATGTTATTATAAACAATAAGGTTCCTTTGGTAGAAGTGAAAGCTTATCGACAGATGGCCCTACTAAGTTCTGCTTTTGCATTTGGTTGG
AGCAAGTGGAACCTACTATGTAATTCTACAAAAGTCGTATTTAAGTGGTGACAGAGCACAAAGACTGAAGATCAAGGAAGAGAGTGAGGCATTTTCTGAAGCACTTAAAGAAGAAACTGAGTTTCATT
CTACTTTATATCACATGGTGAAGGATTTTGCTTCTGAGGAAGCAATGGAGAAAGTCAGGAGTTCCAACTGTCAGTTTGTCAACTCTGTGTGCCACATGCTGCTCTCTACCAGATTGCTCAGCTACTCC
TAACCTCCACTTACAAACTGTATTGTAAGTATGAAGAACCAAGCATGGTGAAAGACAGGTATTTCTGCAACACAATGTAATGAGTGAATGAATACATTTCAAATCAACTATTAAAAATTTTCTAATCT
GCA

hide sequence

RefSeq Acc Id:

XM_047429074 ⟹ XP_047285030

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	25,108,289 - 25,195,160 (-)	NCBI

RefSeq Acc Id:

XM_047429075 ⟹ XP_047285031

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	25,108,289 - 25,195,160 (-)	NCBI

RefSeq Acc Id:

XM_047429076 ⟹ XP_047285032

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	25,114,655 - 25,195,160 (-)	NCBI

RefSeq Acc Id:

XM_047429077 ⟹ XP_047285033

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	25,108,289 - 25,195,160 (-)	NCBI

RefSeq Acc Id:

XM_047429078 ⟹ XP_047285034

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	25,114,655 - 25,195,160 (-)	NCBI

RefSeq Acc Id:

XM_054372411 ⟹ XP_054228386

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	24,979,200 - 25,066,403 (-)	NCBI

RefSeq Acc Id:

XM_054372412 ⟹ XP_054228387

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	24,977,958 - 25,066,403 (-)	NCBI

RefSeq Acc Id:

XM_054372413 ⟹ XP_054228388

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	24,979,200 - 25,066,403 (-)	NCBI

RefSeq Acc Id:

XM_054372414 ⟹ XP_054228389

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	24,979,200 - 25,066,403 (-)	NCBI

RefSeq Acc Id:

XM_054372415 ⟹ XP_054228390

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	24,979,200 - 25,066,403 (-)	NCBI

RefSeq Acc Id:

XM_054372416 ⟹ XP_054228391

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	24,979,200 - 25,066,403 (-)	NCBI

RefSeq Acc Id:

XM_054372417 ⟹ XP_054228392

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	24,979,200 - 25,066,403 (-)	NCBI

RefSeq Acc Id:

XM_054372418 ⟹ XP_054228393

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	24,985,588 - 25,066,403 (-)	NCBI

RefSeq Acc Id:

XM_054372419 ⟹ XP_054228394

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	24,985,720 - 25,066,403 (-)	NCBI

RefSeq Acc Id:

XM_054372420 ⟹ XP_054228395

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	24,985,588 - 25,066,403 (-)	NCBI

RefSeq Acc Id:

XM_054372421 ⟹ XP_054228396

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	24,979,200 - 25,066,403 (-)	NCBI

RefSeq Acc Id:

XM_054372422 ⟹ XP_054228397

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	24,985,588 - 25,066,403 (-)	NCBI


Protein RefSeqs	NP_001076441	(Get FASTA)	NCBI Sequence Viewer
	NP_001076442	(Get FASTA)	NCBI Sequence Viewer
	NP_001191030	(Get FASTA)	NCBI Sequence Viewer
	NP_001191031	(Get FASTA)	NCBI Sequence Viewer
	NP_001306906	(Get FASTA)	NCBI Sequence Viewer
	NP_001306907	(Get FASTA)	NCBI Sequence Viewer
	NP_001338990	(Get FASTA)	NCBI Sequence Viewer
	NP_001338991	(Get FASTA)	NCBI Sequence Viewer
	NP_001338992	(Get FASTA)	NCBI Sequence Viewer
	NP_001338993	(Get FASTA)	NCBI Sequence Viewer
	NP_001338994	(Get FASTA)	NCBI Sequence Viewer
	NP_001338995	(Get FASTA)	NCBI Sequence Viewer
	NP_001338996	(Get FASTA)	NCBI Sequence Viewer
	NP_001338997	(Get FASTA)	NCBI Sequence Viewer
	NP_060742	(Get FASTA)	NCBI Sequence Viewer
	XP_005253463	(Get FASTA)	NCBI Sequence Viewer
	XP_006719164	(Get FASTA)	NCBI Sequence Viewer
	XP_011519025	(Get FASTA)	NCBI Sequence Viewer
	XP_011519028	(Get FASTA)	NCBI Sequence Viewer
	XP_011519029	(Get FASTA)	NCBI Sequence Viewer
	XP_016875049	(Get FASTA)	NCBI Sequence Viewer
	XP_016875054	(Get FASTA)	NCBI Sequence Viewer
	XP_047285030	(Get FASTA)	NCBI Sequence Viewer
	XP_047285031	(Get FASTA)	NCBI Sequence Viewer
	XP_047285032	(Get FASTA)	NCBI Sequence Viewer
	XP_047285033	(Get FASTA)	NCBI Sequence Viewer
	XP_047285034	(Get FASTA)	NCBI Sequence Viewer
	XP_054228386	(Get FASTA)	NCBI Sequence Viewer
	XP_054228387	(Get FASTA)	NCBI Sequence Viewer
	XP_054228388	(Get FASTA)	NCBI Sequence Viewer
	XP_054228389	(Get FASTA)	NCBI Sequence Viewer
	XP_054228390	(Get FASTA)	NCBI Sequence Viewer
	XP_054228391	(Get FASTA)	NCBI Sequence Viewer
	XP_054228392	(Get FASTA)	NCBI Sequence Viewer
	XP_054228393	(Get FASTA)	NCBI Sequence Viewer
	XP_054228394	(Get FASTA)	NCBI Sequence Viewer
	XP_054228395	(Get FASTA)	NCBI Sequence Viewer
	XP_054228396	(Get FASTA)	NCBI Sequence Viewer
	XP_054228397	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH28415	(Get FASTA)	NCBI Sequence Viewer
	AAH47415	(Get FASTA)	NCBI Sequence Viewer
	AAH57795	(Get FASTA)	NCBI Sequence Viewer
	AAI17282	(Get FASTA)	NCBI Sequence Viewer
	AAI17284	(Get FASTA)	NCBI Sequence Viewer
	AAQ93499	(Get FASTA)	NCBI Sequence Viewer
	BAA91908	(Get FASTA)	NCBI Sequence Viewer
	BAG52654	(Get FASTA)	NCBI Sequence Viewer
	BAG60304	(Get FASTA)	NCBI Sequence Viewer
	BAG63223	(Get FASTA)	NCBI Sequence Viewer
	BAG63589	(Get FASTA)	NCBI Sequence Viewer
	BAG65388	(Get FASTA)	NCBI Sequence Viewer
	EAW96507	(Get FASTA)	NCBI Sequence Viewer
	EAW96508	(Get FASTA)	NCBI Sequence Viewer
	EAW96509	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000313141
	ENSP00000313141.9
	ENSP00000346126
	ENSP00000346126.5
	ENSP00000379310
	ENSP00000379313
	ENSP00000379313.2
	ENSP00000437373
	ENSP00000437373.1
	ENSP00000501714
	ENSP00000501814
	ENSP00000502075
GenBank Protein	Q6TDU7	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_060742 ⟸ NM_018272
- Peptide Label:	isoform a
- UniProtKB:	F8W8F9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MGPKAKKSGSKKKKVTKAERLKLLQEEEERRLKEEEEARLKYEKEEMERLEIQRIEKEKWHRLEAKDLERRNEELEELYLLERCFPEAEKLKQETKLLSQWKHYIQCDGSPDPSVAQEMNTFISLWKE KTNETFEEVIEKSKVVLNLIEKLKFILLETPPCDLQDKNIIQYQESILQLQELLHLKFGVATEILLKQASTLADLDSGNMEKVIKDENVTLYVWANLKKNPRHRSVRFSETQIGFEIPRILATSDIAV RLLHTHYDHVSALHPVSTPSKEYTSAVTELVKDDVKNVEKAISKEVEEESKQQERGSHLIQEEEIKVEEEQGDIEVKMSSAEEESEAIKCEREMKVLSETVSAAQLLLVENSSEKPDFFEDNVVDLCQ FTTLGGVYHLDILELPPQCKPVKGWMIVEILKEGLQKYTYPPETTEEFETENAFPPIEVTLEVHENVIFFEDPVVVRWDAEGKHWRTDGISNVSYKPKERLVTFSLDTFGPVTLIQDAHINMPYQSWE LRPLDVNKVLLTVTTVFTEIQIQIKENLCMLSSIKLKDKKHISILEGTWMTPIPFIIALKEAGLNIFPTRHSHFYVIINNKVPLVEVKAYRQMALLSSAFAFGWSKWNLLCNSTKVVFKVREHLTEEC TENPNWALLMFSGDRAQRLKIKEESEAFSEALKEETEFHSTLYHMVKDFASEEAMEKVRSSNCQFVNSVCHMLLSTRLLSYS hide sequence

RefSeq Acc Id:	NP_001076442 ⟸ NM_001082973
- Peptide Label:	isoform b
- UniProtKB:	Q6TDU7 (UniProtKB/Swiss-Prot), Q5U5K5 (UniProtKB/Swiss-Prot), Q4G171 (UniProtKB/Swiss-Prot), Q17RL2 (UniProtKB/Swiss-Prot), F5H6T6 (UniProtKB/Swiss-Prot), B4DNP2 (UniProtKB/Swiss-Prot), Q9NV50 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MSGSKKKKVTKAERLKLLQEEEERRLKEEEEARLKYEKEEMERLEIQRIEKEKWHRLEAKDLERRNEELEELYLLERCFPEAEKLKQETKLLSQWKHYIQCDGSPDPSVAQEMNTFISLWKEKTNETF EEVIEKSKVVLNLIEKLKFILLETPPCDLQDKNIIQYQESILQLQELLHLKFGVATEILLKQASTLADLDSGNMEKVIKDENVTLYVWANLKKNPRHRSVRFSETQIGFEIPRILATSDIAVRLLHTH YDHVSALHPVSTPSKEYTSAVTELVKDDVKNVEKAISKEVEEESKQQERGSHLIQEEEIKVEEEQGDIEVKMSSAEEESEAIKCEREMKVLSETVSAAQLLLVENSSEKPDFFEDNVVDLCQFTTLGG VYHLDILELPPQCKPVKGWMIVEILKEGLQKYTYPPETTEEFETENAFPPIEVTLEVHENVIFFEDPVVVRWDAEGKHWRTDGISNVSYKPKERLVTFSLDTFGPVTLIQDAHINMPYQSWELRPLDV NKVLLTVTTVFTEIQIQIKENLCMLSSIKLKDKKHISILEGTWMTPIPFIIALKEAGLNIFPTRHSHFYVIINNKVPLVEVKAYRQMALLSSAFAFGWSKWNLLCNSTKVVFKVREHLTEECTENPNW ALLMFSGDRAQRLKIKEESEAFSEALKEETEFHSTLYHMVKDFASEEAMEKVRSSNCQFVNSVCHMLLSTRLLSYS hide sequence

RefSeq Acc Id:	NP_001076441 ⟸ NM_001082972
- Peptide Label:	isoform c
- UniProtKB:	Q6TDU7 (UniProtKB/Swiss-Prot), B4E376 (UniProtKB/TrEMBL)
- Sequence:	show sequence MRQTGGGATTDSASPVLNNVIKSQSYFTAKRVGLGNNSYLGVGRPSSQQWLSLPGPGGQGPKAKKSGSKKKKVTKAERLKLLQEEEERRLKEEEEARLKYEKEEMERLEIQRIEKEKWHRLEAKDLER RNEELEELYLLERCFPEAEKLKQETKLLSQWKHYIQCDGSPDPSVAQEMNTFISLWKEKTNETFEEVIEKSKVVLNLIEKLKFILLETPPCDLQDKNIIQYQESILQLQELLHLKFGVATEILLKQAS TLADLDSGNMEKVIKDENVTLYVWANLKKNPRHRSVRFSETQIGFEIPRILATSDIAVRLLHTHYDHVSALHPVSTPSKEYTSAVTELVKDDVKNVEKAISKEVEEESKQQERGSHLIQEEEIKVEEE QGDIEVKMSSAEEESEAIKCEREMKVLSETVSAAQLLLVENSSEKPDFFEDNVVDLCQFTTLGGVYHLDILELPPQCKPVKGWMIVEILKEGLQKYTYPPETTEEFETENAFPPIEVTLEVHENVIFF EDPVVVRWDAEGKHWRTDGISNVSYKPKERLVTFSLDTFGPVTLIQDAHINMPYQSWELRPLDVNKVLLTVTTVFTEIQIQIKENLCMLSSIKLKDKKHISILEGTWMTPIPFIIALKEAGLNIFPTR HSHFYVIINNKVPLVEVKAYRQMALLSSAFAFGWSKWNLLCNSTKVVFKW hide sequence

RefSeq Acc Id:	NP_001191030 ⟸ NM_001204101
- Peptide Label:	isoform e
- UniProtKB:	A0A6Q8PG26 (UniProtKB/TrEMBL)
- Sequence:	show sequence MDLERRNEELEELYLLERCFPEAEKLKQETKLLSQWKHYIQCDGSPDPSVAQEMNTFISLWKEK TNETFEEVIEKSKVVLNLIEKLKFILLETPPCDLQDKNIIQYQESILQLQELLHLKFGVATEILLKQASTLADLDSGNMEKVIKDENVTLYVWANLKKNPRHRSVRFSETQIGFEIPRILATSDIAVR LLHTHYDHVSALHPVSTPSKEYTSAVTELVKDDVKNVEKAISKEVEEESKQQERGSHLIQEEEIKVEEEQGDIEVKMSSAEEESEAIKCEREMKVLSETVSAAQLLLVENSSEKPDFFEDNVVDLCQF TTLGGVYHLDILELPPQCKPVKGWMIVEILKEGLQKYTYPPETTEEFETENAFPPIEVTLEVHENVIFFEDPVVVRWDAEGKHWRTDGISNVSYKPKERLVTFSLDTFGPVTLIQDAHINMPYQSWEL RPLDVNKVLLTVTTVFTEIQIQIKENLCMLSSIKLKDKKHISILEGTWMTPIPFIIALKEAGLNIFPTRHSHFYVIINNKVPLVEVKAYRQMALLSSAFAFGWSKWNLLCNSTKVVFKVREHLTEECT ENPNWALLMFSGDRAQRLKIKEESEAFSEALKEETEFHSTLYHMVKDFASEEAMEKVRSSNCQFVNSVCHMLLSTRLLSYS hide sequence

RefSeq Acc Id:	NP_001191031 ⟸ NM_001204102
- Peptide Label:	isoform d
- UniProtKB:	A0A6Q8PG26 (UniProtKB/TrEMBL)
- Sequence:	show sequence MERLEIQRIEKEKWHRLEAKDLERRNEELEELYLLERCFPEAEKLKQETKLLSQWKHYIQCDGSPDPSVAQEMNTFISLWKEKTNETFEEVIEKSKVVLNLIEKLKFILLETPPCDLQDKNIIQYQES ILQLQELLHLKFGVATEILLKQASTLADLDSGNMEKVIKDENVTLYVWANLKKNPRHRSVRFSETQIGFEIPRILATSDIAVRLLHTHYDHVSALHPVSTPSKEYTSAVTELVKDDVKNVEKAISKEV EEESKQQERGSHLIQEEEIKVEEEQGDIEVKMSSAEEESEAIKCEREMKVLSETVSAAQLLLVENSSEKPDFFEDNVVDLCQFTTLGGVYHLDILELPPQCKPVKGWMIVEILKEGLQKYTYPPETTE EFETENAFPPIEVTLEVHENVIFFEDPVVVRWDAEGKHWRTDGISNVSYKPKERLVTFSLDTFGPVTLIQDAHINMPYQSWELRPLDVNKVLLTVTTVFTEIQIQIKENLCMLSSIKLKDKKHISILE GTWMTPIPFIIALKEAGLNIFPTRHSHFYVIINNKVPLVEVKAYRQMALLSSAFAFGWSKWNLLCNSTKVVFKVREHLTEECTENPNWALLMFSGDRAQRLKIKEESEAFSEALKEETEFHSTLYHMV KDFASEEAMEKVRSSNCQFVNSVCHMLLSTRLLSYS hide sequence

Protein Domains

CASC1 C-terminal IC97/Casc1 N-terminal

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q6TDU7-F1-model_v2	AlphaFold	Q6TDU7	1-716	view protein structure

RGD ID:

7223453

Promoter ID:

EPDNEW_H17473

Type:

initiation region

Name:

CASC1_1

Description:

cancer susceptibility 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	25,195,160 - 25,195,220	EPDNEW

RGD ID:

6789929

Promoter ID:

HG_KWN:15217

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

ENST00000395992, NM_001001660, NM_001082972, NM_001082973, NM_018272, UC001RGJ.1, UC001RGO.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	12	25,239,249 - 25,239,749 (-)	MPROMDB

Database	Acc Id	Source(s)
COSMIC	DNAI7	COSMIC
Ensembl Genes	ENSG00000118307	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000320267	ENTREZGENE
	ENST00000320267.13	UniProtKB/Swiss-Prot
	ENST00000354189	ENTREZGENE
	ENST00000354189.9	UniProtKB/Swiss-Prot
	ENST00000395987	ENTREZGENE
	ENST00000395990	ENTREZGENE
	ENST00000395990.6	UniProtKB/Swiss-Prot
	ENST00000545133	ENTREZGENE
	ENST00000545133.5	UniProtKB/Swiss-Prot
	ENST00000554533	ENTREZGENE
	ENST00000557684	ENTREZGENE
	ENST00000674567	ENTREZGENE
	ENST00000676236	ENTREZGENE
GTEx	ENSG00000118307	GTEx
HGNC ID	HGNC:29599	ENTREZGENE
Human Proteome Map	DNAI7	Human Proteome Map
InterPro	Casc1	UniProtKB/Swiss-Prot
	CASC1_C	UniProtKB/Swiss-Prot
	Casc1_N	UniProtKB/Swiss-Prot
KEGG Report	hsa:55259	UniProtKB/Swiss-Prot
NCBI Gene	55259	ENTREZGENE
OMIM	616906	OMIM
PANTHER	DYNEIN AXONEMAL INTERMEDIATE CHAIN 7	UniProtKB/Swiss-Prot
	PTHR20929	UniProtKB/Swiss-Prot
Pfam	Casc1_C	UniProtKB/Swiss-Prot
	Casc1_N	UniProtKB/Swiss-Prot
PharmGKB	PA166352473	PharmGKB
PRINTS	CANCERSCCP1	UniProtKB/Swiss-Prot
UniProt	A0A6Q8PG26	ENTREZGENE, UniProtKB/TrEMBL
	B3KS92	ENTREZGENE, UniProtKB/TrEMBL
	B4DNP2	ENTREZGENE
	B4DY27	ENTREZGENE, UniProtKB/TrEMBL
	B4E376	ENTREZGENE, UniProtKB/TrEMBL
	CASC1_HUMAN	UniProtKB/Swiss-Prot
	F5H6T6	ENTREZGENE
	F8W8F9	ENTREZGENE, UniProtKB/TrEMBL
	G3V2J3_HUMAN	UniProtKB/TrEMBL
	G3V333_HUMAN	UniProtKB/TrEMBL
	G3V3G6_HUMAN	UniProtKB/TrEMBL
	H0YJM7_HUMAN	UniProtKB/TrEMBL
	Q17RL2	ENTREZGENE
	Q4G171	ENTREZGENE
	Q5U5K5	ENTREZGENE
	Q6TDU7	ENTREZGENE
	Q9NV50	ENTREZGENE
UniProt Secondary	B4DNP2	UniProtKB/Swiss-Prot
	F5H6T6	UniProtKB/Swiss-Prot
	Q17RL2	UniProtKB/Swiss-Prot
	Q4G171	UniProtKB/Swiss-Prot
	Q5U5K5	UniProtKB/Swiss-Prot
	Q9NV50	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2021-02-15	DNAI7	dynein axonemal intermediate chain 7	CFAP94	cilia and flagella associated protein 94	Symbol and/or name change	19259463	PROVISIONAL
2020-05-11	CFAP94	cilia and flagella associated protein 94	CASC1	cancer susceptibility 1	Symbol and/or name change	19259463	PROVISIONAL
2017-01-31	CASC1	cancer susceptibility 1		cancer susceptibility candidate 1	Symbol and/or name change	5135510	APPROVED

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


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


Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
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MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable

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Imported Disease Annotations - CTD