CDK15 (cyclin dependent kinase 15)

Gene: CDK15 (cyclin dependent kinase 15) Homo sapiens

Analyze

Symbol:

CDK15

Name:

cyclin dependent kinase 15

RGD ID:

1314644

HGNC Page

HGNC:14434

Description:

Enables protein serine/threonine kinase activity. Predicted to be involved in regulation of cell cycle. Predicted to be active in cytosol and nucleus.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

ALS2CR7; amyotrophic lateral sclerosis 2 (juvenile) chromosome region, candidate 7; amyotrophic lateral sclerosis 2 chromosomal region candidate gene 7 protein; cell division protein kinase 15; cyclin-dependent kinase 15; PFTAIRE protein kinase 2; PFTAIRE2; PFTK2; serine/threonine protein kinase; serine/threonine-protein kinase ALS2CR7; serine/threonine-protein kinase PFTAIRE-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):	Cdk15 (cyclin dependent kinase 15)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoMCL, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):	Cdk15 (cyclin-dependent kinase 15)	RGD	RGD
Chinchilla lanigera (long-tailed chinchilla):	Cdk15 (cyclin dependent kinase 15)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	CDK15 (cyclin dependent kinase 15)	NCBI	Ortholog
Canis lupus familiaris (dog):	CDK15 (cyclin dependent kinase 15)	HGNC	Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoMCL, Panther, PhylomeDB, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Cdk15 (cyclin dependent kinase 15)	NCBI	Ortholog
Sus scrofa (pig):	CDK15 (cyclin dependent kinase 15)	HGNC	Ensembl, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	CDK15 (cyclin dependent kinase 15)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Cdk15 (cyclin dependent kinase 15)	NCBI	Ortholog
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Cdk15 (cyclin-dependent kinase 15)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Cdk15 (cyclin dependent kinase 15)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	cdk15 (cyclin-dependent kinase 15)	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid\|ZFIN)
Saccharomyces cerevisiae (baker's yeast):	PHO85	Alliance	DIOPT (Ensembl Compara\|OrthoFinder\|PANTHER\|PhylomeDB)
Drosophila melanogaster (fruit fly):	Eip63E	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB)
Caenorhabditis elegans (roundworm):	ZC123.4	Alliance	DIOPT (Ensembl Compara\|OrthoFinder\|PANTHER\|PhylomeDB)
Xenopus tropicalis (tropical clawed frog):	cdk15	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Xenopus laevis (African clawed frog):	cdk15.L	Alliance	DIOPT (Xenbase)

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	2	201,806,429 - 201,895,550 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	2	201,790,461 - 201,895,550 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	2	202,671,152 - 202,760,273 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	2	202,379,443 - 202,466,511 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	2	202,496,703 - 202,583,769	NCBI
Celera	2	196,423,311 - 196,510,043 (+)	NCBI		Celera
Cytogenetic Map	2	q33.1	NCBI
HuRef	2	194,519,358 - 194,609,045 (+)	NCBI		HuRef
CHM1_1	2	202,677,626 - 202,766,857 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	2	202,287,333 - 202,376,437 (+)	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

autoimmune lymphoproliferative syndrome type 2B (IAGP)

Autoimmune Lymphoproliferative Syndrome, Type V (IAGP)

common variable immunodeficiency 1 (IAGP)

genetic disease (IAGP)

Neurodevelopmental Disorders (IAGP)

primary pulmonary hypertension (IAGP)

Primary Pulmonary Hypertension, 1 (IAGP)

Pulmonary Arterial Hypertension (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

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

aflatoxin B1 (EXP)

Aflatoxin B2 alpha (EXP)

all-trans-retinoic acid (ISO)

aristolochic acid A (EXP)

benzo[a]pyrene (EXP)

benzo[e]pyrene (EXP)

bis(2-ethylhexyl) phthalate (ISO)

bisphenol A (EXP)

cadmium atom (EXP)

cadmium dichloride (EXP)

CGP 52608 (EXP)

chlorpyrifos (ISO)

lipopolysaccharide (EXP)

malathion (EXP)

methapyrilene (EXP)

methylisothiazolinone (EXP)

mono(2-ethylhexyl) phthalate (ISO)

nickel atom (EXP)

niclosamide (EXP)

p-chloromercuribenzoic acid (EXP)

paracetamol (EXP)

S-(1,2-dichlorovinyl)-L-cysteine (EXP)

streptozocin (ISO)

titanium dioxide (ISO)

valproic acid (EXP)

vinclozolin (ISO)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

regulation of cell cycle (IEA)

Cellular Component

cytoplasm (IBA)

cytosol (IBA,IEA)

nucleus (IBA,IEA)

Molecular Function

ATP binding (IEA)

cyclin binding (IBA,IEA)

cyclin-dependent protein serine/threonine kinase activity (IBA,IEA)

kinase activity (IEA)

metal ion binding (IEA)

nucleotide binding (IEA)

protein binding (IPI)

protein kinase activity (IEA)

protein serine kinase activity (IEA)

protein serine/threonine kinase activity (IDA,IEA)

transferase activity (IEA)

Molecular Pathway Annotations Click to see Annotation Detail View

Wnt signaling pathway (ISO)

Phenotype Annotations Click to see Annotation Detail View

Human Phenotype

Pulmonary arterial hypertension (IAGP)

References

References - curated

#	Reference Title	Reference Citation
1.	GOAs Human GO annotations	GOA_HUMAN data from the GO Consortium
2.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions
3.	Frizzled 2 and frizzled 7 function redundantly in convergent extension and closure of the ventricular septum and palate: evidence for a network of interacting genes.	Yu H, etal., Development. 2012 Dec 1;139(23):4383-94. doi: 10.1242/dev.083352. Epub 2012 Oct 24.

Additional References at PubMed

PMID:11586298	PMID:12471243	PMID:12477932	PMID:14702039	PMID:15489334	PMID:15815621	PMID:16236519	PMID:16344560	PMID:17353931	PMID:19884882	PMID:21873635	PMID:22939624
PMID:23455922	PMID:23602568	PMID:24866247	PMID:25036637	PMID:26186194	PMID:28514442	PMID:29845934	PMID:30021884	PMID:33961781	PMID:34162268	PMID:34262144

Genomics

Comparative Map Data

CDK15
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	2	201,806,429 - 201,895,550 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	2	201,790,461 - 201,895,550 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	2	202,671,152 - 202,760,273 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	2	202,379,443 - 202,466,511 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	2	202,496,703 - 202,583,769	NCBI
Celera	2	196,423,311 - 196,510,043 (+)	NCBI		Celera
Cytogenetic Map	2	q33.1	NCBI
HuRef	2	194,519,358 - 194,609,045 (+)	NCBI		HuRef
CHM1_1	2	202,677,626 - 202,766,857 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	2	202,287,333 - 202,376,437 (+)	NCBI		T2T-CHM13v2.0

Cdk15
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	1	59,296,029 - 59,391,656 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	1	59,296,065 - 59,392,152 (+)	Ensembl		GRCm39 Ensembl
GRCm38	1	59,256,861 - 59,352,497 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	1	59,256,906 - 59,352,993 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	1	59,313,751 - 59,409,213 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	1	59,201,452 - 59,297,158 (+)	NCBI		MGSCv36	mm8
Celera	1	59,774,052 - 59,869,619 (+)	NCBI		Celera
Cytogenetic Map	1	C1.3- C2	NCBI
cM Map	1	29.47	NCBI

Cdk15
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	9	68,205,759 - 68,299,218 (+)	NCBI		GRCr8
mRatBN7.2	9	60,710,787 - 60,803,638 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	9	60,711,715 - 60,802,777 (+)	Ensembl		mRatBN7.2 Ensembl
Rnor_6.0	9	66,059,765 - 66,153,729 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	9	66,058,047 - 66,148,087 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	9	65,865,897 - 65,958,276 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	9	57,840,625 - 57,930,096 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	9	58,185,126 - 58,214,016 (+)	NCBI
Celera	9	58,148,588 - 58,242,444 (+)	NCBI		Celera
Cytogenetic Map	9	q31	NCBI

Cdk15
(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_004955457	12,880,959 - 12,966,410 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955457	12,878,736 - 12,966,434 (-)	NCBI	ChiLan1.0	ChiLan1.0

CDK15
(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	13	104,429,756 - 104,519,360 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	2B	104,444,798 - 104,534,360 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	2B	89,060,334 - 89,149,106 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	2B	207,198,906 - 207,304,029 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	2B	207,215,058 - 207,304,029 (+)	Ensembl	panpan1.1		panPan2

CDK15
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	37	10,848,789 - 10,929,818 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	37	10,849,003 - 10,926,856 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	37	11,732,588 - 11,814,581 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	37	10,784,792 - 10,867,012 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	37	10,785,070 - 10,866,645 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	37	10,735,784 - 10,818,006 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	37	10,714,305 - 10,796,498 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	37	10,706,802 - 10,789,638 (+)	NCBI		UU_Cfam_GSD_1.0

Cdk15
(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_024405303	159,067,332 - 159,160,261 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936726	1,037,636 - 1,130,571 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936726	1,037,614 - 1,129,961 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

CDK15
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	15	105,401,165 - 105,506,114 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	15	105,401,170 - 105,506,112 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	15	116,938,476 - 116,997,821 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

CDK15
(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	10	87,499,225 - 87,592,748 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	10	87,499,808 - 87,589,730 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666040	111,820,757 - 111,914,138 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Cdk15
(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_004624765	14,555,207 - 14,641,545 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624765	14,550,267 - 14,641,749 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in CDK15
11 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 2q31.1-33.2(chr2:174898848-203941548)x1	copy number loss	See cases [RCV000050980]	Chr2:174898848..203941548 [GRCh38] Chr2:175763576..204806271 [GRCh37] Chr2:175471822..204514516 [NCBI36] Chr2:2q31.1-33.2	pathogenic
GRCh38/hg38 2q32.3-37.3(chr2:194898783-236473913)x3	copy number gain	See cases [RCV000051119]	Chr2:194898783..236473913 [GRCh38] Chr2:195763507..237382556 [GRCh37] Chr2:195471752..237047295 [NCBI36] Chr2:2q32.3-37.3	pathogenic
GRCh38/hg38 2q33.1-34(chr2:198095810-211803453)x1	copy number loss	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052603]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052603]\|See cases [RCV000052603]	Chr2:198095810..211803453 [GRCh38] Chr2:198960534..212668178 [GRCh37] Chr2:198668779..212376423 [NCBI36] Chr2:2q33.1-34	pathogenic
GRCh38/hg38 2q33.1-33.2(chr2:200520961-203566211)x1	copy number loss	See cases [RCV000052605]	Chr2:200520961..203566211 [GRCh38] Chr2:201385684..204430934 [GRCh37] Chr2:201093929..204139179 [NCBI36] Chr2:2q33.1-33.2	pathogenic
GRCh38/hg38 2q33.1(chr2:201537291-201896769)x1	copy number loss	See cases [RCV000052606]	Chr2:201537291..201896769 [GRCh38] Chr2:202402014..202761492 [GRCh37] Chr2:202110259..202469737 [NCBI36] Chr2:2q33.1	pathogenic
GRCh38/hg38 2q31.1-33.1(chr2:176304445-202039790)x1	copy number loss	See cases [RCV000052558]	Chr2:176304445..202039790 [GRCh38] Chr2:177169173..202904513 [GRCh37] Chr2:176877419..202612758 [NCBI36] Chr2:2q31.1-33.1	pathogenic
GRCh38/hg38 2q32.2-37.3(chr2:188818195-242065208)x3	copy number gain	See cases [RCV000052958]	Chr2:188818195..242065208 [GRCh38] Chr2:189682921..243007359 [GRCh37] Chr2:189391166..242656032 [NCBI36] Chr2:2q32.2-37.3	pathogenic
GRCh38/hg38 2q32.2-37.3(chr2:190310736-241892770)x3	copy number gain	See cases [RCV000052959]	Chr2:190310736..241892770 [GRCh38] Chr2:191175462..242834921 [GRCh37] Chr2:190883707..242483594 [NCBI36] Chr2:2q32.2-37.3	pathogenic
GRCh38/hg38 2q32.3-37.3(chr2:193122313-241074980)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052960]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052960]\|See cases [RCV000052960]	Chr2:193122313..241074980 [GRCh38] Chr2:193987039..242014395 [GRCh37] Chr2:193695284..241663068 [NCBI36] Chr2:2q32.3-37.3	pathogenic
GRCh38/hg38 2q33.1(chr2:201674160-202308811)x3	copy number gain	See cases [RCV000134147]	Chr2:201674160..202308811 [GRCh38] Chr2:202538883..203173534 [GRCh37] Chr2:202247128..202881779 [NCBI36] Chr2:2q33.1	uncertain significance
GRCh38/hg38 2q32.3-33.2(chr2:195660594-203969488)x1	copy number loss	See cases [RCV000135341]	Chr2:195660594..203969488 [GRCh38] Chr2:196525318..204834211 [GRCh37] Chr2:196233563..204542456 [NCBI36] Chr2:2q32.3-33.2	pathogenic
GRCh38/hg38 2q33.1(chr2:197400023-202089348)x1	copy number loss	See cases [RCV000135665]	Chr2:197400023..202089348 [GRCh38] Chr2:198264747..202954071 [GRCh37] Chr2:197972992..202662316 [NCBI36] Chr2:2q33.1	likely pathogenic
GRCh38/hg38 2q33.1(chr2:198767347-202353840)x1	copy number loss	See cases [RCV000136596]	Chr2:198767347..202353840 [GRCh38] Chr2:199632071..203218563 [GRCh37] Chr2:199340316..202926808 [NCBI36] Chr2:2q33.1	pathogenic
GRCh38/hg38 2q31.3-36.2(chr2:180513793-224302848)x3	copy number gain	See cases [RCV000139446]	Chr2:180513793..224302848 [GRCh38] Chr2:181378520..225167565 [GRCh37] Chr2:181086765..224875809 [NCBI36] Chr2:2q31.3-36.2	pathogenic
GRCh38/hg38 2q32.3-35(chr2:192938826-215705052)x1	copy number loss	See cases [RCV000141254]	Chr2:192938826..215705052 [GRCh38] Chr2:193803552..216569775 [GRCh37] Chr2:193511797..216278020 [NCBI36] Chr2:2q32.3-35	pathogenic
GRCh38/hg38 2q33.1-34(chr2:199946494-209985195)x1	copy number loss	See cases [RCV000141076]	Chr2:199946494..209985195 [GRCh38] Chr2:200811217..210849919 [GRCh37] Chr2:200519462..210558164 [NCBI36] Chr2:2q33.1-34	pathogenic
GRCh38/hg38 2q32.2-37.3(chr2:189436149-241841232)x3	copy number gain	See cases [RCV000142307]	Chr2:189436149..241841232 [GRCh38] Chr2:190300875..242783384 [GRCh37] Chr2:190009120..242432057 [NCBI36] Chr2:2q32.2-37.3	pathogenic
GRCh38/hg38 2q33.1-34(chr2:199937273-210031924)x1	copy number loss	See cases [RCV000143301]	Chr2:199937273..210031924 [GRCh38] Chr2:200801996..210896648 [GRCh37] Chr2:200510241..210604893 [NCBI36] Chr2:2q33.1-34	pathogenic
GRCh37/hg19 2q33.1(chr2:200776457-203070949)x3	copy number gain	See cases [RCV000240410]	Chr2:200776457..203070949 [GRCh37] Chr2:2q33.1	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
GRCh37/hg19 2q31.1-35(chr2:169829974-215521436)x3	copy number gain	See cases [RCV000448271]	Chr2:169829974..215521436 [GRCh37] Chr2:2q31.1-35	pathogenic
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
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
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
Single allele	duplication	Neurodevelopmental disorder [RCV000787403]	Chr2:188926928..225298653 [GRCh37] Chr2:2q32.1-36.2	pathogenic
GRCh37/hg19 2q33.1(chr2:202639314-202680220)x1	copy number loss	not provided [RCV000846192]	Chr2:202639314..202680220 [GRCh37] Chr2:2q33.1	uncertain significance
GRCh37/hg19 2q24.2-34(chr2:163233162-211927188)x3	copy number gain	not provided [RCV001005349]	Chr2:163233162..211927188 [GRCh37] Chr2:2q24.2-34	pathogenic
NC_000002.11:g.(?_201943606)_(204824322_?)dup	duplication	Autoimmune lymphoproliferative syndrome type 2B [RCV003105677]\|Immunodeficiency, common variable, 1 [RCV003122553]	Chr2:201943606..204824322 [GRCh37] Chr2:2q33.1-33.2	uncertain significance
Single allele	deletion	Pulmonary arterial hypertension [RCV001004033]	Chr2:201106432..204901548 [GRCh37] Chr2:2q33.1-33.3	pathogenic
GRCh37/hg19 2q31.2-37.3(chr2:178397959-243007457)x3	copy number gain	See cases [RCV001263052]	Chr2:178397959..243007457 [GRCh37] Chr2:2q31.2-37.3	pathogenic
GRCh37/hg19 2q33.1(chr2:202011822-202749788)x1	copy number loss	not provided [RCV001258573]	Chr2:202011822..202749788 [GRCh37] Chr2:2q33.1	uncertain significance
GRCh37/hg19 2q32.1-34(chr2:185697659-213002074)	copy number loss	Chromosome 2q32-q33 deletion syndrome [RCV002280608]	Chr2:185697659..213002074 [GRCh37] Chr2:2q32.1-34	pathogenic
NC_000002.11:g.(?_202566574)_(203424669_?)del	deletion	Primary pulmonary hypertension [RCV001946571]	Chr2:202566574..203424669 [GRCh37] Chr2:2q33.1-33.2	pathogenic
GRCh37/hg19 2q31.1-35(chr2:169829974-215521436)	copy number gain	not specified [RCV002053265]	Chr2:169829974..215521436 [GRCh37] Chr2:2q31.1-35	pathogenic
GRCh37/hg19 2q33.1-34(chr2:200851079-209054267)	copy number loss	not specified [RCV002053275]	Chr2:200851079..209054267 [GRCh37] Chr2:2q33.1-34	pathogenic
NC_000002.11:g.(?_201943606)_(204824322_?)del	deletion	Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency [RCV001950956]\|Autoimmune lymphoproliferative syndrome type 2B [RCV001950955]\|Immunodeficiency, common variable, 1 [RCV003120780]	Chr2:201943606..204824322 [GRCh37] Chr2:2q33.1-33.2	pathogenic
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
GRCh37/hg19 2q33.1(chr2:201838259-202711243)x3	copy number gain	CYSTIC HYGROMA, VSD [RCV002282736]	Chr2:201838259..202711243 [GRCh37] Chr2:2q33.1	uncertain significance
GRCh37/hg19 2q32.2-34(chr2:189909904-209468383)x1	copy number loss	not provided [RCV002473800]	Chr2:189909904..209468383 [GRCh37] Chr2:2q32.2-34	pathogenic
NM_001366386.2(CDK15):c.451T>A (p.Ser151Thr)	single nucleotide variant	Inborn genetic diseases [RCV002783468]	Chr2:201822811 [GRCh38] Chr2:202687534 [GRCh37] Chr2:2q33.1	uncertain significance
NM_001366386.2(CDK15):c.1094C>G (p.Ser365Cys)	single nucleotide variant	Inborn genetic diseases [RCV002641536]	Chr2:201880063 [GRCh38] Chr2:202744786 [GRCh37] Chr2:2q33.1	uncertain significance
NM_001366386.2(CDK15):c.286C>G (p.Pro96Ala)	single nucleotide variant	Inborn genetic diseases [RCV002929628]	Chr2:201807870 [GRCh38] Chr2:202672593 [GRCh37] Chr2:2q33.1	uncertain significance
NM_001366386.2(CDK15):c.187G>T (p.Ala63Ser)	single nucleotide variant	Inborn genetic diseases [RCV002808044]	Chr2:201807557 [GRCh38] Chr2:202672280 [GRCh37] Chr2:2q33.1	uncertain significance
NM_001366386.2(CDK15):c.235T>G (p.Cys79Gly)	single nucleotide variant	Inborn genetic diseases [RCV002669571]	Chr2:201807605 [GRCh38] Chr2:202672328 [GRCh37] Chr2:2q33.1	uncertain significance
NM_001366386.2(CDK15):c.965A>G (p.Glu322Gly)	single nucleotide variant	Inborn genetic diseases [RCV003008725]	Chr2:201854893 [GRCh38] Chr2:202719616 [GRCh37] Chr2:2q33.1	uncertain significance
NM_001366386.2(CDK15):c.335G>C (p.Gly112Ala)	single nucleotide variant	Inborn genetic diseases [RCV002714134]	Chr2:201807919 [GRCh38] Chr2:202672642 [GRCh37] Chr2:2q33.1	uncertain significance
NM_001366386.2(CDK15):c.344C>T (p.Ala115Val)	single nucleotide variant	Inborn genetic diseases [RCV002669194]	Chr2:201807928 [GRCh38] Chr2:202672651 [GRCh37] Chr2:2q33.1	uncertain significance
NM_001366386.2(CDK15):c.424G>A (p.Val142Ile)	single nucleotide variant	Inborn genetic diseases [RCV002724779]	Chr2:201812538 [GRCh38] Chr2:202677261 [GRCh37] Chr2:2q33.1	uncertain significance
NM_001366386.2(CDK15):c.1126G>A (p.Val376Ile)	single nucleotide variant	Inborn genetic diseases [RCV003179474]	Chr2:201880095 [GRCh38] Chr2:202744818 [GRCh37] Chr2:2q33.1	uncertain significance
NM_001366386.2(CDK15):c.1000T>C (p.Tyr334His)	single nucleotide variant	Inborn genetic diseases [RCV003281602]	Chr2:201854928 [GRCh38] Chr2:202719651 [GRCh37] Chr2:2q33.1	uncertain significance
GRCh37/hg19 2q32.1-36.1(chr2:186698504-223918111)x3	copy number gain	See cases [RCV003329558]	Chr2:186698504..223918111 [GRCh37] Chr2:2q32.1-36.1	pathogenic
GRCh37/hg19 2q32.3-34(chr2:194305623-215261531)x1	copy number loss	not specified [RCV003986323]	Chr2:194305623..215261531 [GRCh37] Chr2:2q32.3-34	pathogenic

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	2432
Count of miRNA genes:	1070
Interacting mature miRNAs:	1284
Transcripts:	ENST00000260967, ENST00000374598, ENST00000410091, ENST00000434439, ENST00000450471, ENST00000451080, ENST00000460149, ENST00000466337, ENST00000488419, ENST00000493754
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

D2S2214

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	202,730,706 - 202,730,985	UniSTS	GRCh37
Build 36	2	202,438,951 - 202,439,230	RGD	NCBI36
Celera	2	196,482,490 - 196,482,769	RGD
Cytogenetic Map	2	q33.2	UniSTS
HuRef	2	194,579,763 - 194,580,040	UniSTS
Marshfield Genetic Map	2	198.65	RGD
Marshfield Genetic Map	2	198.65	UniSTS
Genethon Genetic Map	2	204.7	UniSTS
deCODE Assembly Map	2	199.28	UniSTS
Whitehead-YAC Contig Map	2		UniSTS

RH99261

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	202,759,903 - 202,760,035	UniSTS	GRCh37
Build 36	2	202,468,148 - 202,468,280	RGD	NCBI36
Celera	2	196,511,678 - 196,511,810	RGD
Cytogenetic Map	2	q33.2	UniSTS
HuRef	2	194,608,675 - 194,608,807	UniSTS
GeneMap99-GB4 RH Map	2	624.47	UniSTS

SHGC-83058

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	202,673,033 - 202,673,322	UniSTS	GRCh37
Build 36	2	202,381,278 - 202,381,567	RGD	NCBI36
Celera	2	196,425,146 - 196,425,435	RGD
Cytogenetic Map	2	q33.2	UniSTS
HuRef	2	194,521,239 - 194,521,528	UniSTS
TNG Radiation Hybrid Map	2	110986.0	UniSTS

G54445

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	202,738,001 - 202,738,323	UniSTS	GRCh37
Build 36	2	202,446,246 - 202,446,568	RGD	NCBI36
Celera	2	196,489,785 - 196,490,107	RGD
Cytogenetic Map	2	q33.2	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

Low

1275

996

163

2512

765

720

982

541

918

1617

Below cutoff

1017

1634

1304

362

907

242

1680

1392

2658

236

318

897

125

285

1163

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001261435	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001261436	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001366386	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_139158	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005246782	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011511650	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011511652	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011511654	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011511655	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011511656	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011511657	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047445552	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047445553	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054343445	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054343446	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054343447	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054343448	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054343449	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054343450	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054343451	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054343452	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_008486494	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_922990	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_922991	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AB053308	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC007242	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC007358	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK091710	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK131512	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK292434	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK310050	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AX772791	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AX772799	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC038807	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX647394	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471063	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068276	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA050598	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000260967 ⟹ ENSP00000260967

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	201,806,375 - 201,893,544 (+)	Ensembl

RefSeq Acc Id:

ENST00000410091 ⟹ ENSP00000386901

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	201,790,461 - 201,893,543 (+)	Ensembl

RefSeq Acc Id:

ENST00000434439 ⟹ ENSP00000412775

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	201,806,621 - 201,889,457 (+)	Ensembl

RefSeq Acc Id:

ENST00000450471 ⟹ ENSP00000406472

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	201,806,579 - 201,895,550 (+)	Ensembl

RefSeq Acc Id:

ENST00000451080 ⟹ ENSP00000389831

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	201,790,461 - 201,876,583 (+)	Ensembl

RefSeq Acc Id:

ENST00000460149

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	201,854,760 - 201,893,360 (+)	Ensembl

RefSeq Acc Id:

ENST00000466337

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	201,854,790 - 201,893,383 (+)	Ensembl

RefSeq Acc Id:

ENST00000488419

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	201,806,579 - 201,861,536 (+)	Ensembl

RefSeq Acc Id:

ENST00000493754

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	201,790,472 - 201,807,938 (+)	Ensembl

RefSeq Acc Id:

ENST00000652192 ⟹ ENSP00000498608

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	201,806,537 - 201,895,550 (+)	Ensembl

RefSeq Acc Id:

NM_001261435 ⟹ NP_001248364

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	201,806,579 - 201,895,550 (+)	NCBI
GRCh37	2	202,655,177 - 202,760,273 (+)	NCBI
HuRef	2	194,519,358 - 194,609,045 (+)	NCBI
CHM1_1	2	202,677,776 - 202,766,857 (+)	NCBI
T2T-CHM13v2.0	2	202,287,483 - 202,376,437 (+)	NCBI

Sequence:

show sequence

CTCTGGCAAAAAGGGAGAGAACAAGGATAGGAGAGGCAGTGGGGGAAAGGTTCAAGTGCGGGTT
TTCTCCTTGAACCTACAAGATTATGGGTCAAGAGCTGTGTGCAAAGACTGTACAGCCTGGATGC
AGCTGCTACCATTGTTCAGAGGGAGGCGAGGCACACAGCTGTCGGAGGAGTCAGCCTGAGACCA
CGGAGGCTGCGTTCAAGCTAACAGACCTAAAAGAAGCATCATGTTCCATGACTTCATTTCACCC
CAGGGGACTTCAAGCTGCCCGTGCCCAGAAGTTCAAGAGTAAAAGGCCACGGAGTAACAGTGAT
TGTTTTCAGGAAGAGGATCTGAGGCAGGGTTTTCAGTGGAGGAAGAGCCTCCCTTTTGGGGCAG
CCTCATCTTACTTGAACTTGGAGAAGCTGGGTGAAGGCTCTTATGCGACAGTTTACAAGGGGAT
TAGCAGAATAAATGGACAACTAGTGGCTTTAAAAGTCATCAGCATGAATGCAGAGGAAGGAGTC
CCATTTACAGCTATCCGAGAAGCTTCTCTCCTGAAGGGTTTGAAACATGCCAATATTGTGCTCC
TGCATGACATAATCCACACCAAAGAGACACTGACATTCGTTTTTGAATACATGCACACAGACCT
GGCCCAGTATATGTCTCAGCATCCAGGAGGGCTTCATCCTCATAATGTCAGACTTTTCATGTTT
CAACTTTTGCGGGGCCTGGCGTACATCCACCACCAACACGTTCTTCACAGGGACCTGAAACCTC
AGAACTTACTCATCAGTCACCTGGGAGAGCTCAAACTGGCTGATTTTGGTCTTGCCCGGGCCAA
GTCCATTCCCAGCCAGACATACTCTTCAGAAGTCGTGACCCTCTGGTACCGGCCCCCTGATGCT
TTGCTGGGAGCCACTGAATATTCCTCTGAGCTGGACATATGGGGTGCAGGCTGCATCTTTATTG
AAATGTTCCAGGGTCAACCTTTGTTTCCTGGGGTTTCCAACATCCTTGAACAGCTGGAGAAAAT
CTGGGAGGTGCTGGGAGTCCCTACAGAGGATACTTGGCCGGGAGTCTCCAAGCTACCTAACTAC
AATCCAGAATGGTTCCCACTGCCTACGCCTCGAAGCCTTCATGTTGTCTGGAACAGGCTGGGCA
GGGTTCCTGAAGCTGAAGACCTGGCCTCCCAGATGCTAAAAGGCTTTCCCAGAGACCGCGTCTC
CGCCCAGGAAGCACTTGTTCATGATTATTTCAGCGCCCTGCCATCTCAGCTGTACCAGCTTCCT
GATGTTTCAGGAGTGAGGCTAAAGCCAGAAATGTGTGACCTTTTGGCCTCCTACCAGAAAGGTC
ACCACCCAGCCCAGTTTAGCAAATGCTGGTGAAAAGAAAGGGCGAGATCACCAAGGTTCTTCCA
GGGCTGTATTTCTGCAGTTTCGGTTTTCATTTGCTTCAGCTTACTAAGAAGCTTCAAATCTAAC
TCCATACTGAACAAGGGGCTTTATGTCCTCACCTATGACCTGGAATAGTTTAAATATGGTGTTC
AAGGCAATAGTACATAATAGTGGAAGAAAATTCAGTGGAAGGTTATTGCTATTGTCATTTGCAT
AGAATTTAAGTGATTGATTTAAAAAAACTGGACATAAACTAAGTCTAAGAAGAGGGCTTCTGAA
TAACTTCATTCATTTTGGCATTTGTTAAGAGATTCCTGGGCTAGAAGGTTGATTTCCCAAAAAG
ACAGATAAGAGACTGACAATTTAAAAGAATCTGGAGACAGAGCTGGTGCTTACAGAGACCTGCC
ACTCCTGTGTTCACTTACAATTTCTCCCAACAAAAGGATTTCTGTGGCAAGGAGAAAACTAGCC
TAAAGTTTAGAAAAAGATGGTTTCTTGGATAACATTGTTAACAAAAGGACTTCCTGAGGACTAT
TTATTATTATTTTGTAGGGGGCACTTCCTCCTTCACTAAACTGGATTATCAGAACGTATTACCA
CCCAACCCATATTTTAGAAGTTTGGATTTGGCTGCTGATTAGAAATGAATTTCAGGCTATCTCC
TCCTACTGAATCTTAATTGTCTGTGATGATGGCAACAGTGATGGGGAATCTAAGCGCTGGTTTG
ATGGTGGAGATATTGAATAAGTAGTTGGGAGCAGAGTTCCAAAGATGTAATTTAAGCCCTGTTG
CACCACCACACACACACACACACACACACACACACACACACACACACCCCTCAAGTAAAATGAG
AGATCTGTCTTAGCTAACACGTGTGCCGTTTTATACAATGACTCCTTCTAAAAGCAGCCAGGGA
AACTCAAATCGCTTCTGTCCAGGGATCATCTCAGGAAATGTAGCAGCCTAGAAACCAGAGACCT
CTGTATATCCTTTGGAAGAGCAAGGAGGAACTAATTAAGAGATAATTAAAAAATAGTAACTATC
CCCCAATGTCTGAGATGGAAAAAGGAAAAAGACACATGGGTAGCCCAAATCAACCTGCCTGAGT
AAGTATCTGATTTTAGTAAGGCATTTGACAAAGACTGTCCAGCTATACCTGAAAGATGAAACAG
TGTAGGCTGGGTGATGGAGCAGATATATGTACTCAAATCATGGTGTTTATTTAACCCAGAGAAA
GGCCAGCCGTGGTGTGCTACAAGGTTCAGTCTTGAGTCCTATTCTGGTCAAATATTTTTATTAA
TTACTCGAATAAATCAGAGTACATGGACAACTTTATACAACTCCTTGAAGTAAGTACTATTATT
ATTAATTTATGACTTCCATTTCACAAAAGAGGAGACTGAGGCTCAGTGAAGTTAGGTAACTCCT
TCATAGTAGCATGCCAGAGTGAAGATGCAAACCTCAGACCTGGTTCTCCAATGTTCCTGACACC
TATCGAATTTAGAGAATACACAACTCTTGCAGAGGCAGCTGCTATTTAGTATTGGATCATGATT
CAAAAGACACCTTGCTAGAAGCCAATGAACAGCAGGCCAAAACAACACTTACTTGCATCAAATT
TCATCTGACTTAAATTCTTACACTTTGGGCTACAACTTAAAAAAGGCTATGACTTAGTGGAAAT
TGGCACTTTTAAGTACAATATGAATTAATAGTATAATTTCGCTGTCCCCCAGAGATAATGCTAG
TACCAATCGAAAGCTCAGGGATGCTACTGTTGACGCATCAGCAAGAGTTCTTGAGCAGTTTTAC
CTGTCCATCAATACAAAGAGTTCCCACAACAGTAGTGGGATTCCTCTGCCTCTCTGAAGATATG
AGAGCTATAGGAGGGATTCCCATGTTGGAGGTTAGAAGAGCTGACCTCCAATGTCCCGTCTAAT
TCCAAGATTCTCCAATAATGACTTTGGAACAGCTGTGTACAGATTATACTTGGAATTATGCTTA
GATACTATTGCTGCAGGAATGAATAGACAAATTTTGTTATTAAAAAATTGATTTTATTAAGTGG
AAGTTGACAGAATTATCCTCTTTATAATGGAGGAACATTATGCTTATGCATATGCATATACCTT
ATGCATATGATTATGCTTGTGCTTCCTTCTTTAATGGATTTACCTATTCAAAAGCTTAATAAAT
GTTATAAGACTCTAAAACATTTAAATCTTTCATTTCTCAATTTTATCAAATAAACATTCCTGGA
ATTTGTGCATAAAAAAAAAAAAAA

hide sequence

RefSeq Acc Id:

NM_001261436 ⟹ NP_001248365

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	201,806,579 - 201,889,452 (+)	NCBI
GRCh37	2	202,655,177 - 202,760,273 (+)	NCBI
HuRef	2	194,519,358 - 194,609,045 (+)	NCBI
CHM1_1	2	202,677,776 - 202,760,761 (+)	NCBI
T2T-CHM13v2.0	2	202,287,483 - 202,370,343 (+)	NCBI

Sequence:

show sequence

CTCTGGCAAAAAGGGAGAGAACAAGGATAGGAGAGGCAGTGGGGGAAAGGTTCAAGTGCGGGTT
TTCTCCTTGAACCTACAAGATTATGGGTCAAGAGCTGTGTGCAAAGACTGTACAGCCTGGATGC
AGCTGCTACCATTGTTCAGAGGGAGGCGAGGCACACAGCTGTCGGAGGAGTCAGCCTGAGACCA
CGGAGGCTGCGTTCAAGCTAACAGACCTAAAAGAAGCATCATGTTCCATGACTTCATTTCACCC
CAGGGGACTTCAAGCTGCCCGTGCCCAGAAGTTCAAGAGTAAAAGGCCACGGAGTAACAGTGAT
TGTTTTCAGGAAGAGGATCTGAGGCAGGGTTTTCAGTGGAGGAAGAGCCTCCCTTTTGGGGCAG
CCTCATCTTACTTGAACTTGGAGAAGCTGGGTGAAGGCTCTTATGCGACAGTTTACAAGGGGAT
TAGCAGAATAAATGGACAACTAGTGGCTTTAAAAGTCATCAGCATGAATGCAGAGGAAGGAGTC
CCATTTACAGCTATCCGAGAAGCTTCTCTCCTGAAGGGTTTGAAACATGCCAATATTGTGCTCC
TGCATGACATAATCCACACCAAAGAGACACTGACATTCGTTTTTGAATACATGCACACAGACCT
GGCCCAGTATATGTCTCAGCATCCAGGAGGGCTTCATCCTCATAATGTCAGACTTTTCATGTTT
CAACTTTTGCGGGGCCTGGCGTACATCCACCACCAACACGTTCTTCACAGGGACCTGAAACCTC
AGAACTTACTCATCAGTCACCTGGGAGAGCTCAAACTGGCTGATTTTGGTCTTGCCCGGGCCAA
GTCCATTCCCAGCCAGACATACTCTTCAGAAGTCGTGACCCTCTGGTACCGGCCCCCTGATGCT
TTGCTGGGAGCCACTGAATATTCCTCTGAGCTGGACATATGGGGTGCAGGCTGCATCTTTATTG
AAATGTTCCAGGGTCAACCTTTGTTTCCTGGGGTTTCCAACATCCTTGAACAGCTGGAGAAAAT
CTGGGAGGTGCTGGGAGTCCCTACAGAGGATACTTGGCCGGGAGTCTCCAAGCTACCTAACTAC
AATCCAGAATGGTTCCCACTGCCTACGCCTCGAAGCCTTCATGTTGTCTGGAACAGGCTGGGCA
GGGTTCCTGAAGCTGAAGACCTGGCCTCCCAGATGCTAAAAGGCTTTCCCAGAGACCGCGTCTC
CGCCCAGGAAGCACTTGTTCATGATTATTTCAGCGCCCTGCCATCTCAGCTGTACCAGCTTCCT
GATGAGTGAAGCAGCTGCGATAATTATGCTGTCAGCCTCGGGAAGCTAATGAGGAGTCACCAGA
GTGGAAGGTTTTGCATTTGTGAGATTGCTGAAGGAGAGCCGCGCTGCAGCTTTTTTCGTTTTTT
ATTTCCCTTTCTTTCTTTCTTCCTCCTTTTTCTTTTTCTATGAGTTGGGAAGGAGAGTCTGGCA
GTCCACAGCCAAATTGGAATCCTTTTGATTAACCGGTTGCCTTCCCAGCATGTTCTGCCAGATA
GTGTCTCTCTCTCTCTCCCTCCCTCCCTGCTTTTGAGGAGCTGCTGCTTTTGAGGGGCAAGGAA
GCCGGAGGGAAATCCCAGCTTTTCATGCCACTGTCCCCAAGGCAAGAGGATACTTCTCCCCGAG
AGAAGTTCCCCAAATGGTTTGGATTTGAGTTGATTTGAGAATAATTGGTAAAGTATACGCACTG
TTTATTTTAGCCATTTAACTGTCTATGCTATGACAAGATCTAATAGAAAGTAGAATACAAAATT
GCATATTATAATATCCGTGTGAAAATGTCTTATGCATATCAACAAATGGTATGATGGCTCCCCT
TTCCAGCCTATTTGGAATATGCGATTCCAAATACAAGACAACGAGACCCCAGATTACCCACAGC
ATTTAAGGGCAGAAGTTTAGGCCAGGCGAGGCAGAGCTGGCAAGTTTATTTCTTCCCTTTGGGT
GTGAGCAGCTTCCAGCAAACAGTATTATTTAAGGCATTTTATGCTTTTGGTGCAGTAATAACAG
AAGGCTCTCTTTTTGTTAAATTGTGAGATATTTTGAGCACCCCAGATTTATGCAAATTGTGAAC
CTGGGAAAAGCAATGCCCAAGTGGAAAGGGGCCCTGAGTAAATTTTGCGGATGTGCTTTGGTGA
CAATGTGGCTGCTGCCTCTTGCTATTTTTCTCAGATATCTGTGCTAATACTTGTAACAATGGCT
ACCATTTATTAAAAACATATTGTGTATCATAAACTAAAAAAAAAAAAAAAAA

hide sequence

RefSeq Acc Id:

NM_001366386 ⟹ NP_001353315

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	201,806,537 - 201,895,550 (+)	NCBI
T2T-CHM13v2.0	2	202,287,441 - 202,376,437 (+)	NCBI

Sequence:

show sequence

AGAGCCATCATGTGAGTCATATGAAAGCTCCACGCTGCTGACCTCTGGCAAAAAGGGAGAGAAC
AAGGATAGGAGAGGCAGTGGGGGAAAGGTTCAAGTGCGGGTTTTCTCCTTGAACCTACAAGATT
ATGGGTCAAGAGCTGTGTGCAAAGACTGTACAGCCTGGATGCAGCTGCTACCATTGTTCAGAGG
GAGGCGAGGCACACAGCTGTCGGAGGAGTCAGCCTGAGACCACGGAGGCTGCGTTCAAGCTAAC
AGACCTAAAAGAAGCATCATGTTCCATGACTTCATTTCACCCCAGGGGACTTCAAGCTGCCCGT
GCCCAGAAGTTCAAGAGTAAAAGGCCACGGAGTAACAGTGATTGTTTTCAGGAAGAGGATCTGA
GGCAGGGTTTTCAGTGGAGGAAGAGCCTCCCTTTTGGGGCAGCCTCATCTTACTTGAACTTGGA
GAAGCTGGGTGAAGGCTCTTATGCGACAGTTTACAAGGGGATTAGCAGAATAAATGGACAACTA
GTGGCTTTAAAAGTCATCAGCATGAATGCAGAGGAAGGAGTCCCATTTACAGCTATCCGAGAAG
CTTCTCTCCTGAAGGGTTTGAAACATGCCAATATTGTGCTCCTGCATGACATAATCCACACCAA
AGAGACACTGACATTCGTTTTTGAATACATGCACACAGACCTGGCCCAGTATATGTCTCAGCAT
CCAGGAGGGCTTCATCCTCATAATGTCAGACTTTTCATGTTTCAACTTTTGCGGGGCCTGGCGT
ACATCCACCACCAACACGTTCTTCACAGGGACCTGAAACCTCAGAACTTACTCATCAGTCACCT
GGGAGAGCTCAAACTGGCTGATTTTGGTCTTGCCCGGGCCAAGTCCATTCCCAGCCAGACATAC
TCTTCAGAAGTCGTGACCCTCTGGTACCGGCCCCCTGATGCTTTGCTGGGAGCCACTGAATATT
CCTCTGAGCTGGACATATGGGGTGCAGGCTGCATCTTTATTGAAATGTTCCAGGGTCAACCTTT
GTTTCCTGGGGTTTCCAACATCCTTGAACAGCTGGAGAAAATCTGGGAGGTGCTGGGAGTCCCT
ACAGAGGATACTTGGCCGGGAGTCTCCAAGCTACCTAACTACAATCCAGAATGGTTCCCACTGC
CTACGCCTCGAAGCCTTCATGTTGTCTGGAACAGGCTGGGCAGGGTTCCTGAAGCTGAAGACCT
GGCCTCCCAGATGCTAAAAGGCTTTCCCAGAGACCGCGTCTCCGCCCAGGAAGCACTTGTTCAT
GATTATTTCAGCGCCCTGCCATCTCAGCTGTACCAGCTTCCTGATGAGGAGTCTTTGTTTACAG
TTTCAGGAGTGAGGCTAAAGCCAGAAATGTGTGACCTTTTGGCCTCCTACCAGAAAGGTCACCA
CCCAGCCCAGTTTAGCAAATGCTGGTGAAAAGAAAGGGCGAGATCACCAAGGTTCTTCCAGGGC
TGTATTTCTGCAGTTTCGGTTTTCATTTGCTTCAGCTTACTAAGAAGCTTCAAATCTAACTCCA
TACTGAACAAGGGGCTTTATGTCCTCACCTATGACCTGGAATAGTTTAAATATGGTGTTCAAGG
CAATAGTACATAATAGTGGAAGAAAATTCAGTGGAAGGTTATTGCTATTGTCATTTGCATAGAA
TTTAAGTGATTGATTTAAAAAAACTGGACATAAACTAAGTCTAAGAAGAGGGCTTCTGAATAAC
TTCATTCATTTTGGCATTTGTTAAGAGATTCCTGGGCTAGAAGGTTGATTTCCCAAAAAGACAG
ATAAGAGACTGACAATTTAAAAGAATCTGGAGACAGAGCTGGTGCTTACAGAGACCTGCCACTC
CTGTGTTCACTTACAATTTCTCCCAACAAAAGGATTTCTGTGGCAAGGAGAAAACTAGCCTAAA
GTTTAGAAAAAGATGGTTTCTTGGATAACATTGTTAACAAAAGGACTTCCTGAGGACTATTTAT
TATTATTTTGTAGGGGGCACTTCCTCCTTCACTAAACTGGATTATCAGAACGTATTACCACCCA
ACCCATATTTTAGAAGTTTGGATTTGGCTGCTGATTAGAAATGAATTTCAGGCTATCTCCTCCT
ACTGAATCTTAATTGTCTGTGATGATGGCAACAGTGATGGGGAATCTAAGCGCTGGTTTGATGG
TGGAGATATTGAATAAGTAGTTGGGAGCAGAGTTCCAAAGATGTAATTTAAGCCCTGTTGCACC
ACCACACACACACACACACACACACACACACACACACACACACCCCTCAAGTAAAATGAGAGAT
CTGTCTTAGCTAACACGTGTGCCGTTTTATACAATGACTCCTTCTAAAAGCAGCCAGGGAAACT
CAAATCGCTTCTGTCCAGGGATCATCTCAGGAAATGTAGCAGCCTAGAAACCAGAGACCTCTGT
ATATCCTTTGGAAGAGCAAGGAGGAACTAATTAAGAGATAATTAAAAAATAGTAACTATCCCCC
AATGTCTGAGATGGAAAAAGGAAAAAGACACATGGGTAGCCCAAATCAACCTGCCTGAGTAAGT
ATCTGATTTTAGTAAGGCATTTGACAAAGACTGTCCAGCTATACCTGAAAGATGAAACAGTGTA
GGCTGGGTGATGGAGCAGATATATGTACTCAAATCATGGTGTTTATTTAACCCAGAGAAAGGCC
AGCCGTGGTGTGCTACAAGGTTCAGTCTTGAGTCCTATTCTGGTCAAATATTTTTATTAATTAC
TCGAATAAATCAGAGTACATGGACAACTTTATACAACTCCTTGAAGTAAGTACTATTATTATTA
ATTTATGACTTCCATTTCACAAAAGAGGAGACTGAGGCTCAGTGAAGTTAGGTAACTCCTTCAT
AGTAGCATGCCAGAGTGAAGATGCAAACCTCAGACCTGGTTCTCCAATGTTCCTGACACCTATC
GAATTTAGAGAATACACAACTCTTGCAGAGGCAGCTGCTATTTAGTATTGGATCATGATTCAAA
AGACACCTTGCTAGAAGCCAATGAACAGCAGGCCAAAACAACACTTACTTGCATCAAATTTCAT
CTGACTTAAATTCTTACACTTTGGGCTACAACTTAAAAAAGGCTATGACTTAGTGGAAATTGGC
ACTTTTAAGTACAATATGAATTAATAGTATAATTTCGCTGTCCCCCAGAGATAATGCTAGTACC
AATCGAAAGCTCAGGGATGCTACTGTTGACGCATCAGCAAGAGTTCTTGAGCAGTTTTACCTGT
CCATCAATACAAAGAGTTCCCACAACAGTAGTGGGATTCCTCTGCCTCTCTGAAGATATGAGAG
CTATAGGAGGGATTCCCATGTTGGAGGTTAGAAGAGCTGACCTCCAATGTCCCGTCTAATTCCA
AGATTCTCCAATAATGACTTTGGAACAGCTGTGTACAGATTATACTTGGAATTATGCTTAGATA
CTATTGCTGCAGGAATGAATAGACAAATTTTGTTATTAAAAAATTGATTTTATTAAGTGGAAGT
TGACAGAATTATCCTCTTTATAATGGAGGAACATTATGCTTATGCATATGCATATACCTTATGC
ATATGATTATGCTTGTGCTTCCTTCTTTAATGGATTTACCTATTCAAAAGCTTAATAAATGTTA
TAAGACTCTAAAACATTTAAATCTTTCATTTCTCAATTTTATCAAATAAACATTCCTGGAATTT
GTGCATA

hide sequence

RefSeq Acc Id:

NM_139158 ⟹ NP_631897

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	201,806,429 - 201,895,550 (+)	NCBI
GRCh37	2	202,655,177 - 202,760,273 (+)	NCBI
Build 36	2	202,379,443 - 202,466,511 (+)	NCBI Archive
Celera	2	196,423,311 - 196,510,043 (+)	RGD
HuRef	2	194,519,358 - 194,609,045 (+)	NCBI
CHM1_1	2	202,677,626 - 202,766,857 (+)	NCBI
T2T-CHM13v2.0	2	202,287,333 - 202,376,437 (+)	NCBI

Sequence:

show sequence

CTGCCTCGTTTTCAGTTGTGCACATCTGAATGCAAGCAATCCCTGTCTGATGTGGAGTTTCTTG
CACTGATAAGGAAAAACTGCTGAAGTTGTGAGGCTGCTCCAGGCAGAGCCATCATCTAACAGAC
CTAAAAGAAGCATCATGTTCCATGACTTCATTTCACCCCAGGGGACTTCAAGCTGCCCGTGCCC
AGAAGTTCAAGAGTAAAAGGCCACGGAGTAACAGTGATTGTTTTCAGGAAGAGGATCTGAGGCA
GGGTTTTCAGTGGAGGAAGAGCCTCCCTTTTGGGGCAGCCTCATCTTACTTGAACTTGGAGAAG
CTGGGTGAAGGCTCTTATGCGACAGTTTACAAGGGGATTAGCAGAATAAATGGACAACTAGTGG
CTTTAAAAGTCATCAGCATGAATGCAGAGGAAGGAGTCCCATTTACAGCTATCCGAGAAGCTTC
TCTCCTGAAGGGTTTGAAACATGCCAATATTGTGCTCCTGCATGACATAATCCACACCAAAGAG
ACACTGACATTCGTTTTTGAATACATGCACACAGACCTGGCCCAGTATATGTCTCAGCATCCAG
GAGGGCTTCATCCTCATAATGTCAGACTTTTCATGTTTCAACTTTTGCGGGGCCTGGCGTACAT
CCACCACCAACACGTTCTTCACAGGGACCTGAAACCTCAGAACTTACTCATCAGTCACCTGGGA
GAGCTCAAACTGGCTGATTTTGGTCTTGCCCGGGCCAAGTCCATTCCCAGCCAGACATACTCTT
CAGAAGTCGTGACCCTCTGGTACCGGCCCCCTGATGCTTTGCTGGGAGCCACTGAATATTCCTC
TGAGCTGGACATATGGGGTGCAGGCTGCATCTTTATTGAAATGTTCCAGGGTCAACCTTTGTTT
CCTGGGGTTTCCAACATCCTTGAACAGCTGGAGAAAATCTGGGAGGTGCTGGGAGTCCCTACAG
AGGATACTTGGCCGGGAGTCTCCAAGCTACCTAACTACAATCCAGAATGGTTCCCACTGCCTAC
GCCTCGAAGCCTTCATGTTGTCTGGAACAGGCTGGGCAGGGTTCCTGAAGCTGAAGACCTGGCC
TCCCAGATGCTAAAAGGCTTTCCCAGAGACCGCGTCTCCGCCCAGGAAGCACTTGTTCATGATT
ATTTCAGCGCCCTGCCATCTCAGCTGTACCAGCTTCCTGATGAGGAGTCTTTGTTTACAGTTTC
AGGAGTGAGGCTAAAGCCAGAAATGTGTGACCTTTTGGCCTCCTACCAGAAAGGTCACCACCCA
GCCCAGTTTAGCAAATGCTGGTGAAAAGAAAGGGCGAGATCACCAAGGTTCTTCCAGGGCTGTA
TTTCTGCAGTTTCGGTTTTCATTTGCTTCAGCTTACTAAGAAGCTTCAAATCTAACTCCATACT
GAACAAGGGGCTTTATGTCCTCACCTATGACCTGGAATAGTTTAAATATGGTGTTCAAGGCAAT
AGTACATAATAGTGGAAGAAAATTCAGTGGAAGGTTATTGCTATTGTCATTTGCATAGAATTTA
AGTGATTGATTTAAAAAAACTGGACATAAACTAAGTCTAAGAAGAGGGCTTCTGAATAACTTCA
TTCATTTTGGCATTTGTTAAGAGATTCCTGGGCTAGAAGGTTGATTTCCCAAAAAGACAGATAA
GAGACTGACAATTTAAAAGAATCTGGAGACAGAGCTGGTGCTTACAGAGACCTGCCACTCCTGT
GTTCACTTACAATTTCTCCCAACAAAAGGATTTCTGTGGCAAGGAGAAAACTAGCCTAAAGTTT
AGAAAAAGATGGTTTCTTGGATAACATTGTTAACAAAAGGACTTCCTGAGGACTATTTATTATT
ATTTTGTAGGGGGCACTTCCTCCTTCACTAAACTGGATTATCAGAACGTATTACCACCCAACCC
ATATTTTAGAAGTTTGGATTTGGCTGCTGATTAGAAATGAATTTCAGGCTATCTCCTCCTACTG
AATCTTAATTGTCTGTGATGATGGCAACAGTGATGGGGAATCTAAGCGCTGGTTTGATGGTGGA
GATATTGAATAAGTAGTTGGGAGCAGAGTTCCAAAGATGTAATTTAAGCCCTGTTGCACCACCA
CACACACACACACACACACACACACACACACACACACACCCCTCAAGTAAAATGAGAGATCTGT
CTTAGCTAACACGTGTGCCGTTTTATACAATGACTCCTTCTAAAAGCAGCCAGGGAAACTCAAA
TCGCTTCTGTCCAGGGATCATCTCAGGAAATGTAGCAGCCTAGAAACCAGAGACCTCTGTATAT
CCTTTGGAAGAGCAAGGAGGAACTAATTAAGAGATAATTAAAAAATAGTAACTATCCCCCAATG
TCTGAGATGGAAAAAGGAAAAAGACACATGGGTAGCCCAAATCAACCTGCCTGAGTAAGTATCT
GATTTTAGTAAGGCATTTGACAAAGACTGTCCAGCTATACCTGAAAGATGAAACAGTGTAGGCT
GGGTGATGGAGCAGATATATGTACTCAAATCATGGTGTTTATTTAACCCAGAGAAAGGCCAGCC
GTGGTGTGCTACAAGGTTCAGTCTTGAGTCCTATTCTGGTCAAATATTTTTATTAATTACTCGA
ATAAATCAGAGTACATGGACAACTTTATACAACTCCTTGAAGTAAGTACTATTATTATTAATTT
ATGACTTCCATTTCACAAAAGAGGAGACTGAGGCTCAGTGAAGTTAGGTAACTCCTTCATAGTA
GCATGCCAGAGTGAAGATGCAAACCTCAGACCTGGTTCTCCAATGTTCCTGACACCTATCGAAT
TTAGAGAATACACAACTCTTGCAGAGGCAGCTGCTATTTAGTATTGGATCATGATTCAAAAGAC
ACCTTGCTAGAAGCCAATGAACAGCAGGCCAAAACAACACTTACTTGCATCAAATTTCATCTGA
CTTAAATTCTTACACTTTGGGCTACAACTTAAAAAAGGCTATGACTTAGTGGAAATTGGCACTT
TTAAGTACAATATGAATTAATAGTATAATTTCGCTGTCCCCCAGAGATAATGCTAGTACCAATC
GAAAGCTCAGGGATGCTACTGTTGACGCATCAGCAAGAGTTCTTGAGCAGTTTTACCTGTCCAT
CAATACAAAGAGTTCCCACAACAGTAGTGGGATTCCTCTGCCTCTCTGAAGATATGAGAGCTAT
AGGAGGGATTCCCATGTTGGAGGTTAGAAGAGCTGACCTCCAATGTCCCGTCTAATTCCAAGAT
TCTCCAATAATGACTTTGGAACAGCTGTGTACAGATTATACTTGGAATTATGCTTAGATACTAT
TGCTGCAGGAATGAATAGACAAATTTTGTTATTAAAAAATTGATTTTATTAAGTGGAAGTTGAC
AGAATTATCCTCTTTATAATGGAGGAACATTATGCTTATGCATATGCATATACCTTATGCATAT
GATTATGCTTGTGCTTCCTTCTTTAATGGATTTACCTATTCAAAAGCTTAATAAATGTTATAAG
ACTCTAAAACATTTAAATCTTTCATTTCTCAATTTTATCAAATAAACATTCCTGGAATTTGTGC
ATA

hide sequence

RefSeq Acc Id:

XM_011511650 ⟹ XP_011509952

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	201,806,537 - 201,882,691 (+)	NCBI

Sequence:

show sequence

CTCTGGCAAAAAGGGAGAGAACAAGGATAGGAGAGGCAGTGGGGGAAAGGTTCAAGTGCGGGTT
TTCTCCTTGAACCTACAAGATTATGGGTCAAGAGCTGTGTGCAAAGACTGTACAGCCTGGATGC
AGCTGCTACCATTGTTCAGAGGGAGGCGAGGCACACAGCTGTCGGAGGAGTCAGCCTGAGACCA
CGGAGGCTGCGTTCAAGCTAACAGACCTAAAAGAAGCATCATGTTCCATGACTTCATTTCACCC
CAGGGGACTTCAAGCTGCCCGTGCCCAGAAGTTCAAGAGTAAAAGGCCACGGAGTAACAGTGAT
TGTTTTCAGGAAGAGGATCTGAGGCAGGGTTTTCAGTGGAGGAAGAGCCTCCCTTTTGGGGCAG
CCTCATCTTACTTGAACTTGGAGAAGCTGGGTGAAGGCTCTTATGCGACAGTTTACAAGGGGAT
TAGCAGAATAAATGGACAACTAGTGGCTTTAAAAGTCATCAGCATGAATGCAGAGGAAGGAGTC
CCATTTACAGCTATCCGAGAAGCTTCTCTCCTGAAGGGTTTGAAACATGCCAATATTGTGCTCC
TGCATGACATAATCCACACCAAAGAGACACTGACATTCGTTTTTGAATACATGCACACAGACCT
GGCCCAGTATATGTCTCAGCATCCAGGAGGGCTTCATCCTCATAATGTCAGACTTTTCATGTTT
CAACTTTTGCGGGGCCTGGCGTACATCCACCACCAACACGTTCTTCACAGGGACCTGAAACCTC
AGAACTTACTCATCAGTCACCTGGGAGAGCTCAAACTGGCTGATTTTGGTCTTGCCCGGGCCAA
GTCCATTCCCAGCCAGACATACTCTTCAGAAGTCGTGACCCTCTGGTACCGGCCCCCTGATGCT
TTGCTGGGAGCCACTGAATATTCCTCTGAGCTGGACATATGGGGTGCAGGCTGCATCTTTATTG
AAATGTTCCAGGGTCAACCTTTGTTTCCTGGGGTTTCCAACATCCTTGAACAGCTGGAGAAAAT
CTGGGAGGTGCTGGGAGTCCCTACAGAGGATACTTGGCCGGGAGTCTCCAAGCTACCTAACTAC
AATCCAGAATGGTTCCCACTGCCTACGCCTCGAAGCCTTCATGTTGTCTGGAACAGGCTGGGCA
GGGTTCCTGAAGCTGAAGACCTGGCCTCCCAGATGCTAAAAGGCTTTCCCAGAGACCGCGTCTC
CGCCCAGGAAGCACTTGTTCATGATTATTTCAGCGCCCTGCCATCTCAGCTGTACCAGCTTCCT
GATGTCACAGAGCCCAAATCTACTTTGACACTTTTAGAAAAATGAAAAGATGGAATCTTGTAGG
AGGCTGCCTGCACTAGCGGGGGAAACCAGGAGTGCTCACAGCAGGAGGGAAGTTGACTTTTCTT
TATACATATAGGGGTTTTTCCATGCAGAGTTTAAATTATGCCTGATAAAAGGAGTTTCGTGGAT
GTTTCAGTTCTTTCAAATTCTCCTGGCTTCCTCCCAATTAAATGAGGTTTGTCAAAGCCACAGG
GCTCTGCTGCTGCTGCCTCGGCGGACAAGCATTTCCTGCAGCGACATCTCGAATCCCCGAGGGA
GAAGATGAAAGCGCCGGTGCCAAGAGACAGGGAAAGGCGGGGGCAAGATTGGGTGTGTGTGCTT
CTGTGTGTGTGTGCTCGTGCACATGAGTGCACGAGCATGTGTGTGTGCTTGTGTATGTGTGTGA
CAGGGTGGTGGGTGTGCAGAAATATGTATATAGACAGATGGACAAGTAGATAGAAAAAGCAAAG
CTACCAGGAAAGAAAAATAGAGGAAGAGACAGAAGCAGCCAGGGCTGGTTTGTGCACCTTCGTG
ACAGTGGCTCTCACCACCAGCACATTATCTACTAAGAGATGCGGTCCTTGGCCTGGCAGTGCCA
GCCTGCTTTTTCATTGCCCCTGGCAATGAGCCTTTATTAACAGCCTCCTTTGCAGACAGAGCAC
ACCAGTGGGTAATCACAGTTCCCAATCTGCAGGGACATAGAAACTCCATCCCTGAGGAGGGCTG
CCCCAGGCATGAGAATTGTGCAAAAATCGGCATGCTCTTGTGAGTGATTTGTAAGGAGAGTTTC
TCTGCCATAATTATGCAAGAAATTTTGCTCTCTGGTGGCATTTCAGTATAAAATTATTTAGGGG
CTTATATTTATATCATTTTATTATTCTGATTTTATTCTGGTTGCAGGATAACAGAGTTGTCACT
TTAAAATATATTCTGTTTCCCCTTTGATCTGGAAGATGCCAGCTCTTATTGTCTGCCCTCTAAA
GAAGACAATTAAAGCATAAAGCCTGGGACTGGGAAATACGTGGAGAGTGGAAGGACAGCCTAAA
TCCCAGTGTAGGAGCGGCATAGAAATTCCACACAAAATGAAAGAATTGTTCCAGTCCATCTCTA
TTTTCATGACGCTGAGAAGTCCCGAACAATGCTTTCCCTAGGTTGTGGCAGTACGCTTAGAGCC
AAAGGGCATTTATCAGGGGGTTATTTGCCATGAAAACCAGGAATTCCAGGATTAGTTTCCTTTT
GGACAGCACCTGAAGTGGAAAAGTGTGAATATTAGAATGGCAAGCATGTGGGAACTTCTGCCAA
GTTCTGACATTTTCCCTTATTGACTCGTGAACACCTGAAGAAACACTTGTTGAAGGAGAAATTA
TTGGTAGTCCCTCTCAAAACACAGCCAACAGCAAGCTAATTGCTTTTGCAGATGGCCAGGGAGT
CGCTCTTCCCACTCAGACACCGGCTTATGGCCACACTTGTGGTCCTCGTGGCTGAGCCAGCAGG
GCAGGACGTCAGCTGGAGCAGCTAGGACCTAAAATTAGGCCCTTGGCAACTCTCTAATCTTAGC
TGCAGGTTCAGCTTCTTCATTTAATTCTCTTTGCCCTCAGCATGAACTTGGGCTCTGGGAAAGG
AACACTGTTTAATGATTTGGGGGTGGGGGTAGTAGGAAATCATTAAGCTGCCCCTTCTTAAAAC
TGGCTCCGCTCTGTTCTTTCAGGAAACCTTCCAAATGTTACCCTTGGAAATTTAAGACTGATTT
TGGAACCTAGCCATTTTGAACTACAGACACTGATCCAGAAAAGTATTTTTTATCTGAGGCAGTA
AATGACACGTGATTTAAGAGTCTGGTCTTTAAGCCATGGTCCTTGATCGTCAGGACATCAAAGG
CTGTCTCTCTTTCTCTCTCTCTCTCTGGGTTGGTCCCATTTTGCTTGCTAGCCAAGTCTCATAC
TTGAGTCTCCCATTCCTTCCTGGACTAAATCCCCTTCTCCTTTAAAACAGGTTTTAGCATCTTA
GGGGGAGAAAATCTAAAAAGCTTGCAATTGTTTCACAAGTAATTTTGCAAAAATGCTGTACCAC
AGCCCCCATTGTTAGAGTATACTTATATACACATAGGGATGGAAGAAAGCATGGCATTTACCTC
TACCTTTGATCACACCATCCCGATATCTATACTCCGAAAGTTCTTCAGCATGCCTCATTGCCCT
GTTAAAATCTGAGTCGTGTTTTGTTTTGGTTCAATAAAATAACTTCAGGCCTTCTTTGAGTGTT
ATCTCCTTAATATATTGGAAGGTCCCTATGATATCACTTCCCAAAGGCCACTTTAGGCTGAATT
CCTTTAACCTTTGTTTCCAAATACAAATTCTGTTTCTCCCACTTTTTAGTCATTTTGTTTTATT
GTTCTCTTCTGAATCTGTTCCAATTATTTTGCTTATCTCTGAGAATATGGAGGCAGCATAGACT
CAAATTTCTTGCATGGTGGGAGAATCATGTTCCATTCATTCATTGGAGGTTTACTGAGTGTCCA
TGAGGTGTGATATTAAAGGATACAAAAATGAATTAGTCATAGACCCTGTCCTCAAAGAGCTTAC
GGTCCTTTAGGAAATAAGACAAGTATATAAACAGCTGCAGATCAAGTATACAAATAAAGTGCTC
TAAGTGTTTGAAGGAGGTGAGATTAACTCCAGCTGTGGGGATCCAGGATGATTTTGTGAGTGGG
CCTTGAAAGATGATGGGTCTGGATGATTGGAGAGGAAGGGCATACGGGCAAAGGAATGTCGTGT
TCCTCTCAATACCATCTAAGATCATTCTGAAGTTGTCTTCTTTTTAATCATAGTGGCTCAGTCT
TAACTCATATACCATTGTAGTTTTTCTTACCATCGTATGCCTTTTTGCAACAATTTAAACATTC
TTTAACATGTACTAATCAAGCTTAGTTTCACTCTGAATGCTTCCACGTAATTTCAAACCTATTC
TGTTTATTGGTTTTTTTGTGTATTCTATTCAAAGTTGAACCAGAATATTTTGTCATTCTATGAG
GCCAGGTTTCAGGGGCTGGGGATGTTGGAAAAGAGGGAGGGAAGATTCTCAGCCATCCTCTTGA
CTCTGTGCTACTTCTAGGAGTTTGTAACGTAACTCAGACCAATCTGTCCACCTTTTAAATCCTC
CATTAATCAGCCCTTAAGAAGCGAATTTGGAGATGTCCTCCATAACACACTTCCTCACCTTCTA
TGCACAAAGTTGTTCTCCATCCATTTCAATATGTTAGAGGAGATACTGGGTTGAGACGTGGTTT
ATGGGGTTGCATAGCATTGTGTTGCTGGGAGAAGTCTGGGAAAACCAAGTCCCTCAGCCCTACC
AAGCCCTTAAGTTGGTTAAATTTGTTACG

hide sequence

RefSeq Acc Id:

XM_011511652 ⟹ XP_011509954

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	201,806,537 - 201,895,550 (+)	NCBI

Sequence:

show sequence

CTCTGGCAAAAAGGGAGAGAACAAGGATAGGAGAGGCAGTGGGGGAAAGGTTCAAGTGCGGGTT
TTCTCCTTGAACCTACAAGATTATGGGTCAAGAGCTGTGTGCAAAGACTGTACAGCCTGGATGC
AGCTGCTACCATTGTTCAGAGGGAGGCGAGGCACACAGCTGTCGGAGGAGTCAGCCTGAGACCA
CGGAGGCTGCGTTCAAGCTAACAGACCTAAAAGAAGCATCATGTTCCATGACTTCATTTCACCC
CAGGGGACTTCAAGCTGCCCGTGCCCAGAAGTTCAAGAGTAAAAGGCCACGGAGTAACAGTGAT
TGTTTTCAGGAAGAGGATCTGAGGCAGGGTTTTCAGTGGAGGAAGAGCCTCCCTTTTGGGGCAG
CCTCATCTTACTTGAACTTGGAGAAGCTGGGTGAAGGCTCTTATGCGACAGTTTACAAGGGGAT
TAGCAGAATAAATGGACAACTAGTGGCTTTAAAAGTCATCAGCATGAATGCAGAGGAAGGAGTC
CCATTTACAGCTATCCGAGAAGCTTCTCTCCTGAAGGGTTTGAAACATGCCAATATTGTGCTCC
TGCATGACATAATCCACACCAAAGAGACACTGACATTCGTTTTTGAATACATGCACACAGACCT
GGCCCAGTATATGTCTCAGCATCCAGGAGGGCTTCATCCTCATAATGTCAGACTTTTCATGTTT
CAACTTTTGCGGGGCCTGGCGTACATCCACCACCAACACGTTCTTCACAGGGACCTGAAACCTC
AGAACTTACTCATCAGTCACCTGGGAGAGCTCAAACTGGCTGATTTTGGTCTTGCCCGGGCCAA
GTCCATTCCCAGCCAGACATACTCTTCAGAAGTCGTGACCCTCTGGTACCGGCCCCCTGATGCT
TTGCTGGGAGCCACTGAATATTCCTCTGAGCTGGACATATGGGGTGCAGGCTGCATCTTTATTG
AAATGTTCCAGGGTCAACCTTTGTTTCCTGGGGTTTCCAACATCCTTGAACAGCTGGAGAAAAT
CTGGGAGGTGCTGGGAGTCCCTACAGAGGATACTTGGCCGGGAGTCTCCAAGCTACCTAACTAC
AATCCAGAGGAGTCTTTGTTTACAGTTTCAGGAGTGAGGCTAAAGCCAGAAATGTGTGACCTTT
TGGCCTCCTACCAGAAAGGTCACCACCCAGCCCAGTTTAGCAAATGCTGGTGAAAAGAAAGGGC
GAGATCACCAAGGTTCTTCCAGGGCTGTATTTCTGCAGTTTCGGTTTTCATTTGCTTCAGCTTA
CTAAGAAGCTTCAAATCTAACTCCATACTGAACAAGGGGCTTTATGTCCTCACCTATGACCTGG
AATAGTTTAAATATGGTGTTCAAGGCAATAGTACATAATAGTGGAAGAAAATTCAGTGGAAGGT
TATTGCTATTGTCATTTGCATAGAATTTAAGTGATTGATTTAAAAAAACTGGACATAAACTAAG
TCTAAGAAGAGGGCTTCTGAATAACTTCATTCATTTTGGCATTTGTTAAGAGATTCCTGGGCTA
GAAGGTTGATTTCCCAAAAAGACAGATAAGAGACTGACAATTTAAAAGAATCTGGAGACAGAGC
TGGTGCTTACAGAGACCTGCCACTCCTGTGTTCACTTACAATTTCTCCCAACAAAAGGATTTCT
GTGGCAAGGAGAAAACTAGCCTAAAGTTTAGAAAAAGATGGTTTCTTGGATAACATTGTTAACA
AAAGGACTTCCTGAGGACTATTTATTATTATTTTGTAGGGGGCACTTCCTCCTTCACTAAACTG
GATTATCAGAACGTATTACCACCCAACCCATATTTTAGAAGTTTGGATTTGGCTGCTGATTAGA
AATGAATTTCAGGCTATCTCCTCCTACTGAATCTTAATTGTCTGTGATGATGGCAACAGTGATG
GGGAATCTAAGCGCTGGTTTGATGGTGGAGATATTGAATAAGTAGTTGGGAGCAGAGTTCCAAA
GATGTAATTTAAGCCCTGTTGCACCACCACACACACACACACACACACACACACACACACACAC
ACACCCCTCAAGTAAAATGAGAGATCTGTCTTAGCTAACACGTGTGCCGTTTTATACAATGACT
CCTTCTAAAAGCAGCCAGGGAAACTCAAATCGCTTCTGTCCAGGGATCATCTCAGGAAATGTAG
CAGCCTAGAAACCAGAGACCTCTGTATATCCTTTGGAAGAGCAAGGAGGAACTAATTAAGAGAT
AATTAAAAAATAGTAACTATCCCCCAATGTCTGAGATGGAAAAAGGAAAAAGACACATGGGTAG
CCCAAATCAACCTGCCTGAGTAAGTATCTGATTTTAGTAAGGCATTTGACAAAGACTGTCCAGC
TATACCTGAAAGATGAAACAGTGTAGGCTGGGTGATGGAGCAGATATATGTACTCAAATCATGG
TGTTTATTTAACCCAGAGAAAGGCCAGCCGTGGTGTGCTACAAGGTTCAGTCTTGAGTCCTATT
CTGGTCAAATATTTTTATTAATTACTCGAATAAATCAGAGTACATGGACAACTTTATACAACTC
CTTGAAGTAAGTACTATTATTATTAATTTATGACTTCCATTTCACAAAAGAGGAGACTGAGGCT
CAGTGAAGTTAGGTAACTCCTTCATAGTAGCATGCCAGAGTGAAGATGCAAACCTCAGACCTGG
TTCTCCAATGTTCCTGACACCTATCGAATTTAGAGAATACACAACTCTTGCAGAGGCAGCTGCT
ATTTAGTATTGGATCATGATTCAAAAGACACCTTGCTAGAAGCCAATGAACAGCAGGCCAAAAC
AACACTTACTTGCATCAAATTTCATCTGACTTAAATTCTTACACTTTGGGCTACAACTTAAAAA
AGGCTATGACTTAGTGGAAATTGGCACTTTTAAGTACAATATGAATTAATAGTATAATTTCGCT
GTCCCCCAGAGATAATGCTAGTACCAATCGAAAGCTCAGGGATGCTACTGTTGACGCATCAGCA
AGAGTTCTTGAGCAGTTTTACCTGTCCATCAATACAAAGAGTTCCCACAACAGTAGTGGGATTC
CTCTGCCTCTCTGAAGATATGAGAGCTATAGGAGGGATTCCCATGTTGGAGGTTAGAAGAGCTG
ACCTCCAATGTCCCGTCTAATTCCAAGATTCTCCAATAATGACTTTGGAACAGCTGTGTACAGA
TTATACTTGGAATTATGCTTAGATACTATTGCTGCAGGAATGAATAGACAAATTTTGTTATTAA
AAAATTGATTTTATTAAGTGGAAGTTGACAGAATTATCCTCTTTATAATGGAGGAACATTATGC
TTATGCATATGCATATACCTTATGCATATGATTATGCTTGTGCTTCCTTCTTTAATGGATTTAC
CTATTCAAAAGCTTAATAAATGTTATAAGACTCTAAAACATTTAAATCTTTCATTTCTCAATTT
TATCAAATAAACATTCCTGGAATTTGTG

hide sequence

RefSeq Acc Id:

XM_011511654 ⟹ XP_011509956

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	201,806,537 - 201,856,926 (+)	NCBI

Sequence:

show sequence

CTCTGGCAAAAAGGGAGAGAACAAGGATAGGAGAGGCAGTGGGGGAAAGGTTCAAGTGCGGGTT
TTCTCCTTGAACCTACAAGATTATGGGTCAAGAGCTGTGTGCAAAGACTGTACAGCCTGGATGC
AGCTGCTACCATTGTTCAGAGGGAGGCGAGGCACACAGCTGTCGGAGGAGTCAGCCTGAGACCA
CGGAGGCTGCGTTCAAGCTAACAGACCTAAAAGAAGCATCATGTTCCATGACTTCATTTCACCC
CAGGGGACTTCAAGCTGCCCGTGCCCAGAAGTTCAAGAGTAAAAGGCCACGGAGTAACAGTGAT
TGTTTTCAGGAAGAGGATCTGAGGCAGGGTTTTCAGTGGAGGAAGAGCCTCCCTTTTGGGGCAG
CCTCATCTTACTTGAACTTGGAGAAGCTGGGTGAAGGCTCTTATGCGACAGTTTACAAGGGGAT
TAGCAGAATAAATGGACAACTAGTGGCTTTAAAAGTCATCAGCATGAATGCAGAGGAAGGAGTC
CCATTTACAGCTATCCGAGAAGCTTCTCTCCTGAAGGGTTTGAAACATGCCAATATTGTGCTCC
TGCATGACATAATCCACACCAAAGAGACACTGACATTCGTTTTTGAATACATGCACACAGACCT
GGCCCAGTATATGTCTCAGCATCCAGGAGGGCTTCATCCTCATAATGTCAGACTTTTCATGTTT
CAACTTTTGCGGGGCCTGGCGTACATCCACCACCAACACGTTCTTCACAGGGACCTGAAACCTC
AGAACTTACTCATCAGTCACCTGGGAGAGCTCAAACTGGCTGATTTTGGTCTTGCCCGGGCCAA
GTCCATTCCCAGCCAGACATACTCTTCAGAAGTCGTGACCCTCTGGTACCGGCCCCCTGATGCT
TTGCTGGGAGCCACTGAATATTCCTCTGAGCTGGACATATGGGGTGCAGGCTGCATCTTTATTG
AAATGTTCCAGGGTCAACCTTTGTTTCCTGGGGTTTCCAACATCCTTGAACAGCTGGAGAAAAT
CTGGGAGGTGCTGGGAGTCCCTACAGAGGATACTTGGCCGGGAGTCTCCAAGCTACCTAACTAC
AATCCAGCTATCCATAGGGATCTGGCATCTTGAACCACCAGGATTATGGAAGCCCTACAGCAAG
CTAAAGACTAACTGTAAAGTCCTTTCAGCTGCTTTGTGAATGGTTATATCTATTGCTAAAAGGC
CTTAATATCATTTGCAAATAGTTTATGATTTCTAACTATTTTTCTAGAGTTTAACACGTGAGAA
AAATGCTACTCTCTGGTCACAGGACTTAGAATAGTGCCTATTTCCATTGGTCTGAGATAGAGAA
AAAAGAACAAGTTTCTTGTGGAGCCGTGGTCCAGTCTGCAAATTGCTCCTATCTCCAGTTGCCA
TGGTTTCCAGGAGAACGTGGCTCTCATCTTTTCCTGCCCTGCCTGTACTTCTCCCTGTCCACTC
TGTTCTCTATTTTCCCTCAGCTTCCTAACTGAGAATGCCAGCAGAAGTTTAGAGTCACAGATGG
ATTGTAGGAAACAATTTGGATGATGCCAATACAAAGCTACTGTGGTGGGCATATGCTGCTCCCC
CAAACTTCAGACATTTGGGTTTCAGGTTGGTCCAGGCAATCAACAGTGATCCTTAATACAAAAT
GTCTTGGTGAGAGCAATAATCAAGAAACTTGGCCAAAGTGCTTCCCTGCCAGATTGTGTGCTTA
ATAAG

hide sequence

RefSeq Acc Id:

XM_011511655 ⟹ XP_011509957

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	201,822,431 - 201,895,550 (+)	NCBI

Sequence:

show sequence

TTTCCTGAAGCCAGAGGTCTTCCTATCTCCAGAAGCTCCAAAGACACACTTTCAAACCCCTCCC
AGTCACTTGGCCTTTTGTGATGACTTCTTTCCTTCAAGGCTGCCTTTAGTAACCGATTATTGAA
GAGGCAAGAGAAAGCCCTCAGCCTTCTCCACTTTCACCTCCCTGGGCTCCCCAAGTTTGGCCGA
CTCCTCTTTTCAAGTTCACATTTTCTCCTTTCCACAGAGGTTTGCAACATTACCTTTAAGAAAT
CATCTCCAGTCTCTATCATGTTTCAACAGTTCTTTACCCCATGCTTTTATCCCTGTCTCCCACC
AATCATATCCACCGGCCCTATTGACCGCTTGTGGGAGTTAGAATTTTGGAGACTGGTCATATGT
CACAAAGTCCTGCTCTAGAAGGCAGAACACTCCATTTCCTGCTCCTCCAAAGCCCTTTATCTCT
CCAGGCCTCTCCTCCTGTAGCTCTGAAGCTGGATTGATGAGATTCCCAGAGGGGAGCATTTAGT
GCTCTGAGTGCTTTGATGAAATTGATTAGCTTCTCTCCTGAAGGGTTTGAAACATGCCAATATT
GTGCTCCTGCATGACATAATCCACACCAAAGAGACACTGACATTCGTTTTTGAATACATGCACA
CAGACCTGGCCCAGTATATGTCTCAGCATCCAGGAGGGCTTCATCCTCATAATGTCAGACTTTT
CATGTTTCAACTTTTGCGGGGCCTGGCGTACATCCACCACCAACACGTTCTTCACAGGGACCTG
AAACCTCAGAACTTACTCATCAGTCACCTGGGAGAGCTCAAACTGGCTGATTTTGGTCTTGCCC
GGGCCAAGTCCATTCCCAGCCAGACATACTCTTCAGAAGTCGTGACCCTCTGGTACCGGCCCCC
TGATGCTTTGCTGGGAGCCACTGAATATTCCTCTGAGCTGGACATATGGGGTGCAGGCTGCATC
TTTATTGAAATGTTCCAGGGTCAACCTTTGTTTCCTGGGGTTTCCAACATCCTTGAACAGCTGG
AGAAAATCTGGGAGGTGCTGGGAGTCCCTACAGAGGATACTTGGCCGGGAGTCTCCAAGCTACC
TAACTACAATCCAGAATGGTTCCCACTGCCTACGCCTCGAAGCCTTCATGTTGTCTGGAACAGG
CTGGGCAGGGTTCCTGAAGCTGAAGACCTGGCCTCCCAGATGCTAAAAGGCTTTCCCAGAGACC
GCGTCTCCGCCCAGGAAGCACTTGTTCATGATTATTTCAGCGCCCTGCCATCTCAGCTGTACCA
GCTTCCTGATGAGGAGTCTTTGTTTACAGTTTCAGGAGTGAGGCTAAAGCCAGAAATGTGTGAC
CTTTTGGCCTCCTACCAGAAAGGTCACCACCCAGCCCAGTTTAGCAAATGCTGGTGAAAAGAAA
GGGCGAGATCACCAAGGTTCTTCCAGGGCTGTATTTCTGCAGTTTCGGTTTTCATTTGCTTCAG
CTTACTAAGAAGCTTCAAATCTAACTCCATACTGAACAAGGGGCTTTATGTCCTCACCTATGAC
CTGGAATAGTTTAAATATGGTGTTCAAGGCAATAGTACATAATAGTGGAAGAAAATTCAGTGGA
AGGTTATTGCTATTGTCATTTGCATAGAATTTAAGTGATTGATTTAAAAAAACTGGACATAAAC
TAAGTCTAAGAAGAGGGCTTCTGAATAACTTCATTCATTTTGGCATTTGTTAAGAGATTCCTGG
GCTAGAAGGTTGATTTCCCAAAAAGACAGATAAGAGACTGACAATTTAAAAGAATCTGGAGACA
GAGCTGGTGCTTACAGAGACCTGCCACTCCTGTGTTCACTTACAATTTCTCCCAACAAAAGGAT
TTCTGTGGCAAGGAGAAAACTAGCCTAAAGTTTAGAAAAAGATGGTTTCTTGGATAACATTGTT
AACAAAAGGACTTCCTGAGGACTATTTATTATTATTTTGTAGGGGGCACTTCCTCCTTCACTAA
ACTGGATTATCAGAACGTATTACCACCCAACCCATATTTTAGAAGTTTGGATTTGGCTGCTGAT
TAGAAATGAATTTCAGGCTATCTCCTCCTACTGAATCTTAATTGTCTGTGATGATGGCAACAGT
GATGGGGAATCTAAGCGCTGGTTTGATGGTGGAGATATTGAATAAGTAGTTGGGAGCAGAGTTC
CAAAGATGTAATTTAAGCCCTGTTGCACCACCACACACACACACACACACACACACACACACAC
ACACACACCCCTCAAGTAAAATGAGAGATCTGTCTTAGCTAACACGTGTGCCGTTTTATACAAT
GACTCCTTCTAAAAGCAGCCAGGGAAACTCAAATCGCTTCTGTCCAGGGATCATCTCAGGAAAT
GTAGCAGCCTAGAAACCAGAGACCTCTGTATATCCTTTGGAAGAGCAAGGAGGAACTAATTAAG
AGATAATTAAAAAATAGTAACTATCCCCCAATGTCTGAGATGGAAAAAGGAAAAAGACACATGG
GTAGCCCAAATCAACCTGCCTGAGTAAGTATCTGATTTTAGTAAGGCATTTGACAAAGACTGTC
CAGCTATACCTGAAAGATGAAACAGTGTAGGCTGGGTGATGGAGCAGATATATGTACTCAAATC
ATGGTGTTTATTTAACCCAGAGAAAGGCCAGCCGTGGTGTGCTACAAGGTTCAGTCTTGAGTCC
TATTCTGGTCAAATATTTTTATTAATTACTCGAATAAATCAGAGTACATGGACAACTTTATACA
ACTCCTTGAAGTAAGTACTATTATTATTAATTTATGACTTCCATTTCACAAAAGAGGAGACTGA
GGCTCAGTGAAGTTAGGTAACTCCTTCATAGTAGCATGCCAGAGTGAAGATGCAAACCTCAGAC
CTGGTTCTCCAATGTTCCTGACACCTATCGAATTTAGAGAATACACAACTCTTGCAGAGGCAGC
TGCTATTTAGTATTGGATCATGATTCAAAAGACACCTTGCTAGAAGCCAATGAACAGCAGGCCA
AAACAACACTTACTTGCATCAAATTTCATCTGACTTAAATTCTTACACTTTGGGCTACAACTTA
AAAAAGGCTATGACTTAGTGGAAATTGGCACTTTTAAGTACAATATGAATTAATAGTATAATTT
CGCTGTCCCCCAGAGATAATGCTAGTACCAATCGAAAGCTCAGGGATGCTACTGTTGACGCATC
AGCAAGAGTTCTTGAGCAGTTTTACCTGTCCATCAATACAAAGAGTTCCCACAACAGTAGTGGG
ATTCCTCTGCCTCTCTGAAGATATGAGAGCTATAGGAGGGATTCCCATGTTGGAGGTTAGAAGA
GCTGACCTCCAATGTCCCGTCTAATTCCAAGATTCTCCAATAATGACTTTGGAACAGCTGTGTA
CAGATTATACTTGGAATTATGCTTAGATACTATTGCTGCAGGAATGAATAGACAAATTTTGTTA
TTAAAAAATTGATTTTATTAAGTGGAAGTTGACAGAATTATCCTCTTTATAATGGAGGAACATT
ATGCTTATGCATATGCATATACCTTATGCATATGATTATGCTTGTGCTTCCTTCTTTAATGGAT
TTACCTATTCAAAAGCTTAATAAATGTTATAAGACTCTAAAACATTTAAATCTTTCATTTCTCA
ATTTTATCAAATAAACATTCCTGGAATTTGTG

hide sequence

RefSeq Acc Id:

XM_011511656 ⟹ XP_011509958

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	201,821,366 - 201,895,550 (+)	NCBI

Sequence:

show sequence

CCATTCTTGGGTAGAGGCCGGGTCAGTTCCACCAGATGAGCATGGTCTGAGGAAGAAGACGGTT
GTTTTTCCAGGGGAAAATAGAAGTGCCCCCGCTAGAAGGGAGAATGGCTGTCAGGAGGGCAAAA
CGACAGATTCACTAAAATAGCTTCTCTCCTGAAGGGTTTGAAACATGCCAATATTGTGCTCCTG
CATGACATAATCCACACCAAAGAGACACTGACATTCGTTTTTGAATACATGCACACAGACCTGG
CCCAGTATATGTCTCAGCATCCAGGAGGGCTTCATCCTCATAATGTCAGACTTTTCATGTTTCA
ACTTTTGCGGGGCCTGGCGTACATCCACCACCAACACGTTCTTCACAGGGACCTGAAACCTCAG
AACTTACTCATCAGTCACCTGGGAGAGCTCAAACTGGCTGATTTTGGTCTTGCCCGGGCCAAGT
CCATTCCCAGCCAGACATACTCTTCAGAAGTCGTGACCCTCTGGTACCGGCCCCCTGATGCTTT
GCTGGGAGCCACTGAATATTCCTCTGAGCTGGACATATGGGGTGCAGGCTGCATCTTTATTGAA
ATGTTCCAGGGTCAACCTTTGTTTCCTGGGGTTTCCAACATCCTTGAACAGCTGGAGAAAATCT
GGGAGGTGCTGGGAGTCCCTACAGAGGATACTTGGCCGGGAGTCTCCAAGCTACCTAACTACAA
TCCAGAATGGTTCCCACTGCCTACGCCTCGAAGCCTTCATGTTGTCTGGAACAGGCTGGGCAGG
GTTCCTGAAGCTGAAGACCTGGCCTCCCAGATGCTAAAAGGCTTTCCCAGAGACCGCGTCTCCG
CCCAGGAAGCACTTGTTCATGATTATTTCAGCGCCCTGCCATCTCAGCTGTACCAGCTTCCTGA
TGAGGAGTCTTTGTTTACAGTTTCAGGAGTGAGGCTAAAGCCAGAAATGTGTGACCTTTTGGCC
TCCTACCAGAAAGGTCACCACCCAGCCCAGTTTAGCAAATGCTGGTGAAAAGAAAGGGCGAGAT
CACCAAGGTTCTTCCAGGGCTGTATTTCTGCAGTTTCGGTTTTCATTTGCTTCAGCTTACTAAG
AAGCTTCAAATCTAACTCCATACTGAACAAGGGGCTTTATGTCCTCACCTATGACCTGGAATAG
TTTAAATATGGTGTTCAAGGCAATAGTACATAATAGTGGAAGAAAATTCAGTGGAAGGTTATTG
CTATTGTCATTTGCATAGAATTTAAGTGATTGATTTAAAAAAACTGGACATAAACTAAGTCTAA
GAAGAGGGCTTCTGAATAACTTCATTCATTTTGGCATTTGTTAAGAGATTCCTGGGCTAGAAGG
TTGATTTCCCAAAAAGACAGATAAGAGACTGACAATTTAAAAGAATCTGGAGACAGAGCTGGTG
CTTACAGAGACCTGCCACTCCTGTGTTCACTTACAATTTCTCCCAACAAAAGGATTTCTGTGGC
AAGGAGAAAACTAGCCTAAAGTTTAGAAAAAGATGGTTTCTTGGATAACATTGTTAACAAAAGG
ACTTCCTGAGGACTATTTATTATTATTTTGTAGGGGGCACTTCCTCCTTCACTAAACTGGATTA
TCAGAACGTATTACCACCCAACCCATATTTTAGAAGTTTGGATTTGGCTGCTGATTAGAAATGA
ATTTCAGGCTATCTCCTCCTACTGAATCTTAATTGTCTGTGATGATGGCAACAGTGATGGGGAA
TCTAAGCGCTGGTTTGATGGTGGAGATATTGAATAAGTAGTTGGGAGCAGAGTTCCAAAGATGT
AATTTAAGCCCTGTTGCACCACCACACACACACACACACACACACACACACACACACACACACC
CCTCAAGTAAAATGAGAGATCTGTCTTAGCTAACACGTGTGCCGTTTTATACAATGACTCCTTC
TAAAAGCAGCCAGGGAAACTCAAATCGCTTCTGTCCAGGGATCATCTCAGGAAATGTAGCAGCC
TAGAAACCAGAGACCTCTGTATATCCTTTGGAAGAGCAAGGAGGAACTAATTAAGAGATAATTA
AAAAATAGTAACTATCCCCCAATGTCTGAGATGGAAAAAGGAAAAAGACACATGGGTAGCCCAA
ATCAACCTGCCTGAGTAAGTATCTGATTTTAGTAAGGCATTTGACAAAGACTGTCCAGCTATAC
CTGAAAGATGAAACAGTGTAGGCTGGGTGATGGAGCAGATATATGTACTCAAATCATGGTGTTT
ATTTAACCCAGAGAAAGGCCAGCCGTGGTGTGCTACAAGGTTCAGTCTTGAGTCCTATTCTGGT
CAAATATTTTTATTAATTACTCGAATAAATCAGAGTACATGGACAACTTTATACAACTCCTTGA
AGTAAGTACTATTATTATTAATTTATGACTTCCATTTCACAAAAGAGGAGACTGAGGCTCAGTG
AAGTTAGGTAACTCCTTCATAGTAGCATGCCAGAGTGAAGATGCAAACCTCAGACCTGGTTCTC
CAATGTTCCTGACACCTATCGAATTTAGAGAATACACAACTCTTGCAGAGGCAGCTGCTATTTA
GTATTGGATCATGATTCAAAAGACACCTTGCTAGAAGCCAATGAACAGCAGGCCAAAACAACAC
TTACTTGCATCAAATTTCATCTGACTTAAATTCTTACACTTTGGGCTACAACTTAAAAAAGGCT
ATGACTTAGTGGAAATTGGCACTTTTAAGTACAATATGAATTAATAGTATAATTTCGCTGTCCC
CCAGAGATAATGCTAGTACCAATCGAAAGCTCAGGGATGCTACTGTTGACGCATCAGCAAGAGT
TCTTGAGCAGTTTTACCTGTCCATCAATACAAAGAGTTCCCACAACAGTAGTGGGATTCCTCTG
CCTCTCTGAAGATATGAGAGCTATAGGAGGGATTCCCATGTTGGAGGTTAGAAGAGCTGACCTC
CAATGTCCCGTCTAATTCCAAGATTCTCCAATAATGACTTTGGAACAGCTGTGTACAGATTATA
CTTGGAATTATGCTTAGATACTATTGCTGCAGGAATGAATAGACAAATTTTGTTATTAAAAAAT
TGATTTTATTAAGTGGAAGTTGACAGAATTATCCTCTTTATAATGGAGGAACATTATGCTTATG
CATATGCATATACCTTATGCATATGATTATGCTTGTGCTTCCTTCTTTAATGGATTTACCTATT
CAAAAGCTTAATAAATGTTATAAGACTCTAAAACATTTAAATCTTTCATTTCTCAATTTTATCA
AATAAACATTCCTGGAATTTGTG

hide sequence

RefSeq Acc Id:

XM_011511657 ⟹ XP_011509959

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	201,828,312 - 201,895,550 (+)	NCBI

Sequence:

show sequence

AGTTTAGAAGACAAGGAGTAGGCAACCAAAAGAGCAAATACACAAAGAGAGGAGGACTGATGAT
GAGACTTTTGCCTTTTAGGATGAGAAGAGGAACAGGAAATGAAGGAATGAAGGGAAGCAGCTTG
TAGGAATGTAGAGCATCTGAAAAAAAAATACACACTGTCATGGAAGTCAAGGGAAGAAGAATTT
CAAGAAGGAGGCTTTTCATGTTTCAACTTTTGCGGGGCCTGGCGTACATCCACCACCAACACGT
TCTTCACAGGGACCTGAAACCTCAGAACTTACTCATCAGTCACCTGGGAGAGCTCAAACTGGCT
GATTTTGGTCTTGCCCGGGCCAAGTCCATTCCCAGCCAGACATACTCTTCAGAAGTCGTGACCC
TCTGGTACCGGCCCCCTGATGCTTTGCTGGGAGCCACTGAATATTCCTCTGAGCTGGACATATG
GGGTGCAGGCTGCATCTTTATTGAAATGTTCCAGGGTCAACCTTTGTTTCCTGGGGTTTCCAAC
ATCCTTGAACAGCTGGAGAAAATCTGGGAGGTGCTGGGAGTCCCTACAGAGGATACTTGGCCGG
GAGTCTCCAAGCTACCTAACTACAATCCAGAATGGTTCCCACTGCCTACGCCTCGAAGCCTTCA
TGTTGTCTGGAACAGGCTGGGCAGGGTTCCTGAAGCTGAAGACCTGGCCTCCCAGATGCTAAAA
GGCTTTCCCAGAGACCGCGTCTCCGCCCAGGAAGCACTTGTTCATGATTATTTCAGCGCCCTGC
CATCTCAGCTGTACCAGCTTCCTGATGAGGAGTCTTTGTTTACAGTTTCAGGAGTGAGGCTAAA
GCCAGAAATGTGTGACCTTTTGGCCTCCTACCAGAAAGGTCACCACCCAGCCCAGTTTAGCAAA
TGCTGGTGAAAAGAAAGGGCGAGATCACCAAGGTTCTTCCAGGGCTGTATTTCTGCAGTTTCGG
TTTTCATTTGCTTCAGCTTACTAAGAAGCTTCAAATCTAACTCCATACTGAACAAGGGGCTTTA
TGTCCTCACCTATGACCTGGAATAGTTTAAATATGGTGTTCAAGGCAATAGTACATAATAGTGG
AAGAAAATTCAGTGGAAGGTTATTGCTATTGTCATTTGCATAGAATTTAAGTGATTGATTTAAA
AAAACTGGACATAAACTAAGTCTAAGAAGAGGGCTTCTGAATAACTTCATTCATTTTGGCATTT
GTTAAGAGATTCCTGGGCTAGAAGGTTGATTTCCCAAAAAGACAGATAAGAGACTGACAATTTA
AAAGAATCTGGAGACAGAGCTGGTGCTTACAGAGACCTGCCACTCCTGTGTTCACTTACAATTT
CTCCCAACAAAAGGATTTCTGTGGCAAGGAGAAAACTAGCCTAAAGTTTAGAAAAAGATGGTTT
CTTGGATAACATTGTTAACAAAAGGACTTCCTGAGGACTATTTATTATTATTTTGTAGGGGGCA
CTTCCTCCTTCACTAAACTGGATTATCAGAACGTATTACCACCCAACCCATATTTTAGAAGTTT
GGATTTGGCTGCTGATTAGAAATGAATTTCAGGCTATCTCCTCCTACTGAATCTTAATTGTCTG
TGATGATGGCAACAGTGATGGGGAATCTAAGCGCTGGTTTGATGGTGGAGATATTGAATAAGTA
GTTGGGAGCAGAGTTCCAAAGATGTAATTTAAGCCCTGTTGCACCACCACACACACACACACAC
ACACACACACACACACACACACACCCCTCAAGTAAAATGAGAGATCTGTCTTAGCTAACACGTG
TGCCGTTTTATACAATGACTCCTTCTAAAAGCAGCCAGGGAAACTCAAATCGCTTCTGTCCAGG
GATCATCTCAGGAAATGTAGCAGCCTAGAAACCAGAGACCTCTGTATATCCTTTGGAAGAGCAA
GGAGGAACTAATTAAGAGATAATTAAAAAATAGTAACTATCCCCCAATGTCTGAGATGGAAAAA
GGAAAAAGACACATGGGTAGCCCAAATCAACCTGCCTGAGTAAGTATCTGATTTTAGTAAGGCA
TTTGACAAAGACTGTCCAGCTATACCTGAAAGATGAAACAGTGTAGGCTGGGTGATGGAGCAGA
TATATGTACTCAAATCATGGTGTTTATTTAACCCAGAGAAAGGCCAGCCGTGGTGTGCTACAAG
GTTCAGTCTTGAGTCCTATTCTGGTCAAATATTTTTATTAATTACTCGAATAAATCAGAGTACA
TGGACAACTTTATACAACTCCTTGAAGTAAGTACTATTATTATTAATTTATGACTTCCATTTCA
CAAAAGAGGAGACTGAGGCTCAGTGAAGTTAGGTAACTCCTTCATAGTAGCATGCCAGAGTGAA
GATGCAAACCTCAGACCTGGTTCTCCAATGTTCCTGACACCTATCGAATTTAGAGAATACACAA
CTCTTGCAGAGGCAGCTGCTATTTAGTATTGGATCATGATTCAAAAGACACCTTGCTAGAAGCC
AATGAACAGCAGGCCAAAACAACACTTACTTGCATCAAATTTCATCTGACTTAAATTCTTACAC
TTTGGGCTACAACTTAAAAAAGGCTATGACTTAGTGGAAATTGGCACTTTTAAGTACAATATGA
ATTAATAGTATAATTTCGCTGTCCCCCAGAGATAATGCTAGTACCAATCGAAAGCTCAGGGATG
CTACTGTTGACGCATCAGCAAGAGTTCTTGAGCAGTTTTACCTGTCCATCAATACAAAGAGTTC
CCACAACAGTAGTGGGATTCCTCTGCCTCTCTGAAGATATGAGAGCTATAGGAGGGATTCCCAT
GTTGGAGGTTAGAAGAGCTGACCTCCAATGTCCCGTCTAATTCCAAGATTCTCCAATAATGACT
TTGGAACAGCTGTGTACAGATTATACTTGGAATTATGCTTAGATACTATTGCTGCAGGAATGAA
TAGACAAATTTTGTTATTAAAAAATTGATTTTATTAAGTGGAAGTTGACAGAATTATCCTCTTT
ATAATGGAGGAACATTATGCTTATGCATATGCATATACCTTATGCATATGATTATGCTTGTGCT
TCCTTCTTTAATGGATTTACCTATTCAAAAGCTTAATAAATGTTATAAGACTCTAAAACATTTA
AATCTTTCATTTCTCAATTTTATCAAATAAACATTCCTGGAATTTGTG

hide sequence

RefSeq Acc Id:

XM_047445552 ⟹ XP_047301508

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	201,806,537 - 201,880,167 (+)	NCBI

RefSeq Acc Id:

XM_047445553 ⟹ XP_047301509

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	201,807,551 - 201,895,550 (+)	NCBI

RefSeq Acc Id:

XM_054343445 ⟹ XP_054199420

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	202,287,441 - 202,363,582 (+)	NCBI

RefSeq Acc Id:

XM_054343446 ⟹ XP_054199421

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	202,287,441 - 202,376,437 (+)	NCBI

RefSeq Acc Id:

XM_054343447 ⟹ XP_054199422

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	202,287,441 - 202,361,059 (+)	NCBI

RefSeq Acc Id:

XM_054343448 ⟹ XP_054199423

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	202,287,441 - 202,337,808 (+)	NCBI

RefSeq Acc Id:

XM_054343449 ⟹ XP_054199424

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	202,288,455 - 202,376,437 (+)	NCBI

RefSeq Acc Id:

XM_054343450 ⟹ XP_054199425

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	202,303,327 - 202,376,437 (+)	NCBI

RefSeq Acc Id:

XM_054343451 ⟹ XP_054199426

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	202,302,262 - 202,376,437 (+)	NCBI

RefSeq Acc Id:

XM_054343452 ⟹ XP_054199427

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	202,309,209 - 202,376,437 (+)	NCBI

RefSeq Acc Id:

XR_008486494

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	202,287,441 - 202,328,340 (+)	NCBI

RefSeq Acc Id:

XR_922991

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	201,806,537 - 201,847,457 (+)	NCBI

Sequence:

show sequence

CTCTGGCAAAAAGGGAGAGAACAAGGATAGGAGAGGCAGTGGGGGAAAGGTTCAAGTGCGGGTT
TTCTCCTTGAACCTACAAGATTATGGGTCAAGAGCTGTGTGCAAAGACTGTACAGCCTGGATGC
AGCTGCTACCATTGTTCAGAGGGAGGCGAGGCACACAGCTGTCGGAGGAGTCAGCCTGAGACCA
CGGAGGCTGCGTTCAAGCTAACAGACCTAAAAGAAGCATCATGTTCCATGACTTCATTTCACCC
CAGGGGACTTCAAGCTGCCCGTGCCCAGAAGTTCAAGAGTAAAAGGCCACGGAGTAACAGTGAT
TGTTTTCAGGAAGAGGATCTGAGGCAGGGTTTTCAGTGGAGGAAGAGCCTCCCTTTTGGGGCAG
CCTCATCTTACTTGAACTTGGAGAAGCTGGGTGAAGGCTCTTATGCGACAGTTTACAAGGGGAT
TAGCAGAATAAATGGACAACTAGTGGCTTTAAAAGTCATCAGCATGAATGCAGAGGAAGGAGTC
CCATTTACAGCTATCCGAGAAGCTTCTCTCCTGAAGGGTTTGAAACATGCCAATATTGTGCTCC
TGCATGACATAATCCACACCAAAGAGACACTGACATTCGTTTTTGAATACATGCACACAGACCT
GGCCCAGTATATGTCTCAGCATCCAGGAGGGCTTCATCCTCATAATGTCAGACTTTTCATGTTT
CAACTTTTGCGGGGCCTGGCGTACATCCACCACCAACACGTTCTTCACAGGGACCTGAAACCTC
AGAACTTACTCATCAGTCACCTGGGAGAGCTCAAACTGGCTGATTTTGGTCTTGCCCGGGCCAA
GTCCATTCCCAGCCAGACATACTCTTCAGAAGTCGTGACCCTCTGGTACCGGCCCCCTGATGCT
TTGCTGGGAGCCACTGAATATTCCTCTGAGCTGGACATATGAGTGATAAGAGGGGAAGTGAGAA
GGGAGAAGATTTCCAGTTGACAAAGAATGAAAAAGAAAGAATAATCCTATTCTGCTAGGCCATG
CAACCCCATAGGGTCCAAAGTGAATGCCCTTGTAGGAGGTAGATGACACTGGGGGTGCAGGCTG
CATCTTTATTGAAATGTTCCAGGGTCAACCTTTGTTTCCTGGGGTTTCCAACATCCTTGAACAG
C

hide sequence

Protein Sequences


Protein RefSeqs	NP_001248364	(Get FASTA)	NCBI Sequence Viewer
	NP_001248365	(Get FASTA)	NCBI Sequence Viewer
	NP_001353315	(Get FASTA)	NCBI Sequence Viewer
	NP_631897	(Get FASTA)	NCBI Sequence Viewer
	XP_011509952	(Get FASTA)	NCBI Sequence Viewer
	XP_011509954	(Get FASTA)	NCBI Sequence Viewer
	XP_011509956	(Get FASTA)	NCBI Sequence Viewer
	XP_011509957	(Get FASTA)	NCBI Sequence Viewer
	XP_011509958	(Get FASTA)	NCBI Sequence Viewer
	XP_011509959	(Get FASTA)	NCBI Sequence Viewer
	XP_047301508	(Get FASTA)	NCBI Sequence Viewer
	XP_047301509	(Get FASTA)	NCBI Sequence Viewer
	XP_054199420	(Get FASTA)	NCBI Sequence Viewer
	XP_054199421	(Get FASTA)	NCBI Sequence Viewer
	XP_054199422	(Get FASTA)	NCBI Sequence Viewer
	XP_054199423	(Get FASTA)	NCBI Sequence Viewer
	XP_054199424	(Get FASTA)	NCBI Sequence Viewer
	XP_054199425	(Get FASTA)	NCBI Sequence Viewer
	XP_054199426	(Get FASTA)	NCBI Sequence Viewer
	XP_054199427	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH38807	(Get FASTA)	NCBI Sequence Viewer
	AAX88914	(Get FASTA)	NCBI Sequence Viewer
	AAX93182	(Get FASTA)	NCBI Sequence Viewer
	BAB69017	(Get FASTA)	NCBI Sequence Viewer
	BAD18656	(Get FASTA)	NCBI Sequence Viewer
	BAF85123	(Get FASTA)	NCBI Sequence Viewer
	CAE06249	(Get FASTA)	NCBI Sequence Viewer
	CAE06250	(Get FASTA)	NCBI Sequence Viewer
	EAW70295	(Get FASTA)	NCBI Sequence Viewer
	EAW70296	(Get FASTA)	NCBI Sequence Viewer
	EAW70297	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000260967
	ENSP00000260967.2
	ENSP00000386901.3
	ENSP00000389831.1
	ENSP00000406472
	ENSP00000406472.2
	ENSP00000412775
	ENSP00000412775.1
	ENSP00000498608
	ENSP00000498608.2
GenBank Protein	Q96Q40	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_631897 ⟸ NM_139158
- Peptide Label:	isoform 3
- UniProtKB:	Q96Q40 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MTSFHPRGLQAARAQKFKSKRPRSNSDCFQEEDLRQGFQWRKSLPFGAASSYLNLEKLGEGSYA TVYKGISRINGQLVALKVISMNAEEGVPFTAIREASLLKGLKHANIVLLHDIIHTKETLTFVFE YMHTDLAQYMSQHPGGLHPHNVRLFMFQLLRGLAYIHHQHVLHRDLKPQNLLISHLGELKLADF GLARAKSIPSQTYSSEVVTLWYRPPDALLGATEYSSELDIWGAGCIFIEMFQGQPLFPGVSNIL EQLEKIWEVLGVPTEDTWPGVSKLPNYNPEWFPLPTPRSLHVVWNRLGRVPEAEDLASQMLKGF PRDRVSAQEALVHDYFSALPSQLYQLPDEESLFTVSGVRLKPEMCDLLASYQKGHHPAQFSKCW hide sequence

RefSeq Acc Id:	NP_001248364 ⟸ NM_001261435
- Peptide Label:	isoform 1
- UniProtKB:	Q96Q40 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MGQELCAKTVQPGCSCYHCSEGGEAHSCRRSQPETTEAAFKLTDLKEASCSMTSFHPRGLQAAR AQKFKSKRPRSNSDCFQEEDLRQGFQWRKSLPFGAASSYLNLEKLGEGSYATVYKGISRINGQL VALKVISMNAEEGVPFTAIREASLLKGLKHANIVLLHDIIHTKETLTFVFEYMHTDLAQYMSQH PGGLHPHNVRLFMFQLLRGLAYIHHQHVLHRDLKPQNLLISHLGELKLADFGLARAKSIPSQTY SSEVVTLWYRPPDALLGATEYSSELDIWGAGCIFIEMFQGQPLFPGVSNILEQLEKIWEVLGVP TEDTWPGVSKLPNYNPEWFPLPTPRSLHVVWNRLGRVPEAEDLASQMLKGFPRDRVSAQEALVH DYFSALPSQLYQLPDVSGVRLKPEMCDLLASYQKGHHPAQFSKCW hide sequence

RefSeq Acc Id:	NP_001248365 ⟸ NM_001261436
- Peptide Label:	isoform 2
- UniProtKB:	Q96Q40 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MGQELCAKTVQPGCSCYHCSEGGEAHSCRRSQPETTEAAFKLTDLKEASCSMTSFHPRGLQAAR AQKFKSKRPRSNSDCFQEEDLRQGFQWRKSLPFGAASSYLNLEKLGEGSYATVYKGISRINGQL VALKVISMNAEEGVPFTAIREASLLKGLKHANIVLLHDIIHTKETLTFVFEYMHTDLAQYMSQH PGGLHPHNVRLFMFQLLRGLAYIHHQHVLHRDLKPQNLLISHLGELKLADFGLARAKSIPSQTY SSEVVTLWYRPPDALLGATEYSSELDIWGAGCIFIEMFQGQPLFPGVSNILEQLEKIWEVLGVP TEDTWPGVSKLPNYNPEWFPLPTPRSLHVVWNRLGRVPEAEDLASQMLKGFPRDRVSAQEALVH DYFSALPSQLYQLPDE hide sequence

RefSeq Acc Id:

XP_011509954 ⟸ XM_011511652

- Peptide Label:

isoform X2

- Sequence:

show sequence

MGQELCAKTVQPGCSCYHCSEGGEAHSCRRSQPETTEAAFKLTDLKEASCSMTSFHPRGLQAAR
AQKFKSKRPRSNSDCFQEEDLRQGFQWRKSLPFGAASSYLNLEKLGEGSYATVYKGISRINGQL
VALKVISMNAEEGVPFTAIREASLLKGLKHANIVLLHDIIHTKETLTFVFEYMHTDLAQYMSQH
PGGLHPHNVRLFMFQLLRGLAYIHHQHVLHRDLKPQNLLISHLGELKLADFGLARAKSIPSQTY
SSEVVTLWYRPPDALLGATEYSSELDIWGAGCIFIEMFQGQPLFPGVSNILEQLEKIWEVLGVP
TEDTWPGVSKLPNYNPEESLFTVSGVRLKPEMCDLLASYQKGHHPAQFSKCW

hide sequence

RefSeq Acc Id:

XP_011509952 ⟸ XM_011511650

- Peptide Label:

isoform X1

- Sequence:

show sequence

MGQELCAKTVQPGCSCYHCSEGGEAHSCRRSQPETTEAAFKLTDLKEASCSMTSFHPRGLQAAR
AQKFKSKRPRSNSDCFQEEDLRQGFQWRKSLPFGAASSYLNLEKLGEGSYATVYKGISRINGQL
VALKVISMNAEEGVPFTAIREASLLKGLKHANIVLLHDIIHTKETLTFVFEYMHTDLAQYMSQH
PGGLHPHNVRLFMFQLLRGLAYIHHQHVLHRDLKPQNLLISHLGELKLADFGLARAKSIPSQTY
SSEVVTLWYRPPDALLGATEYSSELDIWGAGCIFIEMFQGQPLFPGVSNILEQLEKIWEVLGVP
TEDTWPGVSKLPNYNPEWFPLPTPRSLHVVWNRLGRVPEAEDLASQMLKGFPRDRVSAQEALVH
DYFSALPSQLYQLPDVTEPKSTLTLLEK

hide sequence

RefSeq Acc Id:

XP_011509956 ⟸ XM_011511654

- Peptide Label:

isoform X4

- Sequence:

show sequence

MGQELCAKTVQPGCSCYHCSEGGEAHSCRRSQPETTEAAFKLTDLKEASCSMTSFHPRGLQAAR
AQKFKSKRPRSNSDCFQEEDLRQGFQWRKSLPFGAASSYLNLEKLGEGSYATVYKGISRINGQL
VALKVISMNAEEGVPFTAIREASLLKGLKHANIVLLHDIIHTKETLTFVFEYMHTDLAQYMSQH
PGGLHPHNVRLFMFQLLRGLAYIHHQHVLHRDLKPQNLLISHLGELKLADFGLARAKSIPSQTY
SSEVVTLWYRPPDALLGATEYSSELDIWGAGCIFIEMFQGQPLFPGVSNILEQLEKIWEVLGVP
TEDTWPGVSKLPNYNPAIHRDLAS

hide sequence

RefSeq Acc Id:

XP_011509958 ⟸ XM_011511656

- Peptide Label:

isoform X6

- Sequence:

show sequence

MHTDLAQYMSQHPGGLHPHNVRLFMFQLLRGLAYIHHQHVLHRDLKPQNLLISHLGELKLADFG
LARAKSIPSQTYSSEVVTLWYRPPDALLGATEYSSELDIWGAGCIFIEMFQGQPLFPGVSNILE
QLEKIWEVLGVPTEDTWPGVSKLPNYNPEWFPLPTPRSLHVVWNRLGRVPEAEDLASQMLKGFP
RDRVSAQEALVHDYFSALPSQLYQLPDEESLFTVSGVRLKPEMCDLLASYQKGHHPAQFSKCW

hide sequence

RefSeq Acc Id:

XP_011509957 ⟸ XM_011511655

- Peptide Label:

isoform X6

- Sequence:

show sequence

MHTDLAQYMSQHPGGLHPHNVRLFMFQLLRGLAYIHHQHVLHRDLKPQNLLISHLGELKLADFG
LARAKSIPSQTYSSEVVTLWYRPPDALLGATEYSSELDIWGAGCIFIEMFQGQPLFPGVSNILE
QLEKIWEVLGVPTEDTWPGVSKLPNYNPEWFPLPTPRSLHVVWNRLGRVPEAEDLASQMLKGFP
RDRVSAQEALVHDYFSALPSQLYQLPDEESLFTVSGVRLKPEMCDLLASYQKGHHPAQFSKCW

hide sequence

RefSeq Acc Id:

XP_011509959 ⟸ XM_011511657

- Peptide Label:

isoform X7

- Sequence:

show sequence

MEVKGRRISRRRLFMFQLLRGLAYIHHQHVLHRDLKPQNLLISHLGELKLADFGLARAKSIPSQ
TYSSEVVTLWYRPPDALLGATEYSSELDIWGAGCIFIEMFQGQPLFPGVSNILEQLEKIWEVLG
VPTEDTWPGVSKLPNYNPEWFPLPTPRSLHVVWNRLGRVPEAEDLASQMLKGFPRDRVSAQEAL
VHDYFSALPSQLYQLPDEESLFTVSGVRLKPEMCDLLASYQKGHHPAQFSKCW

hide sequence

RefSeq Acc Id:	NP_001353315 ⟸ NM_001366386
- Peptide Label:	isoform 4
- UniProtKB:	Q96Q40 (UniProtKB/Swiss-Prot), Q6ZMR9 (UniProtKB/Swiss-Prot), Q53TV1 (UniProtKB/Swiss-Prot), Q4ZG86 (UniProtKB/Swiss-Prot), F8W6H8 (UniProtKB/Swiss-Prot), C9K003 (UniProtKB/Swiss-Prot), C9J1N8 (UniProtKB/Swiss-Prot), B8ZZX0 (UniProtKB/Swiss-Prot), A8K8R9 (UniProtKB/Swiss-Prot), Q8IUP1 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:

ENSP00000386901 ⟸ ENST00000410091

RefSeq Acc Id:

ENSP00000406472 ⟸ ENST00000450471

RefSeq Acc Id:

ENSP00000389831 ⟸ ENST00000451080

RefSeq Acc Id:

ENSP00000498608 ⟸ ENST00000652192

RefSeq Acc Id:

ENSP00000260967 ⟸ ENST00000260967

RefSeq Acc Id:

ENSP00000412775 ⟸ ENST00000434439

RefSeq Acc Id:	XP_047301508 ⟸ XM_047445552
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_047301509 ⟸ XM_047445553
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054199421 ⟸ XM_054343446
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054199420 ⟸ XM_054343445
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054199422 ⟸ XM_054343447
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054199423 ⟸ XM_054343448
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054199424 ⟸ XM_054343449
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054199426 ⟸ XM_054343451
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_054199425 ⟸ XM_054343450
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_054199427 ⟸ XM_054343452
- Peptide Label:	isoform X7

Protein Domains

Protein kinase

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q96Q40-F1-model_v2	AlphaFold	Q96Q40	1-435	view protein structure

Promoters

RGD ID:

6862556

Promoter ID:

EPDNEW_H4443

Type:

initiation region

Name:

CDK15_1

Description:

cyclin dependent kinase 15

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H4442 EPDNEW_H4444

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	201,806,583 - 201,806,643	EPDNEW

RGD ID:

6862558

Promoter ID:

EPDNEW_H4444

Type:

initiation region

Name:

CDK15_2

Description:

cyclin dependent kinase 15

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H4442 EPDNEW_H4443

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	201,806,714 - 201,806,774	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:14434	AgrOrtholog
COSMIC	CDK15	COSMIC
Ensembl Genes	ENSG00000138395	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000260967	ENTREZGENE
	ENST00000260967.6	UniProtKB/Swiss-Prot
	ENST00000410091.7	UniProtKB/Swiss-Prot
	ENST00000434439	ENTREZGENE
	ENST00000434439.1	UniProtKB/Swiss-Prot
	ENST00000450471	ENTREZGENE
	ENST00000450471.6	UniProtKB/Swiss-Prot
	ENST00000451080.5	UniProtKB/TrEMBL
	ENST00000652192	ENTREZGENE
	ENST00000652192.3	UniProtKB/Swiss-Prot
Gene3D-CATH	Transferase(Phosphotransferase) domain 1	UniProtKB/Swiss-Prot
GTEx	ENSG00000138395	GTEx
HGNC ID	HGNC:14434	ENTREZGENE
Human Proteome Map	CDK15	Human Proteome Map
InterPro	CDK15_STKc	UniProtKB/Swiss-Prot
	Kinase-like_dom_sf	UniProtKB/Swiss-Prot
	Prot_kinase_dom	UniProtKB/Swiss-Prot
	Protein_kinase_ATP_BS	UniProtKB/Swiss-Prot
	Ser/Thr_kinase_AS	UniProtKB/Swiss-Prot
KEGG Report	hsa:65061	UniProtKB/Swiss-Prot
NCBI Gene	65061	ENTREZGENE
OMIM	616147	OMIM
PANTHER	CELL DIVISION PROTEIN KINASE	UniProtKB/Swiss-Prot
	CYCLIN-DEPENDENT KINASE 15	UniProtKB/Swiss-Prot
Pfam	Pkinase	UniProtKB/Swiss-Prot
PharmGKB	PA165696414	PharmGKB
PROSITE	PROTEIN_KINASE_ATP	UniProtKB/Swiss-Prot
	PROTEIN_KINASE_DOM	UniProtKB/Swiss-Prot
	PROTEIN_KINASE_ST	UniProtKB/Swiss-Prot
SMART	S_TKc	UniProtKB/Swiss-Prot
Superfamily-SCOP	SSF56112	UniProtKB/Swiss-Prot
UniProt	A8K8R9	ENTREZGENE
	B8ZZX0	ENTREZGENE
	C9J1N8	ENTREZGENE
	C9K003	ENTREZGENE
	CDK15_HUMAN	UniProtKB/Swiss-Prot
	F8W6H8	ENTREZGENE
	F8WDP7_HUMAN	UniProtKB/TrEMBL
	Q4ZG86	ENTREZGENE
	Q53TV1	ENTREZGENE
	Q6ZMR9	ENTREZGENE
	Q8IUP1	ENTREZGENE
	Q96Q40	ENTREZGENE
UniProt Secondary	A8K8R9	UniProtKB/Swiss-Prot
	B8ZZX0	UniProtKB/Swiss-Prot
	C9J1N8	UniProtKB/Swiss-Prot
	C9K003	UniProtKB/Swiss-Prot
	F8W6H8	UniProtKB/Swiss-Prot
	Q4ZG86	UniProtKB/Swiss-Prot
	Q53TV1	UniProtKB/Swiss-Prot
	Q6ZMR9	UniProtKB/Swiss-Prot
	Q8IUP1	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2016-06-21	CDK15	cyclin dependent kinase 15		cyclin-dependent kinase 15	Symbol and/or name change	5135510	APPROVED
2011-07-27	CDK15	cyclin-dependent kinase 15	PFTK2	PFTAIRE protein 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)

Imported Disease Annotations - ClinVar

RGD Manual Annotations

Imported Human Phenotype Annotations - ClinVar

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Imported Disease Annotations - ClinVar

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Imported Human Phenotype Annotations - ClinVar