VRK2 (VRK serine/threonine kinase 2)

Gene: VRK2 (VRK serine/threonine kinase 2) Homo sapiens

Analyze

Symbol:

VRK2

Name:

VRK serine/threonine kinase 2

RGD ID:

1323120

HGNC Page

HGNC:12719

Description:

Enables protein domain specific binding activity; protein kinase binding activity; and protein serine/threonine kinase activity. Involved in cellular response to oxidative stress; regulation of MAPK cascade; and regulation of interleukin-1-mediated signaling pathway. Located in endoplasmic reticulum membrane; mitochondrial membrane; and nucleus. Part of protein-containing complex.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

serine/threonine-protein kinase VRK2; vaccinia related kinase 2; vaccinia virus B1R-related kinase 2; vaccinia-related kinase 2; vaccinia-related kinase-2

RGD Orthologs

Alliance Genes

More Info

more info ...

More Info

Species	Gene symbol and name	Data Source	Assertion derived from	less info ...
Orthologs ¹				less info ...
Mus musculus (house mouse):	Vrk2 (vaccinia related kinase 2)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):	Vrk2 (VRK serine/threonine kinase 2)	HGNC	Ensembl, HomoloGene, Inparanoid, NCBI, OrthoDB, Panther
Chinchilla lanigera (long-tailed chinchilla):	Vrk2 (VRK serine/threonine kinase 2)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	VRK2 (VRK serine/threonine kinase 2)	NCBI	Ortholog
Canis lupus familiaris (dog):	VRK2 (VRK serine/threonine kinase 2)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Vrk2 (VRK serine/threonine kinase 2)	NCBI	Ortholog
Sus scrofa (pig):	VRK2 (VRK serine/threonine kinase 2)	HGNC	EggNOG, Ensembl, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	VRK2 (VRK serine/threonine kinase 2)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Vrk2 (VRK serine/threonine kinase 2)	NCBI	Ortholog
Other homologs ²
Rattus norvegicus (Norway rat):	Pxdc1 (PX domain containing 1)	HGNC	OMA
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Vrk2 (VRK serine/threonine kinase 2)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Vrk2 (vaccinia related kinase 2)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	vrk2 (VRK serine/threonine kinase 2)	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid\|ZFIN)
Caenorhabditis elegans (roundworm):	vrk-1	Alliance	DIOPT (Ensembl Compara\|InParanoid\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Drosophila melanogaster (fruit fly):	ball	Alliance	DIOPT (Ensembl Compara\|InParanoid\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Xenopus laevis (African clawed frog):	vrk2.L	Alliance	DIOPT (Xenbase)
Xenopus tropicalis (tropical clawed frog):	vrk2	Alliance	DIOPT (Ensembl Compara\|OMA\|OrthoFinder\|PANTHER\|PhylomeDB)

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	2	57,907,592 - 58,159,920 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	2	57,907,629 - 58,159,920 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	2	58,134,727 - 58,387,055 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	2	58,127,224 - 58,240,510 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	2	58,185,476 - 58,298,654	NCBI
Celera	2	58,116,828 - 58,230,225 (+)	NCBI		Celera
Cytogenetic Map	2	p16.1	NCBI
HuRef	2	58,014,875 - 58,128,335 (+)	NCBI		HuRef
CHM1_1	2	58,203,888 - 58,317,318 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	2	57,912,292 - 58,164,754 (+)	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

epilepsy (IAGP)

Fanconi anemia (IAGP)

Fanconi anemia complementation group A (IAGP)

Fanconi anemia complementation group L (IAGP)

genetic disease (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

(+)-catechin (EXP)

(S)-nicotine (EXP)

1,2-dimethylhydrazine (ISO)

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

4-hydroxyphenyl retinamide (ISO)

acrylamide (EXP)

aflatoxin B1 (EXP,ISO)

all-trans-retinoic acid (EXP)

antirheumatic drug (EXP)

aristolochic acid A (EXP)

benzo[a]pyrene (ISO)

benzo[b]fluoranthene (ISO)

bisphenol A (EXP,ISO)

cadmium dichloride (EXP,ISO)

carbon nanotube (ISO)

CGP 52608 (EXP)

chlorpyrifos (ISO)

chrysene (ISO)

copper(II) sulfate (EXP)

cyclosporin A (EXP)

cytarabine (EXP)

DDT (ISO)

dibutyl phthalate (ISO)

dicrotophos (EXP)

doxorubicin (EXP)

epoxiconazole (ISO)

folic acid (ISO)

FR900359 (EXP)

furan (ISO)

glycidyl methacrylate (EXP)

indole-3-methanol (ISO)

N-nitrosodimethylamine (EXP)

nicotine (EXP)

phenobarbital (EXP)

phenol (EXP)

pirinixic acid (ISO)

piroxicam (EXP)

protein kinase inhibitor (EXP)

quercetin (EXP)

sunitinib (EXP)

tamibarotene (EXP)

temozolomide (EXP)

tetraphene (ISO)

thioacetamide (ISO)

titanium dioxide (ISO)

trichostatin A (EXP)

triptonide (ISO)

valproic acid (EXP)

vinclozolin (ISO)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

cellular response to oxidative stress (IMP)

regulation of interleukin-1-mediated signaling pathway (IMP)

regulation of MAPK cascade (IMP)

signal transduction (IBA,IEA)

Cellular Component

cytoplasm (IDA,IEA)

endoplasmic reticulum (IDA,IEA)

endoplasmic reticulum membrane (IDA,IEA)

membrane (IEA)

mitochondrial membrane (IDA,IEA)

mitochondrion (IEA)

nuclear envelope (IEA,ISS)

nucleus (IBA,IDA,IEA)

protein-containing complex (IDA)

Molecular Function

ATP binding (IEA)

kinase activity (IEA)

protein binding (IPI)

protein domain specific binding (IDA)

protein kinase activity (IEA)

protein kinase binding (IDA)

protein serine kinase activity (IEA)

protein serine/threonine kinase activity (IBA,IDA,IEA,TAS)

Phenotype Annotations Click to see Annotation Detail View

Human Phenotype

Seizure (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:8125298	PMID:9344656	PMID:12477932	PMID:14645249	PMID:15489334	PMID:16344560	PMID:16495336	PMID:16704422	PMID:16963744	PMID:17709393	PMID:18286207	PMID:18612383
PMID:18617507	PMID:19141289	PMID:19571808	PMID:20679487	PMID:20936779	PMID:21791550	PMID:21829721	PMID:21873635	PMID:21920476	PMID:22412018	PMID:22572157	PMID:22752157
PMID:22889411	PMID:22949513	PMID:23082977	PMID:23102693	PMID:23105117	PMID:23449449	PMID:23483238	PMID:24298020	PMID:24447338	PMID:25056061	PMID:25079070	PMID:25087078
PMID:25755282	PMID:25852190	PMID:26186194	PMID:26345874	PMID:26389662	PMID:26496610	PMID:26638075	PMID:26941264	PMID:26949251	PMID:27377031	PMID:27382989	PMID:27456229
PMID:27494321	PMID:27880917	PMID:27922604	PMID:28514442	PMID:28515294	PMID:28692057	PMID:28790404	PMID:29100046	PMID:29180619	PMID:29395067	PMID:29509190	PMID:29568061
PMID:29872222	PMID:29987050	PMID:30062698	PMID:30194290	PMID:30463901	PMID:30804502	PMID:31056421	PMID:31073040	PMID:31091453	PMID:31177093	PMID:31527615	PMID:31586073
PMID:31732153	PMID:31871319	PMID:32062451	PMID:32296183	PMID:32344865	PMID:32788342	PMID:32807901	PMID:32877691	PMID:32994395	PMID:33522046	PMID:33545068	PMID:33875785
PMID:33957083	PMID:33961781	PMID:34079125	PMID:34140642	PMID:34369648	PMID:34432599	PMID:34597346	PMID:34672954	PMID:34709727	PMID:35173553	PMID:35271311	PMID:35384245
PMID:35439318	PMID:35944360	PMID:36040810	PMID:36244648	PMID:36424410	PMID:36857408	PMID:37232246	PMID:37452335	PMID:37689310	PMID:37774976	PMID:37931956	PMID:37943248
PMID:38117590

Genomics

Comparative Map Data

VRK2
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	2	57,907,592 - 58,159,920 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	2	57,907,629 - 58,159,920 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	2	58,134,727 - 58,387,055 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	2	58,127,224 - 58,240,510 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	2	58,185,476 - 58,298,654	NCBI
Celera	2	58,116,828 - 58,230,225 (+)	NCBI		Celera
Cytogenetic Map	2	p16.1	NCBI
HuRef	2	58,014,875 - 58,128,335 (+)	NCBI		HuRef
CHM1_1	2	58,203,888 - 58,317,318 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	2	57,912,292 - 58,164,754 (+)	NCBI		T2T-CHM13v2.0

Vrk2
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	11	26,421,398 - 26,544,006 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	11	26,421,322 - 26,543,999 (-)	Ensembl		GRCm39 Ensembl
GRCm38	11	26,471,398 - 26,594,012 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	11	26,471,322 - 26,593,999 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	11	26,371,401 - 26,493,920 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	11	26,503,981 - 26,625,366 (-)	NCBI		MGSCv36	mm8
MGSCv36	11	26,371,404 - 26,493,611 (-)	NCBI		MGSCv36	mm8
Celera	11	28,995,024 - 28,995,410 (+)	NCBI		Celera
Celera	11	37,253,803 - 37,372,542 (-)	NCBI		Celera
Cytogenetic Map	11	A3.3	NCBI
cM Map	11	15.94	NCBI

Vrk2
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	14	104,514,815 - 104,635,549 (-)	NCBI		GRCr8
mRatBN7.2	14	100,313,771 - 100,434,520 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	14	100,313,601 - 100,434,527 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	14	104,646,638 - 104,767,362 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	14	105,890,724 - 106,011,446 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	14	102,362,554 - 102,483,276 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	14	110,739,835 - 110,883,836 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	14	110,739,226 - 110,883,803 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	14	110,554,902 - 110,576,584 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
Rnor_5.0	14	110,444,503 - 110,501,306 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	14	107,287,844 - 107,450,960 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	14	107,300,490 - 107,470,542 (-)	NCBI
Celera	14	99,260,139 - 99,368,196 (-)	NCBI		Celera
Cytogenetic Map	14	q22	NCBI

Vrk2
(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_004955424	25,282,007 - 25,399,348 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955424	25,307,221 - 25,397,900 (-)	NCBI	ChiLan1.0	ChiLan1.0

VRK2
(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	12	68,197,958 - 68,310,907 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	2A	68,201,910 - 68,314,773 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	2A	58,158,347 - 58,271,245 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	2A	59,166,949 - 59,419,895 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	2A	59,305,233 - 59,419,895 (+)	Ensembl	panpan1.1		panPan2

VRK2
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	10	58,432,144 - 58,544,189 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	10	58,431,978 - 58,544,189 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	10	58,280,905 - 58,497,135 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	10	59,332,186 - 59,547,978 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	10	59,435,778 - 59,547,970 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	10	59,029,154 - 59,244,640 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	10	59,313,317 - 59,529,195 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	10	59,606,236 - 59,821,676 (+)	NCBI		UU_Cfam_GSD_1.0

Vrk2
(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_024406292	24,418,835 - 24,615,182 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936491	3,958,588 - 4,057,738 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936491	3,956,171 - 4,057,753 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

VRK2
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	3	83,433,313 - 83,536,980 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	3	83,435,250 - 83,537,022 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	3	88,020,677 - 88,122,044 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

VRK2
(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	14	48,803,149 - 48,909,144 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	14	48,798,499 - 48,906,712 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666045	62,835,754 - 62,944,601 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Vrk2
(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_004624833	3,663,641 - 3,776,404 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624833	3,663,606 - 3,778,598 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in VRK2
68 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 2p16.1-15(chr2:56738054-62473668)x1	copy number loss	See cases [RCV000054020]	Chr2:56738054..62473668 [GRCh38] Chr2:56965189..62700803 [GRCh37] Chr2:56818693..62554307 [NCBI36] Chr2:2p16.1-15	pathogenic
GRCh38/hg38 2p16.1-15(chr2:57249378-61842734)x1	copy number loss	See cases [RCV000054021]	Chr2:57249378..61842734 [GRCh38] Chr2:57476513..62069869 [GRCh37] Chr2:57330017..61923373 [NCBI36] Chr2:2p16.1-15	pathogenic
GRCh38/hg38 2p16.1(chr2:55570578-60519844)x1	copy number loss	See cases [RCV000137092]	Chr2:55570578..60519844 [GRCh38] Chr2:55797714..60746979 [GRCh37] Chr2:55651218..60600483 [NCBI36] Chr2:2p16.1	pathogenic\|uncertain significance
GRCh38/hg38 2p16.3-11.2(chr2:47620388-86702722)x3	copy number gain	See cases [RCV000137586]	Chr2:47620388..86702722 [GRCh38] Chr2:47847527..86929845 [GRCh37] Chr2:47701031..86783356 [NCBI36] Chr2:2p16.3-11.2	uncertain significance
GRCh38/hg38 2p16.1(chr2:57802633-58951698)x3	copy number gain	See cases [RCV000137145]	Chr2:57802633..58951698 [GRCh38] Chr2:58029768..59178833 [GRCh37] Chr2:57883272..59032337 [NCBI36] Chr2:2p16.1	uncertain significance
GRCh38/hg38 2p25.1-11.2(chr2:7495123-87705899)x3	copy number gain	See cases [RCV000141494]	Chr2:7495123..87705899 [GRCh38] Chr2:7635254..88005418 [GRCh37] Chr2:7552705..87786533 [NCBI36] Chr2:2p25.1-11.2	benign
GRCh38/hg38 2p16.1-15(chr2:58031916-63611810)x1	copy number loss	See cases [RCV000143007]	Chr2:58031916..63611810 [GRCh38] Chr2:58259051..63838944 [GRCh37] Chr2:58112555..63692448 [NCBI36] Chr2:2p16.1-15	pathogenic
NM_006296.7(VRK2):c.1303G>A (p.Asp435Asn)	single nucleotide variant	Fanconi anemia complementation group L [RCV000259387]\|Inborn genetic diseases [RCV003168510]	Chr2:58159469 [GRCh38] Chr2:58386604 [GRCh37] Chr2:2p16.1	uncertain significance
NM_006296.7(VRK2):c.102_105dup	duplication	FANCL-related condition [RCV003401051]\|Fanconi anemia [RCV000226300]\|Fanconi anemia complementation group A [RCV000986760]\|Fanconi anemia complementation group L [RCV001195069]\|not provided [RCV000513086]\|not specified [RCV000192919]	Chr2:58159793..58159794 [GRCh38] Chr2:58386928..58386929 [GRCh37] Chr2:2p16.1	pathogenic\|likely pathogenic\|conflicting interpretations of pathogenicity\|uncertain significance
NM_018062.4(FANCL):c.1115G>C (p.Gly372Ala)	single nucleotide variant	Fanconi anemia [RCV000226623]\|Fanconi anemia complementation group L [RCV002494656]\|not specified [RCV000500570]	Chr2:58159778 [GRCh38] Chr2:58386913 [GRCh37] Chr2:2p16.1	likely benign
NM_018062.4(FANCL):c.*165A>G	single nucleotide variant	Fanconi anemia complementation group L [RCV000317720]	Chr2:58159600 [GRCh38] Chr2:58386735 [GRCh37] Chr2:2p16.1	uncertain significance
NM_018062.4(FANCL):c.*333A>G	single nucleotide variant	Fanconi anemia complementation group L [RCV000379699]	Chr2:58159432 [GRCh38] Chr2:58386567 [GRCh37] Chr2:2p16.1	likely benign\|uncertain significance
NM_018062.4(FANCL):c.447_450del	deletion	Fanconi anemia [RCV000322806]	Chr2:58159315..58159318 [GRCh38] Chr2:58386450..58386453 [GRCh37] Chr2:2p16.1	uncertain significance
GRCh37/hg19 2p25.3-q37.3(chr2:14238-243048760)x3	copy number gain	not provided [RCV000752802]	Chr2:14238..243048760 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
NC_000002.12:g.(?_58159755)_(58165884_?)del	deletion	Fanconi anemia [RCV000816627]	Chr2:58159755..58165884 [GRCh38] Chr2:58386890..58393019 [GRCh37] Chr2:2p16.1	likely pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:15672-243101834)x3	copy number gain	not provided [RCV000752804]	Chr2:15672..243101834 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
GRCh37/hg19 2p23.3-16.1(chr2:27861707-60790985)x3	copy number gain	See cases [RCV000454271]	Chr2:27861707..60790985 [GRCh37] Chr2:2p23.3-16.1	pathogenic
GRCh37/hg19 2p16.1(chr2:58190764-58386590)x3	copy number gain	See cases [RCV000447233]	Chr2:58190764..58386590 [GRCh37] Chr2:2p16.1	uncertain significance
GRCh37/hg19 2p16.1(chr2:58347020-58560846)x3	copy number gain	See cases [RCV000446429]	Chr2:58347020..58560846 [GRCh37] Chr2:2p16.1	uncertain significance
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)	copy number gain	See cases [RCV000512056]	Chr2:12771..242783384 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
Single allele	variation	not specified [RCV000508309]	Chr2:58163083..58163084 [GRCh38] Chr2:58390219..58390220 [GRCh37] Chr2:2p16.1	benign
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)x3	copy number gain	See cases [RCV000511212]	Chr2:12771..242783384 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
Single allele	deletion	not provided [RCV000714264]	Chr2:40608411..146900718 [GRCh37] Chr2:2p22.1-q22.3	likely pathogenic
GRCh37/hg19 2p16.1(chr2:57999642-58459232)x3	copy number gain	not provided [RCV000752991]	Chr2:57999642..58459232 [GRCh37] Chr2:2p16.1	benign
GRCh37/hg19 2p16.1(chr2:58386773-58463541)x3	copy number gain	not provided [RCV000752995]	Chr2:58386773..58463541 [GRCh37] Chr2:2p16.1	benign
GRCh37/hg19 2p16.1-15(chr2:57445335-62733206)	copy number loss	not provided [RCV000767552]	Chr2:57445335..62733206 [GRCh37] Chr2:2p16.1-15	likely pathogenic
NC_000002.12:g.(?_58159755)_(58241323_?)del	deletion	Fanconi anemia [RCV000792150]	Chr2:58159755..58241323 [GRCh38] Chr2:58386890..58468458 [GRCh37] Chr2:2p16.1	pathogenic
GRCh37/hg19 2p16.1(chr2:56175876-60780215)x1	copy number loss	not provided [RCV000849729]	Chr2:56175876..60780215 [GRCh37] Chr2:2p16.1	pathogenic
GRCh37/hg19 2p16.1(chr2:57320871-60143201)x1	copy number loss	not provided [RCV000847598]	Chr2:57320871..60143201 [GRCh37] Chr2:2p16.1	uncertain significance
NM_018062.4(FANCL):c.*515A>C	single nucleotide variant	Fanconi anemia complementation group L [RCV001137353]	Chr2:58159250 [GRCh38] Chr2:58386385 [GRCh37] Chr2:2p16.1	uncertain significance
NM_018062.4(FANCL):c.*434A>G	single nucleotide variant	Fanconi anemia complementation group L [RCV001137354]	Chr2:58159331 [GRCh38] Chr2:58386466 [GRCh37] Chr2:2p16.1	uncertain significance
NM_006296.7(VRK2):c.367A>G (p.Arg123Gly)	single nucleotide variant	Inborn genetic diseases [RCV003248243]	Chr2:58088363 [GRCh38] Chr2:58315498 [GRCh37] Chr2:2p16.1	uncertain significance
NM_018062.4(FANCL):c.1093-65G>A	single nucleotide variant	not provided [RCV001687214]	Chr2:58159865 [GRCh38] Chr2:58387000 [GRCh37] Chr2:2p16.1	benign
NM_018062.4(FANCL):c.*89C>T	single nucleotide variant	Fanconi anemia complementation group L [RCV001139585]	Chr2:58159676 [GRCh38] Chr2:58386811 [GRCh37] Chr2:2p16.1	uncertain significance
NM_018062.4(FANCL):c.*95A>G	single nucleotide variant	Fanconi anemia complementation group L [RCV001139584]\|not provided [RCV001537367]	Chr2:58159670 [GRCh38] Chr2:58386805 [GRCh37] Chr2:2p16.1	benign\|likely benign
NC_000002.12:g.(?_58159755)_(58241323_?)dup	duplication	Fanconi anemia [RCV001031857]	Chr2:58386890..58468458 [GRCh37] Chr2:2p16.1	uncertain significance
NM_018062.4(FANCL):c.*281C>G	single nucleotide variant	Fanconi anemia complementation group L [RCV001139581]	Chr2:58159484 [GRCh38] Chr2:58386619 [GRCh37] Chr2:2p16.1	uncertain significance
NM_018062.4(FANCL):c.*165A>C	single nucleotide variant	Fanconi anemia complementation group L [RCV001139582]	Chr2:58159600 [GRCh38] Chr2:58386735 [GRCh37] Chr2:2p16.1	uncertain significance
NM_018062.4(FANCL):c.*128G>A	single nucleotide variant	Fanconi anemia complementation group L [RCV001139583]	Chr2:58159637 [GRCh38] Chr2:58386772 [GRCh37] Chr2:2p16.1	uncertain significance
NC_000002.11:g.58271895_58333429dup	duplication	Seizure [RCV001256141]	Chr2:58271895..58333429 [GRCh37] Chr2:2p16.1	uncertain significance
NC_000002.11:g.(?_58386890)_(58468458_?)dup	duplication	Fanconi anemia [RCV001296456]	Chr2:58386890..58468458 [GRCh37] Chr2:2p16.1	uncertain significance
NM_018062.4(FANCL):c.1124A>C (p.His375Pro)	single nucleotide variant	Fanconi anemia [RCV001441728]	Chr2:58159769 [GRCh38] Chr2:58386904 [GRCh37] Chr2:2p16.1	likely benign
NC_000002.11:g.(?_58386900)_(58468448_?)dup	duplication	Fanconi anemia [RCV001926328]	Chr2:58386900..58468448 [GRCh37] Chr2:2p16.1	uncertain significance
GRCh37/hg19 2p16.1(chr2:58347020-58560846)	copy number gain	not specified [RCV002052770]	Chr2:58347020..58560846 [GRCh37] Chr2:2p16.1	uncertain significance
NM_018062.4(FANCL):c.1109T>C (p.Met370Thr)	single nucleotide variant	Fanconi anemia [RCV001944016]	Chr2:58159784 [GRCh38] Chr2:58386919 [GRCh37] Chr2:2p16.1	uncertain significance
NC_000002.11:g.(?_58386900)_(58390229_?)dup	duplication	Fanconi anemia [RCV001931416]	Chr2:58386900..58390229 [GRCh37] Chr2:2p16.1	uncertain significance
NC_000002.11:g.(?_58386900)_(58393019_?)del	deletion	Fanconi anemia [RCV002028026]	Chr2:58386900..58393019 [GRCh37] Chr2:2p16.1	likely pathogenic
NM_018062.4(FANCL):c.1121A>G (p.Lys374Arg)	single nucleotide variant	Fanconi anemia [RCV001925734]	Chr2:58159772 [GRCh38] Chr2:58386907 [GRCh37] Chr2:2p16.1	uncertain significance
GRCh37/hg19 2p25.3-q37.3(chr2:1-243199373)	copy number gain	Mosaic trisomy 2 [RCV002280628]	Chr2:1..243199373 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
NM_018062.4(FANCL):c.1093-19_1093-9dup	duplication	Fanconi anemia [RCV002114011]\|Fanconi anemia complementation group L [RCV002494372]	Chr2:58159808..58159809 [GRCh38] Chr2:58386943..58386944 [GRCh37] Chr2:2p16.1	likely benign
NM_018062.4(FANCL):c.1093-34_1093-16del	deletion	Fanconi anemia [RCV002155453]	Chr2:58159816..58159834 [GRCh38] Chr2:58386951..58386969 [GRCh37] Chr2:2p16.1	likely benign
NM_018062.4(FANCL):c.1093-15G>T	single nucleotide variant	Fanconi anemia [RCV002155261]	Chr2:58159815 [GRCh38] Chr2:58386950 [GRCh37] Chr2:2p16.1	likely benign
NC_000002.11:g.(?_58386900)_(58459267_?)del	deletion	Fanconi anemia [RCV003119873]	Chr2:58386900..58459267 [GRCh37] Chr2:2p16.1	pathogenic
NC_000002.11:g.(?_58386900)_(58393029_?)dup	duplication	Fanconi anemia [RCV003119874]	Chr2:58386900..58393029 [GRCh37] Chr2:2p16.1	uncertain significance
NM_006296.7(VRK2):c.689G>A (p.Arg230Gln)	single nucleotide variant	Inborn genetic diseases [RCV003275886]	Chr2:58131820 [GRCh38] Chr2:58358955 [GRCh37] Chr2:2p16.1	uncertain significance
NM_018062.4(FANCL):c.1096A>T (p.Ile366Phe)	single nucleotide variant	not specified [RCV003151522]	Chr2:58159797 [GRCh38] Chr2:58386932 [GRCh37] Chr2:2p16.1	uncertain significance
GRCh37/hg19 2p25.1-q13(chr2:11504318-111365996)x1	copy number loss	See cases [RCV002287563]	Chr2:11504318..111365996 [GRCh37] Chr2:2p25.1-q13	pathogenic
NM_006296.7(VRK2):c.1292A>C (p.Glu431Ala)	single nucleotide variant	Inborn genetic diseases [RCV003286547]	Chr2:58159458 [GRCh38] Chr2:58386593 [GRCh37] Chr2:2p16.1	uncertain significance
NM_018062.4(FANCL):c.1093-13T>A	single nucleotide variant	Fanconi anemia [RCV003076753]	Chr2:58159813 [GRCh38] Chr2:58386948 [GRCh37] Chr2:2p16.1	uncertain significance
NM_006296.7(VRK2):c.1253A>C (p.Gln418Pro)	single nucleotide variant	Inborn genetic diseases [RCV002865099]	Chr2:58159419 [GRCh38] Chr2:58386554 [GRCh37] Chr2:2p16.1	uncertain significance
NM_018062.4(FANCL):c.1093-11T>A	single nucleotide variant	Fanconi anemia [RCV002971788]	Chr2:58159811 [GRCh38] Chr2:58386946 [GRCh37] Chr2:2p16.1	likely benign
NM_018062.4(FANCL):c.1093-10_1093-8del	deletion	Fanconi anemia [RCV002923035]	Chr2:58159808..58159810 [GRCh38] Chr2:58386943..58386945 [GRCh37] Chr2:2p16.1	likely benign
NM_006296.7(VRK2):c.1025T>C (p.Val342Ala)	single nucleotide variant	Inborn genetic diseases [RCV002845826]	Chr2:58146317 [GRCh38] Chr2:58373452 [GRCh37] Chr2:2p16.1	uncertain significance
NM_006296.7(VRK2):c.358G>C (p.Val120Leu)	single nucleotide variant	Inborn genetic diseases [RCV002782812]	Chr2:58088354 [GRCh38] Chr2:58315489 [GRCh37] Chr2:2p16.1	uncertain significance
NM_006296.7(VRK2):c.696C>G (p.Asp232Glu)	single nucleotide variant	Inborn genetic diseases [RCV002985883]	Chr2:58131827 [GRCh38] Chr2:58358962 [GRCh37] Chr2:2p16.1	uncertain significance
NM_018062.4(FANCL):c.1123C>G (p.His375Asp)	single nucleotide variant	Fanconi anemia [RCV002572585]	Chr2:58159770 [GRCh38] Chr2:58386905 [GRCh37] Chr2:2p16.1	uncertain significance
NM_006296.7(VRK2):c.1115C>A (p.Ser372Tyr)	single nucleotide variant	Inborn genetic diseases [RCV002802931]	Chr2:58146407 [GRCh38] Chr2:58373542 [GRCh37] Chr2:2p16.1	uncertain significance
NM_018062.4(FANCL):c.1118G>C (p.Arg373Thr)	single nucleotide variant	Fanconi anemia [RCV002953880]	Chr2:58159775 [GRCh38] Chr2:58386910 [GRCh37] Chr2:2p16.1	uncertain significance
NM_018062.4(FANCL):c.1093-15G>A	single nucleotide variant	Fanconi anemia [RCV002914730]	Chr2:58159815 [GRCh38] Chr2:58386950 [GRCh37] Chr2:2p16.1	likely benign
NM_006296.7(VRK2):c.1279A>G (p.Asn427Asp)	single nucleotide variant	Inborn genetic diseases [RCV002712302]	Chr2:58159445 [GRCh38] Chr2:58386580 [GRCh37] Chr2:2p16.1	uncertain significance
NM_006296.7(VRK2):c.649A>G (p.Thr217Ala)	single nucleotide variant	Inborn genetic diseases [RCV002915742]	Chr2:58123206 [GRCh38] Chr2:58350341 [GRCh37] Chr2:2p16.1	uncertain significance
NM_006296.7(VRK2):c.1073G>A (p.Arg358Lys)	single nucleotide variant	Inborn genetic diseases [RCV002766977]	Chr2:58146365 [GRCh38] Chr2:58373500 [GRCh37] Chr2:2p16.1	uncertain significance
NM_006296.7(VRK2):c.446G>A (p.Arg149Gln)	single nucleotide variant	Inborn genetic diseases [RCV002677255]	Chr2:58088442 [GRCh38] Chr2:58315577 [GRCh37] Chr2:2p16.1	uncertain significance
NM_006296.7(VRK2):c.187G>A (p.Glu63Lys)	single nucleotide variant	Inborn genetic diseases [RCV002944369]	Chr2:58084881 [GRCh38] Chr2:58312016 [GRCh37] Chr2:2p16.1	uncertain significance
NM_018062.4(FANCL):c.102_105dup	duplication	not specified [RCV003226830]	Chr2:58159659..58159660 [GRCh38] Chr2:58386794..58386795 [GRCh37] Chr2:2p16.1	uncertain significance
NM_006296.7(VRK2):c.587A>G (p.Asn196Ser)	single nucleotide variant	Inborn genetic diseases [RCV003202912]	Chr2:58123144 [GRCh38] Chr2:58350279 [GRCh37] Chr2:2p16.1	uncertain significance
NM_006296.7(VRK2):c.419A>G (p.Lys140Arg)	single nucleotide variant	Inborn genetic diseases [RCV003352375]	Chr2:58088415 [GRCh38] Chr2:58315550 [GRCh37] Chr2:2p16.1	uncertain significance
NM_018062.4(FANCL):c.1108del (p.Met370fs)	deletion	not provided [RCV003426979]	Chr2:58159785 [GRCh38] Chr2:58386920 [GRCh37] Chr2:2p16.1	uncertain significance
NM_018062.4(FANCL):c.1093-18T>G	single nucleotide variant	Fanconi anemia [RCV003637010]	Chr2:58159818 [GRCh38] Chr2:58386953 [GRCh37] Chr2:2p16.1	likely benign
NM_018062.4(FANCL):c.1093-13T>C	single nucleotide variant	Fanconi anemia [RCV003522351]	Chr2:58159813 [GRCh38] Chr2:58386948 [GRCh37] Chr2:2p16.1	likely benign
NM_018062.4(FANCL):c.1093-10C>A	single nucleotide variant	Fanconi anemia [RCV003637841]	Chr2:58159810 [GRCh38] Chr2:58386945 [GRCh37] Chr2:2p16.1	likely benign
NM_018062.4(FANCL):c.1093-12C>G	single nucleotide variant	Fanconi anemia [RCV003636202]	Chr2:58159812 [GRCh38] Chr2:58386947 [GRCh37] Chr2:2p16.1	likely benign
NM_018062.4(FANCL):c.1093-17A>T	single nucleotide variant	Fanconi anemia [RCV003523928]	Chr2:58159817 [GRCh38] Chr2:58386952 [GRCh37] Chr2:2p16.1	likely benign
NM_018062.4(FANCL):c.1096A>G (p.Ile366Val)	single nucleotide variant	Fanconi anemia [RCV003522576]	Chr2:58159797 [GRCh38] Chr2:58386932 [GRCh37] Chr2:2p16.1	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	1522
Count of miRNA genes:	680
Interacting mature miRNAs:	753
Transcripts:	ENST00000340157, ENST00000412104, ENST00000417641, ENST00000428021, ENST00000432057, ENST00000435505, ENST00000440705, ENST00000463222, ENST00000478687
Prediction methods:	Microtar, Miranda, Rnahybrid, Targetscan
Result types:	miRGate_prediction

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

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

Markers in Region

D2S2913

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	58,386,731 - 58,386,860	UniSTS	GRCh37
Build 36	2	58,240,235 - 58,240,364	RGD	NCBI36
Celera	2	58,229,901 - 58,230,030	RGD
Cytogenetic Map	2	p16.1	UniSTS
HuRef	2	58,128,011 - 58,128,140	UniSTS

RH78793

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	58,386,541 - 58,386,696	UniSTS	GRCh37
Build 36	2	58,240,045 - 58,240,200	RGD	NCBI36
Celera	2	58,229,711 - 58,229,866	RGD
Cytogenetic Map	2	p16.1	UniSTS
HuRef	2	58,127,821 - 58,127,976	UniSTS

VRK2

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	58,275,959 - 58,276,089	UniSTS	GRCh37
Build 36	2	58,129,463 - 58,129,593	RGD	NCBI36
Celera	2	58,119,010 - 58,119,140	RGD
HuRef	2	58,017,057 - 58,017,187	UniSTS

FANCL__7636

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	58,386,253 - 58,386,933	UniSTS	GRCh37
Build 36	2	58,239,757 - 58,240,437	RGD	NCBI36
Celera	2	58,229,423 - 58,230,103	RGD
HuRef	2	58,127,533 - 58,128,213	UniSTS

SHGC-35879

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	58,386,432 - 58,386,532	UniSTS	GRCh37
Build 36	2	58,239,936 - 58,240,036	RGD	NCBI36
Celera	2	58,229,602 - 58,229,702	RGD
Cytogenetic Map	2	p16.1	UniSTS
HuRef	2	58,127,712 - 58,127,812	UniSTS
TNG Radiation Hybrid Map	2	33747.0	UniSTS
Stanford-G3 RH Map	2	2360.0	UniSTS
NCBI RH Map	2	335.7	UniSTS
GeneMap99-G3 RH Map	2	2317.0	UniSTS

RH66429

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	58,278,503 - 58,278,662	UniSTS	GRCh37
Build 36	2	58,132,007 - 58,132,166	RGD	NCBI36
Celera	2	58,121,554 - 58,121,713	RGD
Cytogenetic Map	2	p16.1	UniSTS
HuRef	2	58,019,601 - 58,019,760	UniSTS
GeneMap99-GB4 RH Map	2	178.91	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

adipose tissue

appendage

entire extraembryonic component

High

Medium

231

295

170

757

596

103

155

451

436

261

Low

2201

2633

1551

522

1159

392

3759

2065

3359

263

997

1167

130

1146

2527

Below cutoff

268

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NG_029717	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001130480	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001130481	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001130482	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001130483	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001288836	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001288837	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001288838	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001288839	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_006296	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005264540	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006712090	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006712091	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006712092	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006712093	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011533092	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017004858	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017004859	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017004860	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017004861	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017004862	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017004863	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017004865	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017004866	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047445745	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047445747	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047445748	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054343751	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054343752	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054343753	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054343754	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054343755	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054343756	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054343757	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AB000450	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC007250	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC068193	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC073215	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AJ512204	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK058199	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK223540	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK292727	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK295193	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK296611	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK307113	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK311205	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY228367	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY228368	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY228369	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY228370	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY228371	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY228372	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC021663	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC027854	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC036434	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BI906749	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471053	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068276	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA273734	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB227029	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000340157 ⟹ ENSP00000342381

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	58,046,806 - 58,159,871 (+)	Ensembl

RefSeq Acc Id:

ENST00000412104 ⟹ ENSP00000404156

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	58,046,642 - 58,159,920 (+)	Ensembl

RefSeq Acc Id:

ENST00000417641 ⟹ ENSP00000402375

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	57,907,651 - 58,159,871 (+)	Ensembl

RefSeq Acc Id:

ENST00000428021 ⟹ ENSP00000404961

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	58,046,875 - 58,084,927 (+)	Ensembl

RefSeq Acc Id:

ENST00000432057 ⟹ ENSP00000400006

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	58,046,712 - 58,159,784 (+)	Ensembl

RefSeq Acc Id:

ENST00000435505 ⟹ ENSP00000408002

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	57,907,651 - 58,159,867 (+)	Ensembl

RefSeq Acc Id:

ENST00000440705 ⟹ ENSP00000398323

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	58,046,715 - 58,159,784 (+)	Ensembl

RefSeq Acc Id:

ENST00000463222

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	57,907,656 - 58,033,327 (+)	Ensembl

RefSeq Acc Id:

ENST00000478687

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	57,907,652 - 58,033,663 (+)	Ensembl

RefSeq Acc Id:

ENST00000648897 ⟹ ENSP00000497378

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	57,907,629 - 58,159,840 (+)	Ensembl

RefSeq Acc Id:

NM_001130480 ⟹ NP_001123952

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	58,046,642 - 58,159,920 (+)	NCBI
GRCh37	2	58,273,777 - 58,387,055 (+)	RGD
Celera	2	58,116,828 - 58,230,225 (+)	RGD
HuRef	2	57,875,865 - 58,128,335 (+)	NCBI
CHM1_1	2	58,203,888 - 58,317,318 (+)	NCBI
T2T-CHM13v2.0	2	58,051,331 - 58,164,754 (+)	NCBI

Sequence:

show sequence

GTGGACAGGCCGCTGAAAGGAACCGGCTGCGGCCTGTGTGAGGCTCCGCGGGCCGCTGCACTGC
GAGGCCGACGCAGCTGGAGAGAAGTTAGGCAGGTCCTAGGGAGGGCAGGCTCGAGTGCTGGGCC
CGCCTCCCCGCGGGACTGTAGGCCCGGGGGCTCCGCCTCGTCGCAGCGGCAGAAGTGATGCCAC
CAAAAAGAAATGAAAAATACAAACTTCCTATTCCATTTCCAGAAGGCAAGGTTCTGGATGATAT
GGAAGGCAATCAGTGGGTACTGGGCAAGAAGATTGGCTCTGGAGGATTTGGATTGATATATTTA
GCTTTCCCCACAAATAAACCAGAGAAAGATGCAAGACATGTAGTAAAAGTGGAATATCAAGAAA
ATGGCCCGTTATTTTCAGAACTTAAATTTTATCAGAGAGTTGCAAAAAAAGACTGTATCAAAAA
GTGGATAGAACGCAAACAACTTGATTATTTAGGAATTCCTCTGTTTTATGGATCTGGTCTGACT
GAATTCAAGGGAAGAAGTTACAGATTTATGGTAATGGAAAGACTAGGAATAGATTTACAGAAGA
TCTCAGGCCAGAATGGTACCTTTAAAAAGTCAACTGTCCTGCAATTAGGTATCCGAATGTTGGA
TGTACTGGAATATATACATGAAAATGAATATGTTCATGGTGATATAAAAGCAGCAAATCTACTT
TTGGGTTACAAAAATCCAGACCAGGTTTATCTTGCAGATTATGGACTTTCCTACAGATATTGTC
CCAATGGGAACCACAAACAGTATCAGGAAAATCCTAGAAAAGGCCATAATGGGACAATAGAGTT
TACCAGCTTGGATGCCCACAAGGGAGTAGCCTTGTCCAGACGAAGTGACGTTGAGATCCTCGGC
TACTGCATGCTGCGGTGGTTGTGTGGGAAACTTCCCTGGGAACAGAACCTGAAGGACCCTGTGG
CTGTGCAGACTGCTAAAACAAATCTGTTGGACGAGCTCCCCCAGTCAGTGCTTAAATGGGCTCC
TTCTGGAAGCAGTTGCTGTGAAATAGCCCAATTTTTGGTATGTGCTCATAGTTTAGCATATGAT
GAAAAGCCAAACTATCAAGCCCTCAAGAAAATTTTGAACCCTCATGGAATACCTTTAGGACCAC
TGGACTTTTCCACAAAAGGACAGAGTATAAATGTCCATACTCCAAACAGTCAAAAAGTTGATTC
ACAAAAGGCTGCAACAAAGCAAGTCAACAAGGCACACAATAGGTTAATCGAAAAAAAAGTCCAC
AGTGAGAGAAGCGCTGAGTCCTGTGCAACATGGAAAGTGCAGAAAGAGGAGAAACTGATTGGAT
TGATGAACAATGAAGCAGCTCAGGAAAGCACAAGGAGAAGACAGAAATATCAAGAGTCTCAAGA
ACCTTTGAATGAAGTAAACAGTTTCCCACAAAAAATCAGCTATACACAATTCCCAAACTCATTT
TATGAGCCTCATCAAGATTTTACCAGTCCAGATATATTCAAGAAGTCAAGATCTCCATCTTGGT
ATAAATACACTTCCACAGTCAGCACGGGGATCACAGACTTAGAAAGTTCAACTGGACTTTGGCC
TACAATTTCCCAGTTTACTCTTAGTGAAGAGACAAACGCAGATGTTTATTATTATCGCATCATC
ATACCTGTCCTTTTGATGTTAGTATTTCTTGCTTTATTTTTTCTCTGAAGATGATACCAAAATT
CCTTTTGATAATTTTTTAAGTTTCCAGCTCTTCACCGAAATGTTGTATTCTTATTTCAGTGTTT
CCTTCCAGACATTTTTAAGGTAATTGGCTTTAAAAAGAGAACATATTTTAACAAAGTTTGTGGA
CACTCTAAAAAATAAAATTGCTTTGTACTAGAAATAGTGTCATAGAATAGTGTCATAGTACAGT
TTGGAAAACACTTCTGAAG

hide sequence

RefSeq Acc Id:

NM_001130481 ⟹ NP_001123953

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	58,046,712 - 58,159,920 (+)	NCBI
GRCh37	2	58,273,777 - 58,387,055 (+)	RGD
Celera	2	58,116,828 - 58,230,225 (+)	RGD
HuRef	2	57,875,865 - 58,128,335 (+)	NCBI
CHM1_1	2	58,203,958 - 58,317,318 (+)	NCBI
T2T-CHM13v2.0	2	58,051,401 - 58,164,754 (+)	NCBI

Sequence:

show sequence

GACGCAGCTGGAGAGAAGTTAGAAGTGATGCCACCAAAAAGAAATGAAAAATACAAACTTCCTA
TTCCATTTCCAGAAGGCAAGGTTCTGGATGATATGGAAGGCAATCAGTGGGTACTGGGCAAGAA
GATTGGCTCTGGAGGATTTGGATTGATATATTTAGCTTTCCCCACAAATAAACCAGAGAAAGAT
GCAAGACATGTAGTAAAAGTGGAATATCAAGAAAATGGCCCGTTATTTTCAGAACTTAAATTTT
ATCAGAGAGTTGCAAAAAAAGACTGTATCAAAAAGTGGATAGAACGCAAACAACTTGATTATTT
AGGAATTCCTCTGTTTTATGGATCTGGTCTGACTGAATTCAAGGGAAGAAGTTACAGATTTATG
GTAATGGAAAGACTAGGAATAGATTTACAGAAGATCTCAGGCCAGAATGGTACCTTTAAAAAGT
CAACTGTCCTGCAATTAGGTATCCGAATGTTGGATGTACTGGAATATATACATGAAAATGAATA
TGTTCATGGTGATATAAAAGCAGCAAATCTACTTTTGGGTTACAAAAATCCAGACCAGGTTTAT
CTTGCAGATTATGGACTTTCCTACAGATATTGTCCCAATGGGAACCACAAACAGTATCAGGAAA
ATCCTAGAAAAGGCCATAATGGGACAATAGAGTTTACCAGCTTGGATGCCCACAAGGGAGTAGC
CTTGTCCAGACGAAGTGACGTTGAGATCCTCGGCTACTGCATGCTGCGGTGGTTGTGTGGGAAA
CTTCCCTGGGAACAGAACCTGAAGGACCCTGTGGCTGTGCAGACTGCTAAAACAAATCTGTTGG
ACGAGCTCCCCCAGTCAGTGCTTAAATGGGCTCCTTCTGGAAGCAGTTGCTGTGAAATAGCCCA
ATTTTTGGTATGTGCTCATAGTTTAGCATATGATGAAAAGCCAAACTATCAAGCCCTCAAGAAA
ATTTTGAACCCTCATGGAATACCTTTAGGACCACTGGACTTTTCCACAAAAGGACAGAGTATAA
ATGTCCATACTCCAAACAGTCAAAAAGTTGATTCACAAAAGGCTGCAACAAAGCAAGTCAACAA
GGCACACAATAGGTTAATCGAAAAAAAAGTCCACAGTGAGAGAAGCGCTGAGTCCTGTGCAACA
TGGAAAGTGCAGAAAGAGGAGAAACTGATTGGATTGATGAACAATGAAGCAGCTCAGGAAAGCA
CAAGGAGAAGACAGAAATATCAAGAGTCTCAAGAACCTTTGAATGAAGTAAACAGTTTCCCACA
AAAAATCAGCTATACACAATTCCCAAACTCATTTTATGAGCCTCATCAAGATTTTACCAGTCCA
GATATATTCAAGAAGTCAAGATCTCCATCTTGGTATAAATACACTTCCACAGTCAGCACGGGGA
TCACAGACTTAGAAAGTTCAACTGGACTTTGGCCTACAATTTCCCAGTTTACTCTTAGTGAAGA
GACAAACGCAGATGTTTATTATTATCGCATCATCATACCTGTCCTTTTGATGTTAGTATTTCTT
GCTTTATTTTTTCTCTGAAGATGATACCAAAATTCCTTTTGATAATTTTTTAAGTTTCCAGCTC
TTCACCGAAATGTTGTATTCTTATTTCAGTGTTTCCTTCCAGACATTTTTAAGGTAATTGGCTT
TAAAAAGAGAACATATTTTAACAAAGTTTGTGGACACTCTAAAAAATAAAATTGCTTTGTACTA
GAAATAGTGTCATAGAATAGTGTCATAGTACAGTTTGGAAAACACTTCTGAAG

hide sequence

RefSeq Acc Id:

NM_001130482 ⟹ NP_001123954

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	58,046,642 - 58,159,920 (+)	NCBI
GRCh37	2	58,273,777 - 58,387,055 (+)	RGD
Celera	2	58,116,828 - 58,230,225 (+)	RGD
HuRef	2	57,875,865 - 58,128,335 (+)	NCBI
CHM1_1	2	58,203,888 - 58,317,318 (+)	NCBI
T2T-CHM13v2.0	2	58,051,331 - 58,164,754 (+)	NCBI

Sequence:

show sequence

GTGGACAGGCCGCTGAAAGGAACCGGCTGCGGCCTGTGTGAGGCTCCGCGGGCCGCTGCACTGC
GAGGCCGACGCAGCTGGAGAGAAGTTAGGCAGGTCCTAGGGAGGGCAGGCTCGAGTGCTGGGCC
CGCCTCCCCGCGGGACTGTAGGCCCGGGGGCTCCGCCTCGTCGCAGCGGCAGAAGGCAAGGTTC
TGGATGATATGGAAGGCAATCAGTGGGTACTGGGCAAGAAGATTGGCTCTGGAGGATTTGGATT
GATATATTTAGCTTTCCCCACAAATAAACCAGAGAAAGATGCAAGACATGTAGTAAAAGTGGAA
TATCAAGAAAATGGCCCGTTATTTTCAGAACTTAAATTTTATCAGAGAGTTGCAAAAAAAGACT
GTATCAAAAAGTGGATAGAACGCAAACAACTTGATTATTTAGGAATTCCTCTGTTTTATGGATC
TGGTCTGACTGAATTCAAGGGAAGAAGTTACAGATTTATGGTAATGGAAAGACTAGGAATAGAT
TTACAGAAGATCTCAGGCCAGAATGGTACCTTTAAAAAGTCAACTGTCCTGCAATTAGGTATCC
GAATGTTGGATGTACTGGAATATATACATGAAAATGAATATGTTCATGGTGATATAAAAGCAGC
AAATCTACTTTTGGGTTACAAAAATCCAGACCAGGTTTATCTTGCAGATTATGGACTTTCCTAC
AGATATTGTCCCAATGGGAACCACAAACAGTATCAGGAAAATCCTAGAAAAGGCCATAATGGGA
CAATAGAGTTTACCAGCTTGGATGCCCACAAGGGAGTAGCCTTGTCCAGACGAAGTGACGTTGA
GATCCTCGGCTACTGCATGCTGCGGTGGTTGTGTGGGAAACTTCCCTGGGAACAGAACCTGAAG
GACCCTGTGGCTGTGCAGACTGCTAAAACAAATCTGTTGGACGAGCTCCCCCAGTCAGTGCTTA
AATGGGCTCCTTCTGGAAGCAGTTGCTGTGAAATAGCCCAATTTTTGGTATGTGCTCATAGTTT
AGCATATGATGAAAAGCCAAACTATCAAGCCCTCAAGAAAATTTTGAACCCTCATGGAATACCT
TTAGGACCACTGGACTTTTCCACAAAAGGACAGAGTATAAATGTCCATACTCCAAACAGTCAAA
AAGTTGATTCACAAAAGGCTGCAACAAAGCAAGTCAACAAGGCACACAATAGGTTAATCGAAAA
AAAAGTCCACAGTGAGAGAAGCGCTGAGTCCTGTGCAACATGGAAAGTGCAGAAAGAGGAGAAA
CTGATTGGATTGATGAACAATGAAGCAGCTCAGGAAAGCACAAGGAGAAGACAGAAATATCAAG
AGTCTCAAGAACCTTTGAATGAAGTAAACAGTTTCCCACAAAAAATCAGCTATACACAATTCCC
AAACTCATTTTATGAGCCTCATCAAGATTTTACCAGTCCAGATATATTCAAGAAGTCAAGATCT
CCATCTTGGTATAAATACACTTCCACAGTCAGCACGGGGATCACAGACTTAGAAAGTTCAACTG
GACTTTGGCCTACAATTTCCCAGTTTACTCTTAGTGAAGAGACAAACGCAGATGTTTATTATTA
TCGCATCATCATACCTGTCCTTTTGATGTTAGTATTTCTTGCTTTATTTTTTCTCTGAAGATGA
TACCAAAATTCCTTTTGATAATTTTTTAAGTTTCCAGCTCTTCACCGAAATGTTGTATTCTTAT
TTCAGTGTTTCCTTCCAGACATTTTTAAGGTAATTGGCTTTAAAAAGAGAACATATTTTAACAA
AGTTTGTGGACACTCTAAAAAATAAAATTGCTTTGTACTAGAAATAGTGTCATAGAATAGTGTC
ATAGTACAGTTTGGAAAACACTTCTGAAG

hide sequence

RefSeq Acc Id:

NM_001130483 ⟹ NP_001123955

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	58,046,642 - 58,159,920 (+)	NCBI
GRCh37	2	58,273,777 - 58,387,055 (+)	RGD
Celera	2	58,116,828 - 58,230,225 (+)	RGD
HuRef	2	57,875,865 - 58,128,335 (+)	NCBI
CHM1_1	2	58,203,888 - 58,317,318 (+)	NCBI
T2T-CHM13v2.0	2	58,051,331 - 58,164,754 (+)	NCBI

Sequence:

show sequence

GTGGACAGGCCGCTGAAAGGAACCGGCTGCGGCCTGTGTGAGGCTCCGCGGGCCGCTGCACTGC
GAGGCCGACGCAGCTGGAGAGAAGTTAGGCAGGTCCTAGGGAGGGCAGGCTCGAGTGCTGGGCC
CGCCTCCCCGCGGGACTGTAGGCCCGGGGGCTCCGCCTCGTCGCAGCGGCAGAAGTGATGCCAC
CAAAAAGAAATGAAAAATACAAACTTCCTATTCCATTTCCAGAAGGCAAGGTTCTGGATGATAT
GGAAGGCAATCAGTGGGTACTGGGCAAGAAGATTGGCTCTGGAGGATTTGGATTGATATATTTA
GCTTTCCCCACAAATAAACCAGAGAAAGATGCAAGACATGTAGTAAAAGTGGAATATCAAGAAA
ATGGCCCGTTATTTTCAGAACTTAAATTTTATCAGAGAGTTGCAAAAAAAGACTGTATCAAAAA
GTGGATAGAACGCAAACAACTTGATTATTTAGGAATTCCTCTGTTTTATGGATCTGGTCTGACT
GAATTCAAGGGAAGAAGTTACAGATTTATGGTAATGGAAAGACTAGGAATAGATTTACAGAAGA
TCTCAGGCCAGAATGGTACCTTTAAAAAGTCAACTGTCCTGCAATTAGGTATCCGAATGTTGGA
TGTACTGGAATATATACATGAAAATGAATATGTTCATGGTGATATAAAAGCAGCAAATCTACTT
TTGGGTTACAAAAATCCAGACCAGGTTTATCTTGCAGATTATGGACTTTCCTACAGATATTGTC
CCAATGGGAACCACAAACAGTATCAGGAAAATCCTAGAAAAGGCCATAATGGGACAATAGAGTT
TACCAGCTTGGATGCCCACAAGGGAGTAGCCTTGTCCAGACGAAGTGACGTTGAGATCCTCGGC
TACTGCATGCTGCGGTGGTTGTGTGGGAAACTTCCCTGGGAACAGAACCTGAAGGACCCTGTGG
CTGTGCAGACTGCTAAAACAAATCTGTTGGACGAGCTCCCCCAGTCAGTGCTTAAATGGGCTCC
TTCTGGAAGCAGTTGCTGTGAAATAGCCCAATTTTTGGTATGTGCTCATAGTTTAGCATATGAT
GAAAAGCCAAACTATCAAGCCCTCAAGAAAATTTTGAACCCTCATGGAATACCTTTAGGACCAC
TGGACTTTTCCACAAAAGGACAGAGTATAAATGTCCATACTCCAAACAGTCAAAAAGTTGATTC
ACAAAAGGCTGCAACAAAGCAAGTCAACAAGGCACACAATAGGTTAATCGAAAAAAAAGTCCAC
AGTGAGAGAAGCGCTGAGTCCTGTGCAACATGGAAAGTGCAGAAAGAGGAGAAACTGATTGGAT
TGATGAACAATGAAGCAGCTCAGTTTAGGTAGAAGCTTAGGCTATTGATTTGAACCCACTATTT
TTTCTAATGAAAGCACAAGGAGAAGACAGAAATATCAAGAGTCTCAAGAACCTTTGAATGAAGT
AAACAGTTTCCCACAAAAAATCAGCTATACACAATTCCCAAACTCATTTTATGAGCCTCATCAA
GATTTTACCAGTCCAGATATATTCAAGAAGTCAAGATCTCCATCTTGGTATAAATACACTTCCA
CAGTCAGCACGGGGATCACAGACTTAGAAAGTTCAACTGGACTTTGGCCTACAATTTCCCAGTT
TACTCTTAGTGAAGAGACAAACGCAGATGTTTATTATTATCGCATCATCATACCTGTCCTTTTG
ATGTTAGTATTTCTTGCTTTATTTTTTCTCTGAAGATGATACCAAAATTCCTTTTGATAATTTT
TTAAGTTTCCAGCTCTTCACCGAAATGTTGTATTCTTATTTCAGTGTTTCCTTCCAGACATTTT
TAAGGTAATTGGCTTTAAAAAGAGAACATATTTTAACAAAGTTTGTGGACACTCTAAAAAATAA
AATTGCTTTGTACTAGAAATAGTGTCATAGAATAGTGTCATAGTACAGTTTGGAAAACACTTCT
GAAG

hide sequence

RefSeq Acc Id:

NM_001288836 ⟹ NP_001275765

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	58,046,642 - 58,159,920 (+)	NCBI
HuRef	2	57,875,865 - 58,128,335 (+)	NCBI
CHM1_1	2	58,203,888 - 58,317,318 (+)	NCBI
T2T-CHM13v2.0	2	58,051,331 - 58,164,754 (+)	NCBI

Sequence:

show sequence

GTGGACAGGCCGCTGAAAGGAACCGGCTGCGGCCTGTGTGAGGCTCCGCGGGCCGCTGCACTGC
GAGGCCGACGCAGCTGGAGAGAAGTTAGGCAGGTCCTAGGGAGGGCAGGCTCGAGTGCTGGGCC
CGCCTCCCCGCGGGACTGTAGGCCCGGGGGCTCCGCCTCGTCGCAGCGGCAGAAGTGATGCCAC
CAAAAAGAAATGAAAAATACAAACTTCCTATTCCATTTCCAGAAGGCAAGGTTCTGGATGATAT
GGAAGGCAATCAGTGGGTACTGGGCAAGAAGATTGGCTCTGGAGGATTTGGATTGATATATTTA
GAGACACTGGCCATTTTTCTCTCTCCAATGCTTAGTGTGGAGTAAAGGCAGCTTCCCGCAAATT
TATTTCAAGCAAGAGCAATCGGAAGCTTCGACATGTGTGAAAGAGGCGCATAGAGAACATAGCT
TCCATTTCAGCTTTCCCCACAAATAAACCAGAGAAAGATGCAAGACATGTAGTAAAAGTGGAAT
ATCAAGAAAATGGCCCGTTATTTTCAGAACTTAAATTTTATCAGAGAGTTGCAAAAAAAGACTG
TATCAAAAAGTGGATAGAACGCAAACAACTTGATTATTTAGGAATTCCTCTGTTTTATGGATCT
GGTCTGACTGAATTCAAGGGAAGAAGTTACAGATTTATGGTAATGGAAAGACTAGGAATAGATT
TACAGAAGATCTCAGGCCAGAATGGTACCTTTAAAAAGTCAACTGTCCTGCAATTAGGTATCCG
AATGTTGGATGTACTGGAATATATACATGAAAATGAATATGTTCATGGTGATATAAAAGCAGCA
AATCTACTTTTGGGTTACAAAAATCCAGACCAGGTTTATCTTGCAGATTATGGACTTTCCTACA
GATATTGTCCCAATGGGAACCACAAACAGTATCAGGAAAATCCTAGAAAAGGCCATAATGGGAC
AATAGAGTTTACCAGCTTGGATGCCCACAAGGGAGTAGCCTTGTCCAGACGAAGTGACGTTGAG
ATCCTCGGCTACTGCATGCTGCGGTGGTTGTGTGGGAAACTTCCCTGGGAACAGAACCTGAAGG
ACCCTGTGGCTGTGCAGACTGCTAAAACAAATCTGTTGGACGAGCTCCCCCAGTCAGTGCTTAA
ATGGGCTCCTTCTGGAAGCAGTTGCTGTGAAATAGCCCAATTTTTGGTATGTGCTCATAGTTTA
GCATATGATGAAAAGCCAAACTATCAAGCCCTCAAGAAAATTTTGAACCCTCATGGAATACCTT
TAGGACCACTGGACTTTTCCACAAAAGGACAGAGTATAAATGTCCATACTCCAAACAGTCAAAA
AGTTGATTCACAAAAGGCTGCAACAAAGCAAGTCAACAAGGCACACAATAGGTTAATCGAAAAA
AAAGTCCACAGTGAGAGAAGCGCTGAGTCCTGTGCAACATGGAAAGTGCAGAAAGAGGAGAAAC
TGATTGGATTGATGAACAATGAAGCAGCTCAGGAAAGCACAAGGAGAAGACAGAAATATCAAGA
GTCTCAAGAACCTTTGAATGAAGTAAACAGTTTCCCACAAAAAATCAGCTATACACAATTCCCA
AACTCATTTTATGAGCCTCATCAAGATTTTACCAGTCCAGATATATTCAAGAAGTCAAGATCTC
CATCTTGGTATAAATACACTTCCACAGTCAGCACGGGGATCACAGACTTAGAAAGTTCAACTGG
ACTTTGGCCTACAATTTCCCAGTTTACTCTTAGTGAAGAGACAAACGCAGATGTTTATTATTAT
CGCATCATCATACCTGTCCTTTTGATGTTAGTATTTCTTGCTTTATTTTTTCTCTGAAGATGAT
ACCAAAATTCCTTTTGATAATTTTTTAAGTTTCCAGCTCTTCACCGAAATGTTGTATTCTTATT
TCAGTGTTTCCTTCCAGACATTTTTAAGGTAATTGGCTTTAAAAAGAGAACATATTTTAACAAA
GTTTGTGGACACTCTAAAAAATAAAATTGCTTTGTACTAGAAATAGTGTCATAGAATAGTGTCA
TAGTACAGTTTGGAAAACACTTCTGAAG

hide sequence

RefSeq Acc Id:

NM_001288837 ⟹ NP_001275766

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	57,907,592 - 58,159,871 (+)	NCBI
HuRef	2	57,875,865 - 58,128,335 (+)	NCBI
CHM1_1	2	58,064,879 - 58,317,318 (+)	NCBI
T2T-CHM13v2.0	2	57,912,292 - 58,164,705 (+)	NCBI

Sequence:

show sequence

AGCATTTCCAAACAGAGCAACTACAACCACTTCAAACATCCTAAACTCCCTCCAACCCTGGCTA
TTCACACGCTTCAGTTCACAACTTCCATCCAGAATCCTACTTCTCTGATTGTCCTCATGGGGAA
AGTATGCTATTTCCTTCATCCTACAAGATGCTTCTCACTGACTCTATCCATATTCTTCTCATCC
TTCAAGAGCCAAGTCAAATCTCTCTGCTTCCAATAAGCCTTCCTTGCTACACTCAGAAATGGAA
TGAATCCCCAAGATGGCTTAAGGATGCCCTTCTGTTTTGGAATGCTTTCTCTTGGTGTATATCA
AGGTTGGTTCAGTTTACCAGAGAAAAGATGCCAGGGTCTCATTCTGTCACCCAAGCTGGAGTCC
AGTGACATGGTCACAGCTCACTGAAGCCTCAACCTCCTTGGCTCAAGCAATCCTTTCACCTCAG
CCTTCTAAGTAGCTAGGAGCACAGTGTCATAAAGAAGAATATTTGAAGCTCTATAAATATGTTG
CTTTACGTGGCAAAAAGGACTTTACAGATCTGAGTACACTGGATTATCTGGGTGGGCACAATGT
AATCACAAGGGGCTTTCTAAGAAGGAAGAAGGAGGGTTCAAGGCAGAAAAACCGGAAGAAGTTA
TAACATTGGCTTTGAAGATGGAAGATGGGGACACAAGTCAAGGAATTCAGGTGGCCTCTAGAAG
CCTGAAAAGTCAAAGAAATGAATTCTCCCCTAGAGCCTCAAGAAGGAACACAGCCCTGCTGACA
GCTTGATTTTAGGATTTCTGACCTCCAGACTAAGTGATGCCACCAAAAAGAAATGAAAAATACA
AACTTCCTATTCCATTTCCAGAAGGCAAGGTTCTGGATGATATGGAAGGCAATCAGTGGGTACT
GGGCAAGAAGATTGGCTCTGGAGGATTTGGATTGATATATTTAGCTTTCCCCACAAATAAACCA
GAGAAAGATGCAAGACATGTAGTAAAAGTGGAATATCAAGAAAATGGCCCGTTATTTTCAGAAC
TTAAATTTTATCAGAGAGTTGCAAAAAAAGACTGTATCAAAAAGTGGATAGAACGCAAACAACT
TGATTATTTAGGAATTCCTCTGTTTTATGGATCTGGTCTGACTGAATTCAAGGGAAGAAGTTAC
AGATTTATGGTAATGGAAAGACTAGGAATAGATTTACAGAAGATCTCAGGCCAGAATGGTACCT
TTAAAAAGTCAACTGTCCTGCAATTAGGTATCCGAATGTTGGATGTACTGGAATATATACATGA
AAATGAATATGTTCATGGTGATATAAAAGCAGCAAATCTACTTTTGGGTTACAAAAATCCAGAC
CAGGTTTATCTTGCAGATTATGGACTTTCCTACAGATATTGTCCCAATGGGAACCACAAACAGT
ATCAGGAAAATCCTAGAAAAGGCCATAATGGGACAATAGAGTTTACCAGCTTGGATGCCCACAA
GGGAGTAGCCTTGTCCAGACGAAGTGACGTTGAGATCCTCGGCTACTGCATGCTGCGGTGGTTG
TGTGGGAAACTTCCCTGGGAACAGAACCTGAAGGACCCTGTGGCTGTGCAGACTGCTAAAACAA
ATCTGTTGGACGAGCTCCCCCAGTCAGTGCTTAAATGGGCTCCTTCTGGAAGCAGTTGCTGTGA
AATAGCCCAATTTTTGGTATGTGCTCATAGTTTAGCATATGATGAAAAGCCAAACTATCAAGCC
CTCAAGAAAATTTTGAACCCTCATGGAATACCTTTAGGACCACTGGACTTTTCCACAAAAGGAC
AGAGTATAAATGTCCATACTCCAAACAGTCAAAAAGTTGATTCACAAAAGGCTGCAACAAAGCA
AGTCAACAAGGCACACAATAGGTTAATCGAAAAAAAAGTCCACAGTGAGAGAAGCGCTGAGTCC
TGTGCAACATGGAAAGTGCAGAAAGAGGAGAAACTGATTGGATTGATGAACAATGAAGCAGCTC
AGGAAAGCACAAGGAGAAGACAGAAATATCAAGAGTCTCAAGAACCTTTGAATGAAGTAAACAG
TTTCCCACAAAAAATCAGCTATACACAATTCCCAAACTCATTTTATGAGCCTCATCAAGATTTT
ACCAGTCCAGATATATTCAAGAAGTCAAGATCTCCATCTTGGTATAAATACACTTCCACAGTCA
GCACGGGGATCACAGACTTAGAAAGTTCAACTGGACTTTGGCCTACAATTTCCCAGTTTACTCT
TAGTGAAGAGACAAACGCAGATGTTTATTATTATCGCATCATCATACCTGTCCTTTTGATGTTA
GTATTTCTTGCTTTATTTTTTCTCTGAAGATGATACCAAAATTCCTTTTGATAATTTTTTAAGT
TTCCAGCTCTTCACCGAAATGTTGTATTCTTATTTCAGTGTTTCCTTCCAGACATTTTTAAGGT
AATTGGCTTTAAAAAGAGAACATATTTTAACAAAGTTTGTGGACACTCTAAAAAATAAAATTGC
TTTGTACTAGAAA

hide sequence

RefSeq Acc Id:

NM_001288838 ⟹ NP_001275767

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	57,907,592 - 58,159,871 (+)	NCBI
HuRef	2	57,875,865 - 58,128,335 (+)	NCBI
CHM1_1	2	58,064,879 - 58,317,318 (+)	NCBI
T2T-CHM13v2.0	2	57,912,292 - 58,164,705 (+)	NCBI

Sequence:

show sequence

AGCATTTCCAAACAGAGCAACTACAACCACTTCAAACATCCTAAACTCCCTCCAACCCTGGCTA
TTCACACGCTTCAGTTCACAACTTCCATCCAGAATCCTACTTCTCTGATTGTCCTCATGGGGAA
AGTATGCTATTTCCTTCATCCTACAAGATGCTTCTCACTGACTCTATCCATATTCTTCTCATCC
TTCAAGAGCCAAGTCAAATCTCTCTGCTTCCAATAAGCCTTCCTTGCTACACTCAGAAATGGAA
TGAATCCCCAAGATGGCTTAAGGATGCCCTTCTGTTTTGGAATGCTTTCTCTTGGTGTATATCA
AGGTTGGTTCAGTTTACCAGAGAAAAGATGCCAGTGTCATAAAGAAGAATATTTGAAGCTCTAT
AAATATGTTGCTTTACGTGGCAAAAAGGACTTTACAGATCTGAGTACACTGGATTATCTGGGTG
GGCACAATGTAATCACAAGGGGCTTTCTAAGAAGGAAGAAGGAGGGTTCAAGGCAGAAAAACCG
GAAGAAGTTATAACATTGGCTTTGAAGATGGAAGATGGGGACACAAGTCAAGGAATTCAGGTGG
CCTCTAGAAGCCTGAAAAGTCAAAGAAATGAATTCTCCCCTAGAGCCTCAAGAAGGAACACAGC
CCTGCTGACAGCTTGATTTTAGGATTTCTGACCTCCAGACTAAGTGATGCCACCAAAAAGAAAT
GAAAAATACAAACTTCCTATTCCATTTCCAGAAGGCAAGGTTCTGGATGATATGGAAGGCAATC
AGTGGGTACTGGGCAAGAAGATTGGCTCTGGAGGATTTGGATTGATATATTTAGCTTTCCCCAC
AAATAAACCAGAGAAAGATGCAAGACATGTAGTAAAAGTGGAATATCAAGAAAATGGCCCGTTA
TTTTCAGAACTTAAATTTTATCAGAGAGTTGCAAAAAAAGACTGTATCAAAAAGTGGATAGAAC
GCAAACAACTTGATTATTTAGGAATTCCTCTGTTTTATGGATCTGGTCTGACTGAATTCAAGGG
AAGAAGTTACAGATTTATGGTAATGGAAAGACTAGGAATAGATTTACAGAAGATCTCAGGCCAG
AATGGTACCTTTAAAAAGTCAACTGTCCTGCAATTAGGTATCCGAATGTTGGATGTACTGGAAT
ATATACATGAAAATGAATATGTTCATGGTGATATAAAAGCAGCAAATCTACTTTTGGGTTACAA
AAATCCAGACCAGGTTTATCTTGCAGATTATGGACTTTCCTACAGATATTGTCCCAATGGGAAC
CACAAACAGTATCAGGAAAATCCTAGAAAAGGCCATAATGGGACAATAGAGTTTACCAGCTTGG
ATGCCCACAAGGGAGTAGCCTTGTCCAGACGAAGTGACGTTGAGATCCTCGGCTACTGCATGCT
GCGGTGGTTGTGTGGGAAACTTCCCTGGGAACAGAACCTGAAGGACCCTGTGGCTGTGCAGACT
GCTAAAACAAATCTGTTGGACGAGCTCCCCCAGTCAGTGCTTAAATGGGCTCCTTCTGGAAGCA
GTTGCTGTGAAATAGCCCAATTTTTGGTATGTGCTCATAGTTTAGCATATGATGAAAAGCCAAA
CTATCAAGCCCTCAAGAAAATTTTGAACCCTCATGGAATACCTTTAGGACCACTGGACTTTTCC
ACAAAAGGACAGAGTATAAATGTCCATACTCCAAACAGTCAAAAAGTTGATTCACAAAAGGCTG
CAACAAAGCAAGTCAACAAGGCACACAATAGGTTAATCGAAAAAAAAGTCCACAGTGAGAGAAG
CGCTGAGTCCTGTGCAACATGGAAAGTGCAGAAAGAGGAGAAACTGATTGGATTGATGAACAAT
GAAGCAGCTCAGTTTAGGTAGAAGCTTAGGCTATTGATTTGAACCCACTATTTTTTCTAATGAA
AGCACAAGGAGAAGACAGAAATATCAAGAGTCTCAAGAACCTTTGAATGAAGTAAACAGTTTCC
CACAAAAAATCAGCTATACACAATTCCCAAACTCATTTTATGAGCCTCATCAAGATTTTACCAG
TCCAGATATATTCAAGAAGTCAAGATCTCCATCTTGGTATAAATACACTTCCACAGTCAGCACG
GGGATCACAGACTTAGAAAGTTCAACTGGACTTTGGCCTACAATTTCCCAGTTTACTCTTAGTG
AAGAGACAAACGCAGATGTTTATTATTATCGCATCATCATACCTGTCCTTTTGATGTTAGTATT
TCTTGCTTTATTTTTTCTCTGAAGATGATACCAAAATTCCTTTTGATAATTTTTTAAGTTTCCA
GCTCTTCACCGAAATGTTGTATTCTTATTTCAGTGTTTCCTTCCAGACATTTTTAAGGTAATTG
GCTTTAAAAAGAGAACATATTTTAACAAAGTTTGTGGACACTCTAAAAAATAAAATTGCTTTGT
ACTAGAAA

hide sequence

RefSeq Acc Id:

NM_001288839 ⟹ NP_001275768

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	58,046,806 - 58,159,871 (+)	NCBI
HuRef	2	57,875,865 - 58,128,335 (+)	NCBI
CHM1_1	2	58,203,888 - 58,317,318 (+)	NCBI
T2T-CHM13v2.0	2	58,051,495 - 58,164,705 (+)	NCBI

Sequence:

show sequence

CTCGTCGCAGCGGCAGGTAGGAGGCGGTGCGCGCGGCCCGGCGACGGGGGATCCTGAGGCCCGA
AGTGATGCCACCAAAAAGAAATGAAAAATACAAACTTCCTATTCCATTTCCAGAAGGCAAGGTT
CTGGATGATATGGAAGGCAATCAGTGGGTACTGGGCAAGAAGATTGGCTCTGGAGGATTTGGAT
TGATATATTTAGCTTTCCCCACAAATAAACCAGAGAAAGATGCAAGACATGTAGTAAAAGTGTC
AAAAAGTGGATAGAACGCAAACAACTTGATTATTTAGGAATTCCTCTGTTTTATGGATCTGGTC
TGACTGAATTCAAGGGAAGAAGTTACAGATTTATGGTAATGGAAAGACTAGGAATAGATTTACA
GAAGATCTCAGGCCAGAATGGTACCTTTAAAAAGTCAACTGTCCTGCAATTAGGTATCCGAATG
TTGGATGTACTGGAATATATACATGAAAATGAATATGTTCATGGTGATATAAAAGCAGCAAATC
TACTTTTGGGTTACAAAAATCCAGACCAGGTTTATCTTGCAGATTATGGACTTTCCTACAGATA
TTGTCCCAATGGGAACCACAAACAGTATCAGGAAAATCCTAGAAAAGGCCATAATGGGACAATA
GAGTTTACCAGCTTGGATGCCCACAAGGGAGTAGCCTTGTCCAGACGAAGTGACGTTGAGATCC
TCGGCTACTGCATGCTGCGGTGGTTGTGTGGGAAACTTCCCTGGGAACAGAACCTGAAGGACCC
TGTGGCTGTGCAGACTGCTAAAACAAATCTGTTGGACGAGCTCCCCCAGTCAGTGCTTAAATGG
GCTCCTTCTGGAAGCAGTTGCTGTGAAATAGCCCAATTTTTGGTATGTGCTCATAGTTTAGCAT
ATGATGAAAAGCCAAACTATCAAGCCCTCAAGAAAATTTTGAACCCTCATGGAATACCTTTAGG
ACCACTGGACTTTTCCACAAAAGGACAGAGTATAAATGTCCATACTCCAAACAGTCAAAAAGTT
GATTCACAAAAGGCTGCAACAAAGCAAGTCAACAAGGCACACAATAGGTTAATCGAAAAAAAAG
TCCACAGTGAGAGAAGCGCTGAGTCCTGTGCAACATGGAAAGTGCAGAAAGAGGAGAAACTGAT
TGGATTGATGAACAATGAAGCAGCTCAGGAAAGCACAAGGAGAAGACAGAAATATCAAGAGTCT
CAAGAACCTTTGAATGAAGTAAACAGTTTCCCACAAAAAATCAGCTATACACAATTCCCAAACT
CATTTTATGAGCCTCATCAAGATTTTACCAGTCCAGATATATTCAAGAAGTCAAGATCTCCATC
TTGGTATAAATACACTTCCACAGTCAGCACGGGGATCACAGACTTAGAAAGTTCAACTGGACTT
TGGCCTACAATTTCCCAGTTTACTCTTAGTGAAGAGACAAACGCAGATGTTTATTATTATCGCA
TCATCATACCTGTCCTTTTGATGTTAGTATTTCTTGCTTTATTTTTTCTCTGAAGATGATACCA
AAATTCCTTTTGATAATTTTTTAAGTTTCCAGCTCTTCACCGAAATGTTGTATTCTTATTTCAG
TGTTTCCTTCCAGACATTTTTAAGGTAATTGGCTTTAAAAAGAGAACATATTTTAACAAAGTTT
GTGGACACTCTAAAAAATAAAATTGCTTTGTACTAGAAA

hide sequence

RefSeq Acc Id:

NM_006296 ⟹ NP_006287

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	58,046,806 - 58,159,871 (+)	NCBI
GRCh37	2	58,273,777 - 58,387,055 (+)	RGD
Build 36	2	58,127,224 - 58,240,510 (+)	NCBI Archive
Celera	2	58,116,828 - 58,230,225 (+)	RGD
HuRef	2	57,875,865 - 58,128,335 (+)	NCBI
CHM1_1	2	58,203,888 - 58,317,318 (+)	NCBI
T2T-CHM13v2.0	2	58,051,495 - 58,164,705 (+)	NCBI

Sequence:

show sequence

CTCGTCGCAGCGGCAGGTAGGAGGCGGTGCGCGCGGCCCGGCGACGGGGGATCCTGAGGCCCGA
AGTGATGCCACCAAAAAGAAATGAAAAATACAAACTTCCTATTCCATTTCCAGAAGGCAAGGTT
CTGGATGATATGGAAGGCAATCAGTGGGTACTGGGCAAGAAGATTGGCTCTGGAGGATTTGGAT
TGATATATTTAGCTTTCCCCACAAATAAACCAGAGAAAGATGCAAGACATGTAGTAAAAGTGGA
ATATCAAGAAAATGGCCCGTTATTTTCAGAACTTAAATTTTATCAGAGAGTTGCAAAAAAAGAC
TGTATCAAAAAGTGGATAGAACGCAAACAACTTGATTATTTAGGAATTCCTCTGTTTTATGGAT
CTGGTCTGACTGAATTCAAGGGAAGAAGTTACAGATTTATGGTAATGGAAAGACTAGGAATAGA
TTTACAGAAGATCTCAGGCCAGAATGGTACCTTTAAAAAGTCAACTGTCCTGCAATTAGGTATC
CGAATGTTGGATGTACTGGAATATATACATGAAAATGAATATGTTCATGGTGATATAAAAGCAG
CAAATCTACTTTTGGGTTACAAAAATCCAGACCAGGTTTATCTTGCAGATTATGGACTTTCCTA
CAGATATTGTCCCAATGGGAACCACAAACAGTATCAGGAAAATCCTAGAAAAGGCCATAATGGG
ACAATAGAGTTTACCAGCTTGGATGCCCACAAGGGAGTAGCCTTGTCCAGACGAAGTGACGTTG
AGATCCTCGGCTACTGCATGCTGCGGTGGTTGTGTGGGAAACTTCCCTGGGAACAGAACCTGAA
GGACCCTGTGGCTGTGCAGACTGCTAAAACAAATCTGTTGGACGAGCTCCCCCAGTCAGTGCTT
AAATGGGCTCCTTCTGGAAGCAGTTGCTGTGAAATAGCCCAATTTTTGGTATGTGCTCATAGTT
TAGCATATGATGAAAAGCCAAACTATCAAGCCCTCAAGAAAATTTTGAACCCTCATGGAATACC
TTTAGGACCACTGGACTTTTCCACAAAAGGACAGAGTATAAATGTCCATACTCCAAACAGTCAA
AAAGTTGATTCACAAAAGGCTGCAACAAAGCAAGTCAACAAGGCACACAATAGGTTAATCGAAA
AAAAAGTCCACAGTGAGAGAAGCGCTGAGTCCTGTGCAACATGGAAAGTGCAGAAAGAGGAGAA
ACTGATTGGATTGATGAACAATGAAGCAGCTCAGGAAAGCACAAGGAGAAGACAGAAATATCAA
GAGTCTCAAGAACCTTTGAATGAAGTAAACAGTTTCCCACAAAAAATCAGCTATACACAATTCC
CAAACTCATTTTATGAGCCTCATCAAGATTTTACCAGTCCAGATATATTCAAGAAGTCAAGATC
TCCATCTTGGTATAAATACACTTCCACAGTCAGCACGGGGATCACAGACTTAGAAAGTTCAACT
GGACTTTGGCCTACAATTTCCCAGTTTACTCTTAGTGAAGAGACAAACGCAGATGTTTATTATT
ATCGCATCATCATACCTGTCCTTTTGATGTTAGTATTTCTTGCTTTATTTTTTCTCTGAAGATG
ATACCAAAATTCCTTTTGATAATTTTTTAAGTTTCCAGCTCTTCACCGAAATGTTGTATTCTTA
TTTCAGTGTTTCCTTCCAGACATTTTTAAGGTAATTGGCTTTAAAAAGAGAACATATTTTAACA
AAGTTTGTGGACACTCTAAAAAATAAAATTGCTTTGTACTAGAAA

hide sequence

RefSeq Acc Id:

XM_005264540 ⟹ XP_005264597

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	58,046,806 - 58,159,920 (+)	NCBI
GRCh37	2	58,273,777 - 58,387,055 (+)	NCBI

Sequence:

show sequence

TCTTGGGTGGCGGGCGGCACCTCCGCTTGCAGTGCCGGAGCCGCGGCCCCGCTCGGAAAAGGGC
TGCCGTCGGAGTTAGATGCCGGGGACTCCGGGCCGTCCCAGCCCCCGGGCCTCAGCTCCGGCCC
GGGCAGAGTCGCTGCTTCCGCGTTTGGTTCTTTTTTCCCCGCTGGGAGTGAGAACAAGGCGTCC
CCTTCTACTCACGTTTGCCAAAAGCGGGTCCGACGTGTTAGCGGAAAAAAGTGATGCCACCAAA
AAGAAATGAAAAATACAAACTTCCTATTCCATTTCCAGAAGGCAAGGTTCTGGATGATATGGAA
GGCAATCAGTGGGTACTGGGCAAGAAGATTGGCTCTGGAGGATTTGGATTGATATATTTAGCTT
TCCCCACAAATAAACCAGAGAAAGATGCAAGACATGTAGTAAAAGTGGAATATCAAGAAAATGG
CCCGTTATTTTCAGAACTTAAATTTTATCAGAGAGTTGCAAAAAAAGACTGTATCAAAAAGTGG
ATAGAACGCAAACAACTTGATTATTTAGGAATTCCTCTGTTTTATGGATCTGGTCTGACTGAAT
TCAAGGGAAGAAGTTACAGATTTATGGTAATGGAAAGACTAGGAATAGATTTACAGAAGATCTC
AGGCCAGAATGGTACCTTTAAAAAGTCAACTGTCCTGCAATTAGGTATCCGAATGTTGGATGTA
CTGGAATATATACATGAAAATGAATATGTTCATGGTGATATAAAAGCAGCAAATCTACTTTTGG
GTTACAAAAATCCAGACCAGGTTTATCTTGCAGATTATGGACTTTCCTACAGATATTGTCCCAA
TGGGAACCACAAACAGTATCAGGAAAATCCTAGAAAAGGCCATAATGGGACAATAGAGTTTACC
AGCTTGGATGCCCACAAGGGAGTAGCCTTGTCCAGACGAAGTGACGTTGAGATCCTCGGCTACT
GCATGCTGCGGTGGTTGTGTGGGAAACTTCCCTGGGAACAGAACCTGAAGGACCCTGTGGCTGT
GCAGACTGCTAAAACAAATCTGTTGGACGAGCTCCCCCAGTCAGTGCTTAAATGGGCTCCTTCT
GGAAGCAGTTGCTGTGAAATAGCCCAATTTTTGGTATGTGCTCATAGTTTAGCATATGATGAAA
AGCCAAACTATCAAGCCCTCAAGAAAATTTTGAACCCTCATGGAATACCTTTAGGACCACTGGA
CTTTTCCACAAAAGGACAGAGTATAAATGTCCATACTCCAAACAGTCAAAAAGTTGATTCACAA
AAGGCTGCAACAAAGCAAGTCAACAAGGCACACAATAGGTTAATCGAAAAAAAAGTCCACAGTG
AGAGAAGCGCTGAGTCCTGTGCAACATGGAAAGTGCAGAAAGAGGAGAAACTGATTGGATTGAT
GAACAATGAAGCAGCTCAGGAAAGCACAAGGAGAAGACAGAAATATCAAGAGTCTCAAGAACCT
TTGAATGAAGTAAACAGTTTCCCACAAAAAATCAGCTATACACAATTCCCAAACTCATTTTATG
AGCCTCATCAAGATTTTACCAGTCCAGATATATTCAAGAAGTCAAGATCTCCATCTTGGTATAA
ATACACTTCCACAGTCAGCACGGGGATCACAGACTTAGAAAGTTCAACTGGACTTTGGCCTACA
ATTTCCCAGTTTACTCTTAGTGAAGAGACAAACGCAGATGTTTATTATTATCGCATCATCATAC
CTGTCCTTTTGATGTTAGTATTTCTTGCTTTATTTTTTCTCTGAAGATGATACCAAAATTCCTT
TTGATAATTTTTTAAGTTTCCAGCTCTTCACCGAAATGTTGTATTCTTATTTCAGTGTTTCCTT
CCAGACATTTTTAAGGTAATTGGCTTTAAAAAGAGAACATATTTTAACAAAGTTTGTGGACACT
CTAAAAAATAAAATTGCTTTGTACTAGAAATAGTGTCATAGAATAGTGTCATAGTACAGTTTGG
AAAACACTTCTGAAGTTTCAGATCACCTAGGAAATCTAGAAAAGGAGTTTAATGTTTTTGATCA
GAGAATTTGAAAAATAGAAATACAGAGAATGAGTTTCAAAAGTTTTAGATAAACTGATATACTA
TATAGATCTATCTTCTAGAACATATTACTGAAAGCTAGGCACATTTTATGAGATGTGATTAACA
ATTTGCTTACCTTACTACAATATGGACATTCACCAAATATGATGTTAAAACTCTGTCTACTAGT
TAGTAGTCCTCTCAGCCACTGCAAATTTTAAAAGATAAAGGAGAAGCGTCAGCATGATTACAAA
TTACAGATACTCCAAATGTCATTCCCTTTGTTTTTAAGTGCATTATGTTTTTATTCCAGAAGAC
TTAGCTTAATTTTGTTTTGCAAGAGTAAGGGATGTATTTCCTGAGCCAATAGCAGACTATTAAG
ATGTTGAGTAACAAGGGAAATCAACATGGAATTGAAGGCCTAAACCACTGGTTTATAACCAGAT
TATGGGCCCCTTTAAGAATCTGATAAGAATTACGCATTTTCTTTATCCCCAGAATAGACATACA
TAAAAATAATGCATACTAAGTTCCTGGCATTCATAGACTTTCCCTAAATCCATTAATCACAAAT
TAACAACTCCTGCTGTTAAAGATACTACAGGCTCTTGAAAATTTCCCTCTTAGTTCTGGTCTGA
ATCACTAACAGTGGGTTAATTTTCAACCCATTGATTATAAGCATGAGCCAGTGAATTTTTAAAA
ATTAAATGAATATTCATAATTACAAAAGAAATCACATGTTCCCTTAGAGTATTTCTGTAATTTG
ACCTGTATTTCTGTAATTTCATGATTTTATATAAGGTAAATAGATGCCTCTGCCTAAGTTCTCC
ATTGGCAAAGTACAGACGGCACCAACTGCTACCTCTAATCACAAAAGTAAAGATGTGATATTAA
GGAAGACTGAAACCGAAGGCAACATACAATTGCAAGGTGTTCTGTATATAGTTACACACAGTTT
ATCATGTATCAACTAGGCCCTAAGGTGAAGCCAGGCACTAAAGACAGGAATGAAAGTAGACTTC
ACATACAGTAAGTAAAGTGGCATTGCCTGAGTGCTGTGAGACTCAGATCACAAAAGGCATTCTT
CTCAACATGAAAAGTAGTAGTATTGGATATATTCTATTCTTAAATGCAGCCTGAAAAGTAATAG
ATACTACATAGTACTAATTTCATTTTCACTGTATTACTGCCACTTTCAACCACCTCCACCTCGG
GTAAACCTATGAAGCTTACATTGTGGTAACAAGGAATTTATAGAAAGATTCCAATGTACCATCA
ATTTAATTTGTTATGTGTCAATAAGCTAGTCCATGAATATATTCTGGATAGATTTTCTCCCTTG
GATACTTCAGAACATTTCTCCACTCATTAGTAACTGTGATGAAGAAATGAAGCACATAAGCATC
TGGAATAAACTGGTAAAAGGAGTTAATGGCAAAAGAGAGGATCACTATTGACTCAACAGATTTT
AGATTCTGTGTATTTCAAACAGGAATACTTCCTATGTTGTGTTAGCGGAAAAAAGTCTTGACAA
TATTTTTATTTTTTACCTCATATAAGCATATTTGATGGAAAGGTTGTCCACACTGAGAATTATC
ACACACTTGATCAGGAATGGTACCGTCAAGTTGATAAGCATAACAAATTCCACAATCCATAGTA
AAATCCTTCAAAAGAAAAATATTT

hide sequence

RefSeq Acc Id:

XM_006712090 ⟹ XP_006712153

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	58,046,806 - 58,159,920 (+)	NCBI

Sequence:

show sequence

CCGGGGGCTCCGCCTCGTCGCAGCGGCAGGTAGGAGGCGGTGCGCGCGGCCCGGCGACGGGGGA
TCCTGAGGCCCGAAGTGATGCCACCAAAAAGAAATGAAAAATACAAACTTCCTATTCCATTTCC
AGAAGGCAAGGTTCTGGATGATATGGAAGGCAATCAGTGGGTACTGGGCAAGAAGATTGGCTCT
GGAGGATTTGGATTGATATATTTAGCTTTCCCCACAAATAAACCAGAGAAAGATGCAAGACATG
TAGTAAAAGTGGAATATCAAGAAAATGGCCCGTTATTTTCAGAACTTAAATTTTATCAGAGAGT
TGCAAAAAAAGACTGTATCAAAAAGTGGATAGAACGCAAACAACTTGATTATTTAGGAATTCCT
CTGTTTTATGGATCTGGTCTGACTGAATTCAAGGGAAGAAGTTACAGATTTATGGTAATGGAAA
GACTAGGAATAGATTTACAGAAGATCTCAGGCCAGAATGGTACCTTTAAAAAGTCAACTGTCCT
GCAATTAGGTATCCGAATGTTGGATGTACTGGAATATATACATGAAAATGAATATGTTCATGGT
GATATAAAAGCAGCAAATCTACTTTTGGGTTACAAAAATCCAGACCAGGTTTATCTTGCAGATT
ATGGACTTTCCTACAGATATTGTCCCAATGGGAACCACAAACAGTATCAGGAAAATCCTAGAAA
AGGCCATAATGGGACAATAGAGTTTACCAGCTTGGATGCCCACAAGGGAGTAGCCTTGTCCAGA
CGAAGTGACGTTGAGATCCTCGGCTACTGCATGCTGCGGTGGTTGTGTGGGAAACTTCCCTGGG
AACAGAACCTGAAGGACCCTGTGGCTGTGCAGACTGCTAAAACAAATCTGTTGGACGAGCTCCC
CCAGTCAGTGCTTAAATGGGCTCCTTCTGGAAGCAGTTGCTGTGAAATAGCCCAATTTTTGGTA
TGTGCTCATAGTTTAGCATATGATGAAAAGCCAAACTATCAAGCCCTCAAGAAAATTTTGAACC
CTCATGGAATACCTTTAGGACCACTGGACTTTTCCACAAAAGGACAGAGTATAAATGTCCATAC
TCCAAACAGTCAAAAAGTTGATTCACAAAAGGCTGCAACAAAGCAAGTCAACAAGGCACACAAT
AGGTTAATCGAAAAAAAAGTCCACAGTGAGAGAAGCGCTGAGTCCTGTGCAACATGGAAAGTGC
AGAAAGAGGAGAAACTGATTGGATTGATGAACAATGAAGCAGCTCAGGTAGAAGCTTAGGCTAT
TGATTTGAACCCACTATTTTTTCTAATGAAAGCACAAGGAGAAGACAGAAATATCAAGAGTCTC
AAGAACCTTTGAATGAAGTAAACAGTTTCCCACAAAAAATCAGCTATACACAATTCCCAAACTC
ATTTTATGAGCCTCATCAAGATTTTACCAGTCCAGATATATTCAAGAAGTCAAGATCTCCATCT
TGGTATAAATACACTTCCACAGTCAGCACGGGGATCACAGACTTAGAAAGTTCAACTGGACTTT
GGCCTACAATTTCCCAGTTTACTCTTAGTGAAGAGACAAACGCAGATGTTTATTATTATCGCAT
CATCATACCTGTCCTTTTGATGTTAGTATTTCTTGCTTTATTTTTTCTCTGAAGATGATACCAA
AATTCCTTTTGATAATTTTTTAAGTTTCCAGCTCTTCACCGAAATGTTGTATTCTTATTTCAGT
GTTTCCTTCCAGACATTTTTAAGGTAATTGGCTTTAAAAAGAGAACATATTTTAACAAAGTTTG
TGGACACTCTAAAAAATAAAATTGCTTTGTACTAGAAATAGTGTCATAGAATAGTGTCATAGTA
CAGTTTGGAAAACACTTCTGAAGTTTCAGATCACCTAGGAAATCTAGAAAAGGAGTTTAATGTT
TTTGATCAGAGAATTTGAAAAATAGAAATACAGAGAATGAGTTTCAAAAGTTTTAGATAAACTG
ATATACTATATAGATCTATCTTCTAGAACATATTACTGAAAGCTAGGCACATTTTATGAGATGT
GATTAACAATTTGCTTACCTTACTACAATATGGACATTCACCAAATATGATGTTAAAACTCTGT
CTACTAGTTAGTAGTCCTCTCAGCCACTGCAAATTTTAAAAGATAAAGGAGAAGCGTCAGCATG
ATTACAAATTACAGATACTCCAAATGTCATTCCCTTTGTTTTTAAGTGCATTATGTTTTTATTC
CAGAAGACTTAGCTTAATTTTGTTTTGCAAGAGTAAGGGATGTATTTCCTGAGCCAATAGCAGA
CTATTAAGATGTTGAGTAACAAGGGAAATCAACATGGAATTGAAGGCCTAAACCACTGGTTTAT
AACCAGATTATGGGCCCCTTTAAGAATCTGATAAGAATTACGCATTTTCTTTATCCCCAGAATA
GACATACATAAAAATAATGCATACTAAGTTCCTGGCATTCATAGACTTTCCCTAAATCCATTAA
TCACAAATTAACAACTCCTGCTGTTAAAGATACTACAGGCTCTTGAAAATTTCCCTCTTAGTTC
TGGTCTGAATCACTAACAGTGGGTTAATTTTCAACCCATTGATTATAAGCATGAGCCAGTGAAT
TTTTAAAAATTAAATGAATATTCATAATTACAAAAGAAATCACATGTTCCCTTAGAGTATTTCT
GTAATTTGACCTGTATTTCTGTAATTTCATGATTTTATATAAGGTAAATAGATGCCTCTGCCTA
AGTTCTCCATTGGCAAAGTACAGACGGCACCAACTGCTACCTCTAATCACAAAAGTAAAGATGT
GATATTAAGGAAGACTGAAACCGAAGGCAACATACAATTGCAAGGTGTTCTGTATATAGTTACA
CACAGTTTATCATGTATCAACTAGGCCCTAAGGTGAAGCCAGGCACTAAAGACAGGAATGAAAG
TAGACTTCACATACAGTAAGTAAAGTGGCATTGCCTGAGTGCTGTGAGACTCAGATCACAAAAG
GCATTCTTCTCAACATGAAAAGTAGTAGTATTGGATATATTCTATTCTTAAATGCAGCCTGAAA
AGTAATAGATACTACATAGTACTAATTTCATTTTCACTGTATTACTGCCACTTTCAACCACCTC
CACCTCGGGTAAACCTATGAAGCTTACATTGTGGTAACAAGGAATTTATAGAAAGATTCCAATG
TACCATCAATTTAATTTGTTATGTGTCAATAAGCTAGTCCATGAATATATTCTGGATAGATTTT
CTCCCTTGGATACTTCAGAACATTTCTCCACTCATTAGTAACTGTGATGAAGAAATGAAGCACA
TAAGCATCTGGAATAAACTGGTAAAAGGA

hide sequence

RefSeq Acc Id:

XM_006712091 ⟹ XP_006712154

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	58,046,806 - 58,159,920 (+)	NCBI

Sequence:

show sequence

ATTCCCCATGTAGCCGCGCCCTCTCCTTCCCCTGGGCGTCTCCGGGGCGTGGACAGGCCGCTGA
AAGGAACCGGCTGCGGCCTGTGTGAGGCTCCGCGGGCCGCTGCACTGCGAGGCCGACGCAGCTG
GAGAGAAGTTAGGCAGGTCCTAGGGAGGGCAGGCTCGAGTGCTGGGCCCGCCTCCCCGCGGGAC
TGTAGGCCCGGGGGCTCCGCCTCGTCGCAGCGGCAGGTAGGAGGCGGTGCGCGCGGCCCGGCGA
CGGGGGATCCTGAGGCCCGAAGTGATGCCACCAAAAAGAAATGAAAAATACAAACTTCCTATTC
CATTTCCAGAAGGCAAGGTTCTGGATGATATGGAAGGCAATCAGTGGGTACTGGGCAAGAAGAT
TGGCTCTGGAGGATTTGGATTGATATATTTAGCTTTCCCCACAAATAAACCAGAGAAAGATGCA
AGACATGTAGTAAAAGTGGAATATCAAGAAAATGGCCCGTTATTTTCAGAACTTAAATTTTATC
AGAGAGTTGCAAAAAAAGACTGTATCAAAAAGTGGATAGAACGCAAACAACTTGATTATTTAGG
AATTCCTCTGTTTTATGGATCTGGTCTGACTGAATTCAAGGGAAGAAGTTACAGATTTATGGTA
ATGGAAAGACTAGGAATAGATTTACAGAAGATCTCAGGCCAGAATGGTACCTTTAAAAAGTCAA
CTGTCCTGCAATTAGGTATCCGAATGTTGGATGTACTGGAATATATACATGAAAATGAATATGT
TCATGGTGATATAAAAGCAGCAAATCTACTTTTGGGTTACAAAAATCCAGACCAGGTTTATCTT
GCAGATTATGGACTTTCCTACAGATATTGTCCCAATGGGAACCACAAACAGTATCAGGAAAATC
CTAGAAAAGGCCATAATGGGACAATAGAGTTTACCAGCTTGGATGCCCACAAGGGAGTAGCCTT
GTCCAGACGAAGTGACGTTGAGATCCTCGGCTACTGCATGCTGCGGTGGTTGTGTGGGAAACTT
CCCTGGGAACAGAACCTGAAGGACCCTGTGGCTGTGCAGACTGCTAAAACAAATCTGTTGGACG
AGCTCCCCCAGTCAGTGCTTAAATGGGCTCCTTCTGGAAGCAGTTGCTGTGAAATAGCCCAATT
TTTGGTATGTGCTCATAGTTTAGCATATGATGAAAAGCCAAACTATCAAGCCCTCAAGAAAATT
TTGAACCCTCATGGAATACCTTTAGGACCACTGGACTTTTCCACAAAAGGACAGAGTATAAATG
TCCATACTCCAAACAGTCAAAAAGTTGATTCACAAAAGGCTGCAACAAAGCAAGTCAACAAGGC
ACACAATAGGTTAATCGAAAAAAAAGTCCACAGTGAGAGAAGCGCTGAGTCCTGTGCAACATGG
AAAGTGCAGAAAGAGGAGAAACTGATTGGATTGATGAACAATGAAGCAGCTCAGTTTAGGTAGA
AGCTTAGGCTATTGATTTGAACCCACTATTTTTTCTAATGAAAGCACAAGGAGAAGACAGAAAT
ATCAAGAGTCTCAAGAACCTTTGAATGAAGTAAACAGTTTCCCACAAAAAATCAGCTATACACA
ATTCCCAAACTCATTTTATGAGCCTCATCAAGATTTTACCAGTCCAGATATATTCAAGAAGTCA
AGATCTCCATCTTGGTATAAATACACTTCCACAGTCAGCACGGGGATCACAGACTTAGAAAGTT
CAACTGGACTTTGGCCTACAATTTCCCAGTTTACTCTTAGTGAAGAGACAAACGCAGATGTTTA
TTATTATCGCATCATCATACCTGTCCTTTTGATGTTAGTATTTCTTGCTTTATTTTTTCTCTGA
AGATGATACCAAAATTCCTTTTGATAATTTTTTAAGTTTCCAGCTCTTCACCGAAATGTTGTAT
TCTTATTTCAGTGTTTCCTTCCAGACATTTTTAAGGTAATTGGCTTTAAAAAGAGAACATATTT
TAACAAAGTTTGTGGACACTCTAAAAAATAAAATTGCTTTGTACTAGAAATAGTGTCATAGAA

hide sequence

RefSeq Acc Id:

XM_011533092 ⟹ XP_011531394

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	58,047,195 - 58,159,920 (+)	NCBI

Sequence:

show sequence

CCAGTTTGCTCGGAAACTCGTGTTGAGGACTCATCTTAGCCCTGGGAAGAAGTGATGCCACCAA
AAAGAAATGAAAAATACAAACTTCCTATTCCATTTCCAGAAGGCAAGGTTCTGGATGATATGGA
AGGCAATCAGTGGGTACTGGGCAAGAAGATTGGCTCTGGAGGATTTGGATTGATATATTTAGCT
TTCCCCACAAATAAACCAGAGAAAGATGCAAGACATGTAGTAAAAGTGGAATATCAAGAAAATG
GCCCGTTATTTTCAGAACTTAAATTTTATCAGAGAGTTGCAAAAAAAGACTGTATCAAAAAGTG
GATAGAACGCAAACAACTTGATTATTTAGGAATTCCTCTGTTTTATGGATCTGGTCTGACTGAA
TTCAAGGGAAGAAGTTACAGATTTATGGTAATGGAAAGACTAGGAATAGATTTACAGAAGATCT
CAGGCCAGAATGGTACCTTTAAAAAGTCAACTGTCCTGCAATTAGGTATCCGAATGTTGGATGT
ACTGGAATATATACATGAAAATGAATATGTTCATGGTGATATAAAAGCAGCAAATCTACTTTTG
GGTTACAAAAATCCAGACCAGGTTTATCTTGCAGATTATGGACTTTCCTACAGATATTGTCCCA
ATGGGAACCACAAACAGTATCAGGAAAATCCTAGAAAAGGCCATAATGGGACAATAGAGTTTAC
CAGCTTGGATGCCCACAAGGGAGTAGCCTTGTCCAGACGAAGTGACGTTGAGATCCTCGGCTAC
TGCATGCTGCGGTGGTTGTGTGGGAAACTTCCCTGGGAACAGAACCTGAAGGACCCTGTGGCTG
TGCAGACTGCTAAAACAAATCTGTTGGACGAGCTCCCCCAGTCAGTGCTTAAATGGGCTCCTTC
TGGAAGCAGTTGCTGTGAAATAGCCCAATTTTTGGTATGTGCTCATAGTTTAGCATATGATGAA
AAGCCAAACTATCAAGCCCTCAAGAAAATTTTGAACCCTCATGGAATACCTTTAGGACCACTGG
ACTTTTCCACAAAAGGACAGAGTATAAATGTCCATACTCCAAACAGTCAAAAAGTTGATTCACA
AAAGGCTGCAACAAAGCAAGTCAACAAGGCACACAATAGGTTAATCGAAAAAAAAGTCCACAGT
GAGAGAAGCGCTGAGTCCTGTGCAACATGGAAAGTGCAGAAAGAGGAGAAACTGATTGGATTGA
TGAACAATGAAGCAGCTCAGGAAAGCACAAGGAGAAGACAGAAATATCAAGAGTCTCAAGAACC
TTTGAATGAAGTAAACAGTTTCCCACAAAAAATCAGCTATACACAATTCCCAAACTCATTTTAT
GAGCCTCATCAAGATTTTACCAGTCCAGATATATTCAAGAAGTCAAGATCTCCATCTTGGTATA
AATACACTTCCACAGTCAGCACGGGGATCACAGACTTAGAAAGTTCAACTGGACTTTGGCCTAC
AATTTCCCAGTTTACTCTTAGTGAAGAGACAAACGCAGATGTTTATTATTATCGCATCATCATA
CCTGTCCTTTTGATGTTAGTATTTCTTGCTTTATTTTTTCTCTGAAGATGATACCAAAATTCCT
TTTGATAATTTTTTAAGTTTCCAGCTCTTCACCGAAATGTTGTATTCTTATTTCAGTGTTTCCT
TCCAGACATTTTTAAGGTAATTGGCTTTAAAAAGAGAACATATTTTAACAAAGTTTGTGGACAC
TCTAAAAAATAAAATTGCTTTGTACTAGAAATAGTGTCATAGAATAGTGTCATAGTACAGTTTG
GAAAACACTTCTGAAGTTTCAGATCACCTAGGAAATCTAGAAAAGGAGTTTAATGTTTTTGATC
AGAGAATTTGAAAAATAGAAATACAGAGAATGAGTTTCAAAAGTTTTAGATAAACTGATATACT
ATATAGATCTATCTTCTAGAACATATTACTGAAAGCTAGGCACATTTTATGAGATGTGATTAAC
AATTTGCTTACCTTACTACAATATGGACATTCACCAAATATGATGTTAAAACTCTGTCTACTAG
TTAGTAGTCCTCTCAGCCACTGCAAATTTTAAAAGATAAAGGAGAAGCGTCAGCATGATTACAA
ATTACAGATACTCCAAATGTCATTCCCTTTGTTTTTAAGTGCATTATGTTTTTATTCCAGAAGA
CTTAGCTTAATTTTGTTTTGCAAGAGTAAGGGATGTATTTCCTGAGCCAATAGCAGACTATTAA
GATGTTGAGTAACAAGGGAAATCAACATGGAATTGAAGGCCTAAACCACTGGTTTATAACCAGA
TTATGGGCCCCTTTAAGAATCTGATAAGAATTACGCATTTTCTTTATCCCCAGAATAGACATAC
ATAAAAATAATGCATACTAAGTTCCTGGCATTCATAGACTTTCCCTAAATCCATTAATCACAAA
TTAACAACTCCTGCTGTTAAAGATACTACAGGCTCTTGAAAATTTCCCTCTTAGTTCTGGTCTG
AATCACTAACAGTGGGTTAATTTTCAACCCATTGATTATAAGCATGAGCCAGTGAATTTTTAAA
AATTAAATGAATATTCATAATTACAAAAGAAATCACATGTTCCCTTAGAGTATTTCTGTAATTT
GACCTGTATTTCTGTAATTTCATGATTTTATATAAGGTAAATAGATGCCTCTGCCTAAGTTCTC
CATTGGCAAAGTACAGACGGCACCAACTGCTACCTCTAATCACAAAAGTAAAGATGTGATATTA
AGGAAGACTGAAACCGAAGGCAACATACAATTGCAAGGTGTTCTGTATATAGTTACACACAGTT
TATCATGTATCAACTAGGCCCTAAGGTGAAGCCAGGCACTAAAGACAGGAATGAAAGTAGACTT
CACATACAGTAAGTAAAGTGGCATTGCCTGAGTGCTGTGAGACTCAGATCACAAAAGGCATTCT
TCTCAACATGAAAAGTAGTAGTATTGGATATATTCTATTCTTAAATGCAGCCTGAAAAGTAATA
GATACTACATAGTACTAATTTCATTTTCACTGTATTACTGCCACTTTCAACCACCTCCACCTCG
GGTAAACCTATGAAGCTTACATTGTGGTAACAAGGAATTTATAGAAAGATTCCAATGTACCATC
AATTTAATTTGTTATGTGTCAATAAGCTAGTCCATGAATATATTCTGGATAGATTTTCTCCCTT
GGATACTTCAGAACATTTCTCCACTCATTAGTAACTGTGATGAAGAAATGAAGCACATAAGCAT
CTGGAATAAACTGGTAAAAGGAGTTAATGGCAAAAGAGAGGATCACTATTGACTCAACAGATTT
TAGATTCTGTGTATTTCAAACAGGAATACTTCCTATGTTGTGTTAGCGGAAAAAAGTCTTGACA
ATATTTTTATTTTTTACCTCATATAAGCATATTTGATGGAAAGGTTGTCCACACTGAGAATTAT
CACACACTTGATCAGGAATGGTACCGTCAAGTTGATAAGCATAACAAATTCCACAATCCATAGT
AAAATCCTTCAAAAGAAAAATATTT

hide sequence

RefSeq Acc Id:

XM_047445745 ⟹ XP_047301701

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	58,084,904 - 58,159,920 (+)	NCBI

RefSeq Acc Id:

XM_047445747 ⟹ XP_047301703

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	58,058,352 - 58,159,920 (+)	NCBI

RefSeq Acc Id:

XM_047445748 ⟹ XP_047301704

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	58,048,827 - 58,159,920 (+)	NCBI

RefSeq Acc Id:

XM_054343751 ⟹ XP_054199726

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	58,047,732 - 58,164,754 (+)	NCBI

RefSeq Acc Id:

XM_054343752 ⟹ XP_054199727

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	58,051,863 - 58,164,754 (+)	NCBI

RefSeq Acc Id:

XM_054343753 ⟹ XP_054199728

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	58,051,495 - 58,164,754 (+)	NCBI

RefSeq Acc Id:

XM_054343754 ⟹ XP_054199729

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	58,051,495 - 58,164,754 (+)	NCBI

RefSeq Acc Id:

XM_054343755 ⟹ XP_054199730

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	58,089,581 - 58,164,754 (+)	NCBI

RefSeq Acc Id:

XM_054343756 ⟹ XP_054199731

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	58,063,039 - 58,164,754 (+)	NCBI

RefSeq Acc Id:

XM_054343757 ⟹ XP_054199732

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	58,053,516 - 58,164,754 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_001123952	(Get FASTA)	NCBI Sequence Viewer
	NP_001123953	(Get FASTA)	NCBI Sequence Viewer
	NP_001123954	(Get FASTA)	NCBI Sequence Viewer
	NP_001123955	(Get FASTA)	NCBI Sequence Viewer
	NP_001275765	(Get FASTA)	NCBI Sequence Viewer
	NP_001275766	(Get FASTA)	NCBI Sequence Viewer
	NP_001275767	(Get FASTA)	NCBI Sequence Viewer
	NP_001275768	(Get FASTA)	NCBI Sequence Viewer
	NP_006287	(Get FASTA)	NCBI Sequence Viewer
	XP_005264597	(Get FASTA)	NCBI Sequence Viewer
	XP_006712153	(Get FASTA)	NCBI Sequence Viewer
	XP_006712154	(Get FASTA)	NCBI Sequence Viewer
	XP_011531394	(Get FASTA)	NCBI Sequence Viewer
	XP_047301701	(Get FASTA)	NCBI Sequence Viewer
	XP_047301703	(Get FASTA)	NCBI Sequence Viewer
	XP_047301704	(Get FASTA)	NCBI Sequence Viewer
	XP_054199726	(Get FASTA)	NCBI Sequence Viewer
	XP_054199727	(Get FASTA)	NCBI Sequence Viewer
	XP_054199728	(Get FASTA)	NCBI Sequence Viewer
	XP_054199729	(Get FASTA)	NCBI Sequence Viewer
	XP_054199730	(Get FASTA)	NCBI Sequence Viewer
	XP_054199731	(Get FASTA)	NCBI Sequence Viewer
	XP_054199732	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH21663	(Get FASTA)	NCBI Sequence Viewer
	AAH27854	(Get FASTA)	NCBI Sequence Viewer
	AAO73047	(Get FASTA)	NCBI Sequence Viewer
	AAO73048	(Get FASTA)	NCBI Sequence Viewer
	AAO73049	(Get FASTA)	NCBI Sequence Viewer
	AAO73050	(Get FASTA)	NCBI Sequence Viewer
	AAO73051	(Get FASTA)	NCBI Sequence Viewer
	AAO73052	(Get FASTA)	NCBI Sequence Viewer
	AAX93262	(Get FASTA)	NCBI Sequence Viewer
	AAY14648	(Get FASTA)	NCBI Sequence Viewer
	AAY15019	(Get FASTA)	NCBI Sequence Viewer
	BAA19109	(Get FASTA)	NCBI Sequence Viewer
	BAD97260	(Get FASTA)	NCBI Sequence Viewer
	BAF85416	(Get FASTA)	NCBI Sequence Viewer
	BAG59222	(Get FASTA)	NCBI Sequence Viewer
	BAH12007	(Get FASTA)	NCBI Sequence Viewer
	CAD54446	(Get FASTA)	NCBI Sequence Viewer
	EAX00062	(Get FASTA)	NCBI Sequence Viewer
	EAX00063	(Get FASTA)	NCBI Sequence Viewer
	EAX00064	(Get FASTA)	NCBI Sequence Viewer
	EAX00065	(Get FASTA)	NCBI Sequence Viewer
	EAX00066	(Get FASTA)	NCBI Sequence Viewer
	EAX00067	(Get FASTA)	NCBI Sequence Viewer
	EAX00068	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000342381
	ENSP00000342381.4
	ENSP00000398323
	ENSP00000398323.2
	ENSP00000400006.1
	ENSP00000402375
	ENSP00000402375.2
	ENSP00000404156
	ENSP00000404156.3
	ENSP00000404961.1
	ENSP00000408002
	ENSP00000408002.2
	ENSP00000497378
	ENSP00000497378.1
GenBank Protein	Q86Y07	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_001123952 ⟸ NM_001130480
- Peptide Label:	isoform 1
- UniProtKB:	Q8IXI5 (UniProtKB/Swiss-Prot), Q86Y12 (UniProtKB/Swiss-Prot), Q86Y11 (UniProtKB/Swiss-Prot), Q86Y10 (UniProtKB/Swiss-Prot), Q86Y09 (UniProtKB/Swiss-Prot), Q86Y08 (UniProtKB/Swiss-Prot), Q53TU1 (UniProtKB/Swiss-Prot), Q53S77 (UniProtKB/Swiss-Prot), Q53S39 (UniProtKB/Swiss-Prot), Q53EU9 (UniProtKB/Swiss-Prot), Q49AK9 (UniProtKB/Swiss-Prot), D6W5D6 (UniProtKB/Swiss-Prot), D6W5D4 (UniProtKB/Swiss-Prot), B4DKL0 (UniProtKB/Swiss-Prot), Q99987 (UniProtKB/Swiss-Prot), Q86Y07 (UniProtKB/Swiss-Prot), Q05CR6 (UniProtKB/TrEMBL)
- Sequence:	show sequence MPPKRNEKYKLPIPFPEGKVLDDMEGNQWVLGKKIGSGGFGLIYLAFPTNKPEKDARHVVKVEY QENGPLFSELKFYQRVAKKDCIKKWIERKQLDYLGIPLFYGSGLTEFKGRSYRFMVMERLGIDL QKISGQNGTFKKSTVLQLGIRMLDVLEYIHENEYVHGDIKAANLLLGYKNPDQVYLADYGLSYR YCPNGNHKQYQENPRKGHNGTIEFTSLDAHKGVALSRRSDVEILGYCMLRWLCGKLPWEQNLKD PVAVQTAKTNLLDELPQSVLKWAPSGSSCCEIAQFLVCAHSLAYDEKPNYQALKKILNPHGIPL GPLDFSTKGQSINVHTPNSQKVDSQKAATKQVNKAHNRLIEKKVHSERSAESCATWKVQKEEKL IGLMNNEAAQESTRRRQKYQESQEPLNEVNSFPQKISYTQFPNSFYEPHQDFTSPDIFKKSRSP SWYKYTSTVSTGITDLESSTGLWPTISQFTLSEETNADVYYYRIIIPVLLMLVFLALFFL hide sequence

RefSeq Acc Id:	NP_001123954 ⟸ NM_001130482
- Peptide Label:	isoform 2
- UniProtKB:	Q05CR6 (UniProtKB/TrEMBL)
- Sequence:	show sequence MEGNQWVLGKKIGSGGFGLIYLAFPTNKPEKDARHVVKVEYQENGPLFSELKFYQRVAKKDCIK KWIERKQLDYLGIPLFYGSGLTEFKGRSYRFMVMERLGIDLQKISGQNGTFKKSTVLQLGIRML DVLEYIHENEYVHGDIKAANLLLGYKNPDQVYLADYGLSYRYCPNGNHKQYQENPRKGHNGTIE FTSLDAHKGVALSRRSDVEILGYCMLRWLCGKLPWEQNLKDPVAVQTAKTNLLDELPQSVLKWA PSGSSCCEIAQFLVCAHSLAYDEKPNYQALKKILNPHGIPLGPLDFSTKGQSINVHTPNSQKVD SQKAATKQVNKAHNRLIEKKVHSERSAESCATWKVQKEEKLIGLMNNEAAQESTRRRQKYQESQ EPLNEVNSFPQKISYTQFPNSFYEPHQDFTSPDIFKKSRSPSWYKYTSTVSTGITDLESSTGLW PTISQFTLSEETNADVYYYRIIIPVLLMLVFLALFFL hide sequence

RefSeq Acc Id:	NP_001123955 ⟸ NM_001130483
- Peptide Label:	isoform 3
- UniProtKB:	Q05CR6 (UniProtKB/TrEMBL)
- Sequence:	show sequence MPPKRNEKYKLPIPFPEGKVLDDMEGNQWVLGKKIGSGGFGLIYLAFPTNKPEKDARHVVKVEY QENGPLFSELKFYQRVAKKDCIKKWIERKQLDYLGIPLFYGSGLTEFKGRSYRFMVMERLGIDL QKISGQNGTFKKSTVLQLGIRMLDVLEYIHENEYVHGDIKAANLLLGYKNPDQVYLADYGLSYR YCPNGNHKQYQENPRKGHNGTIEFTSLDAHKGVALSRRSDVEILGYCMLRWLCGKLPWEQNLKD PVAVQTAKTNLLDELPQSVLKWAPSGSSCCEIAQFLVCAHSLAYDEKPNYQALKKILNPHGIPL GPLDFSTKGQSINVHTPNSQKVDSQKAATKQVNKAHNRLIEKKVHSERSAESCATWKVQKEEKL IGLMNNEAAQFR hide sequence

RefSeq Acc Id:	NP_006287 ⟸ NM_006296
- Peptide Label:	isoform 1
- UniProtKB:	Q8IXI5 (UniProtKB/Swiss-Prot), Q86Y12 (UniProtKB/Swiss-Prot), Q86Y11 (UniProtKB/Swiss-Prot), Q86Y10 (UniProtKB/Swiss-Prot), Q86Y09 (UniProtKB/Swiss-Prot), Q86Y08 (UniProtKB/Swiss-Prot), Q53TU1 (UniProtKB/Swiss-Prot), Q53S77 (UniProtKB/Swiss-Prot), Q53S39 (UniProtKB/Swiss-Prot), Q53EU9 (UniProtKB/Swiss-Prot), Q49AK9 (UniProtKB/Swiss-Prot), D6W5D6 (UniProtKB/Swiss-Prot), D6W5D4 (UniProtKB/Swiss-Prot), B4DKL0 (UniProtKB/Swiss-Prot), Q99987 (UniProtKB/Swiss-Prot), Q86Y07 (UniProtKB/Swiss-Prot), Q05CR6 (UniProtKB/TrEMBL)
- Sequence:	show sequence MPPKRNEKYKLPIPFPEGKVLDDMEGNQWVLGKKIGSGGFGLIYLAFPTNKPEKDARHVVKVEY QENGPLFSELKFYQRVAKKDCIKKWIERKQLDYLGIPLFYGSGLTEFKGRSYRFMVMERLGIDL QKISGQNGTFKKSTVLQLGIRMLDVLEYIHENEYVHGDIKAANLLLGYKNPDQVYLADYGLSYR YCPNGNHKQYQENPRKGHNGTIEFTSLDAHKGVALSRRSDVEILGYCMLRWLCGKLPWEQNLKD PVAVQTAKTNLLDELPQSVLKWAPSGSSCCEIAQFLVCAHSLAYDEKPNYQALKKILNPHGIPL GPLDFSTKGQSINVHTPNSQKVDSQKAATKQVNKAHNRLIEKKVHSERSAESCATWKVQKEEKL IGLMNNEAAQESTRRRQKYQESQEPLNEVNSFPQKISYTQFPNSFYEPHQDFTSPDIFKKSRSP SWYKYTSTVSTGITDLESSTGLWPTISQFTLSEETNADVYYYRIIIPVLLMLVFLALFFL hide sequence

RefSeq Acc Id:	NP_001123953 ⟸ NM_001130481
- Peptide Label:	isoform 1
- UniProtKB:	Q8IXI5 (UniProtKB/Swiss-Prot), Q86Y12 (UniProtKB/Swiss-Prot), Q86Y11 (UniProtKB/Swiss-Prot), Q86Y10 (UniProtKB/Swiss-Prot), Q86Y09 (UniProtKB/Swiss-Prot), Q86Y08 (UniProtKB/Swiss-Prot), Q53TU1 (UniProtKB/Swiss-Prot), Q53S77 (UniProtKB/Swiss-Prot), Q53S39 (UniProtKB/Swiss-Prot), Q53EU9 (UniProtKB/Swiss-Prot), Q49AK9 (UniProtKB/Swiss-Prot), D6W5D6 (UniProtKB/Swiss-Prot), D6W5D4 (UniProtKB/Swiss-Prot), B4DKL0 (UniProtKB/Swiss-Prot), Q99987 (UniProtKB/Swiss-Prot), Q86Y07 (UniProtKB/Swiss-Prot), Q05CR6 (UniProtKB/TrEMBL)
- Sequence:	show sequence MPPKRNEKYKLPIPFPEGKVLDDMEGNQWVLGKKIGSGGFGLIYLAFPTNKPEKDARHVVKVEY QENGPLFSELKFYQRVAKKDCIKKWIERKQLDYLGIPLFYGSGLTEFKGRSYRFMVMERLGIDL QKISGQNGTFKKSTVLQLGIRMLDVLEYIHENEYVHGDIKAANLLLGYKNPDQVYLADYGLSYR YCPNGNHKQYQENPRKGHNGTIEFTSLDAHKGVALSRRSDVEILGYCMLRWLCGKLPWEQNLKD PVAVQTAKTNLLDELPQSVLKWAPSGSSCCEIAQFLVCAHSLAYDEKPNYQALKKILNPHGIPL GPLDFSTKGQSINVHTPNSQKVDSQKAATKQVNKAHNRLIEKKVHSERSAESCATWKVQKEEKL IGLMNNEAAQESTRRRQKYQESQEPLNEVNSFPQKISYTQFPNSFYEPHQDFTSPDIFKKSRSP SWYKYTSTVSTGITDLESSTGLWPTISQFTLSEETNADVYYYRIIIPVLLMLVFLALFFL hide sequence

RefSeq Acc Id:	XP_005264597 ⟸ XM_005264540
- Peptide Label:	isoform X1
- UniProtKB:	Q8IXI5 (UniProtKB/Swiss-Prot), Q86Y12 (UniProtKB/Swiss-Prot), Q86Y11 (UniProtKB/Swiss-Prot), Q86Y10 (UniProtKB/Swiss-Prot), Q86Y09 (UniProtKB/Swiss-Prot), Q86Y08 (UniProtKB/Swiss-Prot), Q53TU1 (UniProtKB/Swiss-Prot), Q53S77 (UniProtKB/Swiss-Prot), Q53S39 (UniProtKB/Swiss-Prot), Q53EU9 (UniProtKB/Swiss-Prot), Q49AK9 (UniProtKB/Swiss-Prot), D6W5D6 (UniProtKB/Swiss-Prot), D6W5D4 (UniProtKB/Swiss-Prot), B4DKL0 (UniProtKB/Swiss-Prot), Q99987 (UniProtKB/Swiss-Prot), Q86Y07 (UniProtKB/Swiss-Prot), Q05CR6 (UniProtKB/TrEMBL)
- Sequence:	show sequence MPPKRNEKYKLPIPFPEGKVLDDMEGNQWVLGKKIGSGGFGLIYLAFPTNKPEKDARHVVKVEY QENGPLFSELKFYQRVAKKDCIKKWIERKQLDYLGIPLFYGSGLTEFKGRSYRFMVMERLGIDL QKISGQNGTFKKSTVLQLGIRMLDVLEYIHENEYVHGDIKAANLLLGYKNPDQVYLADYGLSYR YCPNGNHKQYQENPRKGHNGTIEFTSLDAHKGVALSRRSDVEILGYCMLRWLCGKLPWEQNLKD PVAVQTAKTNLLDELPQSVLKWAPSGSSCCEIAQFLVCAHSLAYDEKPNYQALKKILNPHGIPL GPLDFSTKGQSINVHTPNSQKVDSQKAATKQVNKAHNRLIEKKVHSERSAESCATWKVQKEEKL IGLMNNEAAQESTRRRQKYQESQEPLNEVNSFPQKISYTQFPNSFYEPHQDFTSPDIFKKSRSP SWYKYTSTVSTGITDLESSTGLWPTISQFTLSEETNADVYYYRIIIPVLLMLVFLALFFL hide sequence

RefSeq Acc Id:	NP_001275766 ⟸ NM_001288837
- Peptide Label:	isoform 1
- UniProtKB:	Q8IXI5 (UniProtKB/Swiss-Prot), Q86Y12 (UniProtKB/Swiss-Prot), Q86Y11 (UniProtKB/Swiss-Prot), Q86Y10 (UniProtKB/Swiss-Prot), Q86Y09 (UniProtKB/Swiss-Prot), Q86Y08 (UniProtKB/Swiss-Prot), Q53TU1 (UniProtKB/Swiss-Prot), Q53S77 (UniProtKB/Swiss-Prot), Q53S39 (UniProtKB/Swiss-Prot), Q53EU9 (UniProtKB/Swiss-Prot), Q49AK9 (UniProtKB/Swiss-Prot), D6W5D6 (UniProtKB/Swiss-Prot), D6W5D4 (UniProtKB/Swiss-Prot), B4DKL0 (UniProtKB/Swiss-Prot), Q99987 (UniProtKB/Swiss-Prot), Q86Y07 (UniProtKB/Swiss-Prot), Q05CR6 (UniProtKB/TrEMBL)
- Sequence:	show sequence MPPKRNEKYKLPIPFPEGKVLDDMEGNQWVLGKKIGSGGFGLIYLAFPTNKPEKDARHVVKVEY QENGPLFSELKFYQRVAKKDCIKKWIERKQLDYLGIPLFYGSGLTEFKGRSYRFMVMERLGIDL QKISGQNGTFKKSTVLQLGIRMLDVLEYIHENEYVHGDIKAANLLLGYKNPDQVYLADYGLSYR YCPNGNHKQYQENPRKGHNGTIEFTSLDAHKGVALSRRSDVEILGYCMLRWLCGKLPWEQNLKD PVAVQTAKTNLLDELPQSVLKWAPSGSSCCEIAQFLVCAHSLAYDEKPNYQALKKILNPHGIPL GPLDFSTKGQSINVHTPNSQKVDSQKAATKQVNKAHNRLIEKKVHSERSAESCATWKVQKEEKL IGLMNNEAAQESTRRRQKYQESQEPLNEVNSFPQKISYTQFPNSFYEPHQDFTSPDIFKKSRSP SWYKYTSTVSTGITDLESSTGLWPTISQFTLSEETNADVYYYRIIIPVLLMLVFLALFFL hide sequence

RefSeq Acc Id:	NP_001275767 ⟸ NM_001288838
- Peptide Label:	isoform 3
- UniProtKB:	Q05CR6 (UniProtKB/TrEMBL)
- Sequence:	show sequence MPPKRNEKYKLPIPFPEGKVLDDMEGNQWVLGKKIGSGGFGLIYLAFPTNKPEKDARHVVKVEY QENGPLFSELKFYQRVAKKDCIKKWIERKQLDYLGIPLFYGSGLTEFKGRSYRFMVMERLGIDL QKISGQNGTFKKSTVLQLGIRMLDVLEYIHENEYVHGDIKAANLLLGYKNPDQVYLADYGLSYR YCPNGNHKQYQENPRKGHNGTIEFTSLDAHKGVALSRRSDVEILGYCMLRWLCGKLPWEQNLKD PVAVQTAKTNLLDELPQSVLKWAPSGSSCCEIAQFLVCAHSLAYDEKPNYQALKKILNPHGIPL GPLDFSTKGQSINVHTPNSQKVDSQKAATKQVNKAHNRLIEKKVHSERSAESCATWKVQKEEKL IGLMNNEAAQFR hide sequence

RefSeq Acc Id:	NP_001275768 ⟸ NM_001288839
- Peptide Label:	isoform 4
- UniProtKB:	Q86Y07 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MVMERLGIDLQKISGQNGTFKKSTVLQLGIRMLDVLEYIHENEYVHGDIKAANLLLGYKNPDQV YLADYGLSYRYCPNGNHKQYQENPRKGHNGTIEFTSLDAHKGVALSRRSDVEILGYCMLRWLCG KLPWEQNLKDPVAVQTAKTNLLDELPQSVLKWAPSGSSCCEIAQFLVCAHSLAYDEKPNYQALK KILNPHGIPLGPLDFSTKGQSINVHTPNSQKVDSQKAATKQVNKAHNRLIEKKVHSERSAESCA TWKVQKEEKLIGLMNNEAAQESTRRRQKYQESQEPLNEVNSFPQKISYTQFPNSFYEPHQDFTS PDIFKKSRSPSWYKYTSTVSTGITDLESSTGLWPTISQFTLSEETNADVYYYRIIIPVLLMLVF LALFFL hide sequence

RefSeq Acc Id:	NP_001275765 ⟸ NM_001288836
- Peptide Label:	isoform 4
- UniProtKB:	Q86Y07 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MVMERLGIDLQKISGQNGTFKKSTVLQLGIRMLDVLEYIHENEYVHGDIKAANLLLGYKNPDQV YLADYGLSYRYCPNGNHKQYQENPRKGHNGTIEFTSLDAHKGVALSRRSDVEILGYCMLRWLCG KLPWEQNLKDPVAVQTAKTNLLDELPQSVLKWAPSGSSCCEIAQFLVCAHSLAYDEKPNYQALK KILNPHGIPLGPLDFSTKGQSINVHTPNSQKVDSQKAATKQVNKAHNRLIEKKVHSERSAESCA TWKVQKEEKLIGLMNNEAAQESTRRRQKYQESQEPLNEVNSFPQKISYTQFPNSFYEPHQDFTS PDIFKKSRSPSWYKYTSTVSTGITDLESSTGLWPTISQFTLSEETNADVYYYRIIIPVLLMLVF LALFFL hide sequence

RefSeq Acc Id:	XP_006712154 ⟸ XM_006712091
- Peptide Label:	isoform X3
- UniProtKB:	Q05CR6 (UniProtKB/TrEMBL)
- Sequence:	show sequence MPPKRNEKYKLPIPFPEGKVLDDMEGNQWVLGKKIGSGGFGLIYLAFPTNKPEKDARHVVKVEY QENGPLFSELKFYQRVAKKDCIKKWIERKQLDYLGIPLFYGSGLTEFKGRSYRFMVMERLGIDL QKISGQNGTFKKSTVLQLGIRMLDVLEYIHENEYVHGDIKAANLLLGYKNPDQVYLADYGLSYR YCPNGNHKQYQENPRKGHNGTIEFTSLDAHKGVALSRRSDVEILGYCMLRWLCGKLPWEQNLKD PVAVQTAKTNLLDELPQSVLKWAPSGSSCCEIAQFLVCAHSLAYDEKPNYQALKKILNPHGIPL GPLDFSTKGQSINVHTPNSQKVDSQKAATKQVNKAHNRLIEKKVHSERSAESCATWKVQKEEKL IGLMNNEAAQFR hide sequence

RefSeq Acc Id:	XP_006712153 ⟸ XM_006712090
- Peptide Label:	isoform X2
- UniProtKB:	Q05CR6 (UniProtKB/TrEMBL)
- Sequence:	show sequence MPPKRNEKYKLPIPFPEGKVLDDMEGNQWVLGKKIGSGGFGLIYLAFPTNKPEKDARHVVKVEY QENGPLFSELKFYQRVAKKDCIKKWIERKQLDYLGIPLFYGSGLTEFKGRSYRFMVMERLGIDL QKISGQNGTFKKSTVLQLGIRMLDVLEYIHENEYVHGDIKAANLLLGYKNPDQVYLADYGLSYR YCPNGNHKQYQENPRKGHNGTIEFTSLDAHKGVALSRRSDVEILGYCMLRWLCGKLPWEQNLKD PVAVQTAKTNLLDELPQSVLKWAPSGSSCCEIAQFLVCAHSLAYDEKPNYQALKKILNPHGIPL GPLDFSTKGQSINVHTPNSQKVDSQKAATKQVNKAHNRLIEKKVHSERSAESCATWKVQKEEKL IGLMNNEAAQVEA hide sequence

RefSeq Acc Id:	XP_011531394 ⟸ XM_011533092
- Peptide Label:	isoform X1
- UniProtKB:	Q8IXI5 (UniProtKB/Swiss-Prot), Q86Y12 (UniProtKB/Swiss-Prot), Q86Y11 (UniProtKB/Swiss-Prot), Q86Y10 (UniProtKB/Swiss-Prot), Q86Y09 (UniProtKB/Swiss-Prot), Q86Y08 (UniProtKB/Swiss-Prot), Q53TU1 (UniProtKB/Swiss-Prot), Q53S77 (UniProtKB/Swiss-Prot), Q53S39 (UniProtKB/Swiss-Prot), Q53EU9 (UniProtKB/Swiss-Prot), Q49AK9 (UniProtKB/Swiss-Prot), D6W5D6 (UniProtKB/Swiss-Prot), D6W5D4 (UniProtKB/Swiss-Prot), B4DKL0 (UniProtKB/Swiss-Prot), Q99987 (UniProtKB/Swiss-Prot), Q86Y07 (UniProtKB/Swiss-Prot), Q05CR6 (UniProtKB/TrEMBL)
- Sequence:	show sequence MPPKRNEKYKLPIPFPEGKVLDDMEGNQWVLGKKIGSGGFGLIYLAFPTNKPEKDARHVVKVEY QENGPLFSELKFYQRVAKKDCIKKWIERKQLDYLGIPLFYGSGLTEFKGRSYRFMVMERLGIDL QKISGQNGTFKKSTVLQLGIRMLDVLEYIHENEYVHGDIKAANLLLGYKNPDQVYLADYGLSYR YCPNGNHKQYQENPRKGHNGTIEFTSLDAHKGVALSRRSDVEILGYCMLRWLCGKLPWEQNLKD PVAVQTAKTNLLDELPQSVLKWAPSGSSCCEIAQFLVCAHSLAYDEKPNYQALKKILNPHGIPL GPLDFSTKGQSINVHTPNSQKVDSQKAATKQVNKAHNRLIEKKVHSERSAESCATWKVQKEEKL IGLMNNEAAQESTRRRQKYQESQEPLNEVNSFPQKISYTQFPNSFYEPHQDFTSPDIFKKSRSP SWYKYTSTVSTGITDLESSTGLWPTISQFTLSEETNADVYYYRIIIPVLLMLVFLALFFL hide sequence

RefSeq Acc Id:

ENSP00000497378 ⟸ ENST00000648897

RefSeq Acc Id:

ENSP00000404156 ⟸ ENST00000412104

RefSeq Acc Id:

ENSP00000404961 ⟸ ENST00000428021

RefSeq Acc Id:

ENSP00000398323 ⟸ ENST00000440705

RefSeq Acc Id:

ENSP00000402375 ⟸ ENST00000417641

RefSeq Acc Id:

ENSP00000400006 ⟸ ENST00000432057

RefSeq Acc Id:

ENSP00000342381 ⟸ ENST00000340157

RefSeq Acc Id:

ENSP00000408002 ⟸ ENST00000435505

RefSeq Acc Id:	XP_047301704 ⟸ XM_047445748
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_047301703 ⟸ XM_047445747
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_047301701 ⟸ XM_047445745
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054199726 ⟸ XM_054343751
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054199729 ⟸ XM_054343754
- Peptide Label:	isoform X3
- UniProtKB:	A8K9L2 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054199728 ⟸ XM_054343753
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054199727 ⟸ XM_054343752
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054199732 ⟸ XM_054343757
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054199731 ⟸ XM_054343756
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054199730 ⟸ XM_054343755
- Peptide Label:	isoform X4

Protein Domains

Protein kinase

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q86Y07-F1-model_v2	AlphaFold	Q86Y07	1-508	view protein structure

Promoters

RGD ID:

6860374

Promoter ID:

EPDNEW_H3352

Type:

initiation region

Name:

VRK2_3

Description:

vaccinia related kinase 2

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H3353 EPDNEW_H3354

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	57,907,652 - 57,907,712	EPDNEW

RGD ID:

6860376

Promoter ID:

EPDNEW_H3353

Type:

initiation region

Name:

VRK2_2

Description:

vaccinia related kinase 2

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H3352 EPDNEW_H3354

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	58,046,687 - 58,046,747	EPDNEW

RGD ID:

6860378

Promoter ID:

EPDNEW_H3354

Type:

initiation region

Name:

VRK2_1

Description:

vaccinia related kinase 2

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H3352 EPDNEW_H3353

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	58,046,814 - 58,046,874	EPDNEW

RGD ID:

6798435

Promoter ID:

HG_KWN:32739

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

ENST00000340157, ENST00000394539, NM_001130480, NM_001130481, NM_001130482, NM_001130483, OTTHUMT00000325300, UC002RZQ.1, UC002RZR.1, UC002RZT.1, UC002RZU.1, UC010FCC.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	2	58,127,191 - 58,127,742 (+)	MPROMDB

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:12719	AgrOrtholog
COSMIC	VRK2	COSMIC
Ensembl Genes	ENSG00000028116	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000340157	ENTREZGENE
	ENST00000340157.9	UniProtKB/Swiss-Prot
	ENST00000412104	ENTREZGENE
	ENST00000412104.6	UniProtKB/Swiss-Prot
	ENST00000417641	ENTREZGENE
	ENST00000417641.6	UniProtKB/Swiss-Prot
	ENST00000428021.1	UniProtKB/TrEMBL
	ENST00000432057.2	UniProtKB/TrEMBL
	ENST00000435505	ENTREZGENE
	ENST00000435505.6	UniProtKB/Swiss-Prot
	ENST00000440705	ENTREZGENE
	ENST00000440705.6	UniProtKB/Swiss-Prot
	ENST00000648897	ENTREZGENE
	ENST00000648897.1	UniProtKB/Swiss-Prot
Gene3D-CATH	Transferase(Phosphotransferase) domain 1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000028116	GTEx
HGNC ID	HGNC:12719	ENTREZGENE
Human Proteome Map	VRK2	Human Proteome Map
InterPro	Kinase-like_dom_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Prot_kinase_dom	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Ser/Thr_kinase_AS	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:7444	UniProtKB/Swiss-Prot
NCBI Gene	7444	ENTREZGENE
OMIM	602169	OMIM
PANTHER	CASEIN KINASE-RELATED	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SERINE/THREONINE-PROTEIN KINASE VRK2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	Pkinase	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA37331	PharmGKB
PROSITE	PROTEIN_KINASE_DOM	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	PROTEIN_KINASE_ST	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART	S_TKc	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP	SSF56112	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	A8K9L2	ENTREZGENE, UniProtKB/TrEMBL
	B4DKL0	ENTREZGENE
	D6W5D4	ENTREZGENE
	D6W5D6	ENTREZGENE
	E7ERS5_HUMAN	UniProtKB/TrEMBL
	E9PBU1_HUMAN	UniProtKB/TrEMBL
	Q05CR6	ENTREZGENE, UniProtKB/TrEMBL
	Q49AK9	ENTREZGENE
	Q53EU9	ENTREZGENE
	Q53S39	ENTREZGENE
	Q53S77	ENTREZGENE
	Q53TU1	ENTREZGENE
	Q86Y07	ENTREZGENE
	Q86Y08	ENTREZGENE
	Q86Y09	ENTREZGENE
	Q86Y10	ENTREZGENE
	Q86Y11	ENTREZGENE
	Q86Y12	ENTREZGENE
	Q8IXI5	ENTREZGENE
	Q99987	ENTREZGENE
	VRK2_HUMAN	UniProtKB/Swiss-Prot
UniProt Secondary	B4DKL0	UniProtKB/Swiss-Prot
	D6W5D4	UniProtKB/Swiss-Prot
	D6W5D6	UniProtKB/Swiss-Prot
	Q49AK9	UniProtKB/Swiss-Prot
	Q53EU9	UniProtKB/Swiss-Prot
	Q53S39	UniProtKB/Swiss-Prot
	Q53S77	UniProtKB/Swiss-Prot
	Q53TU1	UniProtKB/Swiss-Prot
	Q86Y08	UniProtKB/Swiss-Prot
	Q86Y09	UniProtKB/Swiss-Prot
	Q86Y10	UniProtKB/Swiss-Prot
	Q86Y11	UniProtKB/Swiss-Prot
	Q86Y12	UniProtKB/Swiss-Prot
	Q8IXI5	UniProtKB/Swiss-Prot
	Q99987	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2018-08-21	VRK2	VRK serine/threonine kinase 2	VRK2	vaccinia related kinase 2	Symbol and/or name change	5135510	APPROVED

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

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

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

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

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