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Gene: ARMC3 (armadillo repeat containing 3) Homo sapiens

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Symbol:

ARMC3

Name:

armadillo repeat containing 3

RGD ID:

1312695

HGNC Page

HGNC:30964

Description:

Predicted to be involved in flagellated sperm motility; ribophagy; and spermatid development. Located in extracellular exosome.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

armadillo repeat-containing protein 3; beta-catenin-like protein; cancer/testis antigen 81; CT81; FLJ25845; FLJ32827; KU-CT-1; RP11-300B11.1; VAC8

RGD Orthologs

Alliance Orthologs

More Info

more info ...

More Info

Species	Gene symbol and name	Data Source	Assertion derived from	less info ...
Orthologs ¹				less info ...
Mus musculus (house mouse):	Armc3 (armadillo repeat containing 3)	HGNC	Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):	Armc3 (armadillo repeat containing 3)	RGD	RGD
Chinchilla lanigera (long-tailed chinchilla):	Armc3 (armadillo repeat containing 3)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	ARMC3 (armadillo repeat containing 3)	NCBI	Ortholog
Canis lupus familiaris (dog):	ARMC3 (armadillo repeat containing 3)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Armc3 (armadillo repeat containing 3)	NCBI	Ortholog
Sus scrofa (pig):	ARMC3 (armadillo repeat containing 3)	HGNC	EggNOG, Ensembl, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	ARMC3 (armadillo repeat containing 3)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Armc3 (armadillo repeat containing 3)	NCBI	Ortholog
Other homologs ²
Rattus norvegicus (Norway rat):	Sardh (sarcosine dehydrogenase)	HGNC	OMA
Alliance orthologs ³
Mus musculus (house mouse):	Armc3 (armadillo repeat containing 3)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Rattus norvegicus (Norway rat):	Armc3 (armadillo repeat containing 3)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	armc3 (armadillo repeat containing 3)	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid\|ZFIN)
Drosophila melanogaster (fruit fly):	CG13326	Alliance	DIOPT (OrthoFinder\|OrthoInspector\|PANTHER)
Xenopus tropicalis (tropical clawed frog):	armc3	Alliance	DIOPT (Ensembl Compara\|OMA\|OrthoFinder\|PANTHER\|PhylomeDB)
Xenopus laevis (African clawed frog):	armc3.L	Alliance	DIOPT (Xenbase)

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	10	22,928,053 - 23,038,523 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	10	22,928,024 - 23,038,523 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	10	23,216,982 - 23,327,452 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	10	23,256,966 - 23,366,520 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	10	23,256,965 - 23,366,520	NCBI
Celera	10	22,904,614 - 23,014,160 (+)	NCBI		Celera
Cytogenetic Map	10	p12.2	NCBI
HuRef	10	22,877,824 - 22,986,594 (+)	NCBI		HuRef
CHM1_1	10	23,217,435 - 23,327,017 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	10	22,947,064 - 23,057,478 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
ARMC3	Human	Familial Persistent Stuttering 4		IAGP	(Homo sapiens)	8554872	ClinVar Annotator: match by term: Stuttering more ...	ClinVar

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

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
ARMC3	Human	1,2-dimethylhydrazine	decreases expression	ISO	Armc3 (Mus musculus)	6480464	1 and 2-Dimethylhydrazine results in decreased expression of ARMC3 mRNA	CTD	PMID:22206623
ARMC3	Human	17beta-estradiol	increases expression	EXP		6480464	Estradiol results in increased expression of ARMC3 mRNA	CTD	PMID:31614463
ARMC3	Human	2,3,7,8-Tetrachlorodibenzofuran	decreases expression	ISO	Armc3 (Rattus norvegicus)	6480464	2 more ...	CTD	PMID:32109520
ARMC3	Human	4,4'-sulfonyldiphenol	increases expression	ISO	Armc3 (Mus musculus)	6480464	bisphenol S results in increased expression of ARMC3 mRNA	CTD	PMID:30951980
ARMC3	Human	4,4'-sulfonyldiphenol	affects methylation	ISO	Armc3 (Mus musculus)	6480464	bisphenol S affects the methylation of ARMC3 gene	CTD	PMID:31683443
ARMC3	Human	6-propyl-2-thiouracil	increases expression	ISO	Armc3 (Rattus norvegicus)	6480464	Propylthiouracil results in increased expression of ARMC3 mRNA	CTD	PMID:24780913
ARMC3	Human	acetamide	increases expression	ISO	Armc3 (Rattus norvegicus)	6480464	acetamide results in increased expression of ARMC3 mRNA	CTD	PMID:31881176
ARMC3	Human	acrolein	decreases expression	ISO	Armc3 (Rattus norvegicus)	6480464	Acrolein results in decreased expression of ARMC3 mRNA	CTD	PMID:38090360
ARMC3	Human	aflatoxin B1	decreases methylation	EXP		6480464	Aflatoxin B1 results in decreased methylation of ARMC3 gene	CTD	PMID:27153756
ARMC3	Human	Aflatoxin B2 alpha	decreases methylation	EXP		6480464	aflatoxin B2 results in decreased methylation of ARMC3 intron	CTD	PMID:30157460
ARMC3	Human	aristolochic acid A	decreases expression	EXP		6480464	aristolochic acid I results in decreased expression of ARMC3 mRNA	CTD	PMID:33212167
ARMC3	Human	benzo[a]pyrene	decreases expression	EXP		6480464	Benzo(a)pyrene results in decreased expression of ARMC3 mRNA	CTD	PMID:22316170
ARMC3	Human	benzo[a]pyrene	increases methylation	EXP		6480464	Benzo(a)pyrene results in increased methylation of ARMC3 3' UTR more ...	CTD	PMID:27901495
ARMC3	Human	benzo[a]pyrene	increases expression	ISO	Armc3 (Mus musculus)	6480464	Benzo(a)pyrene results in increased expression of ARMC3 mRNA	CTD	PMID:27195522
ARMC3	Human	bis(2-ethylhexyl) phthalate	increases expression	ISO	Armc3 (Mus musculus)	6480464	Diethylhexyl Phthalate results in increased expression of ARMC3 mRNA	CTD	PMID:34319233
ARMC3	Human	bisphenol A	increases expression	ISO	Armc3 (Mus musculus)	6480464	bisphenol A results in increased expression of ARMC3 mRNA	CTD	PMID:30951980 and PMID:35598803
ARMC3	Human	bisphenol A	increases expression	ISO	Armc3 (Rattus norvegicus)	6480464	bisphenol A results in increased expression of ARMC3 mRNA	CTD	PMID:34947998
ARMC3	Human	bisphenol A	decreases expression	ISO	Armc3 (Rattus norvegicus)	6480464	bisphenol A results in decreased expression of ARMC3 mRNA	CTD	PMID:30816183
ARMC3	Human	bisphenol F	increases expression	ISO	Armc3 (Mus musculus)	6480464	bisphenol F results in increased expression of ARMC3 mRNA	CTD	PMID:30951980
ARMC3	Human	cadmium atom	multiple interactions	EXP		6480464	[Cadmium Chloride results in increased abundance of Cadmium] which results in decreased expression of ARMC3 mRNA	CTD	PMID:35301059
ARMC3	Human	cadmium dichloride	multiple interactions	EXP		6480464	[Cadmium Chloride results in increased abundance of Cadmium] which results in decreased expression of ARMC3 mRNA	CTD	PMID:35301059
ARMC3	Human	carbon nanotube	decreases expression	ISO	Armc3 (Mus musculus)	6480464	Nanotubes more ...	CTD	PMID:25554681
ARMC3	Human	CGP 52608	multiple interactions	EXP		6480464	CGP 52608 promotes the reaction [RORA protein binds to ARMC3 gene]	CTD	PMID:28238834
ARMC3	Human	chloroprene	increases expression	ISO	Armc3 (Mus musculus)	6480464	Chloroprene results in increased expression of ARMC3 mRNA	CTD	PMID:23125180
ARMC3	Human	crocidolite asbestos	increases expression	ISO	Armc3 (Mus musculus)	6480464	Asbestos and Crocidolite results in increased expression of ARMC3 mRNA	CTD	PMID:29279043
ARMC3	Human	fulvestrant	increases methylation	EXP		6480464	Fulvestrant results in increased methylation of ARMC3 gene	CTD	PMID:31601247
ARMC3	Human	glyphosate	decreases expression	ISO	Armc3 (Rattus norvegicus)	6480464	Glyphosate results in decreased expression of ARMC3 mRNA	CTD	PMID:38314887
ARMC3	Human	malathion	decreases expression	EXP		6480464	Malathion results in decreased expression of ARMC3 mRNA	CTD	PMID:37047231
ARMC3	Human	ozone	multiple interactions	ISO	Armc3 (Mus musculus)	6480464	[Air Pollutants results in increased abundance of [Ozone co-treated with Soot]] which results in increased expression of ARMC3 mRNA	CTD	PMID:34911549
ARMC3	Human	pirinixic acid	multiple interactions	EXP		6480464	[pirinixic acid binds to and results in increased activity of PPARA protein] which results in decreased expression of ARMC3 mRNA	CTD	PMID:19710929
ARMC3	Human	propanal	increases expression	EXP		6480464	propionaldehyde results in increased expression of ARMC3 mRNA	CTD	PMID:26079696
ARMC3	Human	sodium arsenite	decreases expression	ISO	Armc3 (Mus musculus)	6480464	sodium arsenite results in decreased expression of ARMC3 mRNA	CTD	PMID:36209798
ARMC3	Human	titanium dioxide	affects expression	ISO	Armc3 (Mus musculus)	6480464	titanium dioxide affects the expression of ARMC3 mRNA	CTD	PMID:23557971
ARMC3	Human	trichloroethene	decreases expression	ISO	Armc3 (Rattus norvegicus)	6480464	Trichloroethylene results in decreased expression of ARMC3 mRNA	CTD	PMID:33387578
ARMC3	Human	triphenyl phosphate	affects expression	EXP		6480464	triphenyl phosphate affects the expression of ARMC3 mRNA	CTD	PMID:37042841
ARMC3	Human	valproic acid	decreases methylation	EXP		6480464	Valproic Acid results in decreased methylation of ARMC3 gene	CTD	PMID:29154799

Biological Process

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

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
ARMC3	Human	autophagy	involved_in	IEA	UniProtKB-KW:KW-0072	150520179		UniProt	GO_REF:0000043
ARMC3	Human	cell differentiation	involved_in	IEA	UniProtKB-KW:KW-0221	150520179		UniProt	GO_REF:0000043
ARMC3	Human	flagellated sperm motility	involved_in	ISS	UniProtKB:A2AU72	150520179		UniProt	GO_REF:0000024
ARMC3	Human	ribophagy	involved_in	ISS	UniProtKB:A2AU72	150520179		UniProt	GO_REF:0000024
ARMC3	Human	spermatid development	involved_in	ISS	UniProtKB:A2AU72	150520179		UniProt	GO_REF:0000024
ARMC3	Human	spermatogenesis	involved_in	IEA	UniProtKB-KW:KW-0744	150520179		UniProt	GO_REF:0000043

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)
ARMC3	Human	extracellular exosome	located_in	HDA		150520179	PMID:19056867	UniProt	PMID:19056867

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)
ARMC3	Human	protein binding	enables	ISO	UniProtKB:O88597 more ...	9068941	PMID:34428398	UniProt	PMID:34428398

#	Reference Title	Reference Citation
1.	ClinVar Automated Import and Annotation Pipeline	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

PMID:8889548	PMID:12477932	PMID:14702039	PMID:16385451	PMID:16397042	PMID:16915934	PMID:19056867	PMID:20379614	PMID:23382691	PMID:26923438	PMID:30021884	PMID:32393512
PMID:32616903	PMID:33961781	PMID:34705610	PMID:35575683	PMID:36553564	PMID:39221575

ARMC3
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	10	22,928,053 - 23,038,523 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	10	22,928,024 - 23,038,523 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	10	23,216,982 - 23,327,452 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	10	23,256,966 - 23,366,520 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	10	23,256,965 - 23,366,520	NCBI
Celera	10	22,904,614 - 23,014,160 (+)	NCBI		Celera
Cytogenetic Map	10	p12.2	NCBI
HuRef	10	22,877,824 - 22,986,594 (+)	NCBI		HuRef
CHM1_1	10	23,217,435 - 23,327,017 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	10	22,947,064 - 23,057,478 (+)	NCBI		T2T-CHM13v2.0

Armc3
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	2	19,203,676 - 19,315,054 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	2	19,204,113 - 19,315,052 (+)	Ensembl		GRCm39 Ensembl
GRCm38	2	19,198,865 - 19,310,243 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	2	19,199,302 - 19,310,241 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	2	19,120,745 - 19,231,861 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	2	19,116,872 - 19,227,988 (+)	NCBI		MGSCv36	mm8
Celera	2	19,104,793 - 19,208,375 (+)	NCBI		Celera
Cytogenetic Map	2	A3	NCBI
cM Map	2	13.2	NCBI

Armc3
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	17	86,722,436 - 86,825,899 (+)	NCBI		GRCr8
mRatBN7.2	17	81,814,087 - 81,917,534 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	17	81,832,518 - 81,917,531 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	17	85,297,704 - 85,382,538 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	17	89,133,120 - 89,217,975 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	17	83,149,878 - 83,234,738 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	17	85,895,841 - 86,009,403 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	17	85,914,410 - 86,009,396 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	17	87,610,808 - 87,726,061 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	17	93,278,359 - 93,361,623 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
Celera	17	81,103,766 - 81,187,813 (+)	NCBI		Celera
Cytogenetic Map	17	q12.3	NCBI

Armc3
(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_004955429	5,947,940 - 6,051,038 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955429	5,949,180 - 6,050,690 (-)	NCBI	ChiLan1.0	ChiLan1.0

ARMC3
(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	8	35,527,861 - 35,721,296 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	10	35,533,182 - 35,724,736 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	10	23,085,591 - 23,196,943 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	10	23,460,342 - 23,570,908 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	10	23,460,348 - 23,570,908 (+)	Ensembl	panpan1.1		panPan2

ARMC3
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	2	10,201,347 - 10,302,951 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	2	10,202,329 - 10,302,733 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	2	8,895,514 - 8,996,035 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	2	8,400,242 - 8,500,787 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	2	8,400,246 - 8,500,665 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	2	7,765,696 - 7,866,137 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	2	7,848,514 - 7,949,051 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	2	8,016,960 - 8,117,519 (-)	NCBI		UU_Cfam_GSD_1.0

Armc3
(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_024409344	22,746,484 - 22,844,963 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936520	5,116,628 - 5,211,163 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936520	5,116,628 - 5,211,163 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

ARMC3
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	10	51,959,610 - 52,049,425 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	10	51,959,571 - 52,050,071 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	10	57,615,066 - 57,704,928 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

ARMC3
(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	9	22,683,911 - 22,800,051 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	9	22,685,028 - 22,800,926 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666051	28,442,972 - 28,564,471 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Armc3
(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_004624796	5,678,701 - 5,778,443 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624796	5,679,159 - 5,781,173 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants in ARMC3
73 total Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
NM_173081.5(ARMC3):c.1676C>G (p.Thr559Ser)	single nucleotide variant	not specified [RCV004157926]	Chr10:23003359 [GRCh38] Chr10:23292288 [GRCh37] Chr10:10p12.2	uncertain significance
GRCh38/hg38 10p15.3-12.1(chr10:90421-29058318)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053512]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053512]\|See cases [RCV000053512]	Chr10:90421..29058318 [GRCh38] Chr10:224406..29347247 [GRCh37] Chr10:126361..29387253 [NCBI36] Chr10:10p15.3-12.1	pathogenic
NM_173081.4(ARMC3):c.1575C>T (p.Ile525=)	single nucleotide variant	Malignant melanoma [RCV000068890]	Chr10:23003258 [GRCh38] Chr10:23292187 [GRCh37] Chr10:23332193 [NCBI36] Chr10:10p12.2	not provided
GRCh38/hg38 10p15.3-12.1(chr10:90205-26339978)x3	copy number gain	See cases [RCV000138428]	Chr10:90205..26339978 [GRCh38] Chr10:224406..26628907 [GRCh37] Chr10:126145..26668913 [NCBI36] Chr10:10p15.3-12.1	pathogenic
GRCh38/hg38 10p12.31-11.22(chr10:19088161-32732293)x3	copy number gain	See cases [RCV000139427]	Chr10:19088161..32732293 [GRCh38] Chr10:19377090..33021221 [GRCh37] Chr10:19417096..33061227 [NCBI36] Chr10:10p12.31-11.22	likely pathogenic
GRCh38/hg38 10p15.1-q11.22(chr10:4604734-48074662)x3	copy number gain	See cases [RCV000141497]	Chr10:4604734..48074662 [GRCh38] Chr10:4646926..47531169 [GRCh37] Chr10:4636926..47125152 [NCBI36] Chr10:10p15.1-q11.22	benign
GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143)	copy number gain	See cases [RCV000511389]	Chr10:100027..135427143 [GRCh37] Chr10:10p15.3-q26.3	pathogenic\|uncertain significance
GRCh37/hg19 10p15.3-11.23(chr10:100026-30278548)x3	copy number gain	See cases [RCV000447131]	Chr10:100026..30278548 [GRCh37] Chr10:10p15.3-11.23	pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:93297-135378918)x3	copy number gain	See cases [RCV000448750]	Chr10:93297..135378918 [GRCh37] Chr10:10p15.3-q26.3	pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143)x3	copy number gain	See cases [RCV000510861]	Chr10:100027..135427143 [GRCh37] Chr10:10p15.3-q26.3	pathogenic
GRCh37/hg19 10p15.3-q11.23(chr10:100026-50961640)x3	copy number gain	See cases [RCV000510893]	Chr10:100026..50961640 [GRCh37] Chr10:10p15.3-q11.23	pathogenic
NM_173081.5(ARMC3):c.916+1G>A	single nucleotide variant	Stuttering, familial persistent, 4 [RCV003164495]	Chr10:22968490 [GRCh38] Chr10:23257419 [GRCh37] Chr10:10p12.2	uncertain significance
GRCh37/hg19 10p15.3-q26.3(chr10:98087-135477883)x3	copy number gain	not provided [RCV000749465]	Chr10:98087..135477883 [GRCh37] Chr10:10p15.3-q26.3	pathogenic
NM_173081.5(ARMC3):c.1712G>T (p.Gly571Val)	single nucleotide variant	not specified [RCV004324663]	Chr10:23003395 [GRCh38] Chr10:23292324 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.99G>A (p.Met33Ile)	single nucleotide variant	not specified [RCV004261946]	Chr10:22946194 [GRCh38] Chr10:23235123 [GRCh37] Chr10:10p12.2	uncertain significance
GRCh37/hg19 10p15.3-q11.22(chr10:135655-47688677)x4	copy number gain	Mosaic supernumerary isodicentric chromosome 10 [RCV001825164]	Chr10:135655..47688677 [GRCh37] Chr10:10p15.3-q11.22	not provided
GRCh37/hg19 10p15.1-11.21(chr10:6273934-34732521)	copy number gain	not specified [RCV002052863]	Chr10:6273934..34732521 [GRCh37] Chr10:10p15.1-11.21	pathogenic
GRCh37/hg19 10p12.31-12.2(chr10:22208767-23220277)x3	copy number gain	not provided [RCV002474612]	Chr10:22208767..23220277 [GRCh37] Chr10:10p12.31-12.2	uncertain significance
NM_173081.5(ARMC3):c.509C>T (p.Ser170Phe)	single nucleotide variant	not specified [RCV004236115]	Chr10:22959546 [GRCh38] Chr10:23248475 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.2494G>C (p.Asp832His)	single nucleotide variant	not specified [RCV004118035]	Chr10:23037354 [GRCh38] Chr10:23326283 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.1333A>G (p.Ile445Val)	single nucleotide variant	not specified [RCV004199503]	Chr10:22998305 [GRCh38] Chr10:23287234 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.1591G>A (p.Val531Ile)	single nucleotide variant	not specified [RCV004080404]	Chr10:23003274 [GRCh38] Chr10:23292203 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.1003G>A (p.Ala335Thr)	single nucleotide variant	not specified [RCV004193259]	Chr10:22981426 [GRCh38] Chr10:23270355 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.263C>T (p.Thr88Ile)	single nucleotide variant	not specified [RCV004140460]	Chr10:22955903 [GRCh38] Chr10:23244832 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.209A>G (p.Glu70Gly)	single nucleotide variant	not specified [RCV004219649]	Chr10:22955849 [GRCh38] Chr10:23244778 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.1180G>T (p.Ala394Ser)	single nucleotide variant	not specified [RCV004080821]	Chr10:22998152 [GRCh38] Chr10:23287081 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.2174T>C (p.Met725Thr)	single nucleotide variant	not specified [RCV004183637]	Chr10:23030724 [GRCh38] Chr10:23319653 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.1323G>A (p.Met441Ile)	single nucleotide variant	not provided [RCV004695453]\|not specified [RCV004123301]	Chr10:22998295 [GRCh38] Chr10:23287224 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.712A>G (p.Ile238Val)	single nucleotide variant	not specified [RCV004191043]	Chr10:22962058 [GRCh38] Chr10:23250987 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.2027C>T (p.Thr676Ile)	single nucleotide variant	not specified [RCV004091560]	Chr10:23008913 [GRCh38] Chr10:23297842 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.1634A>C (p.Asn545Thr)	single nucleotide variant	not specified [RCV004178660]	Chr10:23003317 [GRCh38] Chr10:23292246 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.454T>A (p.Leu152Ile)	single nucleotide variant	not specified [RCV004171460]	Chr10:22959491 [GRCh38] Chr10:23248420 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.1765G>A (p.Glu589Lys)	single nucleotide variant	not specified [RCV004170871]	Chr10:23006917 [GRCh38] Chr10:23295846 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.1409T>C (p.Val470Ala)	single nucleotide variant	not specified [RCV004236967]	Chr10:22998381 [GRCh38] Chr10:23287310 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.1078C>G (p.Gln360Glu)	single nucleotide variant	not specified [RCV004089849]	Chr10:22981603 [GRCh38] Chr10:23270532 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.2333T>C (p.Phe778Ser)	single nucleotide variant	not specified [RCV004193140]	Chr10:23032947 [GRCh38] Chr10:23321876 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.1204C>A (p.Pro402Thr)	single nucleotide variant	not specified [RCV004133582]	Chr10:22998176 [GRCh38] Chr10:23287105 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.1796G>A (p.Arg599Gln)	single nucleotide variant	not specified [RCV004145111]	Chr10:23006948 [GRCh38] Chr10:23295877 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.980C>T (p.Ser327Phe)	single nucleotide variant	not specified [RCV004258985]	Chr10:22981403 [GRCh38] Chr10:23270332 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.86C>G (p.Thr29Ser)	single nucleotide variant	not specified [RCV004275615]	Chr10:22946181 [GRCh38] Chr10:23235110 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.2461G>A (p.Gly821Ser)	single nucleotide variant	not specified [RCV004267172]	Chr10:23037321 [GRCh38] Chr10:23326250 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.2153C>T (p.Pro718Leu)	single nucleotide variant	not specified [RCV004257058]	Chr10:23030703 [GRCh38] Chr10:23319632 [GRCh37] Chr10:10p12.2	uncertain significance
GRCh37/hg19 10p14-q26.3(chr10:11138692-135427143)	copy number gain	Distal trisomy 10q [RCV003319593]	Chr10:11138692..135427143 [GRCh37] Chr10:10p14-q26.3	pathogenic
NM_173081.5(ARMC3):c.2434G>T (p.Gly812Cys)	single nucleotide variant	not specified [RCV004294578]	Chr10:23037294 [GRCh38] Chr10:23326223 [GRCh37] Chr10:10p12.2	uncertain significance
GRCh37/hg19 10p13-q26.3(chr10:12829206-135427143)	copy number loss	Distal 10q deletion syndrome [RCV003319583]	Chr10:12829206..135427143 [GRCh37] Chr10:10p13-q26.3	pathogenic
NM_173081.5(ARMC3):c.20A>C (p.Lys7Thr)	single nucleotide variant	not specified [RCV004348801]	Chr10:22932016 [GRCh38] Chr10:23220945 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.1717T>C (p.Tyr573His)	single nucleotide variant	not specified [RCV004363286]	Chr10:23003400 [GRCh38] Chr10:23292329 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.491C>T (p.Pro164Leu)	single nucleotide variant	not specified [RCV004337030]	Chr10:22959528 [GRCh38] Chr10:23248457 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.902A>G (p.Lys301Arg)	single nucleotide variant	not specified [RCV004350152]	Chr10:22968475 [GRCh38] Chr10:23257404 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.1421C>A (p.Thr474Asn)	single nucleotide variant	not specified [RCV004353963]	Chr10:22998393 [GRCh38] Chr10:23287322 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.1067A>T (p.Gln356Leu)	single nucleotide variant	not specified [RCV004417974]	Chr10:22981490 [GRCh38] Chr10:23270419 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.1052A>T (p.Asp351Val)	single nucleotide variant	not specified [RCV004417973]	Chr10:22981475 [GRCh38] Chr10:23270404 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.1741G>A (p.Gly581Ser)	single nucleotide variant	not specified [RCV004417982]	Chr10:23006893 [GRCh38] Chr10:23295822 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.1318A>C (p.Ile440Leu)	single nucleotide variant	not specified [RCV004417976]	Chr10:22998290 [GRCh38] Chr10:23287219 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.1342C>A (p.Leu448Met)	single nucleotide variant	not specified [RCV004417977]	Chr10:22998314 [GRCh38] Chr10:23287243 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.2042G>T (p.Trp681Leu)	single nucleotide variant	not specified [RCV004417983]	Chr10:23008928 [GRCh38] Chr10:23297857 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.574G>T (p.Ala192Ser)	single nucleotide variant	not specified [RCV004417989]	Chr10:22961920 [GRCh38] Chr10:23250849 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.778T>A (p.Cys260Ser)	single nucleotide variant	not specified [RCV004417991]	Chr10:22968351 [GRCh38] Chr10:23257280 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.2500C>T (p.Arg834Trp)	single nucleotide variant	not specified [RCV004417987]	Chr10:23037360 [GRCh38] Chr10:23326289 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.875A>G (p.Gln292Arg)	single nucleotide variant	not specified [RCV004417992]	Chr10:22968448 [GRCh38] Chr10:23257377 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.964G>T (p.Val322Leu)	single nucleotide variant	not specified [RCV004417993]	Chr10:22981387 [GRCh38] Chr10:23270316 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.294T>C (p.Asn98=)	single nucleotide variant	EBV-positive nodal T- and NK-cell lymphoma [RCV004557816]	Chr10:22959071 [GRCh38] Chr10:23248000 [GRCh37] Chr10:10p12.2	likely benign
NM_173081.5(ARMC3):c.1246G>A (p.Ala416Thr)	single nucleotide variant	not specified [RCV004854494]	Chr10:22998218 [GRCh38] Chr10:23287147 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.1408G>A (p.Val470Ile)	single nucleotide variant	not specified [RCV004854496]	Chr10:22998380 [GRCh38] Chr10:23287309 [GRCh37] Chr10:10p12.2	uncertain significance
GRCh37/hg19 10p15.3-q26.3(chr10:73232-135524321)x3	copy number gain	not provided [RCV000749464]	Chr10:73232..135524321 [GRCh37] Chr10:10p15.3-q26.3	pathogenic
NM_173081.5(ARMC3):c.1277C>T (p.Ala426Val)	single nucleotide variant	not specified [RCV004229814]	Chr10:22998249 [GRCh38] Chr10:23287178 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.632C>T (p.Ala211Val)	single nucleotide variant	not specified [RCV004265293]	Chr10:22961978 [GRCh38] Chr10:23250907 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.1176C>T (p.Asn392=)	single nucleotide variant	not specified [RCV004345654]	Chr10:22998148 [GRCh38] Chr10:23287077 [GRCh37] Chr10:10p12.2	likely benign
NM_173081.5(ARMC3):c.2432T>C (p.Ile811Thr)	single nucleotide variant	not specified [RCV004347898]	Chr10:23037292 [GRCh38] Chr10:23326221 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.2484G>A (p.Met828Ile)	single nucleotide variant	not specified [RCV004334300]	Chr10:23037344 [GRCh38] Chr10:23326273 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.1531G>A (p.Glu511Lys)	single nucleotide variant	not specified [RCV004356391]	Chr10:23002024 [GRCh38] Chr10:23290953 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.1117C>T (p.Arg373Trp)	single nucleotide variant	not specified [RCV004339112]	Chr10:22981642 [GRCh38] Chr10:23270571 [GRCh37] Chr10:10p12.2	likely benign
NM_173081.5(ARMC3):c.1232G>A (p.Arg411Gln)	single nucleotide variant	not specified [RCV004417975]	Chr10:22998204 [GRCh38] Chr10:23287133 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.1682A>G (p.Tyr561Cys)	single nucleotide variant	not specified [RCV004417979]	Chr10:23003365 [GRCh38] Chr10:23292294 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.1700T>C (p.Ile567Thr)	single nucleotide variant	not specified [RCV004417980]	Chr10:23003383 [GRCh38] Chr10:23292312 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.1733T>C (p.Ile578Thr)	single nucleotide variant	not specified [RCV004417981]	Chr10:23006885 [GRCh38] Chr10:23295814 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.2308G>C (p.Glu770Gln)	single nucleotide variant	not specified [RCV004417985]	Chr10:23032922 [GRCh38] Chr10:23321851 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.370G>C (p.Val124Leu)	single nucleotide variant	not specified [RCV004417988]	Chr10:22959407 [GRCh38] Chr10:23248336 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.2462G>T (p.Gly821Val)	single nucleotide variant	not specified [RCV004661012]	Chr10:23037322 [GRCh38] Chr10:23326251 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.29A>T (p.Glu10Val)	single nucleotide variant	not specified [RCV004661020]	Chr10:22932025 [GRCh38] Chr10:23220954 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.1106A>G (p.Asn369Ser)	single nucleotide variant	not specified [RCV004674304]	Chr10:22981631 [GRCh38] Chr10:23270560 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.1261G>A (p.Val421Ile)	single nucleotide variant	not specified [RCV004674305]	Chr10:22998233 [GRCh38] Chr10:23287162 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.1289C>T (p.Pro430Leu)	single nucleotide variant	not specified [RCV004674314]	Chr10:22998261 [GRCh38] Chr10:23287190 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.1678G>T (p.Gly560Cys)	single nucleotide variant	not specified [RCV004860621]	Chr10:23003361 [GRCh38] Chr10:23292290 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.679A>G (p.Met227Val)	single nucleotide variant	not specified [RCV004854493]	Chr10:22962025 [GRCh38] Chr10:23250954 [GRCh37] Chr10:10p12.2	uncertain significance
NM_173081.5(ARMC3):c.344C>A (p.Ala115Asp)	single nucleotide variant	not specified [RCV004854495]	Chr10:22959121 [GRCh38] Chr10:23248050 [GRCh37] Chr10:10p12.2	uncertain significance

Predicted Target Of

	Summary Value
Count of predictions:	1257
Count of miRNA genes:	705
Interacting mature miRNAs:	831
Transcripts:	ENST00000298032, ENST00000376528, ENST00000409049, ENST00000409983, ENST00000447081, ENST00000464017, ENST00000465729, ENST00000468003, ENST00000473919, ENST00000483596, ENST00000484642, ENST00000491803, ENST00000496741
Prediction methods:	Microtar, Miranda, Rnahybrid, Targetscan
Result types:	miRGate_prediction

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

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

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
597438732	GWAS1534806_H	systemic lupus erythematosus QTL GWAS1534806 (human)		0.0000002	systemic lupus erythematosus		10	22960180	22960181	Human
597255064	GWAS1351138_H	age at first sexual intercourse measurement QTL GWAS1351138 (human)		1e-19	age at first sexual intercourse measurement		10	22963922	22963928	Human
1643515	BW287_H	Body Weight QTL 287 (human)	2.45	0.0004	Body weight	BMI	10	18424110	44424110	Human
597380584	GWAS1476658_H	serum IgG glycosylation measurement QTL GWAS1476658 (human)		0.000006	serum IgG glycosylation measurement		10	23014324	23014325	Human
597331999	GWAS1428073_H	S-6-hydroxywarfarin measurement QTL GWAS1428073 (human)		0.000001	S-6-hydroxywarfarin measurement		10	22929519	22929520	Human
597403996	GWAS1500070_H	protein measurement QTL GWAS1500070 (human)		3e-08	protein measurement		10	22960289	22960290	Human
597380259	GWAS1476333_H	serum IgG glycosylation measurement QTL GWAS1476333 (human)		0.0000006	serum IgG glycosylation measurement		10	23014324	23014325	Human
1300009	BW22_H	Body weight QTL 22 (human)	2.32		Body weight	body mass index	10	18424110	44424110	Human
597375623	GWAS1471697_H	serum IgG glycosylation measurement QTL GWAS1471697 (human)		0.000002	serum IgG glycosylation measurement		10	23014324	23014325	Human
597380582	GWAS1476656_H	serum IgG glycosylation measurement QTL GWAS1476656 (human)		0.000003	serum IgG glycosylation measurement		10	23014324	23014325	Human

RH103830

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	10	23,321,338 - 23,321,431	UniSTS	GRCh37
Build 36	10	23,361,344 - 23,361,437	RGD	NCBI36
Celera	10	23,008,984 - 23,009,077	RGD
Cytogenetic Map	10	p12.31	UniSTS
HuRef	10	22,981,418 - 22,981,511	UniSTS
GeneMap99-GB4 RH Map	10	135.41	UniSTS

G65505

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	10	23,256,729 - 23,257,005	UniSTS	GRCh37
Build 36	10	23,296,735 - 23,297,011	RGD	NCBI36
Celera	10	22,944,385 - 22,944,661	RGD
Cytogenetic Map	10	p12.31	UniSTS
HuRef	10	22,917,611 - 22,917,887	UniSTS

AB070084

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	10	23,287,135 - 23,287,234	UniSTS	GRCh37
Build 36	10	23,327,141 - 23,327,240	RGD	NCBI36
Celera	10	22,974,792 - 22,974,891	RGD
HuRef	10	22,948,019 - 22,948,118	UniSTS

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

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
533	1839	1496	1544	3817	1100	1716	1	277	1120	142	1050	4333	3895	12	3521	612	1424	1363	141


RefSeq Transcripts	NM_001282745	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001282746	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001282747	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_173081	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005252380	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005252381	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011519350	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011519351	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017015831	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017015832	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017015833	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054365001	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054365002	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054365003	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054365004	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054365005	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054365006	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054365007	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AA628128	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC079269	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK057389	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK090961	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK098711	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK302104	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK302985	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL139815	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY436643	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC039312	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX115364	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CB240778	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471072	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068268	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB459427	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000298032 ⟹ ENSP00000298032

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	22,928,053 - 23,038,523 (+)	Ensembl

Ensembl Acc Id:

ENST00000376528 ⟹ ENSP00000365711

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	22,928,024 - 23,038,523 (+)	Ensembl

Ensembl Acc Id:

ENST00000409049 ⟹ ENSP00000387288

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	22,928,064 - 23,014,489 (+)	Ensembl

Ensembl Acc Id:

ENST00000409983 ⟹ ENSP00000386943

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	22,928,037 - 23,037,589 (+)	Ensembl

Ensembl Acc Id:

ENST00000447081 ⟹ ENSP00000396629

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	22,928,085 - 22,961,966 (+)	Ensembl

Ensembl Acc Id:

ENST00000464017

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	22,955,196 - 22,961,727 (+)	Ensembl

Ensembl Acc Id:

ENST00000465729

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	22,931,996 - 22,946,683 (+)	Ensembl

Ensembl Acc Id:

ENST00000468003

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	22,928,085 - 22,968,342 (+)	Ensembl

Ensembl Acc Id:

ENST00000473919

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	23,030,631 - 23,031,195 (+)	Ensembl

Ensembl Acc Id:

ENST00000483596

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	22,928,086 - 22,962,067 (+)	Ensembl

Ensembl Acc Id:

ENST00000484642

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	22,928,077 - 22,981,608 (+)	Ensembl

Ensembl Acc Id:

ENST00000491803

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	23,006,735 - 23,008,374 (+)	Ensembl

Ensembl Acc Id:

ENST00000496741

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	22,928,077 - 22,981,453 (+)	Ensembl

RefSeq Acc Id:

NM_001282745 ⟹ NP_001269674

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	22,928,053 - 23,038,523 (+)	NCBI
HuRef	10	22,877,823 - 22,987,532 (+)	NCBI
CHM1_1	10	23,217,434 - 23,327,955 (+)	NCBI
T2T-CHM13v2.0	10	22,947,064 - 23,057,478 (+)	NCBI

Sequence:

show sequence

GTTCGTCTGCTGGGTTTGCGGAGCAGCTAGCTACTCGGCGGGATCTCCCGGCAGGATGGGTAAAAAGATAAAGAAGGAAGTAGAGCCTCCTCCTAAGGATGTGTTTGACCCATTAATGATTGAAAGCA
AAAAAGCAGCAACTGTGGTGTTAATGCTTAATTCTCCAGAAGAGGAAATTTTGGCTAAAGCATGTGAAGCCATTTATAAATTTGCTTTAAAAGGTGAGGAAAATAAAACAACCCTCCTTGAACTTGGA
GCTGTGGAACCTTTAACTAAGCTACTCACCCATGAAGACAAAATTGTAAGAAGAAATGCTACTATGATATTTGGAATCCTGGCTTCTAATAATGATGTTAAAAAATTGTTAAGGGAGTTAGATGTCAT
GAATTCTGTCATTGCCCAGCTCGCTCCAGAAGAAGAAGTAGTTATCCATGAGTTTGCTAGTCTTTGTCTAGCAAACATGTCTGCAGAGTACACCAGTAAAGTGCAAATATTTGAACATGGGGGATTAG
AGCCACTCATCAGACTACTGAGTAGCCCTGACCCGGATGTAAAGAAGAACTCTATGGAATGCATTTACAACTTGGTGCAGGATTTTCAGTGTCGAGCTAAACTTCAAGAACTAAATGCAATACCTCCT
ATCTTAGATCTCTTGAAGTCAGAATATCCAGTGATTCAGTTGTTGGCTCTCAAAACCTTAGGTGTTATTGCAAATGATAAGGAGTCTCGAACAATGCTAAGAGACAATCAAGGATTGGACCATCTTAT
TAAGATCCTAGAAACTAAGGAATTGAATGACCTTCATATAGAAGCACTTGCAGTGATAGCCAATTGCCTTGAAGACATGGATACTATGGTGCAGATTCAGCAGACAGGGGGTCTTAAAAAGCTCCTGT
CATTTGCAGAAAACTCTACAATTCCTGATATTCAGAAGAATGCAGCAAAAGCCATTACTAAAGCAGCTTATGATCCTGAAAATAGAAAACTTTTTCATGAACAAGAGGTTGAAAAGTGCCTTGTAGCC
CTTTTGGGTTCTGAAAATGATGGAACTAAAATTGCTGCTTCCCAAGCTATTTCAGCAATGTGTGAGAATTCAGGCAGCAAAGATTTTTTCAATAATCAGGGGATTCCACAGTTAATTCAGTTGCTAAA
AAGTGACAATGAAGAGGTACGGGAAGCAGCAGCTCTAGCCCTGGCAAACCTAACCACTTGCAACCCTGCTAATGCAAACGCTGCTGCTGAAGCTGATGGTATTGATCCATTAATAAACCTCCTGTCTA
GTAAACGAGATGGAGCCATTGCCAACGCTGCTACAGTATTAACAAACATGGCCATGCAGGAGCCCCTGCGCCTGAACATACAGAATCACGACATCATGCATGCCATCATCAGCCCACTGCGTTCTGCA
AACACAGTCGTGCAGAGCAAAGCTGCTCTCGCTGTCACCGCAACTGCGTGTGACGTTGAAGCCCGGACTGAGTTAAGAAATTCTGGTGGATTGGAGCCCCTGGTAGAGCTGCTACGCTCCAAGAATGA
TGAAGTGAGGAAGCACGCCAGTTGGGCAGTGATGGTCTGTGCTGGTGACGAGCTGACGGCCAATGAATTATGCAGGCTCGGGGCTTTAGATATCCTTGAAGAAGTTAACGTATCAGGAACTCGGAAAA
ATAAATTCAGTGAGGCAGCTTATAATAAGTTGCTCAATAACAATCTTTCCCTGAAATACAGCCAGACTGGCTATTTGTCATCAAGTAACATAATTAACGATGGATTCTATGATTATGGTCGGATAAAT
CCCGGCACCAAACTGTTGCCTTTGAAGGAGCTCTGCTTACAAGAACCAAGTGACCTACGGGCTGTACTCTTAATCAACAGTAAATCTTACGTTTCTCCACCTTCATCTATGGAAGATAAATCAGATGT
TGGTTATGGACGAAGTATTTCTTCTTCATCTTCCTTAAGAAGATCAAGTAAAGAAAAGAACAATGCTGGATTTGGATCTCCCATAGAAGACAAATCAGAGCCAGCTTCTGGACGAAATACTGTTCTCA
GCAAAAGCGCCACCAAAGAAAAAGGATGGAGGAAAAGCAAAGGAAAAAAAGAAGAGGAAAAAGTGAAAGAGGAGGAAGAGGTTATGGTGGTACCAAAATTTGTTGGTGAAGGAAGCTCTGACAAAGAA
TGGTGTCCTCCCTCTGACCCTGATTTCTCTATGTATGTGTATGAGGTGACCAAATCAATACTGCCAATAACCAATATTAAGGAACAGATTGAGGATCTGGCAAAGTATGTAGCAGAAAAAATGGGTGG
TAAGATTCCAAAAGAGAAACTACCTGATTTCAGCTGGGAACTTCACATAAGTGAACTGAAATTTCAACTTAAATCCAATGTTATACCGATTGGACATGTCAAAAAAGGAATCTTCTACCATCGAGCTT
TGCTTTTCAAGGCTCTGGCTGATAGAATTGGCATTGGTTGCTCCCTAGTTCGCGGAGAGTACGGTAGAGCGTGGAATGAAGTCATGCTGCAGAATGACTCTCGGAAGGGAGTGATTGGGGGCCTCCCC
GCTCCTGAGATGTACGTGATTGACCTCATGTTCCATCCAGGTGGACTGATGAAGTTGAGAAGTCGAGAGGCTGATCTTTACAGATTCATTTAAGCCATCAGACGAACACAAGAGAGGCTCAAACAAGA
AATTCACTGTGTACACTCTCTAAGACATTCTCCAAATTGATTTTATCTCTTTAAATAAAAACTTTAAATAAAAGTATTAGAAATGTTTTCTCTGCGTAGAAATTAGGAAGCTTGGAGTGAACTTTGCT
GTGCTTCTGATTTCAGGCTTTTGGCAAGAGTTCTGTCTTATTAGGTCATTTTCCGCTCACTGACCCTCACATAAAGCTGATTGTTGTCGAAATTCATCCAGCCCACTGTGTCCTGAGGAGCGTCTCTG
TCATTTAGGAATCACATGTAGCACTCAGCTGCTGCACCCAGGACAACACTGTGGCCTCATGACTGTCATCTTTCATGCCCAGAATGCTTCAGGCATGCTCAGTTAAGCAAACTAAGTGAATTTTTAGT
ATTTGCAATCACCTTGTCTCAGTTTCATTTAAGATTTTGATAGTTTAGATAGAATAAACACAGATCTGAGTGTTACAAATTCCTTTCTAAAAATTTTTGTTTCTATTTTTAAAAATTCATCATTAAAA
ACACTTTAATATAGTGAATTAAAAATATTTCTAAAGTATATTTCCATAAAATGGTTTTGGTTTCATCTTGTCTGTGTTAGCTTGGAAACATACCTTCAGCTAAAAACAATTCTGATTTGCTCTTCCAC
ATTTTAATGCTGGGCCATTAATATATTATTTTCAATTTATAGAACTAAAAAATTTTTATTTTTTGGAAAACTTTGAAGCATAAAGGTAGAGCAAATCTTTGCTGAGGAATTGTGTTTTAGTATTGAGC
ACAAAATGGGGAGTAAATTCACATTTCAAATGATAAGACAAAAACTACTAATGTGGTTAATCTCGTGAAGTACATATTGCCTAGTCACGCTTAAAGTCCAGTGTTGACCTGTATAGTCATTTTCCTAG
AAGACGTTTTAAAGTGAATTTGATTTTAGAAATTAAAGCTAAGATTATTTTGTATTAATTTGTAATTTCAAATAATATAATTCTTTATTTCAGAATAAATTTATTTCAAATGG

hide sequence

RefSeq Acc Id:

NM_001282746 ⟹ NP_001269675

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	22,928,053 - 23,014,477 (+)	NCBI
HuRef	10	22,877,823 - 22,987,532 (+)	NCBI
CHM1_1	10	23,217,434 - 23,303,912 (+)	NCBI
T2T-CHM13v2.0	10	22,947,064 - 23,033,438 (+)	NCBI

Sequence:

show sequence

GTTCGTCTGCTGGGTTTGCGGAGCAGCTAGCTACTCGGCGGGATCTCCCGGCAGGATGGGTAAAAAGATAAAGAAGGAAGTAGAGCCTCCTCCTAAGGATGTGTTTGACCCATTAATGATTGAAAGCA
AAAAAGCAGCAACTGTGGTGTTAATGCTTAATTCTCCAGAAGAGGAAATTTTGGCTAAAGCATGTGAAGCCATTTATAAATTTGCTTTAAAAGGTGAGGAAAATAAAACAACCCTCCTTGAACTTGGA
GCTGTGGAACCTTTAACTAAGCTACTCACCCATGAAGACAAAATTGTAAGAAGAAATGCTACTATGATATTTGGAATCCTGGCTTCTAATAATGATGTTAAAAAATTGTTAAGGGAGTTAGATGTCAT
GAATTCTGTCATTGCCCAGCTCGCTCCAGAAGAAGAAGTAGTTATCCATGAGTTTGCTAGTCTTTGTCTAGCAAACATGTCTGCAGAGTACACCAGTAAAGTGCAAATATTTGAACATGGGGGATTAG
AGCCACTCATCAGACTACTGAGTAGCCCTGACCCGGATGTAAAGAAGAACTCTATGGAATGCATTTACAACTTGGTGCAGGATTTTCAGTGTCGAGCTAAACTTCAAGAACTAAATGCAATACCTCCT
ATCTTAGATCTCTTGAAGTCAGAATATCCAGTGATTCAGTTGTTGGCTCTCAAAACCTTAGGTGTTATTGCAAATGATAAGGAGTCTCGAACAATGCTAAGAGACAATCAAGGATTGGACCATCTTAT
TAAGATCCTAGAAACTAAGGAATTGAATGACCTTCATATAGAAGCACTTGCAGTGATAGCCAATTGCCTTGAAGACATGGATACTATGGTGCAGATTCAGCAGACAGGGGGTCTTAAAAAGCTCCTGT
CATTTGCAGAAAACTCTACAATTCCTGATATTCAGAAGAATGCAGCAAAAGCCATTACTAAAGCAGCTTATGATCCTGAAAATAGAAAACTTTTTCATGAACAAGAGGTTGAAAAGTGCCTTGTAGCC
CTTTTGGGTTCTGAAAATGATGGAACTAAAATTGCTGCTTCCCAAGCTATTTCAGCAATGTGTGAGAATTCAGGCAGCAAAGATTTTTTCAATAATCAGGGGATTCCACAGTTAATTCAGTTGCTAAA
AAGTGACAATGAAGAGGTACGGGAAGCAGCAGCTCTAGCCCTGGCAAACCTAACCACTTGCAACCCTGCTAATGCAAACGCTGCTGCTGAAGCTGATGGTATTGATCCATTAATAAACCTCCTGTCTA
GTAAACGAGATGGAGCCATTGCCAACGCTGCTACAGTATTAACAAACATGGCCATGCAGGAGCCCCTGCGCCTGAACATACAGAATCACGACATCATGCATGCCATCATCAGCCCACTGCGTTCTGCA
AACACAGTCGTGCAGAGCAAAGCTGCTCTCGCTGTCACCGCAACTGCGTGTGACGTTGAAGCCCGGACTGAGTTAAGAAATTCTGGTGGATTGGAGCCCCTGGTAGAGCTGCTACGCTCCAAGAATGA
TGAAGTGAGGAAGCACGCCAGTTGGGCAGTGATGGTCTGTGCTGGTGACGAGCTGACGGCCAATGAATTATGCAGGCTCGGGGCTTTAGATATCCTTGAAGAAGTTAACGTATCAGGAACTCGGAAAA
ATAAATTCAGTGAGGCAGCTTATAATAAGTTGCTCAATAACAATCTTTCCCTGAAATACAGCCAGACTGGCTATTTGTCATCAAGTAACATAATTAACGATGGATTCTATGATTATGGTCGGATAAAT
CCCGGCACCAAACTGTTGCCTTTGAAGGAGCTCTGCTTACAAGAACCAAGTGACCTACGGGCTGTACTCTTAATCAACAGTAAATCTTACGTTTCTCCACCTTCATCTATGGAAGATAAATCAGATGT
TGGTTATGGACGAAGTATTTCTTCTTCATCTTCCTTAAGAAGATCAAGTAAAGAAAAGAACAAAAAAAATAGTTATCATTTTAGTGCTGGATTTGGATCTCCCATAGAAGACAAATCAGAGCCAGCTT
CTGGACGAAATACTGTTCTCAGCAAAAGCGCCACCAAAGAAAAAGGATGGAGCTCACTCCCCACTTCAAGATAAACCCTGAAGCACTCCTAGGATTTAAGAGGATTGTTGGCATGAGGAGAACACAGA
GACTTTGGATTCAGACACAACTGGGCCTTGGTCTTCTGAATTGTAAATGAAAATGATGATCCCTGCCTCAAAGAGCTGCTGTAAGAGGAGAGATGGTGTCAGGAAAGTGCCTGACCATCACCTAGCAC
ACTTAGGGGCTCAATGTGCGTCCCTTCTCTCTTCCCTTCTTAGCCTTTGGTCCATTGAGGGGTAGATTAGCCATAGCCCTGTTGTCCTGTTGCCTGTCTTTTGGTCAACCCTTCTTGTCTTATGACTA
TTAAAACTTTGGACTCCTGGAAATAGAATAAAATATTTTAACTGCA

hide sequence

RefSeq Acc Id:

NM_001282747 ⟹ NP_001269676

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	22,928,053 - 23,038,523 (+)	NCBI
HuRef	10	22,877,823 - 22,987,532 (+)	NCBI
CHM1_1	10	23,217,434 - 23,327,955 (+)	NCBI
T2T-CHM13v2.0	10	22,947,064 - 23,057,478 (+)	NCBI

Sequence:

show sequence

GTTCGTCTGCTGGGTTTGCGGAGCAGCTAGCTACTCGGCGGGATCTCCCGGCAGGATGGGTAAA
AAGATAAAGAAGGAAGTAGAGCCTCCTCCTAAGGATGTGGTGAGGAAAATAAAACAACCCTCCTTGAACTTGGAGCTGTGGAACCTTTAACTAAGCTACTCACCCATGAAGACAAAATTGTAAGAAGA
AATGCTACTATGATATTTGGAATCCTGGCTTCTAATAATGATGTTAAAAAATTGTTAAGGGAGTTAGATGTCATGAATTCTGTCATTGCCCAGCTCGCTCCAGAAGGAATTGAATGACCTTCATATAG
AAGCACTTGCAGTGATAGCCAATTGCCTTGAAGACATGGATACTATGGTGCAGATTCAGCAGACAGGGGGTCTTAAAAAGCTCCTGTCATTTGCAGAAAACTCTACAATTCCTGATATTCAGAAGAAT
GCAGCAAAAGCCATTACTAAAGCAGCTTATGATCCTGAAAATAGAAAACTTTTTCATGAACAAGAGGTTGAAAAGTGCCTTGTAGCCCTTTTGGGTTCTGAAAATGATGGAACTAAAATTGCTGCTTC
CCAAGCTATTTCAGCAATGTGTGAGAATTCAGGCAGCAAAGATTTTTTCAATAATCAGGGGATTCCACAGTTAATTCAGTTGCTAAAAAGTGACAATGAAGAGGTACGGGAAGCAGCAGCTCTAGCCC
TGGCAAACCTAACCACTTGCAACCCTGCTAATGCAAACGCTGCTGCTGAAGCTGATGGTATTGATCCATTAATAAACCTCCTGTCTAGTAAACGAGATGGAGCCATTGCCAACGCTGCTACAGTATTA
ACAAACATGGCCATGCAGGAGCCCCTGCGCCTGAACATACAGAATCACGACATCATGCATGCCATCATCAGCCCACTGCGTTCTGCAAACACAGTCGTGCAGAGCAAAGCTGCTCTCGCTGTCACCGC
AACTGCGTGTGACGTTGAAGCCCGGACTGAGTTAAGAAATTCTGGTGGATTGGAGCCCCTGGTAGAGCTGCTACGCTCCAAGAATGATGAAGTGAGGAAGCACGCCAGTTGGGCAGTGATGGTCTGTG
CTGGTGACGAGCTGACGGCCAATGAATTATGCAGGCTCGGGGCTTTAGATATCCTTGAAGAAGTTAACGTATCAGGAACTCGGAAAAATAAATTCAGTGAGGCAGCTTATAATAAGTTGCTCAATAAC
AATCTTTCCCTGAAATACAGCCAGACTGGCTATTTGTCATCAAGTAACATAATTAACGATGGATTCTATGATTATGGTCGGATAAATCCCGGCACCAAACTGTTGCCTTTGAAGGAGCTCTGCTTACA
AGAACCAAGTGACCTACGGGCTGTACTCTTAATCAACAGTAAATCTTACGTTTCTCCACCTTCATCTATGGAAGATAAATCAGATGTTGGTTATGGACGAAGTATTTCTTCTTCATCTTCCTTAAGAA
GATCAAGTAAAGAAAAGAACAAAAAAAATAGTTATCATTTTAGTGCTGGATTTGGATCTCCCATAGAAGACAAATCAGAGCCAGCTTCTGGACGAAATACTGTTCTCAGCAAAAGCGCCACCAAAGAA
AAAGGATGGAGGAAAAGCAAAGGAAAAAAAGAAGAGGAAAAAGTGAAAGAGGAGGAAGAGGTTATGGTGGTACCAAAATTTGTTGGTGAAGGAAGCTCTGACAAAGAATGGTGTCCTCCCTCTGACCC
TGATTTCTCTATGTATGTGTATGAGGTGACCAAATCAATACTGCCAATAACCAATATTAAGGAACAGATTGAGGATCTGGCAAAGTATGTAGCAGAAAAAATGGGTGGTAAGATTCCAAAAGAGAAAC
TACCTGATTTCAGCTGGGAACTTCACATAAGTGAACTGAAATTTCAACTTAAATCCAATGTTATACCGATTGGACATGTCAAAAAAGGAATCTTCTACCATCGAGCTTTGCTTTTCAAGGCTCTGGCT
GATAGAATTGGCATTGGTTGCTCCCTAGTTCGCGGAGAGTACGGTAGAGCGTGGAATGAAGTCATGCTGCAGAATGACTCTCGGAAGGGAGTGATTGGGGGCCTCCCCGCTCCTGAGATGTACGTGAT
TGACCTCATGTTCCATCCAGGTGGACTGATGAAGTTGAGAAGTCGAGAGGCTGATCTTTACAGATTCATTTAAGCCATCAGACGAACACAAGAGAGGCTCAAACAAGAAATTCACTGTGTACACTCTC
TAAGACATTCTCCAAATTGATTTTATCTCTTTAAATAAAAACTTTAAATAAAAGTATTAGAAATGTTTTCTCTGCGTAGAAATTAGGAAGCTTGGAGTGAACTTTGCTGTGCTTCTGATTTCAGGCTT
TTGGCAAGAGTTCTGTCTTATTAGGTCATTTTCCGCTCACTGACCCTCACATAAAGCTGATTGTTGTCGAAATTCATCCAGCCCACTGTGTCCTGAGGAGCGTCTCTGTCATTTAGGAATCACATGTA
GCACTCAGCTGCTGCACCCAGGACAACACTGTGGCCTCATGACTGTCATCTTTCATGCCCAGAATGCTTCAGGCATGCTCAGTTAAGCAAACTAAGTGAATTTTTAGTATTTGCAATCACCTTGTCTC
AGTTTCATTTAAGATTTTGATAGTTTAGATAGAATAAACACAGATCTGAGTGTTACAAATTCCTTTCTAAAAATTTTTGTTTCTATTTTTAAAAATTCATCATTAAAAACACTTTAATATAGTGAATT
AAAAATATTTCTAAAGTATATTTCCATAAAATGGTTTTGGTTTCATCTTGTCTGTGTTAGCTTGGAAACATACCTTCAGCTAAAAACAATTCTGATTTGCTCTTCCACATTTTAATGCTGGGCCATTA
ATATATTATTTTCAATTTATAGAACTAAAAAATTTTTATTTTTTGGAAAACTTTGAAGCATAAAGGTAGAGCAAATCTTTGCTGAGGAATTGTGTTTTAGTATTGAGCACAAAATGGGGAGTAAATTC
ACATTTCAAATGATAAGACAAAAACTACTAATGTGGTTAATCTCGTGAAGTACATATTGCCTAGTCACGCTTAAAGTCCAGTGTTGACCTGTATAGTCATTTTCCTAGAAGACGTTTTAAAGTGAATT
TGATTTTAGAAATTAAAGCTAAGATTATTTTGTATTAATTTGTAATTTCAAATAATATAATTCTTTATTTCAGAATAAATTTATTTCAAATGG

hide sequence

RefSeq Acc Id:

NM_173081 ⟹ NP_775104

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	22,928,053 - 23,038,523 (+)	NCBI
GRCh37	10	23,216,954 - 23,327,452 (+)	NCBI
Build 36	10	23,256,966 - 23,366,520 (+)	NCBI Archive
Celera	10	22,904,614 - 23,014,160 (+)	RGD
HuRef	10	22,877,823 - 22,987,532 (+)	NCBI
CHM1_1	10	23,217,434 - 23,327,955 (+)	NCBI
T2T-CHM13v2.0	10	22,947,064 - 23,057,478 (+)	NCBI

Sequence:

show sequence

GTTCGTCTGCTGGGTTTGCGGAGCAGCTAGCTACTCGGCGGGATCTCCCGGCAGGATGGGTAAAAAGATAAAGAAGGAAGTAGAGCCTCCTCCTAAGGATGTGTTTGACCCATTAATGATTGAAAGCA
AAAAAGCAGCAACTGTGGTGTTAATGCTTAATTCTCCAGAAGAGGAAATTTTGGCTAAAGCATGTGAAGCCATTTATAAATTTGCTTTAAAAGGTGAGGAAAATAAAACAACCCTCCTTGAACTTGGA
GCTGTGGAACCTTTAACTAAGCTACTCACCCATGAAGACAAAATTGTAAGAAGAAATGCTACTATGATATTTGGAATCCTGGCTTCTAATAATGATGTTAAAAAATTGTTAAGGGAGTTAGATGTCAT
GAATTCTGTCATTGCCCAGCTCGCTCCAGAAGAAGAAGTAGTTATCCATGAGTTTGCTAGTCTTTGTCTAGCAAACATGTCTGCAGAGTACACCAGTAAAGTGCAAATATTTGAACATGGGGGATTAG
AGCCACTCATCAGACTACTGAGTAGCCCTGACCCGGATGTAAAGAAGAACTCTATGGAATGCATTTACAACTTGGTGCAGGATTTTCAGTGTCGAGCTAAACTTCAAGAACTAAATGCAATACCTCCT
ATCTTAGATCTCTTGAAGTCAGAATATCCAGTGATTCAGTTGTTGGCTCTCAAAACCTTAGGTGTTATTGCAAATGATAAGGAGTCTCGAACAATGCTAAGAGACAATCAAGGATTGGACCATCTTAT
TAAGATCCTAGAAACTAAGGAATTGAATGACCTTCATATAGAAGCACTTGCAGTGATAGCCAATTGCCTTGAAGACATGGATACTATGGTGCAGATTCAGCAGACAGGGGGTCTTAAAAAGCTCCTGT
CATTTGCAGAAAACTCTACAATTCCTGATATTCAGAAGAATGCAGCAAAAGCCATTACTAAAGCAGCTTATGATCCTGAAAATAGAAAACTTTTTCATGAACAAGAGGTTGAAAAGTGCCTTGTAGCC
CTTTTGGGTTCTGAAAATGATGGAACTAAAATTGCTGCTTCCCAAGCTATTTCAGCAATGTGTGAGAATTCAGGCAGCAAAGATTTTTTCAATAATCAGGGGATTCCACAGTTAATTCAGTTGCTAAA
AAGTGACAATGAAGAGGTACGGGAAGCAGCAGCTCTAGCCCTGGCAAACCTAACCACTTGCAACCCTGCTAATGCAAACGCTGCTGCTGAAGCTGATGGTATTGATCCATTAATAAACCTCCTGTCTA
GTAAACGAGATGGAGCCATTGCCAACGCTGCTACAGTATTAACAAACATGGCCATGCAGGAGCCCCTGCGCCTGAACATACAGAATCACGACATCATGCATGCCATCATCAGCCCACTGCGTTCTGCA
AACACAGTCGTGCAGAGCAAAGCTGCTCTCGCTGTCACCGCAACTGCGTGTGACGTTGAAGCCCGGACTGAGTTAAGAAATTCTGGTGGATTGGAGCCCCTGGTAGAGCTGCTACGCTCCAAGAATGA
TGAAGTGAGGAAGCACGCCAGTTGGGCAGTGATGGTCTGTGCTGGTGACGAGCTGACGGCCAATGAATTATGCAGGCTCGGGGCTTTAGATATCCTTGAAGAAGTTAACGTATCAGGAACTCGGAAAA
ATAAATTCAGTGAGGCAGCTTATAATAAGTTGCTCAATAACAATCTTTCCCTGAAATACAGCCAGACTGGCTATTTGTCATCAAGTAACATAATTAACGATGGATTCTATGATTATGGTCGGATAAAT
CCCGGCACCAAACTGTTGCCTTTGAAGGAGCTCTGCTTACAAGAACCAAGTGACCTACGGGCTGTACTCTTAATCAACAGTAAATCTTACGTTTCTCCACCTTCATCTATGGAAGATAAATCAGATGT
TGGTTATGGACGAAGTATTTCTTCTTCATCTTCCTTAAGAAGATCAAGTAAAGAAAAGAACAAAAAAAATAGTTATCATTTTAGTGCTGGATTTGGATCTCCCATAGAAGACAAATCAGAGCCAGCTT
CTGGACGAAATACTGTTCTCAGCAAAAGCGCCACCAAAGAAAAAGGATGGAGGAAAAGCAAAGGAAAAAAAGAAGAGGAAAAAGTGAAAGAGGAGGAAGAGGTTATGGTGGTACCAAAATTTGTTGGT
GAAGGAAGCTCTGACAAAGAATGGTGTCCTCCCTCTGACCCTGATTTCTCTATGTATGTGTATGAGGTGACCAAATCAATACTGCCAATAACCAATATTAAGGAACAGATTGAGGATCTGGCAAAGTA
TGTAGCAGAAAAAATGGGTGGTAAGATTCCAAAAGAGAAACTACCTGATTTCAGCTGGGAACTTCACATAAGTGAACTGAAATTTCAACTTAAATCCAATGTTATACCGATTGGACATGTCAAAAAAG
GAATCTTCTACCATCGAGCTTTGCTTTTCAAGGCTCTGGCTGATAGAATTGGCATTGGTTGCTCCCTAGTTCGCGGAGAGTACGGTAGAGCGTGGAATGAAGTCATGCTGCAGAATGACTCTCGGAAG
GGAGTGATTGGGGGCCTCCCCGCTCCTGAGATGTACGTGATTGACCTCATGTTCCATCCAGGTGGACTGATGAAGTTGAGAAGTCGAGAGGCTGATCTTTACAGATTCATTTAAGCCATCAGACGAAC
ACAAGAGAGGCTCAAACAAGAAATTCACTGTGTACACTCTCTAAGACATTCTCCAAATTGATTTTATCTCTTTAAATAAAAACTTTAAATAAAAGTATTAGAAATGTTTTCTCTGCGTAGAAATTAGG
AAGCTTGGAGTGAACTTTGCTGTGCTTCTGATTTCAGGCTTTTGGCAAGAGTTCTGTCTTATTAGGTCATTTTCCGCTCACTGACCCTCACATAAAGCTGATTGTTGTCGAAATTCATCCAGCCCACT
GTGTCCTGAGGAGCGTCTCTGTCATTTAGGAATCACATGTAGCACTCAGCTGCTGCACCCAGGACAACACTGTGGCCTCATGACTGTCATCTTTCATGCCCAGAATGCTTCAGGCATGCTCAGTTAAG
CAAACTAAGTGAATTTTTAGTATTTGCAATCACCTTGTCTCAGTTTCATTTAAGATTTTGATAGTTTAGATAGAATAAACACAGATCTGAGTGTTACAAATTCCTTTCTAAAAATTTTTGTTTCTATT
TTTAAAAATTCATCATTAAAAACACTTTAATATAGTGAATTAAAAATATTTCTAAAGTATATTTCCATAAAATGGTTTTGGTTTCATCTTGTCTGTGTTAGCTTGGAAACATACCTTCAGCTAAAAAC
AATTCTGATTTGCTCTTCCACATTTTAATGCTGGGCCATTAATATATTATTTTCAATTTATAGAACTAAAAAATTTTTATTTTTTGGAAAACTTTGAAGCATAAAGGTAGAGCAAATCTTTGCTGAGG
AATTGTGTTTTAGTATTGAGCACAAAATGGGGAGTAAATTCACATTTCAAATGATAAGACAAAAACTACTAATGTGGTTAATCTCGTGAAGTACATATTGCCTAGTCACGCTTAAAGTCCAGTGTTGA
CCTGTATAGTCATTTTCCTAGAAGACGTTTTAAAGTGAATTTGATTTTAGAAATTAAAGCTAAGATTATTTTGTATTAATTTGTAATTTCAAATAATATAATTCTTTATTTCAGAATAAATTTATTTC
AAATGG

hide sequence

RefSeq Acc Id:

XM_005252380 ⟹ XP_005252437

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	22,928,053 - 23,038,523 (+)	NCBI
GRCh37	10	23,216,954 - 23,327,452 (+)	NCBI

Sequence:

show sequence

AACGAGGCACAACAAGGGACTGGGGGTTCGTCTGCTGGGTTTGCGGAGCAGCTAGCTACTCGGC
GGGATCTCCCGGCAGGATGGGTAAAAAGATAAAGAAGGAAGTAGAGCCTCCTCCTAAGGATGTGTTTGACCCATTAATGATTGAAAGCAAAAAAGCAGCAACTGTGGTGTTAATGCTTAATTCTCCAG
AAGAGGAAATTTTGGCTAAAGCATGTGAAGCCATTTATAAATTTGCTTTAAAAGGTGAGGAAAATAAAACAACCCTCCTTGAACTTGGAGCTGTGGAACCTTTAACTAAGCTACTCACCCATGAAGAC
AAAATTGTAAGAAGAAATGCTACTATGATATTTGGAATCCTGGCTTCTAATAATGATGTTAAAAAATTGTTAAGGGAGTTAGATGTCATGAATTCTGTCATTGCCCAGCTCGCTCCAGAAGAAGAAGT
AGTTATCCATGAGTTTGCTAGTCTTTGTCTAGCAAACATGTCTGCAGAGTACACCAGTAAAGTGCAAATATTTGAACATGGGGGATTAGAGCCACTCATCAGACTACTGAGTAGCCCTGACCCGGATG
TAAAGAAGAACTCTATGGAATGCATTTACAACTTGGTGCAGGAATTGAATGACCTTCATATAGAAGCACTTGCAGTGATAGCCAATTGCCTTGAAGACATGGATACTATGGTGCAGATTCAGCAGACA
GGGGGTCTTAAAAAGCTCCTGTCATTTGCAGAAAACTCTACAATTCCTGATATTCAGAAGAATGCAGCAAAAGCCATTACTAAAGCAGCTTATGATCCTGAAAATAGAAAACTTTTTCATGAACAAGA
GGTTGAAAAGTGCCTTGTAGCCCTTTTGGGTTCTGAAAATGATGGAACTAAAATTGCTGCTTCCCAAGCTATTTCAGCAATGTGTGAGAATTCAGGCAGCAAAGATTTTTTCAATAATCAGGGGATTC
CACAGTTAATTCAGTTGCTAAAAAGTGACAATGAAGAGGTACGGGAAGCAGCAGCTCTAGCCCTGGCAAACCTAACCACTTGCAACCCTGCTAATGCAAACGCTGCTGCTGAAGCTGATGGTATTGAT
CCATTAATAAACCTCCTGTCTAGTAAACGAGATGGAGCCATTGCCAACGCTGCTACAGTATTAACAAACATGGCCATGCAGGAGCCCCTGCGCCTGAACATACAGAATCACGACATCATGCATGCCAT
CATCAGCCCACTGCGTTCTGCAAACACAGTCGTGCAGAGCAAAGCTGCTCTCGCTGTCACCGCAACTGCGTGTGACGTTGAAGCCCGGACTGAGTTAAGAAATTCTGGTGGATTGGAGCCCCTGGTAG
AGCTGCTACGCTCCAAGAATGATGAAGTGAGGAAGCACGCCAGTTGGGCAGTGATGGTCTGTGCTGGTGACGAGCTGACGGCCAATGAATTATGCAGGCTCGGGGCTTTAGATATCCTTGAAGAAGTT
AACGTATCAGGAACTCGGAAAAATAAATTCAGTGAGGCAGCTTATAATAAGTTGCTCAATAACAATCTTTCCCTGAAATACAGCCAGACTGGCTATTTGTCATCAAGTAACATAATTAACGATGGATT
CTATGATTATGGTCGGATAAATCCCGGCACCAAACTGTTGCCTTTGAAGGAGCTCTGCTTACAAGAACCAAGTGACCTACGGGCTGTACTCTTAATCAACAGTAAATCTTACGTTTCTCCACCTTCAT
CTATGGAAGATAAATCAGATGTTGGTTATGGACGAAGTATTTCTTCTTCATCTTCCTTAAGAAGATCAAGTAAAGAAAAGAACAAAAAAAATAGTTATCATTTTAGTGCTGGATTTGGATCTCCCATA
GAAGACAAATCAGAGCCAGCTTCTGGACGAAATACTGTTCTCAGCAAAAGCGCCACCAAAGAAAAAGGATGGAGGAAAAGCAAAGGAAAAAAAGAAGAGGAAAAAGTGAAAGAGGAGGAAGAGGTTAT
GGTGGTACCAAAATTTGTTGGTGAAGGAAGCTCTGACAAAGAATGGTGTCCTCCCTCTGACCCTGATTTCTCTATGTATGTGTATGAGGTGACCAAATCAATACTGCCAATAACCAATATTAAGGAAC
AGATTGAGGATCTGGCAAAGTATGTAGCAGAAAAAATGGGTGGTAAGATTCCAAAAGAGAAACTACCTGATTTCAGCTGGGAACTTCACATAAGTGAACTGAAATTTCAACTTAAATCCAATGTTATA
CCGATTGGACATGTCAAAAAAGGAATCTTCTACCATCGAGCTTTGCTTTTCAAGGCTCTGGCTGATAGAATTGGCATTGGTTGCTCCCTAGTTCGCGGAGAGTACGGTAGAGCGTGGAATGAAGTCAT
GCTGCAGAATGACTCTCGGAAGGGAGTGATTGGGGGCCTCCCCGCTCCTGAGATGTACGTGATTGACCTCATGTTCCATCCAGGTGGACTGATGAAGTTGAGAAGTCGAGAGGCTGATCTTTACAGAT
TCATTTAAGCCATCAGACGAACACAAGAGAGGCTCAAACAAGAAATTCACTGTGTACACTCTCTAAGACATTCTCCAAATTGATTTTATCTCTTTAAATAAAAACTTTAAATAAAAGTATTAGAAATG
TTTTCTCTGCGTAGAAATTAGGAAGCTTGGAGTGAACTTTGCTGTGCTTCTGATTTCAGGCTTTTGGCAAGAGTTCTGTCTTATTAGGTCATTTTCCGCTCACTGACCCTCACATAAAGCTGATTGTT
GTCGAAATTCATCCAGCCCACTGTGTCCTGAGGAGCGTCTCTGTCATTTAGGAATCACATGTAGCACTCAGCTGCTGCACCCAGGACAACACTGTGGCCTCATGACTGTCATCTTTCATGCCCAGAAT
GCTTCAGGCATGCTCAGTTAAGCAAACTAAGTGAATTTTTAGTATTTGCAATCACCTTGTCTCAGTTTCATTTAAGATTTTGATAGTTTAGATAGAATAAACACAGATCTGAGTGTTACAAATTCCTT
TCTAAAAATTTTTGTTTCTATTTTTAAAAATTCATCATTAAAAACACTTTAATATAGTGAATTAAAAATATTTCTAAAGTATATTTCCATAAAATGGTTTTGGTTTCATCTTGTCTGTGTTAGCTTGG
AAACATACCTTCAGCTAAAAACAATTCTGATTTGCTCTTCCACATTTTAATGCTGGGCCATTAATATATTATTTTCAATTTATAGAACTAAAAAATTTTTATTTTTTGGAAAACTTTGAAGCATAAAG
GTAGAGCAAATCTTTGCTGAGGAATTGTGTTTTAGTATTGAGCACAAAATGGGGAGTAAATTCACATTTCAAATGATAAGACAAAAACTACTAATGTGGTTAATCTCGTGAAGTACATATTGCCTAGT
CACGCTTAAAGTCCAGTGTTGACCTGTATAGTCATTTTCCTAGAAGACGTTTTAAAGTGAATTTGATTTTAGAAATTAAAGCTAAGATTATTTTGTATTAATTTGTAATTTCAAATAATATAATTCTT
TATTTCAGAATAAATTTATTTCAAATGGCGTG

hide sequence

RefSeq Acc Id:

XM_005252381 ⟹ XP_005252438

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	22,928,053 - 23,038,523 (+)	NCBI
GRCh37	10	23,216,954 - 23,327,452 (+)	NCBI

Sequence:

show sequence

ACTCGGCGGGATCTCCCGGCAGGATGGGTAAAAAGATAAAGAAGGAAGTAGAGCCTCCTCCTAA
GGATGTGGTGAGGAAAATAAAACAACCCTCCTTGAACTTGGAGCTGTGGAACCTTTAACTAAGCTACTCACCCATGAAGACAAAATTGTAAGAAGAAATGCTACTATGATATTTGGAATCCTGGCTTC
TAATAATGATGTTAAAAAATTGTTAAGGGAGTTAGATGTCATGAATTCTGTCATTGCCCAGCTCGCTCCAGAAGAAGAAGTAGTTATCCATGAGTTTGCTAGTCTTTGTCTAGCAAACATGTCTGCAG
AGTACACCAGTAAAGTGCAAATATTTGAACATGGGGGATTAGAGCCACTCATCAGACTACTGAGTAGCCCTGACCCGGATGTAAAGAAGAACTCTATGGAATGCATTTACAACTTGGTGCAGGATTTT
CAGTGTCGAGCTAAACTTCAAGAACTAAATGCAATACCTCCTATCTTAGATCTCTTGAAGTCAGAATATCCAGTGATTCAGTTGTTGGCTCTCAAAACCTTAGGTGTTATTGCAAATGATAAGGAGTC
TCGAACAATGCTAAGAGACAATCAAGGATTGGACCATCTTATTAAGATCCTAGAAACTAAGGAATTGAATGACCTTCATATAGAAGCACTTGCAGTGATAGCCAATTGCCTTGAAGACATGGATACTA
TGGTGCAGATTCAGCAGACAGGGGGTCTTAAAAAGCTCCTGTCATTTGCAGAAAACTCTACAATTCCTGATATTCAGAAGAATGCAGCAAAAGCCATTACTAAAGCAGCTTATGATCCTGAAAATAGA
AAACTTTTTCATGAACAAGAGGTTGAAAAGTGCCTTGTAGCCCTTTTGGGTTCTGAAAATGATGGAACTAAAATTGCTGCTTCCCAAGCTATTTCAGCAATGTGTGAGAATTCAGGCAGCAAAGATTT
TTTCAATAATCAGGGGATTCCACAGTTAATTCAGTTGCTAAAAAGTGACAATGAAGAGGTACGGGAAGCAGCAGCTCTAGCCCTGGCAAACCTAACCACTTGCAACCCTGCTAATGCAAACGCTGCTG
CTGAAGCTGATGGTATTGATCCATTAATAAACCTCCTGTCTAGTAAACGAGATGGAGCCATTGCCAACGCTGCTACAGTATTAACAAACATGGCCATGCAGGAGCCCCTGCGCCTGAACATACAGAAT
CACGACATCATGCATGCCATCATCAGCCCACTGCGTTCTGCAAACACAGTCGTGCAGAGCAAAGCTGCTCTCGCTGTCACCGCAACTGCGTGTGACGTTGAAGCCCGGACTGAGTTAAGAAATTCTGG
TGGATTGGAGCCCCTGGTAGAGCTGCTACGCTCCAAGAATGATGAAGTGAGGAAGCACGCCAGTTGGGCAGTGATGGTCTGTGCTGGTGACGAGCTGACGGCCAATGAATTATGCAGGCTCGGGGCTT
TAGATATCCTTGAAGAAGTTAACGTATCAGGAACTCGGAAAAATAAATTCAGTGAGGCAGCTTATAATAAGTTGCTCAATAACAATCTTTCCCTGAAATACAGCCAGACTGGCTATTTGTCATCAAGT
AACATAATTAACGATGGATTCTATGATTATGGTCGGATAAATCCCGGCACCAAACTGTTGCCTTTGAAGGAGCTCTGCTTACAAGAACCAAGTGACCTACGGGCTGTACTCTTAATCAACAGTAAATC
TTACGTTTCTCCACCTTCATCTATGGAAGATAAATCAGATGTTGGTTATGGACGAAGTATTTCTTCTTCATCTTCCTTAAGAAGATCAAGTAAAGAAAAGAACAAAAAAAATAGTTATCATTTTAGTG
CTGGATTTGGATCTCCCATAGAAGACAAATCAGAGCCAGCTTCTGGACGAAATACTGTTCTCAGCAAAAGCGCCACCAAAGAAAAAGGATGGAGGAAAAGCAAAGGAAAAAAAGAAGAGGAAAAAGTG
AAAGAGGAGGAAGAGGTTATGGTGGTACCAAAATTTGTTGGTGAAGGAAGCTCTGACAAAGAATGGTGTCCTCCCTCTGACCCTGATTTCTCTATGTATGTGTATGAGGTGACCAAATCAATACTGCC
AATAACCAATATTAAGGAACAGATTGAGGATCTGGCAAAGTATGTAGCAGAAAAAATGGGTGGTAAGATTCCAAAAGAGAAACTACCTGATTTCAGCTGGGAACTTCACATAAGTGAACTGAAATTTC
AACTTAAATCCAATGTTATACCGATTGGACATGTCAAAAAAGGAATCTTCTACCATCGAGCTTTGCTTTTCAAGGCTCTGGCTGATAGAATTGGCATTGGTTGCTCCCTAGTTCGCGGAGAGTACGGT
AGAGCGTGGAATGAAGTCATGCTGCAGAATGACTCTCGGAAGGGAGTGATTGGGGGCCTCCCCGCTCCTGAGATGTACGTGATTGACCTCATGTTCCATCCAGGTGGACTGATGAAGTTGAGAAGTCG
AGAGGCTGATCTTTACAGATTCATTTAAGCCATCAGACGAACACAAGAGAGGCTCAAACAAGAAATTCACTGTGTACACTCTCTAAGACATTCTCCAAATTGATTTTATCTCTTTAAATAAAAACTTT
AAATAAAAGTATTAGAAATGTTTTCTCTGCGTAGAAATTAGGAAGCTTGGAGTGAACTTTGCTGTGCTTCTGATTTCAGGCTTTTGGCAAGAGTTCTGTCTTATTAGGTCATTTTCCGCTCACTGACC
CTCACATAAAGCTGATTGTTGTCGAAATTCATCCAGCCCACTGTGTCCTGAGGAGCGTCTCTGTCATTTAGGAATCACATGTAGCACTCAGCTGCTGCACCCAGGACAACACTGTGGCCTCATGACTG
TCATCTTTCATGCCCAGAATGCTTCAGGCATGCTCAGTTAAGCAAACTAAGTGAATTTTTAGTATTTGCAATCACCTTGTCTCAGTTTCATTTAAGATTTTGATAGTTTAGATAGAATAAACACAGAT
CTGAGTGTTACAAATTCCTTTCTAAAAATTTTTGTTTCTATTTTTAAAAATTCATCATTAAAAACACTTTAATATAGTGAATTAAAAATATTTCTAAAGTATATTTCCATAAAATGGTTTTGGTTTCA
TCTTGTCTGTGTTAGCTTGGAAACATACCTTCAGCTAAAAACAATTCTGATTTGCTCTTCCACATTTTAATGCTGGGCCATTAATATATTATTTTCAATTTATAGAACTAAAAAATTTTTATTTTTTG
GAAAACTTTGAAGCATAAAGGTAGAGCAAATCTTTGCTGAGGAATTGTGTTTTAGTATTGAGCACAAAATGGGGAGTAAATTCACATTTCAAATGATAAGACAAAAACTACTAATGTGGTTAATCTCG
TGAAGTACATATTGCCTAGTCACGCTTAAAGTCCAGTGTTGACCTGTATAGTCATTTTCCTAGAAGACGTTTTAAAGTGAATTTGATTTTAGAAATTAAAGCTAAGATTATTTTGTATTAATTTGTAA
TTTCAAATAATATAATTCTTTATTTCAGAATAAATTTATTTCAAATGGCGTG

hide sequence

RefSeq Acc Id:

XM_011519350 ⟹ XP_011517652

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	22,928,053 - 23,016,939 (+)	NCBI

Sequence:

show sequence

AACGAGGCACAACAAGGGACTGGGGGTTCGTCTGCTGGGTTTGCGGAGCAGCTAGCTACTCGGC
GGGATCTCCCGGCAGGATGGGTAAAAAGATAAAGAAGGAAGTAGAGCCTCCTCCTAAGGATGTGTTTGACCCATTAATGATTGAAAGCAAAAAAGCAGCAACTGTGGTGTTAATGCTTAATTCTCCAG
AAGAGGAAATTTTGGCTAAAGCATGTGAAGCCATTTATAAATTTGCTTTAAAAGGTGAGGAAAATAAAACAACCCTCCTTGAACTTGGAGCTGTGGAACCTTTAACTAAGCTACTCACCCATGAAGAC
AAAATTGTAAGAAGAAATGCTACTATGATATTTGGAATCCTGGCTTCTAATAATGATGTTAAAAAATTGTTAAGGGAGTTAGATGTCATGAATTCTGTCATTGCCCAGCTCGCTCCAGAAGAAGAAGT
AGTTATCCATGAGTTTGCTAGTCTTTGTCTAGCAAACATGTCTGCAGAGTACACCAGTAAAGTGCAAATATTTGAACATGGGGGATTAGAGCCACTCATCAGACTACTGAGTAGCCCTGACCCGGATG
TAAAGAAGAACTCTATGGAATGCATTTACAACTTGGTGCAGGATTTTCAGTGTCGAGCTAAACTTCAAGAACTAAATGCAATACCTCCTATCTTAGATCTCTTGAAGTCAGAATATCCAGTGATTCAG
TTGTTGGCTCTCAAAACCTTAGGTGTTATTGCAAATGATAAGGAGTCTCGAACAATGCTAAGAGACAATCAAGGATTGGACCATCTTATTAAGATCCTAGAAACTAAGGAATTGAATGACCTTCATAT
AGAAGCACTTGCAGTGATAGCCAATTGCCTTGAAGACATGGATACTATGGTGCAGATTCAGCAGACAGGGGGTCTTAAAAAGCTCCTGTCATTTGCAGAAAACTCTACAATTCCTGATATTCAGAAGA
ATGCAGCAAAAGCCATTACTAAAGCAGCTTATGATCCTGAAAATAGAAAACTTTTTCATGAACAAGAGGTTGAAAAGTGCCTTGTAGCCCTTTTGGGTTCTGAAAATGATGGAACTAAAATTGCTGCT
TCCCAAGCTATTTCAGCAATGTGTGAGAATTCAGGCAGCAAAGATTTTTTCAATAATCAGGGGATTCCACAGTTAATTCAGTTGCTAAAAAGTGACAATGAAGAGGTACGGGAAGCAGCAGCTCTAGC
CCTGGCAAACCTAACCACTTGCAACCCTGCTAATGCAAACGCTGCTGCTGAAGCTGATGGTATTGATCCATTAATAAACCTCCTGTCTAGTAAACGAGATGGAGCCATTGCCAACGCTGCTACAGTAT
TAACAAACATGGCCATGCAGGAGCCCCTGCGCCTGAACATACAGAATCACGACATCATGCATGCCATCATCAGCCCACTGCGTTCTGCAAACACAGTCGTGCAGAGCAAAGCTGCTCTCGCTGTCACC
GCAACTGCGTGTGACGTTGAAGCCCGGACTGAGTTAAGAAATTCTGGTGGATTGGAGCCCCTGGTAGAGCTGCTACGCTCCAAGAATGATGAAGTGAGGAAGCACGCCAGTTGGGCAGTGATGGTCTG
TGCTGGTGACGAGCTGACGGCCAATGAATTATGCAGGCTCGGGGCTTTAGATATCCTTGAAGAAGTTAACGTATCAGGAACTCGGAAAAATAAATTCAGTGAGGCAGCTTATAATAAGTTGCTCAATA
ACAATCTTTCCCTGAAATACAGCCAGACTGGCTATTTGTCATCAAGTAACATAATTAACGATGGATTCTATGATTATGGTCGGATAAATCCCGGCACCAAACTGTTGCCTTTGAAGGAGCTCTGCTTA
CAAGAACCAAGTGACCTACGGGCTGTACTCTTAATCAACAGTAAATCTTACGTTTCTCCACCTTCATCTATGGAAGATAAATCAGATGTTGGTTATGGACGAAGTATTTCTTCTTCATCTTCCTTAAG
AAGATCAAGTAAAGAAAAGAACAAAAAAAATAGTTATCATTTTAGTGCTGGATTTGGATCTCCCATAGAAGACAAATCAGAGCCAGCTTCTGGACGAAATACTGTTCTCAGCAAAAGCGCCACCAAAG
AAAAAGGATGGAGGTAACTCTGAATAGTCACTCTATTCAGTGACGAAGTATTGGACTGACTGTTGGAACTGAGCTCTCCAATCTTACACCACCACCTTGCAATTT

hide sequence

RefSeq Acc Id:

XM_011519351 ⟹ XP_011517653

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	22,995,953 - 23,038,523 (+)	NCBI

Sequence:

show sequence

AAAGTGAACATTCTCGAGGGAAAACCACCAAGTGACAAAGGAATCATGCATTTTGGCCAAGCATATTTATAATGATTAACAAATACAAGCGCTGCTGCTGAAGCTGATGGTATTGATCCATTAATAAA
CCTCCTGTCTAGTAAACGAGATGGAGCCATTGCCAACGCTGCTACAGTATTAACAAACATGGCCATGCAGGAGCCCCTGCGCCTGAACATACAGAATCACGACATCATGCATGCCATCATCAGCCCAC
TGCGTTCTGCAAACACAGTCGTGCAGAGCAAAGCTGCTCTCGCTGTCACCGCAACTGCGTGTGACGTTGAAGCCCGGACTGAGTTAAGAAATTCTGGTGGATTGGAGCCCCTGGTAGAGCTGCTACGC
TCCAAGAATGATGAAGTGAGGAAGCACGCCAGTTGGGCAGTGATGGTCTGTGCTGGTGACGAGCTGACGGCCAATGAATTATGCAGGCTCGGGGCTTTAGATATCCTTGAAGAAGTTAACGTATCAGG
AACTCGGAAAAATAAATTCAGTGAGGCAGCTTATAATAAGTTGCTCAATAACAATCTTTCCCTGAAATACAGCCAGACTGGCTATTTGTCATCAAGTAACATAATTAACGATGGATTCTATGATTATG
GTCGGATAAATCCCGGCACCAAACTGTTGCCTTTGAAGGAGCTCTGCTTACAAGAACCAAGTGACCTACGGGCTGTACTCTTAATCAACAGTAAATCTTACGTTTCTCCACCTTCATCTATGGAAGAT
AAATCAGATGTTGGTTATGGACGAAGTATTTCTTCTTCATCTTCCTTAAGAAGATCAAGTAAAGAAAAGAACAAAAAAAATAGTTATCATTTTAGTGCTGGATTTGGATCTCCCATAGAAGACAAATC
AGAGCCAGCTTCTGGACGAAATACTGTTCTCAGCAAAAGCGCCACCAAAGAAAAAGGATGGAGGAAAAGCAAAGGAAAAAAAGAAGAGGAAAAAGTGAAAGAGGAGGAAGAGGTTATGGTGGTACCAA
AATTTGTTGGTGAAGGAAGCTCTGACAAAGAATGGTGTCCTCCCTCTGACCCTGATTTCTCTATGTATGTGTATGAGGTGACCAAATCAATACTGCCAATAACCAATATTAAGGAACAGATTGAGGAT
CTGGCAAAGTATGTAGCAGAAAAAATGGGTGGTAAGATTCCAAAAGAGAAACTACCTGATTTCAGCTGGGAACTTCACATAAGTGAACTGAAATTTCAACTTAAATCCAATGTTATACCGATTGGACA
TGTCAAAAAAGGAATCTTCTACCATCGAGCTTTGCTTTTCAAGGCTCTGGCTGATAGAATTGGCATTGGTTGCTCCCTAGTTCGCGGAGAGTACGGTAGAGCGTGGAATGAAGTCATGCTGCAGAATG
ACTCTCGGAAGGGAGTGATTGGGGGCCTCCCCGCTCCTGAGATGTACGTGATTGACCTCATGTTCCATCCAGGTGGACTGATGAAGTTGAGAAGTCGAGAGGCTGATCTTTACAGATTCATTTAAGCC
ATCAGACGAACACAAGAGAGGCTCAAACAAGAAATTCACTGTGTACACTCTCTAAGACATTCTCCAAATTGATTTTATCTCTTTAAATAAAAACTTTAAATAAAAGTATTAGAAATGTTTTCTCTGCG
TAGAAATTAGGAAGCTTGGAGTGAACTTTGCTGTGCTTCTGATTTCAGGCTTTTGGCAAGAGTTCTGTCTTATTAGGTCATTTTCCGCTCACTGACCCTCACATAAAGCTGATTGTTGTCGAAATTCA
TCCAGCCCACTGTGTCCTGAGGAGCGTCTCTGTCATTTAGGAATCACATGTAGCACTCAGCTGCTGCACCCAGGACAACACTGTGGCCTCATGACTGTCATCTTTCATGCCCAGAATGCTTCAGGCAT
GCTCAGTTAAGCAAACTAAGTGAATTTTTAGTATTTGCAATCACCTTGTCTCAGTTTCATTTAAGATTTTGATAGTTTAGATAGAATAAACACAGATCTGAGTGTTACAAATTCCTTTCTAAAAATTT
TTGTTTCTATTTTTAAAAATTCATCATTAAAAACACTTTAATATAGTGAATTAAAAATATTTCTAAAGTATATTTCCATAAAATGGTTTTGGTTTCATCTTGTCTGTGTTAGCTTGGAAACATACCTT
CAGCTAAAAACAATTCTGATTTGCTCTTCCACATTTTAATGCTGGGCCATTAATATATTATTTTCAATTTATAGAACTAAAAAATTTTTATTTTTTGGAAAACTTTGAAGCATAAAGGTAGAGCAAAT
CTTTGCTGAGGAATTGTGTTTTAGTATTGAGCACAAAATGGGGAGTAAATTCACATTTCAAATGATAAGACAAAAACTACTAATGTGGTTAATCTCGTGAAGTACATATTGCCTAGTCACGCTTAAAG
TCCAGTGTTGACCTGTATAGTCATTTTCCTAGAAGACGTTTTAAAGTGAATTTGATTTTAGAAATTAAAGCTAAGATTATTTTGTATTAATTTGTAATTTCAAATAATATAATTCTTTATTTCAGAAT
AAATTTATTTCAAATGGCGTG

hide sequence

RefSeq Acc Id:

XM_017015831 ⟹ XP_016871320

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	22,928,053 - 23,038,523 (+)	NCBI

Sequence:

show sequence

AACGAGGCACAACAAGGGACTGGGGGTTCGTCTGCTGGGTTTGCGGAGCAGCTAGCTACTCGGC
GGGATCTCCCGGCAGGATGGGTAAAAAGATAAAGAAGGAAGTAGAGCCTCCTCCTAAGGATGTGTTTGACCCATTAATGATTGAAAGCAAAAAAGCAGCAACTGTGGTGTTAATGCTTAATTCTCCAG
AAGAGGAAATTTTGGCTAAAGCATGTGAAGCCATTTATAAATTTGCTTTAAAAGGTGAGGAAAATAAAACAACCCTCCTTGAACTTGGAGCTGTGGAACCTTTAACTAAGCTACTCACCCATGAAGAC
AAAATTGTAAGAAGAAATGCTACTATGATATTTGGAATCCTGGCTTCTAATAATGATGTTAAAAAATTGTTAAGGGAGTTAGATGTCATGAATTCTGTCATTGCCCAGCTCGCTCCAGAAGAAGAAGT
AGTTATCCATGAGTTTGCTAGTCTTTGTCTAGCAAACATGTCTGCAGAGTACACCAGTAAAGTGCAAATATTTGAACATGGGGGATTAGAGCCACTCATCAGACTACTGAGTAGCCCTGACCCGGATG
TAAAGAAGAACTCTATGGAATGCATTTACAACTTGGTGCAGGAATTGAATGACCTTCATATAGAAGCACTTGCAGTGATAGCCAATTGCCTTGAAGACATGGATACTATGGTGCAGATTCAGCAGACA
GGGGGTCTTAAAAAGCTCCTGTCATTTGCAGAAAACTCTACAATTCCTGATATTCAGAAGAATGCAGCAAAAGCCATTACTAAAGCAGCTTATGATCCTGAAAATAGAAAACTTTTTCATGAACAAGA
GGTTGAAAAGTGCCTTGTAGCCCTTTTGGGTTCTGAAAATGATGGAACTAAAATTGCTGCTTCCCAAGCTATTTCAGCAATGTGTGAGAATTCAGGCAGCAAAGATTTTTTCAATAATCAGGGGATTC
CACAGTTAATTCAGTTGCTAAAAAGTGACAATGAAGAGGTACGGGAAGCAGCAGCTCTAGCCCTGGCAAACCTAACCACTTGCAACCCTGCTAATGCAAACGCTGCTGCTGAAGCTGATGGTATTGAT
CCATTAATAAACCTCCTGTCTAGTAAACGAGATGGAGCCATTGCCAACGCTGCTACAGTATTAACAAACATGGCCATGCAGGAGCCCCTGCGCCTGAACATACAGAATCACGACATCATGCATGCCAT
CATCAGCCCACTGCGTTCTGCAAACACAGTCGTGCAGAGCAAAGCTGCTCTCGCTGTCACCGCAACTGCGTGTGACGTTGAAGCCCGGACTGAGTTAAGAAATTCTGGTGGATTGGAGCCCCTGGTAG
AGCTGCTACGCTCCAAGAATGATGAAGTGAGGAAGCACGCCAGTTGGGCAGTGATGGTCTGTGCTGGTGACGAGCTGACGGCCAATGAATTATGCAGGCTCGGGGCTTTAGATATCCTTGAAGAAGTT
AACGTATCAGGAACTCGGAAAAATAAATTCAGTGAGGCAGCTTATAATAAGTTGCTCAATAACAATCTTTCCCTGAAATACAGCCAGACTGGCTATTTGTCATCAAGTAACATAATTAACGATGGATT
CTATGATTATGGTCGGATAAATCCCGGCACCAAACTGTTGCCTTTGAAGGAGCTCTGCTTACAAGAACCAAGTGACCTACGGGCTGTACTCTTAATCAACAGTAAATCTTACGTTTCTCCACCTTCAT
CTATGGAAGATAAATCAGATGTTGGTTATGGACGAAGTATTTCTTCTTCATCTTCCTTAAGAAGATCAAGTAAAGAAAAGAACAATGCTGGATTTGGATCTCCCATAGAAGACAAATCAGAGCCAGCT
TCTGGACGAAATACTGTTCTCAGCAAAAGCGCCACCAAAGAAAAAGGATGGAGGAAAAGCAAAGGAAAAAAAGAAGAGGAAAAAGTGAAAGAGGAGGAAGAGGTTATGGTGGTACCAAAATTTGTTGG
TGAAGGAAGCTCTGACAAAGAATGGTGTCCTCCCTCTGACCCTGATTTCTCTATGTATGTGTATGAGGTGACCAAATCAATACTGCCAATAACCAATATTAAGGAACAGATTGAGGATCTGGCAAAGT
ATGTAGCAGAAAAAATGGGTGGTAAGATTCCAAAAGAGAAACTACCTGATTTCAGCTGGGAACTTCACATAAGTGAACTGAAATTTCAACTTAAATCCAATGTTATACCGATTGGACATGTCAAAAAA
GGAATCTTCTACCATCGAGCTTTGCTTTTCAAGGCTCTGGCTGATAGAATTGGCATTGGTTGCTCCCTAGTTCGCGGAGAGTACGGTAGAGCGTGGAATGAAGTCATGCTGCAGAATGACTCTCGGAA
GGGAGTGATTGGGGGCCTCCCCGCTCCTGAGATGTACGTGATTGACCTCATGTTCCATCCAGGTGGACTGATGAAGTTGAGAAGTCGAGAGGCTGATCTTTACAGATTCATTTAAGCCATCAGACGAA
CACAAGAGAGGCTCAAACAAGAAATTCACTGTGTACACTCTCTAAGACATTCTCCAAATTGATTTTATCTCTTTAAATAAAAACTTTAAATAAAAGTATTAGAAATGTTTTCTCTGCGTAGAAATTAG
GAAGCTTGGAGTGAACTTTGCTGTGCTTCTGATTTCAGGCTTTTGGCAAGAGTTCTGTCTTATTAGGTCATTTTCCGCTCACTGACCCTCACATAAAGCTGATTGTTGTCGAAATTCATCCAGCCCAC
TGTGTCCTGAGGAGCGTCTCTGTCATTTAGGAATCACATGTAGCACTCAGCTGCTGCACCCAGGACAACACTGTGGCCTCATGACTGTCATCTTTCATGCCCAGAATGCTTCAGGCATGCTCAGTTAA
GCAAACTAAGTGAATTTTTAGTATTTGCAATCACCTTGTCTCAGTTTCATTTAAGATTTTGATAGTTTAGATAGAATAAACACAGATCTGAGTGTTACAAATTCCTTTCTAAAAATTTTTGTTTCTAT
TTTTAAAAATTCATCATTAAAAACACTTTAATATAGTGAATTAAAAATATTTCTAAAGTATATTTCCATAAAATGGTTTTGGTTTCATCTTGTCTGTGTTAGCTTGGAAACATACCTTCAGCTAAAAA
CAATTCTGATTTGCTCTTCCACATTTTAATGCTGGGCCATTAATATATTATTTTCAATTTATAGAACTAAAAAATTTTTATTTTTTGGAAAACTTTGAAGCATAAAGGTAGAGCAAATCTTTGCTGAG
GAATTGTGTTTTAGTATTGAGCACAAAATGGGGAGTAAATTCACATTTCAAATGATAAGACAAAAACTACTAATGTGGTTAATCTCGTGAAGTACATATTGCCTAGTCACGCTTAAAGTCCAGTGTTG
ACCTGTATAGTCATTTTCCTAGAAGACGTTTTAAAGTGAATTTGATTTTAGAAATTAAAGCTAAGATTATTTTGTATTAATTTGTAATTTCAAATAATATAATTCTTTATTTCAGAATAAATTTATTT
CAAATGGCGTG

hide sequence

RefSeq Acc Id:

XM_017015832 ⟹ XP_016871321

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	22,928,053 - 23,014,477 (+)	NCBI

Sequence:

show sequence

AACGAGGCACAACAAGGGACTGGGGGTTCGTCTGCTGGGTTTGCGGAGCAGCTAGCTACTCGGC
GGGATCTCCCGGCAGGATGGGTAAAAAGATAAAGAAGGAAGTAGAGCCTCCTCCTAAGGATGTGTTTGACCCATTAATGATTGAAAGCAAAAAAGCAGCAACTGTGGTGTTAATGCTTAATTCTCCAG
AAGAGGAAATTTTGGCTAAAGCATGTGAAGCCATTTATAAATTTGCTTTAAAAGGTGAGGAAAATAAAACAACCCTCCTTGAACTTGGAGCTGTGGAACCTTTAACTAAGCTACTCACCCATGAAGAC
AAAATTGTAAGAAGAAATGCTACTATGATATTTGGAATCCTGGCTTCTAATAATGATGTTAAAAAATTGTTAAGGGAGTTAGATGTCATGAATTCTGTCATTGCCCAGCTCGCTCCAGAAGAAGAAGT
AGTTATCCATGAGTTTGCTAGTCTTTGTCTAGCAAACATGTCTGCAGAGTACACCAGTAAAGTGCAAATATTTGAACATGGGGGATTAGAGCCACTCATCAGACTACTGAGTAGCCCTGACCCGGATG
TAAAGAAGAACTCTATGGAATGCATTTACAACTTGGTGCAGGATTTTCAGTGTCGAGCTAAACTTCAAGAACTAAATGCAATACCTCCTATCTTAGATCTCTTGAAGTCAGAATATCCAGTGATTCAG
TTGTTGGCTCTCAAAACCTTAGGTGTTATTGCAAATGATAAGGAGTCTCGAACAATGCTAAGAGACAATCAAGGATTGGACCATCTTATTAAGATCCTAGAAACTAAGGAATTGAATGACCTTCATAT
AGAAGCACTTGCAGTGATAGCCAATTGCCTTGAAGACATGGATACTATGGTGCAGATTCAGCAGACAGGGGGTCTTAAAAAGCTCCTGTCATTTGCAGAAAACTCTACAATTCCTGATATTCAGAAGA
ATGCAGCAAAAGCCATTACTAAAGCAGCTTATGATCCTGAAAATAGAAAACTTTTTCATGAACAAGAGGTTGAAAAGTGCCTTGTAGCCCTTTTGGGTTCTGAAAATGATGGAACTAAAATTGCTGCT
TCCCAAGCTATTTCAGCAATGTGTGAGAATTCAGGCAGCAAAGATTTTTTCAATAATCAGGGGATTCCACAGTTAATTCAGTTGCTAAAAAGTGACAATGAAGAGGTACGGGAAGCAGCAGCTCTAGC
CCTGGCAAACCTAACCACTTGCAACCCTGCTAATGCAAACGCTGCTGCTGAAGCTGATGGTATTGATCCATTAATAAACCTCCTGTCTAGTAAACGAGATGGAGCCATTGCCAACGCTGCTACAGTAT
TAACAAACATGGCCATGCAGGAGCCCCTGCGCCTGAACATACAGAATCACGACATCATGCATGCCATCATCAGCCCACTGCGTTCTGCAAACACAGTCGTGCAGAGCAAAGCTGCTCTCGCTGTCACC
GCAACTGCGTGTGACGTTGAAGCCCGGACTGAGTTAAGAAATTCTGGTGGATTGGAGCCCCTGGTAGAGCTGCTACGCTCCAAGAATGATGAAGTGAGGAAGCACGCCAGTTGGGCAGTGATGGTCTG
TGCTGGTGACGAGCTGACGGCCAATGAATTATGCAGGCTCGGGGCTTTAGATATCCTTGAAGAAGTTAACGTATCAGGAACTCGGAAAAATAAATTCAGTGAGGCAGCTTATAATAAGTTGCTCAATA
ACAATCTTTCCCTGAAATACAGCCAGACTGGCTATTTGTCATCAAGTAACATAATTAACGATGGATTCTATGATTATGGTCGGATAAATCCCGGCACCAAACTGTTGCCTTTGAAGGAGCTCTGCTTA
CAAGAACCAAGTGACCTACGGGCTGTACTCTTAATCAACAGTAAATCTTACGTTTCTCCACCTTCATCTATGGAAGATAAATCAGATGTTGGTTATGGACGAAGTATTTCTTCTTCATCTTCCTTAAG
AAGATCAAGTAAAGAAAAGAACAATGCTGGATTTGGATCTCCCATAGAAGACAAATCAGAGCCAGCTTCTGGACGAAATACTGTTCTCAGCAAAAGCGCCACCAAAGAAAAAGGATGGAGCTCACTCC
CCACTTCAAGATAAACCCTGAAGCACTCCTAGGATTTAAGAGGATTGTTGGCATGAGGAGAACACAGAGACTTTGGATTCAGACACAACTGGGCCTTGGTCTTCTGAATTGTAAATGAAAATGATGAT
CCCTGCCTCAAAGAGCTGCTGTAAGAGGAGAGATGGTGTCAGGAAAGTGCCTGACCATCACCTAGCACACTTAGGGGCTCAATGTGCGTCCCTTCTCTCTTCCCTTCTTAGCCTTTGGTCCATTGAGG
GGTAGATTAGCCATAGCCCTGTTGTCCTGTTGCCTGTCTTTTGGTCAACCCTTCTTGTCTTATGACTATTAAAACTTTGGACTCCTGGAAATAGAATAAAATATTTTAACTGCATTCGTCTGAAAA

hide sequence

RefSeq Acc Id:

XM_017015833 ⟹ XP_016871322

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	22,928,053 - 23,014,477 (+)	NCBI

Sequence:

show sequence

AACGAGGCACAACAAGGGACTGGGGGTTCGTCTGCTGGGTTTGCGGAGCAGCTAGCTACTCGGCGGGATCTCCCGGCAGGATGGGTAAAAAGATAAAGAAGGAAGTAGAGCCTCCTCCTAAGGATGTG
TTTGACCCATTAATGATTGAAAGCAAAAAAGCAGCAACTGTGGTGTTAATGCTTAATTCTCCAGAAGAGGAAATTTTGGCTAAAGCATGTGAAGCCATTTATAAATTTGCTTTAAAAGGTGAGGAAAA
TAAAACAACCCTCCTTGAACTTGGAGCTGTGGAACCTTTAACTAAGCTACTCACCCATGAAGACAAAATTGTAAGAAGAAATGCTACTATGATATTTGGAATCCTGGCTTCTAATAATGATGTTAAAA
AATTGTTAAGGGAGTTAGATGTCATGAATTCTGTCATTGCCCAGCTCGCTCCAGAAGAAGAAGTAGTTATCCATGAGTTTGCTAGTCTTTGTCTAGCAAACATGTCTGCAGAGTACACCAGTAAAGTG
CAAATATTTGAACATGGGGGATTAGAGCCACTCATCAGACTACTGAGTAGCCCTGACCCGGATGTAAAGAAGAACTCTATGGAATGCATTTACAACTTGGTGCAGGAATTGAATGACCTTCATATAGA
AGCACTTGCAGTGATAGCCAATTGCCTTGAAGACATGGATACTATGGTGCAGATTCAGCAGACAGGGGGTCTTAAAAAGCTCCTGTCATTTGCAGAAAACTCTACAATTCCTGATATTCAGAAGAATG
CAGCAAAAGCCATTACTAAAGCAGCTTATGATCCTGAAAATAGAAAACTTTTTCATGAACAAGAGGTTGAAAAGTGCCTTGTAGCCCTTTTGGGTTCTGAAAATGATGGAACTAAAATTGCTGCTTCC
CAAGCTATTTCAGCAATGTGTGAGAATTCAGGCAGCAAAGATTTTTTCAATAATCAGGGGATTCCACAGTTAATTCAGTTGCTAAAAAGTGACAATGAAGAGGTACGGGAAGCAGCAGCTCTAGCCCT
GGCAAACCTAACCACTTGCAACCCTGCTAATGCAAACGCTGCTGCTGAAGCTGATGGTATTGATCCATTAATAAACCTCCTGTCTAGTAAACGAGATGGAGCCATTGCCAACGCTGCTACAGTATTAA
CAAACATGGCCATGCAGGAGCCCCTGCGCCTGAACATACAGAATCACGACATCATGCATGCCATCATCAGCCCACTGCGTTCTGCAAACACAGTCGTGCAGAGCAAAGCTGCTCTCGCTGTCACCGCA
ACTGCGTGTGACGTTGAAGCCCGGACTGAGTTAAGAAATTCTGGTGGATTGGAGCCCCTGGTAGAGCTGCTACGCTCCAAGAATGATGAAGTGAGGAAGCACGCCAGTTGGGCAGTGATGGTCTGTGC
TGGTGACGAGCTGACGGCCAATGAATTATGCAGGCTCGGGGCTTTAGATATCCTTGAAGAAGTTAACGTATCAGGAACTCGGAAAAATAAATTCAGTGAGGCAGCTTATAATAAGTTGCTCAATAACA
ATCTTTCCCTGAAATACAGCCAGACTGGCTATTTGTCATCAAGTAACATAATTAACGATGGATTCTATGATTATGGTCGGATAAATCCCGGCACCAAACTGTTGCCTTTGAAGGAGCTCTGCTTACAA
GAACCAAGTGACCTACGGGCTGTACTCTTAATCAACAGTAAATCTTACGTTTCTCCACCTTCATCTATGGAAGATAAATCAGATGTTGGTTATGGACGAAGTATTTCTTCTTCATCTTCCTTAAGAAG
ATCAAGTAAAGAAAAGAACAAAAAAAATAGTTATCATTTTAGTGCTGGATTTGGATCTCCCATAGAAGACAAATCAGAGCCAGCTTCTGGACGAAATACTGTTCTCAGCAAAAGCGCCACCAAAGAAA
AAGGATGGAGCTCACTCCCCACTTCAAGATAAACCCTGAAGCACTCCTAGGATTTAAGAGGATTGTTGGCATGAGGAGAACACAGAGACTTTGGATTCAGACACAACTGGGCCTTGGTCTTCTGAATT
GTAAATGAAAATGATGATCCCTGCCTCAAAGAGCTGCTGTAAGAGGAGAGATGGTGTCAGGAAAGTGCCTGACCATCACCTAGCACACTTAGGGGCTCAATGTGCGTCCCTTCTCTCTTCCCTTCTTA
GCCTTTGGTCCATTGAGGGGTAGATTAGCCATAGCCCTGTTGTCCTGTTGCCTGTCTTTTGGTCAACCCTTCTTGTCTTATGACTATTAAAACTTTGGACTCCTGGAAATAGAATAAAATATTTTAAC
TGCATTCGTCTGAAAA

hide sequence

RefSeq Acc Id:

XM_054365001 ⟹ XP_054220976

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	22,947,064 - 23,057,478 (+)	NCBI

RefSeq Acc Id:

XM_054365002 ⟹ XP_054220977

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	22,947,064 - 23,057,478 (+)	NCBI

RefSeq Acc Id:

XM_054365003 ⟹ XP_054220978

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	22,947,064 - 23,057,478 (+)	NCBI

RefSeq Acc Id:

XM_054365004 ⟹ XP_054220979

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	22,947,064 - 23,035,900 (+)	NCBI

RefSeq Acc Id:

XM_054365005 ⟹ XP_054220980

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	22,947,064 - 23,033,438 (+)	NCBI

RefSeq Acc Id:

XM_054365006 ⟹ XP_054220981

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	22,947,064 - 23,033,438 (+)	NCBI

RefSeq Acc Id:

XM_054365007 ⟹ XP_054220982

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	23,014,965 - 23,057,478 (+)	NCBI


Protein RefSeqs	NP_001269674	(Get FASTA)	NCBI Sequence Viewer
	NP_001269675	(Get FASTA)	NCBI Sequence Viewer
	NP_001269676	(Get FASTA)	NCBI Sequence Viewer
	NP_775104	(Get FASTA)	NCBI Sequence Viewer
	XP_005252437	(Get FASTA)	NCBI Sequence Viewer
	XP_005252438	(Get FASTA)	NCBI Sequence Viewer
	XP_011517652	(Get FASTA)	NCBI Sequence Viewer
	XP_011517653	(Get FASTA)	NCBI Sequence Viewer
	XP_016871320	(Get FASTA)	NCBI Sequence Viewer
	XP_016871321	(Get FASTA)	NCBI Sequence Viewer
	XP_016871322	(Get FASTA)	NCBI Sequence Viewer
	XP_054220976	(Get FASTA)	NCBI Sequence Viewer
	XP_054220977	(Get FASTA)	NCBI Sequence Viewer
	XP_054220978	(Get FASTA)	NCBI Sequence Viewer
	XP_054220979	(Get FASTA)	NCBI Sequence Viewer
	XP_054220980	(Get FASTA)	NCBI Sequence Viewer
	XP_054220981	(Get FASTA)	NCBI Sequence Viewer
	XP_054220982	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH39312	(Get FASTA)	NCBI Sequence Viewer
	AAR99738	(Get FASTA)	NCBI Sequence Viewer
	BAB71463	(Get FASTA)	NCBI Sequence Viewer
	BAC05389	(Get FASTA)	NCBI Sequence Viewer
	BAG63485	(Get FASTA)	NCBI Sequence Viewer
	BAG64125	(Get FASTA)	NCBI Sequence Viewer
	EAW86137	(Get FASTA)	NCBI Sequence Viewer
	EAW86138	(Get FASTA)	NCBI Sequence Viewer
	EAW86139	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000298032
	ENSP00000298032.5
	ENSP00000365711
	ENSP00000386943
	ENSP00000386943.3
	ENSP00000387288
	ENSP00000387288.3
GenBank Protein	Q5W041	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_775104 ⟸ NM_173081
- Peptide Label:	isoform 1
- UniProtKB:	Q8N7B0 (UniProtKB/Swiss-Prot), Q8IXS5 (UniProtKB/Swiss-Prot), B7ZBN7 (UniProtKB/Swiss-Prot), B7ZBN6 (UniProtKB/Swiss-Prot), B4DZL3 (UniProtKB/Swiss-Prot), A6NH64 (UniProtKB/Swiss-Prot), A0PG76 (UniProtKB/Swiss-Prot), Q96M49 (UniProtKB/Swiss-Prot), Q5W041 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MGKKIKKEVEPPPKDVFDPLMIESKKAATVVLMLNSPEEEILAKACEAIYKFALKGEENKTTLLELGAVEPLTKLLTHEDKIVRRNATMIFGILASNNDVKKLLRELDVMNSVIAQLAPEEEVVIHEF ASLCLANMSAEYTSKVQIFEHGGLEPLIRLLSSPDPDVKKNSMECIYNLVQDFQCRAKLQELNAIPPILDLLKSEYPVIQLLALKTLGVIANDKESRTMLRDNQGLDHLIKILETKELNDLHIEALAV IANCLEDMDTMVQIQQTGGLKKLLSFAENSTIPDIQKNAAKAITKAAYDPENRKLFHEQEVEKCLVALLGSENDGTKIAASQAISAMCENSGSKDFFNNQGIPQLIQLLKSDNEEVREAAALALANLT TCNPANANAAAEADGIDPLINLLSSKRDGAIANAATVLTNMAMQEPLRLNIQNHDIMHAIISPLRSANTVVQSKAALAVTATACDVEARTELRNSGGLEPLVELLRSKNDEVRKHASWAVMVCAGDEL TANELCRLGALDILEEVNVSGTRKNKFSEAAYNKLLNNNLSLKYSQTGYLSSSNIINDGFYDYGRINPGTKLLPLKELCLQEPSDLRAVLLINSKSYVSPPSSMEDKSDVGYGRSISSSSSLRRSSKE KNKKNSYHFSAGFGSPIEDKSEPASGRNTVLSKSATKEKGWRKSKGKKEEEKVKEEEEVMVVPKFVGEGSSDKEWCPPSDPDFSMYVYEVTKSILPITNIKEQIEDLAKYVAEKMGGKIPKEKLPDFS WELHISELKFQLKSNVIPIGHVKKGIFYHRALLFKALADRIGIGCSLVRGEYGRAWNEVMLQNDSRKGVIGGLPAPEMYVIDLMFHPGGLMKLRSREADLYRFI hide sequence

RefSeq Acc Id:

XP_005252437 ⟸ XM_005252380

- Peptide Label:

isoform X1

- Sequence:

show sequence

MGKKIKKEVEPPPKDVFDPLMIESKKAATVVLMLNSPEEEILAKACEAIYKFALKGEENKTTLLELGAVEPLTKLLTHEDKIVRRNATMIFGILASNNDVKKLLRELDVMNSVIAQLAPEEEVVIHEF
ASLCLANMSAEYTSKVQIFEHGGLEPLIRLLSSPDPDVKKNSMECIYNLVQELNDLHIEALAVIANCLEDMDTMVQIQQTGGLKKLLSFAENSTIPDIQKNAAKAITKAAYDPENRKLFHEQEVEKCL
VALLGSENDGTKIAASQAISAMCENSGSKDFFNNQGIPQLIQLLKSDNEEVREAAALALANLTTCNPANANAAAEADGIDPLINLLSSKRDGAIANAATVLTNMAMQEPLRLNIQNHDIMHAIISPLR
SANTVVQSKAALAVTATACDVEARTELRNSGGLEPLVELLRSKNDEVRKHASWAVMVCAGDELTANELCRLGALDILEEVNVSGTRKNKFSEAAYNKLLNNNLSLKYSQTGYLSSSNIINDGFYDYGR
INPGTKLLPLKELCLQEPSDLRAVLLINSKSYVSPPSSMEDKSDVGYGRSISSSSSLRRSSKEKNKKNSYHFSAGFGSPIEDKSEPASGRNTVLSKSATKEKGWRKSKGKKEEEKVKEEEEVMVVPKF
VGEGSSDKEWCPPSDPDFSMYVYEVTKSILPITNIKEQIEDLAKYVAEKMGGKIPKEKLPDFSWELHISELKFQLKSNVIPIGHVKKGIFYHRALLFKALADRIGIGCSLVRGEYGRAWNEVMLQNDS
RKGVIGGLPAPEMYVIDLMFHPGGLMKLRSREADLYRFI

hide sequence

RefSeq Acc Id:

XP_005252438 ⟸ XM_005252381

- Peptide Label:

isoform X3

- Sequence:

show sequence

MIFGILASNNDVKKLLRELDVMNSVIAQLAPEEEVVIHEFASLCLANMSAEYTSKVQIFEHGGL
EPLIRLLSSPDPDVKKNSMECIYNLVQDFQCRAKLQELNAIPPILDLLKSEYPVIQLLALKTLGVIANDKESRTMLRDNQGLDHLIKILETKELNDLHIEALAVIANCLEDMDTMVQIQQTGGLKKLL
SFAENSTIPDIQKNAAKAITKAAYDPENRKLFHEQEVEKCLVALLGSENDGTKIAASQAISAMCENSGSKDFFNNQGIPQLIQLLKSDNEEVREAAALALANLTTCNPANANAAAEADGIDPLINLLS
SKRDGAIANAATVLTNMAMQEPLRLNIQNHDIMHAIISPLRSANTVVQSKAALAVTATACDVEARTELRNSGGLEPLVELLRSKNDEVRKHASWAVMVCAGDELTANELCRLGALDILEEVNVSGTRK
NKFSEAAYNKLLNNNLSLKYSQTGYLSSSNIINDGFYDYGRINPGTKLLPLKELCLQEPSDLRAVLLINSKSYVSPPSSMEDKSDVGYGRSISSSSSLRRSSKEKNKKNSYHFSAGFGSPIEDKSEPA
SGRNTVLSKSATKEKGWRKSKGKKEEEKVKEEEEVMVVPKFVGEGSSDKEWCPPSDPDFSMYVYEVTKSILPITNIKEQIEDLAKYVAEKMGGKIPKEKLPDFSWELHISELKFQLKSNVIPIGHVKK
GIFYHRALLFKALADRIGIGCSLVRGEYGRAWNEVMLQNDSRKGVIGGLPAPEMYVIDLMFHPGGLMKLRSREADLYRFI

hide sequence

RefSeq Acc Id:	NP_001269674 ⟸ NM_001282745
- Peptide Label:	isoform 2
- UniProtKB:	Q5W041 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MGKKIKKEVEPPPKDVFDPLMIESKKAATVVLMLNSPEEEILAKACEAIYKFALKGEENKTTLLELGAVEPLTKLLTHEDKIVRRNATMIFGILASNNDVKKLLRELDVMNSVIAQLAPEEEVVIHEF ASLCLANMSAEYTSKVQIFEHGGLEPLIRLLSSPDPDVKKNSMECIYNLVQDFQCRAKLQELNAIPPILDLLKSEYPVIQLLALKTLGVIANDKESRTMLRDNQGLDHLIKILETKELNDLHIEALAV IANCLEDMDTMVQIQQTGGLKKLLSFAENSTIPDIQKNAAKAITKAAYDPENRKLFHEQEVEKCLVALLGSENDGTKIAASQAISAMCENSGSKDFFNNQGIPQLIQLLKSDNEEVREAAALALANLT TCNPANANAAAEADGIDPLINLLSSKRDGAIANAATVLTNMAMQEPLRLNIQNHDIMHAIISPLRSANTVVQSKAALAVTATACDVEARTELRNSGGLEPLVELLRSKNDEVRKHASWAVMVCAGDEL TANELCRLGALDILEEVNVSGTRKNKFSEAAYNKLLNNNLSLKYSQTGYLSSSNIINDGFYDYGRINPGTKLLPLKELCLQEPSDLRAVLLINSKSYVSPPSSMEDKSDVGYGRSISSSSSLRRSSKE KNNAGFGSPIEDKSEPASGRNTVLSKSATKEKGWRKSKGKKEEEKVKEEEEVMVVPKFVGEGSSDKEWCPPSDPDFSMYVYEVTKSILPITNIKEQIEDLAKYVAEKMGGKIPKEKLPDFSWELHISE LKFQLKSNVIPIGHVKKGIFYHRALLFKALADRIGIGCSLVRGEYGRAWNEVMLQNDSRKGVIGGLPAPEMYVIDLMFHPGGLMKLRSREADLYRFI hide sequence

RefSeq Acc Id:	NP_001269676 ⟸ NM_001282747
- Peptide Label:	isoform 4
- UniProtKB:	B4DXS3 (UniProtKB/TrEMBL)
- Sequence:	show sequence MDTMVQIQQTGGLKKLLSFAENSTIPDIQKNAAKAITKAAYDPENRKLFHEQEVEKCLVALLGSENDGTKIAASQAISAMCENSGSKDFFNNQGIPQLIQLLKSDNEEVREAAALALANLTTCNPANA NAAAEADGIDPLINLLSSKRDGAIANAATVLTNMAMQEPLRLNIQNHDIMHAIISPLRSANTVVQSKAALAVTATACDVEARTELRNSGGLEPLVELLRSKNDEVRKHASWAVMVCAGDELTANELCR LGALDILEEVNVSGTRKNKFSEAAYNKLLNNNLSLKYSQTGYLSSSNIINDGFYDYGRINPGTKLLPLKELCLQEPSDLRAVLLINSKSYVSPPSSMEDKSDVGYGRSISSSSSLRRSSKEKNKKNSY HFSAGFGSPIEDKSEPASGRNTVLSKSATKEKGWRKSKGKKEEEKVKEEEEVMVVPKFVGEGSSDKEWCPPSDPDFSMYVYEVTKSILPITNIKEQIEDLAKYVAEKMGGKIPKEKLPDFSWELHISE LKFQLKSNVIPIGHVKKGIFYHRALLFKALADRIGIGCSLVRGEYGRAWNEVMLQNDSRKGVIGGLPAPEMYVIDLMFHPGGLMKLRSREADLYRFI hide sequence

Protein Domains

EDR1/CTR1/ARMC3-like peptidase-like

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q5W041-F1-model_v2	AlphaFold	Q5W041	1-872	view protein structure

RGD ID:

7217173

Promoter ID:

EPDNEW_H14333

Type:

initiation region

Name:

ARMC3_2

Description:

armadillo repeat containing 3

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H14334

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	22,927,924 - 22,927,984	EPDNEW

RGD ID:

7217175

Promoter ID:

EPDNEW_H14334

Type:

initiation region

Name:

ARMC3_1

Description:

armadillo repeat containing 3

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H14333

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	22,928,074 - 22,928,134	EPDNEW

RGD ID:

6787359

Promoter ID:

HG_KWN:8848

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

K562, Lymphoblastoid

Transcripts:

ENST00000376523, ENST00000376528, ENST00000409049, ENST00000409983, OTTHUMT00000047197, OTTHUMT00000047203, OTTHUMT00000334597, OTTHUMT00000334598, OTTHUMT00000334599, OTTHUMT00000334600

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	10	23,256,616 - 23,257,116 (+)	MPROMDB

Database	Acc Id	Source(s)
COSMIC	ARMC3	COSMIC
Ensembl Genes	ENSG00000165309	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000298032	ENTREZGENE
	ENST00000298032.10	UniProtKB/Swiss-Prot
	ENST00000376528	ENTREZGENE
	ENST00000409049	ENTREZGENE
	ENST00000409049.7	UniProtKB/Swiss-Prot
	ENST00000409983	ENTREZGENE
	ENST00000409983.7	UniProtKB/Swiss-Prot
Gene3D-CATH	1.25.10.10	UniProtKB/Swiss-Prot
GTEx	ENSG00000165309	GTEx
HGNC ID	HGNC:30964	ENTREZGENE
Human Proteome Map	ARMC3	Human Proteome Map
InterPro	ARM-like	UniProtKB/Swiss-Prot
	ARM-type_fold	UniProtKB/Swiss-Prot
	Armadillo	UniProtKB/Swiss-Prot
	Armadillo-Ser/Thr_Kinase	UniProtKB/Swiss-Prot
	EDR1/CTR1/ARMC3-like_pept-like	UniProtKB/Swiss-Prot
KEGG Report	hsa:219681	UniProtKB/Swiss-Prot
NCBI Gene	219681	ENTREZGENE
OMIM	611226	OMIM
PANTHER	ARMADILLO REPEAT-CONTAINING PROTEIN 3	UniProtKB/Swiss-Prot
	ARMADILLO REPEAT-CONTAINING PROTEIN 3	UniProtKB/Swiss-Prot
Pfam	Arm	UniProtKB/Swiss-Prot
	EDR1	UniProtKB/Swiss-Prot
PharmGKB	PA134917281	PharmGKB
PROSITE	ARM_REPEAT	UniProtKB/Swiss-Prot
SMART	ARM	UniProtKB/Swiss-Prot
Superfamily-SCOP	SSF48371	UniProtKB/Swiss-Prot
UniProt	A0PG76	ENTREZGENE
	A6NH64	ENTREZGENE
	ARMC3_HUMAN	UniProtKB/Swiss-Prot
	B4DXS3	ENTREZGENE, UniProtKB/TrEMBL
	B4DZL3	ENTREZGENE
	B7ZBN6	ENTREZGENE
	B7ZBN7	ENTREZGENE
	C9JC46_HUMAN	UniProtKB/TrEMBL
	Q5W041	ENTREZGENE
	Q8IXS5	ENTREZGENE
	Q8N7B0	ENTREZGENE
	Q96M49	ENTREZGENE
UniProt Secondary	A0PG76	UniProtKB/Swiss-Prot
	A6NH64	UniProtKB/Swiss-Prot
	B4DZL3	UniProtKB/Swiss-Prot
	B7ZBN6	UniProtKB/Swiss-Prot
	B7ZBN7	UniProtKB/Swiss-Prot
	Q8IXS5	UniProtKB/Swiss-Prot
	Q8N7B0	UniProtKB/Swiss-Prot
	Q96M49	UniProtKB/Swiss-Prot

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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Imported Disease Annotations - ClinVar