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Gene: RCOR3 (REST corepressor 3) Homo sapiens

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Symbol:

RCOR3

Name:

REST corepressor 3

RGD ID:

1350848

HGNC Page

HGNC:25594

Description:

Predicted to enable enzyme binding activity and transcription corepressor activity. Predicted to be involved in negative regulation of DNA-templated transcription and regulation of transcription by RNA polymerase II. Located in cytosol and nucleoplasm.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

FLJ10876; FLJ16298; RP11-318L16.1

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):	Rcor3 (REST corepressor 3)	HGNC	EggNOG, Ensembl, HGNC, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):	Rcor3 (REST corepressor 3)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, OMA, OrthoDB, Panther
Chinchilla lanigera (long-tailed chinchilla):	Rcor3 (REST corepressor 3)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	RCOR3 (REST corepressor 3)	NCBI	Ortholog
Canis lupus familiaris (dog):	RCOR3 (REST corepressor 3)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Rcor3 (REST corepressor 3)	NCBI	Ortholog
Sus scrofa (pig):	RCOR3 (REST corepressor 3)	HGNC	Ensembl, NCBI, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	RCOR3 (REST corepressor 3)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Rcor3 (REST corepressor 3)	NCBI	Ortholog
Other homologs ²
Rattus norvegicus (Norway rat):	Spata18 (spermatogenesis associated 18)	HGNC	OMA
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Rcor3 (REST corepressor 3)	Alliance	DIOPT (HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Rcor3 (REST corepressor 3)	Alliance	DIOPT (HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	rcor3 (REST corepressor 3)	Alliance	DIOPT (Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid\|ZFIN)
Caenorhabditis elegans (roundworm):	rcor-1	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OrthoFinder\|OrthoInspector\|PANTHER)
Drosophila melanogaster (fruit fly):	CoRest	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OrthoFinder\|OrthoInspector\|PANTHER\|SonicParanoid)
Caenorhabditis elegans (roundworm):	spr-1	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OrthoFinder\|OrthoInspector\|PANTHER)
Xenopus laevis (African clawed frog):	rcor3.S	Alliance	DIOPT (Xenbase)
Xenopus tropicalis (tropical clawed frog):	rcor3	Alliance	DIOPT (Ensembl Compara\|OMA\|OrthoFinder\|PANTHER\|PhylomeDB)
Xenopus laevis (African clawed frog):	rcor3.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	1	211,259,366 - 211,316,385 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	1	211,258,377 - 211,316,385 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	1	211,432,708 - 211,489,727 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	1	209,499,949 - 209,556,200 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	1	207,821,720 - 207,877,972	NCBI
Celera	1	184,656,707 - 184,716,396 (+)	NCBI		Celera
Cytogenetic Map	1	q32.2-q32.3	NCBI
HuRef	1	182,109,654 - 182,166,679 (+)	NCBI		HuRef
CHM1_1	1	212,705,251 - 212,762,151 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	1	210,504,931 - 210,561,986 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

gastrointestinal stromal tumor (IAGP)

parathyroid carcinoma (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

1,2-dimethylhydrazine (ISO)

17alpha-ethynylestradiol (ISO)

2,2',4,4',5,5'-hexachlorobiphenyl (ISO)

2,2',5,5'-tetrachlorobiphenyl (ISO)

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

3-isobutyl-1-methyl-7H-xanthine (EXP)

4,4'-diaminodiphenylmethane (ISO)

4,4'-sulfonyldiphenol (EXP)

acrolein (EXP)

aflatoxin B1 (ISO)

alpha-pinene (EXP)

alpha-Zearalanol (ISO)

antirheumatic drug (EXP)

bisphenol A (EXP,ISO)

bisphenol F (EXP)

cadmium dichloride (EXP)

caffeine (EXP)

casticin (ISO)

coumarin (EXP)

coumestrol (EXP)

crocidolite asbestos (ISO)

crotonaldehyde (EXP)

dexamethasone (EXP)

Dibutyl phosphate (EXP)

dibutyl phthalate (ISO)

elemental selenium (EXP)

Enterolactone (EXP)

epoxiconazole (ISO)

ethanol (EXP)

folic acid (ISO)

FR900359 (EXP)

fulvestrant (EXP)

geraniol (EXP)

hydrogen peroxide (EXP)

indometacin (EXP)

leflunomide (EXP)

menadione (EXP)

methyl methanesulfonate (EXP)

ozone (EXP)

PCB138 (ISO)

pentachlorophenol (ISO)

perfluorooctanoic acid (ISO)

phenobarbital (ISO)

raloxifene (EXP)

selenium atom (EXP)

sodium arsenate (ISO)

sodium arsenite (EXP)

sodium fluoride (ISO)

tamoxifen (EXP,ISO)

tert-butyl hydroperoxide (EXP)

tetrachloromethane (ISO)

thioacetamide (ISO)

titanium dioxide (ISO)

trichostatin A (EXP)

triptonide (ISO)

troglitazone (ISO)

tunicamycin (EXP)

valproic acid (ISO)

vitamin E (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

negative regulation of DNA-templated transcription (IBA)

regulation of transcription by RNA polymerase II (IBA)

Cellular Component

cytosol (IDA)

histone deacetylase complex (IBA)

nucleoplasm (IDA)

nucleus (IEA)

transcription regulator complex (IBA)

Molecular Function

enzyme binding (ISO)

protein binding (IPI)

transcription corepressor activity (IBA)

Phenotype Annotations Click to see Annotation Detail View

Human Phenotype

Gastrointestinal stroma tumor (IAGP)

Parathyroid carcinoma (IAGP)

References

References - curated

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

Additional References at PubMed

PMID:8889548	PMID:10718198	PMID:10737800	PMID:14702039	PMID:15342556	PMID:15489334	PMID:16189514	PMID:16344560	PMID:16710414	PMID:17081983	PMID:18029348	PMID:19060904
PMID:19274049	PMID:19322201	PMID:19394292	PMID:19773279	PMID:20360068	PMID:21150319	PMID:21258344	PMID:21516116	PMID:21765449	PMID:21832049	PMID:21873635	PMID:21988832
PMID:23414517	PMID:23455924	PMID:23752268	PMID:24981860	PMID:25416956	PMID:25798074	PMID:26186194	PMID:26344197	PMID:26496610	PMID:26593974	PMID:26638075	PMID:26871637
PMID:27107014	PMID:27634302	PMID:27684187	PMID:27705803	PMID:27926873	PMID:28242625	PMID:28514442	PMID:28611215	PMID:28883622	PMID:29395067	PMID:29778605	PMID:29892012
PMID:30804502	PMID:30886144	PMID:30894540	PMID:31182584	PMID:31586073	PMID:31753913	PMID:32296183	PMID:32814053	PMID:32891193	PMID:33640491	PMID:33961781	PMID:34079125
PMID:34383978	PMID:34709266	PMID:35140242	PMID:35271311	PMID:35831314	PMID:36129980	PMID:36543142	PMID:37314216	PMID:37536630

Genomics

Comparative Map Data

RCOR3
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	1	211,259,366 - 211,316,385 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	1	211,258,377 - 211,316,385 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	1	211,432,708 - 211,489,727 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	1	209,499,949 - 209,556,200 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	1	207,821,720 - 207,877,972	NCBI
Celera	1	184,656,707 - 184,716,396 (+)	NCBI		Celera
Cytogenetic Map	1	q32.2-q32.3	NCBI
HuRef	1	182,109,654 - 182,166,679 (+)	NCBI		HuRef
CHM1_1	1	212,705,251 - 212,762,151 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	1	210,504,931 - 210,561,986 (+)	NCBI		T2T-CHM13v2.0

Rcor3
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	1	191,782,842 - 191,822,371 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	1	191,782,846 - 191,822,359 (-)	Ensembl		GRCm39 Ensembl
GRCm38	1	192,098,546 - 192,138,074 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	1	192,098,546 - 192,138,062 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	1	193,924,340 - 193,961,669 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	1	193,800,994 - 193,838,511 (-)	NCBI		MGSCv36	mm8
Celera	1	198,993,375 - 199,030,668 (-)	NCBI		Celera
Cytogenetic Map	1	H6	NCBI
cM Map	1	97.23	NCBI

Rcor3
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	13	106,156,166 - 106,196,542 (-)	NCBI		GRCr8
mRatBN7.2	13	103,624,966 - 103,665,565 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	13	103,624,971 - 103,665,565 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	13	106,147,164 - 106,185,492 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	13	107,530,997 - 107,569,325 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	13	104,745,999 - 104,784,327 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	13	110,822,149 - 110,864,469 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	13	110,822,150 - 110,864,469 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	13	115,381,178 - 115,422,102 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
Celera	13	103,066,186 - 103,096,345 (-)	NCBI		Celera
Cytogenetic Map	13	q27	NCBI

Rcor3
(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_004955489	1,018,529 - 1,066,807 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955489	1,016,124 - 1,059,795 (-)	NCBI	ChiLan1.0	ChiLan1.0

RCOR3
(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	1	38,091,704 - 38,148,935 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	1	38,056,730 - 38,114,012 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	1	186,822,259 - 186,879,534 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	1	191,686,975 - 191,743,497 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	1	191,686,125 - 191,743,487 (+)	Ensembl	panpan1.1		panPan2

RCOR3
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	7	9,720,401 - 9,773,223 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	7	9,719,411 - 9,789,700 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	7	9,295,402 - 9,348,530 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	7	9,422,869 - 9,476,144 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	7	9,422,814 - 9,475,915 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	7	9,346,213 - 9,399,331 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	7	9,447,751 - 9,501,005 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	7	9,572,124 - 9,625,603 (+)	NCBI		UU_Cfam_GSD_1.0

Rcor3
(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	64,746,303 - 64,790,969 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936557	1,986,630 - 2,031,078 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936557	1,986,587 - 2,031,251 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

RCOR3
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	9	131,833,399 - 131,890,799 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	9	131,833,395 - 131,890,822 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	9	144,906,668 - 144,924,011 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

RCOR3
(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	25	18,184,375 - 18,247,432 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	25	18,184,011 - 18,247,398 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666055	18,716,347 - 18,774,169 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Rcor3
(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_004624807	945,783 - 983,581 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624807	943,599 - 990,205 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in RCOR3
23 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 1q31.1-42.11(chr1:187143981-224299417)x3	copy number gain	See cases [RCV000051857]	Chr1:187143981..224299417 [GRCh38] Chr1:187113113..224487119 [GRCh37] Chr1:185379736..222553742 [NCBI36] Chr1:1q31.1-42.11	pathogenic
GRCh38/hg38 1q32.2-44(chr1:209646207-248931113)x3	copy number gain	See cases [RCV000051861]	Chr1:209646207..248931113 [GRCh38] Chr1:209819552..249225312 [GRCh37] Chr1:207886175..247191935 [NCBI36] Chr1:1q32.2-44	pathogenic
NM_001136223.1(RCOR3):c.940-467T>C	single nucleotide variant	Lung cancer [RCV000090419]	Chr1:211295209 [GRCh38] Chr1:211468551 [GRCh37] Chr1:1q32.2	uncertain significance
GRCh38/hg38 1q32.2-44(chr1:209963625-248918469)x3	copy number gain	See cases [RCV000134979]	Chr1:209963625..248918469 [GRCh38] Chr1:210136970..249212668 [GRCh37] Chr1:208203593..247179291 [NCBI36] Chr1:1q32.2-44	pathogenic
GRCh38/hg38 1q32.2-32.3(chr1:208063461-211907812)x1	copy number loss	See cases [RCV000138122]	Chr1:208063461..211907812 [GRCh38] Chr1:208236806..212081154 [GRCh37] Chr1:206303429..210147777 [NCBI36] Chr1:1q32.2-32.3	likely benign
GRCh38/hg38 1q32.1-42.12(chr1:204764914-225408698)x3	copy number gain	See cases [RCV000142054]	Chr1:204764914..225408698 [GRCh38] Chr1:204734042..225596400 [GRCh37] Chr1:203000665..223663023 [NCBI36] Chr1:1q32.1-42.12	pathogenic
GRCh38/hg38 1q32.2-44(chr1:207346642-248930485)x3	copy number gain	See cases [RCV000143727]	Chr1:207346642..248930485 [GRCh38] Chr1:207519987..249224684 [GRCh37] Chr1:205586610..247191307 [NCBI36] Chr1:1q32.2-44	pathogenic
GRCh37/hg19 1q31.3-42.13(chr1:197811907-228997888)x3	copy number gain	See cases [RCV000240137]	Chr1:197811907..228997888 [GRCh37] Chr1:1q31.3-42.13	pathogenic
GRCh37/hg19 1q31.3-44(chr1:195483439-249213000)x3	copy number gain	See cases [RCV000449172]	Chr1:195483439..249213000 [GRCh37] Chr1:1q31.3-44	pathogenic
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 1p36.33-q44(chr1:849467-249224684)	copy number gain	See cases [RCV000510926]	Chr1:849467..249224684 [GRCh37] Chr1:1p36.33-q44	pathogenic
NM_001136223.3(RCOR3):c.125A>T (p.Tyr42Phe)	single nucleotide variant	not specified [RCV004333856]	Chr1:211259685 [GRCh38] Chr1:211433027 [GRCh37] Chr1:1q32.2	uncertain significance
GRCh37/hg19 1q32.1-32.3(chr1:204682513-212815646)	copy number loss	Global developmental delay [RCV000626524]	Chr1:204682513..212815646 [GRCh37] Chr1:1q32.1-32.3	pathogenic
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 1q25.3-41(chr1:185644663-221698833)x3	copy number gain	not provided [RCV000749265]	Chr1:185644663..221698833 [GRCh37] Chr1:1q25.3-41	pathogenic
GRCh37/hg19 1q32.1-32.3(chr1:206329070-213263817)x3	copy number gain	not provided [RCV000848713]	Chr1:206329070..213263817 [GRCh37] Chr1:1q32.1-32.3	uncertain significance
GRCh37/hg19 1q25.3-44(chr1:182388773-249111240)x3	copy number gain	not provided [RCV000845852]	Chr1:182388773..249111240 [GRCh37] Chr1:1q25.3-44	pathogenic
GRCh37/hg19 1q32.2-44(chr1:210152794-249218992)x3	copy number gain	See cases [RCV001194578]	Chr1:210152794..249218992 [GRCh37] Chr1:1q32.2-44	pathogenic
GRCh37/hg19 1q32.1-44(chr1:204045948-249218992)x3	copy number gain	See cases [RCV001007407]	Chr1:204045948..249218992 [GRCh37] Chr1:1q32.1-44	pathogenic
NC_000001.10:g.(?_130980840)_(248900000_?)dup	duplication	Gastrointestinal stromal tumor [RCV001300221]\|Parathyroid carcinoma [RCV001341077]	Chr1:130980840..248900000 [GRCh37] Chr1:1q12-44	uncertain significance
GRCh37/hg19 1q31.3-44(chr1:197867914-249224684)x3	copy number gain	See cases [RCV002287837]	Chr1:197867914..249224684 [GRCh37] Chr1:1q31.3-44	pathogenic
NM_001136223.3(RCOR3):c.1535C>T (p.Pro512Leu)	single nucleotide variant	not specified [RCV004103660]	Chr1:211313641 [GRCh38] Chr1:211486983 [GRCh37] Chr1:1q32.3	uncertain significance
GRCh37/hg19 1q25.3-32.3(chr1:181453460-213107248)x3	copy number gain	not provided [RCV002475637]	Chr1:181453460..213107248 [GRCh37] Chr1:1q25.3-32.3	pathogenic
GRCh38/hg38 1q32.2-42.13(chr1:228006998-228061271)x2	copy number loss	Orofacial cleft 2 [RCV002481175]	Chr1:228006998..228061271 [GRCh38] Chr1:1q32.2-42.13	association
NM_001136223.3(RCOR3):c.1471C>T (p.Pro491Ser)	single nucleotide variant	not specified [RCV004139441]	Chr1:211313577 [GRCh38] Chr1:211486919 [GRCh37] Chr1:1q32.3	uncertain significance
NM_001136223.3(RCOR3):c.1236T>G (p.Asn412Lys)	single nucleotide variant	not specified [RCV004172076]	Chr1:211312880 [GRCh38] Chr1:211486222 [GRCh37] Chr1:1q32.3	uncertain significance
NM_001136223.3(RCOR3):c.224G>A (p.Gly75Asp)	single nucleotide variant	not specified [RCV004173753]	Chr1:211271232 [GRCh38] Chr1:211444574 [GRCh37] Chr1:1q32.2	uncertain significance
NM_001136223.3(RCOR3):c.74C>T (p.Pro25Leu)	single nucleotide variant	not specified [RCV004096303]	Chr1:211259634 [GRCh38] Chr1:211432976 [GRCh37] Chr1:1q32.2	uncertain significance
NM_001136223.3(RCOR3):c.935G>A (p.Arg312His)	single nucleotide variant	not specified [RCV004270865]	Chr1:211289392 [GRCh38] Chr1:211462734 [GRCh37] Chr1:1q32.2	uncertain significance
NM_001136223.3(RCOR3):c.525T>A (p.Asp175Glu)	single nucleotide variant	not specified [RCV004276464]	Chr1:211278125 [GRCh38] Chr1:211451467 [GRCh37] Chr1:1q32.2	uncertain significance
NM_001136223.3(RCOR3):c.755T>C (p.Ile252Thr)	single nucleotide variant	not specified [RCV004355411]	Chr1:211289212 [GRCh38] Chr1:211462554 [GRCh37] Chr1:1q32.2	uncertain significance
NM_001136223.3(RCOR3):c.700A>C (p.Lys234Gln)	single nucleotide variant	not specified [RCV004353346]	Chr1:211279296 [GRCh38] Chr1:211452638 [GRCh37] Chr1:1q32.2	uncertain significance
NM_001136223.3(RCOR3):c.64G>A (p.Ala22Thr)	single nucleotide variant	not specified [RCV004358686]	Chr1:211259624 [GRCh38] Chr1:211432966 [GRCh37] Chr1:1q32.2	uncertain significance
NM_001136223.3(RCOR3):c.1339C>T (p.Arg447Trp)	single nucleotide variant	not specified [RCV004443668]	Chr1:211313445 [GRCh38] Chr1:211486787 [GRCh37] Chr1:1q32.3	uncertain significance
NM_001136223.3(RCOR3):c.1463G>A (p.Arg488Gln)	single nucleotide variant	not specified [RCV004443670]	Chr1:211313569 [GRCh38] Chr1:211486911 [GRCh37] Chr1:1q32.3	uncertain significance
NM_001136223.3(RCOR3):c.1595C>T (p.Thr532Met)	single nucleotide variant	not specified [RCV004443671]	Chr1:211313701 [GRCh38] Chr1:211487043 [GRCh37] Chr1:1q32.3	uncertain significance
NM_001136223.3(RCOR3):c.248A>C (p.Asp83Ala)	single nucleotide variant	not specified [RCV004443672]	Chr1:211271256 [GRCh38] Chr1:211444598 [GRCh37] Chr1:1q32.2	uncertain significance
NM_001136223.3(RCOR3):c.890A>T (p.Asn297Ile)	single nucleotide variant	not specified [RCV004443673]	Chr1:211289347 [GRCh38] Chr1:211462689 [GRCh37] Chr1:1q32.2	uncertain significance
NM_001136223.3(RCOR3):c.1363G>T (p.Ala455Ser)	single nucleotide variant	not specified [RCV004443669]	Chr1:211313469 [GRCh38] Chr1:211486811 [GRCh37] Chr1:1q32.3	uncertain significance
NM_001136223.3(RCOR3):c.895A>G (p.Ile299Val)	single nucleotide variant	not specified [RCV004443674]	Chr1:211289352 [GRCh38] Chr1:211462694 [GRCh37] Chr1:1q32.2	uncertain significance
NC_000001.10:g.(?_190829412)_(216061974_?)del	deletion	not provided [RCV004579260]	Chr1:190829412..216061974 [GRCh37] Chr1:1q31.2-41	pathogenic
NM_001136223.3(RCOR3):c.473C>G (p.Ala158Gly)	single nucleotide variant	not specified [RCV004671757]	Chr1:211276375 [GRCh38] Chr1:211449717 [GRCh37] Chr1:1q32.2	uncertain significance
NM_001136223.3(RCOR3):c.728C>A (p.Thr243Asn)	single nucleotide variant	not specified [RCV004657992]	Chr1:211289185 [GRCh38] Chr1:211462527 [GRCh37] Chr1:1q32.2	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	2757
Count of miRNA genes:	1093
Interacting mature miRNAs:	1338
Transcripts:	ENST00000367005, ENST00000367006, ENST00000419091, ENST00000452621, ENST00000472734, ENST00000485186, ENST00000486666, ENST00000526255, ENST00000528066, ENST00000528408, ENST00000528926, ENST00000529572, ENST00000529763, ENST00000533469, ENST00000534460, ENST00000534478
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.

QTLs in Region (GRCh38)

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
597351777	GWAS1447851_H	body height QTL GWAS1447851 (human)		3e-35	body height (VT:0001253)	body height (CMO:0000106)	1	211260330	211260331	Human
597103052	GWAS1199126_H	platelet crit QTL GWAS1199126 (human)		1e-09	platelet crit	plateletcrit (CMO:0001349)	1	211268844	211268845	Human

Markers in Region

SHGC-76308

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	211,489,304 - 211,489,510	UniSTS	GRCh37
Build 36	1	209,555,927 - 209,556,133	RGD	NCBI36
Celera	1	184,715,973 - 184,716,179	RGD
Cytogenetic Map	1	q32.2	UniSTS
HuRef	1	182,166,256 - 182,166,462	UniSTS
TNG Radiation Hybrid Map	1	103900.0	UniSTS
GeneMap99-GB4 RH Map	1	694.61	UniSTS
Whitehead-RH Map	1	845.3	UniSTS

RH103497

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	211,434,283 - 211,434,404	UniSTS	GRCh37
Build 36	1	209,500,906 - 209,501,027	RGD	NCBI36
Celera	1	184,660,967 - 184,661,088	RGD
Cytogenetic Map	1	q32.2	UniSTS
HuRef	1	182,111,275 - 182,111,396	UniSTS
GeneMap99-GB4 RH Map	1	694.61	UniSTS

SHGC-76311

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	211,488,735 - 211,488,823	UniSTS	GRCh37
Build 36	1	209,555,358 - 209,555,446	RGD	NCBI36
Celera	1	184,715,404 - 184,715,492	RGD
Cytogenetic Map	1	q32.2	UniSTS
HuRef	1	182,165,687 - 182,165,775	UniSTS
TNG Radiation Hybrid Map	1	103900.0	UniSTS
GeneMap99-GB4 RH Map	1	694.71	UniSTS

D1S527E

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	211,488,817 - 211,488,896	UniSTS	GRCh37
Build 36	1	209,555,440 - 209,555,519	RGD	NCBI36
Celera	1	184,715,486 - 184,715,565	RGD
Cytogenetic Map	1	q32.2	UniSTS
HuRef	1	182,165,769 - 182,165,848	UniSTS

AL009661

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	211,474,993 - 211,475,073	UniSTS	GRCh37
Build 36	1	209,541,616 - 209,541,696	RGD	NCBI36
Celera	1	184,701,674 - 184,701,754	RGD
Cytogenetic Map	1	q32.2	UniSTS
HuRef	1	182,151,946 - 182,152,026	UniSTS

SHGC-53772

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	211,487,840 - 211,488,076	UniSTS	GRCh37
Build 36	1	209,554,463 - 209,554,699	RGD	NCBI36
Celera	1	184,714,509 - 184,714,745	RGD
Cytogenetic Map	1	q32.2	UniSTS
HuRef	1	182,164,792 - 182,165,028	UniSTS

AL009693

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	211,443,902 - 211,444,078	UniSTS	GRCh37
Build 36	1	209,510,525 - 209,510,701	RGD	NCBI36
Celera	1	184,670,584 - 184,670,760	RGD
Cytogenetic Map	1	q32.2	UniSTS
HuRef	1	182,120,844 - 182,121,020	UniSTS

D1S3586

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	1	211,489,169 - 211,489,314	UniSTS	GRCh37
Build 36	1	209,555,792 - 209,555,937	RGD	NCBI36
Celera	1	184,715,838 - 184,715,983	RGD
Cytogenetic Map	1	q32.2	UniSTS
HuRef	1	182,166,121 - 182,166,266	UniSTS
TNG Radiation Hybrid Map	1	103900.0	UniSTS
GeneMap99-GB4 RH Map	1	694.71	UniSTS

Expression

RNA-SEQ Expression

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

Download All Expressed Objects for this Gene

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	entire extraembryonic component	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	pharyngeal arch	renal system	reproductive system	respiratory system	sensory system	visual system
1204	2439	2788	2251	4972	1726	2351	5	623	1951	465	2269	7303	6469	53	3734	1	852	1744	1617	174	1

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001136223	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001136224	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001136225	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001350069	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001350070	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_018254	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_146432	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_146433	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_146434	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005273191	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006711442	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011509748	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011509749	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017001758	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017001760	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017001761	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017001762	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017001763	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017001764	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017001765	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017001767	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024448330	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024448331	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024448332	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047425011	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047425021	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047425032	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047425038	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047425043	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047425046	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047425051	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047425052	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047425053	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054337618	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054337619	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054337620	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054337621	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054337622	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054337623	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054337624	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054337625	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054337626	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054337627	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054337628	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054337629	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054337630	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001737300	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001737301	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001737302	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001737303	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001737304	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001737305	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001737306	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001737307	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001737308	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001737310	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_007061955	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_007061956	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_007061957	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_007061958	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_008486104	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_008486105	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_008486106	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_008486107	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AA831517	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AB037764	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AI380424	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK001738	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK057001	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK057163	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK125810	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK131312	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK300942	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK302664	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK311644	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL590101	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL611964	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC031608	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BI051857	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BP221223	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BQ218032	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BU689437	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471100	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068277	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA224160	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA334880	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA478986	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA925839	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB164963	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DC387352	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HY024910	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KT584854	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000367005 ⟹ ENSP00000355972

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	211,259,975 - 211,316,385 (+)	Ensembl

Ensembl Acc Id:

ENST00000367006 ⟹ ENSP00000355973

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	211,259,279 - 211,314,591 (+)	Ensembl

Ensembl Acc Id:

ENST00000419091 ⟹ ENSP00000413929

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	211,259,366 - 211,316,385 (+)	Ensembl

Ensembl Acc Id:

ENST00000452621 ⟹ ENSP00000398558

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	211,259,388 - 211,313,298 (+)	Ensembl

Ensembl Acc Id:

ENST00000472734

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	211,259,606 - 211,261,202 (+)	Ensembl

Ensembl Acc Id:

ENST00000485186 ⟹ ENSP00000434181

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	211,289,332 - 211,312,819 (+)	Ensembl

Ensembl Acc Id:

ENST00000486666

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	211,301,461 - 211,314,587 (+)	Ensembl

Ensembl Acc Id:

ENST00000526255

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	211,312,237 - 211,313,839 (+)	Ensembl

Ensembl Acc Id:

ENST00000528066

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	211,304,011 - 211,313,025 (+)	Ensembl

Ensembl Acc Id:

ENST00000528408

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	211,259,553 - 211,271,570 (+)	Ensembl

Ensembl Acc Id:

ENST00000528926 ⟹ ENSP00000432779

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	211,259,396 - 211,312,804 (+)	Ensembl

Ensembl Acc Id:

ENST00000529572 ⟹ ENSP00000434605

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	211,259,947 - 211,279,276 (+)	Ensembl

Ensembl Acc Id:

ENST00000529763 ⟹ ENSP00000437048

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	211,289,178 - 211,313,672 (+)	Ensembl

Ensembl Acc Id:

ENST00000533469 ⟹ ENSP00000436838

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	211,258,408 - 211,278,223 (+)	Ensembl

Ensembl Acc Id:

ENST00000534460 ⟹ ENSP00000433441

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	211,279,238 - 211,313,474 (+)	Ensembl

Ensembl Acc Id:

ENST00000534478 ⟹ ENSP00000436057

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	1	211,258,377 - 211,276,335 (+)	Ensembl

RefSeq Acc Id:

NM_001136223 ⟹ NP_001129695

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	211,259,366 - 211,316,385 (+)	NCBI
GRCh37	1	211,432,708 - 211,489,727 (+)	RGD
Celera	1	184,656,707 - 184,716,396 (+)	RGD
HuRef	1	182,109,654 - 182,166,679 (+)	ENTREZGENE
CHM1_1	1	212,705,251 - 212,762,151 (+)	NCBI
T2T-CHM13v2.0	1	210,504,931 - 210,561,986 (+)	NCBI

Sequence:

show sequence

GTTGTTGTGAGGCGACTGCGCTACTGCCGGAGCGGGGCGGTTATGGCGGCTCCATATTAACAGC
CTCCTCCTCCTCCGCCGCCGCCGCCGTCTCCTCCTCCTCCTCCTTTCCCTCCCGCCCGCGCTCT
AAGCCATCTCCGCCTTCACCCTGACGCCTGCCTCTTCCCCTCACCTTTCCCCCTCCCCTGTTCT
ACCATGCCCGGCATGATGGAGAAAGGGCCCGAGTTACTGGGGAAGAACCGATCGGCCAACGGCA
GCGCCAAGAGCCCGGCAGGCGGCGGCGGCAGCGGCGCCTCGTCCACCAACGGCGGGCTGCACTA
CTCAGAGCCCGAGAGCGGCTGCAGCAGCGACGACGAGCACGATGTTGGGATGAGAGTCGGAGCC
GAATACCAAGCTCGGATCCCTGAATTTGATCCAGGTGCTACAAAGTACACAGATAAAGACAATG
GAGGGATGCTTGTATGGTCTCCATATCACAGTATCCCAGATGCCAAATTGGATGAATACATTGC
AATTGCAAAGGAAAAGCATGGCTACAATGTGGAACAGGCACTTGGCATGTTGTTCTGGCATAAA
CATAACATTGAGAAGTCCCTTGCTGATCTCCCTAATTTCACTCCCTTTCCGGATGAGTGGACAG
TGGAAGATAAAGTCCTATTTGAACAAGCCTTTAGTTTTCATGGAAAGAGCTTTCACAGGATTCA
GCAAATGCTTCCAGATAAGACAATTGCAAGCCTTGTAAAATATTACTATTCTTGGAAAAAAACT
CGCTCTAGGACAAGTTTGATGGATCGCCAGGCTCGTAAACTAGCTAATAGACATAATCAGGGTG
ACAGTGATGATGATGTAGAAGAAACACATCCAATGGATGGGAATGATAGTGATTATGATCCCAA
AAAAGAAGCCAAAAAAGAGGGTAATACTGAACAACCTGTCCAAACTAGCAAGATTGGACTTGGA
AGAAGAGAGTATCAGAGTTTACAACATCGCCATCATTCTCAGCGTTCTAAGTGCCGTCCACCTA
AGGGCATGTATTTAACCCAGGAAGATGTGGTAGCAGTTTCCTGTAGTCCCAATGCAGCCAACAC
CATCCTGAGGCAACTGGACATGGAGTTGATCTCTCTAAAACGTCAGGTTCAGAATGCTAAGCAA
GTAAACAGTGCACTTAAACAGAAAATGGAAGGTGGAATTGAAGAATTCAAACCTCCTGAGTCAA
ATCAGAAAATTAATGCCCGTTGGACCACAGAGGAGCAGCTTCTAGCAGTGCAAGGTGTCCGCAA
ATATGGTAAAGATTTTCAAGCTATTGCAGATGTAATTGGCAACAAGACTGTTGGCCAAGTGAAG
AACTTCTTTGTAAACTACAGGCGTCGGTTTAACTTAGAGGAGGTATTGCAGGAGTGGGAAGCAG
AACAAGGAACCCAGGCTTCTAATGGTGATGCTTCTACTTTAGGGGAGGAGACAAAAAGTGCTTC
TAATGTGCCATCAGGGAAGAGCACTGATGAAGAAGAGGAGGCACAGACCCCACAGGCTCCTCGG
ACACTGGGTCCATCACCTCCTGCCCCATCATCCACTCCAACACCAACAGCCCCTATTGCCACTC
TGAACCAGCCTCCACCACTTCTTCGTCCAACACTGCCTGCTGCCCCGGCTCTTCACCGGCAGCC
TCCTCCACTCCAGCAGCAGGCTCGGTTCATCCAGCCCCGGCCAACTTTAAATCAGCCTCCACCA
CCTCTTATTCGCCCTGCTAATTCCATGCCACCCCGTCTAAACCCAAGACCGGTGTTGTCCACGG
TTGGTGGTCAACAGCCACCATCACTTATTGGAATTCAGACAGATTCACAGTCCTCACTGCACTA
AAAATTAAATTGGACACAGCTGCAGTAACTTTTCACCCCATCATTATACCAGTGCTCATCTGAC
TGATGAAAAAGAGGAAAGAATAATCATTTCTAGATACTGAGGCTGCGAACTAGTTCTGTGGCAG
TGGACTAGCATAAGTGGATGTCTAAGAAATTTTTCAGTTCACTAGACTAAAATGTTTTACAACA
AAAAGCCTCCAGTTAGCCTCCTTTCTAGAGTATATGTTCAGCAATGTTGATCTCATAAAAGGAA
AAACAAAAGATTTAAGTATTCTATATACCAAGTTTTTGTTTTGTTTTTACTGTATTTATTTTAT
TGAGGTTCTTTATATTCCTGCCTCTTCATAGTCAAGGCTCTTAGTACAGGAATATTGACTTAGG
AATTGTGAAAACTCCTTAAGTTTCTTAAGTTAAGGATGTTTGGCTTTTTTCTTTAATTTTTTAA
AAACCATTTTCCTATGTTAGGAGTGCAAGAATAGCCAGCATTTCCGATTTTGACATATGTTCAT
TTTATGCATATTTAAGAAATTATAGCTGCATATCCCTTCTTTCAAAAAATGTTGCTTTTTTTTT
TAAAGGAATTTTAATATATTCCTTTAAAAGAAAGCAATTTAATCAATTGCAAAGCAATTATATA
AAACCACAAAGAATGTACTGAACCTACTAACCCTTTAACATACAGTTTAGGGTCCTAGCGCAGA
GTCCTTGTTTAAAGGTCATTGACTCATCATCTGTCAGTAATGAGAGGATTGGAAGAATAATTTT
GCATACAAATGAGGACTTAATTTGTTGAAATATAATCTCTTTAAGTTCCTTGAAAATGGAGTTG
GTTTTTTTTGTTTCTAAATGCTATCTGCTTTTAACTAGTAGTTGCCTACATCTGGGGACTTCAG
AGAAGAATTATATTTTGTTAGTTAAGTAGACACAGTGGTTATGGAAGCATTTCTTTACAGTACC
CTTTACATGTTTGGTTTCTGAACTTAAAATTGCCCTCATACTTAATAATATGGTCTGCATTTAA
TATGAAAGGTGTTTTATTGATAAATCTATTGTACTATTTGGATACATTTGTGTATTCCTTGCAG
CCAACCTGTATTCGTGGGATTGGTGTAGGGTTAAATCATCAACATTATTTCATAAAATAAGAAT
TTGTTCTGTGTTATCTAAAGATGTATCAGTATATTGTCACAGTTGTGCTGTTAACTAAAAATGC
TGAGACCCCTTTTTATAGAAAAACAAAAAGACATCAAGTCTTCTTAATTCAACCCATAATCATT
AAGTACTTAACAAAGAATATTTTACAAGTGATAGTATTTCAACAATGTGTAATTAATATTTTTG
ATACAGTGATTTCATATTGGAATCATTATTTGTGCAAAGGGACAGACAGATCACTTAGATTGCT
ATACTAGTGGACATAGGCTACATGTTTGCACATTCACATTCTTATCACGTGTAGAATACTTCAC
AAAATAGTCAACATCTAAGGCCCTAATTTATGTTTTGAAAGATCATGTGTTCCCAAAGTATTCC
CTATTGTTGGCTCCACAGCCTTAAAGTGCTATAGATTTAAATTCATTGATTAGTTTTAATTTTT
AATTTTAGACTGTGTATTTCCATAAATACCCTACGTACTGGCATATTTGAAACTCTTTTTCCAG
GTTAGGTCCTTTTCTTTCTCATTGAATCATCTTAAATAGTTCTTGGCCCTGAATTTAGCTGATT
TAAAATTCTTAATATTCAAGAATTTATACTTATTTTTTCCTTAAAAGCCACAGGGGACAGTTAA
ATATCTTAAAATATCTAAAACATTTTTTAAAGCACTTAGATTGTCTTACGTATGTGCATACTAT
ACCTTTACAGCGTTTATTGTCTTGTCTCTTGTCAGTAGACCTTCAGTACACAGTATGTGGGATA
TGTCAGTCAAGTTGGTCAGCACCAGCATCTGTCCAGCTGTTCAGTATATTGTGATTCATTAAAA
AATCTCTTCTATCCCAGACATGGGCCAAGGTGCTGTATCTGAGGGATGTGCTGTAATTTGATTT
ACATGCATTAGAGCACACAGTAGAAAAACTTTAGCTTCATTAGTAATATGACACATGTATATAG
TGAGATGTCTTTATTGTGTGCTTTGCATATTTTGTAAATATTTTGCACGTCATTATTTTTCTTT
TTTGTTTAAGCAGTGTTTGGCCTGGAAGAGTGATATGCTTGCTGCTTAATCAAAGGATTAAAGA
TTTAAAGATGTCTATGTCTTCTATTTTTATATAATTTCATGTTCTATGAGGAATTTAGTACCTC
TTCACTGTGAAATTCGAAATAATGATTTTTATAAAAGCAAAACTAGAAATCTTTTAATGACAAT
TTTCATTAATTTCAGGGTTATCATTTTTGAGAAATCTACACCAAAGTGGTTTTTTAAAATTACA
TAACTAAAAATAAACCACACTGTGGATACATCTTATAAAACTAATGGAAACAATGTTTTTCTAT
ATGATTTAATTCTAGTGTAATATGGATGAGGTAAGAGTAAGTTATGATCAAACTTTTTATGTTC
TTAATAAGCTTGCAATTGAGTAAAATAGAATATAAAATAAAGGTGAAATAATATAAAA

hide sequence

RefSeq Acc Id:

NM_001136224 ⟹ NP_001129696

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	211,259,366 - 211,316,385 (+)	NCBI
GRCh37	1	211,432,708 - 211,489,727 (+)	RGD
Celera	1	184,656,707 - 184,716,396 (+)	RGD
HuRef	1	182,109,654 - 182,166,679 (+)	ENTREZGENE
CHM1_1	1	212,705,251 - 212,762,151 (+)	NCBI
T2T-CHM13v2.0	1	210,504,931 - 210,561,986 (+)	NCBI

Sequence:

show sequence

GTTGTTGTGAGGCGACTGCGCTACTGCCGGAGCGGGGCGGTTATGGCGGCTCCATATTAACAGC
CTCCTCCTCCTCCGCCGCCGCCGCCGTCTCCTCCTCCTCCTCCTTTCCCTCCCGCCCGCGCTCT
AAGCCATCTCCGCCTTCACCCTGACGCCTGCCTCTTCCCCTCACCTTTCCCCCTCCCCTGTTCT
ACCATGCCCGGCATGATGGAGAAAGGGCCCGAGTTACTGGGGAAGAACCGATCGGCCAACGGCA
GCGCCAAGAGCCCGGCAGGCGGCGGCGGCAGCGGCGCCTCGTCCACCAACGGCGGGCTGCACTA
CTCAGAGCCCGAGAGCGGCTGCAGCAGCGACGACGAGCACGATGTTGGGATGAGAGTCGGAGCC
GAATACCAAGCTCGGATCCCTGAATTTGATCCAGGTGCTACAAAGTACACAGATAAAGACAATG
GAGGGATGCTTGTATGGTCTCCATATCACAGTATCCCAGATGCCAAATTGGATGAATACATTGC
AATTGCAAAGGAAAAGCATGGCTACAATGTGGAACAGGCACTTGGCATGTTGTTCTGGCATAAA
CATAACATTGAGAAGTCCCTTGCTGATCTCCCTAATTTCACTCCCTTTCCGGATGAGTGGACAG
TGGAAGATAAAGTCCTATTTGAACAAGCCTTTAGTTTTCATGGAAAGAGCTTTCACAGGATTCA
GCAAATGCTTCCAGATAAGACAATTGCAAGCCTTGTAAAATATTACTATTCTTGGAAAAAAACT
CGCTCTAGGACAAGTTTGATGGATCGCCAGGCTCGTAAACTAGCTAATAGACATAATCAGGGTG
ACAGTGATGATGATGTAGAAGAAACACATCCAATGGATGGGAATGATAGTGATTATGATCCCAA
AAAAGAAGCCAAAAAAGAGGGTAATACTGAACAACCTGTCCAAACTAGCAAGATTGGACTTGGA
AGAAGAGAGTATCAGAGTTTACAACATCGCCATCATTCTCAGCGTTCTAAGTGCCGTCCACCTA
AGGGCATGTATTTAACCCAGGAAGATGTGGTAGCAGTTTCCTGTAGTCCCAATGCAGCCAACAC
CATCCTGAGGCAACTGGACATGGAGTTGATCTCTCTAAAACGTCAGGTTCAGAATGCTAAGCAA
GTAAACAGTGCACTTAAACAGAAAATGGAAGGTGGAATTGAAGAATTCAAACCTCCTGAGTCAA
ATCAGAAAATTAATGCCCGTTGGACCACAGAGGAGCAGCTTCTAGCAGTGCAAGGCACAGACCC
CACAGGCTCCTCGGACACTGGGTCCATCACCTCCTGCCCCATCATCCACTCCAACACCAACAGC
CCCTATTGCCACTCTGAACCAGCCTCCACCACTTCTTCGTCCAACACTGCCTGCTGCCCCGGCT
CTTCACCGGCAGCCTCCTCCACTCCAGCAGCAGGCTCGGTTCATCCAGCCCCGGCCAACTTTAA
ATCAGCCTCCACCACCTCTTATTCGCCCTGCTAATTCCATGCCACCCCGTCTAAACCCAAGACC
GGTGTTGTCCACGGTTGGTGGTCAACAGCCACCATCACTTATTGGAATTCAGACAGATTCACAG
TCCTCACTGCACTAAAAATTAAATTGGACACAGCTGCAGTAACTTTTCACCCCATCATTATACC
AGTGCTCATCTGACTGATGAAAAAGAGGAAAGAATAATCATTTCTAGATACTGAGGCTGCGAAC
TAGTTCTGTGGCAGTGGACTAGCATAAGTGGATGTCTAAGAAATTTTTCAGTTCACTAGACTAA
AATGTTTTACAACAAAAAGCCTCCAGTTAGCCTCCTTTCTAGAGTATATGTTCAGCAATGTTGA
TCTCATAAAAGGAAAAACAAAAGATTTAAGTATTCTATATACCAAGTTTTTGTTTTGTTTTTAC
TGTATTTATTTTATTGAGGTTCTTTATATTCCTGCCTCTTCATAGTCAAGGCTCTTAGTACAGG
AATATTGACTTAGGAATTGTGAAAACTCCTTAAGTTTCTTAAGTTAAGGATGTTTGGCTTTTTT
CTTTAATTTTTTAAAAACCATTTTCCTATGTTAGGAGTGCAAGAATAGCCAGCATTTCCGATTT
TGACATATGTTCATTTTATGCATATTTAAGAAATTATAGCTGCATATCCCTTCTTTCAAAAAAT
GTTGCTTTTTTTTTTAAAGGAATTTTAATATATTCCTTTAAAAGAAAGCAATTTAATCAATTGC
AAAGCAATTATATAAAACCACAAAGAATGTACTGAACCTACTAACCCTTTAACATACAGTTTAG
GGTCCTAGCGCAGAGTCCTTGTTTAAAGGTCATTGACTCATCATCTGTCAGTAATGAGAGGATT
GGAAGAATAATTTTGCATACAAATGAGGACTTAATTTGTTGAAATATAATCTCTTTAAGTTCCT
TGAAAATGGAGTTGGTTTTTTTTGTTTCTAAATGCTATCTGCTTTTAACTAGTAGTTGCCTACA
TCTGGGGACTTCAGAGAAGAATTATATTTTGTTAGTTAAGTAGACACAGTGGTTATGGAAGCAT
TTCTTTACAGTACCCTTTACATGTTTGGTTTCTGAACTTAAAATTGCCCTCATACTTAATAATA
TGGTCTGCATTTAATATGAAAGGTGTTTTATTGATAAATCTATTGTACTATTTGGATACATTTG
TGTATTCCTTGCAGCCAACCTGTATTCGTGGGATTGGTGTAGGGTTAAATCATCAACATTATTT
CATAAAATAAGAATTTGTTCTGTGTTATCTAAAGATGTATCAGTATATTGTCACAGTTGTGCTG
TTAACTAAAAATGCTGAGACCCCTTTTTATAGAAAAACAAAAAGACATCAAGTCTTCTTAATTC
AACCCATAATCATTAAGTACTTAACAAAGAATATTTTACAAGTGATAGTATTTCAACAATGTGT
AATTAATATTTTTGATACAGTGATTTCATATTGGAATCATTATTTGTGCAAAGGGACAGACAGA
TCACTTAGATTGCTATACTAGTGGACATAGGCTACATGTTTGCACATTCACATTCTTATCACGT
GTAGAATACTTCACAAAATAGTCAACATCTAAGGCCCTAATTTATGTTTTGAAAGATCATGTGT
TCCCAAAGTATTCCCTATTGTTGGCTCCACAGCCTTAAAGTGCTATAGATTTAAATTCATTGAT
TAGTTTTAATTTTTAATTTTAGACTGTGTATTTCCATAAATACCCTACGTACTGGCATATTTGA
AACTCTTTTTCCAGGTTAGGTCCTTTTCTTTCTCATTGAATCATCTTAAATAGTTCTTGGCCCT
GAATTTAGCTGATTTAAAATTCTTAATATTCAAGAATTTATACTTATTTTTTCCTTAAAAGCCA
CAGGGGACAGTTAAATATCTTAAAATATCTAAAACATTTTTTAAAGCACTTAGATTGTCTTACG
TATGTGCATACTATACCTTTACAGCGTTTATTGTCTTGTCTCTTGTCAGTAGACCTTCAGTACA
CAGTATGTGGGATATGTCAGTCAAGTTGGTCAGCACCAGCATCTGTCCAGCTGTTCAGTATATT
GTGATTCATTAAAAAATCTCTTCTATCCCAGACATGGGCCAAGGTGCTGTATCTGAGGGATGTG
CTGTAATTTGATTTACATGCATTAGAGCACACAGTAGAAAAACTTTAGCTTCATTAGTAATATG
ACACATGTATATAGTGAGATGTCTTTATTGTGTGCTTTGCATATTTTGTAAATATTTTGCACGT
CATTATTTTTCTTTTTTGTTTAAGCAGTGTTTGGCCTGGAAGAGTGATATGCTTGCTGCTTAAT
CAAAGGATTAAAGATTTAAAGATGTCTATGTCTTCTATTTTTATATAATTTCATGTTCTATGAG
GAATTTAGTACCTCTTCACTGTGAAATTCGAAATAATGATTTTTATAAAAGCAAAACTAGAAAT
CTTTTAATGACAATTTTCATTAATTTCAGGGTTATCATTTTTGAGAAATCTACACCAAAGTGGT
TTTTTAAAATTACATAACTAAAAATAAACCACACTGTGGATACATCTTATAAAACTAATGGAAA
CAATGTTTTTCTATATGATTTAATTCTAGTGTAATATGGATGAGGTAAGAGTAAGTTATGATCA
AACTTTTTATGTTCTTAATAAGCTTGCAATTGAGTAAAATAGAATATAAAATAAAGGTGAAATA
ATATAAAA

hide sequence

RefSeq Acc Id:

NM_001136225 ⟹ NP_001129697

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	211,259,366 - 211,313,298 (+)	NCBI
GRCh37	1	211,432,708 - 211,489,727 (+)	RGD
Celera	1	184,656,707 - 184,716,396 (+)	RGD
HuRef	1	182,109,654 - 182,166,679 (+)	ENTREZGENE
CHM1_1	1	212,705,251 - 212,759,079 (+)	NCBI
T2T-CHM13v2.0	1	210,504,931 - 210,558,899 (+)	NCBI

Sequence:

show sequence

GTTGTTGTGAGGCGACTGCGCTACTGCCGGAGCGGGGCGGTTATGGCGGCTCCATATTAACAGC
CTCCTCCTCCTCCGCCGCCGCCGCCGTCTCCTCCTCCTCCTCCTTTCCCTCCCGCCCGCGCTCT
AAGCCATCTCCGCCTTCACCCTGACGCCTGCCTCTTCCCCTCACCTTTCCCCCTCCCCTGTTCT
ACCATGCCCGGCATGATGGAGAAAGGGCCCGAGTTACTGGGGAAGAACCGATCGGCCAACGGCA
GCGCCAAGAGCCCGGCAGGCGGCGGCGGCAGCGGCGCCTCGTCCACCAACGGCGGGCTGCACTA
CTCAGAGCCCGAGAGCGGCTGCAGCAGCGACGACGAGCACGATGTTGGGATGAGAGTCGGAGCC
GAATACCAAGCTCGGATCCCTGAATTTGATCCAGGTGCTACAAAGTACACAGATAAAGACAATG
GAGGGATGCTTGTATGGTCTCCATATCACAGTATCCCAGATGCCAAATTGGATGAATACATTGC
AATTGCAAAGGAAAAGCATGGCTACAATGTGGAACAGGCACTTGGCATGTTGTTCTGGCATAAA
CATAACATTGAGAAGTCCCTTGCTGATCTCCCTAATTTCACTCCCTTTCCGGATGAGTGGACAG
TGGAAGATAAAGTCCTATTTGAACAAGCCTTTAGTTTTCATGGAAAGAGCTTTCACAGGATTCA
GCAAATGCTTCCAGATAAGACAATTGCAAGCCTTGTAAAATATTACTATTCTTGGAAAAAAACT
CGCTCTAGGACAAGTTTGATGGATCGCCAGGCTCGTAAACTAGCTAATAGACATAATCAGGGTG
ACAGTGATGATGATGTAGAAGAAACACATCCAATGGATGGGAATGATAGTGATTATGATCCCAA
AAAAGAAGCCAAAAAAGAGGGTAATACTGAACAACCTGTCCAAACTAGCAAGATTGGACTTGGA
AGAAGAGAGTATCAGAGTTTACAACATCGCCATCATTCTCAGCGTTCTAAGTGCCGTCCACCTA
AGGGCATGTATTTAACCCAGGAAGATGTGGTAGCAGTTTCCTGTAGTCCCAATGCAGCCAACAC
CATCCTGAGGCAACTGGACATGGAGTTGATCTCTCTAAAACGTCAGGTTCAGAATGCTAAGCAA
GTAAACAGTGCACTTAAACAGAAAATGGAAGGTGGAATTGAAGAATTCAAACCTCCTGAGTCAA
ATCAGAAAATTAATGCCCGTTGGACCACAGAGGAGCAGCTTCTAGCAGTGCAAGGTGTCCGCAA
ATATGGTAAAGATTTTCAAGCTATTGCAGATGTAATTGGCAACAAGACTGTTGGCCAAGTGAAG
AACTTCTTTGTAAACTACAGGCGTCGGTTTAACTTAGAGGAGGTATTGCAGGAGTGGGAAGCAG
AACAAGGAACCCAGGCTTCTAATGGTGATGCTTCTACTTTAGGGGAGGAGACAAAAAGTGCTTC
TAATGTGCCATCAGGGAAGAGCACTGATGAAGAAGAGGAGGTGTGTTTGTGTATGGAATTTGAG
CTAATATGAGTTGAGGAATCACCATTTTGTGTGGTATTCTGTAAGGTTAATTTGTCAAGAGGAC
TAGCTAAATTGAGCATGAAAGGTTGACAATACACTTCTTCAGTGGTGCATCTCTCGTGACTCTT
AAGTCATAATGACATGCTAAGTTCTGATTCTAGAAGAATGGAGAGTGTATTGTTCTTTCATAGT
CTTATTTTTATTTTCAGTGTTAAGCTGTTTACAAATAAAGATGCCTGTTTGGTAGCCTCATTGG
TTTTTGGTTTTTGGTTTTGTTTTGTTTAAAATAAAAGAAGCTTGTGCTTCCAATAAA

hide sequence

RefSeq Acc Id:

NM_001350069 ⟹ NP_001336998

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	211,259,366 - 211,316,385 (+)	NCBI
T2T-CHM13v2.0	1	210,504,931 - 210,561,986 (+)	NCBI

Sequence:

show sequence

GTTGTTGTGAGGCGACTGCGCTACTGCCGGAGCGGGGCGGTTATGGCGGCTCCATATTAACAGC
CTCCTCCTCCTCCGCCGCCGCCGCCGTCTCCTCCTCCTCCTCCTTTCCCTCCCGCCCGCGCTCT
AAGCCATCTCCGCCTTCACCCTGACGCCTGCCTCTTCCCCTCACCTTTCCCCCTCCCCTGTTCT
ACCATGCCCGGCATGATGGAGAAAGGGCCCGAGTTACTGGGGAAGAACCGATCGGCCAACGGCA
GCGCCAAGAGCCCGGCAGGCGGCGGCGGCAGCGGCGCCTCGTCCACCAACGGCGGGCTGCACTA
CTCAGAGCCCGAGAGCGGCTGCAGCAGCGACGACGAGCACGATGTTGGGATGAGAGTCGGAGCC
GAATACCAAGCTCGGATCCCTGAATTTGATCCAGTAGAGACAAGGTCTTGCTATGTTTCCCAGG
CTGGTCTCAAACTCCGGGGCTCAAGCCATCCGCCCTCCTTGGCCTCCCAAAGTGCTGGGATTAT
AGGTGCTACAAAGTACACAGATAAAGACAATGGAGGGATGCTTGTATGGTCTCCATATCACAGT
ATCCCAGATGCCAAATTGGATGAATACATTGCAATTGCAAAGGAAAAGCATGGCTACAATGTGG
AACAGGCACTTGGCATGTTGTTCTGGCATAAACATAACATTGAGAAGTCCCTTGCTGATCTCCC
TAATTTCACTCCCTTTCCGGATGAGTGGACAGTGGAAGATAAAGTCCTATTTGAACAAGCCTTT
AGTTTTCATGGAAAGAGCTTTCACAGGATTCAGCAAATGCTTCCAGATAAGACAATTGCAAGCC
TTGTAAAATATTACTATTCTTGGAAAAAAACTCGCTCTAGGACAAGTTTGATGGATCGCCAGGC
TCGTAAACTAGCTAATAGACATAATCAGGGTGACAGTGATGATGATGTAGAAGAAACACATCCA
ATGGATGGGAATGATAGTGATTATGATCCCAAAAAAGAAGCCAAAAAAGAGGGTAATACTGAAC
AACCTGTCCAAACTAGCAAGATTGGACTTGGAAGAAGAGAGTATCAGAGTTTACAACATCGCCA
TCATTCTCAGCGTTCTAAGTGCCGTCCACCTAAGGGCATGTATTTAACCCAGGAAGATGTGGTA
GCAGTTTCCTGTAGTCCCAATGCAGCCAACACCATCCTGAGGCAACTGGACATGGAGTTGATCT
CTCTAAAACGTCAGGTTCAGAATGCTAAGCAAGTAAACAGTGCACTTAAACAGAAAATGGAAGG
TGGAATTGAAGAATTCAAACCTCCTGAGTCAAATCAGAAAATTAATGCCCGTTGGACCACAGAG
GAGCAGCTTCTAGCAGTGCAAGGTGTCCGCAAATATGGTAAAGATTTTCAAGCTATTGCAGATG
TAATTGGCAACAAGACTGTTGGCCAAGTGAAGAACTTCTTTGTAAACTACAGGCGTCGGTTTAA
CTTAGAGGAGGTATTGCAGGAGTGGGAAGCAGAACAAGGAACCCAGGCTTCTAATGGTGATGCT
TCTACTTTAGGGGAGGAGACAAAAAGTGCTTCTAATGTGCCATCAGGGAAGAGCACTGATGAAG
AAGAGGAGGCACAGACCCCACAGGCTCCTCGGACACTGGGTCCATCACCTCCTGCCCCATCATC
CACTCCAACACCAACAGCCCCTATTGCCACTCTGAACCAGCCTCCACCACTTCTTCGTCCAACA
CTGCCTGCTGCCCCGGCTCTTCACCGGCAGCCTCCTCCACTCCAGCAGCAGGCTCGGTTCATCC
AGCCCCGGCCAACTTTAAATCAGCCTCCACCACCTCTTATTCGCCCTGCTAATTCCATGCCACC
CCGTCTAAACCCAAGACCGGTGTTGTCCACGGTTGGTGGTCAACAGCCACCATCACTTATTGGA
ATTCAGACAGATTCACAGTCCTCACTGCACTAAAAATTAAATTGGACACAGCTGCAGTAACTTT
TCACCCCATCATTATACCAGTGCTCATCTGACTGATGAAAAAGAGGAAAGAATAATCATTTCTA
GATACTGAGGCTGCGAACTAGTTCTGTGGCAGTGGACTAGCATAAGTGGATGTCTAAGAAATTT
TTCAGTTCACTAGACTAAAATGTTTTACAACAAAAAGCCTCCAGTTAGCCTCCTTTCTAGAGTA
TATGTTCAGCAATGTTGATCTCATAAAAGGAAAAACAAAAGATTTAAGTATTCTATATACCAAG
TTTTTGTTTTGTTTTTACTGTATTTATTTTATTGAGGTTCTTTATATTCCTGCCTCTTCATAGT
CAAGGCTCTTAGTACAGGAATATTGACTTAGGAATTGTGAAAACTCCTTAAGTTTCTTAAGTTA
AGGATGTTTGGCTTTTTTCTTTAATTTTTTAAAAACCATTTTCCTATGTTAGGAGTGCAAGAAT
AGCCAGCATTTCCGATTTTGACATATGTTCATTTTATGCATATTTAAGAAATTATAGCTGCATA
TCCCTTCTTTCAAAAAATGTTGCTTTTTTTTTTAAAGGAATTTTAATATATTCCTTTAAAAGAA
AGCAATTTAATCAATTGCAAAGCAATTATATAAAACCACAAAGAATGTACTGAACCTACTAACC
CTTTAACATACAGTTTAGGGTCCTAGCGCAGAGTCCTTGTTTAAAGGTCATTGACTCATCATCT
GTCAGTAATGAGAGGATTGGAAGAATAATTTTGCATACAAATGAGGACTTAATTTGTTGAAATA
TAATCTCTTTAAGTTCCTTGAAAATGGAGTTGGTTTTTTTTGTTTCTAAATGCTATCTGCTTTT
AACTAGTAGTTGCCTACATCTGGGGACTTCAGAGAAGAATTATATTTTGTTAGTTAAGTAGACA
CAGTGGTTATGGAAGCATTTCTTTACAGTACCCTTTACATGTTTGGTTTCTGAACTTAAAATTG
CCCTCATACTTAATAATATGGTCTGCATTTAATATGAAAGGTGTTTTATTGATAAATCTATTGT
ACTATTTGGATACATTTGTGTATTCCTTGCAGCCAACCTGTATTCGTGGGATTGGTGTAGGGTT
AAATCATCAACATTATTTCATAAAATAAGAATTTGTTCTGTGTTATCTAAAGATGTATCAGTAT
ATTGTCACAGTTGTGCTGTTAACTAAAAATGCTGAGACCCCTTTTTATAGAAAAACAAAAAGAC
ATCAAGTCTTCTTAATTCAACCCATAATCATTAAGTACTTAACAAAGAATATTTTACAAGTGAT
AGTATTTCAACAATGTGTAATTAATATTTTTGATACAGTGATTTCATATTGGAATCATTATTTG
TGCAAAGGGACAGACAGATCACTTAGATTGCTATACTAGTGGACATAGGCTACATGTTTGCACA
TTCACATTCTTATCACGTGTAGAATACTTCACAAAATAGTCAACATCTAAGGCCCTAATTTATG
TTTTGAAAGATCATGTGTTCCCAAAGTATTCCCTATTGTTGGCTCCACAGCCTTAAAGTGCTAT
AGATTTAAATTCATTGATTAGTTTTAATTTTTAATTTTAGACTGTGTATTTCCATAAATACCCT
ACGTACTGGCATATTTGAAACTCTTTTTCCAGGTTAGGTCCTTTTCTTTCTCATTGAATCATCT
TAAATAGTTCTTGGCCCTGAATTTAGCTGATTTAAAATTCTTAATATTCAAGAATTTATACTTA
TTTTTTCCTTAAAAGCCACAGGGGACAGTTAAATATCTTAAAATATCTAAAACATTTTTTAAAG
CACTTAGATTGTCTTACGTATGTGCATACTATACCTTTACAGCGTTTATTGTCTTGTCTCTTGT
CAGTAGACCTTCAGTACACAGTATGTGGGATATGTCAGTCAAGTTGGTCAGCACCAGCATCTGT
CCAGCTGTTCAGTATATTGTGATTCATTAAAAAATCTCTTCTATCCCAGACATGGGCCAAGGTG
CTGTATCTGAGGGATGTGCTGTAATTTGATTTACATGCATTAGAGCACACAGTAGAAAAACTTT
AGCTTCATTAGTAATATGACACATGTATATAGTGAGATGTCTTTATTGTGTGCTTTGCATATTT
TGTAAATATTTTGCACGTCATTATTTTTCTTTTTTGTTTAAGCAGTGTTTGGCCTGGAAGAGTG
ATATGCTTGCTGCTTAATCAAAGGATTAAAGATTTAAAGATGTCTATGTCTTCTATTTTTATAT
AATTTCATGTTCTATGAGGAATTTAGTACCTCTTCACTGTGAAATTCGAAATAATGATTTTTAT
AAAAGCAAAACTAGAAATCTTTTAATGACAATTTTCATTAATTTCAGGGTTATCATTTTTGAGA
AATCTACACCAAAGTGGTTTTTTAAAATTACATAACTAAAAATAAACCACACTGTGGATACATC
TTATAAAACTAATGGAAACAATGTTTTTCTATATGATTTAATTCTAGTGTAATATGGATGAGGT
AAGAGTAAGTTATGATCAAACTTTTTATGTTCTTAATAAGCTTGCAATTGAGTAAAATAGAATA
TAAAATAAAGGTGAAATAATATAAAA

hide sequence

RefSeq Acc Id:

NM_001350070 ⟹ NP_001336999

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	211,259,366 - 211,316,385 (+)	NCBI
T2T-CHM13v2.0	1	210,504,931 - 210,561,986 (+)	NCBI

Sequence:

show sequence

GTTGTTGTGAGGCGACTGCGCTACTGCCGGAGCGGGGCGGTTATGGCGGCTCCATATTAACAGC
CTCCTCCTCCTCCGCCGCCGCCGCCGTCTCCTCCTCCTCCTCCTTTCCCTCCCGCCCGCGCTCT
AAGCCATCTCCGCCTTCACCCTGACGCCTGCCTCTTCCCCTCACCTTTCCCCCTCCCCTGTTCT
ACCATGCCCGGCATGATGGAGAAAGGGCCCGAGTTACTGGGGAAGAACCGATCGGCCAACGGCA
GCGCCAAGAGCCCGGCAGGCGGCGGCGGCAGCGGCGCCTCGTCCACCAACGGCGGGCTGCACTA
CTCAGAGCCCGAGAGCGGCTGCAGCAGCGACGACGAGCACGATGTTGGGATGAGAGTCGGAGCC
GAATACCAAGCTCGGATCCCTGAATTTGATCCAGGTGCTACAAAGTACACAGATAAAGACAATG
GAGGGATGCTTGTATGGTCTCCATATCACAGTATCCCAGATGCCAAATGCCCATGAAGAATGAA
AAAACCTAGGATCTGATGGCATTGCTGCTTAAATCCTCAAGCAGGGGAGGGAGTTACTATGTAG
ACATCTGCCCAGGCTTTTCCTCAGTATATGGAGCGGTAAAGACATGCCTTCAAACTTCAAAGAG
CCCACTATCATTACCATTTTAAAGAGGAAAGGGGAAAGAACTGACTTCAGCAGCCATCAGGTCA
TCTTTGTGCTCTCCATTTCTGGACGGAGACCTTCTGGATCATTGACCATGCACTTCTTGAATCA
TGGTGTGGCTTTAGACTTCAATGTGATGTAGCGGACCTGATCCTTTGCGGCACATCAGATATAG
GAAACGTGCAGTGGATGAATACATTGCAATTGCAAAGGAAAAGCATGGCTACAATGTGGAACAG
GCACTTGGCATGTTGTTCTGGCATAAACATAACATTGAGAAGTCCCTTGCTGATCTCCCTAATT
TCACTCCCTTTCCGGATGAGTGGACAGTGGAAGATAAAGTCCTATTTGAACAAGCCTTTAGTTT
TCATGGAAAGAGCTTTCACAGGATTCAGCAAATGCTTCCAGATAAGACAATTGCAAGCCTTGTA
AAATATTACTATTCTTGGAAAAAAACTCGCTCTAGGACAAGTTTGATGGATCGCCAGGCTCGTA
AACTAGCTAATAGACATAATCAGGGTGACAGTGATGATGATGTAGAAGAAACACATCCAATGGA
TGGGAATGATAGTGATTATGATCCCAAAAAAGAAGCCAAAAAAGAGGGTAATACTGAACAACCT
GTCCAAACTAGCAAGATTGGACTTGGAAGAAGAGAGTATCAGAGTTTACAACATCGCCATCATT
CTCAGCGTTCTAAGTGCCGTCCACCTAAGGGCATGTATTTAACCCAGGAAGATGTGGTAGCAGT
TTCCTGTAGTCCCAATGCAGCCAACACCATCCTGAGGCAACTGGACATGGAGTTGATCTCTCTA
AAACGTCAGGTTCAGAATGCTAAGCAAGTAAACAGTGCACTTAAACAGAAAATGGAAGGTGGAA
TTGAAGAATTCAAACCTCCTGAGTCAAATCAGAAAATTAATGCCCGTTGGACCACAGAGGAGCA
GCTTCTAGCAGTGCAAGGTGTCCGCAAATATGGTAAAGATTTTCAAGCTATTGCAGATGTAATT
GGCAACAAGACTGTTGGCCAAGTGAAGAACTTCTTTGTAAACTACAGGCGTCGGTTTAACTTAG
AGGAGGTATTGCAGGAGTGGGAAGCAGAACAAGGAACCCAGGCTTCTAATGGTGATGCTTCTAC
TTTAGGGGAGGAGACAAAAAGTGCTTCTAATGTGCCATCAGGGAAGAGCACTGATGAAGAAGAG
GAGGCACAGACCCCACAGGCTCCTCGGACACTGGGTCCATCACCTCCTGCCCCATCATCCACTC
CAACACCAACAGCCCCTATTGCCACTCTGAACCAGCCTCCACCACTTCTTCGTCCAACACTGCC
TGCTGCCCCGGCTCTTCACCGGCAGCCTCCTCCACTCCAGCAGCAGGCTCGGTTCATCCAGCCC
CGGCCAACTTTAAATCAGCCTCCACCACCTCTTATTCGCCCTGCTAATTCCATGCCACCCCGTC
TAAACCCAAGACCGGTGTTGTCCACGGTTGGTGGTCAACAGCCACCATCACTTATTGGAATTCA
GACAGATTCACAGTCCTCACTGCACTAAAAATTAAATTGGACACAGCTGCAGTAACTTTTCACC
CCATCATTATACCAGTGCTCATCTGACTGATGAAAAAGAGGAAAGAATAATCATTTCTAGATAC
TGAGGCTGCGAACTAGTTCTGTGGCAGTGGACTAGCATAAGTGGATGTCTAAGAAATTTTTCAG
TTCACTAGACTAAAATGTTTTACAACAAAAAGCCTCCAGTTAGCCTCCTTTCTAGAGTATATGT
TCAGCAATGTTGATCTCATAAAAGGAAAAACAAAAGATTTAAGTATTCTATATACCAAGTTTTT
GTTTTGTTTTTACTGTATTTATTTTATTGAGGTTCTTTATATTCCTGCCTCTTCATAGTCAAGG
CTCTTAGTACAGGAATATTGACTTAGGAATTGTGAAAACTCCTTAAGTTTCTTAAGTTAAGGAT
GTTTGGCTTTTTTCTTTAATTTTTTAAAAACCATTTTCCTATGTTAGGAGTGCAAGAATAGCCA
GCATTTCCGATTTTGACATATGTTCATTTTATGCATATTTAAGAAATTATAGCTGCATATCCCT
TCTTTCAAAAAATGTTGCTTTTTTTTTTAAAGGAATTTTAATATATTCCTTTAAAAGAAAGCAA
TTTAATCAATTGCAAAGCAATTATATAAAACCACAAAGAATGTACTGAACCTACTAACCCTTTA
ACATACAGTTTAGGGTCCTAGCGCAGAGTCCTTGTTTAAAGGTCATTGACTCATCATCTGTCAG
TAATGAGAGGATTGGAAGAATAATTTTGCATACAAATGAGGACTTAATTTGTTGAAATATAATC
TCTTTAAGTTCCTTGAAAATGGAGTTGGTTTTTTTTGTTTCTAAATGCTATCTGCTTTTAACTA
GTAGTTGCCTACATCTGGGGACTTCAGAGAAGAATTATATTTTGTTAGTTAAGTAGACACAGTG
GTTATGGAAGCATTTCTTTACAGTACCCTTTACATGTTTGGTTTCTGAACTTAAAATTGCCCTC
ATACTTAATAATATGGTCTGCATTTAATATGAAAGGTGTTTTATTGATAAATCTATTGTACTAT
TTGGATACATTTGTGTATTCCTTGCAGCCAACCTGTATTCGTGGGATTGGTGTAGGGTTAAATC
ATCAACATTATTTCATAAAATAAGAATTTGTTCTGTGTTATCTAAAGATGTATCAGTATATTGT
CACAGTTGTGCTGTTAACTAAAAATGCTGAGACCCCTTTTTATAGAAAAACAAAAAGACATCAA
GTCTTCTTAATTCAACCCATAATCATTAAGTACTTAACAAAGAATATTTTACAAGTGATAGTAT
TTCAACAATGTGTAATTAATATTTTTGATACAGTGATTTCATATTGGAATCATTATTTGTGCAA
AGGGACAGACAGATCACTTAGATTGCTATACTAGTGGACATAGGCTACATGTTTGCACATTCAC
ATTCTTATCACGTGTAGAATACTTCACAAAATAGTCAACATCTAAGGCCCTAATTTATGTTTTG
AAAGATCATGTGTTCCCAAAGTATTCCCTATTGTTGGCTCCACAGCCTTAAAGTGCTATAGATT
TAAATTCATTGATTAGTTTTAATTTTTAATTTTAGACTGTGTATTTCCATAAATACCCTACGTA
CTGGCATATTTGAAACTCTTTTTCCAGGTTAGGTCCTTTTCTTTCTCATTGAATCATCTTAAAT
AGTTCTTGGCCCTGAATTTAGCTGATTTAAAATTCTTAATATTCAAGAATTTATACTTATTTTT
TCCTTAAAAGCCACAGGGGACAGTTAAATATCTTAAAATATCTAAAACATTTTTTAAAGCACTT
AGATTGTCTTACGTATGTGCATACTATACCTTTACAGCGTTTATTGTCTTGTCTCTTGTCAGTA
GACCTTCAGTACACAGTATGTGGGATATGTCAGTCAAGTTGGTCAGCACCAGCATCTGTCCAGC
TGTTCAGTATATTGTGATTCATTAAAAAATCTCTTCTATCCCAGACATGGGCCAAGGTGCTGTA
TCTGAGGGATGTGCTGTAATTTGATTTACATGCATTAGAGCACACAGTAGAAAAACTTTAGCTT
CATTAGTAATATGACACATGTATATAGTGAGATGTCTTTATTGTGTGCTTTGCATATTTTGTAA
ATATTTTGCACGTCATTATTTTTCTTTTTTGTTTAAGCAGTGTTTGGCCTGGAAGAGTGATATG
CTTGCTGCTTAATCAAAGGATTAAAGATTTAAAGATGTCTATGTCTTCTATTTTTATATAATTT
CATGTTCTATGAGGAATTTAGTACCTCTTCACTGTGAAATTCGAAATAATGATTTTTATAAAAG
CAAAACTAGAAATCTTTTAATGACAATTTTCATTAATTTCAGGGTTATCATTTTTGAGAAATCT
ACACCAAAGTGGTTTTTTAAAATTACATAACTAAAAATAAACCACACTGTGGATACATCTTATA
AAACTAATGGAAACAATGTTTTTCTATATGATTTAATTCTAGTGTAATATGGATGAGGTAAGAG
TAAGTTATGATCAAACTTTTTATGTTCTTAATAAGCTTGCAATTGAGTAAAATAGAATATAAAA
TAAAGGTGAAATAATATAAAA

hide sequence

RefSeq Acc Id:

NM_018254 ⟹ NP_060724

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	211,259,947 - 211,316,385 (+)	NCBI
GRCh37	1	211,432,708 - 211,489,727 (+)	RGD
Build 36	1	209,499,949 - 209,556,200 (+)	NCBI Archive
Celera	1	184,656,707 - 184,716,396 (+)	RGD
HuRef	1	182,109,654 - 182,166,679 (+)	ENTREZGENE
CHM1_1	1	212,705,760 - 212,762,151 (+)	NCBI
T2T-CHM13v2.0	1	210,505,512 - 210,561,986 (+)	NCBI

Sequence:

show sequence

AATCCGCTGCCATCTCCCGGAGTGCCCCGAGTTGATATCTTCCCATCCACCCGCCGCTTCTTTC
CTCCATCTAGCGATTTTTATTTTTTAAGTGTCTCTTCCTTTTTCTTTCTTTTCTTCTTTTTTAT
TTTTTATATATATTTTTTGGCATTGCTTTGCAGATGTTGGGATGAGAGTCGGAGCCGAATACCA
AGCTCGGATCCCTGAATTTGATCCAGGTGCTACAAAGTACACAGATAAAGACAATGGAGGGATG
CTTGTATGGTCTCCATATCACAGTATCCCAGATGCCAAATTGGATGAATACATTGCAATTGCAA
AGGAAAAGCATGGCTACAATGTGGAACAGGCACTTGGCATGTTGTTCTGGCATAAACATAACAT
TGAGAAGTCCCTTGCTGATCTCCCTAATTTCACTCCCTTTCCGGATGAGTGGACAGTGGAAGAT
AAAGTCCTATTTGAACAAGCCTTTAGTTTTCATGGAAAGAGCTTTCACAGGATTCAGCAAATGC
TTCCAGATAAGACAATTGCAAGCCTTGTAAAATATTACTATTCTTGGAAAAAAACTCGCTCTAG
GACAAGTTTGATGGATCGCCAGGCTCGTAAACTAGCTAATAGACATAATCAGGGTGACAGTGAT
GATGATGTAGAAGAAACACATCCAATGGATGGGAATGATAGTGATTATGATCCCAAAAAAGAAG
CCAAAAAAGAGGGTAATACTGAACAACCTGTCCAAACTAGCAAGATTGGACTTGGAAGAAGAGA
GTATCAGAGTTTACAACATCGCCATCATTCTCAGCGTTCTAAGTGCCGTCCACCTAAGGGCATG
TATTTAACCCAGGAAGATGTGGTAGCAGTTTCCTGTAGTCCCAATGCAGCCAACACCATCCTGA
GGCAACTGGACATGGAGTTGATCTCTCTAAAACGTCAGGTTCAGAATGCTAAGCAAGTAAACAG
TGCACTTAAACAGAAAATGGAAGGTGGAATTGAAGAATTCAAACCTCCTGAGTCAAATCAGAAA
ATTAATGCCCGTTGGACCACAGAGGAGCAGCTTCTAGCAGTGCAAGGTGTCCGCAAATATGGTA
AAGATTTTCAAGCTATTGCAGATGTAATTGGCAACAAGACTGTTGGCCAAGTGAAGAACTTCTT
TGTAAACTACAGGCGTCGGTTTAACTTAGAGGAGGTATTGCAGGAGTGGGAAGCAGAACAAGGA
ACCCAGGCTTCTAATGGTGATGCTTCTACTTTAGGGGAGGAGACAAAAAGTGCTTCTAATGTGC
CATCAGGGAAGAGCACTGATGAAGAAGAGGAGGCACAGACCCCACAGGCTCCTCGGACACTGGG
TCCATCACCTCCTGCCCCATCATCCACTCCAACACCAACAGCCCCTATTGCCACTCTGAACCAG
CCTCCACCACTTCTTCGTCCAACACTGCCTGCTGCCCCGGCTCTTCACCGGCAGCCTCCTCCAC
TCCAGCAGCAGGCTCGGTTCATCCAGCCCCGGCCAACTTTAAATCAGCCTCCACCACCTCTTAT
TCGCCCTGCTAATTCCATGCCACCCCGTCTAAACCCAAGACCGGTGTTGTCCACGGTTGGTGGT
CAACAGCCACCATCACTTATTGGAATTCAGACAGATTCACAGTCCTCACTGCACTAAAAATTAA
ATTGGACACAGCTGCAGTAACTTTTCACCCCATCATTATACCAGTGCTCATCTGACTGATGAAA
AAGAGGAAAGAATAATCATTTCTAGATACTGAGGCTGCGAACTAGTTCTGTGGCAGTGGACTAG
CATAAGTGGATGTCTAAGAAATTTTTCAGTTCACTAGACTAAAATGTTTTACAACAAAAAGCCT
CCAGTTAGCCTCCTTTCTAGAGTATATGTTCAGCAATGTTGATCTCATAAAAGGAAAAACAAAA
GATTTAAGTATTCTATATACCAAGTTTTTGTTTTGTTTTTACTGTATTTATTTTATTGAGGTTC
TTTATATTCCTGCCTCTTCATAGTCAAGGCTCTTAGTACAGGAATATTGACTTAGGAATTGTGA
AAACTCCTTAAGTTTCTTAAGTTAAGGATGTTTGGCTTTTTTCTTTAATTTTTTAAAAACCATT
TTCCTATGTTAGGAGTGCAAGAATAGCCAGCATTTCCGATTTTGACATATGTTCATTTTATGCA
TATTTAAGAAATTATAGCTGCATATCCCTTCTTTCAAAAAATGTTGCTTTTTTTTTTAAAGGAA
TTTTAATATATTCCTTTAAAAGAAAGCAATTTAATCAATTGCAAAGCAATTATATAAAACCACA
AAGAATGTACTGAACCTACTAACCCTTTAACATACAGTTTAGGGTCCTAGCGCAGAGTCCTTGT
TTAAAGGTCATTGACTCATCATCTGTCAGTAATGAGAGGATTGGAAGAATAATTTTGCATACAA
ATGAGGACTTAATTTGTTGAAATATAATCTCTTTAAGTTCCTTGAAAATGGAGTTGGTTTTTTT
TGTTTCTAAATGCTATCTGCTTTTAACTAGTAGTTGCCTACATCTGGGGACTTCAGAGAAGAAT
TATATTTTGTTAGTTAAGTAGACACAGTGGTTATGGAAGCATTTCTTTACAGTACCCTTTACAT
GTTTGGTTTCTGAACTTAAAATTGCCCTCATACTTAATAATATGGTCTGCATTTAATATGAAAG
GTGTTTTATTGATAAATCTATTGTACTATTTGGATACATTTGTGTATTCCTTGCAGCCAACCTG
TATTCGTGGGATTGGTGTAGGGTTAAATCATCAACATTATTTCATAAAATAAGAATTTGTTCTG
TGTTATCTAAAGATGTATCAGTATATTGTCACAGTTGTGCTGTTAACTAAAAATGCTGAGACCC
CTTTTTATAGAAAAACAAAAAGACATCAAGTCTTCTTAATTCAACCCATAATCATTAAGTACTT
AACAAAGAATATTTTACAAGTGATAGTATTTCAACAATGTGTAATTAATATTTTTGATACAGTG
ATTTCATATTGGAATCATTATTTGTGCAAAGGGACAGACAGATCACTTAGATTGCTATACTAGT
GGACATAGGCTACATGTTTGCACATTCACATTCTTATCACGTGTAGAATACTTCACAAAATAGT
CAACATCTAAGGCCCTAATTTATGTTTTGAAAGATCATGTGTTCCCAAAGTATTCCCTATTGTT
GGCTCCACAGCCTTAAAGTGCTATAGATTTAAATTCATTGATTAGTTTTAATTTTTAATTTTAG
ACTGTGTATTTCCATAAATACCCTACGTACTGGCATATTTGAAACTCTTTTTCCAGGTTAGGTC
CTTTTCTTTCTCATTGAATCATCTTAAATAGTTCTTGGCCCTGAATTTAGCTGATTTAAAATTC
TTAATATTCAAGAATTTATACTTATTTTTTCCTTAAAAGCCACAGGGGACAGTTAAATATCTTA
AAATATCTAAAACATTTTTTAAAGCACTTAGATTGTCTTACGTATGTGCATACTATACCTTTAC
AGCGTTTATTGTCTTGTCTCTTGTCAGTAGACCTTCAGTACACAGTATGTGGGATATGTCAGTC
AAGTTGGTCAGCACCAGCATCTGTCCAGCTGTTCAGTATATTGTGATTCATTAAAAAATCTCTT
CTATCCCAGACATGGGCCAAGGTGCTGTATCTGAGGGATGTGCTGTAATTTGATTTACATGCAT
TAGAGCACACAGTAGAAAAACTTTAGCTTCATTAGTAATATGACACATGTATATAGTGAGATGT
CTTTATTGTGTGCTTTGCATATTTTGTAAATATTTTGCACGTCATTATTTTTCTTTTTTGTTTA
AGCAGTGTTTGGCCTGGAAGAGTGATATGCTTGCTGCTTAATCAAAGGATTAAAGATTTAAAGA
TGTCTATGTCTTCTATTTTTATATAATTTCATGTTCTATGAGGAATTTAGTACCTCTTCACTGT
GAAATTCGAAATAATGATTTTTATAAAAGCAAAACTAGAAATCTTTTAATGACAATTTTCATTA
ATTTCAGGGTTATCATTTTTGAGAAATCTACACCAAAGTGGTTTTTTAAAATTACATAACTAAA
AATAAACCACACTGTGGATACATCTTATAAAACTAATGGAAACAATGTTTTTCTATATGATTTA
ATTCTAGTGTAATATGGATGAGGTAAGAGTAAGTTATGATCAAACTTTTTATGTTCTTAATAAG
CTTGCAATTGAGTAAAATAGAATATAAAATAAAGGTGAAATAATATAAAA

hide sequence

RefSeq Acc Id:

NR_146432

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	211,259,366 - 211,316,385 (+)	NCBI
T2T-CHM13v2.0	1	210,504,931 - 210,561,986 (+)	NCBI

Sequence:

show sequence

GTTGTTGTGAGGCGACTGCGCTACTGCCGGAGCGGGGCGGTTATGGCGGCTCCATATTAACAGC
CTCCTCCTCCTCCGCCGCCGCCGCCGTCTCCTCCTCCTCCTCCTTTCCCTCCCGCCCGCGCTCT
AAGCCATCTCCGCCTTCACCCTGACGCCTGCCTCTTCCCCTCACCTTTCCCCCTCCCCTGTTCT
ACCATGCCCGGCATGATGGAGAAAGGGCCCGAGTTACTGGGGAAGAACCGATCGGCCAACGGCA
GCGCCAAGAGCCCGGCAGGCGGCGGCGGCAGCGGCGCCTCGTCCACCAACGGCGGGCTGCACTA
CTCAGAGCCCGAGAGCGGCTGCAGCAGCGACGACGAGCACGGTGATGTTGGGATGAGAGTCGGA
GCCGAATACCAAGCTCGGATCCCTGAATTTGATCCAGGTGCTACAAAGTACACAGATAAAGACA
ATGGAGGGATGCTTGTATGGTCTCCATATCACAGTATCCCAGATGCCAAATTGGATGAATACAT
TGCAATTGCAAAGGAAAAGCATGGCTACAATGTGGAACAGGCACTTGGCATGTTGTTCTGGCAT
AAACATAACATTGAGAAGTCCCTTGCTGATCTCCCTAATTTCACTCCCTTTCCGGATGAGTGGA
CAGTGGAAGATAAAGTCCTATTTGAACAAGCCTTTAGTTTTCATGGAAAGAGCTTTCACAGGAT
TCAGCAAATGCTTCCAGATAAGACAATTGCAAGCCTTGTAAAATATTACTATTCTTGGAAAAAA
ACTCGCTCTAGGACAAGTTTGATGGATCGCCAGGCTCGTAAACTAGCTAATAGACATAATCAGG
GTGACAGTGATGATGATGTAGAAGAAACACATCCAATGGATGGGAATGATAGTGATTATGATCC
CAAAAAAGAAGCCAAAAAAGAGGGTAATACTGAACAACCTGTCCAAACTAGCAAGATTGGACTT
GGAAGAAGAGAGTATCAGAGTTTACAACATCGCCATCATTCTCAGCGTTCTAAGTGCCGTCCAC
CTAAGGGCATGTATTTAACCCAGGAAGATGTGGTAGCAGTTTCCTGTAGTCCCAATGCAGCCAA
CACCATCCTGAGGCAACTGGACATGGAGTTGATCTCTCTAAAACGTCAGGTTCAGAATGCTAAG
CAAGTAAACAGTGCACTTAAACAGAAAATGGAAGGTGGAATTGAAGAATTCAAACCTCCTGAGT
CAAATCAGAAAATTAATGCCCGTTGGACCACAGAGGAGCAGCTTCTAGCAGTGCAAGGTGACTG
GCTACTAGGGAAATAAATGAATGTGGAATTGAGGATGGAACAAAGAATTCAATGCTTTACAATA
AATGGACTGTATTTGAGAGTTCAAGAGAGGATTGGAGAAAATAACTGAGTATGTAAAAAATGGT
GTCCGCAAATATGGTAAAGATTTTCAAGCTATTGCAGATGTAATTGGCAACAAGACTGTTGGCC
AAGTGAAGAACTTCTTTGTAAACTACAGGCGTCGGTTTAACTTAGAGGAGGTATTGCAGGAGTG
GGAAGCAGAACAAGGAACCCAGGCTTCTAATGGTGATGCTTCTACTTTAGGGGAGGAGACAAAA
AGTGCTTCTAATGTGCCATCAGGGAAGAGCACTGATGAAGAAGAGGAGGCACAGACCCCACAGG
CTCCTCGGACACTGGGTCCATCACCTCCTGCCCCATCATCCACTCCAACACCAACAGCCCCTAT
TGCCACTCTGAACCAGCCTCCACCACTTCTTCGTCCAACACTGCCTGCTGCCCCGGCTCTTCAC
CGGCAGCCTCCTCCACTCCAGCAGCAGGCTCGGTTCATCCAGCCCCGGCCAACTTTAAATCAGC
CTCCACCACCTCTTATTCGCCCTGCTAATTCCATGCCACCCCGTCTAAACCCAAGACCGGTGTT
GTCCACGGTTGGTGGTCAACAGCCACCATCACTTATTGGAATTCAGACAGATTCACAGTCCTCA
CTGCACTAAAAATTAAATTGGACACAGCTGCAGTAACTTTTCACCCCATCATTATACCAGTGCT
CATCTGACTGATGAAAAAGAGGAAAGAATAATCATTTCTAGATACTGAGGCTGCGAACTAGTTC
TGTGGCAGTGGACTAGCATAAGTGGATGTCTAAGAAATTTTTCAGTTCACTAGACTAAAATGTT
TTACAACAAAAAGCCTCCAGTTAGCCTCCTTTCTAGAGTATATGTTCAGCAATGTTGATCTCAT
AAAAGGAAAAACAAAAGATTTAAGTATTCTATATACCAAGTTTTTGTTTTGTTTTTACTGTATT
TATTTTATTGAGGTTCTTTATATTCCTGCCTCTTCATAGTCAAGGCTCTTAGTACAGGAATATT
GACTTAGGAATTGTGAAAACTCCTTAAGTTTCTTAAGTTAAGGATGTTTGGCTTTTTTCTTTAA
TTTTTTAAAAACCATTTTCCTATGTTAGGAGTGCAAGAATAGCCAGCATTTCCGATTTTGACAT
ATGTTCATTTTATGCATATTTAAGAAATTATAGCTGCATATCCCTTCTTTCAAAAAATGTTGCT
TTTTTTTTTAAAGGAATTTTAATATATTCCTTTAAAAGAAAGCAATTTAATCAATTGCAAAGCA
ATTATATAAAACCACAAAGAATGTACTGAACCTACTAACCCTTTAACATACAGTTTAGGGTCCT
AGCGCAGAGTCCTTGTTTAAAGGTCATTGACTCATCATCTGTCAGTAATGAGAGGATTGGAAGA
ATAATTTTGCATACAAATGAGGACTTAATTTGTTGAAATATAATCTCTTTAAGTTCCTTGAAAA
TGGAGTTGGTTTTTTTTGTTTCTAAATGCTATCTGCTTTTAACTAGTAGTTGCCTACATCTGGG
GACTTCAGAGAAGAATTATATTTTGTTAGTTAAGTAGACACAGTGGTTATGGAAGCATTTCTTT
ACAGTACCCTTTACATGTTTGGTTTCTGAACTTAAAATTGCCCTCATACTTAATAATATGGTCT
GCATTTAATATGAAAGGTGTTTTATTGATAAATCTATTGTACTATTTGGATACATTTGTGTATT
CCTTGCAGCCAACCTGTATTCGTGGGATTGGTGTAGGGTTAAATCATCAACATTATTTCATAAA
ATAAGAATTTGTTCTGTGTTATCTAAAGATGTATCAGTATATTGTCACAGTTGTGCTGTTAACT
AAAAATGCTGAGACCCCTTTTTATAGAAAAACAAAAAGACATCAAGTCTTCTTAATTCAACCCA
TAATCATTAAGTACTTAACAAAGAATATTTTACAAGTGATAGTATTTCAACAATGTGTAATTAA
TATTTTTGATACAGTGATTTCATATTGGAATCATTATTTGTGCAAAGGGACAGACAGATCACTT
AGATTGCTATACTAGTGGACATAGGCTACATGTTTGCACATTCACATTCTTATCACGTGTAGAA
TACTTCACAAAATAGTCAACATCTAAGGCCCTAATTTATGTTTTGAAAGATCATGTGTTCCCAA
AGTATTCCCTATTGTTGGCTCCACAGCCTTAAAGTGCTATAGATTTAAATTCATTGATTAGTTT
TAATTTTTAATTTTAGACTGTGTATTTCCATAAATACCCTACGTACTGGCATATTTGAAACTCT
TTTTCCAGGTTAGGTCCTTTTCTTTCTCATTGAATCATCTTAAATAGTTCTTGGCCCTGAATTT
AGCTGATTTAAAATTCTTAATATTCAAGAATTTATACTTATTTTTTCCTTAAAAGCCACAGGGG
ACAGTTAAATATCTTAAAATATCTAAAACATTTTTTAAAGCACTTAGATTGTCTTACGTATGTG
CATACTATACCTTTACAGCGTTTATTGTCTTGTCTCTTGTCAGTAGACCTTCAGTACACAGTAT
GTGGGATATGTCAGTCAAGTTGGTCAGCACCAGCATCTGTCCAGCTGTTCAGTATATTGTGATT
CATTAAAAAATCTCTTCTATCCCAGACATGGGCCAAGGTGCTGTATCTGAGGGATGTGCTGTAA
TTTGATTTACATGCATTAGAGCACACAGTAGAAAAACTTTAGCTTCATTAGTAATATGACACAT
GTATATAGTGAGATGTCTTTATTGTGTGCTTTGCATATTTTGTAAATATTTTGCACGTCATTAT
TTTTCTTTTTTGTTTAAGCAGTGTTTGGCCTGGAAGAGTGATATGCTTGCTGCTTAATCAAAGG
ATTAAAGATTTAAAGATGTCTATGTCTTCTATTTTTATATAATTTCATGTTCTATGAGGAATTT
AGTACCTCTTCACTGTGAAATTCGAAATAATGATTTTTATAAAAGCAAAACTAGAAATCTTTTA
ATGACAATTTTCATTAATTTCAGGGTTATCATTTTTGAGAAATCTACACCAAAGTGGTTTTTTA
AAATTACATAACTAAAAATAAACCACACTGTGGATACATCTTATAAAACTAATGGAAACAATGT
TTTTCTATATGATTTAATTCTAGTGTAATATGGATGAGGTAAGAGTAAGTTATGATCAAACTTT
TTATGTTCTTAATAAGCTTGCAATTGAGTAAAATAGAATATAAAATAAAGGTGAAATAATATAA
AA

hide sequence

RefSeq Acc Id:

NR_146433

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	211,259,366 - 211,316,385 (+)	NCBI
T2T-CHM13v2.0	1	210,504,931 - 210,561,986 (+)	NCBI

Sequence:

show sequence

GTTGTTGTGAGGCGACTGCGCTACTGCCGGAGCGGGGCGGTTATGGCGGCTCCATATTAACAGC
CTCCTCCTCCTCCGCCGCCGCCGCCGTCTCCTCCTCCTCCTCCTTTCCCTCCCGCCCGCGCTCT
AAGCCATCTCCGCCTTCACCCTGACGCCTGCCTCTTCCCCTCACCTTTCCCCCTCCCCTGTTCT
ACCATGCCCGGCATGATGGAGAAAGGGCCCGAGTTACTGGGGAAGAACCGATCGGCCAACGGCA
GCGCCAAGAGCCCGGCAGGCGGCGGCGGCAGCGGCGCCTCGTCCACCAACGGCGGGCTGCACTA
CTCAGAGCCCGAGAGCGGCTGCAGCAGCGACGACGAGCACGATGTTGGGATGAGAGTCGGAGCC
GAATACCAAGCTCGGATCCCTGAATTTGATCCAGGTGCTACAAAGTACACAGATAAAGACAATG
GAGGGATGCTTGTATGGTCTCCATATCACAGTATCCCAGATGCCAAATTGGATGAATACATTGC
AATTGCAAAGGAAAAGCATGGCTACAATGTGGAACAGGCACTTGGCATGTTGTTCTGGCATAAA
CATAACATTGAGAAGTCCCTTGCTGATCTCCCTAATTTCACTCCCTTTCCGGATGAGTGGACAG
TGGAAGATAAAGTCCTATTTGAACAAGCCTTTAGTTTTCATGGAAAGAGCTTTCACAGGATTCA
GCAAATGCTTCCAGATAAGACAATTGCAAGCCTTGTAAAATATTACTATTCTTGGAAAAAAACT
CGCTCTAGGACAAGTTTGATGGATCGCCAGGCTCGTAAACTAGCTAATAGACATAATCAGGGTG
ACAGTGATGATGATGTAGAAGAAACACATCCAATGGATGGGAATGATAGTGATTATGATCCCAA
AAAAGAAGCCAAAAAAGAGGGTAATACTGAACAACCTGTCCAAACTAGCAAGATTGGACTTGGA
AGAAGAGAGTATCAGAGTTTACAACATCGCCATCATTCTCAGCGTTCTAAGTGCCGTCCACCTA
AGGGCATGTATTTAACCCAGGAAGATGTGGTAGCAGTTTCCTGTAGTCCCAATGCAGCCAACAC
CATCCTGAGGCAACTGGACATGGAGTTGATCTCTCTAAAACGTCAGGTTCAGAATGCTAAGCAA
GTAAACAGTGCACTTAAACAGAAAATGGAAGGTGGAATTGAAGAATTCAAACCTCCTGAGTCAA
ATCAGAAAATTAATGCCCGTTGGACCACAGAGGAGCAGCTTCTAGCAGTGCAAGGTGACTGGCT
ACTAGGGAAATAAATGAATGTGGAATTGAGGATGGAACAAAGAATTCAATGCTTTACAATAAAT
GGACTGTATTTGAGAGTTCAAGAGAGGATTGGAGAAAATAACTGAGTATGTAAAAAATGGTGTC
CGCAAATATGGTAAAGATTTTCAAGCTATTGCAGATGTAATTGGCAACAAGACTGTTGGCCAAG
TGAAGAACTTCTTTGTAAACTACAGGCGTCGGTTTAACTTAGAGGAGGTATTGCAGGAGTGGGA
AGCAGAACAAGGAACCCAGGCTTCTAATGGTGATGCTTCTACTTTAGGGGAGGAGACAAAAAGT
GCTTCTAATGTGCCATCAGGGAAGAGCACTGATGAAGAAGAGGAGGCACAGACCCCACAGGCTC
CTCGGACACTGGGTCCATCACCTCCTGCCCCATCATCCACTCCAACACCAACAGCCCCTATTGC
CACTCTGAACCAGCCTCCACCACTTCTTCGTCCAACACTGCCTGCTGCCCCGGCTCTTCACCGG
CAGCCTCCTCCACTCCAGCAGCAGGCTCGGTTCATCCAGCCCCGGCCAACTTTAAATCAGCCTC
CACCACCTCTTATTCGCCCTGCTAATTCCATGCCACCCCGTCTAAACCCAAGACCGGTGTTGTC
CACGGTTGGTGGTCAACAGCCACCATCACTTATTGGAATTCAGACAGATTCACAGTCCTCACTG
CACTAAAAATTAAATTGGACACAGCTGCAGTAACTTTTCACCCCATCATTATACCAGTGCTCAT
CTGACTGATGAAAAAGAGGAAAGAATAATCATTTCTAGATACTGAGGCTGCGAACTAGTTCTGT
GGCAGTGGACTAGCATAAGTGGATGTCTAAGAAATTTTTCAGTTCACTAGACTAAAATGTTTTA
CAACAAAAAGCCTCCAGTTAGCCTCCTTTCTAGAGTATATGTTCAGCAATGTTGATCTCATAAA
AGGAAAAACAAAAGATTTAAGTATTCTATATACCAAGTTTTTGTTTTGTTTTTACTGTATTTAT
TTTATTGAGGTTCTTTATATTCCTGCCTCTTCATAGTCAAGGCTCTTAGTACAGGAATATTGAC
TTAGGAATTGTGAAAACTCCTTAAGTTTCTTAAGTTAAGGATGTTTGGCTTTTTTCTTTAATTT
TTTAAAAACCATTTTCCTATGTTAGGAGTGCAAGAATAGCCAGCATTTCCGATTTTGACATATG
TTCATTTTATGCATATTTAAGAAATTATAGCTGCATATCCCTTCTTTCAAAAAATGTTGCTTTT
TTTTTTAAAGGAATTTTAATATATTCCTTTAAAAGAAAGCAATTTAATCAATTGCAAAGCAATT
ATATAAAACCACAAAGAATGTACTGAACCTACTAACCCTTTAACATACAGTTTAGGGTCCTAGC
GCAGAGTCCTTGTTTAAAGGTCATTGACTCATCATCTGTCAGTAATGAGAGGATTGGAAGAATA
ATTTTGCATACAAATGAGGACTTAATTTGTTGAAATATAATCTCTTTAAGTTCCTTGAAAATGG
AGTTGGTTTTTTTTGTTTCTAAATGCTATCTGCTTTTAACTAGTAGTTGCCTACATCTGGGGAC
TTCAGAGAAGAATTATATTTTGTTAGTTAAGTAGACACAGTGGTTATGGAAGCATTTCTTTACA
GTACCCTTTACATGTTTGGTTTCTGAACTTAAAATTGCCCTCATACTTAATAATATGGTCTGCA
TTTAATATGAAAGGTGTTTTATTGATAAATCTATTGTACTATTTGGATACATTTGTGTATTCCT
TGCAGCCAACCTGTATTCGTGGGATTGGTGTAGGGTTAAATCATCAACATTATTTCATAAAATA
AGAATTTGTTCTGTGTTATCTAAAGATGTATCAGTATATTGTCACAGTTGTGCTGTTAACTAAA
AATGCTGAGACCCCTTTTTATAGAAAAACAAAAAGACATCAAGTCTTCTTAATTCAACCCATAA
TCATTAAGTACTTAACAAAGAATATTTTACAAGTGATAGTATTTCAACAATGTGTAATTAATAT
TTTTGATACAGTGATTTCATATTGGAATCATTATTTGTGCAAAGGGACAGACAGATCACTTAGA
TTGCTATACTAGTGGACATAGGCTACATGTTTGCACATTCACATTCTTATCACGTGTAGAATAC
TTCACAAAATAGTCAACATCTAAGGCCCTAATTTATGTTTTGAAAGATCATGTGTTCCCAAAGT
ATTCCCTATTGTTGGCTCCACAGCCTTAAAGTGCTATAGATTTAAATTCATTGATTAGTTTTAA
TTTTTAATTTTAGACTGTGTATTTCCATAAATACCCTACGTACTGGCATATTTGAAACTCTTTT
TCCAGGTTAGGTCCTTTTCTTTCTCATTGAATCATCTTAAATAGTTCTTGGCCCTGAATTTAGC
TGATTTAAAATTCTTAATATTCAAGAATTTATACTTATTTTTTCCTTAAAAGCCACAGGGGACA
GTTAAATATCTTAAAATATCTAAAACATTTTTTAAAGCACTTAGATTGTCTTACGTATGTGCAT
ACTATACCTTTACAGCGTTTATTGTCTTGTCTCTTGTCAGTAGACCTTCAGTACACAGTATGTG
GGATATGTCAGTCAAGTTGGTCAGCACCAGCATCTGTCCAGCTGTTCAGTATATTGTGATTCAT
TAAAAAATCTCTTCTATCCCAGACATGGGCCAAGGTGCTGTATCTGAGGGATGTGCTGTAATTT
GATTTACATGCATTAGAGCACACAGTAGAAAAACTTTAGCTTCATTAGTAATATGACACATGTA
TATAGTGAGATGTCTTTATTGTGTGCTTTGCATATTTTGTAAATATTTTGCACGTCATTATTTT
TCTTTTTTGTTTAAGCAGTGTTTGGCCTGGAAGAGTGATATGCTTGCTGCTTAATCAAAGGATT
AAAGATTTAAAGATGTCTATGTCTTCTATTTTTATATAATTTCATGTTCTATGAGGAATTTAGT
ACCTCTTCACTGTGAAATTCGAAATAATGATTTTTATAAAAGCAAAACTAGAAATCTTTTAATG
ACAATTTTCATTAATTTCAGGGTTATCATTTTTGAGAAATCTACACCAAAGTGGTTTTTTAAAA
TTACATAACTAAAAATAAACCACACTGTGGATACATCTTATAAAACTAATGGAAACAATGTTTT
TCTATATGATTTAATTCTAGTGTAATATGGATGAGGTAAGAGTAAGTTATGATCAAACTTTTTA
TGTTCTTAATAAGCTTGCAATTGAGTAAAATAGAATATAAAATAAAGGTGAAATAATATAAAA

hide sequence

RefSeq Acc Id:

NR_146434

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	211,259,366 - 211,313,298 (+)	NCBI
T2T-CHM13v2.0	1	210,504,931 - 210,558,899 (+)	NCBI

Sequence:

show sequence

GTTGTTGTGAGGCGACTGCGCTACTGCCGGAGCGGGGCGGTTATGGCGGCTCCATATTAACAGC
CTCCTCCTCCTCCGCCGCCGCCGCCGTCTCCTCCTCCTCCTCCTTTCCCTCCCGCCCGCGCTCT
AAGCCATCTCCGCCTTCACCCTGACGCCTGCCTCTTCCCCTCACCTTTCCCCCTCCCCTGTTCT
ACCATGCCCGGCATGATGGAGAAAGGGCCCGAGTTACTGGGGAAGAACCGATCGGCCAACGGCA
GCGCCAAGAGCCCGGCAGGCGGCGGCGGCAGCGGCGCCTCGTCCACCAACGGCGGGCTGCACTA
CTCAGAGCCCGAGAGCGGCTGCAGCAGCGACGACGAGCACGATGTTGGGATGAGAGTCGGAGCC
GAATACCAAGCTCGGATCCCTGAATTTGATCCAGGTGCTACAAAGTACACAGATAAAGACAATG
GAGGGATGCTTGTATGGTCTCCATATCACAGTATCCCAGATGCCAAATTGGATGAATACATTGC
AATTGCAAAGGAAAAGCATGGCTACAATGTGGAACAGGCACTTGGCATGTTGTTCTGGCATAAA
CATAACATTGAGAAGTCCCTTGCTGATCTCCCTAATTTCACTCCCTTTCCGGATGAGTGGACAG
TGGAAGATAAAGTCCTATTTGAACAAGCCTTTAGTTTTCATGGAAAGAGCTTTCACAGGATTCA
GCAAATGCTTCCAGATAAGACAATTGCAAGCCTTGTAAAATATTACTATTCTTGGAAAAAAACT
CGCTCTAGGACAAGTTTGATGGATCGCCAGGCTCGTAAACTAGCTAATAGACATAATCAGGGTG
ACAGTGATGATGATGTAGAAGAAACACATCCAATGGATGGGAATGATAGTGATTATGATCCCAA
AAAAGAAGCCAAAAAAGAGGGTAATACTGAACAACCTGTCCAAACTAGCAAGATTGGACTTGGA
AGAAGAGAGTATCAGAGTTTACAACATCGCCATCATTCTCAGCGTTCTAAGTGCCGTCCACCTA
AGGGCATGTATTTAACCCAGGAAGATGTGGTAGCAGTTTCCTGTAGTCCCAATGCAGCCAACAC
CATCCTGAGGCAACTGGACATGGAGTTGATCTCTCTAAAACGTCAGGTTCAGAATGCTAAGCAA
GTAAACAGTGCACTTAAACAGAAAATGGAAGGTGGAATTGAAGAATTCAAACCTCCTGAGTCAA
ATCAGAAAATTAATGCCCGTTGGACCACAGAGGAGCAGCTTCTAGCAGTGCAAGGTGACTGGCT
ACTAGGGAAATAAATGAATGTGGAATTGAGGATGGAACAAAGAATTCAATGCTTTACAATAAAT
GGACTGTATTTGAGAGTTCAAGAGAGGATTGGAGAAAATAACTGAGTATGTAAAAAATGGTGTC
CGCAAATATGGTAAAGATTTTCAAGCTATTGCAGATGTAATTGGCAACAAGACTGTTGGCCAAG
TGAAGAACTTCTTTGTAAACTACAGGCGTCGGTTTAACTTAGAGGAGGTATTGCAGGAGTGGGA
AGCAGAACAAGGAACCCAGGCTTCTAATGGTGATGCTTCTACTTTAGGGGAGGAGACAAAAAGT
GCTTCTAATGTGCCATCAGGGAAGAGCACTGATGAAGAAGAGGAGGTGTGTTTGTGTATGGAAT
TTGAGCTAATATGAGTTGAGGAATCACCATTTTGTGTGGTATTCTGTAAGGTTAATTTGTCAAG
AGGACTAGCTAAATTGAGCATGAAAGGTTGACAATACACTTCTTCAGTGGTGCATCTCTCGTGA
CTCTTAAGTCATAATGACATGCTAAGTTCTGATTCTAGAAGAATGGAGAGTGTATTGTTCTTTC
ATAGTCTTATTTTTATTTTCAGTGTTAAGCTGTTTACAAATAAAGATGCCTGTTTGGTAGCCTC
ATTGGTTTTTGGTTTTTGGTTTTGTTTTGTTTAAAATAAAAGAAGCTTGTGCTTCCAATAAA

hide sequence

RefSeq Acc Id:

XM_005273191 ⟹ XP_005273248

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	211,259,366 - 211,316,385 (+)	NCBI
GRCh37	1	211,432,708 - 211,489,727 (+)	NCBI

Sequence:

show sequence

GCTACTGCCGGAGCGGGGCGGTTATGGCGGCTCCATATTAACAGCCTCCTCCTCCTCCGCCGCC
GCCGCCGTCTCCTCCTCCTCCTCCTTTCCCTCCCGCCCGCGCTCTAAGCCATCTCCGCCTTCAC
CCTGACGCCTGCCTCTTCCCCTCACCTTTCCCCCTCCCCTGTTCTACCATGCCCGGCATGATGG
AGAAAGGGCCCGAGTTACTGGGGAAGAACCGATCGGCCAACGGCAGCGCCAAGAGCCCGGCAGG
CGGCGGCGGCAGCGGCGCCTCGTCCACCAACGGCGGGCTGCACTACTCAGAGCCCGAGAGCGGC
TGCAGCAGCGACGACGAGCACGGTGATGTTGGGATGAGAGTCGGAGCCGAATACCAAGCTCGGA
TCCCTGAATTTGATCCAGGTGCTACAAAGTACACAGATAAAGACAATGGAGGGATGCTTGTATG
GTCTCCATATCACAGTATCCCAGATGCCAAATTGGATGAATACATTGCAATTGCAAAGGAAAAG
CATGGCTACAATGTGGAACAGGCACTTGGCATGTTGTTCTGGCATAAACATAACATTGAGAAGT
CCCTTGCTGATCTCCCTAATTTCACTCCCTTTCCGGATGAGTGGACAGTGGAAGATAAAGTCCT
ATTTGAACAAGCCTTTAGTTTTCATGGAAAGAGCTTTCACAGGATTCAGCAAATGCTTCCAGAT
AAGACAATTGCAAGCCTTGTAAAATATTACTATTCTTGGAAAAAAACTCGCTCTAGGACAAGTT
TGATGGATCGCCAGGCTCGTAAACTAGCTAATAGACATAATCAGGGTGACAGTGATGATGATGT
AGAAGAAACACATCCAATGGATGGGAATGATAGTGATTATGATCCCAAAAAAGAAGCCAAAAAA
GAGGGTAATACTGAACAACCTGTCCAAACTAGCAAGATTGGACTTGGAAGAAGAGAGTATCAGA
GTTTACAACATCGCCATCATTCTCAGCGTTCTAAGTGCCGTCCACCTAAGGGCATGTATTTAAC
CCAGGAAGATGTGGTAGCAGTTTCCTGTAGTCCCAATGCAGCCAACACCATCCTGAGGCAACTG
GACATGGAGTTGATCTCTCTAAAACGTCAGGTTCAGAATGCTAAGCAAGTAAACAGTGCACTTA
AACAGAAAATGGAAGGTGGAATTGAAGAATTCAAACCTCCTGAGTCAAATCAGAAAATTAATGC
CCGTTGGACCACAGAGGAGCAGCTTCTAGCAGTGCAAGGTGTCCGCAAATATGGTAAAGATTTT
CAAGCTATTGCAGATGTAATTGGCAACAAGACTGTTGGCCAAGTGAAGAACTTCTTTGTAAACT
ACAGGCGTCGGTTTAACTTAGAGGAGGTATTGCAGGAGTGGGAAGCAGAACAAGGAACCCAGGC
TTCTAATGGTGATGCTTCTACTTTAGGGGAGGAGACAAAAAGTGCTTCTAATGTGCCATCAGGG
AAGAGCACTGATGAAGAAGAGGAGGCACAGACCCCACAGGCTCCTCGGACACTGGGTCCATCAC
CTCCTGCCCCATCATCCACTCCAACACCAACAGCCCCTATTGCCACTCTGAACCAGCCTCCACC
ACTTCTTCGTCCAACACTGCCTGCTGCCCCGGCTCTTCACCGGCAGCCTCCTCCACTCCAGCAG
CAGGCTCGGTTCATCCAGCCCCGGCCAACTTTAAATCAGCCTCCACCACCTCTTATTCGCCCTG
CTAATTCCATGCCACCCCGTCTAAACCCAAGACCGGTGTTGTCCACGGTTGGTGGTCAACAGCC
ACCATCACTTATTGGAATTCAGACAGATTCACAGTCCTCACTGCACTAAAAATTAAATTGGACA
CAGCTGCAGTAACTTTTCACCCCATCATTATACCAGTGCTCATCTGACTGATGAAAAAGAGGAA
AGAATAATCATTTCTAGATACTGAGGCTGCGAACTAGTTCTGTGGCAGTGGACTAGCATAAGTG
GATGTCTAAGAAATTTTTCAGTTCACTAGACTAAAATGTTTTACAACAAAAAGCCTCCAGTTAG
CCTCCTTTCTAGAGTATATGTTCAGCAATGTTGATCTCATAAAAGGAAAAACAAAAGATTTAAG
TATTCTATATACCAAGTTTTTGTTTTGTTTTTACTGTATTTATTTTATTGAGGTTCTTTATATT
CCTGCCTCTTCATAGTCAAGGCTCTTAGTACAGGAATATTGACTTAGGAATTGTGAAAACTCCT
TAAGTTTCTTAAGTTAAGGATGTTTGGCTTTTTTCTTTAATTTTTTAAAAACCATTTTCCTATG
TTAGGAGTGCAAGAATAGCCAGCATTTCCGATTTTGACATATGTTCATTTTATGCATATTTAAG
AAATTATAGCTGCATATCCCTTCTTTCAAAAAATGTTGCTTTTTTTTTTAAAGGAATTTTAATA
TATTCCTTTAAAAGAAAGCAATTTAATCAATTGCAAAGCAATTATATAAAACCACAAAGAATGT
ACTGAACCTACTAACCCTTTAACATACAGTTTAGGGTCCTAGCGCAGAGTCCTTGTTTAAAGGT
CATTGACTCATCATCTGTCAGTAATGAGAGGATTGGAAGAATAATTTTGCATACAAATGAGGAC
TTAATTTGTTGAAATATAATCTCTTTAAGTTCCTTGAAAATGGAGTTGGTTTTTTTTGTTTCTA
AATGCTATCTGCTTTTAACTAGTAGTTGCCTACATCTGGGGACTTCAGAGAAGAATTATATTTT
GTTAGTTAAGTAGACACAGTGGTTATGGAAGCATTTCTTTACAGTACCCTTTACATGTTTGGTT
TCTGAACTTAAAATTGCCCTCATACTTAATAATATGGTCTGCATTTAATATGAAAGGTGTTTTA
TTGATAAATCTATTGTACTATTTGGATACATTTGTGTATTCCTTGCAGCCAACCTGTATTCGTG
GGATTGGTGTAGGGTTAAATCATCAACATTATTTCATAAAATAAGAATTTGTTCTGTGTTATCT
AAAGATGTATCAGTATATTGTCACAGTTGTGCTGTTAACTAAAAATGCTGAGACCCCTTTTTAT
AGAAAAACAAAAAGACATCAAGTCTTCTTAATTCAACCCATAATCATTAAGTACTTAACAAAGA
ATATTTTACAAGTGATAGTATTTCAACAATGTGTAATTAATATTTTTGATACAGTGATTTCATA
TTGGAATCATTATTTGTGCAAAGGGACAGACAGATCACTTAGATTGCTATACTAGTGGACATAG
GCTACATGTTTGCACATTCACATTCTTATCACGTGTAGAATACTTCACAAAATAGTCAACATCT
AAGGCCCTAATTTATGTTTTGAAAGATCATGTGTTCCCAAAGTATTCCCTATTGTTGGCTCCAC
AGCCTTAAAGTGCTATAGATTTAAATTCATTGATTAGTTTTAATTTTTAATTTTAGACTGTGTA
TTTCCATAAATACCCTACGTACTGGCATATTTGAAACTCTTTTTCCAGGTTAGGTCCTTTTCTT
TCTCATTGAATCATCTTAAATAGTTCTTGGCCCTGAATTTAGCTGATTTAAAATTCTTAATATT
CAAGAATTTATACTTATTTTTTCCTTAAAAGCCACAGGGGACAGTTAAATATCTTAAAATATCT
AAAACATTTTTTAAAGCACTTAGATTGTCTTACGTATGTGCATACTATACCTTTACAGCGTTTA
TTGTCTTGTCTCTTGTCAGTAGACCTTCAGTACACAGTATGTGGGATATGTCAGTCAAGTTGGT
CAGCACCAGCATCTGTCCAGCTGTTCAGTATATTGTGATTCATTAAAAAATCTCTTCTATCCCA
GACATGGGCCAAGGTGCTGTATCTGAGGGATGTGCTGTAATTTGATTTACATGCATTAGAGCAC
ACAGTAGAAAAACTTTAGCTTCATTAGTAATATGACACATGTATATAGTGAGATGTCTTTATTG
TGTGCTTTGCATATTTTGTAAATATTTTGCACGTCATTATTTTTCTTTTTTGTTTAAGCAGTGT
TTGGCCTGGAAGAGTGATATGCTTGCTGCTTAATCAAAGGATTAAAGATTTAAAGATGTCTATG
TCTTCTATTTTTATATAATTTCATGTTCTATGAGGAATTTAGTACCTCTTCACTGTGAAATTCG
AAATAATGATTTTTATAAAAGCAAAACTAGAAATC

hide sequence

RefSeq Acc Id:

XM_006711442 ⟹ XP_006711505

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	211,259,366 - 211,316,385 (+)	NCBI

Sequence:

show sequence

GCTACTGCCGGAGCGGGGCGGTTATGGCGGCTCCATATTAACAGCCTCCTCCTCCTCCGCCGCC
GCCGCCGTCTCCTCCTCCTCCTCCTTTCCCTCCCGCCCGCGCTCTAAGCCATCTCCGCCTTCAC
CCTGACGCCTGCCTCTTCCCCTCACCTTTCCCCCTCCCCTGTTCTACCATGCCCGGCATGATGG
AGAAAGGGCCCGAGTTACTGGGGAAGAACCGATCGGCCAACGGCAGCGCCAAGAGCCCGGCAGG
CGGCGGCGGCAGCGGCGCCTCGTCCACCAACGGCGGGCTGCACTACTCAGAGCCCGAGAGCGGC
TGCAGCAGCGACGACGAGCACGGTGATGTTGGGATGAGAGTCGGAGCCGAATACCAAGCTCGGA
TCCCTGAATTTGATCCAGGTGCTACAAAGTACACAGATAAAGACAATGGAGGGATGCTTGTATG
GTCTCCATATCACAGTATCCCAGATGCCAAATTGGATGAATACATTGCAATTGCAAAGGAAAAG
CATGGCTACAATGTGGAACAGGCACTTGGCATGTTGTTCTGGCATAAACATAACATTGAGAAGT
CCCTTGCTGATCTCCCTAATTTCACTCCCTTTCCGGATGAGTGGACAGTGGAAGATAAAGTCCT
ATTTGAACAAGCCTTTAGTTTTCATGGAAAGAGCTTTCACAGGATTCAGCAAATGCTTCCAGAT
AAGACAATTGCAAGCCTTGTAAAATATTACTATTCTTGGAAAAAAACTCGCTCTAGGACAAGTT
TGATGGATCGCCAGGCTCGTAAACTAGCTAATAGACATAATCAGGGTGACAGTGATGATGATGT
AGAAGAAACACATCCAATGGATGGGAATGATAGTGATTATGATCCCAAAAAAGAAGCCAAAAAA
GAGGGTAATACTGAACAACCTGTCCAAACTAGCAAGATTGGACTTGGAAGAAGAGAGTATCAGA
GTTTACAACATCGCCATCATTCTCAGCGTTCTAAGTGCCGTCCACCTAAGGGCATGTATTTAAC
CCAGGAAGATGTGGTAGCAGTTTCCTGTAGTCCCAATGCAGCCAACACCATCCTGAGGCAACTG
GACATGGAGTTGATCTCTCTAAAACGTCAGGTTCAGAATGCTAAGCAAGTAAACAGTGCACTTA
AACAGAAAATGGAAGGTGGAATTGAAGAATTCAAACCTCCTGAGTCAAATCAGAAAATTAATGC
CCGTTGGACCACAGAGGAGCAGCTTCTAGCAGTGCAAGGCACAGACCCCACAGGCTCCTCGGAC
ACTGGGTCCATCACCTCCTGCCCCATCATCCACTCCAACACCAACAGCCCCTATTGCCACTCTG
AACCAGCCTCCACCACTTCTTCGTCCAACACTGCCTGCTGCCCCGGCTCTTCACCGGCAGCCTC
CTCCACTCCAGCAGCAGGCTCGGTTCATCCAGCCCCGGCCAACTTTAAATCAGCCTCCACCACC
TCTTATTCGCCCTGCTAATTCCATGCCACCCCGTCTAAACCCAAGACCGGTGTTGTCCACGGTT
GGTGGTCAACAGCCACCATCACTTATTGGAATTCAGACAGATTCACAGTCCTCACTGCACTAAA
AATTAAATTGGACACAGCTGCAGTAACTTTTCACCCCATCATTATACCAGTGCTCATCTGACTG
ATGAAAAAGAGGAAAGAATAATCATTTCTAGATACTGAGGCTGCGAACTAGTTCTGTGGCAGTG
GACTAGCATAAGTGGATGTCTAAGAAATTTTTCAGTTCACTAGACTAAAATGTTTTACAACAAA
AAGCCTCCAGTTAGCCTCCTTTCTAGAGTATATGTTCAGCAATGTTGATCTCATAAAAGGAAAA
ACAAAAGATTTAAGTATTCTATATACCAAGTTTTTGTTTTGTTTTTACTGTATTTATTTTATTG
AGGTTCTTTATATTCCTGCCTCTTCATAGTCAAGGCTCTTAGTACAGGAATATTGACTTAGGAA
TTGTGAAAACTCCTTAAGTTTCTTAAGTTAAGGATGTTTGGCTTTTTTCTTTAATTTTTTAAAA
ACCATTTTCCTATGTTAGGAGTGCAAGAATAGCCAGCATTTCCGATTTTGACATATGTTCATTT
TATGCATATTTAAGAAATTATAGCTGCATATCCCTTCTTTCAAAAAATGTTGCTTTTTTTTTTA
AAGGAATTTTAATATATTCCTTTAAAAGAAAGCAATTTAATCAATTGCAAAGCAATTATATAAA
ACCACAAAGAATGTACTGAACCTACTAACCCTTTAACATACAGTTTAGGGTCCTAGCGCAGAGT
CCTTGTTTAAAGGTCATTGACTCATCATCTGTCAGTAATGAGAGGATTGGAAGAATAATTTTGC
ATACAAATGAGGACTTAATTTGTTGAAATATAATCTCTTTAAGTTCCTTGAAAATGGAGTTGGT
TTTTTTTGTTTCTAAATGCTATCTGCTTTTAACTAGTAGTTGCCTACATCTGGGGACTTCAGAG
AAGAATTATATTTTGTTAGTTAAGTAGACACAGTGGTTATGGAAGCATTTCTTTACAGTACCCT
TTACATGTTTGGTTTCTGAACTTAAAATTGCCCTCATACTTAATAATATGGTCTGCATTTAATA
TGAAAGGTGTTTTATTGATAAATCTATTGTACTATTTGGATACATTTGTGTATTCCTTGCAGCC
AACCTGTATTCGTGGGATTGGTGTAGGGTTAAATCATCAACATTATTTCATAAAATAAGAATTT
GTTCTGTGTTATCTAAAGATGTATCAGTATATTGTCACAGTTGTGCTGTTAACTAAAAATGCTG
AGACCCCTTTTTATAGAAAAACAAAAAGACATCAAGTCTTCTTAATTCAACCCATAATCATTAA
GTACTTAACAAAGAATATTTTACAAGTGATAGTATTTCAACAATGTGTAATTAATATTTTTGAT
ACAGTGATTTCATATTGGAATCATTATTTGTGCAAAGGGACAGACAGATCACTTAGATTGCTAT
ACTAGTGGACATAGGCTACATGTTTGCACATTCACATTCTTATCACGTGTAGAATACTTCACAA
AATAGTCAACATCTAAGGCCCTAATTTATGTTTTGAAAGATCATGTGTTCCCAAAGTATTCCCT
ATTGTTGGCTCCACAGCCTTAAAGTGCTATAGATTTAAATTCATTGATTAGTTTTAATTTTTAA
TTTTAGACTGTGTATTTCCATAAATACCCTACGTACTGGCATATTTGAAACTCTTTTTCCAGGT
TAGGTCCTTTTCTTTCTCATTGAATCATCTTAAATAGTTCTTGGCCCTGAATTTAGCTGATTTA
AAATTCTTAATATTCAAGAATTTATACTTATTTTTTCCTTAAAAGCCACAGGGGACAGTTAAAT
ATCTTAAAATATCTAAAACATTTTTTAAAGCACTTAGATTGTCTTACGTATGTGCATACTATAC
CTTTACAGCGTTTATTGTCTTGTCTCTTGTCAGTAGACCTTCAGTACACAGTATGTGGGATATG
TCAGTCAAGTTGGTCAGCACCAGCATCTGTCCAGCTGTTCAGTATATTGTGATTCATTAAAAAA
TCTCTTCTATCCCAGACATGGGCCAAGGTGCTGTATCTGAGGGATGTGCTGTAATTTGATTTAC
ATGCATTAGAGCACACAGTAGAAAAACTTTAGCTTCATTAGTAATATGACACATGTATATAGTG
AGATGTCTTTATTGTGTGCTTTGCATATTTTGTAAATATTTTGCACGTCATTATTTTTCTTTTT
TGTTTAAGCAGTGTTTGGCCTGGAAGAGTGATATGCTTGCTGCTTAATCAAAGGATTAAAGATT
TAAAGATGTCTATGTC

hide sequence

RefSeq Acc Id:

XM_011509748 ⟹ XP_011508050

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	211,259,366 - 211,316,385 (+)	NCBI

Sequence:

show sequence

GCTACTGCCGGAGCGGGGCGGTTATGGCGGCTCCATATTAACAGCCTCCTCCTCCTCCGCCGCC
GCCGCCGTCTCCTCCTCCTCCTCCTTTCCCTCCCGCCCGCGCTCTAAGCCATCTCCGCCTTCAC
CCTGACGCCTGCCTCTTCCCCTCACCTTTCCCCCTCCCCTGTTCTACCATGCCCGGCATGATGG
AGAAAGGGCCCGAGTTACTGGGGAAGAACCGATCGGCCAACGGCAGCGCCAAGAGCCCGGCAGG
CGGCGGCGGCAGCGGCGCCTCGTCCACCAACGGCGGGCTGCACTACTCAGAGCCCGAGAGCGGC
TGCAGCAGCGACGACGAGCACGGTGATGTTGGGATGAGAGTCGGAGCCGAATACCAAGCTCGGA
TCCCTGAATTTGATCCAGGTGCTACAAAGTACACAGATAAAGACAATGGAGGGATGCTTGTATG
GTCTCCATATCACAGTATCCCAGATGCCAAATTGGATGAATACATTGCAATTGCAAAGGAAAAG
CATGGCTACAATGTGGAACAGGCACTTGGCATGTTGTTCTGGCATAAACATAACATTGAGAAGT
CCCTTGCTGATCTCCCTAATTTCACTCCCTTTCCGGATGAGTGGACAGTGGAAGATAAAGTCCT
ATTTGAACAAGCCTTTAGTTTTCATGGAAAGAGCTTTCACAGGATTCAGCAAATGCTTCCAGAT
AAGACAATTGCAAGCCTTGTAAAATATTACTATTCTTGGAAAAAAACTCGCTCTAGGACAAGTT
TGATGGATCGCCAGGCTCGTAAACTAGCTAATAGACATAATCAGGGTGACAGTGATGATGATGT
AGAAGAAACACATCCAATGGATGGGAATGATAGTGATTATGATCCCAAAAAAGAAGCCAAAAAA
GAGGGTAATACTGAACAACCTGTCCAAACTAGCAAGATTGGACTTGGAAGAAGAGAGTATCAGA
GTTTACAACATCGCCATCATTCTCAGCGTTCTAAGTGCCGTCCACCTAAGGGCATGTATTTAAC
CCAGGAAGATGTGGTAGCAGTTTCCTGTAGTCCCAATGCAGCCAACACCATCCTGAGGCAACTG
GACATGGAGTTGATCTCTCTAAAACGTCAGTCAAATCAGAAAATTAATGCCCGTTGGACCACAG
AGGAGCAGCTTCTAGCAGTGCAAGGTGTCCGCAAATATGGTAAAGATTTTCAAGCTATTGCAGA
TGTAATTGGCAACAAGACTGTTGGCCAAGTGAAGAACTTCTTTGTAAACTACAGGCGTCGGTTT
AACTTAGAGGAGGTATTGCAGGAGTGGGAAGCAGAACAAGGAACCCAGGCTTCTAATGGTGATG
CTTCTACTTTAGGGGAGGAGACAAAAAGTGCTTCTAATGTGCCATCAGGGAAGAGCACTGATGA
AGAAGAGGAGGCACAGACCCCACAGGCTCCTCGGACACTGGGTCCATCACCTCCTGCCCCATCA
TCCACTCCAACACCAACAGCCCCTATTGCCACTCTGAACCAGCCTCCACCACTTCTTCGTCCAA
CACTGCCTGCTGCCCCGGCTCTTCACCGGCAGCCTCCTCCACTCCAGCAGCAGGCTCGGTTCAT
CCAGCCCCGGCCAACTTTAAATCAGCCTCCACCACCTCTTATTCGCCCTGCTAATTCCATGCCA
CCCCGTCTAAACCCAAGACCGGTGTTGTCCACGGTTGGTGGTCAACAGCCACCATCACTTATTG
GAATTCAGACAGATTCACAGTCCTCACTGCACTAAAAATTAAATTGGACACAGCTGCAGTAACT
TTTCACCCCATCATTATACCAGTGCTCATCTGACTGATGAAAAAGAGGAAAGAATAATCATTTC
TAGATACTGAGGCTGCGAACTAGTTCTGTGGCAGTGGACTAGCATAAGTGGATGTCTAAGAAAT
TTTTCAGTTCACTAGACTAAAATGTTTTACAACAAAAAGCCTCCAGTTAGCCTCCTTTCTAGAG
TATATGTTCAGCAATGTTGATCTCATAAAAGGAAAAACAAAAGATTTAAGTATTCTATATACCA
AGTTTTTGTTTTGTTTTTACTGTATTTATTTTATTGAGGTTCTTTATATTCCTGCCTCTTCATA
GTCAAGGCTCTTAGTACAGGAATATTGACTTAGGAATTGTGAAAACTCCTTAAGTTTCTTAAGT
TAAGGATGTTTGGCTTTTTTCTTTAATTTTTTAAAAACCATTTTCCTATGTTAGGAGTGCAAGA
ATAGCCAGCATTTCCGATTTTGACATATGTTCATTTTATGCATATTTAAGAAATTATAGCTGCA
TATCCCTTCTTTCAAAAAATGTTGCTTTTTTTTTTAAAGGAATTTTAATATATTCCTTTAAAAG
AAAGCAATTTAATCAATTGCAAAGCAATTATATAAAACCACAAAGAATGTACTGAACCTACTAA
CCCTTTAACATACAGTTTAGGGTCCTAGCGCAGAGTCCTTGTTTAAAGGTCATTGACTCATCAT
CTGTCAGTAATGAGAGGATTGGAAGAATAATTTTGCATACAAATGAGGACTTAATTTGTTGAAA
TATAATCTCTTTAAGTTCCTTGAAAATGGAGTTGGTTTTTTTTGTTTCTAAATGCTATCTGCTT
TTAACTAGTAGTTGCCTACATCTGGGGACTTCAGAGAAGAATTATATTTTGTTAGTTAAGTAGA
CACAGTGGTTATGGAAGCATTTCTTTACAGTACCCTTTACATGTTTGGTTTCTGAACTTAAAAT
TGCCCTCATACTTAATAATATGGTCTGCATTTAATATGAAAGGTGTTTTATTGATAAATCTATT
GTACTATTTGGATACATTTGTGTATTCCTTGCAGCCAACCTGTATTCGTGGGATTGGTGTAGGG
TTAAATCATCAACATTATTTCATAAAATAAGAATTTGTTCTGTGTTATCTAAAGATGTATCAGT
ATATTGTCACAGTTGTGCTGTTAACTAAAAATGCTGAGACCCCTTTTTATAGAAAAACAAAAAG
ACATCAAGTCTTCTTAATTCAACCCATAATCATTAAGTACTTAACAAAGAATATTTTACAAGTG
ATAGTATTTCAACAATGTGTAATTAATATTTTTGATACAGTGATTTCATATTGGAATCATTATT
TGTGCAAAGGGACAGACAGATCACTTAGATTGCTATACTAGTGGACATAGGCTACATGTTTGCA
CATTCACATTCTTATCACGTGTAGAATACTTCACAAAATAGTCAACATCTAAGGCCCTAATTTA
TGTTTTGAAAGATCATGTGTTCCCAAAGTATTCCCTATTGTTGGCTCCACAGCCTTAAAGTGCT
ATAGATTTAAATTCATTGATTAGTTTTAATTTTTAATTTTAGACTGTGTATTTCCATAAATACC
CTACGTACTGGCATATTTGAAACTCTTTTTCCAGGTTAGGTCCTTTTCTTTCTCATTGAATCAT
CTTAAATAGTTCTTGGCCCTGAATTTAGCTGATTTAAAATTCTTAATATTCAAGAATTTATACT
TATTTTTTCCTTAAAAGCCACAGGGGACAGTTAAATATCTTAAAATATCTAAAACATTTTTTAA
AGCACTTAGATTGTCTTACGTATGTGCATACTATACCTTTACAGCGTTTATTGTCTTGTCTCTT
GTCAGTAGACCTTCAGTACACAGTATGTGGGATATGTCAGTCAAGTTGGTCAGCACCAGCATCT
GTCCAGCTGTTCAGTATATTGTGATTCATTAAAAAATCTCTTCTATCCCAGACATGGGCCAAGG
TGCTGTATCTGAGGGATGTGCTGTAATTTGATTTACATGCATTAGAGCACACAGTAGAAAAACT
TTAGCTTCATTAGTAATATGACACATGTATATAGTGAGATGTCTTTATTGTGTGCTTTGCATAT
TTTGTAAATATTTTGCACGTCATTATTTTTCTTTTTTGTTTAAGCAGTGTTTGGCCTGGAAGAG
TGATATGCTTGCTGCTTAATCAAAGGATTAAAGATTTAAAGATGTCTATGTC

hide sequence

RefSeq Acc Id:

XM_017001761 ⟹ XP_016857250

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	211,259,366 - 211,316,385 (+)	NCBI

Sequence:

show sequence

GCTACTGCCGGAGCGGGGCGGTTATGGCGGCTCCATATTAACAGCCTCCTCCTCCTCCGCCGCC
GCCGCCGTCTCCTCCTCCTCCTCCTTTCCCTCCCGCCCGCGCTCTAAGCCATCTCCGCCTTCAC
CCTGACGCCTGCCTCTTCCCCTCACCTTTCCCCCTCCCCTGTTCTACCATGCCCGGCATGATGG
AGAAAGGGCCCGAGTTACTGGGGAAGAACCGATCGGCCAACGGCAGCGCCAAGAGCCCGGCAGG
CGGCGGCGGCAGCGGCGCCTCGTCCACCAACGGCGGGCTGCACTACTCAGAGCCCGAGAGCGGC
TGCAGCAGCGACGACGAGCACGATGTTGGGATGAGAGTCGGAGCCGAATACCAAGCTCGGATCC
CTGAATTTGATCCAGGTGCTACAAAGTACACAGATAAAGACAATGGAGGGATGCTTGTATGGTC
TCCATATCACAGTATCCCAGATGCCAAATTGGATGAATACATTGCAATTGCAAAGGAAAAGCAT
GGCTACAATGTGGAACAGGCACTTGGCATGTTGTTCTGGCATAAACATAACATTGAGAAGTCCC
TTGCTGATCTCCCTAATTTCACTCCCTTTCCGGATGAGTGGACAGTGGAAGATAAAGTCCTATT
TGAACAAGCCTTTAGTTTTCATGGAAAGAGCTTTCACAGGATTCAGCAAATGCTTCCAGATAAG
ACAATTGCAAGCCTTGTAAAATATTACTATTCTTGGAAAAAAACTCGCTCTAGGACAAGTTTGA
TGGATCGCCAGGCTCGTAAACTAGCTAATAGACATAATCAGGGTGACAGTGATGATGATGTAGA
AGAAACACATCCAATGGATGGGAATGATAGTGATTATGATCCCAAAAAAGAAGCCAAAAAAGAG
GGTAATACTGAACAACCTGTCCAAACTAGCAAGATTGGACTTGGAAGAAGAGAGTATCAGAGTT
TACAACATCGCCATCATTCTCAGCGTTCTAAGTGCCGTCCACCTAAGGGCATGTATTTAACCCA
GGAAGATGTGGTAGCAGTTTCCTGTAGTCCCAATGCAGCCAACACCATCCTGAGGCAACTGGAC
ATGGAGTTGATCTCTCTAAAACGTCAGTCAAATCAGAAAATTAATGCCCGTTGGACCACAGAGG
AGCAGCTTCTAGCAGTGCAAGGTGTCCGCAAATATGGTAAAGATTTTCAAGCTATTGCAGATGT
AATTGGCAACAAGACTGTTGGCCAAGTGAAGAACTTCTTTGTAAACTACAGGCGTCGGTTTAAC
TTAGAGGAGGTATTGCAGGAGTGGGAAGCAGAACAAGGAACCCAGGCTTCTAATGGTGATGCTT
CTACTTTAGGGGAGGAGACAAAAAGTGCTTCTAATGTGCCATCAGGGAAGAGCACTGATGAAGA
AGAGGAGGCACAGACCCCACAGGCTCCTCGGACACTGGGTCCATCACCTCCTGCCCCATCATCC
ACTCCAACACCAACAGCCCCTATTGCCACTCTGAACCAGCCTCCACCACTTCTTCGTCCAACAC
TGCCTGCTGCCCCGGCTCTTCACCGGCAGCCTCCTCCACTCCAGCAGCAGGCTCGGTTCATCCA
GCCCCGGCCAACTTTAAATCAGCCTCCACCACCTCTTATTCGCCCTGCTAATTCCATGCCACCC
CGTCTAAACCCAAGACCGGTGTTGTCCACGGTTGGTGGTCAACAGCCACCATCACTTATTGGAA
TTCAGACAGATTCACAGTCCTCACTGCACTAAAAATTAAATTGGACACAGCTGCAGTAACTTTT
CACCCCATCATTATACCAGTGCTCATCTGACTGATGAAAAAGAGGAAAGAATAATCATTTCTAG
ATACTGAGGCTGCGAACTAGTTCTGTGGCAGTGGACTAGCATAAGTGGATGTCTAAGAAATTTT
TCAGTTCACTAGACTAAAATGTTTTACAACAAAAAGCCTCCAGTTAGCCTCCTTTCTAGAGTAT
ATGTTCAGCAATGTTGATCTCATAAAAGGAAAAACAAAAGATTTAAGTATTCTATATACCAAGT
TTTTGTTTTGTTTTTACTGTATTTATTTTATTGAGGTTCTTTATATTCCTGCCTCTTCATAGTC
AAGGCTCTTAGTACAGGAATATTGACTTAGGAATTGTGAAAACTCCTTAAGTTTCTTAAGTTAA
GGATGTTTGGCTTTTTTCTTTAATTTTTTAAAAACCATTTTCCTATGTTAGGAGTGCAAGAATA
GCCAGCATTTCCGATTTTGACATATGTTCATTTTATGCATATTTAAGAAATTATAGCTGCATAT
CCCTTCTTTCAAAAAATGTTGCTTTTTTTTTTAAAGGAATTTTAATATATTCCTTTAAAAGAAA
GCAATTTAATCAATTGCAAAGCAATTATATAAAACCACAAAGAATGTACTGAACCTACTAACCC
TTTAACATACAGTTTAGGGTCCTAGCGCAGAGTCCTTGTTTAAAGGTCATTGACTCATCATCTG
TCAGTAATGAGAGGATTGGAAGAATAATTTTGCATACAAATGAGGACTTAATTTGTTGAAATAT
AATCTCTTTAAGTTCCTTGAAAATGGAGTTGGTTTTTTTTGTTTCTAAATGCTATCTGCTTTTA
ACTAGTAGTTGCCTACATCTGGGGACTTCAGAGAAGAATTATATTTTGTTAGTTAAGTAGACAC
AGTGGTTATGGAAGCATTTCTTTACAGTACCCTTTACATGTTTGGTTTCTGAACTTAAAATTGC
CCTCATACTTAATAATATGGTCTGCATTTAATATGAAAGGTGTTTTATTGATAAATCTATTGTA
CTATTTGGATACATTTGTGTATTCCTTGCAGCCAACCTGTATTCGTGGGATTGGTGTAGGGTTA
AATCATCAACATTATTTCATAAAATAAGAATTTGTTCTGTGTTATCTAAAGATGTATCAGTATA
TTGTCACAGTTGTGCTGTTAACTAAAAATGCTGAGACCCCTTTTTATAGAAAAACAAAAAGACA
TCAAGTCTTCTTAATTCAACCCATAATCATTAAGTACTTAACAAAGAATATTTTACAAGTGATA
GTATTTCAACAATGTGTAATTAATATTTTTGATACAGTGATTTCATATTGGAATCATTATTTGT
GCAAAGGGACAGACAGATCACTTAGATTGCTATACTAGTGGACATAGGCTACATGTTTGCACAT
TCACATTCTTATCACGTGTAGAATACTTCACAAAATAGTCAACATCTAAGGCCCTAATTTATGT
TTTGAAAGATCATGTGTTCCCAAAGTATTCCCTATTGTTGGCTCCACAGCCTTAAAGTGCTATA
GATTTAAATTCATTGATTAGTTTTAATTTTTAATTTTAGACTGTGTATTTCCATAAATACCCTA
CGTACTGGCATATTTGAAACTCTTTTTCCAGGTTAGGTCCTTTTCTTTCTCATTGAATCATCTT
AAATAGTTCTTGGCCCTGAATTTAGCTGATTTAAAATTCTTAATATTCAAGAATTTATACTTAT
TTTTTCCTTAAAAGCCACAGGGGACAGTTAAATATCTTAAAATATCTAAAACATTTTTTAAAGC
ACTTAGATTGTCTTACGTATGTGCATACTATACCTTTACAGCGTTTATTGTCTTGTCTCTTGTC
AGTAGACCTTCAGTACACAGTATGTGGGATATGTCAGTCAAGTTGGTCAGCACCAGCATCTGTC
CAGCTGTTCAGTATATTGTGATTCATTAAAAAATCTCTTCTATCCCAGACATGGGCCAAGGTGC
TGTATCTGAGGGATGTGCTGTAATTTGATTTACATGCATTAGAGCACACAGTAGAAAAACTTTA
GCTTCATTAGTAATATGACACATGTATATAGTGAGATGTCTTTATTGTGTGCTTTGCATATTTT
GTAAATATTTTGCACGTCATTATTTTTCTTTTTTGTTTAAGCAGTGTTTGGCCTGGAAGAGTGA
TATGCTTGCTGCTTAATCAAAGGATTAAAGATTTAAAGATGTCTATGTC

hide sequence

RefSeq Acc Id:

XM_047425011 ⟹ XP_047280967

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	211,271,228 - 211,316,385 (+)	NCBI

RefSeq Acc Id:

XM_047425021 ⟹ XP_047280977

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	211,259,366 - 211,316,385 (+)	NCBI

RefSeq Acc Id:

XM_047425032 ⟹ XP_047280988

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	211,259,366 - 211,316,385 (+)	NCBI

RefSeq Acc Id:

XM_047425038 ⟹ XP_047280994

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	211,259,366 - 211,294,585 (+)	NCBI

RefSeq Acc Id:

XM_047425043 ⟹ XP_047280999

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	211,259,366 - 211,313,298 (+)	NCBI

RefSeq Acc Id:

XM_047425046 ⟹ XP_047281002

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	211,259,366 - 211,316,385 (+)	NCBI

RefSeq Acc Id:

XM_047425051 ⟹ XP_047281007

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	211,267,780 - 211,316,385 (+)	NCBI

RefSeq Acc Id:

XM_047425052 ⟹ XP_047281008

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	211,259,366 - 211,295,731 (+)	NCBI

RefSeq Acc Id:

XM_047425053 ⟹ XP_047281009

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	211,259,366 - 211,295,731 (+)	NCBI

RefSeq Acc Id:

XM_054337618 ⟹ XP_054193593

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	1	210,504,931 - 210,561,986 (+)	NCBI

RefSeq Acc Id:

XM_054337619 ⟹ XP_054193594

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	1	210,504,931 - 210,561,986 (+)	NCBI

RefSeq Acc Id:

XM_054337620 ⟹ XP_054193595

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	1	210,504,931 - 210,561,986 (+)	NCBI

RefSeq Acc Id:

XM_054337621 ⟹ XP_054193596

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	1	210,504,931 - 210,561,986 (+)	NCBI

RefSeq Acc Id:

XM_054337622 ⟹ XP_054193597

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	1	210,516,803 - 210,561,986 (+)	NCBI

RefSeq Acc Id:

XM_054337623 ⟹ XP_054193598

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	1	210,504,931 - 210,561,986 (+)	NCBI

RefSeq Acc Id:

XM_054337624 ⟹ XP_054193599

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	1	210,504,931 - 210,561,986 (+)	NCBI

RefSeq Acc Id:

XM_054337625 ⟹ XP_054193600

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	1	210,504,931 - 210,540,170 (+)	NCBI

RefSeq Acc Id:

XM_054337626 ⟹ XP_054193601

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	1	210,504,931 - 210,558,899 (+)	NCBI

RefSeq Acc Id:

XM_054337627 ⟹ XP_054193602

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	1	210,504,931 - 210,561,986 (+)	NCBI

RefSeq Acc Id:

XM_054337628 ⟹ XP_054193603

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	1	210,513,362 - 210,561,986 (+)	NCBI

RefSeq Acc Id:

XM_054337629 ⟹ XP_054193604

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	1	210,504,931 - 210,541,319 (+)	NCBI

RefSeq Acc Id:

XM_054337630 ⟹ XP_054193605

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	1	210,504,931 - 210,541,319 (+)	NCBI

RefSeq Acc Id:

XR_007061955

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	211,259,366 - 211,313,298 (+)	NCBI

RefSeq Acc Id:

XR_007061956

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	211,259,366 - 211,313,298 (+)	NCBI

RefSeq Acc Id:

XR_007061957

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	211,259,366 - 211,312,399 (+)	NCBI

RefSeq Acc Id:

XR_007061958

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	211,259,366 - 211,313,298 (+)	NCBI

RefSeq Acc Id:

XR_008486104

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	1	210,504,931 - 210,558,899 (+)	NCBI

RefSeq Acc Id:

XR_008486105

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	1	210,504,931 - 210,558,899 (+)	NCBI

RefSeq Acc Id:

XR_008486106

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	1	210,504,931 - 210,558,000 (+)	NCBI

RefSeq Acc Id:

XR_008486107

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	1	210,504,931 - 210,558,899 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_001129695	(Get FASTA)	NCBI Sequence Viewer
	NP_001129696	(Get FASTA)	NCBI Sequence Viewer
	NP_001129697	(Get FASTA)	NCBI Sequence Viewer
	NP_001336998	(Get FASTA)	NCBI Sequence Viewer
	NP_001336999	(Get FASTA)	NCBI Sequence Viewer
	NP_060724	(Get FASTA)	NCBI Sequence Viewer
	XP_005273248	(Get FASTA)	NCBI Sequence Viewer
	XP_006711505	(Get FASTA)	NCBI Sequence Viewer
	XP_011508050	(Get FASTA)	NCBI Sequence Viewer
	XP_016857250	(Get FASTA)	NCBI Sequence Viewer
	XP_047280967	(Get FASTA)	NCBI Sequence Viewer
	XP_047280977	(Get FASTA)	NCBI Sequence Viewer
	XP_047280988	(Get FASTA)	NCBI Sequence Viewer
	XP_047280994	(Get FASTA)	NCBI Sequence Viewer
	XP_047280999	(Get FASTA)	NCBI Sequence Viewer
	XP_047281002	(Get FASTA)	NCBI Sequence Viewer
	XP_047281007	(Get FASTA)	NCBI Sequence Viewer
	XP_047281008	(Get FASTA)	NCBI Sequence Viewer
	XP_047281009	(Get FASTA)	NCBI Sequence Viewer
	XP_054193593	(Get FASTA)	NCBI Sequence Viewer
	XP_054193594	(Get FASTA)	NCBI Sequence Viewer
	XP_054193595	(Get FASTA)	NCBI Sequence Viewer
	XP_054193596	(Get FASTA)	NCBI Sequence Viewer
	XP_054193597	(Get FASTA)	NCBI Sequence Viewer
	XP_054193598	(Get FASTA)	NCBI Sequence Viewer
	XP_054193599	(Get FASTA)	NCBI Sequence Viewer
	XP_054193600	(Get FASTA)	NCBI Sequence Viewer
	XP_054193601	(Get FASTA)	NCBI Sequence Viewer
	XP_054193602	(Get FASTA)	NCBI Sequence Viewer
	XP_054193603	(Get FASTA)	NCBI Sequence Viewer
	XP_054193604	(Get FASTA)	NCBI Sequence Viewer
	XP_054193605	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH31608	(Get FASTA)	NCBI Sequence Viewer
	BAA91872	(Get FASTA)	NCBI Sequence Viewer
	BAA92581	(Get FASTA)	NCBI Sequence Viewer
	BAG54764	(Get FASTA)	NCBI Sequence Viewer
	BAG62571	(Get FASTA)	NCBI Sequence Viewer
	BAG63899	(Get FASTA)	NCBI Sequence Viewer
	EAW93423	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000355972
	ENSP00000355972.4
	ENSP00000355973
	ENSP00000355973.4
	ENSP00000398558
	ENSP00000398558.2
	ENSP00000413929
	ENSP00000413929.2
	ENSP00000432779
	ENSP00000432779.1
	ENSP00000433441.1
	ENSP00000434181.1
	ENSP00000434605.1
	ENSP00000436057.1
	ENSP00000436838.1
	ENSP00000437048.1
GenBank Protein	Q9P2K3	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_001129695 ⟸ NM_001136223
- Peptide Label:	isoform a
- UniProtKB:	Q9P2K3 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MPGMMEKGPELLGKNRSANGSAKSPAGGGGSGASSTNGGLHYSEPESGCSSDDEHDVGMRVGAE YQARIPEFDPGATKYTDKDNGGMLVWSPYHSIPDAKLDEYIAIAKEKHGYNVEQALGMLFWHKH NIEKSLADLPNFTPFPDEWTVEDKVLFEQAFSFHGKSFHRIQQMLPDKTIASLVKYYYSWKKTR SRTSLMDRQARKLANRHNQGDSDDDVEETHPMDGNDSDYDPKKEAKKEGNTEQPVQTSKIGLGR REYQSLQHRHHSQRSKCRPPKGMYLTQEDVVAVSCSPNAANTILRQLDMELISLKRQVQNAKQV NSALKQKMEGGIEEFKPPESNQKINARWTTEEQLLAVQGVRKYGKDFQAIADVIGNKTVGQVKN FFVNYRRRFNLEEVLQEWEAEQGTQASNGDASTLGEETKSASNVPSGKSTDEEEEAQTPQAPRT LGPSPPAPSSTPTPTAPIATLNQPPPLLRPTLPAAPALHRQPPPLQQQARFIQPRPTLNQPPPP LIRPANSMPPRLNPRPVLSTVGGQQPPSLIGIQTDSQSSLH hide sequence

RefSeq Acc Id:	NP_001129696 ⟸ NM_001136224
- Peptide Label:	isoform b
- UniProtKB:	Q9P2K3 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MPGMMEKGPELLGKNRSANGSAKSPAGGGGSGASSTNGGLHYSEPESGCSSDDEHDVGMRVGAE YQARIPEFDPGATKYTDKDNGGMLVWSPYHSIPDAKLDEYIAIAKEKHGYNVEQALGMLFWHKH NIEKSLADLPNFTPFPDEWTVEDKVLFEQAFSFHGKSFHRIQQMLPDKTIASLVKYYYSWKKTR SRTSLMDRQARKLANRHNQGDSDDDVEETHPMDGNDSDYDPKKEAKKEGNTEQPVQTSKIGLGR REYQSLQHRHHSQRSKCRPPKGMYLTQEDVVAVSCSPNAANTILRQLDMELISLKRQVQNAKQV NSALKQKMEGGIEEFKPPESNQKINARWTTEEQLLAVQGTDPTGSSDTGSITSCPIIHSNTNSP YCHSEPASTTSSSNTACCPGSSPAASSTPAAGSVHPAPANFKSASTTSYSPC hide sequence

RefSeq Acc Id:	NP_060724 ⟸ NM_018254
- Peptide Label:	isoform d
- UniProtKB:	Q8N5U3 (UniProtKB/Swiss-Prot), Q7L9I5 (UniProtKB/Swiss-Prot), Q5VT47 (UniProtKB/Swiss-Prot), B4DYY7 (UniProtKB/Swiss-Prot), B3KYA2 (UniProtKB/Swiss-Prot), Q9NV83 (UniProtKB/Swiss-Prot), Q9P2K3 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MRVGAEYQARIPEFDPGATKYTDKDNGGMLVWSPYHSIPDAKLDEYIAIAKEKHGYNVEQALGM LFWHKHNIEKSLADLPNFTPFPDEWTVEDKVLFEQAFSFHGKSFHRIQQMLPDKTIASLVKYYY SWKKTRSRTSLMDRQARKLANRHNQGDSDDDVEETHPMDGNDSDYDPKKEAKKEGNTEQPVQTS KIGLGRREYQSLQHRHHSQRSKCRPPKGMYLTQEDVVAVSCSPNAANTILRQLDMELISLKRQV QNAKQVNSALKQKMEGGIEEFKPPESNQKINARWTTEEQLLAVQGVRKYGKDFQAIADVIGNKT VGQVKNFFVNYRRRFNLEEVLQEWEAEQGTQASNGDASTLGEETKSASNVPSGKSTDEEEEAQT PQAPRTLGPSPPAPSSTPTPTAPIATLNQPPPLLRPTLPAAPALHRQPPPLQQQARFIQPRPTL NQPPPPLIRPANSMPPRLNPRPVLSTVGGQQPPSLIGIQTDSQSSLH hide sequence

RefSeq Acc Id:	NP_001129697 ⟸ NM_001136225
- Peptide Label:	isoform c
- UniProtKB:	Q9P2K3 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MPGMMEKGPELLGKNRSANGSAKSPAGGGGSGASSTNGGLHYSEPESGCSSDDEHDVGMRVGAE YQARIPEFDPGATKYTDKDNGGMLVWSPYHSIPDAKLDEYIAIAKEKHGYNVEQALGMLFWHKH NIEKSLADLPNFTPFPDEWTVEDKVLFEQAFSFHGKSFHRIQQMLPDKTIASLVKYYYSWKKTR SRTSLMDRQARKLANRHNQGDSDDDVEETHPMDGNDSDYDPKKEAKKEGNTEQPVQTSKIGLGR REYQSLQHRHHSQRSKCRPPKGMYLTQEDVVAVSCSPNAANTILRQLDMELISLKRQVQNAKQV NSALKQKMEGGIEEFKPPESNQKINARWTTEEQLLAVQGVRKYGKDFQAIADVIGNKTVGQVKN FFVNYRRRFNLEEVLQEWEAEQGTQASNGDASTLGEETKSASNVPSGKSTDEEEEVCLCMEFEL I hide sequence

RefSeq Acc Id:

XP_005273248 ⟸ XM_005273191

- Peptide Label:

isoform X1

- Sequence:

show sequence

MPGMMEKGPELLGKNRSANGSAKSPAGGGGSGASSTNGGLHYSEPESGCSSDDEHGDVGMRVGA
EYQARIPEFDPGATKYTDKDNGGMLVWSPYHSIPDAKLDEYIAIAKEKHGYNVEQALGMLFWHK
HNIEKSLADLPNFTPFPDEWTVEDKVLFEQAFSFHGKSFHRIQQMLPDKTIASLVKYYYSWKKT
RSRTSLMDRQARKLANRHNQGDSDDDVEETHPMDGNDSDYDPKKEAKKEGNTEQPVQTSKIGLG
RREYQSLQHRHHSQRSKCRPPKGMYLTQEDVVAVSCSPNAANTILRQLDMELISLKRQVQNAKQ
VNSALKQKMEGGIEEFKPPESNQKINARWTTEEQLLAVQGVRKYGKDFQAIADVIGNKTVGQVK
NFFVNYRRRFNLEEVLQEWEAEQGTQASNGDASTLGEETKSASNVPSGKSTDEEEEAQTPQAPR
TLGPSPPAPSSTPTPTAPIATLNQPPPLLRPTLPAAPALHRQPPPLQQQARFIQPRPTLNQPPP
PLIRPANSMPPRLNPRPVLSTVGGQQPPSLIGIQTDSQSSLH

hide sequence

RefSeq Acc Id:

XP_006711505 ⟸ XM_006711442

- Peptide Label:

isoform X4

- Sequence:

show sequence

MPGMMEKGPELLGKNRSANGSAKSPAGGGGSGASSTNGGLHYSEPESGCSSDDEHGDVGMRVGA
EYQARIPEFDPGATKYTDKDNGGMLVWSPYHSIPDAKLDEYIAIAKEKHGYNVEQALGMLFWHK
HNIEKSLADLPNFTPFPDEWTVEDKVLFEQAFSFHGKSFHRIQQMLPDKTIASLVKYYYSWKKT
RSRTSLMDRQARKLANRHNQGDSDDDVEETHPMDGNDSDYDPKKEAKKEGNTEQPVQTSKIGLG
RREYQSLQHRHHSQRSKCRPPKGMYLTQEDVVAVSCSPNAANTILRQLDMELISLKRQVQNAKQ
VNSALKQKMEGGIEEFKPPESNQKINARWTTEEQLLAVQGTDPTGSSDTGSITSCPIIHSNTNS
PYCHSEPASTTSSSNTACCPGSSPAASSTPAAGSVHPAPANFKSASTTSYSPC

hide sequence

RefSeq Acc Id:

XP_011508050 ⟸ XM_011509748

- Peptide Label:

isoform X2

- Sequence:

show sequence

MPGMMEKGPELLGKNRSANGSAKSPAGGGGSGASSTNGGLHYSEPESGCSSDDEHGDVGMRVGA
EYQARIPEFDPGATKYTDKDNGGMLVWSPYHSIPDAKLDEYIAIAKEKHGYNVEQALGMLFWHK
HNIEKSLADLPNFTPFPDEWTVEDKVLFEQAFSFHGKSFHRIQQMLPDKTIASLVKYYYSWKKT
RSRTSLMDRQARKLANRHNQGDSDDDVEETHPMDGNDSDYDPKKEAKKEGNTEQPVQTSKIGLG
RREYQSLQHRHHSQRSKCRPPKGMYLTQEDVVAVSCSPNAANTILRQLDMELISLKRQSNQKIN
ARWTTEEQLLAVQGVRKYGKDFQAIADVIGNKTVGQVKNFFVNYRRRFNLEEVLQEWEAEQGTQ
ASNGDASTLGEETKSASNVPSGKSTDEEEEAQTPQAPRTLGPSPPAPSSTPTPTAPIATLNQPP
PLLRPTLPAAPALHRQPPPLQQQARFIQPRPTLNQPPPPLIRPANSMPPRLNPRPVLSTVGGQQ
PPSLIGIQTDSQSSLH

hide sequence

RefSeq Acc Id:

XP_016857250 ⟸ XM_017001761

- Peptide Label:

isoform X3

- Sequence:

show sequence

MPGMMEKGPELLGKNRSANGSAKSPAGGGGSGASSTNGGLHYSEPESGCSSDDEHDVGMRVGAE
YQARIPEFDPGATKYTDKDNGGMLVWSPYHSIPDAKLDEYIAIAKEKHGYNVEQALGMLFWHKH
NIEKSLADLPNFTPFPDEWTVEDKVLFEQAFSFHGKSFHRIQQMLPDKTIASLVKYYYSWKKTR
SRTSLMDRQARKLANRHNQGDSDDDVEETHPMDGNDSDYDPKKEAKKEGNTEQPVQTSKIGLGR
REYQSLQHRHHSQRSKCRPPKGMYLTQEDVVAVSCSPNAANTILRQLDMELISLKRQSNQKINA
RWTTEEQLLAVQGVRKYGKDFQAIADVIGNKTVGQVKNFFVNYRRRFNLEEVLQEWEAEQGTQA
SNGDASTLGEETKSASNVPSGKSTDEEEEAQTPQAPRTLGPSPPAPSSTPTPTAPIATLNQPPP
LLRPTLPAAPALHRQPPPLQQQARFIQPRPTLNQPPPPLIRPANSMPPRLNPRPVLSTVGGQQP
PSLIGIQTDSQSSLH

hide sequence

RefSeq Acc Id:

NP_001336998 ⟸ NM_001350069

- Peptide Label:

isoform e

- Sequence:

show sequence

MPGMMEKGPELLGKNRSANGSAKSPAGGGGSGASSTNGGLHYSEPESGCSSDDEHDVGMRVGAE
YQARIPEFDPVETRSCYVSQAGLKLRGSSHPPSLASQSAGIIGATKYTDKDNGGMLVWSPYHSI
PDAKLDEYIAIAKEKHGYNVEQALGMLFWHKHNIEKSLADLPNFTPFPDEWTVEDKVLFEQAFS
FHGKSFHRIQQMLPDKTIASLVKYYYSWKKTRSRTSLMDRQARKLANRHNQGDSDDDVEETHPM
DGNDSDYDPKKEAKKEGNTEQPVQTSKIGLGRREYQSLQHRHHSQRSKCRPPKGMYLTQEDVVA
VSCSPNAANTILRQLDMELISLKRQVQNAKQVNSALKQKMEGGIEEFKPPESNQKINARWTTEE
QLLAVQGVRKYGKDFQAIADVIGNKTVGQVKNFFVNYRRRFNLEEVLQEWEAEQGTQASNGDAS
TLGEETKSASNVPSGKSTDEEEEAQTPQAPRTLGPSPPAPSSTPTPTAPIATLNQPPPLLRPTL
PAAPALHRQPPPLQQQARFIQPRPTLNQPPPPLIRPANSMPPRLNPRPVLSTVGGQQPPSLIGI
QTDSQSSLH

hide sequence

RefSeq Acc Id:

NP_001336999 ⟸ NM_001350070

- Peptide Label:

isoform f

- Sequence:

show sequence

MLFWHKHNIEKSLADLPNFTPFPDEWTVEDKVLFEQAFSFHGKSFHRIQQMLPDKTIASLVKYY
YSWKKTRSRTSLMDRQARKLANRHNQGDSDDDVEETHPMDGNDSDYDPKKEAKKEGNTEQPVQT
SKIGLGRREYQSLQHRHHSQRSKCRPPKGMYLTQEDVVAVSCSPNAANTILRQLDMELISLKRQ
VQNAKQVNSALKQKMEGGIEEFKPPESNQKINARWTTEEQLLAVQGVRKYGKDFQAIADVIGNK
TVGQVKNFFVNYRRRFNLEEVLQEWEAEQGTQASNGDASTLGEETKSASNVPSGKSTDEEEEAQ
TPQAPRTLGPSPPAPSSTPTPTAPIATLNQPPPLLRPTLPAAPALHRQPPPLQQQARFIQPRPT
LNQPPPPLIRPANSMPPRLNPRPVLSTVGGQQPPSLIGIQTDSQSSLH

hide sequence

Ensembl Acc Id:

ENSP00000398558 ⟸ ENST00000452621

Ensembl Acc Id:

ENSP00000436838 ⟸ ENST00000533469

Ensembl Acc Id:

ENSP00000433441 ⟸ ENST00000534460

Ensembl Acc Id:

ENSP00000436057 ⟸ ENST00000534478

Ensembl Acc Id:

ENSP00000413929 ⟸ ENST00000419091

Ensembl Acc Id:

ENSP00000434181 ⟸ ENST00000485186

Ensembl Acc Id:

ENSP00000355972 ⟸ ENST00000367005

Ensembl Acc Id:

ENSP00000355973 ⟸ ENST00000367006

Ensembl Acc Id:

ENSP00000432779 ⟸ ENST00000528926

Ensembl Acc Id:

ENSP00000437048 ⟸ ENST00000529763

Ensembl Acc Id:

ENSP00000434605 ⟸ ENST00000529572

RefSeq Acc Id:	XP_047281002 ⟸ XM_047425046
- Peptide Label:	isoform X9
- UniProtKB:	B4DV59 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047280977 ⟸ XM_047425021
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_047280988 ⟸ XM_047425032
- Peptide Label:	isoform X7

RefSeq Acc Id:	XP_047280999 ⟸ XM_047425043
- Peptide Label:	isoform X9
- UniProtKB:	B4DV59 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047281008 ⟸ XM_047425052
- Peptide Label:	isoform X11
- UniProtKB:	B4DV59 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047281009 ⟸ XM_047425053
- Peptide Label:	isoform X12
- UniProtKB:	B4DV59 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047280994 ⟸ XM_047425038
- Peptide Label:	isoform X8
- UniProtKB:	B4DV59 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047281007 ⟸ XM_047425051
- Peptide Label:	isoform X10

RefSeq Acc Id:	XP_047280967 ⟸ XM_047425011
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054193602 ⟸ XM_054337627
- Peptide Label:	isoform X9
- UniProtKB:	B4DV59 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054193593 ⟸ XM_054337618
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054193596 ⟸ XM_054337621
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054193594 ⟸ XM_054337619
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054193598 ⟸ XM_054337623
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_054193595 ⟸ XM_054337620
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054193599 ⟸ XM_054337624
- Peptide Label:	isoform X7

RefSeq Acc Id:	XP_054193601 ⟸ XM_054337626
- Peptide Label:	isoform X9
- UniProtKB:	B4DV59 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054193604 ⟸ XM_054337629
- Peptide Label:	isoform X11
- UniProtKB:	B4DV59 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054193605 ⟸ XM_054337630
- Peptide Label:	isoform X12
- UniProtKB:	B4DV59 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054193600 ⟸ XM_054337625
- Peptide Label:	isoform X8
- UniProtKB:	B4DV59 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054193603 ⟸ XM_054337628
- Peptide Label:	isoform X10

RefSeq Acc Id:	XP_054193597 ⟸ XM_054337622
- Peptide Label:	isoform X5

Protein Domains

ELM2 REST corepressor helical SANT

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q9P2K3-F1-model_v2	AlphaFold	Q9P2K3	1-495	view protein structure

Promoters

RGD ID:

6786409

Promoter ID:

HG_KWN:7202

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

NM_001136223, NM_001136225, OTTHUMT00000089821, OTTHUMT00000089822, OTTHUMT00000089823

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	1	209,498,766 - 209,499,497 (+)	MPROMDB

RGD ID:

6814853

Promoter ID:

HG_MRA:1468

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

K562

Transcripts:

AK057001

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	1	209,555,481 - 209,555,981 (+)	MPROMDB

RGD ID:

6858898

Promoter ID:

EPDNEW_H2614

Type:

initiation region

Name:

RCOR3_1

Description:

REST corepressor 3

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H2615 EPDNEW_H2616

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	211,259,369 - 211,259,429	EPDNEW

RGD ID:

6858900

Promoter ID:

EPDNEW_H2615

Type:

initiation region

Name:

RCOR3_2

Description:

REST corepressor 3

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H2614 EPDNEW_H2616

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	211,259,975 - 211,260,035	EPDNEW

RGD ID:

6858902

Promoter ID:

EPDNEW_H2616

Type:

initiation region

Name:

RCOR3_3

Description:

REST corepressor 3

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H2614 EPDNEW_H2615

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	1	211,312,260 - 211,312,320	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:25594	AgrOrtholog
COSMIC	RCOR3	COSMIC
Ensembl Genes	ENSG00000117625	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000367005	ENTREZGENE
	ENST00000367005.8	UniProtKB/Swiss-Prot
	ENST00000367006	ENTREZGENE
	ENST00000367006.8	UniProtKB/Swiss-Prot
	ENST00000419091	ENTREZGENE
	ENST00000419091.7	UniProtKB/Swiss-Prot
	ENST00000452621	ENTREZGENE
	ENST00000452621.6	UniProtKB/Swiss-Prot
	ENST00000485186.1	UniProtKB/TrEMBL
	ENST00000528926	ENTREZGENE
	ENST00000528926.5	UniProtKB/TrEMBL
	ENST00000529572.5	UniProtKB/TrEMBL
	ENST00000529763.5	UniProtKB/TrEMBL
	ENST00000533469.5	UniProtKB/TrEMBL
	ENST00000534460.5	UniProtKB/TrEMBL
	ENST00000534478.5	UniProtKB/TrEMBL
Gene3D-CATH	1.20.58.1880	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	4.10.1240.50	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Homeodomain-like	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000117625	GTEx
HGNC ID	HGNC:25594	ENTREZGENE
Human Proteome Map	RCOR3	Human Proteome Map
InterPro	ELM2_dom	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Homeobox-like_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	REST_helical	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SANT/Myb	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SANT_dom	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Trans_reg/Corepressor	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:55758	UniProtKB/Swiss-Prot
NCBI Gene	55758	ENTREZGENE
OMIM	620464	OMIM
PANTHER	REST COREPRESSOR 3	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	REST COREPRESSOR COREST PROTEIN-RELATED	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	ELM2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Myb_DNA-binding	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	REST_helical	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA134917623	PharmGKB
PRINTS	F138DOMAIN	UniProtKB/TrEMBL
PROSITE	ELM2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SANT	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART	ELM2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SANT	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP	SSF46689	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	B3KYA2	ENTREZGENE
	B4DV59	ENTREZGENE, UniProtKB/TrEMBL
	B4DYY7	ENTREZGENE
	E9PPC5_HUMAN	UniProtKB/TrEMBL
	E9PQE5_HUMAN	UniProtKB/TrEMBL
	E9PR63_HUMAN	UniProtKB/TrEMBL
	H0YDD7_HUMAN	UniProtKB/TrEMBL
	H0YDR8_HUMAN	UniProtKB/TrEMBL
	H0YF22_HUMAN	UniProtKB/TrEMBL
	Q5VT47	ENTREZGENE
	Q7L9I5	ENTREZGENE
	Q8N5U3	ENTREZGENE
	Q9NV83	ENTREZGENE
	Q9P2K3	ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary	B3KYA2	UniProtKB/Swiss-Prot
	B4DYY7	UniProtKB/Swiss-Prot
	Q5VT47	UniProtKB/Swiss-Prot
	Q7L9I5	UniProtKB/Swiss-Prot
	Q8N5U3	UniProtKB/Swiss-Prot
	Q9NV83	UniProtKB/Swiss-Prot

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

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

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

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

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