GPR137 (G protein-coupled receptor 137)

Gene: GPR137 (G protein-coupled receptor 137) Homo sapiens

Analyze

Symbol:

GPR137

Name:

G protein-coupled receptor 137

RGD ID:

1604608

HGNC Page

HGNC:24300

Description:

Predicted to be involved in several processes, including negative regulation of bone resorption; negative regulation of osteoclast differentiation; and positive regulation of TORC1 signaling. Located in lysosomal membrane.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

C11orf4; GPR137A; integral membrane protein GPR137; TM7SF1L1; transmembrane 7 superfamily member 1-like 1 protein

RGD Orthologs

Alliance Genes

More Info

more info ...

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	11	64,270,531 - 64,289,500 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	11	64,270,062 - 64,289,494 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	11	64,038,003 - 64,056,972 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	11	63,809,907 - 63,813,539 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	11	61,378,710 - 61,383,871 (+)	NCBI		Celera
Cytogenetic Map	11	q13.1	NCBI
HuRef	11	60,379,535 - 60,384,696 (+)	NCBI		HuRef
CHM1_1	11	63,934,808 - 63,939,969 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	11	64,260,559 - 64,279,464 (+)	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

genetic disease (IAGP)

high grade glioma (IAGP)

intellectual disability (IAGP)

leukocyte adhesion deficiency 3 (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

(+)-schisandrin B (ISO)

(1->4)-beta-D-glucan (ISO)

1,2-dimethylhydrazine (ISO)

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

4,4'-sulfonyldiphenol (ISO)

6-propyl-2-thiouracil (ISO)

amphetamine (ISO)

aristolochic acid A (EXP)

arsane (EXP)

arsenic atom (EXP)

benzo[a]pyrene (EXP,ISO)

bisphenol A (ISO)

chlorpyrifos (ISO)

cyclosporin A (EXP)

decabromodiphenyl ether (EXP)

elemental selenium (EXP)

ethanol (ISO)

folic acid (ISO)

FR900359 (EXP)

isobutanol (EXP)

N-ethyl-N-nitrosourea (ISO)

ozone (EXP)

paracetamol (EXP,ISO)

perfluorooctane-1-sulfonic acid (ISO)

resveratrol (EXP)

selenium atom (EXP)

sunitinib (EXP)

tetrachloromethane (ISO)

trichloroethene (ISO)

urethane (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

autophagy (IEA)

biological_process (ND)

negative regulation of bone resorption (IBA,IEA)

negative regulation of osteoclast differentiation (IBA,IEA)

positive regulation of TORC1 signaling (IBA,IEA)

regulation of autophagy (IBA,IEA)

Cellular Component

lysosomal membrane (IBA,IDA,IEA)

lysosome (IEA)

membrane (IEA)

Molecular Function

molecular_function (ND)

Phenotype Annotations Click to see Annotation Detail View

Human Phenotype

Ependymoma (IAGP)

Intellectual disability (IAGP)

References

References - curated

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

Additional References at PubMed

PMID:8889548	PMID:10873569	PMID:12477932	PMID:14702039	PMID:15489334	PMID:21873635	PMID:22837380	PMID:24870220	PMID:25490967	PMID:25496438	PMID:26669804	PMID:28298427
PMID:28514442	PMID:28975893	PMID:29739299	PMID:31036939	PMID:31464892	PMID:33961781	PMID:35271311	PMID:36920340

Genomics

Comparative Map Data

GPR137
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	11	64,270,531 - 64,289,500 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	11	64,270,062 - 64,289,494 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	11	64,038,003 - 64,056,972 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	11	63,809,907 - 63,813,539 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	11	61,378,710 - 61,383,871 (+)	NCBI		Celera
Cytogenetic Map	11	q13.1	NCBI
HuRef	11	60,379,535 - 60,384,696 (+)	NCBI		HuRef
CHM1_1	11	63,934,808 - 63,939,969 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	11	64,260,559 - 64,279,464 (+)	NCBI		T2T-CHM13v2.0

Gpr137
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	19	6,915,425 - 6,919,818 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	19	6,915,425 - 6,919,848 (-)	Ensembl		GRCm39 Ensembl
GRCm38	19	6,938,057 - 6,942,450 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	19	6,938,057 - 6,942,480 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	19	7,012,560 - 7,016,940 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	19	7,005,114 - 7,008,523 (-)	NCBI		MGSCv36	mm8
Celera	19	6,715,154 - 6,719,541 (-)	NCBI		Celera
Cytogenetic Map	19	A	NCBI
cM Map	19	5.09	NCBI

Gpr137
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	1	213,558,846 - 213,562,422 (-)	NCBI		GRCr8
mRatBN7.2	1	204,129,636 - 204,132,622 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	1	204,129,636 - 204,133,082 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	1	212,479,805 - 212,482,791 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	1	219,574,899 - 219,577,885 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	1	212,265,952 - 212,268,938 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	1	222,194,266 - 222,197,252 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	1	222,194,266 - 222,197,252 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	1	229,185,120 - 229,188,106 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	1	209,613,157 - 209,616,143 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
Celera	1	201,663,636 - 201,666,622 (-)	NCBI		Celera
Cytogenetic Map	1	q43	NCBI

Gpr137
(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_004955422	20,790,104 - 20,795,423 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955422	20,791,144 - 20,795,451 (-)	NCBI	ChiLan1.0	ChiLan1.0

GPR137
(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	9	65,511,895 - 65,516,602 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	11	66,557,035 - 66,561,749 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	11	59,627,488 - 59,646,556 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	11	62,985,909 - 62,990,950 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	11	62,985,909 - 62,990,950 (+)	Ensembl	panpan1.1		panPan2

GPR137
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	18	52,776,857 - 52,781,050 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	18	52,776,858 - 52,779,783 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	18	51,383,928 - 51,388,205 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	18	53,822,260 - 53,826,536 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	18	53,822,263 - 53,826,865 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	18	52,924,928 - 52,929,204 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	18	52,500,680 - 52,504,956 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	18	53,284,584 - 53,288,860 (-)	NCBI		UU_Cfam_GSD_1.0

Gpr137
(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_024404947	8,477,998 - 8,481,549 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936599	4,919,897 - 4,923,655 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936599	4,920,347 - 4,923,655 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

GPR137
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	2	7,826,456 - 7,830,969 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	2	7,826,454 - 7,831,010 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	2	6,893,223 - 6,897,787 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

GPR137
(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	1	9,944,971 - 9,949,623 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	1	9,944,579 - 9,949,624 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666038	107,284,936 - 107,289,645 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Gpr137
(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_004624767	22,019,257 - 22,025,686 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624767	22,021,596 - 22,025,362 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in GPR137
26 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
NM_001170726.1(GPR137):c.1143C>T (p.Asp381=)	single nucleotide variant	Malignant melanoma [RCV000069589]	Chr11:64288659 [GRCh38] Chr11:64056131 [GRCh37] Chr11:63812707 [NCBI36] Chr11:11q13.1	not provided
Single allele	deletion	Intellectual disability [RCV001293382]	Chr11:118359328..118372573 [GRCh37] Chr11:11p15.3-q23.3	pathogenic
NM_032989.3(BAD):c.246C>G (p.Asp82Glu)	single nucleotide variant	Inborn genetic diseases [RCV003179244]	Chr11:64271745 [GRCh38] Chr11:64039217 [GRCh37] Chr11:11q13.1	likely benign
GRCh38/hg38 11q12.3-13.1(chr11:62893226-64335043)x1	copy number loss	See cases [RCV000140879]	Chr11:62893226..64335043 [GRCh38] Chr11:62660698..64102515 [GRCh37] Chr11:62417274..63859091 [NCBI36] Chr11:11q12.3-13.1	likely pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)	copy number gain	See cases [RCV000511729]	Chr11:230616..134938470 [GRCh37] Chr11:11p15.5-q25	pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)x3	copy number gain	See cases [RCV000510881]	Chr11:230616..134938470 [GRCh37] Chr11:11p15.5-q25	pathogenic
GRCh37/hg19 11p15.5-q25(chr11:198510-134934063)x3	copy number gain	not provided [RCV000737348]	Chr11:198510..134934063 [GRCh37] Chr11:11p15.5-q25	pathogenic
GRCh37/hg19 11p15.5-q25(chr11:70864-134938470)x3	copy number gain	not provided [RCV000749874]	Chr11:70864..134938470 [GRCh37] Chr11:11p15.5-q25	pathogenic
dup(11)(q13.1q13.1)	duplication	Ependymoma [RCV000785872]	Chr11:63533279..65429676 [GRCh37] Chr11:11q13.1	likely pathogenic
NC_000011.9:g.(?_59596957)_(68707199_?)dup	duplication	Familial temporal lobe epilepsy 8 [RCV001372442]	Chr11:59596957..68707199 [GRCh37] Chr11:11q12.1-13.3	uncertain significance
NC_000011.9:g.(?_58916346)_(64972349_?)dup	duplication	Leukocyte adhesion deficiency 3 [RCV003113394]\|not provided [RCV003113393]	Chr11:58916346..64972349 [GRCh37] Chr11:11q12.1-13.1	uncertain significance\|no classifications from unflagged records
GRCh37/hg19 11p13-q25(chr11:32799481-134938470)x3	copy number gain	MISSED ABORTION [RCV002282973]	Chr11:32799481..134938470 [GRCh37] Chr11:11p13-q25	pathogenic
NM_001170880.2(GPR137):c.386G>A (p.Arg129Gln)	single nucleotide variant	Inborn genetic diseases [RCV002973545]	Chr11:64286993 [GRCh38] Chr11:64054465 [GRCh37] Chr11:11q13.1	uncertain significance
NM_001170880.2(GPR137):c.*54C>T	single nucleotide variant	Inborn genetic diseases [RCV002683015]	Chr11:64289250 [GRCh38] Chr11:64056722 [GRCh37] Chr11:11q13.1	uncertain significance
NM_001170880.2(GPR137):c.*84C>T	single nucleotide variant	Inborn genetic diseases [RCV002683115]	Chr11:64289280 [GRCh38] Chr11:64056752 [GRCh37] Chr11:11q13.1	uncertain significance
NM_001170880.2(GPR137):c.919A>G (p.Ser307Gly)	single nucleotide variant	Inborn genetic diseases [RCV002865212]	Chr11:64288609 [GRCh38] Chr11:64056081 [GRCh37] Chr11:11q13.1	uncertain significance
NM_001170880.2(GPR137):c.1188G>A (p.Thr396=)	single nucleotide variant	Inborn genetic diseases [RCV002868260]	Chr11:64289193 [GRCh38] Chr11:64056665 [GRCh37] Chr11:11q13.1	uncertain significance
NM_001170880.2(GPR137):c.397A>G (p.Ser133Gly)	single nucleotide variant	Inborn genetic diseases [RCV002694643]	Chr11:64287004 [GRCh38] Chr11:64054476 [GRCh37] Chr11:11q13.1	uncertain significance
NM_001170880.2(GPR137):c.*75C>T	single nucleotide variant	Inborn genetic diseases [RCV002979998]	Chr11:64289271 [GRCh38] Chr11:64056743 [GRCh37] Chr11:11q13.1	likely benign
NM_001170880.2(GPR137):c.724T>A (p.Leu242Met)	single nucleotide variant	Inborn genetic diseases [RCV002692255]	Chr11:64288155 [GRCh38] Chr11:64055627 [GRCh37] Chr11:11q13.1	uncertain significance
NM_001170880.2(GPR137):c.463G>A (p.Val155Met)	single nucleotide variant	Inborn genetic diseases [RCV002981926]	Chr11:64287776 [GRCh38] Chr11:64055248 [GRCh37] Chr11:11q13.1	uncertain significance
NM_032989.3(BAD):c.97G>A (p.Gly33Ser)	single nucleotide variant	Inborn genetic diseases [RCV002931248]	Chr11:64284272 [GRCh38] Chr11:64051744 [GRCh37] Chr11:11q13.1	uncertain significance
NM_032989.3(BAD):c.-8-15A>G	single nucleotide variant	Inborn genetic diseases [RCV002703126]	Chr11:64284391 [GRCh38] Chr11:64051863 [GRCh37] Chr11:11q13.1	uncertain significance
NM_032989.3(BAD):c.146G>A (p.Ser49Asn)	single nucleotide variant	Inborn genetic diseases [RCV002936416]	Chr11:64284223 [GRCh38] Chr11:64051695 [GRCh37] Chr11:11q13.1	uncertain significance
NM_032989.3(BAD):c.244G>A (p.Asp82Asn)	single nucleotide variant	Inborn genetic diseases [RCV002717933]	Chr11:64271747 [GRCh38] Chr11:64039219 [GRCh37] Chr11:11q13.1	uncertain significance
NM_001170880.2(GPR137):c.740G>A (p.Arg247Gln)	single nucleotide variant	Inborn genetic diseases [RCV003189261]	Chr11:64288171 [GRCh38] Chr11:64055643 [GRCh37] Chr11:11q13.1	uncertain significance
NM_001170880.2(GPR137):c.485A>C (p.His162Pro)	single nucleotide variant	Inborn genetic diseases [RCV003195923]	Chr11:64287798 [GRCh38] Chr11:64055270 [GRCh37] Chr11:11q13.1	uncertain significance
NM_001170880.2(GPR137):c.1187C>T (p.Thr396Met)	single nucleotide variant	Inborn genetic diseases [RCV003218112]	Chr11:64289192 [GRCh38] Chr11:64056664 [GRCh37] Chr11:11q13.1	uncertain significance
NM_032989.3(BAD):c.236G>T (p.Gly79Val)	single nucleotide variant	Inborn genetic diseases [RCV003204640]	Chr11:64271755 [GRCh38] Chr11:64039227 [GRCh37] Chr11:11q13.1	uncertain significance
NM_032989.3(BAD):c.193G>A (p.Gly65Arg)	single nucleotide variant	Inborn genetic diseases [RCV003213084]	Chr11:64271798 [GRCh38] Chr11:64039270 [GRCh37] Chr11:11q13.1	uncertain significance
NM_001170880.2(GPR137):c.970C>T (p.Arg324Trp)	single nucleotide variant	Inborn genetic diseases [RCV003360164]	Chr11:64288660 [GRCh38] Chr11:64056132 [GRCh37] Chr11:11q13.1	uncertain significance
GRCh37/hg19 11q13.1(chr11:63643711-64533636)x1	copy number loss	not provided [RCV003483125]	Chr11:63643711..64533636 [GRCh37] Chr11:11q13.1	uncertain significance
GRCh37/hg19 11q12.2-13.5(chr11:59923608-76272324)x3	copy number gain	not provided [RCV003484842]	Chr11:59923608..76272324 [GRCh37] Chr11:11q12.2-13.5	pathogenic
GRCh37/hg19 11q12.1-13.3(chr11:56895955-69295402)x3	copy number gain	not specified [RCV003986944]	Chr11:56895955..69295402 [GRCh37] Chr11:11q12.1-13.3	likely pathogenic

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	6810
Count of miRNA genes:	977
Interacting mature miRNAs:	1210
Transcripts:	ENST00000313074, ENST00000377702, ENST00000411458, ENST00000438980, ENST00000535675, ENST00000536017, ENST00000536282, ENST00000536667, ENST00000538032, ENST00000538244, ENST00000539833, ENST00000539851, ENST00000540370, ENST00000541952, ENST00000542190, ENST00000543383, ENST00000545366, ENST00000546139, ENST00000546201
Prediction methods:	Miranda, Rnahybrid, Targetscan
Result types:	miRGate_prediction

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

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

Markers in Region

RH47513

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,055,577 - 64,055,829	UniSTS	GRCh37
Build 36	11	63,812,153 - 63,812,405	RGD	NCBI36
Celera	11	61,382,476 - 61,382,728	RGD
Cytogenetic Map	11	cen-q22.3	UniSTS
HuRef	11	60,383,301 - 60,383,553	UniSTS
GeneMap99-GB4 RH Map	11	249.53	UniSTS
NCBI RH Map	11	573.2	UniSTS

RH98400

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,056,813 - 64,056,947	UniSTS	GRCh37
Build 36	11	63,813,389 - 63,813,523	RGD	NCBI36
Celera	11	61,383,712 - 61,383,846	RGD
Cytogenetic Map	11	q13	UniSTS
Cytogenetic Map	11	cen-q22.3	UniSTS
HuRef	11	60,384,537 - 60,384,671	UniSTS
GeneMap99-GB4 RH Map	11	238.55	UniSTS

WI-17324

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,055,387 - 64,055,517	UniSTS	GRCh37
Build 36	11	63,811,963 - 63,812,093	RGD	NCBI36
Celera	11	61,382,286 - 61,382,416	RGD
Cytogenetic Map	11	cen-q22.3	UniSTS
HuRef	11	60,383,111 - 60,383,241	UniSTS
GeneMap99-GB4 RH Map	11	238.55	UniSTS
Whitehead-RH Map	11	317.9	UniSTS

PMC230316P4

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,037,549 - 64,037,809	UniSTS	GRCh37
Build 36	11	63,794,125 - 63,794,385	RGD	NCBI36
Celera	11	61,364,433 - 61,364,693	RGD
Cytogenetic Map	11	cen-q22.3	UniSTS
Cytogenetic Map	11	q13.1	UniSTS
HuRef	11	60,365,342 - 60,365,602	UniSTS

RH78541

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	64,037,556 - 64,037,689	UniSTS	GRCh37
Build 36	11	63,794,132 - 63,794,265	RGD	NCBI36
Celera	11	61,364,440 - 61,364,573	RGD
Cytogenetic Map	11	cen-q22.3	UniSTS
Cytogenetic Map	11	q13.1	UniSTS
HuRef	11	60,365,349 - 60,365,482	UniSTS
GeneMap99-GB4 RH Map	11	238.55	UniSTS

Expression

RNA-SEQ Expression

High: > 1000 TPM value Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system

circulatory system

endocrine system

exocrine system

hemolymphoid system

hepatobiliary system

integumental system

musculoskeletal system

nervous system

renal system

reproductive system

respiratory system

sensory system

visual system

adipose tissue

appendage

entire extraembryonic component

High

Medium

2297

1963

1483

379

1343

242

3546

1100

3586

363

1433

1564

151

1112

2022

Low

138

1026

241

243

604

223

809

1095

131

766

Below cutoff

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001170880	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001170881	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001177358	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001378076	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001378077	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001378078	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001378079	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001378080	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001378081	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001378082	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001378083	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001378084	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001378085	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001378086	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001378087	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001378088	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001378089	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_020155	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_165394	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_165395	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_165396	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_165397	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005274100	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005274102	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005274104	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011545168	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011545169	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017018016	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024448611	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047427263	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047427264	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047427265	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054369369	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054369370	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054369371	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054369372	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054369373	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054369374	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054369375	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054369376	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054369377	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_002957154	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AJ250392	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK056094	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK300209	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK302256	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AP001453	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AX211494	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC020396	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC029297	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC033920	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC035002	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BI830247	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BU730608	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BU730610	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX119209	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471076	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068267	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HF584129	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000313074 ⟹ ENSP00000321698

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,286,420 - 64,289,491 (+)	Ensembl

RefSeq Acc Id:

ENST00000377702 ⟹ ENSP00000366931

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,285,257 - 64,289,494 (+)	Ensembl

RefSeq Acc Id:

ENST00000411458 ⟹ ENSP00000411827

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,284,339 - 64,289,404 (+)	Ensembl

RefSeq Acc Id:

ENST00000438980 ⟹ ENSP00000415698

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,285,848 - 64,289,494 (+)	Ensembl

RefSeq Acc Id:

ENST00000535675 ⟹ ENSP00000446342

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,285,477 - 64,287,003 (+)	Ensembl

RefSeq Acc Id:

ENST00000536017

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,286,110 - 64,288,013 (+)	Ensembl

RefSeq Acc Id:

ENST00000536282 ⟹ ENSP00000443443

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,288,363 - 64,289,292 (+)	Ensembl

RefSeq Acc Id:

ENST00000536667 ⟹ ENSP00000440928

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,284,880 - 64,287,744 (+)	Ensembl

RefSeq Acc Id:

ENST00000538032 ⟹ ENSP00000445000

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,285,699 - 64,287,814 (+)	Ensembl

RefSeq Acc Id:

ENST00000538244 ⟹ ENSP00000442322

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,275,688 - 64,286,713 (+)	Ensembl

RefSeq Acc Id:

ENST00000539833 ⟹ ENSP00000438716

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,285,057 - 64,288,090 (+)	Ensembl

RefSeq Acc Id:

ENST00000539851 ⟹ ENSP00000442792

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,284,811 - 64,289,500 (+)	Ensembl

RefSeq Acc Id:

ENST00000540370 ⟹ ENSP00000446387

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,285,859 - 64,286,760 (+)	Ensembl

RefSeq Acc Id:

ENST00000541952 ⟹ ENSP00000442929

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,286,521 - 64,288,089 (+)	Ensembl

RefSeq Acc Id:

ENST00000542190 ⟹ ENSP00000441034

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,286,512 - 64,288,005 (+)	Ensembl

RefSeq Acc Id:

ENST00000543383 ⟹ ENSP00000441003

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,285,495 - 64,288,151 (+)	Ensembl

RefSeq Acc Id:

ENST00000545366

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,288,083 - 64,288,680 (+)	Ensembl

RefSeq Acc Id:

ENST00000546139 ⟹ ENSP00000445570

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,270,062 - 64,288,090 (+)	Ensembl

RefSeq Acc Id:

ENST00000546201 ⟹ ENSP00000438146

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	64,285,254 - 64,288,714 (+)	Ensembl

RefSeq Acc Id:

NM_001170880 ⟹ NP_001164351

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,285,848 - 64,289,494 (+)	NCBI
GRCh37	11	64,051,781 - 64,056,972 (+)	NCBI
Celera	11	61,378,710 - 61,383,871 (+)	RGD
HuRef	11	60,379,535 - 60,384,696 (+)	RGD
CHM1_1	11	63,936,579 - 63,939,969 (+)	NCBI
T2T-CHM13v2.0	11	64,275,812 - 64,279,458 (+)	NCBI

Sequence:

show sequence

GGAGCAGCGGGAGCCGGGGAGCCGGAGCCCCGGGTCCCCACGACCTGAGCCGGCTCTCCCATCA
GCGGCCTGAGGACCTGGCGTCCGCCTCCTCCCTCCCCTTGAGGCTGGAGCGTGGACGCGGTGGG
GGAGGGTGGGGCGGGGGCAGCTTTCGAGAATTACGAGGACAGGAGGCAGAGGCCCTCCCCATCC
GCATTATTGGAGGAGAGAGAGCCTCCCCCAGCTTGGGGAGGGGGAGAGCGGGGCATTGGGCGCC
CCTCGCAGCGGCCGCTGCCCTGACCCGACGGGTATCAGCCGGCTCTCCCCCTCCACCCAGGACG
ACATGAACGACCGAGGCCAGGGAGTCCTCTCCTTGGGCCTCTGCATCCCCCCATCCTTGGCTCT
GGGGTAGGCCCAGGGAGGAGACACCCCCAACCCCTATCCGGTCTGTCCTGGAGAAAAGAGACTG
CCCTTCCATGCCCCTGAGTGAGGGGCCTGGGGCCCAGGCTGCCTGTGTTCCCCAAGGGCAAGGG
TCTCTCTGTTGAGGAGGAGGGGCCTGTCAGCCACAACTTCTTTCCTCCTGAGCGCCCCATCTCC
CTCTCTGCACCCTGCAATTCCCACCCCTCCGTATTTATTTCCCTGGTCCCGCCGACAGTCCCTC
CTTGTCTGTCTCCGGGATTCAGGCCTCCCTCCCTGACATGGAGAGTAACCTGTCTGGCCTGGTG
CCTGCTGCCGGGCTGGTGCCTGCGCTGCCACCTGCTGTGACCCTGGGGCTGACAGCTGCCTACA
CCACCCTGTATGCCCTGCTCTTCTTCTCCGTCTATGCCCAGCTCTGGCTGGTGCTTCTGTATGG
GCACAAGCGTCTCAGCTATCAGACGGTGTTCCTGGCCCTCTGTCTGCTCTGGGCCGCCTTGCGT
ACCACCCTCTTCTCCTTCTACTTCCGAGATACTCCCCGCGCCAACCGCCTGGGGCCCTTGCCCT
TCTGGCTTCTCTACTGCTGCCCCGTCTGCCTGCAGTTCTTCACCTTGACGCTTATGAACCTCTA
CTTTGCCCAGGTGGTGTTCAAGGCCAAGGTGAAGCGTCGGCCGGAGATGAGCCGAGGCTTGCTC
GCTGTCCGAGGGGCCTTTGTGGGGGCCTCGCTGCTCTTTCTGCTGGTGAACGTGCTGTGTGCTG
TGCTCTCCCATCGGCGCCGGGCACAGCCCTGGGCCCTGCTGCTTGTCCGCGTCCTGGTGAGCGA
CTCCCTGTTCGTCATCTGCGCGCTGTCTCTTGCTGCCTGCCTCTGCCTCGTCGCCAGGCGGGCG
CCCTCCACTAGCATCTACCTGGAGGCCAAGGGGACCAGTGTGTGCCAGGCGGCCGCGATGGGTG
GCGCCATGGTCCTGCTCTATGCCAGCCGGGCCTGCTACAACCTGACAGCACTGGCCTTGGCCCC
CCAGAGCCGGCTGGACACCTTCGATTACGACTGGTACAATGTGTCTGACCAGGCGGACCTGGTG
AATGACCTGGGGAACAAAGGCTACCTGGTATTTGGCCTCATCCTCTTCGTGTGGGAGCTACTGC
CCACCACCCTGCTGGTGGGCTTCTTCCGGGTGCACCGGCCCCCACAGGACCTGAGCACCAGCCA
CATCCTCAATGGGCAGGTCTTTGCCTCTCGGTCCTACTTCTTTGACCGGGCTGGGCACTGTGAA
GATGAGGGCTGCTCCTGGGAGCACAGCCGGGGTGAGAGCACCAGTATGTCGGGCAGTCTAGGCT
CTGGGAGCTGGTATGGTGCCATCGGGCGTGAGCCGGGCTGGTATGGGGGCAGCCAGACGAAGAC
CACTCCTCTGCTCTTCTCCCAGGTGCCAGGACCAGGCGGCCACCACCACAGTCTCTACTCCACC
CCACAGACGTGATCCCCCTCCCTCCCCCACAGAATACCCAGGCCCCAGTCCCCCTCACCCTAGG
CCCCTGTGCCAAGTTTGTCTGCCGCTTCTTGCCCAGGATCCTGGGGGTCGTGGCTACCCCCTCC
TCTGGCCGGCTCCTTGCTGCTCCTGTCATAGTGAGCTTGTGCCGTCCCCCTAGGATGGGGGGCA
TGGCCCTGGCTGCCAGATGCCCACAGCACCCTGGCATGACCTGCCACCTCTGCTTCCACACCGG
AGCCAGCTACCTCTCCTGTGCCTGCCACTCAATAAACAGTGTCTGCGCCCCACA

hide sequence

RefSeq Acc Id:

NM_001170881 ⟹ NP_001164352

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,284,843 - 64,289,494 (+)	NCBI
GRCh37	11	64,051,781 - 64,056,972 (+)	NCBI
Celera	11	61,378,710 - 61,383,871 (+)	RGD
HuRef	11	60,379,535 - 60,384,696 (+)	RGD
CHM1_1	11	63,935,282 - 63,939,969 (+)	NCBI
T2T-CHM13v2.0	11	64,274,807 - 64,279,458 (+)	NCBI

Sequence:

show sequence

CTCCCTCCTTCGGCCCCGGGGCTCACATCCTCGCTGCCTCACACCTTGGGCGTGTGTGGGAGCA
GGAGAGGGATTCTCTGGGGTCCCCATTTGGAACCTGGAGACCCACTTCTGCCAACAAGTCCTTC
AGCCCCTCTGGGCCTTAGTTTCCCCCCAGTGAAGTGGGGATAGTGACAGCTCCCCCGGGAGCCA
GTGAAAACTTTGTGAAGGGAGTGATTACTGCGGGCGAAGGCGCTTGGCACAGCCACAACTGAAG
CTCAGCCGTCGGATGTGATTATTGTTGCTATTGTTACCGCTCCGCCTGGACTGGGTGCCCGGTC
GGAAAGTCCCGCTCCCCGCTCCTCCTCCCAGGCGCGGAAGCTTCGCGCCGCCCGCCTCGGGGGA
CACCTCCCGCGCCATCTCGGGGGCACTGGAGATAAGGAAAGGAACCTCCTCCCTGGCTGGGATG
GCTGCCCGGGCGCGGGAGGAGGGCCGGGGACCCGGTGAGGGAGGACCGTAGGGCCCGTGGGGGC
TTCACGCCTGGCAGGCGGCCGGCCAGGCCTCCCTCCCTGACATGGAGAGTAACCTGTCTGGCCT
GGTGCCTGCTGCCGGGCTGGTGCCTGCGCTGCCACCTGCTGTGACCCTGGGGCTGACAGCTGCC
TACACCACCCTGTATGCCCTGCTCTTCTTCTCCGTCTATGCCCAGCTCTGGCTGGTGCTTCTGT
ATGGGCACAAGCGTCTCAGCTATCAGACGGTGTTCCTGGCCCTCTGTCTGCTCTGGGCCGCCTT
GCGTACCACCCTCTTCTCCTTCTACTTCCGAGATACTCCCCGCGCCAACCGCCTGGGGCCCTTG
CCCTTCTGGCTTCTCTACTGCTGCCCCGTCTGCCTGCAGTTCTTCACCTTGACGCTTATGAACC
TCTACTTTGCCCAGGTGGTGTTCAAGGCCAAGGTGAAGCGTCGGCCGGAGATGAGCCGAGGCTT
GCTCGCTGTCCGAGGGGCCTTTGTGGGGGCCTCGCTGCTCTTTCTGCTGGTGAACGTGCTGTGT
GCTGTGCTCTCCCATCGGCGCCGGGCACAGCCCTGGGCCCTGCTGCTTGTCCGCGTCCTGGTGA
GCGACTCCCTGTTCGTCATCTGCGCGCTGTCTCTTGCTGCCTGCCTCTGCCTCGTCGCCAGGCG
GGCGCCCTCCACTAGCATCTACCTGGAGGCCAAGGCGGACCTGGTGAATGACCTGGGGAACAAA
GGCTACCTGGTATTTGGCCTCATCCTCTTCGTGTGGGAGCTACTGCCCACCACCCTGCTGGTGG
GCTTCTTCCGGGTGCACCGGCCCCCACAGGACCTGAGCACCAGCCACATCCTCAATGGGCAGGT
CTTTGCCTCTCGGTCCTACTTCTTTGACCGGGCTGGGCACTGTGAAGATGAGGGCTGCTCCTGG
GAGCACAGCCGGGGTGAGAGCACCAGTATGTCGGGCAGTCTAGGCTCTGGGAGCTGGTATGGTG
CCATCGGGCGTGAGCCGGGCTGGTATGGGGGCAGCCAGACGAAGACCACTCCTCTGCTCTTCTC
CCAGGTGCCAGGACCAGGCGGCCACCACCACAGTCTCTACTCCACCCCACAGACGTGATCCCCC
TCCCTCCCCCACAGAATACCCAGGCCCCAGTCCCCCTCACCCTAGGCCCCTGTGCCAAGTTTGT
CTGCCGCTTCTTGCCCAGGATCCTGGGGGTCGTGGCTACCCCCTCCTCTGGCCGGCTCCTTGCT
GCTCCTGTCATAGTGAGCTTGTGCCGTCCCCCTAGGATGGGGGGCATGGCCCTGGCTGCCAGAT
GCCCACAGCACCCTGGCATGACCTGCCACCTCTGCTTCCACACCGGAGCCAGCTACCTCTCCTG
TGCCTGCCACTCAATAAACAGTGTCTGCGCCCCACA

hide sequence

RefSeq Acc Id:

NM_001177358 ⟹ NP_001170829

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,284,843 - 64,289,500 (+)	NCBI
GRCh37	11	64,051,781 - 64,056,972 (+)	NCBI
Celera	11	61,378,710 - 61,383,871 (+)	RGD
HuRef	11	60,379,535 - 60,384,696 (+)	RGD
CHM1_1	11	63,935,280 - 63,939,969 (+)	NCBI
T2T-CHM13v2.0	11	64,274,807 - 64,279,464 (+)	NCBI

Sequence:

show sequence

CTCCCTCCTTCGGCCCCGGGGCTCACATCCTCGCTGCCTCACACCTTGGGCGTGTGTGGGAGCA
GGAGAGGGATTCTCTGGGGTCCCCATTTGGAACCTGGAGACCCACTTCTGCCAACAAGTCCTTC
AGCCCCTCTGGGCCTTAGTTTCCCCCCAGTGAAGTGGGGATAGTGACAGCTCCCCCGGGAGCCA
GTGAAAACTTTGTGAAGGGAGTGATTACTGCGGGCGAAGGCGCTTGGCACAGCCACAACTGAAG
CTCAGCCGTCGGATGTGATTATTGTTGCTATTGTTACCGCTCCGCCTGGACTGGGTGCCCGGTC
GGAAAGTCCCGCTCCCCGCTCCTCCTCCCAGGCGCGGAAGCTTCGCGCCGCCCGCCTCGGGGGA
CACCTCCCGCGCCATCTCGGGGGCACTGGAGATAAGGCCTCCCTCCCTGACATGGAGAGTAACC
TGTCTGGCCTGGTGCCTGCTGCCGGGCTGGTGCCTGCGCTGCCACCTGCTGTGACCCTGGGGCT
GACAGCTGCCTACACCACCCTGTATGCCCTGCTCTTCTTCTCCGTCTATGCCCAGCTCTGGCTG
GTGCTTCTGTATGGGCACAAGCGTCTCAGCTATCAGACGGTGTTCCTGGCCCTCTGTCTGCTCT
GGGCCGCCTTGCGTACCACCCTCTTCTCCTTCTACTTCCGAGATACTCCCCGCGCCAACCGCCT
GGGGCCCTTGCCCTTCTGGCTTCTCTACTGCTGCCCCGTCTGCCTGCAGTTCTTCACCTTGACG
CTTATGAACCTCTACTTTGCCCAGGTGGTGTTCAAGGCCAAGGTGAAGCGTCGGCCGGAGATGA
GCCGAGGCTTGCTCGCTGTCCGAGGGGCCTTTGTGGGGGCCTCGCTGCTCTTTCTGCTGGTGAA
CGTGCTGTGTGCTGTGCTCTCCCATCGGCGCCGGGCACAGCCCTGGGCCCTGCTGCTTGTCCGC
GTCCTGGTGAGCGACTCCCTGTTCGTCATCTGCGCGCTGTCTCTTGCTGCCTGCCTCTGCCTCG
TCGCCAGGCGGGCGCCCTCCACTAGCATCTACCTGGAGGCCAAGGGGACCAGTGTGTGCCAGGC
GGCCGCGATGGGTGGCGCCATGGTCCTGCTCTATGCCAGCCGGGCCTGCTACAACCTGACAGCA
CTGGCCTTGGCCCCCCAGAGCCGGCTGGACACCTTCGATTACGACTGGTACAATGTGTCTGACC
AGGCGGACCTGGTGAATGACCTGGGGAACAAAGGCTACCTGGTATTTGGCCTCATCCTCTTCGT
GTGGGAGCTACTGCCCACCACCCTGCTGGTGGGCTTCTTCCGGGTGCACCGGCCCCCACAGGAC
CTGTATGTCGGGCAGTCTAGGCTCTGGGAGCTGGTATGGTGCCATCGGGCGTGAGCCGGGCTGG
TATGGGGGCAGCCAGACGAAGACCACTCCTCTGCTCTTCTCCCAGGTGCCAGGACCAGGCGGCC
ACCACCACAGTCTCTACTCCACCCCACAGACGTGATCCCCCTCCCTCCCCCACAGAATACCCAG
GCCCCAGTCCCCCTCACCCTAGGCCCCTGTGCCAAGTTTGTCTGCCGCTTCTTGCCCAGGATCC
TGGGGGTCGTGGCTACCCCCTCCTCTGGCCGGCTCCTTGCTGCTCCTGTCATAGTGAGCTTGTG
CCGTCCCCCTAGGATGGGGGGCATGGCCCTGGCTGCCAGATGCCCACAGCACCCTGGCATGACC
TGCCACCTCTGCTTCCACACCGGAGCCAGCTACCTCTCCTGTGCCTGCCACTCAATAAACAGTG
TCTGCGCCCCACAGTTGTG

hide sequence

RefSeq Acc Id:

NM_001378076 ⟹ NP_001365005

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,270,531 - 64,289,494 (+)	NCBI
T2T-CHM13v2.0	11	64,260,559 - 64,279,458 (+)	NCBI

Sequence:

show sequence

AGATCCCAGGAACTCCGTGCCGGAGACGGGAAGAGAGGATGCCTAGGGCCCTAAATGGAAAGGC
CAGAGCTGGAGACCTAGCACCCAGAAGATGAGACCGCAATTCGAGAATCAAAGGGCCGGGAGCG
ATGGCCTCCCTCCCTGACATGGAGAGTAACCTGTCTGGCCTGGTGCCTGCTGCCGGGCTGGTGC
CTGCGCTGCCACCTGCTGTGACCCTGGGGCTGACAGCTGCCTACACCACCCTGTATGCCCTGCT
CTTCTTCTCCGTCTATGCCCAGCTCTGGCTGGTGCTTCTGTATGGGCACAAGCGTCTCAGCTAT
CAGACGGTGTTCCTGGCCCTCTGTCTGCTCTGGGCCGCCTTGCGTACCACCCTCTTCTCCTTCT
ACTTCCGAGATACTCCCCGCGCCAACCGCCTGGGGCCCTTGCCCTTCTGGCTTCTCTACTGCTG
CCCCGTCTGCCTGCAGTTCTTCACCTTGACGCTTATGAACCTCTACTTTGCCCAGGTGGTGTTC
AAGGCCAAGGTGAAGCGTCGGCCGGAGATGAGCCGAGGCTTGCTCGCTGTCCGAGGGGCCTTTG
TGGGGGCCTCGCTGCTCTTTCTGCTGGTGAACGTGCTGTGTGCTGTGCTCTCCCATCGGCGCCG
GGCACAGCCCTGGGCCCTGCTGCTTGTCCGCGTCCTGGTGAGCGACTCCCTGTTCGTCATCTGC
GCGCTGTCTCTTGCTGCCTGCCTCTGCCTCGTCGCCAGGCGGGCGCCCTCCACTAGCATCTACC
TGGAGGCCAAGGCGGACCTGGTGAATGACCTGGGGAACAAAGGCTACCTGGTATTTGGCCTCAT
CCTCTTCGTGTGGGAGCTACTGCCCACCACCCTGCTGGTGGGCTTCTTCCGGGTGCACCGGCCC
CCACAGGACCTGAGCACCAGCCACATCCTCAATGGGCAGGTCTTTGCCTCTCGGTCCTACTTCT
TTGACCGGGCTGGGCACTGTGAAGATGAGGGCTGCTCCTGGGAGCACAGCCGGGGTGAGAGCAC
CAGTATGTCGGGCAGTCTAGGCTCTGGGAGCTGGTATGGTGCCATCGGGCGTGAGCCGGGCTGG
TATGGGGGCAGCCAGACGAAGACCACTCCTCTGCTCTTCTCCCAGGTGCCAGGACCAGGCGGCC
ACCACCACAGTCTCTACTCCACCCCACAGACGTGATCCCCCTCCCTCCCCCACAGAATACCCAG
GCCCCAGTCCCCCTCACCCTAGGCCCCTGTGCCAAGTTTGTCTGCCGCTTCTTGCCCAGGATCC
TGGGGGTCGTGGCTACCCCCTCCTCTGGCCGGCTCCTTGCTGCTCCTGTCATAGTGAGCTTGTG
CCGTCCCCCTAGGATGGGGGGCATGGCCCTGGCTGCCAGATGCCCACAGCACCCTGGCATGACC
TGCCACCTCTGCTTCCACACCGGAGCCAGCTACCTCTCCTGTGCCTGCCACTCAATAAACAGTG
TCTGCGCCCCACA

hide sequence

RefSeq Acc Id:

NM_001378077 ⟹ NP_001365006

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,285,848 - 64,289,494 (+)	NCBI
T2T-CHM13v2.0	11	64,275,812 - 64,279,458 (+)	NCBI

Sequence:

show sequence

GGAGCAGCGGGAGCCGGGGAGCCGGAGCCCCGGGTCCCCACGACCTGAGCCGGCTCTCCCATCA
GCGGCCTGAGGACCTGGCGTCCGCCTCCTCCCTCCCCTTGAGGCTGGAGCGTGGACGCGGTGGG
GGAGGGTGGGGCGGGGGCAGCTTTCGAGAATTACGAGGACAGGAGGCAGAGGCCCTCCCCATCC
GCATTATTGGAGGAGAGAGAGCCTCCCCCAGCTTGGGGAGGGGGAGAGCGGGGCATTGGGCGCC
CCTCGCAGCGGCCGCTGCCCTGACCCGACGGGTATCAGCCGGCTCTCCCCCTCCACCCAGGACG
ACATGAACGACCGAGGCCAGGGAGTCCTCTCCTTGGGCCTCTGCATCCCCCCATCCTTGGCTCT
GGGGTAGGCCCAGGGAGGAGACACCCCCAACCCCTATCCGGTCTGTCCTGGAGAAAAGAGACTG
CCCTTCCATGCCCCTGAGTGAGGGGCCTGGGGCCCAGGCTGCCTGTGTTCCCCAAGGGCAAGGG
TCTCTCTGTTGAGGAGGAGGGGCCTGTCAGCCACAACTTCTTTCCTCCTGAGCGCCCCATCTCC
CTCTCTGCACCCTGCAATTCCCACCCCTCCGTATTTATTTCCCTGGTCCCGCCGACAGTCCCTC
CTTGTCTGTCTCCGGGATTCAGGCCTCCCTCCCTGACATGGAGAGTAACCTGTCTGGCCTGGTG
CCTGCTGCCGGGCTGGTGCCTGCGCTGCCACCTGCTGTGACCCTGGGGCTGACAGCTGCCTACA
CCACCCTGTATGCCCTGCTCTTCTTCTCCGTCTATGCCCAGCTCTGGCTGGTGCTTCTGTATGG
GCACAAGCGTCTCAGCTATCAGACGGTGTTCCTGGCCCTCTGTCTGCTCTGGGCCGCCTTGCGT
ACCACCCTCTTCTCCTTCTACTTCCGAGATACTCCCCGCGCCAACCGCCTGGGGCCCTTGCCCT
TCTGGCTTCTCTACTGCTGCCCCGTCTGCCTGCAGTTCTTCACCTTGACGCTTATGAACCTCTA
CTTTGCCCAGGTGGTGTTCAAGGCCAAGGTGAAGCGTCGGCCGGAGATGAGCCGAGGCTTGCTC
GCTGTCCGAGGGGCCTTTGTGGGGGCCTCGCTGCTCTTTCTGCTGGTGAACGTGCTGTGTGCTG
TGCTCTCCCATCGGCGCCGGGCACAGCCCTGGGCCCTGCTGCTTGTCCGCGTCCTGGTGAGCGA
CTCCCTGTTCGTCATCTGCGCGCTGTCTCTTGCTGCCTGCCTCTGCCTCGTCGCCAGGCGGGCG
CCCTCCACTAGCATCTACCTGGAGGCCAAGGCGGACCTGGTGAATGACCTGGGGAACAAAGGCT
ACCTGGTATTTGGCCTCATCCTCTTCGTGTGGGAGCTACTGCCCACCACCCTGCTGGTGGGCTT
CTTCCGGGTGCACCGGCCCCCACAGGACCTGAGCACCAGCCACATCCTCAATGGGCAGGTCTTT
GCCTCTCGGTCCTACTTCTTTGACCGGGCTGGGCACTGTGAAGATGAGGGCTGCTCCTGGGAGC
ACAGCCGGGGTGAGAGCACCAGTATGTCGGGCAGTCTAGGCTCTGGGAGCTGGTATGGTGCCAT
CGGGCGTGAGCCGGGCTGGTATGGGGGCAGCCAGACGAAGACCACTCCTCTGCTCTTCTCCCAG
GTGCCAGGACCAGGCGGCCACCACCACAGTCTCTACTCCACCCCACAGACGTGATCCCCCTCCC
TCCCCCACAGAATACCCAGGCCCCAGTCCCCCTCACCCTAGGCCCCTGTGCCAAGTTTGTCTGC
CGCTTCTTGCCCAGGATCCTGGGGGTCGTGGCTACCCCCTCCTCTGGCCGGCTCCTTGCTGCTC
CTGTCATAGTGAGCTTGTGCCGTCCCCCTAGGATGGGGGGCATGGCCCTGGCTGCCAGATGCCC
ACAGCACCCTGGCATGACCTGCCACCTCTGCTTCCACACCGGAGCCAGCTACCTCTCCTGTGCC
TGCCACTCAATAAACAGTGTCTGCGCCCCACA

hide sequence

RefSeq Acc Id:

NM_001378078 ⟹ NP_001365007

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,270,531 - 64,289,494 (+)	NCBI
T2T-CHM13v2.0	11	64,260,559 - 64,279,458 (+)	NCBI

Sequence:

show sequence

AGATCCCAGGAACTCCGTGCCGGAGACGGGAAGAGAGGATGCCTAGGGCCCTAAATGGAAAGGC
CAGAGCTGGAGACCTAGCACCCAGAAGATGAGACCGCAATTCGAGAATCAAAGGGCCGGGAGCG
ATGGCCTCCCTCCCTGACATGGAGAGTAACCTGTCTGGCCTGGTGCCTGCTGCCGGGCTGGTGC
CTGCGCTGCCACCTGCTGTGACCCTGGGGCTGACAGCTGCCTACACCACCCTGTATGCCCTGCT
CTTCTTCTCCGTCTATGCCCAGCTCTGGCTGGTGCTTCTGTATGGGCACAAGCGTCTCAGCTAT
CAGACGGTGTTCCTGGCCCTCTGTCTGCTCTGGGCCGCCTTGCGTACCACCCTCTTCTCCTTCT
ACTTCCGAGATACTCCCCGCGCCAACCGCCTGGGGCCCTTGCCCTTCTGGCTTCTCTACTGCTG
CCCCGTCTGCCTGCAGTTCTTCACCTTGACGCTTATGAACCTCTACTTTGCCCAGGTGGTGTTC
AAGGCCAAGGTGAAGCGTCGGCCGGAGATGAGCCGAGGCTTGCTCGCTGTCCGAGGGGCCTTTG
TGGGGGCCTCGCTGCTCTTTCTGCTGGTGAACGTGCTGTGTGCTGTGCTCTCCCATCGGCGCCG
GGCACAGCCCTGGGCCCTGCTGCTTGTCCGCGTCCTGGTGAGCGACTCCCTGTTCGTCATCTGC
GCGCTGTCTCTTGCTGCCTGCCTCTGCCTCGTCGCCAGGCGGGCGCCCTCCACTAGCATCTACC
TGGAGGCCAAGGGGACCAGTGTGTGCCAGGCGGCCGCGATGGGTGGCGCCATGGTCCTGCTCTA
TGCCAGCCGGGCCTGCTACAACCTGACAGCACTGGCCTTGGCCCCCCAGAGCCGGCTGGACACC
TTCGATTACGACTGGTACAATGTGTCTGACCAGGCGGACCTGGTGAATGACCTGGGGAACAAAG
GCTACCTGGTATTTGGCCTCATCCTCTTCGTGTGGGAGCTACTGCCCACCACCCTGCTGGTGGG
CTTCTTCCGGGTGCACCGGCCCCCACAGGACCTGAGCACCAGCCACATCCTCAATGGGCAGGTC
TTTGCCTCTCGGTCCTACTTCTTTGACCGGGCTGGGCACTGTGAAGATGAGGGCTGCTCCTGGG
AGCACAGCCGGGGTGAGAGCACCAGTATGTCGGGCAGTCTAGGCTCTGGGAGCTGGTATGGTGC
CATCGGGCGTGAGCCGGGCTGGTATGGGGGCAGCCAGACGAAGACCACTCCTCTGCTCTTCTCC
CAGGTGCCAGGACCAGGCGGCCACCACCACAGTCTCTACTCCACCCCACAGACGTGATCCCCCT
CCCTCCCCCACAGAATACCCAGGCCCCAGTCCCCCTCACCCTAGGCCCCTGTGCCAAGTTTGTC
TGCCGCTTCTTGCCCAGGATCCTGGGGGTCGTGGCTACCCCCTCCTCTGGCCGGCTCCTTGCTG
CTCCTGTCATAGTGAGCTTGTGCCGTCCCCCTAGGATGGGGGGCATGGCCCTGGCTGCCAGATG
CCCACAGCACCCTGGCATGACCTGCCACCTCTGCTTCCACACCGGAGCCAGCTACCTCTCCTGT
GCCTGCCACTCAATAAACAGTGTCTGCGCCCCACA

hide sequence

RefSeq Acc Id:

NM_001378079 ⟹ NP_001365008

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,284,843 - 64,289,494 (+)	NCBI
T2T-CHM13v2.0	11	64,274,807 - 64,279,458 (+)	NCBI

Sequence:

show sequence

CTCCCTCCTTCGGCCCCGGGGCTCACATCCTCGCTGCCTCACACCTTGGGCGTGTGTGGGAGCA
GGAGAGGGATTCTCTGGGGTCCCCATTTGGAACCTGGAGACCCACTTCTGCCAACAAGTCCTTC
AGCCCCTCTGGGCCTTAGTTTCCCCCCAGTGAAGTGGGGATAGTGACAGCTCCCCCGGGAGCCA
GTGAAAACTTTGTGAAGGGAGTGATTACTGCGGGCGAAGGCGCTTGGCACAGCCACAACTGAAG
CTCAGCCGTCGGATGTGATTATTGTTGCTATTGTTACCGCTCCGCCTGGACTGGGTGCCCGGTC
GGAAAGTCCCGCTCCCCGCTCCTCCTCCCAGGCGCGGAAGCTTCGCGCCGCCCGCCTCGGGGGA
CACCTCCCGCGCCATCTCGGGGGCACTGGAGATAAGGAAAGGAACCTCCTCCCTGGCTGGGATG
GCTGCCCGGGCGCGGGAGGAGGGCCGGGGACCCGGTGAGGGAGGACCGTAGGGCCCGTGGGGGC
TTCACGCCTGGCAGGCGGCCGGCCAGGCCTCCCTCCCTGACATGGAGAGTAACCTGTCTGGCCT
GGTGCCTGCTGCCGGGCTGGTGCCTGCGCTGCCACCTGCTGTGACCCTGGGGCTGACAGCTGCC
TACACCACCCTGTATGCCCTGCTCTTCTTCTCCGTCTATGCCCAGCTCTGGCTGGTGCTTCTGT
ATGGGCACAAGCGTCTCAGCTATCAGACGGTGTTCCTGGCCCTCTGTCTGCTCTGGGCCGCCTT
GCGTACCACCCTCTTCTCCTTCTACTTCCGAGATACTCCCCGCGCCAACCGCCTGGGGCCCTTG
CCCTTCTGGCTTCTCTACTGCTGCCCCGTCTGCCTGCAGTTCTTCACCTTGACGCTTATGAACC
TCTACTTTGCCCAGGTGGTGTTCAAGGCCAAGGTGAAGCGTCGGCCGGAGATGAGCCGAGGCTT
GCTCGCTGTCCGAGGGGCCTTTGTGGGGGCCTCGCTGCTCTTTCTGCTGGTGAACGTGCTGTGT
GCTGTGCTCTCCCATCGGCGCCGGGCACAGCCCTGGGCCCTGCTGCTTGTCCGCGTCCTGGTGA
GCGACTCCCTGTTCGTCATCTGCGCGCTGTCTCTTGCTGCCTGCCTCTGCCTCGTCGCCAGGCG
GGCGCCCTCCACTAGCATCTACCTGGAGGCCAAGGGGACCAGTGTGTGCCAGGCGGCCGCGATG
GGTGGCGCCATGGTCCTGCTCTATGCCAGCCGGGCCTGCTACAACCTGACAGCACTGGCCTTGG
CCCCCCAGAGCCGGCTGGACACCTTCGATTACGACTGGTACAATGTGTCTGACCAGGCGGACCT
GGTGAATGACCTGGGGAACAAAGGCTACCTGGTATTTGGCCTCATCCTCTTCGTGTGGGAGCTA
CTGCCCACCACCCTGCTGGTGGGCTTCTTCCGGGTGCACCGGCCCCCACAGGACCTGAGCACCA
GCCACATCCTCAATGGGCAGGTCTTTGCCTCTCGGTCCTACTTCTTTGACCGGGCTGGGCACTG
TGAAGATGAGGGCTGCTCCTGGGAGCACAGCCGGGGTGAGAGCACCAGTATGTCGGGCAGTCTA
GGCTCTGGGAGCTGGTATGGTGCCATCGGGCGTGAGCCGGGCTGGTATGGGGGCAGCCAGACGA
AGACCACTCCTCTGCTCTTCTCCCAGGTGCCAGGACCAGGCGGCCACCACCACAGTCTCTACTC
CACCCCACAGACGTGATCCCCCTCCCTCCCCCACAGAATACCCAGGCCCCAGTCCCCCTCACCC
TAGGCCCCTGTGCCAAGTTTGTCTGCCGCTTCTTGCCCAGGATCCTGGGGGTCGTGGCTACCCC
CTCCTCTGGCCGGCTCCTTGCTGCTCCTGTCATAGTGAGCTTGTGCCGTCCCCCTAGGATGGGG
GGCATGGCCCTGGCTGCCAGATGCCCACAGCACCCTGGCATGACCTGCCACCTCTGCTTCCACA
CCGGAGCCAGCTACCTCTCCTGTGCCTGCCACTCAATAAACAGTGTCTGCGCCCCACA

hide sequence

RefSeq Acc Id:

NM_001378080 ⟹ NP_001365009

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,285,505 - 64,289,494 (+)	NCBI
T2T-CHM13v2.0	11	64,275,469 - 64,279,458 (+)	NCBI

Sequence:

show sequence

AGAGACCGAGGGACGGGAATCCGTTGCCGCCCCCGGCCGGGCGGCACGACCCCGATTTGGGTAT
AGGAGAGAGGAGCGTGGGAACTGGCGGACCCCCATACAAGCCTCCCTCCCTGACATGGAGAGTA
ACCTGTCTGGCCTGGTGCCTGCTGCCGGGCTGGTGCCTGCGCTGCCACCTGCTGTGACCCTGGG
GCTGACAGCTGCCTACACCACCCTGTATGCCCTGCTCTTCTTCTCCGTCTATGCCCAGCTCTGG
CTGGTGCTTCTGTATGGGCACAAGCGTCTCAGCTATCAGACGGTGTTCCTGGCCCTCTGTCTGC
TCTGGGCCGCCTTGCGTACCACCCTCTTCTCCTTCTACTTCCGAGATACTCCCCGCGCCAACCG
CCTGGGGCCCTTGCCCTTCTGGCTTCTCTACTGCTGCCCCGTCTGCCTGCAGTTCTTCACCTTG
ACGCTTATGAACCTCTACTTTGCCCAGGTGGTGTTCAAGGCCAAGGTGAAGCGTCGGCCGGAGA
TGAGCCGAGGCTTGCTCGCTGTCCGAGGGGCCTTTGTGGGGGCCTCGCTGCTCTTTCTGCTGGT
GAACGTGCTGTGTGCTGTGCTCTCCCATCGGCGCCGGGCACAGCCCTGGGCCCTGCTGCTTGTC
CGCGTCCTGGTGAGCGACTCCCTGTTCGTCATCTGCGCGCTGTCTCTTGCTGCCTGCCTCTGCC
TCGTCGCCAGGCGGGCGCCCTCCACTAGCATCTACCTGGAGGCCAAGGGGACCAGTGTGTGCCA
GGCGGCCGCGATGGGTGGCGCCATGGTCCTGCTCTATGCCAGCCGGGCCTGCTACAACCTGACA
GCACTGGCCTTGGCCCCCCAGAGCCGGCTGGACACCTTCGATTACGACTGGTACAATGTGTCTG
ACCAGGCGGACCTGGTGAATGACCTGGGGAACAAAGGCTACCTGGTATTTGGCCTCATCCTCTT
CGTGTGGGAGCTACTGCCCACCACCCTGCTGGTGGGCTTCTTCCGGGTGCACCGGCCCCCACAG
GACCTGAGCACCAGCCACATCCTCAATGGGCAGGTCTTTGCCTCTCGGTCCTACTTCTTTGACC
GGGCTGGGCACTGTGAAGATGAGGGCTGCTCCTGGGAGCACAGCCGGGGTGAGAGCACCAGTAT
GTCGGGCAGTCTAGGCTCTGGGAGCTGGTATGGTGCCATCGGGCGTGAGCCGGGCTGGTATGGG
GGCAGCCAGACGAAGACCACTCCTCTGCTCTTCTCCCAGGTGCCAGGACCAGGCGGCCACCACC
ACAGTCTCTACTCCACCCCACAGACGTGATCCCCCTCCCTCCCCCACAGAATACCCAGGCCCCA
GTCCCCCTCACCCTAGGCCCCTGTGCCAAGTTTGTCTGCCGCTTCTTGCCCAGGATCCTGGGGG
TCGTGGCTACCCCCTCCTCTGGCCGGCTCCTTGCTGCTCCTGTCATAGTGAGCTTGTGCCGTCC
CCCTAGGATGGGGGGCATGGCCCTGGCTGCCAGATGCCCACAGCACCCTGGCATGACCTGCCAC
CTCTGCTTCCACACCGGAGCCAGCTACCTCTCCTGTGCCTGCCACTCAATAAACAGTGTCTGCG
CCCCACA

hide sequence

RefSeq Acc Id:

NM_001378081 ⟹ NP_001365010

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,285,505 - 64,289,494 (+)	NCBI
T2T-CHM13v2.0	11	64,275,469 - 64,279,458 (+)	NCBI

Sequence:

show sequence

AGAGACCGAGGGACGGGAATCCGTTGCCGCCCCCGGCCGGGCGGCACGACCCCGATTTGGGTAT
AGGAGAGAGGAGCGTGGGAACTGGCGGACCCCCATACAAGTAAAGGCGGGCGGCACGGGGCACG
GCCCACCCGGGGACCCCCTGGATGCGGCACGGCCCCCGCAACTCGGCCGCCCTCCTGCCGCCTC
CCGTAACCCCGGGCGCCCGCCAGCGGCGCAGCTCGCGCCAATTCTCGCCTCCCTCCCTGACATG
GAGAGTAACCTGTCTGGCCTGGTGCCTGCTGCCGGGCTGGTGCCTGCGCTGCCACCTGCTGTGA
CCCTGGGGCTGACAGCTGCCTACACCACCCTGTATGCCCTGCTCTTCTTCTCCGTCTATGCCCA
GCTCTGGCTGGTGCTTCTGTATGGGCACAAGCGTCTCAGCTATCAGACGGTGTTCCTGGCCCTC
TGTCTGCTCTGGGCCGCCTTGCGTACCACCCTCTTCTCCTTCTACTTCCGAGATACTCCCCGCG
CCAACCGCCTGGGGCCCTTGCCCTTCTGGCTTCTCTACTGCTGCCCCGTCTGCCTGCAGTTCTT
CACCTTGACGCTTATGAACCTCTACTTTGCCCAGGTGGTGTTCAAGGCCAAGGTGAAGCGTCGG
CCGGAGATGAGCCGAGGCTTGCTCGCTGTCCGAGGGGCCTTTGTGGGGGCCTCGCTGCTCTTTC
TGCTGGTGAACGTGCTGTGTGCTGTGCTCTCCCATCGGCGCCGGGCACAGCCCTGGGCCCTGCT
GCTTGTCCGCGTCCTGGTGAGCGACTCCCTGTTCGTCATCTGCGCGCTGTCTCTTGCTGCCTGC
CTCTGCCTCGTCGCCAGGCGGGCGCCCTCCACTAGCATCTACCTGGAGGCCAAGGGGACCAGTG
TGTGCCAGGCGGCCGCGATGGGTGGCGCCATGGTCCTGCTCTATGCCAGCCGGGCCTGCTACAA
CCTGACAGCACTGGCCTTGGCCCCCCAGAGCCGGCTGGACACCTTCGATTACGACTGGTACAAT
GTGTCTGACCAGGCGGACCTGGTGAATGACCTGGGGAACAAAGGCTACCTGGTATTTGGCCTCA
TCCTCTTCGTGTGGGAGCTACTGCCCACCACCCTGCTGGTGGGCTTCTTCCGGGTGCACCGGCC
CCCACAGGACCTGAGCACCAGCCACATCCTCAATGGGCAGGTCTTTGCCTCTCGGTCCTACTTC
TTTGACCGGGCTGGGCACTGTGAAGATGAGGGCTGCTCCTGGGAGCACAGCCGGGGTGAGAGCA
CCAGTATGTCGGGCAGTCTAGGCTCTGGGAGCTGGTATGGTGCCATCGGGCGTGAGCCGGGCTG
GTATGGGGGCAGCCAGACGAAGACCACTCCTCTGCTCTTCTCCCAGGTGCCAGGACCAGGCGGC
CACCACCACAGTCTCTACTCCACCCCACAGACGTGATCCCCCTCCCTCCCCCACAGAATACCCA
GGCCCCAGTCCCCCTCACCCTAGGCCCCTGTGCCAAGTTTGTCTGCCGCTTCTTGCCCAGGATC
CTGGGGGTCGTGGCTACCCCCTCCTCTGGCCGGCTCCTTGCTGCTCCTGTCATAGTGAGCTTGT
GCCGTCCCCCTAGGATGGGGGGCATGGCCCTGGCTGCCAGATGCCCACAGCACCCTGGCATGAC
CTGCCACCTCTGCTTCCACACCGGAGCCAGCTACCTCTCCTGTGCCTGCCACTCAATAAACAGT
GTCTGCGCCCCACA

hide sequence

RefSeq Acc Id:

NM_001378082 ⟹ NP_001365011

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,285,848 - 64,289,494 (+)	NCBI
T2T-CHM13v2.0	11	64,275,812 - 64,279,458 (+)	NCBI

Sequence:

show sequence

GGAGCAGCGGGAGCCGGGGAGCCGGAGCCCCGGGTCCCCACGACCTGAGCCGGCTCTCCCATCA
GCGGCCTGAGGACCTGGCGTCCGCCTCCTCCCTCCCCTTGAGGCTGGAGCGTGGACGCGGTGGG
GGAGGGTGGGGCGGGGGCAGCTTTCGAGAATTACGAGGACAGGAGGCAGAGGCCCTCCCCATCC
GCATTATTGGAGGAGAGAGAGCCTCCCCCAGCTTGGGGAGGGGGAGAGCGGGGCATTGGGCGCC
CCTCGCAGCGGCCGCTGCCCTGACCCGACGGGTATCAGCCGGCTCTCCCCCTCCACCCAGGACG
ACATGAACGACCGAGGCCAGGGAGTCCTCTCCTTGGGCCTCTGCATCCCCCCATCCTTGGCTCT
GGGGCCTCCCTCCCTGACATGGAGAGTAACCTGTCTGGCCTGGTGCCTGCTGCCGGGCTGGTGC
CTGCGCTGCCACCTGCTGTGACCCTGGGGCTGACAGCTGCCTACACCACCCTGTATGCCCTGCT
CTTCTTCTCCGTCTATGCCCAGCTCTGGCTGGTGCTTCTGTATGGGCACAAGCGTCTCAGCTAT
CAGACGGTGTTCCTGGCCCTCTGTCTGCTCTGGGCCGCCTTGCGTACCACCCTCTTCTCCTTCT
ACTTCCGAGATACTCCCCGCGCCAACCGCCTGGGGCCCTTGCCCTTCTGGCTTCTCTACTGCTG
CCCCGTCTGCCTGCAGTTCTTCACCTTGACGCTTATGAACCTCTACTTTGCCCAGGTGGTGTTC
AAGGCCAAGGTGAAGCGTCGGCCGGAGATGAGCCGAGGCTTGCTCGCTGTCCGAGGGGCCTTTG
TGGGGGCCTCGCTGCTCTTTCTGCTGGTGAACGTGCTGTGTGCTGTGCTCTCCCATCGGCGCCG
GGCACAGCCCTGGGCCCTGCTGCTTGTCCGCGTCCTGGTGAGCGACTCCCTGTTCGTCATCTGC
GCGCTGTCTCTTGCTGCCTGCCTCTGCCTCGTCGCCAGGCGGGCGCCCTCCACTAGCATCTACC
TGGAGGCCAAGGGGACCAGTGTGTGCCAGGCGGCCGCGATGGGTGGCGCCATGGTCCTGCTCTA
TGCCAGCCGGGCCTGCTACAACCTGACAGCACTGGCCTTGGCCCCCCAGAGCCGGCTGGACACC
TTCGATTACGACTGGTACAATGTGTCTGACCAGGCGGACCTGGTGAATGACCTGGGGAACAAAG
GCTACCTGGTATTTGGCCTCATCCTCTTCGTGTGGGAGCTACTGCCCACCACCCTGCTGGTGGG
CTTCTTCCGGGTGCACCGGCCCCCACAGGACCTGAGCACCAGCCACATCCTCAATGGGCAGGTC
TTTGCCTCTCGGTCCTACTTCTTTGACCGGGCTGGGCACTGTGAAGATGAGGGCTGCTCCTGGG
AGCACAGCCGGGGTGAGAGCACCAGTATGTCGGGCAGTCTAGGCTCTGGGAGCTGGTATGGTGC
CATCGGGCGTGAGCCGGGCTGGTATGGGGGCAGCCAGACGAAGACCACTCCTCTGCTCTTCTCC
CAGGTGCCAGGACCAGGCGGCCACCACCACAGTCTCTACTCCACCCCACAGACGTGATCCCCCT
CCCTCCCCCACAGAATACCCAGGCCCCAGTCCCCCTCACCCTAGGCCCCTGTGCCAAGTTTGTC
TGCCGCTTCTTGCCCAGGATCCTGGGGGTCGTGGCTACCCCCTCCTCTGGCCGGCTCCTTGCTG
CTCCTGTCATAGTGAGCTTGTGCCGTCCCCCTAGGATGGGGGGCATGGCCCTGGCTGCCAGATG
CCCACAGCACCCTGGCATGACCTGCCACCTCTGCTTCCACACCGGAGCCAGCTACCTCTCCTGT
GCCTGCCACTCAATAAACAGTGTCTGCGCCCCACA

hide sequence

RefSeq Acc Id:

NM_001378083 ⟹ NP_001365012

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,284,843 - 64,289,494 (+)	NCBI
T2T-CHM13v2.0	11	64,274,807 - 64,279,458 (+)	NCBI

Sequence:

show sequence

CTCCCTCCTTCGGCCCCGGGGCTCACATCCTCGCTGCCTCACACCTTGGGCGTGTGTGGGAGCA
GGAGAGGGATTCTCTGGGGTCCCCATTTGGAACCTGGAGACCCACTTCTGCCAACAAGTCCTTC
AGCCCCTCTGGGCCTTAGTTTCCCCCCAGTGAAGTGGGGATAGTGACAGCTCCCCCGGGAGCCA
GTGAAAACTTTGTGAAGGGAGTGATTACTGCGGGCGAAGGCGCTTGGCACAGCCACAACTGAAG
CTCAGCCGTCGGATGTGATTATTGTTGCTATTGTTACCGCTCCGCCTGGACTGGGTGCCCGGTC
GGAAAGTCCCGCTCCCCGCTCCTCCTCCCAGGCGCGGAAGCTTCGCGCCGCCCGCCTCGGGGGA
CACCTCCCGCGCCATCTCGGGGGCACTGGAGATAAGGAAAGGAACCTCCTCCCTGGCTGGGATG
GCTGCCCGGGCGCGGGAGGAGGGCCGGGGACCCGGTGAGGGAGGACCGTAGGGCCCGTGGGGGC
TTCACGCCTGGCAGGCGGCCGGCCAGGCCTCCCTCCCTGACATGGAGAGTAACCTGTCTGGCCT
GGTGCCTGCTGCCGGGCTGGTGCCTGCGCTGCCACCTGCTGTGACCCTGGGGCTGACAGCTGCC
TACACCACCCTGTATGCCCTGCTCTTCTTCTCCGTCTATGCCCAGCTCTGGCTGGTGCTTCTGT
ATGGGCACAAGCGTCTCAGCTATCAGACGGTGTTCCTGGCCCTCTGTCTGCTCTGGGCCGCCTT
GCGTACCACCCTCTTCTCCTTCTACTTCCGAGATACTCCCCGCGCCAACCGCCTGGGGCCCTTG
CCCTTCTGGCTTCTCTACTGCTGCCCCGTCTGCCTGCAGTTCTTCACCTTGACGCTTATGAACC
TCTACTTTGCCCAGGTGGTGTTCAAGGCCAAGGTGAAGCGTCGGCCGGAGATGAGCCGAGGCTT
GCTCGCTGTCCGAGGGGCCTTTGTGGGGGCCTCGCTGCTCTTTCTGCTGGTGAACGTGCTGTGT
GCTGTGCTCTCCCATCGGCGCCGGGCACAGCCCTGGGCCCTGCTGCTTGTCCGCGTCCTGGTGA
GCGACTCCCTGTTCGTCATCTGCGCGCTGTCTCTTGCTGCCTGCCTCTGCCTCGTCGCCAGGCG
GGCGCCCTCCACTAGCATCTACCTGGAGGCCAAGGGGACCAGTGTGTGCCAGGCGGCCGCGATG
GGTGGCGCCATGGTCCTGCTCTATGCCAGCCGGGCCTGCTACAACCTGACAGCACTGGCCTTGG
CCCCCCAGAGCCGGCTGGACACCTTCGATTACGACTGGTACAATGTGTCTGACCAGGCGGACCT
GGTGAATGACCTGGGGAACAAAGGCTACCTGGTATTTGGCCTCATCCTCTTCGTGTGGGAGCTA
CTGCCCACCACCCTGCTGGTGGGCTTCTTCCGGGTGCACCGGCCCCCACAGGACCTGAGCACCA
GCCACATCCTCAATGGGCAGGTCTTTGCCTCTCGGTCCTACTTCTTTGACCGGGCTGGGCACTG
TGAAGATGAGGGCTGCTCCTGGGAGCACAGCCGGGGTGAGAGCACCAGGTGCCAGGACCAGGCG
GCCACCACCACAGTCTCTACTCCACCCCACAGACGTGATCCCCCTCCCTCCCCCACAGAATACC
CAGGCCCCAGTCCCCCTCACCCTAGGCCCCTGTGCCAAGTTTGTCTGCCGCTTCTTGCCCAGGA
TCCTGGGGGTCGTGGCTACCCCCTCCTCTGGCCGGCTCCTTGCTGCTCCTGTCATAGTGAGCTT
GTGCCGTCCCCCTAGGATGGGGGGCATGGCCCTGGCTGCCAGATGCCCACAGCACCCTGGCATG
ACCTGCCACCTCTGCTTCCACACCGGAGCCAGCTACCTCTCCTGTGCCTGCCACTCAATAAACA
GTGTCTGCGCCCCACA

hide sequence

RefSeq Acc Id:

NM_001378084 ⟹ NP_001365013

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,270,531 - 64,289,494 (+)	NCBI
T2T-CHM13v2.0	11	64,260,559 - 64,279,458 (+)	NCBI

Sequence:

show sequence

AGATCCCAGGAACTCCGTGCCGGAGACGGGAAGAGAGGATGCCTAGGGCCCTAAATGGAAAGGC
CAGAGCTGGAGACCTAGCACCCAGAAGATGAGACCGCAATTCGAGAATCAAAGGGCCGGGAGCG
ATGGCCTCCCTCCCTGACATGGAGAGTAACCTGTCTGGCCTGGTGCCTGCTGCCGGGCTGGTGC
CTGCGCTGCCACCTGCTGTGACCCTGGGGCTGACAGCTGCCTACACCACCCTGTATGCCCTGCT
CTTCTTCTCCGTCTATGCCCAGCTCTGGCTGGTGCTTCTGTATGGGCACAAGCGTCTCAGCTAT
CAGACGGTGTTCCTGGCCCTCTGTCTGCTCTGGGCCGCCTTGCGTACCACCCTCTTCTCCTTCT
ACTTCCGAGATACTCCCCGCGCCAACCGCCTGGGGCCCTTGCCCTTCTGGCTTCTCTACTGCTG
CCCCGTCTGCCTGCAGTTCTTCACCTTGACGCTTATGAACCTCTACTTTGCCCAGGTGGTGTTC
AAGGCCAAGGTGAAGCGTCGGCCGGAGATGAGCCGAGGCTTGCTCGCTGTCCGAGGGGCCTTTG
TGGGGGCCTCGCTGCTCTTTCTGCTGGTGAACGTGCTGTGTGCTGTGCTCTCCCATCGGCGCCG
GGCACAGCCCTGGGCCCTGCTGCTTGTCCGCGTCCTGGTGAGCGACTCCCTGTTCGTCATCTGC
GCGCTGTCTCTTGCTGCCTGCCTCTGCCTCGTCGCCAGGCGGGCGCCCTCCACTAGCATCTACC
TGGAGGCCAAGGGGACCAGTGTGTGCCAGGCGGCCGCGATGGGTGGCGCCATGGTCCTGCTCTA
TGCCAGCCGGGCCTGCTACAACCTGACAGCACTGGCCTTGGCCCCCCAGAGCCGGCTGGACACC
TTCGATTACGACTGGTACAATGTGTCTGACCAGGCGGACCTGGTGAATGACCTGGGGAACAAAG
GCTACCTGGTATTTGGCCTCATCCTCTTCGTGTGGGAGCTACTGCCCACCACCCTGCTGGTGGG
CTTCTTCCGGGTGCACCGGCCCCCACAGGACCTGTATGTCGGGCAGTCTAGGCTCTGGGAGCTG
GTATGGTGCCATCGGGCGTGAGCCGGGCTGGTATGGGGGCAGCCAGACGAAGACCACTCCTCTG
CTCTTCTCCCAGGTGCCAGGACCAGGCGGCCACCACCACAGTCTCTACTCCACCCCACAGACGT
GATCCCCCTCCCTCCCCCACAGAATACCCAGGCCCCAGTCCCCCTCACCCTAGGCCCCTGTGCC
AAGTTTGTCTGCCGCTTCTTGCCCAGGATCCTGGGGGTCGTGGCTACCCCCTCCTCTGGCCGGC
TCCTTGCTGCTCCTGTCATAGTGAGCTTGTGCCGTCCCCCTAGGATGGGGGGCATGGCCCTGGC
TGCCAGATGCCCACAGCACCCTGGCATGACCTGCCACCTCTGCTTCCACACCGGAGCCAGCTAC
CTCTCCTGTGCCTGCCACTCAATAAACAGTGTCTGCGCCCCACA

hide sequence

RefSeq Acc Id:

NM_001378085 ⟹ NP_001365014

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,285,848 - 64,289,494 (+)	NCBI
T2T-CHM13v2.0	11	64,275,812 - 64,279,458 (+)	NCBI

Sequence:

show sequence

GGAGCAGCGGGAGCCGGGGAGCCGGAGCCCCGGGTCCCCACGACCTGAGCCGGCTCTCCCATCA
GCGGCCTGAGGACCTGGCGTCCGCCTCCTCCCTCCCCTTGAGGCTGGAGCGTGGACGCGGTGGG
GGAGGGTGGGGCGGGGGCAGCTTTCGAGAATTACGAGGACAGGAGGCAGAGGCCCTCCCCATCC
GCATTATTGGAGGAGAGAGAGCCTCCCCCAGCTTGGGGAGGGGGAGAGCGGGGCATTGGGCGCC
CCTCGCAGCGGCCGCTGCCCTGACCCGACGGGTATCAGCCGGCTCTCCCCCTCCACCCAGGACG
ACATGAACGACCGAGGCCAGGGAGTCCTCTCCTTGGGCCTCTGCATCCCCCCATCCTTGGCTCT
GGGGTAGGCCCAGGGAGGAGACACCCCCAACCCCTATCCGGTCTGTCCTGGAGAAAAGAGACTG
CCCTTCCATGCCCCTGAGTGAGGGGCCTGGGGCCCAGGCTGCCTGTGTTCCCCAAGGGCAAGGG
TCTCTCTGTTGAGGAGGAGGGGCCTGTCAGCCACAACTTCTTTCCTCCTGAGCGCCCCATCTCC
CTCTCTGCACCCTGCAATTCCCACCCCTCCGTATTTATTTCCCTGGTCCCGCCGACAGTCCCTC
CTTGTCTGTCTCCGGGATTCAGGCCTCCCTCCCTGACATGGAGAGTAACCTGTCTGGCCTGGTG
CCTGCTGCCGGGCTGGTGCCTGCGCTGCCACCTGCTGTGACCCTGGGGCTGACAGCTGCCTACA
CCACCCTGTATGCCCTGCTCTTCTTCTCCGTCTATGCCCAGCTCTGGCTGGTGCTTCTGTATGG
GCACAAGCGTCTCAGCTATCAGACGGTGTTCCTGGCCCTCTGTCTGCTCTGGGCCGCCTTGCGT
ACCACCCTCTTCTCCTTCTACTTCCGAGATACTCCCCGCGCCAACCGCCTGGGGCCCTTGCCCT
TCTGGCTTCTCTACTGCTGCCCCGTCTGCCTGCAGTTCTTCACCTTGACGCTTATGAACCTCTA
CTTTGCCCAGGTGGTGTTCAAGGCCAAGGTGAAGCGTCGGCCGGAGATGAGCCGAGGCTTGCTC
GCTGTCCGAGGGGCCTTTGTGGGGGCCTCGCTGCTCTTTCTGCTGGTGAACGTGCTGTGTGCTG
TGCTCTCCCATCGGCGCCGGGCACAGCCCTGGGCCCTGCTGCTTGTCCGCGTCCTGGTGAGCGA
CTCCCTGTTCGTCATCTGCGCGCTGTCTCTTGCTGCCTGCCTCTGCCTCGTCGCCAGGCGGGCG
CCCTCCACTAGCATCTACCTGGAGGCCAAGGGGACCAGTGTGTGCCAGGCGGCCGCGATGGGTG
GCGCCATGGTCCTGCTCTATGCCAGCCGGGCCTGCTACAACCTGACAGCACTGGCCTTGGCCCC
CCAGAGCCGGCTGGACACCTTCGATTACGACTGGTACAATGTGTCTGACCAGGCGGACCTGGTG
AATGACCTGGGGAACAAAGGCTACCTGGTATTTGGCCTCATCCTCTTCGTGTGGGAGCTACTGC
CCACCACCCTGCTGGTGGGCTTCTTCCGGGTGCACCGGCCCCCACAGGACCTGTATGTCGGGCA
GTCTAGGCTCTGGGAGCTGGTATGGTGCCATCGGGCGTGAGCCGGGCTGGTATGGGGGCAGCCA
GACGAAGACCACTCCTCTGCTCTTCTCCCAGGTGCCAGGACCAGGCGGCCACCACCACAGTCTC
TACTCCACCCCACAGACGTGATCCCCCTCCCTCCCCCACAGAATACCCAGGCCCCAGTCCCCCT
CACCCTAGGCCCCTGTGCCAAGTTTGTCTGCCGCTTCTTGCCCAGGATCCTGGGGGTCGTGGCT
ACCCCCTCCTCTGGCCGGCTCCTTGCTGCTCCTGTCATAGTGAGCTTGTGCCGTCCCCCTAGGA
TGGGGGGCATGGCCCTGGCTGCCAGATGCCCACAGCACCCTGGCATGACCTGCCACCTCTGCTT
CCACACCGGAGCCAGCTACCTCTCCTGTGCCTGCCACTCAATAAACAGTGTCTGCGCCCCACA

hide sequence

RefSeq Acc Id:

NM_001378086 ⟹ NP_001365015

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,284,843 - 64,289,494 (+)	NCBI
T2T-CHM13v2.0	11	64,274,807 - 64,279,458 (+)	NCBI

Sequence:

show sequence

CTCCCTCCTTCGGCCCCGGGGCTCACATCCTCGCTGCCTCACACCTTGGGCGTGTGTGGGAGCA
GGAGAGGGATTCTCTGGGGTCCCCATTTGGAACCTGGAGACCCACTTCTGCCAACAAGTCCTTC
AGCCCCTCTGGGCCTTAGTTTCCCCCCAGTGAAGTGGGGATAGTGACAGCTCCCCCGGGAGCCA
GTGAAAACTTTGTGAAGGGAGTGATTACTGCGGGCGAAGGCGCTTGGCACAGCCACAACTGAAG
CTCAGCCGTCGGATGTGATTATTGTTGCTATTGTTACCGCTCCGCCTGGACTGGGTGCCCGGTC
GGAAAGTCCCGCTCCCCGCTCCTCCTCCCAGGCGCGGAAGCTTCGCGCCGCCCGCCTCGGGGGA
CACCTCCCGCGCCATCTCGGGGGCACTGGAGATAAGGAAAGGAACCTCCTCCCTGGCTGGGATG
GCTGCCCGGGCGCGGGAGGAGGGCCGGGGACCCGGTGAGGGAGGACCGTAGGGCCCGTGGGGGC
TTCACGCCTGGCAGGCGGCCGGCCAGGCCTCCCTCCCTGACATGGAGAGTAACCTGTCTGGCCT
GGTGCCTGCTGCCGGGCTGGTGCCTGCGCTGCCACCTGCTGTGACCCTGGGGCTGACAGCTGCC
TACACCACCCTGTATGCCCTGCTCTTCTTCTCCGTCTATGCCCAGCTCTGGCTGGTGCTTCTGT
ATGGGCACAAGCGTCTCAGCTATCAGACGGTGTTCCTGGCCCTCTGTCTGCTCTGGGCCGCCTT
GCGTACCACCCTCTTCTCCTTCTACTTCCGAGATACTCCCCGCGCCAACCGCCTGGGGCCCTTG
CCCTTCTGGCTTCTCTACTGCTGCCCCGTCTGCCTGCAGTTCTTCACCTTGACGCTTATGAACC
TCTACTTTGCCCAGGTGGTGTTCAAGGCCAAGGTGAAGCGTCGGCCGGAGATGAGCCGAGGCTT
GCTCGCTGTCCGAGGGGCCTTTGTGGGGGCCTCGCTGCTCTTTCTGCTGGTGAACGTGCTGTGT
GCTGTGCTCTCCCATCGGCGCCGGGCACAGCCCTGGGCCCTGCTGCTTGTCCGCGTCCTGGTGA
GCGACTCCCTGTTCGTCATCTGCGCGCTGTCTCTTGCTGCCTGCCTCTGCCTCGTCGCCAGGCG
GGCGCCCTCCACTAGCATCTACCTGGAGGCCAAGGGGACCAGTGTGTGCCAGGCGGCCGCGATG
GGTGGCGCCATGGTCCTGCTCTATGCCAGCCGGGCCTGCTACAACCTGACAGCACTGGCCTTGG
CCCCCCAGAGCCGGCTGGACACCTTCGATTACGACTGGTACAATGTGTCTGACCAGGCGGACCT
GGTGAATGACCTGGGGAACAAAGGCTACCTGGTATTTGGCCTCATCCTCTTCGTGTGGGAGCTA
CTGCCCACCACCCTGCTGGTGGGCTTCTTCCGGGTGCACCGGCCCCCACAGGACCTGTATGTCG
GGCAGTCTAGGCTCTGGGAGCTGGTATGGTGCCATCGGGCGTGAGCCGGGCTGGTATGGGGGCA
GCCAGACGAAGACCACTCCTCTGCTCTTCTCCCAGGTGCCAGGACCAGGCGGCCACCACCACAG
TCTCTACTCCACCCCACAGACGTGATCCCCCTCCCTCCCCCACAGAATACCCAGGCCCCAGTCC
CCCTCACCCTAGGCCCCTGTGCCAAGTTTGTCTGCCGCTTCTTGCCCAGGATCCTGGGGGTCGT
GGCTACCCCCTCCTCTGGCCGGCTCCTTGCTGCTCCTGTCATAGTGAGCTTGTGCCGTCCCCCT
AGGATGGGGGGCATGGCCCTGGCTGCCAGATGCCCACAGCACCCTGGCATGACCTGCCACCTCT
GCTTCCACACCGGAGCCAGCTACCTCTCCTGTGCCTGCCACTCAATAAACAGTGTCTGCGCCCC
ACA

hide sequence

RefSeq Acc Id:

NM_001378087 ⟹ NP_001365016

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,284,843 - 64,289,494 (+)	NCBI
T2T-CHM13v2.0	11	64,274,807 - 64,279,458 (+)	NCBI

Sequence:

show sequence

CTCCCTCCTTCGGCCCCGGGGCTCACATCCTCGCTGCCTCACACCTTGGGCGTGTGTGGGAGCA
GGAGAGGGATTCTCTGGGGTCCCCATTTGGAACCTGGAGACCCACTTCTGCCAACAAGTCCTTC
AGCCCCTCTGGGCCTTAGTTTCCCCCCAGTGAAGTGGGGATAGTGACAGCTCCCCCGGGAGCCA
GTGAAAACTTTGTGAAGGGAGTGATTACTGCGGGCGAAGGCGCTTGGCACAGCCACAACTGAAG
CTCAGCCGTCGGATGTGATTATTGTTGCTATTGTTACCGCTCCGCCTGGACTGGGTGCCCGGTC
GGAAAGTCCCGCTCCCCGCTCCTCCTCCCAGGCGCGGAAGCTTCGCGCCGCCCGCCTCGGGGGA
CACCTCCCGCGCCATCTCGGGGGCACTGGAGATAAGGAAAGGAACCTCCTCCCTGGCTGGGATG
GCTGCCCGGGCGCGGGAGGAGGGCCGGGGACCCGGTGAGGGAGGACCGTAGGGCCCGTGGGGGC
TTCACGCCTGGCAGGCGGCCGGCCAGGCCTCCCTCCCTGACATGGAGAGTAACCTGTCTGGCCT
GGTGCCTGCTGCCGGGCTGGTGCCTGCGCTGCCACCTGCTGTGACCCTGGGGCTGACAGCTGCC
TACACCACCCTGTATGCCCTGCTCTTCTTCTCCGTCTATGCCCAGCTCTGGCTGGTGCTTCTGT
ATGGGCACAAGCGTCTCAGCTATCAGACGGTGTTCCTGGCCCTCTGTCTGCTCTGGGCCGCCTT
GCGTACCACCCTCTTCTCCTTCTACTTCCGAGATACTCCCCGCGCCAACCGCCTGGGGCCCTTG
CCCTTCTGGCTTCTCTACTGCTGCCCCGTCTGCCTGCAGTTCTTCACCTTGACGCTTATGAACC
TCTACTTTGCCCAGGTGGTGTTCAAGGCCAAGGTGAAGCGTCGGCCGGAGATGAGCCGAGGCTT
GCTCGCTGTCCGAGGGGCCTTTGTGGGGGCCTCGCTGCTCTTTCTGCTGGTGAACGTGCTGTGT
GCTGTGCTCTCCCATCGGCGCCGGGCACAGCCCTGGGCCCTGCTGCTTGTCCGCGTCCTGGTGA
GCGACTCCCTGTTCGTCATCTGCGCGCTGTCTCTTGCTGCCTGCCTCTGCCTCGTCGCCAGGCG
GGCGCCCTCCACTAGCATCTACCTGGAGGCCAAGGCGGACCTGGTGAATGACCTGGGGAACAAA
GGCTACCTGGTATTTGGCCTCATCCTCTTCGTGTGGGAGCTACTGCCCACCACCCTGCTGGTGG
GCTTCTTCCGGGTGCACCGGCCCCCACAGGACCTGAGCACCAGCCACATCCTCAATGGGCAGGT
CTTTGCCTCTCGGTCCTACTTCTTTGACCGGGCTGGGCACTGTGAAGATGAGGGCTGCTCCTGG
GAGCACAGCCGGGGTGAGAGCACCAGGTGCCAGGACCAGGCGGCCACCACCACAGTCTCTACTC
CACCCCACAGACGTGATCCCCCTCCCTCCCCCACAGAATACCCAGGCCCCAGTCCCCCTCACCC
TAGGCCCCTGTGCCAAGTTTGTCTGCCGCTTCTTGCCCAGGATCCTGGGGGTCGTGGCTACCCC
CTCCTCTGGCCGGCTCCTTGCTGCTCCTGTCATAGTGAGCTTGTGCCGTCCCCCTAGGATGGGG
GGCATGGCCCTGGCTGCCAGATGCCCACAGCACCCTGGCATGACCTGCCACCTCTGCTTCCACA
CCGGAGCCAGCTACCTCTCCTGTGCCTGCCACTCAATAAACAGTGTCTGCGCCCCACA

hide sequence

RefSeq Acc Id:

NM_001378088 ⟹ NP_001365017

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,285,848 - 64,289,494 (+)	NCBI
T2T-CHM13v2.0	11	64,275,812 - 64,279,458 (+)	NCBI

Sequence:

show sequence

GGAGCAGCGGGAGCCGGGGAGCCGGAGCCCCGGGTCCCCACGACCTGAGCCGGCTCTCCCATCA
GCGGCCTGAGGACCTGGCGTCCGCCTCCTCCCTCCCCTTGAGGCTGGAGCGTGGACGCGGTGGG
GGAGGGTGGGGCGGGGGCAGCTTTCGAGAATTACGAGGACAGGAGGCAGAGGCCCTCCCCATCC
GCATTATTGGAGGAGAGAGAGCCTCCCCCAGCTTGGGGAGGGGGAGAGCGGGGCATTGGGCGCC
CCTCGCAGCGGCCGCTGCCCTGACCCGACGGGTATCAGCCGGCTCTCCCCCTCCACCCAGGACG
ACATGAACGACCGAGGCCAGGGAGTCCTCTCCTTGGGCCTCTGCATCCCCCCATCCTTGGCTCT
GGGGTAGGCCCAGGGAGGAGACACCCCCAACCCCTATCCGGTCTGTCCTGGAGAAAAGAGACTG
CCCTTCCATGCCCCTGAGTGAGGGGCCTGGGGCCCAGGCTGCCTGTGTTCCCCAAGGGCAAGGG
TCTCTCTGTTGAGGAGGAGGGGCCTGTCAGCCACAACTTCTTTCCTCCTGAGCGCCCCATCTCC
CTCTCTGCACCCTGCAATTCCCACCCCTCCGTATTTATTTCCCTGGTCCCGCCGACAGTCCCTC
CTTGTCTGTCTCCGGGATTCAGGCCTCCCTCCCTGACATGGAGAGTAACCTGTCTGGCCTGGTG
CCTGCTGCCGGGCTGGTGCCTGCGCTGCCACCTGCTGTGACCCTGGGGCTGACAGCTGCCTACA
CCACCCTGTATGCCCTGCTCTTCTTCTCCGTCTATGCCCAGCTCTGGCTGGTGCTTCTGTATGG
GCACAAGCGTCTCAGCTATCAGACGGTGTTCCTGGCCCTCTGTCTGCTCTGGGCCGCCTTGCGT
ACCACCCTCTTCTCCTTCTACTTCCGAGATACTCCCCGCGCCAACCGCCTGGGGCCCTTGCCCT
TCTGGCTTCTCTACTGCTGCCCCGTCTGCCTGCAGTTCTTCACCTTGACGCTTATGAACCTCTA
CTTTGCCCAGGTGGTGTTCAAGGCCAAGGTGAAGCGTCGGCCGGAGATGAGCCGAGGCTTGCTC
GCTGTCCGAGGGGCCTTTGTGGGGGCCTCGCTGCTCTTTCTGCTGGTGAACGTGCTGTGTGCTG
TGCTCTCCCATCGGCGCCGGGCACAGCCCTGGGCCCTGCTGCTTGTCCGCGTCCTGGTGAGCGA
CTCCCTGTTCGTCATCTGCGCGCTGTCTCTTGCTGCCTGCCTCTGCCTCGTCGCCAGGCGGGCG
CCCTCCACTAGCATCTACCTGGAGGCCAAGGCGGACCTGGTGAATGACCTGGGGAACAAAGGCT
ACCTGGTATTTGGCCTCATCCTCTTCGTGTGGGAGCTACTGCCCACCACCCTGCTGGTGGGCTT
CTTCCGGGTGCACCGGCCCCCACAGGACCTGAGCACCAGCCACATCCTCAATGGGCAGGTCTTT
GCCTCTCGGTCCTACTTCTTTGACCGGGCTGGGCACTGTGAAGATGAGGGCTGCTCCTGGGAGC
ACAGCCGGGGTGAGAGCACCAGGTGCCAGGACCAGGCGGCCACCACCACAGTCTCTACTCCACC
CCACAGACGTGATCCCCCTCCCTCCCCCACAGAATACCCAGGCCCCAGTCCCCCTCACCCTAGG
CCCCTGTGCCAAGTTTGTCTGCCGCTTCTTGCCCAGGATCCTGGGGGTCGTGGCTACCCCCTCC
TCTGGCCGGCTCCTTGCTGCTCCTGTCATAGTGAGCTTGTGCCGTCCCCCTAGGATGGGGGGCA
TGGCCCTGGCTGCCAGATGCCCACAGCACCCTGGCATGACCTGCCACCTCTGCTTCCACACCGG
AGCCAGCTACCTCTCCTGTGCCTGCCACTCAATAAACAGTGTCTGCGCCCCACA

hide sequence

RefSeq Acc Id:

NM_001378089 ⟹ NP_001365018

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,285,848 - 64,289,494 (+)	NCBI
T2T-CHM13v2.0	11	64,275,812 - 64,279,458 (+)	NCBI

Sequence:

show sequence

GGAGCAGCGGGAGCCGGGGAGCCGGAGCCCCGGGTCCCCACGACCTGAGCCGGCTCTCCCATCA
GCGGCCTGAGGACCTGGCGTCCGCCTCCTCCCTCCCCTTGAGGCTGGAGCGTGGACGCGGTGGG
GGAGGGTGGGGCGGGGGCAGCTTTCGAGAATTACGAGGACAGGAGGCAGAGGCCCTCCCCATCC
GCATTATTGGAGGAGAGAGAGCCTCCCCCAGCTTGGGGAGGGGGAGAGCGGGGCATTGGGCGCC
CCTCGCAGCGGCCGCTGCCCTGACCCGACGGGTATCAGCCGGCTCTCCCCCTCCACCCAGGACG
ACATGAACGACCGAGGCCAGGGAGTCCTCTCCTTGGGCCTCTGCATCCCCCCATCCTTGGCTCT
GGGGCCTCCCTCCCTGACATGGAGAGTAACCTGTCTGGCCTGGTGCCTGCTGCCGGGCTGGTGC
CTGCGCTGCCACCTGCTGTGACCCTGGGGCTGACAGCTGCCTACACCACCCTGTATGCCCTGCT
CTTCTTCTCCGTCTATGCCCAGCTCTGGCTGGTGCTTCTGTATGGGCACAAGCGTCTCAGCTAT
CAGACGGTGTTCCTGGCCCTCTGTCTGCTCTGGGCCGCCTTGCGTACCACCCTCTTCTCCTTCT
ACTTCCGAGATACTCCCCGCGCCAACCGCCTGGGGCCCTTGCCCTTCTGGCTTCTCTACTGCTG
CCCCGTCTGCCTGCAGTTCTTCACCTTGACGCTTATGAACCTCTACTTTGCCCAGGTGGTGTTC
AAGGCCAAGGTGAAGCGTCGGCCGGAGATGAGCCGAGGCTTCGGTTCTCAGGGTGTAGAGGAAG
CTGGGAGCCTTCTCTCCCTGAGGGTCCTCTGTTGTTACCTGTGCCAGGGGACCAGTGTGTGCCA
GGCGGCCGCGATGGGTGGCGCCATGGTCCTGCTCTATGCCAGCCGGGCCTGCTACAACCTGACA
GCACTGGCCTTGGCCCCCCAGAGCCGGCTGGACACCTTCGATTACGACTGGTACAATGTGTCTG
ACCAGGCGGACCTGGTGAATGACCTGGGGAACAAAGGCTACCTGGTATTTGGCCTCATCCTCTT
CGTGTGGGAGCTACTGCCCACCACCCTGCTGGTGGGCTTCTTCCGGGTGCACCGGCCCCCACAG
GACCTGAGCACCAGCCACATCCTCAATGGGCAGGTCTTTGCCTCTCGGTCCTACTTCTTTGACC
GGGCTGGGCACTGTGAAGATGAGGGCTGCTCCTGGGAGCACAGCCGGGGTGAGAGCACCAGTAT
GTCGGGCAGTCTAGGCTCTGGGAGCTGGTATGGTGCCATCGGGCGTGAGCCGGGCTGGTATGGG
GGCAGCCAGACGAAGACCACTCCTCTGCTCTTCTCCCAGGTGCCAGGACCAGGCGGCCACCACC
ACAGTCTCTACTCCACCCCACAGACGTGATCCCCCTCCCTCCCCCACAGAATACCCAGGCCCCA
GTCCCCCTCACCCTAGGCCCCTGTGCCAAGTTTGTCTGCCGCTTCTTGCCCAGGATCCTGGGGG
TCGTGGCTACCCCCTCCTCTGGCCGGCTCCTTGCTGCTCCTGTCATAGTGAGCTTGTGCCGTCC
CCCTAGGATGGGGGGCATGGCCCTGGCTGCCAGATGCCCACAGCACCCTGGCATGACCTGCCAC
CTCTGCTTCCACACCGGAGCCAGCTACCTCTCCTGTGCCTGCCACTCAATAAACAGTGTCTGCG
CCCCACA

hide sequence

RefSeq Acc Id:

NM_020155 ⟹ NP_064540

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,285,848 - 64,289,494 (+)	NCBI
GRCh37	11	64,051,781 - 64,056,972 (+)	NCBI
Build 36	11	63,809,907 - 63,813,539 (+)	NCBI Archive
Celera	11	61,378,710 - 61,383,871 (+)	RGD
HuRef	11	60,379,535 - 60,384,696 (+)	RGD
CHM1_1	11	63,936,579 - 63,939,969 (+)	NCBI
T2T-CHM13v2.0	11	64,275,812 - 64,279,458 (+)	NCBI

Sequence:

show sequence

GGAGCAGCGGGAGCCGGGGAGCCGGAGCCCCGGGTCCCCACGACCTGAGCCGGCTCTCCCATCA
GCGGCCTGAGGACCTGGCGTCCGCCTCCTCCCTCCCCTTGAGGCTGGAGCGTGGACGCGGTGGG
GGAGGGTGGGGCGGGGGCAGCTTTCGAGAATTACGAGGACAGGAGGCAGAGGCCCTCCCCATCC
GCATTATTGGAGGAGAGAGAGCCTCCCCCAGCTTGGGGAGGGGGAGAGCGGGGCATTGGGCGCC
CCTCGCAGCGGCCGCTGCCCTGACCCGACGGGTATCAGCCGGCTCTCCCCCTCCACCCAGGACG
ACATGAACGACCGAGGCCAGGGAGTCCTCTCCTTGGGCCTCTGCATCCCCCCATCCTTGGCTCT
GGGGTAGGCCCAGGGAGGAGACACCCCCAACCCCTATCCGGTCTGTCCTGGAGAAAAGAGACTG
CCCTTCCATGCCCCTGAGTGAGGGGCCTGGGGCCCAGGCTGCCTGTGTTCCCCAAGGGCAAGGG
TCTCTCTGTTGAGGAGGAGGGGCCTGTCAGCCACAACTTCTTTCCTCCTGAGCGCCCCATCTCC
CTCTCTGCACCCTGCAATTCCCACCCCTCCGTATTTATTTCCCTGGTCCCGCCGACAGTCCCTC
CTTGTCTGTCTCCGGGATTCAGGCCTCCCTCCCTGACATGGAGAGTAACCTGTCTGGCCTGGTG
CCTGCTGCCGGGCTGGTGCCTGCGCTGCCACCTGCTGTGACCCTGGGGCTGACAGCTGCCTACA
CCACCCTGTATGCCCTGCTCTTCTTCTCCGTCTATGCCCAGCTCTGGCTGGTGCTTCTGTATGG
GCACAAGCGTCTCAGCTATCAGACGGTGTTCCTGGCCCTCTGTCTGCTCTGGGCCGCCTTGCGT
ACCACCCTCTTCTCCTTCTACTTCCGAGATACTCCCCGCGCCAACCGCCTGGGGCCCTTGCCCT
TCTGGCTTCTCTACTGCTGCCCCGTCTGCCTGCAGTTCTTCACCTTGACGCTTATGAACCTCTA
CTTTGCCCAGGTGGTGTTCAAGGCCAAGGTGAAGCGTCGGCCGGAGATGAGCCGAGGCTTGCTC
GCTGTCCGAGGGGCCTTTGTGGGGGCCTCGCTGCTCTTTCTGCTGGTGAACGTGCTGTGTGCTG
TGCTCTCCCATCGGCGCCGGGCACAGCCCTGGGCCCTGCTGCTTGTCCGCGTCCTGGTGAGCGA
CTCCCTGTTCGTCATCTGCGCGCTGTCTCTTGCTGCCTGCCTCTGCCTCGTCGCCAGGCGGGCG
CCCTCCACTAGCATCTACCTGGAGGCCAAGGGGACCAGTGTGTGCCAGGCGGCCGCGATGGGTG
GCGCCATGGTCCTGCTCTATGCCAGCCGGGCCTGCTACAACCTGACAGCACTGGCCTTGGCCCC
CCAGAGCCGGCTGGACACCTTCGATTACGACTGGTACAATGTGTCTGACCAGGCGGACCTGGTG
AATGACCTGGGGAACAAAGGCTACCTGGTATTTGGCCTCATCCTCTTCGTGTGGGAGCTACTGC
CCACCACCCTGCTGGTGGGCTTCTTCCGGGTGCACCGGCCCCCACAGGACCTGAGCACCAGCCA
CATCCTCAATGGGCAGGTCTTTGCCTCTCGGTCCTACTTCTTTGACCGGGCTGGGCACTGTGAA
GATGAGGGCTGCTCCTGGGAGCACAGCCGGGGTGAGAGCACCAGGTGCCAGGACCAGGCGGCCA
CCACCACAGTCTCTACTCCACCCCACAGACGTGATCCCCCTCCCTCCCCCACAGAATACCCAGG
CCCCAGTCCCCCTCACCCTAGGCCCCTGTGCCAAGTTTGTCTGCCGCTTCTTGCCCAGGATCCT
GGGGGTCGTGGCTACCCCCTCCTCTGGCCGGCTCCTTGCTGCTCCTGTCATAGTGAGCTTGTGC
CGTCCCCCTAGGATGGGGGGCATGGCCCTGGCTGCCAGATGCCCACAGCACCCTGGCATGACCT
GCCACCTCTGCTTCCACACCGGAGCCAGCTACCTCTCCTGTGCCTGCCACTCAATAAACAGTGT
CTGCGCCCCACA

hide sequence

RefSeq Acc Id:

NR_165394

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,284,843 - 64,289,494 (+)	NCBI
T2T-CHM13v2.0	11	64,274,807 - 64,279,458 (+)	NCBI

Sequence:

show sequence

CTCCCTCCTTCGGCCCCGGGGCTCACATCCTCGCTGCCTCACACCTTGGGCGTGTGTGGGAGCA
GGAGAGGGATTCTCTGGGGTCCCCATTTGGAACCTGGAGACCCACTTCTGCCAACAAGTCCTTC
AGCCCCTCTGGGCCTTAGTTTCCCCCCAGTGAAGTGGGGATAGTGACAGCTCCCCCGGGAGCCA
GTGAAAACTTTGTGAAGGGAGTGATTACTGCGGGCGAAGGCGCTTGGCACAGCCACAACTGAAG
CTCAGCCGTCGGATGTGATTATTGTTGCTATTGTTACCGCTCCGCCTGGACTGGGTGCCCGGTC
GGAAAGTCCCGCTCCCCGCTCCTCCTCCCAGGCGCGGAAGCTTCGCGCCGCCCGCCTCGGGGGA
CACCTCCCGCGCCATCTCGGGGGCACTGGAGATAAGGAAAGGAACCTCCTCCCTGGCTGGGATG
GCTGCCCGGGCGCGGGAGGAGGGCCGGGGACCCGGTGAGGGAGGACCGTAGGGCCCGTGGGGGC
TTCACGCCTGGCAGGCGGCCGGCCAGGCCTCCCTCCCTGACATGGAGAGTAACCTGTCTGGCCT
GGTGCCTGCTGCCGGGCTGGTGCCTGCGCTGCCACCTGCTGTGACCCTGGGGCTGACAGCTGCC
TACACCACCCTGTATGCCCTGCTCTTCTTCTCCGTCTATGCCCAGCTCTGGCTGGTGCTTCTGT
ATGGGCACAAGCGTCTCAGCTATCAGACGGTGTTCCTGGCCCTCTGTCTGCTCTGGGCCGCCTT
GCGTACCACCCTCTTCTCCTTCTACTTCCGAGATACTCCCCGCGCCAACCGCCTGGGGCCCTTG
CCCTTCTGGCTTCTCTACTGCTGCCCCGTCTGCCTGCAGTTCTTCACCTTGACGCTTATGAACC
TCTACTTTGCCCAGGTGGTGTTCAAGGCCAAGGTGAAGCGTCGGCCGGAGATGAGCCGAGGCTT
GCGGACCTGGTGAATGACCTGGGGAACAAAGGCTACCTGGTATTTGGCCTCATCCTCTTCGTGT
GGGAGCTACTGCCCACCACCCTGCTGGTGGGCTTCTTCCGGGTGCACCGGCCCCCACAGGACCT
GAGCACCAGCCACATCCTCAATGGGCAGGTCTTTGCCTCTCGGTCCTACTTCTTTGACCGGGCT
GGGCACTGTGAAGATGAGGGCTGCTCCTGGGAGCACAGCCGGGGTGAGAGCACCAGTATGTCGG
GCAGTCTAGGCTCTGGGAGCTGGTATGGTGCCATCGGGCGTGAGCCGGGCTGGTATGGGGGCAG
CCAGACGAAGACCACTCCTCTGCTCTTCTCCCAGGTGCCAGGACCAGGCGGCCACCACCACAGT
CTCTACTCCACCCCACAGACGTGATCCCCCTCCCTCCCCCACAGAATACCCAGGCCCCAGTCCC
CCTCACCCTAGGCCCCTGTGCCAAGTTTGTCTGCCGCTTCTTGCCCAGGATCCTGGGGGTCGTG
GCTACCCCCTCCTCTGGCCGGCTCCTTGCTGCTCCTGTCATAGTGAGCTTGTGCCGTCCCCCTA
GGATGGGGGGCATGGCCCTGGCTGCCAGATGCCCACAGCACCCTGGCATGACCTGCCACCTCTG
CTTCCACACCGGAGCCAGCTACCTCTCCTGTGCCTGCCACTCAATAAACAGTGTCTGCGCCCCA
CA

hide sequence

RefSeq Acc Id:

NR_165395

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,284,843 - 64,289,494 (+)	NCBI
T2T-CHM13v2.0	11	64,274,807 - 64,279,458 (+)	NCBI

Sequence:

show sequence

CTCCCTCCTTCGGCCCCGGGGCTCACATCCTCGCTGCCTCACACCTTGGGCGTGTGTGGGAGCA
GGAGAGGGATTCTCTGGGGTCCCCATTTGGAACCTGGAGACCCACTTCTGCCAACAAGTCCTTC
AGCCCCTCTGGGCCTTAGTTTCCCCCCAGTGAAGTGGGGATAGTGACAGCTCCCCCGGGAGCCA
GTGAAAACTTTGTGAAGGGAGTGATTACTGCGGGCGAAGGCGCTTGGCACAGCCACAACTGAAG
CTCAGCCGTCGGATGTGATTATTGTTGCTATTGTTACCGCTCCGCCTGGACTGGGTGCCCGGTC
GGAAAGTCCCGCTCCCCGCTCCTCCTCCCAGGCGCGGAAGCTTCGCGCCGCCCGCCTCGGGGGA
CACCTCCCGCGCCATCTCGGGGGCACTGGAGATAAGGAAAGGAACCTCCTCCCTGGCTGGGATG
GCTGCCCGGGCGCGGGAGGAGGGCCGGGGACCCGGTGAGGGAGGACCGTAGGGCCCGTGGGGGC
TTCACGCCTGGCAGGCGGCCGGCCAGGCCTCCCTCCCTGACATGGAGAGTAACCTGTCTGGCCT
GGTGCCTGCTGCCGGGCTGGTGCCTGCGCTGCCACCTGCTGTGACCCTGGGGCTGACAGCTGCC
TACACCACCCTGTATGCCCTGCTCTTCTTCTCCGTCTATGCCCAGCTCTGGCTGGTGCTTCTGT
ATGGGCACAAGCGTCTCAGCTATCAGACGGTGTTCCTGGCCCTCTGTCTGCTCTGGGCCGCCTT
GCGTACCACCCTCTTCTCCTTCTACTTCCGAGATACTCCCCGCGCCAACCGCCTGGGGCCCTTG
CCCTTCTGGCTTCTCTACTGCTGCCCCGTCTGCCTGCAGTTCTTCACCTTGACGCTTATGAACC
TCTACTTTGCCCAGGTGGTGTTCAAGGCCAAGGTGAAGCGTCGGCCGGAGATGAGCCGAGGCTT
GGGACCAGTGTGTGCCAGGCGGCCGCGATGGGTGGCGCCATGGTCCTGCTCTATGCCAGCCGGG
CCTGCTACAACCTGACAGCACTGGCCTTGGCCCCCCAGAGCCGGCTGGACACCTTCGATTACGA
CTGGTACAATGTGTCTGACCAGGCGGACCTGGTGAATGACCTGGGGAACAAAGGCTACCTGGTA
TTTGGCCTCATCCTCTTCGTGTGGGAGCTACTGCCCACCACCCTGCTGGTGGGCTTCTTCCGGG
TGCACCGGCCCCCACAGGACCTGAGCACCAGCCACATCCTCAATGGGCAGGTCTTTGCCTCTCG
GTCCTACTTCTTTGACCGGGCTGGGCACTGTGAAGATGAGGGCTGCTCCTGGGAGCACAGCCGG
GGTGAGAGCACCAGTATGTCGGGCAGTCTAGGCTCTGGGAGCTGGTATGGTGCCATCGGGCGTG
AGCCGGGCTGGTATGGGGGCAGCCAGACGAAGACCACTCCTCTGCTCTTCTCCCAGGTGCCAGG
ACCAGGCGGCCACCACCACAGTCTCTACTCCACCCCACAGACGTGATCCCCCTCCCTCCCCCAC
AGAATACCCAGGCCCCAGTCCCCCTCACCCTAGGCCCCTGTGCCAAGTTTGTCTGCCGCTTCTT
GCCCAGGATCCTGGGGGTCGTGGCTACCCCCTCCTCTGGCCGGCTCCTTGCTGCTCCTGTCATA
GTGAGCTTGTGCCGTCCCCCTAGGATGGGGGGCATGGCCCTGGCTGCCAGATGCCCACAGCACC
CTGGCATGACCTGCCACCTCTGCTTCCACACCGGAGCCAGCTACCTCTCCTGTGCCTGCCACTC
AATAAACAGTGTCTGCGCCCCACA

hide sequence

RefSeq Acc Id:

NR_165396

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,285,848 - 64,289,494 (+)	NCBI
T2T-CHM13v2.0	11	64,275,812 - 64,279,458 (+)	NCBI

Sequence:

show sequence

GGAGCAGCGGGAGCCGGGGAGCCGGAGCCCCGGGTCCCCACGACCTGAGCCGGCTCTCCCATCA
GCGGCCTGAGGACCTGGCGTCCGCCTCCTCCCTCCCCTTGAGGCTGGAGCGTGGACGCGGTGGG
GGAGGGTGGGGCGGGGGCAGCTTTCGAGAATTACGAGGACAGGAGGCAGAGGCCCTCCCCATCC
GCATTATTGGAGGAGAGAGAGCCTCCCCCAGCTTGGGGAGGGGGAGAGCGGGGCATTGGGCGCC
CCTCGCAGCGGCCGCTGCCCTGACCCGACGGGTATCAGCCGGCTCTCCCCCTCCACCCAGGACG
ACATGAACGACCGAGGCCAGGGAGTCCTCTCCTTGGGCCTCTGCATCCCCCCATCCTTGGCTCT
GGGGTAGGCCCAGGGAGGAGACACCCCCAACCCCTATCCGGTCTGTCCTGGAGAAAAGAGACTG
CCCTTCCATGCCCCTGAGTGAGGGGCCTGGGGCCCAGGCTGCCTGTGTTCCCCAAGGGCAAGGG
TCTCTCTGTTGAGGAGGAGGGGCCTGTCAGCCACAACTTCTTTCCTCCTGAGCGCCCCATCTCC
CTCTCTGCACCCTGCAATTCCCACCCCTCCGTATTTATTTCCCTGGTCCCGCCGACAGTCCCTC
CTTGTCTGTCTCCGGGATTCAGGCCTCCCTCCCTGACATGGAGAGTAACCTGTCTGGCCTGGTG
CCTGCTGCCGGGCTGGTGCCTGCGCTGCCACCTGCTGTGACCCTGGGGCTGACAGCTGCCTACA
CCACCCTGTATGCCCTGCTCTTCTTCTCCGTCTATGCCCAGCTCTGGCTGGTGCTTCTGTATGG
GCACAAGCGTCTCAGCTATCAGACGGTGTTCCTGGCCCTCTGTCTGCTCTGGGCCGCCTTGCGT
ACCACCCTCTTCTCCTTCTACTTCCGAGATACTCCCCGCGCCAACCGCCTGGGGCCCTTGCCCT
TCTGGCTTCTCTACTGCTGCCCCGTCTGCCTGCAGTTCTTCACCTTGACGCTTATGAACCTCTA
CTTTGCCCAGGTGGTGTTCAAGGCCAAGGTGAAGCGTCGGCCGGAGATGAGCCGAGGCTTGCGG
ACCTGGTGAATGACCTGGGGAACAAAGGCTACCTGGTATTTGGCCTCATCCTCTTCGTGTGGGA
GCTACTGCCCACCACCCTGCTGGTGGGCTTCTTCCGGGTGCACCGGCCCCCACAGGACCTGAGC
ACCAGCCACATCCTCAATGGGCAGGTCTTTGCCTCTCGGTCCTACTTCTTTGACCGGGCTGGGC
ACTGTGAAGATGAGGGCTGCTCCTGGGAGCACAGCCGGGGTGAGAGCACCAGTATGTCGGGCAG
TCTAGGCTCTGGGAGCTGGTATGGTGCCATCGGGCGTGAGCCGGGCTGGTATGGGGGCAGCCAG
ACGAAGACCACTCCTCTGCTCTTCTCCCAGGTGCCAGGACCAGGCGGCCACCACCACAGTCTCT
ACTCCACCCCACAGACGTGATCCCCCTCCCTCCCCCACAGAATACCCAGGCCCCAGTCCCCCTC
ACCCTAGGCCCCTGTGCCAAGTTTGTCTGCCGCTTCTTGCCCAGGATCCTGGGGGTCGTGGCTA
CCCCCTCCTCTGGCCGGCTCCTTGCTGCTCCTGTCATAGTGAGCTTGTGCCGTCCCCCTAGGAT
GGGGGGCATGGCCCTGGCTGCCAGATGCCCACAGCACCCTGGCATGACCTGCCACCTCTGCTTC
CACACCGGAGCCAGCTACCTCTCCTGTGCCTGCCACTCAATAAACAGTGTCTGCGCCCCACA

hide sequence

RefSeq Acc Id:

NR_165397

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,285,848 - 64,289,494 (+)	NCBI
T2T-CHM13v2.0	11	64,275,812 - 64,279,458 (+)	NCBI

Sequence:

show sequence

GGAGCAGCGGGAGCCGGGGAGCCGGAGCCCCGGGTCCCCACGACCTGAGCCGGCTCTCCCATCA
GCGGCCTGAGGACCTGGCGTCCGCCTCCTCCCTCCCCTTGAGGCTGGAGCGTGGACGCGGTGGG
GGAGGGTGGGGCGGGGGCAGCTTTCGAGAATTACGAGGACAGGAGGCAGAGGCCCTCCCCATCC
GCATTATTGGAGGAGAGAGAGCCTCCCCCAGCTTGGGGAGGGGGAGAGCGGGGCATTGGGCGCC
CCTCGCAGCGGCCGCTGCCCTGACCCGACGGGTATCAGCCGGCTCTCCCCCTCCACCCAGGACG
ACATGAACGACCGAGGCCAGGGAGTCCTCTCCTTGGGCCTCTGCATCCCCCCATCCTTGGCTCT
GGGGTAGGCCCAGGGAGGAGACACCCCCAACCCCTATCCGGTCTGTCCTGGAGAAAAGAGACTG
CCCTTCCATGCCCCTGAGTGAGGGGCCTGGGGCCCAGGCTGCCTGTGTTCCCCAAGGGCAAGGG
TCTCTCTGTTGAGGAGGAGGGGCCTGTCAGCCACAACTTCTTTCCTCCTGAGCGCCCCATCTCC
CTCTCTGCACCCTGCAATTCCCACCCCTCCGTATTTATTTCCCTGGTCCCGCCGACAGTCCCTC
CTTGTCTGTCTCCGGGATTCAGGCCTCCCTCCCTGACATGGAGAGTAACCTGTCTGGCCTGGTG
CCTGCTGCCGGGCTGGTGCCTGCGCTGCCACCTGCTGTGACCCTGGGGCTGACAGCTGCCTACA
CCACCCTGTATGCCCTGCTCTTCTTCTCCGTCTATGCCCAGCTCTGGCTGGTGCTTCTGTATGG
GCACAAGCGTCTCAGCTATCAGACGGTGTTCCTGGCCCTCTGTCTGCTCTGGGCCGCCTTGCGT
ACCACCCTCTTCTCCTTCTACTTCCGAGATACTCCCCGCGCCAACCGCCTGGGGCCCTTGCCCT
TCTGGCTTCTCTACTGCTGCCCCGTCTGCCTGCAGTTCTTCACCTTGACGCTTATGAACCTCTA
CTTTGCCCAGGTGGTGTTCAAGGCCAAGGTGAAGCGTCGGCCGGAGATGAGCCGAGGCTTGCTC
GCTGTCCGAGGGGCCTTTGTGGGGGCCTCGCTGCTCTTTCTGCTGGTGAACGTGCTGTGTGCTG
TGCTCTCCCATCGGCGCCGGGCACAGCCCTGGGCCCTGCTGCTTGTCCGCGTCCTGCGGTTCTC
AGGGTGTAGAGGAAGCTGGGAGCCTTCTCTCCCTGAGGGTCCTCTGTTGTTACCTGTGCCAGGG
GACCAGTGTGTGCCAGGCGGCCGCGATGGGTGGCGCCATGGTCCTGCTCTATGCCAGCCGGGCC
TGCTACAACCTGACAGCACTGGCCTTGGCCCCCCAGAGCCGGCTGGACACCTTCGATTACGACT
GGTACAATGTGTCTGACCAGGCGGACCTGGTGAATGACCTGGGGAACAAAGGCTACCTGGTATT
TGGCCTCATCCTCTTCGTGTGGGAGCTACTGCCCACCACCCTGCTGGTGGGCTTCTTCCGGGTG
CACCGGCCCCCACAGGACCTGTATGTCGGGCAGTCTAGGCTCTGGGAGCTGGTATGGTGCCATC
GGGCGTGAGCCGGGCTGGTATGGGGGCAGCCAGACGAAGACCACTCCTCTGCTCTTCTCCCAGG
TGCCAGGACCAGGCGGCCACCACCACAGTCTCTACTCCACCCCACAGACGTGATCCCCCTCCCT
CCCCCACAGAATACCCAGGCCCCAGTCCCCCTCACCCTAGGCCCCTGTGCCAAGTTTGTCTGCC
GCTTCTTGCCCAGGATCCTGGGGGTCGTGGCTACCCCCTCCTCTGGCCGGCTCCTTGCTGCTCC
TGTCATAGTGAGCTTGTGCCGTCCCCCTAGGATGGGGGGCATGGCCCTGGCTGCCAGATGCCCA
CAGCACCCTGGCATGACCTGCCACCTCTGCTTCCACACCGGAGCCAGCTACCTCTCCTGTGCCT
GCCACTCAATAAACAGTGTCTGCGCCCCACA

hide sequence

RefSeq Acc Id:

XM_005274100 ⟹ XP_005274157

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,285,848 - 64,289,494 (+)	NCBI
GRCh37	11	64,051,781 - 64,056,972 (+)	NCBI

Sequence:

show sequence

CCGCGCAGGCGCGGAGGGGGAGGGGGGCGGAGCAGCGGGAGCCGGGGAGCCGGAGCCCCGGGTC
CCCACGACCTGAGCCGGCTCTCCCATCAGCGGCCTGAGGACCTGGCGTCCGCCTCCTCCCTCCC
CTTGAGGCTGGAGCGTGGACGCGGTGGGGGAGGGTGGGGCGGGGGCAGCTTTCGAGAATTACGA
GGACAGGAGGCAGAGGCCCTCCCCATCCGCATTATTGGAGGAGAGAGAGCCTCCCCCAGCTTGG
GGAGGGGGAGAGCGGGGCATTGGGCGCCCCTCGCAGCGGCCGCTGCCCTGACCCGACGGGTATC
AGCCGGCTCTCCCCCTCCACCCAGGACGACATGAACGACCGAGGCCAGGGAGTCCTCTCCTTGG
GCCTCTGCATCCCCCCATCCTTGGCTCTGGGGCCTCCCTCCCTGACATGGAGAGTAACCTGTCT
GGCCTGGTGCCTGCTGCCGGGCTGGTGCCTGCGCTGCCACCTGCTGTGACCCTGGGGCTGACAG
CTGCCTACACCACCCTGTATGCCCTGCTCTTCTTCTCCGTCTATGCCCAGCTCTGGCTGGTGCT
TCTGTATGGGCACAAGCGTCTCAGCTATCAGACGGTGTTCCTGGCCCTCTGTCTGCTCTGGGCC
GCCTTGCGTACCACCCTCTTCTCCTTCTACTTCCGAGATACTCCCCGCGCCAACCGCCTGGGGC
CCTTGCCCTTCTGGCTTCTCTACTGCTGCCCCGTCTGCCTGCAGTTCTTCACCTTGACGCTTAT
GAACCTCTACTTTGCCCAGGTGGTGTTCAAGGCCAAGGTGAAGCGTCGGCCGGAGATGAGCCGA
GGCTTGCTCGCTGTCCGAGGGGCCTTTGTGGGGGCCTCGCTGCTCTTTCTGCTGGTGAACGTGC
TGTGTGCTGTGCTCTCCCATCGGCGCCGGGCACAGCCCTGGGCCCTGCTGCTTGTCCGCGTCCT
GGTGAGCGACTCCCTGTTCGTCATCTGCGCGCTGTCTCTTGCTGCCTGCCTCTGCCTCGTCGCC
AGGCGGGCGCCCTCCACTAGCATCTACCTGGAGGCCAAGGGGACCAGTGTGTGCCAGGCGGCCG
CGATGGGTGGCGCCATGGTCCTGCTCTATGCCAGCCGGGCCTGCTACAACCTGACAGCACTGGC
CTTGGCCCCCCAGAGCCGGCTGGACACCTTCGATTACGACTGGTACAATGTGTCTGACCAGGCG
GACCTGGTGAATGACCTGGGGAACAAAGGCTACCTGGTATTTGGCCTCATCCTCTTCGTGTGGG
AGCTACTGCCCACCACCCTGCTGGTGGGCTTCTTCCGGGTGCACCGGCCCCCACAGGACCTGAG
CACCAGCCACATCCTCAATGGGCAGGTCTTTGCCTCTCGGTCCTACTTCTTTGACCGGGCTGGG
CACTGTGAAGATGAGGGCTGCTCCTGGGAGCACAGCCGGGGTGAGAGCACCAGGTGCCAGGACC
AGGCGGCCACCACCACAGTCTCTACTCCACCCCACAGACGTGATCCCCCTCCCTCCCCCACAGA
ATACCCAGGCCCCAGTCCCCCTCACCCTAGGCCCCTGTGCCAAGTTTGTCTGCCGCTTCTTGCC
CAGGATCCTGGGGGTCGTGGCTACCCCCTCCTCTGGCCGGCTCCTTGCTGCTCCTGTCATAGTG
AGCTTGTGCCGTCCCCCTAGGATGGGGGGCATGGCCCTGGCTGCCAGATGCCCACAGCACCCTG
GCATGACCTGCCACCTCTGCTTCCACACCGGAGCCAGCTACCTCTCCTGTGCCTGCCACTCAAT
AAACAGTGTCTGCGCCCCACA

hide sequence

RefSeq Acc Id:

XM_005274102 ⟹ XP_005274159

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,285,505 - 64,289,494 (+)	NCBI
GRCh37	11	64,051,781 - 64,056,972 (+)	NCBI

Sequence:

show sequence

ATCTTGGCTATGGGCGGAAGTTTTCTTCAGAGACCGAGGGACGGGAATCCGTTGCCGCCCCCGG
CCGGGCGGCACGACCCCGATTTGGGTATAGGAGAGAGGAGCGTGGGAACTGGCGGACCCCCATA
CAAGCCTCCCTCCCTGACATGGAGAGTAACCTGTCTGGCCTGGTGCCTGCTGCCGGGCTGGTGC
CTGCGCTGCCACCTGCTGTGACCCTGGGGCTGACAGCTGCCTACACCACCCTGTATGCCCTGCT
CTTCTTCTCCGTCTATGCCCAGCTCTGGCTGGTGCTTCTGTATGGGCACAAGCGTCTCAGCTAT
CAGACGGTGTTCCTGGCCCTCTGTCTGCTCTGGGCCGCCTTGCGTACCACCCTCTTCTCCTTCT
ACTTCCGAGATACTCCCCGCGCCAACCGCCTGGGGCCCTTGCCCTTCTGGCTTCTCTACTGCTG
CCCCGTCTGCCTGCAGTTCTTCACCTTGACGCTTATGAACCTCTACTTTGCCCAGGTGGTGTTC
AAGGCCAAGGTGAAGCGTCGGCCGGAGATGAGCCGAGGCTTGCTCGCTGTCCGAGGGGCCTTTG
TGGGGGCCTCGCTGCTCTTTCTGCTGGTGAACGTGCTGTGTGCTGTGCTCTCCCATCGGCGCCG
GGCACAGCCCTGGGCCCTGCTGCTTGTCCGCGTCCTGGTGAGCGACTCCCTGTTCGTCATCTGC
GCGCTGTCTCTTGCTGCCTGCCTCTGCCTCGTCGCCAGGCGGGCGCCCTCCACTAGCATCTACC
TGGAGGCCAAGGGGACCAGTGTGTGCCAGGCGGCCGCGATGGGTGGCGCCATGGTCCTGCTCTA
TGCCAGCCGGGCCTGCTACAACCTGACAGCACTGGCCTTGGCCCCCCAGAGCCGGCTGGACACC
TTCGATTACGACTGGTACAATGTGTCTGACCAGGCGGACCTGGTGAATGACCTGGGGAACAAAG
GCTACCTGGTATTTGGCCTCATCCTCTTCGTGTGGGAGCTACTGCCCACCACCCTGCTGGTGGG
CTTCTTCCGGGTGCACCGGCCCCCACAGGACCTGAGCACCAGCCACATCCTCAATGGGCAGGTC
TTTGCCTCTCGGTCCTACTTCTTTGACCGGGCTGGGCACTGTGAAGATGAGGGCTGCTCCTGGG
AGCACAGCCGGGGTGAGAGCACCAGGTGCCAGGACCAGGCGGCCACCACCACAGTCTCTACTCC
ACCCCACAGACGTGATCCCCCTCCCTCCCCCACAGAATACCCAGGCCCCAGTCCCCCTCACCCT
AGGCCCCTGTGCCAAGTTTGTCTGCCGCTTCTTGCCCAGGATCCTGGGGGTCGTGGCTACCCCC
TCCTCTGGCCGGCTCCTTGCTGCTCCTGTCATAGTGAGCTTGTGCCGTCCCCCTAGGATGGGGG
GCATGGCCCTGGCTGCCAGATGCCCACAGCACCCTGGCATGACCTGCCACCTCTGCTTCCACAC
CGGAGCCAGCTACCTCTCCTGTGCCTGCCACTCAATAAACAGTGTCTGCGCCCCACA

hide sequence

RefSeq Acc Id:

XM_005274104 ⟹ XP_005274161

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,285,505 - 64,289,494 (+)	NCBI
GRCh37	11	64,051,781 - 64,056,972 (+)	NCBI

Sequence:

show sequence

ATGGGCGGAAGTTTTCTTCAGAGACCGAGGGACGGGAATCCGTTGCCGCCCCCGGCCGGGCGGC
ACGACCCCGATTTGGGCCTCCCTCCCTGACATGGAGAGTAACCTGTCTGGCCTGGTGCCTGCTG
CCGGGCTGGTGCCTGCGCTGCCACCTGCTGTGACCCTGGGGCTGACAGCTGCCTACACCACCCT
GTATGCCCTGCTCTTCTTCTCCGTCTATGCCCAGCTCTGGCTGGTGCTTCTGTATGGGCACAAG
CGTCTCAGCTATCAGACGGTGTTCCTGGCCCTCTGTCTGCTCTGGGCCGCCTTGCGTACCACCC
TCTTCTCCTTCTACTTCCGAGATACTCCCCGCGCCAACCGCCTGGGGCCCTTGCCCTTCTGGCT
TCTCTACTGCTGCCCCGTCTGCCTGCAGTTCTTCACCTTGACGCTTATGAACCTCTACTTTGCC
CAGGTGGTGTTCAAGGCCAAGGTGAAGCGTCGGCCGGAGATGAGCCGAGGCTTGCTCGCTGTCC
GAGGGGCCTTTGTGGGGGCCTCGCTGCTCTTTCTGCTGGTGAACGTGCTGTGTGCTGTGCTCTC
CCATCGGCGCCGGGCACAGCCCTGGGCCCTGCTGCTTGTCCGCGTCCTGGTGAGCGACTCCCTG
TTCGTCATCTGCGCGCTGTCTCTTGCTGCCTGCCTCTGCCTCGTCGCCAGGCGGGCGCCCTCCA
CTAGCATCTACCTGGAGGCCAAGGGGACCAGTGTGTGCCAGGCGGCCGCGATGGGTGGCGCCAT
GGTCCTGCTCTATGCCAGCCGGGCCTGCTACAACCTGACAGCACTGGCCTTGGCCCCCCAGAGC
CGGCTGGACACCTTCGATTACGACTGGTACAATGTGTCTGACCAGGCGGACCTGGTGAATGACC
TGGGGAACAAAGGCTACCTGGTATTTGGCCTCATCCTCTTCGTGTGGGAGCTACTGCCCACCAC
CCTGCTGGTGGGCTTCTTCCGGGTGCACCGGCCCCCACAGGACCTGAGCACCAGCCACATCCTC
AATGGGCAGGTCTTTGCCTCTCGGTCCTACTTCTTTGACCGGGCTGGGCACTGTGAAGATGAGG
GCTGCTCCTGGGAGCACAGCCGGGGTGAGAGCACCAGGTGCCAGGACCAGGCGGCCACCACCAC
AGTCTCTACTCCACCCCACAGACGTGATCCCCCTCCCTCCCCCACAGAATACCCAGGCCCCAGT
CCCCCTCACCCTAGGCCCCTGTGCCAAGTTTGTCTGCCGCTTCTTGCCCAGGATCCTGGGGGTC
GTGGCTACCCCCTCCTCTGGCCGGCTCCTTGCTGCTCCTGTCATAGTGAGCTTGTGCCGTCCCC
CTAGGATGGGGGGCATGGCCCTGGCTGCCAGATGCCCACAGCACCCTGGCATGACCTGCCACCT
CTGCTTCCACACCGGAGCCAGCTACCTCTCCTGTGCCTGCCACTCAATAAACAGTGTCTGCGCC
CCACA

hide sequence

RefSeq Acc Id:

XM_011545168 ⟹ XP_011543470

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,270,531 - 64,289,494 (+)	NCBI

Sequence:

show sequence

TCTGGTGGAGGGAGAAAAGGGTTACATGAGTTAGATTACCATGGCAGCTCGAGCCAGGCTCTCC
ACTTCCGTGAGCCTTCCTCTAAGTGAGATCGGGGGGGAGATAATGAAGGCCACAACTCCCAGGA
GGCTCCACGCCGGGCGGTCAGGGACGCTCGCGAGGACGCATGGGCCCCCAGGAATGGGAACTGG
TTAGATCCCAGGAACTCCGTGCCGGAGACGGGAAGAGAGGATGCCTAGGGCCCTAAATGGAAAG
GCCAGAGCTGGAGACCTAGCACCCAGAAGATGAGACCGCAATTCGAGAATCAAAGGGCCGGGAG
CGATGGCCTCCCTCCCTGACATGGAGAGTAACCTGTCTGGCCTGGTGCCTGCTGCCGGGCTGGT
GCCTGCGCTGCCACCTGCTGTGACCCTGGGGCTGACAGCTGCCTACACCACCCTGTATGCCCTG
CTCTTCTTCTCCGTCTATGCCCAGCTCTGGCTGGTGCTTCTGTATGGGCACAAGCGTCTCAGCT
ATCAGACGGTGTTCCTGGCCCTCTGTCTGCTCTGGGCCGCCTTGCGTACCACCCTCTTCTCCTT
CTACTTCCGAGATACTCCCCGCGCCAACCGCCTGGGGCCCTTGCCCTTCTGGCTTCTCTACTGC
TGCCCCGTCTGCCTGCAGTTCTTCACCTTGACGCTTATGAACCTCTACTTTGCCCAGGTGGTGT
TCAAGGCCAAGGTGAAGCGTCGGCCGGAGATGAGCCGAGGCTTGCTCGCTGTCCGAGGGGCCTT
TGTGGGGGCCTCGCTGCTCTTTCTGCTGGTGAACGTGCTGTGTGCTGTGCTCTCCCATCGGCGC
CGGGCACAGCCCTGGGCCCTGCTGCTTGTCCGCGTCCTGGTGAGCGACTCCCTGTTCGTCATCT
GCGCGCTGTCTCTTGCTGCCTGCCTCTGCCTCGTCGCCAGGCGGGCGCCCTCCACTAGCATCTA
CCTGGAGGCCAAGGGGACCAGTGTGTGCCAGGCGGCCGCGATGGGTGGCGCCATGGTCCTGCTC
TATGCCAGCCGGGCCTGCTACAACCTGACAGCACTGGCCTTGGCCCCCCAGAGCCGGCTGGACA
CCTTCGATTACGACTGGTACAATGTGTCTGACCAGGCGGACCTGGTGAATGACCTGGGGAACAA
AGGCTACCTGGTATTTGGCCTCATCCTCTTCGTGTGGGAGCTACTGCCCACCACCCTGCTGGTG
GGCTTCTTCCGGGTGCACCGGCCCCCACAGGACCTGAGCACCAGCCACATCCTCAATGGGCAGG
TCTTTGCCTCTCGGTCCTACTTCTTTGACCGGGCTGGGCACTGTGAAGATGAGGGCTGCTCCTG
GGAGCACAGCCGGGGTGAGAGCACCAGGTGCCAGGACCAGGCGGCCACCACCACAGTCTCTACT
CCACCCCACAGACGTGATCCCCCTCCCTCCCCCACAGAATACCCAGGCCCCAGTCCCCCTCACC
CTAGGCCCCTGTGCCAAGTTTGTCTGCCGCTTCTTGCCCAGGATCCTGGGGGTCGTGGCTACCC
CCTCCTCTGGCCGGCTCCTTGCTGCTCCTGTCATAGTGAGCTTGTGCCGTCCCCCTAGGATGGG
GGGCATGGCCCTGGCTGCCAGATGCCCACAGCACCCTGGCATGACCTGCCACCTCTGCTTCCAC
ACCGGAGCCAGCTACCTCTCCTGTGCCTGCCACTCAATAAACAGTGTCTGCGCCCCACA

hide sequence

RefSeq Acc Id:

XM_011545169 ⟹ XP_011543471

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,285,505 - 64,289,494 (+)	NCBI

Sequence:

show sequence

GTAACCCCGGGCGCCCGCCAGCGGCGCAGCTCGCGCCAATTCTCGCCTCCCTCCCTGACATGGA
GAGTAACCTGTCTGGCCTGGTGCCTGCTGCCGGGCTGGTGCCTGCGCTGCCACCTGCTGTGACC
CTGGGGCTGACAGCTGCCTACACCACCCTGTATGCCCTGCTCTTCTTCTCCGTCTATGCCCAGC
TCTGGCTGGTGCTTCTGTATGGGCACAAGCGTCTCAGCTATCAGACGGTGTTCCTGGCCCTCTG
TCTGCTCTGGGCCGCCTTGCGTACCACCCTCTTCTCCTTCTACTTCCGAGATACTCCCCGCGCC
AACCGCCTGGGGCCCTTGCCCTTCTGGCTTCTCTACTGCTGCCCCGTCTGCCTGCAGTTCTTCA
CCTTGACGCTTATGAACCTCTACTTTGCCCAGGTGGTGTTCAAGGCCAAGGTGAAGCGTCGGCC
GGAGATGAGCCGAGGCTTGCTCGCTGTCCGAGGGGCCTTTGTGGGGGCCTCGCTGCTCTTTCTG
CTGGTGAACGTGCTGTGTGCTGTGCTCTCCCATCGGCGCCGGGCACAGCCCTGGGCCCTGCTGC
TTGTCCGCGTCCTGGTGAGCGACTCCCTGTTCGTCATCTGCGCGCTGTCTCTTGCTGCCTGCCT
CTGCCTCGTCGCCAGGCGGGCGCCCTCCACTAGCATCTACCTGGAGGCCAAGGGGACCAGTGTG
TGCCAGGCGGCCGCGATGGGTGGCGCCATGGTCCTGCTCTATGCCAGCCGGGCCTGCTACAACC
TGACAGCACTGGCCTTGGCCCCCCAGAGCCGGCTGGACACCTTCGATTACGACTGGTACAATGT
GTCTGACCAGGCGGACCTGGTGAATGACCTGGGGAACAAAGGCTACCTGGTATTTGGCCTCATC
CTCTTCGTGTGGGAGCTACTGCCCACCACCCTGCTGGTGGGCTTCTTCCGGGTGCACCGGCCCC
CACAGGACCTGAGCACCAGCCACATCCTCAATGGGCAGGTCTTTGCCTCTCGGTCCTACTTCTT
TGACCGGGCTGGGCACTGTGAAGATGAGGGCTGCTCCTGGGAGCACAGCCGGGGTGAGAGCACC
AGGTGCCAGGACCAGGCGGCCACCACCACAGTCTCTACTCCACCCCACAGACGTGATCCCCCTC
CCTCCCCCACAGAATACCCAGGCCCCAGTCCCCCTCACCCTAGGCCCCTGTGCCAAGTTTGTCT
GCCGCTTCTTGCCCAGGATCCTGGGGGTCGTGGCTACCCCCTCCTCTGGCCGGCTCCTTGCTGC
TCCTGTCATAGTGAGCTTGTGCCGTCCCCCTAGGATGGGGGGCATGGCCCTGGCTGCCAGATGC
CCACAGCACCCTGGCATGACCTGCCACCTCTGCTTCCACACCGGAGCCAGCTACCTCTCCTGTG
CCTGCCACTCAATAAACAGTGTCTGCGCCCCACA

hide sequence

RefSeq Acc Id:

XM_017018016 ⟹ XP_016873505

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,270,531 - 64,289,494 (+)	NCBI

Sequence:

show sequence

TCTGGTGGAGGGAGAAAAGGGTTACATGAGTTAGATTACCATGGCAGCTCGAGCCAGGCTCTCC
ACTTCCGTGAGCCTTCCTCTAAGTGAGATCGGGGGGGAGATAATGAAGGCCACAACTCCCAGGA
GGCTCCACGCCGGGCGGTCAGGGACGCTCGCGAGGACGCATGGGCCCCCAGGAATGGGAACTGG
TTAGATCCCAGGAACTCCGTGCCGGAGACGGGAAGAGAGGATGCCTAGGGCCCTAAATGGAAAG
GCCAGAGCTGGAGACCTAGCACCCAGAAGATGAGACCGCAATTCGAGAATCAAAGGGCCGGGAG
CGATGGCCTCCCTCCCTGACATGGAGAGTAACCTGTCTGGCCTGGTGCCTGCTGCCGGGCTGGT
GCCTGCGCTGCCACCTGCTGTGACCCTGGGGCTGACAGCTGCCTACACCACCCTGTATGCCCTG
CTCTTCTTCTCCGTCTATGCCCAGCTCTGGCTGGTGCTTCTGTATGGGCACAAGCGTCTCAGCT
ATCAGACGGTGTTCCTGGCCCTCTGTCTGCTCTGGGCCGCCTTGCGTACCACCCTCTTCTCCTT
CTACTTCCGAGATACTCCCCGCGCCAACCGCCTGGGGCCCTTGCCCTTCTGGCTTCTCTACTGC
TGCCCCGTCTGCCTGCAGTTCTTCACCTTGACGCTTATGAACCTCTACTTTGCCCAGGTGGTGT
TCAAGGCCAAGGTGAAGCGTCGGCCGGAGATGAGCCGAGGCTTGCTCGCTGTCCGAGGGGCCTT
TGTGGGGGCCTCGCTGCTCTTTCTGCTGGTGAACGTGCTGTGTGCTGTGCTCTCCCATCGGCGC
CGGGCACAGCCCTGGGCCCTGCTGCTTGTCCGCGTCCTGGTGAGCGACTCCCTGTTCGTCATCT
GCGCGCTGTCTCTTGCTGCCTGCCTCTGCCTCGTCGCCAGGCGGGCGCCCTCCACTAGCATCTA
CCTGGAGGCCAAGGCGGACCTGGTGAATGACCTGGGGAACAAAGGCTACCTGGTATTTGGCCTC
ATCCTCTTCGTGTGGGAGCTACTGCCCACCACCCTGCTGGTGGGCTTCTTCCGGGTGCACCGGC
CCCCACAGGACCTGAGCACCAGCCACATCCTCAATGGGCAGGTCTTTGCCTCTCGGTCCTACTT
CTTTGACCGGGCTGGGCACTGTGAAGATGAGGGCTGCTCCTGGGAGCACAGCCGGGGTGAGAGC
ACCAGGTGCCAGGACCAGGCGGCCACCACCACAGTCTCTACTCCACCCCACAGACGTGATCCCC
CTCCCTCCCCCACAGAATACCCAGGCCCCAGTCCCCCTCACCCTAGGCCCCTGTGCCAAGTTTG
TCTGCCGCTTCTTGCCCAGGATCCTGGGGGTCGTGGCTACCCCCTCCTCTGGCCGGCTCCTTGC
TGCTCCTGTCATAGTGAGCTTGTGCCGTCCCCCTAGGATGGGGGGCATGGCCCTGGCTGCCAGA
TGCCCACAGCACCCTGGCATGACCTGCCACCTCTGCTTCCACACCGGAGCCAGCTACCTCTCCT
GTGCCTGCCACTCAATAAACAGTGTCTGCGCCCCACA

hide sequence

RefSeq Acc Id:

XM_047427263 ⟹ XP_047283219

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,285,505 - 64,289,500 (+)	NCBI

RefSeq Acc Id:

XM_047427264 ⟹ XP_047283220

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,270,531 - 64,289,500 (+)	NCBI

RefSeq Acc Id:

XM_047427265 ⟹ XP_047283221

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,285,505 - 64,289,500 (+)	NCBI

RefSeq Acc Id:

XM_054369369 ⟹ XP_054225344

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	64,260,559 - 64,279,458 (+)	NCBI

RefSeq Acc Id:

XM_054369370 ⟹ XP_054225345

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	64,275,469 - 64,279,458 (+)	NCBI

RefSeq Acc Id:

XM_054369371 ⟹ XP_054225346

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	64,275,469 - 64,279,458 (+)	NCBI

RefSeq Acc Id:

XM_054369372 ⟹ XP_054225347

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	64,275,428 - 64,279,458 (+)	NCBI

RefSeq Acc Id:

XM_054369373 ⟹ XP_054225348

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	64,275,812 - 64,279,458 (+)	NCBI

RefSeq Acc Id:

XM_054369374 ⟹ XP_054225349

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	64,260,559 - 64,279,458 (+)	NCBI

RefSeq Acc Id:

XM_054369375 ⟹ XP_054225350

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	64,275,469 - 64,279,464 (+)	NCBI

RefSeq Acc Id:

XM_054369376 ⟹ XP_054225351

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	64,260,559 - 64,279,464 (+)	NCBI

RefSeq Acc Id:

XM_054369377 ⟹ XP_054225352

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	64,275,426 - 64,279,464 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_001164351	(Get FASTA)	NCBI Sequence Viewer
	NP_001164352	(Get FASTA)	NCBI Sequence Viewer
	NP_001170829	(Get FASTA)	NCBI Sequence Viewer
	NP_001365005	(Get FASTA)	NCBI Sequence Viewer
	NP_001365006	(Get FASTA)	NCBI Sequence Viewer
	NP_001365007	(Get FASTA)	NCBI Sequence Viewer
	NP_001365008	(Get FASTA)	NCBI Sequence Viewer
	NP_001365009	(Get FASTA)	NCBI Sequence Viewer
	NP_001365010	(Get FASTA)	NCBI Sequence Viewer
	NP_001365011	(Get FASTA)	NCBI Sequence Viewer
	NP_001365012	(Get FASTA)	NCBI Sequence Viewer
	NP_001365013	(Get FASTA)	NCBI Sequence Viewer
	NP_001365014	(Get FASTA)	NCBI Sequence Viewer
	NP_001365015	(Get FASTA)	NCBI Sequence Viewer
	NP_001365016	(Get FASTA)	NCBI Sequence Viewer
	NP_001365017	(Get FASTA)	NCBI Sequence Viewer
	NP_001365018	(Get FASTA)	NCBI Sequence Viewer
	NP_064540	(Get FASTA)	NCBI Sequence Viewer
	XP_005274157	(Get FASTA)	NCBI Sequence Viewer
	XP_005274159	(Get FASTA)	NCBI Sequence Viewer
	XP_005274161	(Get FASTA)	NCBI Sequence Viewer
	XP_011543470	(Get FASTA)	NCBI Sequence Viewer
	XP_011543471	(Get FASTA)	NCBI Sequence Viewer
	XP_016873505	(Get FASTA)	NCBI Sequence Viewer
	XP_047283219	(Get FASTA)	NCBI Sequence Viewer
	XP_047283220	(Get FASTA)	NCBI Sequence Viewer
	XP_047283221	(Get FASTA)	NCBI Sequence Viewer
	XP_054225344	(Get FASTA)	NCBI Sequence Viewer
	XP_054225345	(Get FASTA)	NCBI Sequence Viewer
	XP_054225346	(Get FASTA)	NCBI Sequence Viewer
	XP_054225347	(Get FASTA)	NCBI Sequence Viewer
	XP_054225348	(Get FASTA)	NCBI Sequence Viewer
	XP_054225349	(Get FASTA)	NCBI Sequence Viewer
	XP_054225350	(Get FASTA)	NCBI Sequence Viewer
	XP_054225351	(Get FASTA)	NCBI Sequence Viewer
	XP_054225352	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH33920	(Get FASTA)	NCBI Sequence Viewer
	AAH35002	(Get FASTA)	NCBI Sequence Viewer
	BAB71093	(Get FASTA)	NCBI Sequence Viewer
	BAG61979	(Get FASTA)	NCBI Sequence Viewer
	BAH13657	(Get FASTA)	NCBI Sequence Viewer
	CAB96540	(Get FASTA)	NCBI Sequence Viewer
	CAC69286	(Get FASTA)	NCBI Sequence Viewer
	CCQ43626	(Get FASTA)	NCBI Sequence Viewer
	EAW74237	(Get FASTA)	NCBI Sequence Viewer
	EAW74238	(Get FASTA)	NCBI Sequence Viewer
	EAW74239	(Get FASTA)	NCBI Sequence Viewer
	EAW74240	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000321698
	ENSP00000321698.3
	ENSP00000366931
	ENSP00000366931.4
	ENSP00000411827
	ENSP00000411827.2
	ENSP00000415698
	ENSP00000415698.2
	ENSP00000438146.1
	ENSP00000438716.1
	ENSP00000440928.1
	ENSP00000441003.1
	ENSP00000441034.1
	ENSP00000442322.1
	ENSP00000442929.1
	ENSP00000443443.1
	ENSP00000445000.1
	ENSP00000445570.1
	ENSP00000446342.1
	ENSP00000446387.1
GenBank Protein	Q96N19	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_001170829 ⟸ NM_001177358
- Peptide Label:	isoform 5
- UniProtKB:	Q96N19 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MESNLSGLVPAAGLVPALPPAVTLGLTAAYTTLYALLFFSVYAQLWLVLLYGHKRLSYQTVFLA LCLLWAALRTTLFSFYFRDTPRANRLGPLPFWLLYCCPVCLQFFTLTLMNLYFAQVVFKAKVKR RPEMSRGLLAVRGAFVGASLLFLLVNVLCAVLSHRRRAQPWALLLVRVLVSDSLFVICALSLAA CLCLVARRAPSTSIYLEAKGTSVCQAAAMGGAMVLLYASRACYNLTALALAPQSRLDTFDYDWY NVSDQADLVNDLGNKGYLVFGLILFVWELLPTTLLVGFFRVHRPPQDLYVGQSRLWELVWCHRA hide sequence

RefSeq Acc Id:	NP_001164352 ⟸ NM_001170881
- Peptide Label:	isoform 1
- UniProtKB:	Q96N19 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MESNLSGLVPAAGLVPALPPAVTLGLTAAYTTLYALLFFSVYAQLWLVLLYGHKRLSYQTVFLA LCLLWAALRTTLFSFYFRDTPRANRLGPLPFWLLYCCPVCLQFFTLTLMNLYFAQVVFKAKVKR RPEMSRGLLAVRGAFVGASLLFLLVNVLCAVLSHRRRAQPWALLLVRVLVSDSLFVICALSLAA CLCLVARRAPSTSIYLEAKADLVNDLGNKGYLVFGLILFVWELLPTTLLVGFFRVHRPPQDLST SHILNGQVFASRSYFFDRAGHCEDEGCSWEHSRGESTSMSGSLGSGSWYGAIGREPGWYGGSQT KTTPLLFSQVPGPGGHHHSLYSTPQT hide sequence

RefSeq Acc Id:	NP_064540 ⟸ NM_020155
- Peptide Label:	isoform 3
- UniProtKB:	Q4G0Y9 (UniProtKB/Swiss-Prot), B7Z7M1 (UniProtKB/Swiss-Prot), B4DTG7 (UniProtKB/Swiss-Prot), Q8N4K6 (UniProtKB/Swiss-Prot), Q96N19 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MESNLSGLVPAAGLVPALPPAVTLGLTAAYTTLYALLFFSVYAQLWLVLLYGHKRLSYQTVFLA LCLLWAALRTTLFSFYFRDTPRANRLGPLPFWLLYCCPVCLQFFTLTLMNLYFAQVVFKAKVKR RPEMSRGLLAVRGAFVGASLLFLLVNVLCAVLSHRRRAQPWALLLVRVLVSDSLFVICALSLAA CLCLVARRAPSTSIYLEAKGTSVCQAAAMGGAMVLLYASRACYNLTALALAPQSRLDTFDYDWY NVSDQADLVNDLGNKGYLVFGLILFVWELLPTTLLVGFFRVHRPPQDLSTSHILNGQVFASRSY FFDRAGHCEDEGCSWEHSRGESTRCQDQAATTTVSTPPHRRDPPPSPTEYPGPSPPHPRPLCQV CLPLLAQDPGGRGYPLLWPAPCCSCHSELVPSP hide sequence

RefSeq Acc Id:	NP_001164351 ⟸ NM_001170880
- Peptide Label:	isoform 2
- UniProtKB:	Q96N19 (UniProtKB/Swiss-Prot), Q9NQC5 (UniProtKB/TrEMBL)
- Sequence:	show sequence MESNLSGLVPAAGLVPALPPAVTLGLTAAYTTLYALLFFSVYAQLWLVLLYGHKRLSYQTVFLA LCLLWAALRTTLFSFYFRDTPRANRLGPLPFWLLYCCPVCLQFFTLTLMNLYFAQVVFKAKVKR RPEMSRGLLAVRGAFVGASLLFLLVNVLCAVLSHRRRAQPWALLLVRVLVSDSLFVICALSLAA CLCLVARRAPSTSIYLEAKGTSVCQAAAMGGAMVLLYASRACYNLTALALAPQSRLDTFDYDWY NVSDQADLVNDLGNKGYLVFGLILFVWELLPTTLLVGFFRVHRPPQDLSTSHILNGQVFASRSY FFDRAGHCEDEGCSWEHSRGESTSMSGSLGSGSWYGAIGREPGWYGGSQTKTTPLLFSQVPGPG GHHHSLYSTPQT hide sequence

RefSeq Acc Id:	XP_005274159 ⟸ XM_005274102
- Peptide Label:	isoform X2
- UniProtKB:	Q4G0Y9 (UniProtKB/Swiss-Prot), B7Z7M1 (UniProtKB/Swiss-Prot), B4DTG7 (UniProtKB/Swiss-Prot), Q8N4K6 (UniProtKB/Swiss-Prot), Q96N19 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MESNLSGLVPAAGLVPALPPAVTLGLTAAYTTLYALLFFSVYAQLWLVLLYGHKRLSYQTVFLA LCLLWAALRTTLFSFYFRDTPRANRLGPLPFWLLYCCPVCLQFFTLTLMNLYFAQVVFKAKVKR RPEMSRGLLAVRGAFVGASLLFLLVNVLCAVLSHRRRAQPWALLLVRVLVSDSLFVICALSLAA CLCLVARRAPSTSIYLEAKGTSVCQAAAMGGAMVLLYASRACYNLTALALAPQSRLDTFDYDWY NVSDQADLVNDLGNKGYLVFGLILFVWELLPTTLLVGFFRVHRPPQDLSTSHILNGQVFASRSY FFDRAGHCEDEGCSWEHSRGESTRCQDQAATTTVSTPPHRRDPPPSPTEYPGPSPPHPRPLCQV CLPLLAQDPGGRGYPLLWPAPCCSCHSELVPSP hide sequence

RefSeq Acc Id:	XP_005274161 ⟸ XM_005274104
- Peptide Label:	isoform X2
- UniProtKB:	Q4G0Y9 (UniProtKB/Swiss-Prot), B7Z7M1 (UniProtKB/Swiss-Prot), B4DTG7 (UniProtKB/Swiss-Prot), Q8N4K6 (UniProtKB/Swiss-Prot), Q96N19 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MESNLSGLVPAAGLVPALPPAVTLGLTAAYTTLYALLFFSVYAQLWLVLLYGHKRLSYQTVFLA LCLLWAALRTTLFSFYFRDTPRANRLGPLPFWLLYCCPVCLQFFTLTLMNLYFAQVVFKAKVKR RPEMSRGLLAVRGAFVGASLLFLLVNVLCAVLSHRRRAQPWALLLVRVLVSDSLFVICALSLAA CLCLVARRAPSTSIYLEAKGTSVCQAAAMGGAMVLLYASRACYNLTALALAPQSRLDTFDYDWY NVSDQADLVNDLGNKGYLVFGLILFVWELLPTTLLVGFFRVHRPPQDLSTSHILNGQVFASRSY FFDRAGHCEDEGCSWEHSRGESTRCQDQAATTTVSTPPHRRDPPPSPTEYPGPSPPHPRPLCQV CLPLLAQDPGGRGYPLLWPAPCCSCHSELVPSP hide sequence

RefSeq Acc Id:	XP_005274157 ⟸ XM_005274100
- Peptide Label:	isoform X2
- UniProtKB:	Q4G0Y9 (UniProtKB/Swiss-Prot), B7Z7M1 (UniProtKB/Swiss-Prot), B4DTG7 (UniProtKB/Swiss-Prot), Q8N4K6 (UniProtKB/Swiss-Prot), Q96N19 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MESNLSGLVPAAGLVPALPPAVTLGLTAAYTTLYALLFFSVYAQLWLVLLYGHKRLSYQTVFLA LCLLWAALRTTLFSFYFRDTPRANRLGPLPFWLLYCCPVCLQFFTLTLMNLYFAQVVFKAKVKR RPEMSRGLLAVRGAFVGASLLFLLVNVLCAVLSHRRRAQPWALLLVRVLVSDSLFVICALSLAA CLCLVARRAPSTSIYLEAKGTSVCQAAAMGGAMVLLYASRACYNLTALALAPQSRLDTFDYDWY NVSDQADLVNDLGNKGYLVFGLILFVWELLPTTLLVGFFRVHRPPQDLSTSHILNGQVFASRSY FFDRAGHCEDEGCSWEHSRGESTRCQDQAATTTVSTPPHRRDPPPSPTEYPGPSPPHPRPLCQV CLPLLAQDPGGRGYPLLWPAPCCSCHSELVPSP hide sequence

RefSeq Acc Id:

XP_011543470 ⟸ XM_011545168

- Peptide Label:

isoform X1

- Sequence:

show sequence

MASLPDMESNLSGLVPAAGLVPALPPAVTLGLTAAYTTLYALLFFSVYAQLWLVLLYGHKRLSY
QTVFLALCLLWAALRTTLFSFYFRDTPRANRLGPLPFWLLYCCPVCLQFFTLTLMNLYFAQVVF
KAKVKRRPEMSRGLLAVRGAFVGASLLFLLVNVLCAVLSHRRRAQPWALLLVRVLVSDSLFVIC
ALSLAACLCLVARRAPSTSIYLEAKGTSVCQAAAMGGAMVLLYASRACYNLTALALAPQSRLDT
FDYDWYNVSDQADLVNDLGNKGYLVFGLILFVWELLPTTLLVGFFRVHRPPQDLSTSHILNGQV
FASRSYFFDRAGHCEDEGCSWEHSRGESTRCQDQAATTTVSTPPHRRDPPPSPTEYPGPSPPHP
RPLCQVCLPLLAQDPGGRGYPLLWPAPCCSCHSELVPSP

hide sequence

RefSeq Acc Id:	XP_011543471 ⟸ XM_011545169
- Peptide Label:	isoform X2
- UniProtKB:	Q4G0Y9 (UniProtKB/Swiss-Prot), B7Z7M1 (UniProtKB/Swiss-Prot), B4DTG7 (UniProtKB/Swiss-Prot), Q8N4K6 (UniProtKB/Swiss-Prot), Q96N19 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MESNLSGLVPAAGLVPALPPAVTLGLTAAYTTLYALLFFSVYAQLWLVLLYGHKRLSYQTVFLA LCLLWAALRTTLFSFYFRDTPRANRLGPLPFWLLYCCPVCLQFFTLTLMNLYFAQVVFKAKVKR RPEMSRGLLAVRGAFVGASLLFLLVNVLCAVLSHRRRAQPWALLLVRVLVSDSLFVICALSLAA CLCLVARRAPSTSIYLEAKGTSVCQAAAMGGAMVLLYASRACYNLTALALAPQSRLDTFDYDWY NVSDQADLVNDLGNKGYLVFGLILFVWELLPTTLLVGFFRVHRPPQDLSTSHILNGQVFASRSY FFDRAGHCEDEGCSWEHSRGESTRCQDQAATTTVSTPPHRRDPPPSPTEYPGPSPPHPRPLCQV CLPLLAQDPGGRGYPLLWPAPCCSCHSELVPSP hide sequence

RefSeq Acc Id:

XP_016873505 ⟸ XM_017018016

- Peptide Label:

isoform X3

- Sequence:

show sequence

MASLPDMESNLSGLVPAAGLVPALPPAVTLGLTAAYTTLYALLFFSVYAQLWLVLLYGHKRLSY
QTVFLALCLLWAALRTTLFSFYFRDTPRANRLGPLPFWLLYCCPVCLQFFTLTLMNLYFAQVVF
KAKVKRRPEMSRGLLAVRGAFVGASLLFLLVNVLCAVLSHRRRAQPWALLLVRVLVSDSLFVIC
ALSLAACLCLVARRAPSTSIYLEAKADLVNDLGNKGYLVFGLILFVWELLPTTLLVGFFRVHRP
PQDLSTSHILNGQVFASRSYFFDRAGHCEDEGCSWEHSRGESTRCQDQAATTTVSTPPHRRDPP
PSPTEYPGPSPPHPRPLCQVCLPLLAQDPGGRGYPLLWPAPCCSCHSELVPSP

hide sequence

RefSeq Acc Id:	NP_001365007 ⟸ NM_001378078
- Peptide Label:	isoform 2

RefSeq Acc Id:	NP_001365013 ⟸ NM_001378084
- Peptide Label:	isoform 5

RefSeq Acc Id:	NP_001365005 ⟸ NM_001378076
- Peptide Label:	isoform 1

RefSeq Acc Id:	NP_001365008 ⟸ NM_001378079
- Peptide Label:	isoform 2

RefSeq Acc Id:	NP_001365012 ⟸ NM_001378083
- Peptide Label:	isoform 3
- UniProtKB:	Q96N19 (UniProtKB/Swiss-Prot), Q4G0Y9 (UniProtKB/Swiss-Prot), B7Z7M1 (UniProtKB/Swiss-Prot), B4DTG7 (UniProtKB/Swiss-Prot), Q8N4K6 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	NP_001365015 ⟸ NM_001378086
- Peptide Label:	isoform 5

RefSeq Acc Id:	NP_001365016 ⟸ NM_001378087
- Peptide Label:	isoform 6

RefSeq Acc Id:	NP_001365010 ⟸ NM_001378081
- Peptide Label:	isoform 2

RefSeq Acc Id:	NP_001365009 ⟸ NM_001378080
- Peptide Label:	isoform 2

RefSeq Acc Id:	NP_001365014 ⟸ NM_001378085
- Peptide Label:	isoform 5

RefSeq Acc Id:	NP_001365006 ⟸ NM_001378077
- Peptide Label:	isoform 1

RefSeq Acc Id:	NP_001365017 ⟸ NM_001378088
- Peptide Label:	isoform 6

RefSeq Acc Id:	NP_001365011 ⟸ NM_001378082
- Peptide Label:	isoform 2

RefSeq Acc Id:	NP_001365018 ⟸ NM_001378089
- Peptide Label:	isoform 7

RefSeq Acc Id:

ENSP00000442929 ⟸ ENST00000541952

RefSeq Acc Id:

ENSP00000415698 ⟸ ENST00000438980

RefSeq Acc Id:

ENSP00000441034 ⟸ ENST00000542190

RefSeq Acc Id:

ENSP00000441003 ⟸ ENST00000543383

RefSeq Acc Id:

ENSP00000411827 ⟸ ENST00000411458

RefSeq Acc Id:

ENSP00000438146 ⟸ ENST00000546201

RefSeq Acc Id:

ENSP00000445570 ⟸ ENST00000546139

RefSeq Acc Id:

ENSP00000366931 ⟸ ENST00000377702

RefSeq Acc Id:

ENSP00000446342 ⟸ ENST00000535675

RefSeq Acc Id:

ENSP00000440928 ⟸ ENST00000536667

RefSeq Acc Id:

ENSP00000443443 ⟸ ENST00000536282

RefSeq Acc Id:

ENSP00000442322 ⟸ ENST00000538244

RefSeq Acc Id:

ENSP00000445000 ⟸ ENST00000538032

RefSeq Acc Id:

ENSP00000321698 ⟸ ENST00000313074

RefSeq Acc Id:

ENSP00000442792 ⟸ ENST00000539851

RefSeq Acc Id:

ENSP00000438716 ⟸ ENST00000539833

RefSeq Acc Id:

ENSP00000446387 ⟸ ENST00000540370

RefSeq Acc Id:	XP_047283220 ⟸ XM_047427264
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_047283219 ⟸ XM_047427263
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_047283221 ⟸ XM_047427265
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_054225351 ⟸ XM_054369376
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054225344 ⟸ XM_054369369
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054225349 ⟸ XM_054369374
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054225352 ⟸ XM_054369377
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_054225347 ⟸ XM_054369372
- Peptide Label:	isoform X2
- UniProtKB:	Q96N19 (UniProtKB/Swiss-Prot), Q4G0Y9 (UniProtKB/Swiss-Prot), B7Z7M1 (UniProtKB/Swiss-Prot), B4DTG7 (UniProtKB/Swiss-Prot), Q8N4K6 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054225350 ⟸ XM_054369375
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054225346 ⟸ XM_054369371
- Peptide Label:	isoform X2
- UniProtKB:	Q96N19 (UniProtKB/Swiss-Prot), Q4G0Y9 (UniProtKB/Swiss-Prot), B7Z7M1 (UniProtKB/Swiss-Prot), B4DTG7 (UniProtKB/Swiss-Prot), Q8N4K6 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054225345 ⟸ XM_054369370
- Peptide Label:	isoform X2
- UniProtKB:	Q96N19 (UniProtKB/Swiss-Prot), Q4G0Y9 (UniProtKB/Swiss-Prot), B7Z7M1 (UniProtKB/Swiss-Prot), B4DTG7 (UniProtKB/Swiss-Prot), Q8N4K6 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054225348 ⟸ XM_054369373
- Peptide Label:	isoform X2
- UniProtKB:	Q96N19 (UniProtKB/Swiss-Prot), Q4G0Y9 (UniProtKB/Swiss-Prot), B7Z7M1 (UniProtKB/Swiss-Prot), B4DTG7 (UniProtKB/Swiss-Prot), Q8N4K6 (UniProtKB/Swiss-Prot)

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q96N19-F1-model_v2	AlphaFold	Q96N19	1-417	view protein structure

Promoters

RGD ID:

6788966

Promoter ID:

HG_KWN:13206

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

ENST00000313074, ENST00000377702, NM_001170726, NM_001170880, NM_001170881, NM_001177358, NM_020155, UC001NZE.1, UC001NZH.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	11	63,808,781 - 63,809,812 (+)	MPROMDB

RGD ID:

7220855

Promoter ID:

EPDNEW_H16173

Type:

initiation region

Name:

GPR137_4

Description:

G protein-coupled receptor 137

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H16175 EPDNEW_H16176 EPDNEW_H16177

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,285,130 - 64,285,190	EPDNEW

RGD ID:

7220859

Promoter ID:

EPDNEW_H16175

Type:

initiation region

Name:

GPR137_1

Description:

G protein-coupled receptor 137

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H16173 EPDNEW_H16176 EPDNEW_H16177

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,285,260 - 64,285,320	EPDNEW

RGD ID:

7220861

Promoter ID:

EPDNEW_H16176

Type:

initiation region

Name:

GPR137_3

Description:

G protein-coupled receptor 137

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H16173 EPDNEW_H16175 EPDNEW_H16177

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,285,853 - 64,285,913	EPDNEW

RGD ID:

7220863

Promoter ID:

EPDNEW_H16177

Type:

initiation region

Name:

GPR137_2

Description:

G protein-coupled receptor 137

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H16173 EPDNEW_H16175 EPDNEW_H16176

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	64,286,380 - 64,286,440	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:24300	AgrOrtholog
COSMIC	GPR137	COSMIC
Ensembl Genes	ENSG00000173264	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000313074	ENTREZGENE
	ENST00000313074.7	UniProtKB/Swiss-Prot
	ENST00000377702	ENTREZGENE
	ENST00000377702.8	UniProtKB/Swiss-Prot
	ENST00000411458	ENTREZGENE
	ENST00000411458.5	UniProtKB/Swiss-Prot
	ENST00000438980	ENTREZGENE
	ENST00000438980.7	UniProtKB/Swiss-Prot
	ENST00000535675.5	UniProtKB/TrEMBL
	ENST00000536282.1	UniProtKB/TrEMBL
	ENST00000536667.5	UniProtKB/TrEMBL
	ENST00000538032.5	UniProtKB/TrEMBL
	ENST00000538244.1	UniProtKB/TrEMBL
	ENST00000539833.5	UniProtKB/TrEMBL
	ENST00000540370.1	UniProtKB/TrEMBL
	ENST00000541952.1	UniProtKB/TrEMBL
	ENST00000542190.5	UniProtKB/TrEMBL
	ENST00000543383.5	UniProtKB/TrEMBL
	ENST00000546139.5	UniProtKB/TrEMBL
	ENST00000546201.5	UniProtKB/TrEMBL
GTEx	ENSG00000173264	GTEx
HGNC ID	HGNC:24300	ENTREZGENE
Human Proteome Map	GPR137	Human Proteome Map
InterPro	GPR137	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:56834	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene	56834	ENTREZGENE
PANTHER	INTEGRAL MEMBRANE PROTEIN GPR137	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	PTHR15146	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA143485482	PharmGKB
UniProt	B4DTG7	ENTREZGENE
	B7Z7M1	ENTREZGENE
	F5GXD9_HUMAN	UniProtKB/TrEMBL
	F5GXI8_HUMAN	UniProtKB/TrEMBL
	F5GXW8_HUMAN	UniProtKB/TrEMBL
	F5H097_HUMAN	UniProtKB/TrEMBL
	F5H0Q1_HUMAN	UniProtKB/TrEMBL
	F5H1T3_HUMAN	UniProtKB/TrEMBL
	F5H1V9_HUMAN	UniProtKB/TrEMBL
	F5H234_HUMAN	UniProtKB/TrEMBL
	F5H4R8_HUMAN	UniProtKB/TrEMBL
	F5H6Y8_HUMAN	UniProtKB/TrEMBL
	F5H7S0_HUMAN	UniProtKB/TrEMBL
	G137A_HUMAN	UniProtKB/Swiss-Prot
	H0YGJ1_HUMAN	UniProtKB/TrEMBL
	L8EA54_HUMAN	UniProtKB/TrEMBL
	Q4G0Y9	ENTREZGENE
	Q8N4K6	ENTREZGENE
	Q96N19	ENTREZGENE
	Q9NQC5	ENTREZGENE, UniProtKB/TrEMBL
UniProt Secondary	B4DTG7	UniProtKB/Swiss-Prot
	B7Z7M1	UniProtKB/Swiss-Prot
	Q4G0Y9	UniProtKB/Swiss-Prot
	Q8N4K6	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)

Imported Disease Annotations - ClinVar

Imported Human Phenotype Annotations - ClinVar

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Imported Disease Annotations - ClinVar

Imported Human Phenotype Annotations - ClinVar