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Gene: CAMK1D (calcium/calmodulin dependent protein kinase ID) Homo sapiens

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Symbol:

CAMK1D

Name:

calcium/calmodulin dependent protein kinase ID

RGD ID:

1603628

HGNC Page

HGNC:19341

Description:

Enables calcium/calmodulin-dependent protein kinase activity. Involved in several processes, including positive regulation of CREB transcription factor activity; positive regulation of phagocytosis; and positive regulation of respiratory burst. Located in cytoplasm and nucleus.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

calcium/calmodulin-dependent protein kinase ID; calcium/calmodulin-dependent protein kinase type 1D; caM kinase I delta; CaM kinase ID; CaM-K1; caM-KI delta; CAMK1D/ANAPC5 fusion; caMKI delta; CamKI-like protein kinase; CaMKID; CKLiK

RGD Orthologs

Alliance Orthologs

More Info

more info ...

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	10	12,349,547 - 12,835,545 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	10	12,349,547 - 12,835,545 (+)	Ensembl			hg38	GRCh38
GRCh37	10	12,391,546 - 12,877,545 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	10	12,431,589 - 12,911,741 (+)	NCBI	Build 36	Build 36	hg18	NCBI36
Celera	10	12,320,755 - 12,797,502 (+)	NCBI		Celera
Cytogenetic Map	10	p13	NCBI
HuRef	10	12,307,786 - 12,784,748 (+)	NCBI		HuRef
CHM1_1	10	12,391,537 - 12,871,781 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	10	12,360,834 - 12,849,903 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Annotation Click to see Annotation Detail View

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

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

(2,4,5-trichlorophenoxy)acetic acid (ISO)

1,2-dimethylhydrazine (ISO)

17alpha-ethynylestradiol (ISO)

17beta-estradiol (ISO)

2,3',4,4',5-Pentachlorobiphenyl (ISO)

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

2-hydroxypropanoic acid (EXP)

3,4-methylenedioxymethamphetamine (ISO)

4,4'-sulfonyldiphenol (EXP,ISO)

4-hydroxynon-2-enal (ISO)

6-propyl-2-thiouracil (ISO)

acetamide (ISO)

aflatoxin B1 (EXP,ISO)

Aflatoxin B2 alpha (EXP)

aldrin (ISO)

all-trans-retinoic acid (EXP)

aristolochic acid A (EXP)

atrazine (ISO)

avobenzone (EXP)

benzo[a]pyrene (EXP,ISO)

benzo[e]pyrene (EXP)

bis(2-ethylhexyl) phthalate (EXP,ISO)

bisphenol A (EXP,ISO)

bisphenol F (ISO)

buta-1,3-diene (ISO)

butanal (EXP)

cadmium atom (ISO)

cadmium dichloride (ISO)

calcitriol (EXP)

carbon nanotube (ISO)

chlordecone (ISO)

ciguatoxin CTX1B (ISO)

cisplatin (EXP)

copper(II) sulfate (ISO)

coumestrol (EXP)

Cuprizon (ISO)

cyclosporin A (ISO)

Dibutyl phosphate (EXP)

dibutyl phthalate (ISO)

diclofenac (ISO)

dorsomorphin (EXP)

doxorubicin (EXP,ISO)

endosulfan (ISO)

folic acid (ISO)

fulvestrant (EXP)

glyphosate (ISO)

hypochlorous acid (ISO)

inulin (ISO)

methapyrilene (EXP)

methoxychlor (ISO)

methylmercury chloride (EXP)

mono(2-ethylhexyl) phthalate (ISO)

N,N-diethyl-m-toluamide (ISO)

O-methyleugenol (EXP)

okadaic acid (EXP)

paracetamol (ISO)

perfluorooctane-1-sulfonic acid (ISO)

permethrin (ISO)

phenobarbital (ISO)

phenylmercury acetate (EXP)

pirinixic acid (ISO)

potassium chromate (EXP)

progesterone (ISO)

rac-lactic acid (EXP)

rotenone (ISO)

SB 431542 (EXP)

sodium arsenate (ISO)

sodium arsenite (EXP)

sodium fluoride (ISO)

succimer (ISO)

sulforaphane (EXP)

sunitinib (EXP)

tacrolimus hydrate (ISO)

tamoxifen (ISO)

testosterone (EXP)

tetrachloromethane (ISO)

thioacetamide (ISO)

titanium dioxide (ISO)

trichloroethene (ISO)

trichostatin A (EXP)

triphenyl phosphate (EXP)

troglitazone (ISO)

tungsten (ISO)

tunicamycin (ISO)

valproic acid (EXP)

vinclozolin (ISO)

zoledronic acid (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

inflammatory response (IEA)

negative regulation of apoptotic process (ISO)

nervous system development (IEA)

positive regulation of apoptotic process (ISO)

positive regulation of neuron projection development (IEA,ISS)

positive regulation of neutrophil chemotaxis (IEA,ISS)

positive regulation of phagocytosis (IMP)

positive regulation of respiratory burst (IMP)

regulation of dendrite development (IMP)

regulation of granulocyte chemotaxis (IBA,IMP)

regulation of neuron projection development (IBA,IEA)

signal transduction (IBA)

Cellular Component

cytoplasm (IBA,IDA,IEA)

nucleus (IDA,IEA)

Molecular Function

ATP binding (IEA)

calcium/calmodulin-dependent protein kinase activity (IBA,IDA,IEA)

calmodulin binding (IBA,IEA)

catalytic activity (IEA)

kinase activity (IEA)

nucleotide binding (IEA)

protein binding (IPI)

protein kinase activity (IEA)

protein serine kinase activity (IEA)

protein serine/threonine kinase activity (IEA)

transferase activity (IEA)

References

References - curated

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

Additional References at PubMed

PMID:8889548	PMID:11050006	PMID:11264466	PMID:12477932	PMID:12935886	PMID:14702039	PMID:15164054	PMID:15489334	PMID:15840691	PMID:16324104	PMID:16344560	PMID:16385451
PMID:17056143	PMID:18029348	PMID:18372903	PMID:18976975	PMID:19020323	PMID:19020324	PMID:19139842	PMID:19324937	PMID:19383354	PMID:19602701	PMID:19670153	PMID:19720844
PMID:19741467	PMID:19794065	PMID:19833888	PMID:19933996	PMID:19953087	PMID:20080650	PMID:20161779	PMID:20379614	PMID:20418484	PMID:20571754	PMID:20677014	PMID:20712903
PMID:20862305	PMID:20879858	PMID:20889853	PMID:20927120	PMID:21044950	PMID:21832049	PMID:21873635	PMID:21909839	PMID:21988832	PMID:22863883	PMID:22923468	PMID:23251661
PMID:23459443	PMID:23568457	PMID:23824909	PMID:23840313	PMID:24159190	PMID:24510904	PMID:25009623	PMID:25201988	PMID:25366777	PMID:25410890	PMID:25468996	PMID:26186194
PMID:26760575	PMID:28079868	PMID:28319085	PMID:28514442	PMID:29507755	PMID:29533498	PMID:32665263	PMID:32707033	PMID:33127268	PMID:33660800	PMID:33961781	PMID:34857952
PMID:37788672	PMID:39079530	PMID:40437099

Genomics

Comparative Map Data

CAMK1D
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	10	12,349,547 - 12,835,545 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	10	12,349,547 - 12,835,545 (+)	Ensembl			hg38	GRCh38
GRCh37	10	12,391,546 - 12,877,545 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	10	12,431,589 - 12,911,741 (+)	NCBI	Build 36	Build 36	hg18	NCBI36
Celera	10	12,320,755 - 12,797,502 (+)	NCBI		Celera
Cytogenetic Map	10	p13	NCBI
HuRef	10	12,307,786 - 12,784,748 (+)	NCBI		HuRef
CHM1_1	10	12,391,537 - 12,871,781 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	10	12,360,834 - 12,849,903 (+)	NCBI		T2T-CHM13v2.0

Camk1d
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	2	5,298,268 - 5,719,665 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	2	5,298,268 - 5,719,326 (-)	Ensembl		GRCm39 Ensembl		GRCm39
GRCm38	2	5,293,457 - 5,714,860 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	2	5,293,457 - 5,714,515 (-)	Ensembl			mm10	GRCm38
MGSCv37	2	5,214,503 - 5,635,710 (-)	NCBI	MGSCv37	MGSCv37	mm9	NCBIm37
MGSCv36	2	5,210,729 - 5,631,936 (-)	NCBI		MGSCv36	mm8
Celera	2	5,248,039 - 5,664,845 (-)	NCBI		Celera
Cytogenetic Map	2	A1	NCBI
cM Map	2	3.39	NCBI

Camk1d
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	17	77,491,191 - 77,892,018 (+)	NCBI	GRCr8	GRCr8		GRCr8
GRCr8 Ensembl	17	77,491,220 - 77,892,012 (+)	Ensembl				GRCr8
mRatBN7.2	17	72,581,899 - 72,982,704 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	17	72,581,979 - 72,980,556 (+)	Ensembl				mRatBN7.2
UTH_Rnor_SHR_Utx	17	76,089,042 - 76,490,160 (+)	NCBI	UTH_Rnor_SHR_Utx	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	17	79,910,489 - 80,310,785 (+)	NCBI	UTH_Rnor_SHRSP_BbbUtx_1.0	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	17	73,960,745 - 74,360,775 (+)	NCBI	UTH_Rnor_WKY_Bbb_1.0	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	17	76,532,611 - 76,938,956 (+)	NCBI	Rnor_6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	17	76,532,611 - 76,938,956 (+)	Ensembl			rn6	Rnor6.0
Rnor_5.0	17	78,552,005 - 78,591,805 (+)	NCBI	Rnor_5.0	Rnor_5.0	rn5
Rnor_5.0	17	78,187,614 - 78,538,315 (+)	NCBI	Rnor_5.0	Rnor_5.0	rn5
RGSC_v3.4	17	83,649,720 - 84,061,160 (+)	NCBI	RGSC_v3.4	RGSC_v3.4	rn4
Celera	17	72,029,264 - 72,426,573 (+)	NCBI		Celera
Cytogenetic Map	17	q12.3	NCBI

Camk1d
(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_004955462	391,235 - 813,598 (+)	Ensembl
ChiLan1.0	NW_004955462	391,235 - 819,240 (+)	NCBI	ChiLan1.0	ChiLan1.0

CAMK1D
(Pan paniscus - bonobo/pygmy chimpanzee)

Bonobo Assembly	Chr	Position (strand)	Source	Genome Browsers
Bonobo Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
NHGRI_mPanPan1-v2	8	24,879,343 - 25,360,851 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	10	24,884,690 - 25,366,182 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	10	12,359,213 - 12,840,464 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	10	12,471,340 - 12,809,098 (+)	NCBI	PanPan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	10	12,540,854 - 12,808,599 (+)	Ensembl			panPan2	panpan1.1

CAMK1D
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	2	23,680,395 - 24,113,922 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	2	23,685,672 - 24,114,084 (-)	Ensembl			canFam3	CanFam3.1
Dog10K_Boxer_Tasha	2	20,698,974 - 21,138,879 (-)	NCBI	Dog10K_Boxer_Tasha	Dog10K_Boxer_Tasha
ROS_Cfam_1.0	2	24,052,518 - 24,484,818 (-)	NCBI	ROS_Cfam_1.0	ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	2	24,052,523 - 24,484,827 (-)	Ensembl				ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	2	21,178,935 - 21,612,394 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	2	22,021,253 - 22,454,982 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	2	22,737,896 - 23,169,796 (-)	NCBI	UU_Cfam_GSD_1.0	UU_Cfam_GSD_1.0

Camk1d
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)

Squirrel Assembly	Chr	Position (strand)	Source	Genome Browsers
Squirrel Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HiC_Itri_2	NW_024409344	26,461,700 - 26,858,995 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936484	2,632,107 - 3,023,869 (-)	Ensembl		SpeTri2.0 Ensembl
SpeTri2.0	NW_004936484	2,626,909 - 2,768,304 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

CAMK1D
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	10	59,204,724 - 59,630,285 (-)	Ensembl			susScr11	Sscrofa11.1
Sscrofa11.1	10	59,199,541 - 59,630,191 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	10	64,912,917 - 64,969,603 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

CAMK1D
(Chlorocebus sabaeus - green monkey)

Green Monkey Assembly	Chr	Position (strand)	Source	Genome Browsers
Green Monkey Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChlSab1.1	9	12,392,452 - 12,873,294 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	9	12,809,028 - 12,872,778 (+)	Ensembl		ChlSab1.1 Ensembl	chlSab2	Vervet-AGM
Vero_WHO_p1.0	NW_023666051	17,902,237 - 18,395,258 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Camk1d
(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_004624805	5,193,397 - 5,408,011 (+)	Ensembl		HetGla_female_1.0 Ensembl	hetGla2	HetGla_female_1.0 Ensembl
HetGla 1.0	NW_004624805	5,047,885 - 5,413,264 (+)	NCBI	HetGla 1.0	HetGla 1.0	hetGla2

Camk1d
(Rattus rattus - black rat)

Black Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Black Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Rrattus_CSIRO_v1	14	11,643,288 - 12,042,927 (-)	NCBI		Rrattus_CSIRO_v1

Variants

Variants in CAMK1D
67 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 10p13(chr10:12377967-12692594)x3	copy number gain	See cases [RCV000051595]	Chr10:12377967..12692594 [GRCh38] Chr10:12419966..12734593 [GRCh37] Chr10:12459972..12774599 [NCBI36] Chr10:10p13	uncertain significance
GRCh38/hg38 10p15.3-13(chr10:90421-15569528)x1	copy number loss	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052496]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052496]\|See cases [RCV000052496]	Chr10:90421..15569528 [GRCh38] Chr10:224406..15611527 [GRCh37] Chr10:126361..15651533 [NCBI36] Chr10:10p15.3-13	pathogenic
GRCh38/hg38 10p15.1-13(chr10:4802753-16823491)x1	copy number loss	See cases [RCV000052500]	Chr10:4802753..16823491 [GRCh38] Chr10:4844945..16865490 [GRCh37] Chr10:4834945..16905496 [NCBI36] Chr10:10p15.1-13	pathogenic
GRCh38/hg38 10p15.3-12.31(chr10:69261-19184047)x3	copy number gain	See cases [RCV000053507]	Chr10:69261..19184047 [GRCh38] Chr10:224406..19472976 [GRCh37] Chr10:105201..19512982 [NCBI36] Chr10:10p15.3-12.31	pathogenic
GRCh38/hg38 10p15.3-12.2(chr10:90221-22567425)x3	copy number gain	See cases [RCV000053508]	Chr10:90221..22567425 [GRCh38] Chr10:224406..22856354 [GRCh37] Chr10:126161..22896360 [NCBI36] Chr10:10p15.3-12.2	pathogenic
GRCh38/hg38 10p15.3-12.1(chr10:90421-29058318)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053512]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053512]\|See cases [RCV000053512]	Chr10:90421..29058318 [GRCh38] Chr10:224406..29347247 [GRCh37] Chr10:126361..29387253 [NCBI36] Chr10:10p15.3-12.1	pathogenic
NM_020397.3(CAMK1D):c.301G>A (p.Val101Met)	single nucleotide variant	Malignant melanoma [RCV000068852]	Chr10:12760949 [GRCh38] Chr10:12802948 [GRCh37] Chr10:12842954 [NCBI36] Chr10:10p13	not provided
NM_020397.3(CAMK1D):c.452T>C (p.Leu151Ser)	single nucleotide variant	Malignant melanoma [RCV000068853]	Chr10:12769686 [GRCh38] Chr10:12811685 [GRCh37] Chr10:12851691 [NCBI36] Chr10:10p13	not provided
GRCh38/hg38 10p13(chr10:12333253-13948472)x1	copy number loss	See cases [RCV000134396]	Chr10:12333253..13948472 [GRCh38] Chr10:12375252..13990472 [GRCh37] Chr10:12415258..14030478 [NCBI36] Chr10:10p13	likely pathogenic
GRCh38/hg38 10p15.3-13(chr10:73856-12815915)x3	copy number gain	See cases [RCV000135340]	Chr10:73856..12815915 [GRCh38] Chr10:119796..12857914 [GRCh37] Chr10:109796..12897920 [NCBI36] Chr10:10p15.3-13	pathogenic
GRCh38/hg38 10p14-12.31(chr10:7428770-21587752)x1	copy number loss	See cases [RCV000137307]	Chr10:7428770..21587752 [GRCh38] Chr10:7470732..21876681 [GRCh37] Chr10:7510738..21916687 [NCBI36] Chr10:10p14-12.31	pathogenic\|uncertain significance
GRCh38/hg38 10p15.3-13(chr10:70478-15373336)x3	copy number gain	See cases [RCV000137384]	Chr10:70478..15373336 [GRCh38] Chr10:224406..15415335 [GRCh37] Chr10:106418..15455341 [NCBI36] Chr10:10p15.3-13	uncertain significance
GRCh38/hg38 10p15.3-12.1(chr10:90205-26339978)x3	copy number gain	See cases [RCV000138428]	Chr10:90205..26339978 [GRCh38] Chr10:224406..26628907 [GRCh37] Chr10:126145..26668913 [NCBI36] Chr10:10p15.3-12.1	pathogenic
GRCh38/hg38 10p15.3-13(chr10:70478-13736564)x1	copy number loss	See cases [RCV000138960]	Chr10:70478..13736564 [GRCh38] Chr10:224406..13778564 [GRCh37] Chr10:106418..13818570 [NCBI36] Chr10:10p15.3-13	pathogenic
GRCh38/hg38 10p15.1-q11.22(chr10:4604734-48074662)x3	copy number gain	See cases [RCV000141497]	Chr10:4604734..48074662 [GRCh38] Chr10:4646926..47531169 [GRCh37] Chr10:4636926..47125152 [NCBI36] Chr10:10p15.1-q11.22	benign
GRCh38/hg38 10p15.3-13(chr10:54086-13205916)x3	copy number gain	See cases [RCV000142292]	Chr10:54086..13205916 [GRCh38] Chr10:100026..13247916 [GRCh37] Chr10:90026..13287922 [NCBI36] Chr10:10p15.3-13	pathogenic
GRCh38/hg38 10p15.3-12.31(chr10:54086-19336980)x1	copy number loss	See cases [RCV000143703]	Chr10:54086..19336980 [GRCh38] Chr10:100026..19625909 [GRCh37] Chr10:90026..19665915 [NCBI36] Chr10:10p15.3-12.31	pathogenic\|likely pathogenic
GRCh37/hg19 10p13-q26.3(chr10:12829206-135427143)	copy number loss	Distal 10q deletion syndrome [RCV003319583]	Chr10:12829206..135427143 [GRCh37] Chr10:10p13-q26.3	pathogenic
GRCh37/hg19 10p13(chr10:12821353-13275585)x3	copy number gain	See cases [RCV000449238]	Chr10:12821353..13275585 [GRCh37] Chr10:10p13	likely benign
GRCh37/hg19 10p14-13(chr10:9180833-12424863)x3	copy number gain	See cases [RCV000446118]	Chr10:9180833..12424863 [GRCh37] Chr10:10p14-13	uncertain significance
GRCh37/hg19 10p15.3-11.23(chr10:100026-30278548)x3	copy number gain	See cases [RCV000447131]	Chr10:100026..30278548 [GRCh37] Chr10:10p15.3-11.23	pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:93297-135378918)x3	copy number gain	See cases [RCV000448750]	Chr10:93297..135378918 [GRCh37] Chr10:10p15.3-q26.3	pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143)	copy number gain	See cases [RCV000511389]	Chr10:100027..135427143 [GRCh37] Chr10:10p15.3-q26.3	pathogenic\|uncertain significance
GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143)x3	copy number gain	See cases [RCV000510861]	Chr10:100027..135427143 [GRCh37] Chr10:10p15.3-q26.3	pathogenic
GRCh37/hg19 10p15.3-q11.23(chr10:100026-50961640)x3	copy number gain	See cases [RCV000510893]	Chr10:100026..50961640 [GRCh37] Chr10:10p15.3-q11.23	pathogenic
NM_153498.4(CAMK1D):c.274A>C (p.Asn92His)	single nucleotide variant	not specified [RCV004305998]	Chr10:12666785 [GRCh38] Chr10:12708784 [GRCh37] Chr10:10p13	uncertain significance
GRCh37/hg19 10p15.3-13(chr10:100026-12842179)x1	copy number loss	See cases [RCV000512541]	Chr10:100026..12842179 [GRCh37] Chr10:10p15.3-13	pathogenic
GRCh37/hg19 10p13(chr10:12802555-14847149)x1	copy number loss	not provided [RCV000683270]	Chr10:12802555..14847149 [GRCh37] Chr10:10p13	uncertain significance
NC_000010.10:g.(?_12833157)_(13178866_?)del	deletion	Primary open angle glaucoma [RCV000708259]	Chr10:12833157..13178866 [GRCh37] Chr10:10p13	pathogenic
Single allele	deletion	Hypoparathyroidism, deafness, renal disease syndrome [RCV000735901]	Chr10:4689760..19120882 [GRCh37] Chr10:10p15.1-12.31	pathogenic
GRCh37/hg19 10p13(chr10:12601504-12662552)x1	copy number loss	not provided [RCV000737023]	Chr10:12601504..12662552 [GRCh37] Chr10:10p13	benign
GRCh37/hg19 10p15.3-13(chr10:69083-12887271)x3	copy number gain	not provided [RCV000749463]	Chr10:69083..12887271 [GRCh37] Chr10:10p15.3-13	pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:73232-135524321)x3	copy number gain	not provided [RCV000749464]	Chr10:73232..135524321 [GRCh37] Chr10:10p15.3-q26.3	pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:98087-135477883)x3	copy number gain	not provided [RCV000749465]	Chr10:98087..135477883 [GRCh37] Chr10:10p15.3-q26.3	pathogenic
NM_153498.4(CAMK1D):c.324C>T (p.Asp108=)	single nucleotide variant	not provided [RCV000883927]	Chr10:12760972 [GRCh38] Chr10:12802971 [GRCh37] Chr10:10p13	benign
NM_153498.4(CAMK1D):c.876C>T (p.Ser292=)	single nucleotide variant	not provided [RCV000905263]	Chr10:12824507 [GRCh38] Chr10:12866506 [GRCh37] Chr10:10p13	likely benign
GRCh37/hg19 10p15.3-13(chr10:100026-15273144)x3	copy number gain	not provided [RCV000848062]	Chr10:100026..15273144 [GRCh37] Chr10:10p15.3-13	pathogenic
GRCh37/hg19 10p13(chr10:12805430-13306566)x3	copy number gain	See cases [RCV001194562]	Chr10:12805430..13306566 [GRCh37] Chr10:10p13	uncertain significance
GRCh37/hg19 10p15.3-13(chr10:100026-15273144)x3	copy number gain	not provided [RCV000848090]	Chr10:100026..15273144 [GRCh37] Chr10:10p15.3-13	pathogenic
GRCh37/hg19 10p14-13(chr10:12165983-12957560)x3	copy number gain	not provided [RCV001006295]	Chr10:12165983..12957560 [GRCh37] Chr10:10p14-13	uncertain significance
NM_153498.4(CAMK1D):c.450_451del (p.Leu151fs)	microsatellite	Intellectual disability [RCV004785242]	Chr10:12769681..12769682 [GRCh38] Chr10:12811680..12811681 [GRCh37] Chr10:10p13	likely pathogenic
NM_153498.4(CAMK1D):c.198A>G (p.Ile66Met)	single nucleotide variant	not provided [RCV000972596]	Chr10:12553330 [GRCh38] Chr10:12595329 [GRCh37] Chr10:10p13	benign
GRCh37/hg19 10p13(chr10:12810570-13149670)x3	copy number gain	not provided [RCV002472466]	Chr10:12810570..13149670 [GRCh37] Chr10:10p13	uncertain significance
GRCh37/hg19 10p14-13(chr10:9137489-17227168)	copy number loss	Neurodevelopmental delay [RCV001352639]	Chr10:9137489..17227168 [GRCh37] Chr10:10p14-13	pathogenic
GRCh37/hg19 10p15.3-q11.22(chr10:135655-47688677)x4	copy number gain	Mosaic supernumerary isodicentric chromosome 10 [RCV001825164]	Chr10:135655..47688677 [GRCh37] Chr10:10p15.3-q11.22	not provided
GRCh37/hg19 10p15.1-11.21(chr10:6273934-34732521)	copy number gain	not specified [RCV002052863]	Chr10:6273934..34732521 [GRCh37] Chr10:10p15.1-11.21	pathogenic
NC_000010.10:g.(?_12111033)_(13342042_?)dup	duplication	not provided [RCV001979753]	Chr10:12111033..13342042 [GRCh37] Chr10:10p14-13	uncertain significance
GRCh37/hg19 10p15.3-13(chr10:100027-12648149)x3	copy number gain	not provided [RCV002472393]	Chr10:100027..12648149 [GRCh37] Chr10:10p15.3-13	uncertain significance
NM_153498.4(CAMK1D):c.173C>T (p.Ala58Val)	single nucleotide variant	not specified [RCV004226714]	Chr10:12553305 [GRCh38] Chr10:12595304 [GRCh37] Chr10:10p13	uncertain significance
NM_153498.4(CAMK1D):c.1105G>A (p.Glu369Lys)	single nucleotide variant	not specified [RCV004254666]	Chr10:12828834 [GRCh38] Chr10:12870833 [GRCh37] Chr10:10p13	uncertain significance
NM_153498.4(CAMK1D):c.1067T>C (p.Phe356Ser)	single nucleotide variant	not specified [RCV004271500]	Chr10:12828796 [GRCh38] Chr10:12870795 [GRCh37] Chr10:10p13	uncertain significance
GRCh37/hg19 10p14-q26.3(chr10:11138692-135427143)	copy number gain	Distal trisomy 10q [RCV003319593]	Chr10:11138692..135427143 [GRCh37] Chr10:10p14-q26.3	pathogenic
NM_153498.4(CAMK1D):c.121G>A (p.Glu41Lys)	single nucleotide variant	not specified [RCV004343623]	Chr10:12553253 [GRCh38] Chr10:12595252 [GRCh37] Chr10:10p13	uncertain significance
GRCh37/hg19 10p14-13(chr10:10175327-13529362)x3	copy number gain	not provided [RCV003484791]	Chr10:10175327..13529362 [GRCh37] Chr10:10p14-13	uncertain significance
NM_153498.4(CAMK1D):c.806C>T (p.Thr269Met)	single nucleotide variant	not specified [RCV004434624]	Chr10:12816301 [GRCh38] Chr10:12858300 [GRCh37] Chr10:10p13	uncertain significance
NM_153498.4(CAMK1D):c.300G>C (p.Leu100=)	single nucleotide variant	not specified [RCV004434621]	Chr10:12760948 [GRCh38] Chr10:12802947 [GRCh37] Chr10:10p13	likely benign
NM_153498.4(CAMK1D):c.577C>G (p.Leu193Val)	single nucleotide variant	not specified [RCV004434623]	Chr10:12791169 [GRCh38] Chr10:12833168 [GRCh37] Chr10:10p13	uncertain significance
NM_153498.4(CAMK1D):c.208A>G (p.Ile70Val)	single nucleotide variant	not specified [RCV004434620]	Chr10:12553340 [GRCh38] Chr10:12595339 [GRCh37] Chr10:10p13	uncertain significance
NM_153498.4(CAMK1D):c.824G>A (p.Arg275Gln)	single nucleotide variant	not specified [RCV004434625]	Chr10:12816319 [GRCh38] Chr10:12858318 [GRCh37] Chr10:10p13	uncertain significance
GRCh37/hg19 10p15.3-12.31(chr10:100027-18976780)x3	copy number gain	not provided [RCV004819307]	Chr10:100027..18976780 [GRCh37] Chr10:10p15.3-12.31	pathogenic
GRCh37/hg19 10p15.1-13(chr10:3983598-13457969)x3	copy number gain	not provided [RCV004819555]	Chr10:3983598..13457969 [GRCh37] Chr10:10p15.1-13	uncertain significance
NM_153498.4(CAMK1D):c.1082C>T (p.Ser361Leu)	single nucleotide variant	not specified [RCV004895483]	Chr10:12828811 [GRCh38] Chr10:12870810 [GRCh37] Chr10:10p13	uncertain significance
NM_153498.4(CAMK1D):c.214G>A (p.Val72Ile)	single nucleotide variant	not specified [RCV005314697]	Chr10:12553346 [GRCh38] Chr10:12595345 [GRCh37] Chr10:10p13	uncertain significance

miRNA Target Status (No longer updated)

Predicted Target Of

	Summary Value
Count of predictions:	3494
Count of miRNA genes:	1278
Interacting mature miRNAs:	1622
Transcripts:	ENST00000378845, ENST00000378847, ENST00000487696
Prediction methods:	Miranda, Rnahybrid
Result types:	miRGate_prediction

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

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

QTLs in Region (GRCh38)

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
597988769	GWAS1708068_H	asymmetrical dimethylarginine measurement, serum dimethylarginine amount QTL GWAS1708068 (human)		0.000009	asymmetrical dimethylarginine measurement, serum dimethylarginine amount		10	12830881	12830882	Human
407043660	GWAS692636_H	body composition measurement QTL GWAS692636 (human)		0.000004	body mass (VT:0001259)		10	12396784	12396785	Human
598002602	GWAS1721901_H	body height QTL GWAS1721901 (human)		1e-12	body height		10	12778212	12778213	Human
628479342	GWAS2387571_H	Headache QTL GWAS2387571 (human)		5e-10	Headache		10	12684062	12684063	Human
598053765	GWAS1773064_H	body height QTL GWAS1773064 (human)		1e-11	body height		10	12406089	12406090	Human
598034305	GWAS1753604_H	body height QTL GWAS1753604 (human)		0.0000003	body height		10	12782716	12782717	Human
628675935	GWAS2584164_H	bone tissue density QTL GWAS2584164 (human)		8e-09	bone tissue density		10	12463869	12463870	Human
629004119	GWAS2912348_H	body height QTL GWAS2912348 (human)		2e-38	body height		10	12822395	12822396	Human
629004118	GWAS2912347_H	body height QTL GWAS2912347 (human)		3e-12	body height		10	12794840	12794841	Human
406996590	GWAS645566_H	frontal fibrosing alopecia QTL GWAS645566 (human)		0.000005	frontal fibrosing alopecia		10	12462314	12462315	Human
407050349	GWAS699325_H	eating disorder QTL GWAS699325 (human)		0.000004	eating behavior trait (VT:0001431)		10	12833208	12833209	Human
597302187	GWAS1398261_H	systemic lupus erythematosus QTL GWAS1398261 (human)		3e-08	systemic lupus erythematosus		10	12446137	12446138	Human
598076311	GWAS1795610_H	socioeconomic status QTL GWAS1795610 (human)		6e-09	socioeconomic status		10	12669950	12669951	Human
597053346	GWAS1149420_H	household income QTL GWAS1149420 (human)		5e-09	household income		10	12650578	12650579	Human
407380095	GWAS1029071_H	acute myeloid leukemia QTL GWAS1029071 (human)		0.0000003	acute myeloid leukemia		10	12649577	12649578	Human
597464484	GWAS1560558_H	age of onset of Parkinson disease QTL GWAS1560558 (human)		0.000005	age of onset of Parkinson disease		10	12364534	12364535	Human
597139887	GWAS1235961_H	smoking initiation QTL GWAS1235961 (human)		1e-11	smoking initiation		10	12698083	12698084	Human
406904442	GWAS553418_H	Borderline personality disorder QTL GWAS553418 (human)		0.000003	Borderline personality disorder		10	12623139	12623140	Human
628610379	GWAS2518608_H	lipid measurement QTL GWAS2518608 (human)		0.000009	lipid amount (VT:0001547)	blood lipid measurement (CMO:0000050)	10	12729681	12729682	Human
628886840	GWAS2795069_H	educational attainment QTL GWAS2795069 (human)		4e-14	educational attainment		10	12698083	12698084	Human
406929925	GWAS578901_H	body height QTL GWAS578901 (human)		5e-09	body height		10	12786454	12786455	Human
597240796	GWAS1336870_H	educational attainment QTL GWAS1336870 (human)		2e-08	educational attainment		10	12351489	12351490	Human
617109134	GWAS2126633_H	Alzheimer disease, family history of Alzheimer’s disease QTL GWAS2126633 (human)		8e-09	Alzheimer disease, family history of Alzheimer’s disease		10	12380003	12380004	Human
407040010	GWAS688986_H	calcium measurement QTL GWAS688986 (human)		0.000008	calcium amount (VT:0010499)	blood calcium level (CMO:0000502)	10	12559440	12559441	Human
407052808	GWAS701784_H	age at assessment, pelvic organ prolapse QTL GWAS701784 (human)		0.000003	age at assessment, pelvic organ prolapse		10	12493378	12493379	Human
625829121	GWAS2250043_H	type 2 diabetes mellitus QTL GWAS2250043 (human)		0.000003	type 2 diabetes mellitus		10	12481698	12481699	Human
597142489	GWAS1238563_H	educational attainment QTL GWAS1238563 (human)		4e-15	educational attainment		10	12392743	12392744	Human
597142488	GWAS1238562_H	educational attainment QTL GWAS1238562 (human)		2e-18	educational attainment		10	12353101	12353102	Human
597612494	GWAS1669354_H	anaphylaxis QTL GWAS1669354 (human)		3e-11	anaphylaxis		10	12585681	12585682	Human
407121950	GWAS770926_H	mathematical ability QTL GWAS770926 (human)		1e-08	mathematical ability		10	12353101	12353102	Human
407121951	GWAS770927_H	mathematical ability QTL GWAS770927 (human)		3e-11	mathematical ability		10	12714714	12714715	Human
406997023	GWAS645999_H	intelligence QTL GWAS645999 (human)		0.000007	intelligence		10	12654563	12654564	Human
597109751	GWAS1205825_H	self reported educational attainment QTL GWAS1205825 (human)		3e-09	self reported educational attainment		10	12669950	12669951	Human
597600767	GWAS1657627_H	myo-inositol measurement QTL GWAS1657627 (human)		0.000008	myo-inositol measurement		10	12793228	12793229	Human
597109749	GWAS1205823_H	self reported educational attainment QTL GWAS1205823 (human)		1e-12	self reported educational attainment		10	12353101	12353102	Human
406929443	GWAS578419_H	smoking initiation QTL GWAS578419 (human)		1e-11	smoking initiation		10	12698083	12698084	Human
598082498	GWAS1801797_H	socioeconomic status QTL GWAS1801797 (human)		4e-09	socioeconomic status		10	12669950	12669951	Human
597109234	GWAS1205308_H	self reported educational attainment QTL GWAS1205308 (human)		3e-11	self reported educational attainment		10	12669950	12669951	Human
597109233	GWAS1205307_H	self reported educational attainment QTL GWAS1205307 (human)		9e-13	self reported educational attainment		10	12353101	12353102	Human
598082497	GWAS1801796_H	socioeconomic status QTL GWAS1801796 (human)		7e-09	socioeconomic status		10	12353101	12353102	Human
628719902	GWAS2628131_H	systemic lupus erythematosus QTL GWAS2628131 (human)		3e-08	systemic lupus erythematosus		10	12446137	12446138	Human
597102591	GWAS1198665_H	schizophrenia, intelligence, self reported educational attainment QTL GWAS1198665 (human)		2e-09	schizophrenia, intelligence, self reported educational attainment		10	12353101	12353102	Human
407277614	GWAS926590_H	body height QTL GWAS926590 (human)		5e-85	body height		10	12784034	12784035	Human
407277612	GWAS926588_H	body height QTL GWAS926588 (human)		1e-11	body height		10	12406089	12406090	Human
407277613	GWAS926589_H	body height QTL GWAS926589 (human)		9e-09	body height		10	12505385	12505386	Human
628649749	GWAS2557978_H	retinal nerve fibre layer thickness QTL GWAS2557978 (human)		0.000003	retinal nerve fibre layer thickness		10	12470320	12470321	Human
598058453	GWAS1777752_H	body height QTL GWAS1777752 (human)		5e-20	body height		10	12786454	12786455	Human
597165033	GWAS1261107_H	lipid measurement QTL GWAS1261107 (human)		0.000009	lipid measurement		10	12729681	12729682	Human
597234156	GWAS1330230_H	obstructive sleep apnea QTL GWAS1330230 (human)		0.000009	obstructive sleep apnea		10	12656440	12656441	Human
628381442	GWAS2301666_H	socioeconomic status QTL GWAS2301666 (human)		1e-08	socioeconomic status		10	12353101	12353102	Human
597034475	GWAS1130549_H	body height QTL GWAS1130549 (human)		5e-09	body height		10	12786454	12786455	Human
598064421	GWAS1783720_H	body height QTL GWAS1783720 (human)		9e-09	body height		10	12777038	12777039	Human
628747259	GWAS2655488_H	educational attainment QTL GWAS2655488 (human)		2e-08	educational attainment		10	12351489	12351490	Human
628628474	GWAS2536703_H	bipolar disorder QTL GWAS2536703 (human)		0.000006	bipolar disorder		10	12489159	12489160	Human
628415984	GWAS2324213_H	body height QTL GWAS2324213 (human)		5e-09	body height		10	12786454	12786455	Human
597025041	GWAS1121115_H	acute myeloid leukemia QTL GWAS1121115 (human)		0.0000005	acute myeloid leukemia		10	12814776	12814777	Human
628460016	GWAS2368245_H	mathematical ability QTL GWAS2368245 (human)		3e-11	cognitive behavior trait (VT:0010450)		10	12714714	12714715	Human
597025040	GWAS1121114_H	acute myeloid leukemia QTL GWAS1121114 (human)		1e-10	acute myeloid leukemia		10	12814776	12814777	Human
407041732	GWAS690708_H	asymmetrical dimethylarginine measurement, serum dimethylarginine measurement QTL GWAS690708 (human)		0.000009	asymmetrical dimethylarginine measurement, serum dimethylarginine measurement		10	12830881	12830882	Human
597355795	GWAS1451869_H	body height QTL GWAS1451869 (human)		1e-11	body height		10	12406089	12406090	Human
406920392	GWAS569368_H	systemic lupus erythematosus QTL GWAS569368 (human)		3e-08	systemic lupus erythematosus		10	12446137	12446138	Human
597311760	GWAS1407834_H	vaginal microbiome measurement QTL GWAS1407834 (human)		0.000007	vaginal microbiome measurement		10	12368456	12368457	Human
597355796	GWAS1451870_H	body height QTL GWAS1451870 (human)		9e-09	body height		10	12505385	12505386	Human
597355797	GWAS1451871_H	body height QTL GWAS1451871 (human)		5e-85	body height		10	12784034	12784035	Human
598064437	GWAS1783736_H	blood zinc amount QTL GWAS1783736 (human)		0.000002	blood zinc amount		10	12635615	12635616	Human
597252875	GWAS1348949_H	psychotic symptoms QTL GWAS1348949 (human)		0.000007	psychotic symptoms		10	12794764	12794765	Human
628824558	GWAS2732787_H	aseptic loosening, revision of total knee arthroplasty QTL GWAS2732787 (human)		0.0000001	aseptic loosening, revision of total knee arthroplasty		10	12491097	12491098	Human
406900949	GWAS549925_H	alpha-hydroxyisovalerate measurement QTL GWAS549925 (human)		0.0000003	alpha-hydroxyisovalerate measurement		10	12598073	12598074	Human
597092608	GWAS1188682_H	response to cyclophosphamide QTL GWAS1188682 (human)		0.0000009	response to cyclophosphamide		10	12455748	12455749	Human
628460015	GWAS2368244_H	mathematical ability QTL GWAS2368244 (human)		1e-08	cognitive behavior trait (VT:0010450)		10	12353101	12353102	Human
597025039	GWAS1121113_H	acute myeloid leukemia QTL GWAS1121113 (human)		0.0000003	acute myeloid leukemia		10	12649577	12649578	Human
628916198	GWAS2824427_H	trait in response to apixaban QTL GWAS2824427 (human)		0.000002	trait in response to apixaban		10	12747893	12747894	Human
628701157	GWAS2609386_H	vaginal microbiome measurement QTL GWAS2609386 (human)		0.000007	vaginal microbiome measurement		10	12368456	12368457	Human
407154392	GWAS803368_H	gut microbiome measurement QTL GWAS803368 (human)		0.000007	gut microbiome measurement		10	12538665	12538666	Human
407280344	GWAS929320_H	vaginal microbiome measurement QTL GWAS929320 (human)		0.000007	vaginal microbiome measurement		10	12368456	12368457	Human
407013085	GWAS662061_H	bone density QTL GWAS662061 (human)		8e-09	bone density		10	12463869	12463870	Human
407040743	GWAS689719_H	self reported educational attainment QTL GWAS689719 (human)		0.000001	self reported educational attainment		10	12389368	12389369	Human
407262435	GWAS911411_H	obstructive sleep apnea QTL GWAS911411 (human)		0.000009	obstructive sleep apnea		10	12656440	12656441	Human
597141309	GWAS1237383_H	alpha-hydroxyisovalerate measurement QTL GWAS1237383 (human)		0.0000003	alpha-hydroxyisovalerate measurement		10	12598073	12598074	Human
406907627	GWAS556603_H	bipolar disorder QTL GWAS556603 (human)		0.000006	bipolar disorder		10	12489159	12489160	Human
597112122	GWAS1208196_H	tea consumption measurement QTL GWAS1208196 (human)		0.000002	drinking behavior trait (VT:0001422)	drink intake measurement (CMO:0000771)	10	12631011	12631012	Human
406945519	GWAS594495_H	gut microbiome measurement QTL GWAS594495 (human)		0.000005	gut microbiome measurement		10	12397477	12397478	Human
628906450	GWAS2814679_H	labyrinthitis QTL GWAS2814679 (human)		9e-08	labyrinthitis		10	12479914	12479915	Human
406962417	GWAS611393_H	anorexia nervosa QTL GWAS611393 (human)		0.000006	anorexia nervosa		10	12660570	12660571	Human
626444770	GWAS2258703_H	frailty measurement QTL GWAS2258703 (human)		1e-09	frailty measurement		10	12643654	12643655	Human
597100322	GWAS1196396_H	gut microbiome measurement QTL GWAS1196396 (human)		0.000001	gut microbiome measurement		10	12478664	12478665	Human
597187886	GWAS1283960_H	age at initiation of smoking QTL GWAS1283960 (human)		7e-10	age at initiation of smoking		10	12703649	12703650	Human
598110481	GWAS1819364_H	oligodendroglioma QTL GWAS1819364 (human)		1e-08	oligodendroglioma		10	12406846	12406847	Human
407304957	GWAS953933_H	schizophrenia, intelligence, self reported educational attainment QTL GWAS953933 (human)		2e-09	schizophrenia, intelligence, self reported educational attainment		10	12353101	12353102	Human
407320827	GWAS969803_H	aseptic loosening, revision of total knee arthroplasty QTL GWAS969803 (human)		0.0000001	aseptic loosening, revision of total knee arthroplasty		10	12491097	12491098	Human
597603106	GWAS1659966_H	type 2 diabetes mellitus QTL GWAS1659966 (human)		5e-10	type 2 diabetes mellitus		10	12506711	12506712	Human
628653509	GWAS2561738_H	age at assessment, pelvic organ prolapse QTL GWAS2561738 (human)		0.000003	age at assessment, pelvic organ prolapse		10	12493378	12493379	Human
597129514	GWAS1225588_H	body height QTL GWAS1225588 (human)		5e-20	body height		10	12786454	12786455	Human
598071652	GWAS1790951_H	body height QTL GWAS1790951 (human)		3e-12	body height		10	12794840	12794841	Human
597058898	GWAS1154972_H	FEV/FVC ratio QTL GWAS1154972 (human)		2e-09	FEV/FVC ratio		10	12698083	12698084	Human
407197827	GWAS846803_H	cholate measurement QTL GWAS846803 (human)		0.000004	cholate measurement		10	12455771	12455772	Human
597080926	GWAS1177000_H	gut microbiome measurement QTL GWAS1177000 (human)		0.000005	gut microbiome measurement		10	12397477	12397478	Human
628644272	GWAS2552501_H	delivery measurement, gut microbiome measurement QTL GWAS2552501 (human)		4e-08	delivery measurement, gut microbiome measurement		10	12554670	12554671	Human
407380096	GWAS1029072_H	acute myeloid leukemia QTL GWAS1029072 (human)		1e-10	acute myeloid leukemia		10	12814776	12814777	Human
616388724	GWAS1868966_H	trait in response to apixaban QTL GWAS1868966 (human)		0.000002	trait in response to apixaban		10	12747893	12747894	Human
407380097	GWAS1029073_H	acute myeloid leukemia QTL GWAS1029073 (human)		0.0000005	acute myeloid leukemia		10	12814776	12814777	Human
406983311	GWAS632287_H	tea consumption measurement QTL GWAS632287 (human)		0.000002	tea consumption measurement		10	12631011	12631012	Human
597311306	GWAS1407380_H	vaginal microbiome measurement QTL GWAS1407380 (human)		0.000007	vaginal microbiome measurement		10	12418947	12418948	Human
406945938	GWAS594914_H	gut microbiome measurement QTL GWAS594914 (human)		0.000001	gut microbiome measurement		10	12394895	12394896	Human
628609441	GWAS2517670_H	lipid measurement QTL GWAS2517670 (human)		0.000002	lipid amount (VT:0001547)	blood lipid measurement (CMO:0000050)	10	12480145	12480146	Human
407163538	GWAS812514_H	color vision disorder QTL GWAS812514 (human)		0.0000001	color vision disorder		10	12789795	12789796	Human
628886439	GWAS2794668_H	tea consumption measurement QTL GWAS2794668 (human)		4e-09	drinking behavior trait (VT:0001422)	drink intake measurement (CMO:0000771)	10	12650903	12650904	Human
407017625	GWAS666601_H	body height QTL GWAS666601 (human)		5e-20	body height		10	12786454	12786455	Human
597195076	GWAS1291150_H	bone density QTL GWAS1291150 (human)		8e-09	bone density		10	12463869	12463870	Human
598071675	GWAS1790974_H	body height QTL GWAS1790974 (human)		2e-38	body height		10	12822395	12822396	Human
597323589	GWAS1419663_H	body height QTL GWAS1419663 (human)		0.0000003	body height		10	12782716	12782717	Human
407025315	GWAS674291_H	mitochondrial heteroplasmy measurement QTL GWAS674291 (human)		4e-08	mitochondrial heteroplasmy measurement		10	12656440	12656441	Human
407109282	GWAS758258_H	body height QTL GWAS758258 (human)		1e-12	body height		10	12778212	12778213	Human
597062515	GWAS1158589_H	Borderline personality disorder QTL GWAS1158589 (human)		0.000003	Borderline personality disorder		10	12623139	12623140	Human
407090859	GWAS739835_H	Headache QTL GWAS739835 (human)		5e-10	Headache		10	12684062	12684063	Human
407177388	GWAS826364_H	amblyopia QTL GWAS826364 (human)		0.000005	amblyopia		10	12440371	12440372	Human
628879250	GWAS2787479_H	insomnia QTL GWAS2787479 (human)		2e-09	sleep behavior trait (VT:0001501)		10	12714714	12714715	Human
597190004	GWAS1286078_H	age at assessment, pelvic organ prolapse QTL GWAS1286078 (human)		0.000003	age at assessment, pelvic organ prolapse		10	12493378	12493379	Human
628508550	GWAS2416779_H	Headache, HOMA-IR QTL GWAS2416779 (human)		1e-08	Headache, HOMA-IR	Homeostatic Model Assessment of Insulin Resistance (CMO:0003002)	10	12677221	12677222	Human
628653961	GWAS2562190_H	systemic lupus erythematosus QTL GWAS2562190 (human)		3e-08	systemic lupus erythematosus		10	12445997	12445998	Human
407178932	GWAS827908_H	FEV/FVC ratio QTL GWAS827908 (human)		2e-09	FEV/FVC ratio		10	12698083	12698084	Human
628508548	GWAS2416777_H	Headache, HOMA-B QTL GWAS2416777 (human)		8e-09	Headache, HOMA-B	Homeostatic Model Assessment of Beta cell function (CMO:0003211)	10	12677221	12677222	Human
597142371	GWAS1238445_H	educational attainment QTL GWAS1238445 (human)		4e-14	educational attainment		10	12698083	12698084	Human
597814614	GWAS1682005_H	asymmetrical dimethylarginine measurement QTL GWAS1682005 (human)		0.000009	asymmetrical dimethylarginine measurement		10	12830881	12830882	Human
407254852	GWAS903828_H	vaginal microbiome measurement QTL GWAS903828 (human)		0.000007	vaginal microbiome measurement		10	12418947	12418948	Human
597112478	GWAS1208552_H	type 2 diabetes mellitus QTL GWAS1208552 (human)		0.0000003	type 2 diabetes mellitus		10	12555882	12555883	Human
407251276	GWAS900252_H	type 2 diabetes mellitus QTL GWAS900252 (human)		0.0000003	type 2 diabetes mellitus		10	12555882	12555883	Human
625829981	GWAS2250903_H	labyrinthitis QTL GWAS2250903 (human)		9e-08	labyrinthitis		10	12479914	12479915	Human
628428389	GWAS2336618_H	intelligence QTL GWAS2336618 (human)		0.000007	intelligence		10	12654563	12654564	Human
407130961	GWAS779937_H	response to cyclophosphamide QTL GWAS779937 (human)		0.0000009	response to cyclophosphamide		10	12455748	12455749	Human
628778095	GWAS2686324_H	psychotic symptoms QTL GWAS2686324 (human)		0.000007	psychotic symptoms		10	12794764	12794765	Human
628885605	GWAS2793834_H	educational attainment QTL GWAS2793834 (human)		2e-18	educational attainment		10	12353101	12353102	Human
597030028	GWAS1126102_H	coronary aneurysm QTL GWAS1126102 (human)		0.000005	coronary aneurysm		10	12603942	12603943	Human
628885606	GWAS2793835_H	educational attainment QTL GWAS2793835 (human)		4e-15	educational attainment		10	12392743	12392744	Human
628453481	GWAS2361710_H	self reported educational attainment QTL GWAS2361710 (human)		9e-13	self reported educational attainment		10	12353101	12353102	Human
628867687	GWAS2775916_H	alpha-hydroxyisovalerate measurement QTL GWAS2775916 (human)		0.0000003	alpha-hydroxyisovalerate measurement		10	12598073	12598074	Human
628453482	GWAS2361711_H	self reported educational attainment QTL GWAS2361711 (human)		3e-11	self reported educational attainment		10	12669950	12669951	Human
407056227	GWAS705203_H	self reported educational attainment QTL GWAS705203 (human)		1e-12	self reported educational attainment		10	12353101	12353102	Human
407212389	GWAS861365_H	body height QTL GWAS861365 (human)		0.0000003	body height		10	12782716	12782717	Human
616354718	GWAS1839433_H	gut microbiome measurement, environmental exposure measurement QTL GWAS1839433 (human)		3e-08	gut microbiome measurement, environmental exposure measurement		10	12659847	12659848	Human
616360863	GWAS1845578_H	gut microbiome measurement, tobacco smoke exposure measurement QTL GWAS1845578 (human)		0.000004	gut microbiome measurement, tobacco smoke exposure measurement		10	12467477	12467478	Human
597202620	GWAS1298694_H	body height QTL GWAS1298694 (human)		2e-09	body height		10	12784034	12784035	Human
407029095	GWAS678071_H	respiratory quotient QTL GWAS678071 (human)		0.0000006	respiration trait (VT:0001943)		10	12393380	12393381	Human
407198560	GWAS847536_H	lipid measurement QTL GWAS847536 (human)		0.000002	lipid measurement		10	12480145	12480146	Human
628727388	GWAS2635617_H	frailty measurement QTL GWAS2635617 (human)		1e-09	frailty measurement		10	12643654	12643655	Human
407056228	GWAS705204_H	self reported educational attainment QTL GWAS705204 (human)		3e-09	self reported educational attainment		10	12669950	12669951	Human
406993258	GWAS642234_H	age at initiation of smoking QTL GWAS642234 (human)		7e-10	age at initiation of smoking		10	12703649	12703650	Human
597354674	GWAS1450748_H	body height QTL GWAS1450748 (human)		3e-12	body height		10	12794840	12794841	Human
597354675	GWAS1450749_H	body height QTL GWAS1450749 (human)		2e-38	body height		10	12822395	12822396	Human
616373142	GWAS1853384_H	obsolete_blood copper measurement QTL GWAS1853384 (human)		0.000004	obsolete_blood copper measurement		10	12602815	12602816	Human
628521563	GWAS2429792_H	age of onset of Parkinson disease QTL GWAS2429792 (human)		0.000005	age of onset of Parkinson disease		10	12364534	12364535	Human
628484186	GWAS2392415_H	coronary aneurysm QTL GWAS2392415 (human)		0.000005	coronary artery integrity trait (VT:0010746)		10	12603942	12603943	Human
407191402	GWAS840378_H	blood zinc measurement QTL GWAS840378 (human)		0.000002	blood zinc measurement		10	12635615	12635616	Human
407142772	GWAS791748_H	coronary aneurysm QTL GWAS791748 (human)		0.000005	coronary aneurysm		10	12603942	12603943	Human
406943090	GWAS592066_H	trait in response to thiazide, QT interval QTL GWAS592066 (human)		0.000006	trait in response to thiazide, QT interval		10	12633062	12633063	Human
628427328	GWAS2335557_H	household income QTL GWAS2335557 (human)		5e-09	household income		10	12650578	12650579	Human
616361353	GWAS1846068_H	gut microbiome measurement, breastfeeding duration QTL GWAS1846068 (human)		2e-08	gut microbiome measurement, breastfeeding duration		10	12659847	12659848	Human
597040803	GWAS1136877_H	body height QTL GWAS1136877 (human)		1e-12	body height		10	12778212	12778213	Human
616527240	GWAS1923823_H	IGF-1 measurement QTL GWAS1923823 (human)		1e-11	IGF-1 measurement		10	12417774	12417775	Human
616490377	GWAS1886960_H	blood copper level QTL GWAS1886960 (human)		0.000004	blood copper level		10	12602815	12602816	Human
407192956	GWAS841932_H	psychotic symptoms QTL GWAS841932 (human)		0.000007	psychotic symptoms		10	12794764	12794765	Human
628531276	GWAS2439505_H	IGF-1 measurement QTL GWAS2439505 (human)		1e-11	IGF-1 measurement	blood insulin-like growth factor 1 level (CMO:0001297)	10	12417774	12417775	Human
597189282	GWAS1285356_H	systemic lupus erythematosus QTL GWAS1285356 (human)		3e-08	systemic lupus erythematosus		10	12445997	12445998	Human
407291770	GWAS940746_H	body height QTL GWAS940746 (human)		3e-12	body height		10	12794840	12794841	Human
407291771	GWAS940747_H	body height QTL GWAS940747 (human)		2e-38	body height		10	12822395	12822396	Human
597294297	GWAS1390371_H	aseptic loosening, revision of total knee arthroplasty QTL GWAS1390371 (human)		0.0000001	aseptic loosening, revision of total knee arthroplasty		10	12491097	12491098	Human
407027463	GWAS676439_H	body composition measurement QTL GWAS676439 (human)		0.000001	body mass (VT:0001259)		10	12396784	12396785	Human
628753469	GWAS2661698_H	oligodendroglioma QTL GWAS2661698 (human)		1e-08	oligodendroglioma		10	12406846	12406847	Human
597185233	GWAS1281307_H	mitochondrial heteroplasmy measurement QTL GWAS1281307 (human)		4e-08	mitochondrial heteroplasmy measurement		10	12656440	12656441	Human
407362318	GWAS1011294_H	insomnia QTL GWAS1011294 (human)		2e-09	insomnia		10	12714714	12714715	Human
407316749	GWAS965725_H	tea consumption measurement QTL GWAS965725 (human)		4e-09	tea consumption measurement		10	12650903	12650904	Human
597160156	GWAS1256230_H	lipid measurement QTL GWAS1256230 (human)		0.000002	lipid measurement		10	12480145	12480146	Human
406970122	GWAS619098_H	trait in response to efavirenz, virologic response measurement QTL GWAS619098 (human)		0.000008	trait in response to efavirenz, virologic response measurement		10	12707063	12707064	Human
597162201	GWAS1258275_H	paraxanthine measurement QTL GWAS1258275 (human)		0.000006	paraxanthine measurement		10	12502853	12502854	Human
598081258	GWAS1800557_H	socioeconomic status QTL GWAS1800557 (human)		7e-09	socioeconomic status		10	12672270	12672271	Human
596977351	GWAS1096870_H	body height QTL GWAS1096870 (human)		9e-09	body height		10	12777038	12777039	Human
597160142	GWAS1256216_H	cholate measurement QTL GWAS1256216 (human)		0.000004	cholate measurement		10	12455771	12455772	Human
597620423	GWAS1677283_H	Meniere disease QTL GWAS1677283 (human)		3e-11	Meniere disease		10	12658341	12658342	Human
598058751	GWAS1778050_H	body height QTL GWAS1778050 (human)		2e-09	body height		10	12784034	12784035	Human
597293252	GWAS1389326_H	blood copper measurement QTL GWAS1389326 (human)		0.000004	blood copper measurement		10	12602815	12602816	Human
597184199	GWAS1280273_H	migraine disorder, Headache QTL GWAS1280273 (human)		7e-09	migraine disorder, Headache		10	12650903	12650904	Human
598143175	GWAS1829903_H	bone tissue density QTL GWAS1829903 (human)		8e-09	bone tissue density		10	12463869	12463870	Human
407051552	GWAS700528_H	lung disease severity measurement QTL GWAS700528 (human)		0.0000007	lung disease severity measurement		10	12371661	12371662	Human
406930215	GWAS579191_H	educational attainment QTL GWAS579191 (human)		4e-14	educational attainment		10	12698083	12698084	Human
597072121	GWAS1168195_H	Headache QTL GWAS1168195 (human)		5e-10	Headache		10	12684062	12684063	Human
628794378	GWAS2702607_H	age at initiation of smoking QTL GWAS2702607 (human)		7e-10	age at initiation of smoking		10	12703649	12703650	Human
406977843	GWAS626819_H	gut microbiome measurement QTL GWAS626819 (human)		0.000001	gut microbiome measurement		10	12478664	12478665	Human
597278445	GWAS1374519_H	tea consumption measurement QTL GWAS1374519 (human)		4e-09	tea consumption measurement		10	12650903	12650904	Human
628751872	GWAS2660101_H	dementia QTL GWAS2660101 (human)		0.000005	dementia		10	12381745	12381746	Human
628414989	GWAS2323218_H	gut microbiome measurement QTL GWAS2323218 (human)		0.000007	gut microbiome measurement		10	12538665	12538666	Human
616494530	GWAS1891113_H	quinolinate measurement QTL GWAS1891113 (human)		0.000009	quinolinate measurement		10	12559097	12559098	Human
628909569	GWAS2817798_H	body height QTL GWAS2817798 (human)		2e-09	body height		10	12784034	12784035	Human
628641287	GWAS2549516_H	gut microbiome measurement, breastfeeding duration QTL GWAS2549516 (human)		2e-08	lactation duration (VT:1000653)		10	12659847	12659848	Human
617101129	GWAS2118628_H	IGF-1 measurement QTL GWAS2118628 (human)		1e-11	IGF-1 measurement		10	12417774	12417775	Human
598041638	GWAS1760937_H	retinal nerve fibre layer thickness QTL GWAS1760937 (human)		0.000003	retinal nerve fibre layer thickness		10	12470320	12470321	Human
407134144	GWAS783120_H	3-hydroxy-1-methylpropylmercapturic acid measurement QTL GWAS783120 (human)		0.0000004	3-hydroxy-1-methylpropylmercapturic acid measurement		10	12440908	12440909	Human
628399344	GWAS2307573_H	body height QTL GWAS2307573 (human)		5e-85	body height		10	12784034	12784035	Human
628825854	GWAS2734083_H	blood copper level QTL GWAS2734083 (human)		0.000004	blood copper level		10	12602815	12602816	Human
596951070	GWAS1070589_H	dementia QTL GWAS1070589 (human)		0.000005	dementia		10	12381745	12381746	Human
628760310	GWAS2668539_H	mitochondrial heteroplasmy measurement QTL GWAS2668539 (human)		4e-08	mitochondrial heteroplasmy measurement		10	12656440	12656441	Human
597298197	GWAS1394271_H	blood zinc measurement QTL GWAS1394271 (human)		0.000002	blood zinc measurement		10	12635615	12635616	Human
597296138	GWAS1392212_H	body height QTL GWAS1392212 (human)		9e-09	body height		10	12777038	12777039	Human
628655341	GWAS2563570_H	color vision disorder QTL GWAS2563570 (human)		0.0000001	color vision disorder		10	12789795	12789796	Human
407111644	GWAS760620_H	self reported educational attainment QTL GWAS760620 (human)		9e-13	self reported educational attainment		10	12353101	12353102	Human
597261313	GWAS1357387_H	dementia QTL GWAS1357387 (human)		0.000005	dementia		10	12381745	12381746	Human
407111645	GWAS760621_H	self reported educational attainment QTL GWAS760621 (human)		3e-11	self reported educational attainment		10	12669950	12669951	Human
628399342	GWAS2307571_H	body height QTL GWAS2307571 (human)		1e-11	body height		10	12406089	12406090	Human
628399343	GWAS2307572_H	body height QTL GWAS2307572 (human)		9e-09	body height		10	12505385	12505386	Human
407017948	GWAS666924_H	body height QTL GWAS666924 (human)		2e-09	body height		10	12784034	12784035	Human
628722393	GWAS2630622_H	vaginal microbiome measurement QTL GWAS2630622 (human)		0.000007	vaginal microbiome measurement		10	12418947	12418948	Human
628476629	GWAS2384858_H	self reported educational attainment QTL GWAS2384858 (human)		3e-09	self reported educational attainment		10	12669950	12669951	Human
628476628	GWAS2384857_H	self reported educational attainment QTL GWAS2384857 (human)		1e-12	self reported educational attainment		10	12353101	12353102	Human
406944739	GWAS593715_H	gut microbiome measurement QTL GWAS593715 (human)		0.000002	gut microbiome measurement		10	12489287	12489288	Human
597205564	GWAS1301638_H	frontal fibrosing alopecia QTL GWAS1301638 (human)		0.000005	frontal fibrosing alopecia		10	12462314	12462315	Human
406991334	GWAS640310_H	migraine disorder, Headache QTL GWAS640310 (human)		7e-09	migraine disorder, Headache		10	12650903	12650904	Human
628647647	GWAS2555876_H	gut microbiome measurement, environmental exposure measurement QTL GWAS2555876 (human)		3e-08	gut microbiome measurement, environmental exposure measurement		10	12659847	12659848	Human
407194093	GWAS843069_H	paraxanthine measurement QTL GWAS843069 (human)		0.000006	paraxanthine measurement		10	12502853	12502854	Human
628913876	GWAS2822105_H	body height QTL GWAS2822105 (human)		5e-20	body height		10	12786454	12786455	Human
597275691	GWAS1371765_H	insomnia QTL GWAS1371765 (human)		2e-09	insomnia		10	12714714	12714715	Human
598005265	GWAS1724564_H	body height QTL GWAS1724564 (human)		5e-09	body height		10	12786454	12786455	Human
597214254	GWAS1310328_H	mathematical ability QTL GWAS1310328 (human)		1e-08	mathematical ability		10	12353101	12353102	Human
597214255	GWAS1310329_H	mathematical ability QTL GWAS1310329 (human)		3e-11	mathematical ability		10	12714714	12714715	Human
407196668	GWAS845644_H	educational attainment QTL GWAS845644 (human)		2e-08	educational attainment		10	12351489	12351490	Human
407056890	GWAS705866_H	systemic lupus erythematosus QTL GWAS705866 (human)		3e-08	systemic lupus erythematosus		10	12445997	12445998	Human
628829378	GWAS2737607_H	body height QTL GWAS2737607 (human)		9e-09	body height		10	12777038	12777039	Human
407185919	GWAS834895_H	lipid measurement QTL GWAS834895 (human)		0.000009	lipid measurement		10	12729681	12729682	Human
407271932	GWAS920908_H	migraine disorder, endometriosis QTL GWAS920908 (human)		0.000001	uterus integrity trait (VT:0010575)		10	12814058	12814059	Human
406944762	GWAS593738_H	gut microbiome measurement QTL GWAS593738 (human)		0.000004	gut microbiome measurement		10	12489287	12489288	Human
628609227	GWAS2517456_H	cholate measurement QTL GWAS2517456 (human)		0.000004	cholate measurement		10	12455771	12455772	Human
616358780	GWAS1843495_H	delivery measurement, gut microbiome measurement QTL GWAS1843495 (human)		4e-08	delivery measurement, gut microbiome measurement		10	12554670	12554671	Human
625815692	GWAS2236614_H	body height QTL GWAS2236614 (human)		1e-08	body height		10	12777038	12777039	Human
597191770	GWAS1287844_H	lung disease severity measurement QTL GWAS1287844 (human)		0.0000007	lung integrity trait (VT:0010906)		10	12371661	12371662	Human
628987071	GWAS2895300_H	Meniere disease QTL GWAS2895300 (human)		3e-11	Meniere disease		10	12658341	12658342	Human
626449042	GWAS2262975_H	treatment-resistant hypertension QTL GWAS2262975 (human)		0.000005	treatment-resistant hypertension		10	12820778	12820779	Human
597082195	GWAS1178269_H	gut microbiome measurement QTL GWAS1178269 (human)		0.000002	gut microbiome measurement		10	12489287	12489288	Human
597082719	GWAS1178793_H	gut microbiome measurement QTL GWAS1178793 (human)		0.000001	gut microbiome measurement		10	12394895	12394896	Human
407174543	GWAS823519_H	Headache, HOMA-IR QTL GWAS823519 (human)		1e-08	Headache, HOMA-IR		10	12677221	12677222	Human
628907187	GWAS2815416_H	type 2 diabetes mellitus QTL GWAS2815416 (human)		0.000003	type 2 diabetes mellitus		10	12481698	12481699	Human
598077556	GWAS1796855_H	bone density QTL GWAS1796855 (human)		8e-09	bone density		10	12463869	12463870	Human
407053719	GWAS702695_H	household income QTL GWAS702695 (human)		5e-09	household income		10	12650578	12650579	Human
628612771	GWAS2521000_H	body height QTL GWAS2521000 (human)		1e-08	body height		10	12777038	12777039	Human
628848301	GWAS2756530_H	smoking initiation QTL GWAS2756530 (human)		1e-11	behavior trait (VT:0010442)		10	12698083	12698084	Human
628636835	GWAS2545064_H	gut microbiome measurement, tobacco smoke exposure measurement QTL GWAS2545064 (human)		0.000004	gut microbiome measurement, tobacco smoke exposure measurement		10	12467477	12467478	Human
628625573	GWAS2533802_H	FEV/FVC ratio QTL GWAS2533802 (human)		2e-09	lung capacity (VT:0001942)	forced expiratory volume to forced vital capacity ratio (CMO:0000241)	10	12698083	12698084	Human
597032565	GWAS1128639_H	bipolar disorder QTL GWAS1128639 (human)		0.000006	bipolar disorder		10	12489159	12489160	Human
407189922	GWAS838898_H	blood copper measurement QTL GWAS838898 (human)		0.000004	blood copper measurement		10	12602815	12602816	Human
628836502	GWAS2744731_H	paraxanthine measurement QTL GWAS2744731 (human)		0.000006	paraxanthine measurement		10	12502853	12502854	Human
628472472	GWAS2380701_H	obstructive sleep apnea QTL GWAS2380701 (human)		0.000009	obstructive sleep apnea		10	12656440	12656441	Human
628876949	GWAS2785178_H	migraine disorder, Headache QTL GWAS2785178 (human)		7e-09	migraine disorder, Headache		10	12650903	12650904	Human
597094009	GWAS1190083_H	3-hydroxy-1-methylpropylmercapturic acid measurement QTL GWAS1190083 (human)		0.0000004	3-hydroxy-1-methylpropylmercapturic acid measurement		10	12440908	12440909	Human
628984466	GWAS2892695_H	anaphylaxis QTL GWAS2892695 (human)		3e-11	anaphylaxis		10	12585681	12585682	Human
628555399	GWAS2463628_H	body height QTL GWAS2463628 (human)		0.0000003	body height		10	12782716	12782717	Human
406930867	GWAS579843_H	educational attainment QTL GWAS579843 (human)		2e-18	educational attainment		10	12353101	12353102	Human
407174070	GWAS823046_H	Headache, HOMA-B QTL GWAS823046 (human)		8e-09	Headache, HOMA-B		10	12677221	12677222	Human
597081698	GWAS1177772_H	gut microbiome measurement QTL GWAS1177772 (human)		0.000004	gut microbiome measurement		10	12489287	12489288	Human
598053969	GWAS1773268_H	body height QTL GWAS1773268 (human)		9e-09	body height		10	12505385	12505386	Human
597345390	GWAS1441464_H	color vision disorder QTL GWAS1441464 (human)		0.0000001	color vision disorder		10	12789795	12789796	Human
598053970	GWAS1773269_H	body height QTL GWAS1773269 (human)		5e-85	body height		10	12784034	12784035	Human
628905092	GWAS2813321_H	Alzheimer disease, family history of Alzheimer’s disease QTL GWAS2813321 (human)		8e-09	Alzheimer disease, family history of Alzheimer’s disease		10	12380003	12380004	Human
406930872	GWAS579848_H	educational attainment QTL GWAS579848 (human)		4e-15	educational attainment		10	12392743	12392744	Human
628825222	GWAS2733451_H	blood zinc amount QTL GWAS2733451 (human)		0.000002	blood zinc amount		10	12635615	12635616	Human
597329511	GWAS1425585_H	Headache, HOMA-IR QTL GWAS1425585 (human)		1e-08	Headache, HOMA-IR		10	12677221	12677222	Human
597329509	GWAS1425583_H	Headache, HOMA-B QTL GWAS1425583 (human)		8e-09	Headache, HOMA-B		10	12677221	12677222	Human

Markers in Region

D10S2325

Human Assembly	Chr	Position (strand)	Source
Cytogenetic Map	10	p13	UniSTS
HuRef	10	12,706,205 - 12,706,347	UniSTS
Marshfield Genetic Map	10	32.8	UniSTS
Marshfield Genetic Map	10	32.8	RGD
deCODE Assembly Map	10	31.07	UniSTS

D10S1705

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	10	12,589,545 - 12,589,746	UniSTS	GRCh37
Build 36	10	12,629,551 - 12,629,752	RGD	NCBI36
Celera	10	12,516,215 - 12,516,416	RGD
Cytogenetic Map	10	p13	UniSTS
HuRef	10	12,503,256 - 12,503,457	UniSTS
Marshfield Genetic Map	10	32.8	RGD
Marshfield Genetic Map	10	32.8	UniSTS
Genethon Genetic Map	10	32.0	UniSTS
TNG Radiation Hybrid Map	10	6712.0	UniSTS
GeneMap99-GB4 RH Map	10	95.14	UniSTS
Whitehead-YAC Contig Map	10		UniSTS

D10S1430

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	10	12,736,989 - 12,737,134	UniSTS	GRCh37
Build 36	10	12,776,995 - 12,777,140	RGD	NCBI36
Celera	10	12,663,474 - 12,663,635	RGD
Cytogenetic Map	10	p13	UniSTS
Cytogenetic Map	10	p	UniSTS
HuRef	10	12,650,207 - 12,650,368	UniSTS
Marshfield Genetic Map	10	33.18	RGD
Marshfield Genetic Map	10	33.18	UniSTS
deCODE Assembly Map	10	31.07	UniSTS
Whitehead-YAC Contig Map	10		UniSTS

GDB:315097

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	10	12,547,736 - 12,547,985	UniSTS	GRCh37
Build 36	10	12,587,742 - 12,587,991	RGD	NCBI36
Celera	10	12,476,917 - 12,477,166	RGD
Cytogenetic Map	10	p13	UniSTS
HuRef	10	12,464,044 - 12,464,293	UniSTS

D10S2365

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	10	12,791,151 - 12,791,388	UniSTS	GRCh37
Build 36	10	12,831,157 - 12,831,394	RGD	NCBI36
Celera	10	12,717,619 - 12,717,856	RGD
Cytogenetic Map	10	p13	UniSTS
HuRef	10	12,704,359 - 12,704,596	UniSTS
Stanford-G3 RH Map	10	586.0	UniSTS
GeneMap99-G3 RH Map	10	586.0	UniSTS

SHGC-32225

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	10	12,425,918 - 12,426,067	UniSTS	GRCh37
Build 36	10	12,465,924 - 12,466,073	RGD	NCBI36
Celera	10	12,355,087 - 12,355,236	RGD
Cytogenetic Map	10	p13	UniSTS
HuRef	10	12,342,209 - 12,342,358	UniSTS
GeneMap99-GB4 RH Map	10	95.04	UniSTS
Whitehead-RH Map	10	87.1	UniSTS
NCBI RH Map	10	187.1	UniSTS
GeneMap99-G3 RH Map	10	586.0	UniSTS

SHGC-79342

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	10	12,549,423 - 12,549,757	UniSTS	GRCh37
Build 36	10	12,589,429 - 12,589,763	RGD	NCBI36
Celera	10	12,478,604 - 12,478,938	RGD
Cytogenetic Map	10	p13	UniSTS
HuRef	10	12,465,731 - 12,466,065	UniSTS
TNG Radiation Hybrid Map	10	6683.0	UniSTS

SHGC-84721

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	10	12,864,711 - 12,864,902	UniSTS	GRCh37
Build 36	10	12,904,717 - 12,904,908	RGD	NCBI36
Celera	10	12,790,515 - 12,790,706	RGD
Cytogenetic Map	10	p13	UniSTS
HuRef	10	12,777,389 - 12,777,580	UniSTS
TNG Radiation Hybrid Map	10	6899.0	UniSTS

D10S236E

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	10	12,651,881 - 12,651,970	UniSTS	GRCh37
GRCh37	10	12,651,810 - 12,651,989	UniSTS	GRCh37
GRCh37	10	12,651,892 - 12,651,996	UniSTS	GRCh37
Build 36	10	12,691,898 - 12,692,002	RGD	NCBI36
Celera	10	12,578,174 - 12,578,263	UniSTS
Celera	10	12,578,103 - 12,578,282	UniSTS
Celera	10	12,578,185 - 12,578,289	RGD
Cytogenetic Map	10	p13	UniSTS
HuRef	10	12,565,271 - 12,565,360	UniSTS
HuRef	10	12,565,282 - 12,565,386	UniSTS
HuRef	10	12,565,200 - 12,565,379	UniSTS
TNG Radiation Hybrid Map	10	6746.0	UniSTS
Stanford-G3 RH Map	10	582.0	UniSTS
NCBI RH Map	10	194.9	UniSTS
GeneMap99-G3 RH Map	10	582.0	UniSTS

SHGC-132068

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	10	12,791,109 - 12,791,398	UniSTS	GRCh37
Build 36	10	12,831,115 - 12,831,404	RGD	NCBI36
Celera	10	12,717,577 - 12,717,866	RGD
Cytogenetic Map	10	p13	UniSTS
HuRef	10	12,704,317 - 12,704,606	UniSTS
TNG Radiation Hybrid Map	10	6855.0	UniSTS

SHGC-146855

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	10	12,393,047 - 12,393,362	UniSTS	GRCh37
Build 36	10	12,433,053 - 12,433,368	RGD	NCBI36
Celera	10	12,322,219 - 12,322,534	RGD
Cytogenetic Map	10	p13	UniSTS
HuRef	10	12,309,248 - 12,309,563	UniSTS
TNG Radiation Hybrid Map	10	63651.0	UniSTS

SHGC-148366

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	10	12,754,991 - 12,755,320	UniSTS	GRCh37
Build 36	10	12,794,997 - 12,795,326	RGD	NCBI36
Celera	10	12,681,497 - 12,681,826	RGD
Cytogenetic Map	10	p13	UniSTS
HuRef	10	12,668,231 - 12,668,560	UniSTS
TNG Radiation Hybrid Map	10	6841.0	UniSTS

SHGC-149390

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	10	12,820,886 - 12,821,199	UniSTS	GRCh37
Build 36	10	12,860,892 - 12,861,205	RGD	NCBI36
Celera	10	12,746,716 - 12,747,029	RGD
Cytogenetic Map	10	p13	UniSTS
HuRef	10	12,733,795 - 12,734,108	UniSTS
TNG Radiation Hybrid Map	10	6869.0	UniSTS

G17442

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	10	12,821,330 - 12,821,432	UniSTS	GRCh37
Build 36	10	12,861,336 - 12,861,438	RGD	NCBI36
Celera	10	12,747,160 - 12,747,262	RGD
Cytogenetic Map	10	p13	UniSTS
HuRef	10	12,734,239 - 12,734,341	UniSTS

SHGC-153341

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	10	12,640,772 - 12,641,119	UniSTS	GRCh37
Build 36	10	12,680,778 - 12,681,125	RGD	NCBI36
Celera	10	12,567,067 - 12,567,414	RGD
Cytogenetic Map	10	p13	UniSTS
HuRef	10	12,554,129 - 12,554,476	UniSTS
TNG Radiation Hybrid Map	10	6782.0	UniSTS

SHGC-141926

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	10	12,749,350 - 12,749,669	UniSTS	GRCh37
Build 36	10	12,789,356 - 12,789,675	RGD	NCBI36
Celera	10	12,675,856 - 12,676,175	RGD
Cytogenetic Map	10	p13	UniSTS
HuRef	10	12,662,590 - 12,662,909	UniSTS
TNG Radiation Hybrid Map	10	6834.0	UniSTS

SHGC-6785

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	10	12,602,662 - 12,602,797	UniSTS	GRCh37
Build 36	10	12,642,668 - 12,642,803	RGD	NCBI36
Celera	10	12,528,949 - 12,529,084	RGD
Cytogenetic Map	10	p13	UniSTS
HuRef	10	12,515,992 - 12,516,127	UniSTS

RH47896

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	10	12,744,093 - 12,744,218	UniSTS	GRCh37
Build 36	10	12,784,099 - 12,784,224	RGD	NCBI36
Celera	10	12,670,600 - 12,670,725	RGD
Cytogenetic Map	10	p13	UniSTS
HuRef	10	12,657,334 - 12,657,459	UniSTS
GeneMap99-GB4 RH Map	10	95.14	UniSTS
NCBI RH Map	10	202.5	UniSTS

D11S2560

Human Assembly	Chr	Position (strand)	Source
Cytogenetic Map	10	p12.1-p11.2	UniSTS
Cytogenetic Map	22	q13.1	UniSTS
Cytogenetic Map	12	p13.3	UniSTS
Cytogenetic Map	20	q13.3	UniSTS
Cytogenetic Map	19	p13.12	UniSTS
Cytogenetic Map	8	q21.13	UniSTS
Cytogenetic Map	18	p11.22	UniSTS
Cytogenetic Map	9	p13.3-p12	UniSTS
Cytogenetic Map	10	p12.1	UniSTS
Cytogenetic Map	19	q13.11	UniSTS
Cytogenetic Map	22	q11.23	UniSTS
Cytogenetic Map	5	q23.3	UniSTS
Cytogenetic Map	15	q21.1	UniSTS
Cytogenetic Map	14	q24.2	UniSTS
Cytogenetic Map	15	q13	UniSTS
Cytogenetic Map	6	q25.3	UniSTS
Cytogenetic Map	8	p22-p21	UniSTS
Cytogenetic Map	1	p34.1	UniSTS
Cytogenetic Map	4	p16.3	UniSTS
Cytogenetic Map	17	q12	UniSTS
Cytogenetic Map	15	q21.3	UniSTS
Cytogenetic Map	12	q24.31	UniSTS
Cytogenetic Map	2	p13.1	UniSTS
Cytogenetic Map	19	q13.12	UniSTS
Cytogenetic Map	10	q24.2	UniSTS
Cytogenetic Map	2	p23.3	UniSTS
Cytogenetic Map	19	q13.42	UniSTS
Cytogenetic Map	6	q16.2	UniSTS
Cytogenetic Map	X	q26.3	UniSTS
Cytogenetic Map	9	q22.33	UniSTS
Cytogenetic Map	7	q21.2	UniSTS
Cytogenetic Map	16	p11.2	UniSTS
Cytogenetic Map	8	q24.13	UniSTS
Cytogenetic Map	4	q25	UniSTS
Cytogenetic Map	12	p13.33	UniSTS
Cytogenetic Map	19	p13.3	UniSTS
Cytogenetic Map	5	q23	UniSTS
Cytogenetic Map	16	p13.3	UniSTS
Cytogenetic Map	1	q32.1	UniSTS
Cytogenetic Map	3	p21.2	UniSTS
Cytogenetic Map	19	q13.32	UniSTS
Cytogenetic Map	1	p13.2	UniSTS
Cytogenetic Map	6	q27	UniSTS
Cytogenetic Map	2	p13.3	UniSTS
Cytogenetic Map	2	p25.1	UniSTS
Cytogenetic Map	16	q24.1	UniSTS
Cytogenetic Map	7	q22.1	UniSTS
Cytogenetic Map	22	q11.21	UniSTS
Cytogenetic Map	17	q21.31	UniSTS
Cytogenetic Map	2	q12.1	UniSTS
Cytogenetic Map	9	q13-q21	UniSTS
Cytogenetic Map	19	p12	UniSTS
Cytogenetic Map	2	p15	UniSTS
Cytogenetic Map	8	q11.21	UniSTS
Cytogenetic Map	15	q15	UniSTS
Cytogenetic Map	1	p36.21	UniSTS
Cytogenetic Map	12	q23-q24.1	UniSTS
Cytogenetic Map	1	p34.2	UniSTS
Cytogenetic Map	10	q23.2	UniSTS
Cytogenetic Map	3	q23	UniSTS
Cytogenetic Map	19	p13.2	UniSTS
Cytogenetic Map	15	q21	UniSTS
Cytogenetic Map	9	q34.2	UniSTS
Cytogenetic Map	17	q25.1	UniSTS
Cytogenetic Map	2	q35	UniSTS
Cytogenetic Map	6	p21.1	UniSTS
Cytogenetic Map	22	q12.2	UniSTS
Cytogenetic Map	1	p32	UniSTS
Cytogenetic Map	1	p35.1	UniSTS
Cytogenetic Map	7	p15.2	UniSTS
Cytogenetic Map	12	p13.2	UniSTS
Cytogenetic Map	16	q12.2	UniSTS
Cytogenetic Map	3	q26.2-q27	UniSTS
Cytogenetic Map	2	p21	UniSTS
Cytogenetic Map	8	p23.1	UniSTS
Cytogenetic Map	17	p11.2	UniSTS
Cytogenetic Map	X	p11.2	UniSTS
Cytogenetic Map	20	q11.2	UniSTS
Cytogenetic Map	3	q26.2	UniSTS
Cytogenetic Map	4	q22.1	UniSTS
Cytogenetic Map	4	p15.32	UniSTS
Cytogenetic Map	7	q36.3	UniSTS
Cytogenetic Map	2	q33.2	UniSTS
Cytogenetic Map	20	q13.13	UniSTS
Cytogenetic Map	10	p13	UniSTS
Cytogenetic Map	19	q13.4	UniSTS
Cytogenetic Map	1	p36.11-p34.2	UniSTS
Cytogenetic Map	1	q21.3	UniSTS
Cytogenetic Map	8	p21.3	UniSTS
Cytogenetic Map	18	p11.32	UniSTS
Cytogenetic Map	17	p13.2	UniSTS
Cytogenetic Map	8	q22.1	UniSTS
Cytogenetic Map	16	q22.1	UniSTS
Cytogenetic Map	3	p21	UniSTS
Cytogenetic Map	14	q13.2	UniSTS
Cytogenetic Map	8	q12.1	UniSTS
Cytogenetic Map	3	p22.3	UniSTS
Cytogenetic Map	8	q24.3	UniSTS
Cytogenetic Map	13	q12.11	UniSTS
Cytogenetic Map	12	p12	UniSTS
Cytogenetic Map	22	q13.33	UniSTS
Cytogenetic Map	14	q31.1	UniSTS
Cytogenetic Map	21	q22.2	UniSTS
Cytogenetic Map	2	p11.2	UniSTS
Cytogenetic Map	18	q12.3	UniSTS
Cytogenetic Map	12	q13.3	UniSTS
Cytogenetic Map	2	p16.1	UniSTS
Cytogenetic Map	9	q34.11	UniSTS
Cytogenetic Map	12	q13.13	UniSTS
Cytogenetic Map	8	q24.21	UniSTS
Cytogenetic Map	12	q22-q23.1	UniSTS
Cytogenetic Map	3	q26.33	UniSTS
Cytogenetic Map	1	q23	UniSTS
Cytogenetic Map	11	p15.1	UniSTS
Cytogenetic Map	7	q32	UniSTS
Cytogenetic Map	11	p13	UniSTS
Cytogenetic Map	5	p13.1	UniSTS
Cytogenetic Map	18	q21	UniSTS
Cytogenetic Map	7	p14-p13	UniSTS
Cytogenetic Map	11	q13	UniSTS
Cytogenetic Map	11	q22-q23	UniSTS
Cytogenetic Map	19	p13.3-p13.2	UniSTS
Cytogenetic Map	6	q22-q23	UniSTS
Cytogenetic Map	7	p14.3	UniSTS
Cytogenetic Map	1	q21.1	UniSTS
Cytogenetic Map	14	q32.31	UniSTS
Cytogenetic Map	11	q13.1-q13.3	UniSTS
Cytogenetic Map	1	q32	UniSTS
Cytogenetic Map	6	p24	UniSTS
Cytogenetic Map	10	q25	UniSTS
Cytogenetic Map	8	q22.3	UniSTS
Cytogenetic Map	2	p14	UniSTS
Cytogenetic Map	1	p36.31	UniSTS
Cytogenetic Map	6	q13	UniSTS
Cytogenetic Map	2	p25.2	UniSTS
Cytogenetic Map	1	p31.1	UniSTS
Cytogenetic Map	15	q14-q15	UniSTS
Cytogenetic Map	9	q31.1	UniSTS
Cytogenetic Map	21	q22.11	UniSTS
Cytogenetic Map	7	p15.3	UniSTS
Cytogenetic Map	5	q35.3	UniSTS
Cytogenetic Map	1	p36.32	UniSTS
Cytogenetic Map	15	q11.2	UniSTS
Cytogenetic Map	12	p12.1	UniSTS
Cytogenetic Map	X	q25	UniSTS
Cytogenetic Map	X	q28	UniSTS
Cytogenetic Map	19	q13.3	UniSTS
Cytogenetic Map	8	p21.1	UniSTS
Cytogenetic Map	3	p26.1-p25.1	UniSTS
Cytogenetic Map	6	q16.3	UniSTS
Cytogenetic Map	3	q21.3	UniSTS
Cytogenetic Map	X	q27.1	UniSTS
Cytogenetic Map	3	q12.3	UniSTS
Cytogenetic Map	3	q25.31	UniSTS
Cytogenetic Map	17	q25.3	UniSTS
Cytogenetic Map	17	p13.3	UniSTS
Cytogenetic Map	11	q12.3	UniSTS
Cytogenetic Map	11	q13.4	UniSTS
Cytogenetic Map	19	q13.1	UniSTS
Cytogenetic Map	1	q42.3	UniSTS
Cytogenetic Map	22	q13.2	UniSTS
Cytogenetic Map	12	q13.12	UniSTS
Cytogenetic Map	2	q33.1	UniSTS
Cytogenetic Map	11	q23.3	UniSTS
Cytogenetic Map	4	q31.1	UniSTS
Cytogenetic Map	14	q32.33	UniSTS
Cytogenetic Map	9	q33.2	UniSTS
Cytogenetic Map	5	q13	UniSTS
Cytogenetic Map	8	q12	UniSTS
Cytogenetic Map	15	q22.31	UniSTS
Cytogenetic Map	17	q24.3	UniSTS
Cytogenetic Map	5	q12.3	UniSTS
Cytogenetic Map	1	p32.3	UniSTS
Cytogenetic Map	6	q21	UniSTS
Cytogenetic Map	10	q24.32	UniSTS
Cytogenetic Map	19	q13	UniSTS
Cytogenetic Map	17	q21	UniSTS
Cytogenetic Map	14	q32.32	UniSTS
Cytogenetic Map	16	p13.2	UniSTS
Cytogenetic Map	1	p36.33	UniSTS
Cytogenetic Map	10	q11.22	UniSTS
Cytogenetic Map	1	p34	UniSTS
Cytogenetic Map	6	q14.1	UniSTS
Cytogenetic Map	14	q32	UniSTS
Cytogenetic Map	1	p36.3-p36.2	UniSTS
Cytogenetic Map	2	q11.2	UniSTS
Cytogenetic Map	1	p32-p31	UniSTS
Cytogenetic Map	7	q34	UniSTS
Cytogenetic Map	5	q33.1	UniSTS
Cytogenetic Map	2	q21.1	UniSTS
Cytogenetic Map	19	q13.41	UniSTS
Cytogenetic Map	18	p11.21	UniSTS
Cytogenetic Map	10	q26.11	UniSTS
Cytogenetic Map	12	q14.3	UniSTS
Cytogenetic Map	5	q34	UniSTS
Cytogenetic Map	2	q36.1	UniSTS
Cytogenetic Map	15	q25.2	UniSTS
Cytogenetic Map	1	q21	UniSTS
Cytogenetic Map	4	p16.1	UniSTS
Cytogenetic Map	9	q32	UniSTS
Cytogenetic Map	15	q24	UniSTS
Cytogenetic Map	1	p34.3	UniSTS
Cytogenetic Map	12	q21	UniSTS
Cytogenetic Map	19	q13.43	UniSTS
Cytogenetic Map	1	p35-p34	UniSTS
Cytogenetic Map	9	q34.1	UniSTS
Cytogenetic Map	9	q22.2	UniSTS
Cytogenetic Map	X	p22	UniSTS
Cytogenetic Map	13	q14	UniSTS
Cytogenetic Map	2	q33	UniSTS
Cytogenetic Map	16	p12.2	UniSTS
Cytogenetic Map	10	q11.23	UniSTS
Cytogenetic Map	20	q13.31	UniSTS
Cytogenetic Map	3	p25.2	UniSTS
Cytogenetic Map	5	q11	UniSTS

D10S236E

Human Assembly	Chr	Position (strand)	Source	JBrowse
Cytogenetic Map	10	p13	UniSTS

D10S236E

Human Assembly	Chr	Position (strand)	Source
Cytogenetic Map	10	p13	UniSTS
TNG Radiation Hybrid Map	10	6746.0	UniSTS
Stanford-G3 RH Map	10	582.0	UniSTS
NCBI RH Map	10	194.9	UniSTS
GeneMap99-G3 RH Map	10	582.0	UniSTS

Expression

RNA-SEQ Expression

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

Download All Expressed Objects for this Gene

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	entire extraembryonic component	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	pharyngeal arch	renal system	reproductive system	respiratory system	sensory system	visual system
1204	2439	2788	2251	4971	1725	2351	5	624	1951	465	2268	7302	6468	53	3733	1	852	1744	1617	174	1

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001351032	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_020397	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_153498	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006717482	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006717483	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011519591	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011519592	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011519593	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011519594	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011519595	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017016438	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024448087	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047425537	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054366366	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054366367	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054366368	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054366369	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054366370	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054366371	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AA601559	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AA903749	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AB081726	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF286366	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AI821714	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK097377	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK289393	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL391314	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL512284	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL512783	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL603717	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL731559	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AV760219	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC035745	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC073155	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BM930742	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BQ059621	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BU542765	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471072	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068268	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB114811	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	EF444962	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HH961742	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HY156642	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HY168807	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KF510334	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KY966262	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000378845 ⟹ ENSP00000368122

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	12,349,733 - 12,826,143 (+)	Ensembl

Ensembl Acc Id:

ENST00000487696

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	12,349,652 - 12,666,949 (+)	Ensembl

Ensembl Acc Id:

ENST00000615792 ⟹ ENSP00000478861

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	12,760,576 - 12,829,736 (+)	Ensembl

Ensembl Acc Id:

ENST00000619168 ⟹ ENSP00000478874

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	12,349,547 - 12,835,545 (+)	Ensembl

RefSeq Acc Id:

NM_001351032 ⟹ NP_001337961

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	12,388,982 - 12,826,464 (+)	NCBI
T2T-CHM13v2.0	10	12,400,227 - 12,840,845 (+)	NCBI

Sequence:

show sequence

GTGTGATTTACATCCCGCAGCTGATGGAGACACCACCATACTCCATGGAAGGTCCTTCCTGTCC
GATCTGTCCAAGGTCTGGAGGAAGAGGCGAGATGGGTCAACTGTCAGTGGAAGGGATGAATTCA
TCATAGGCACTTGTAGTAGAACATCTCCTTGAGCCTCAAAGAGAAGGCTATTTTTCCTGTGGGT
CATCTTTGTGCTGTGCATGGGAGGTCCTGCCCCATGGGGCAAGAAAAGGAACAAGCAGCAAATG
TGTGGAAGTACTCAGGAAGAAGGCAGAAGCCCTAATGATGCGATCTGAGGACCACGTTGGACAC
GTGAAGCCAGATGCAGTGAAAAGTTGTGAGCTGGTGTTTGAAAGTGATTTACAACAAGTTGGCA
TCCGCTTGCCAGCTTGTGTTCACATGGACATCTGCCCTGCAGAACTGCAGAATGGCTTAGAACA
CCGGTTCTGGTTTCAGGTGGACGTTGTTCACCCCTTCATGGGTGTGGGACCTTGGCGGGGCCTT
TTCCGAAGTGGTTTTAGCTGAAGAGAAGGCAACTGGCAAGCTCTTTGCTGTGAAGTGTATCCCT
AAGAAGGCGCTGAAGGGCAAGGAAAGCAGCATAGAGAATGAGATAGCCGTCCTGAGAAAGATTA
AGCATGAAAATATTGTTGCCCTGGAAGACATTTATGAAAGCCCAAATCACCTGTACTTGGTCAT
GCAGCTGGTGTCCGGTGGAGAGCTGTTTGACCGGATAGTGGAGAAGGGGTTTTATACAGAGAAG
GATGCCAGCACTCTGATCCGCCAAGTCTTGGACGCCGTGTACTATCTCCACAGAATGGGCATCG
TCCACAGAGACCTCAAGCCCGAAAATCTCTTGTACTACAGTCAAGATGAGGAGTCCAAAATAAT
GATCAGTGACTTTGGATTGTCAAAAATGGAGGGCAAAGGAGATGTGATGTCCACTGCCTGTGGA
ACTCCAGGCTATGTCGCTCCTGAAGTCCTCGCCCAGAAACCTTACAGCAAAGCCGTTGACTGCT
GGTCCATCGGAGTGATTGCCTACATCTTGCTCTGCGGCTACCCTCCTTTTTATGATGAAAATGA
CTCCAAGCTCTTTGAGCAGATCCTCAAGGCGGAATATGAGTTTGACTCTCCCTACTGGGATGAC
ATCTCCGACTCTGCAAAAGACTTCATTCGGAACCTGATGGAGAAGGACCCGAATAAAAGATACA
CGTGTGAGCAGGCAGCTCGGCACCCATGGATCGCTGGTGACACAGCCCTCAACAAAAACATCCA
CGAGTCCGTCAGCGCCCAGATCCGGAAAAACTTTGCCAAGAGCAAATGGAGACAAGCATTTAAT
GCCACGGCCGTCGTCAGACATATGAGAAAACTACACCTCGGCAGCAGCCTGGACAGTTCAAATG
CAAGTGTTTCGAGCAGCCTCAGTTTGGCCAGCCAAAAAGACTGTGCGTATGTAGCAAAACCAGA
ATCCCTCAGCTGACACTGAAGACGAGCCTGGGGTGGAGAGGAGGGAGCCGGCATCTGCCGAGCA
CCTCCTGTTTGCCAGGCGCTTTCTATACTTAATCCCATGTCATGCGACCCTAGGACTTTTTTTA
ACATGTAATCACTGGGCTGGGTGCAGTGGCTCACGCCTGTAATCCCAACACTTTGGGAGGCTGA
GGCAGGAGGACTGTTTGAGTTCAGGAGTTTTAAGACCAGCCTGACCAACATGGTGAAACCCCAT
CTCTACTAAAATATAAAAATTAGCCGGGTGTGGTGGCGAGCACCTGTAATGTCAGCTACTTGGG
AGGCTGAGGCAGGAGAATCACTTGAACCCAGGAAGCGGAGGTTGCAATGAGCTGAGATCACACC
ACTGCACTCCAGCCTGGGTGACAGATTGAGACTCCCTCTCAAAAAAAAAAAAGAAAAATCATTG
AACACTCGTGGAACCCTAGGTATTGCTATTTCCATTTACAGTTGAGGAATCCAGGGCTCAAGTC
CTCGCAGCCATGTCTGTCTGGATAAAGGCCTGGACTCTTTCTCATCTCCATCCTTCCCTCTGAT
TTACCTCTCATTGTACAGTCACTCTTGCGGATTGAGGAAGGGAGAGCAGAGCCTCAGGACAGCC
TCCTGCCATTGACTTCCATAATGTATATATTTTGGATGCAGACAATGATAATTTGAGCTCATTT
ATGTGAAGTGCATTGACTTTGCAATAAAAGTAATAGTATTTCATTGTC

hide sequence

RefSeq Acc Id:

NM_020397 ⟹ NP_065130

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	12,349,547 - 12,826,464 (+)	NCBI
GRCh37	10	12,391,583 - 12,871,735 (+)	ENTREZGENE
Build 36	10	12,431,589 - 12,908,148 (+)	NCBI Archive
HuRef	10	12,307,786 - 12,784,748 (+)	ENTREZGENE
CHM1_1	10	12,391,496 - 12,868,491 (+)	NCBI
T2T-CHM13v2.0	10	12,360,834 - 12,840,845 (+)	NCBI

Sequence:

show sequence

AGTAGCAGAAAGTGAGGCTGGCAGGCGGCGGCAAAGGAGCCGGCGCGCGGCGGCGGCAGGAAGT
CTGTGCCCGAGAACAGCAGAAATAAGAGCCAGGGAGGGACCGCGGCCGCGGCGGCGGCGGCGAG
AGCGAAAGAGGAAACTGCAGAGGAGGAAGCTGCGCCGCAGCCCGAGCCGCCCGGCATCCCCGCC
GCCTCTGCGCCCGCGCCGCGCCCCCGGCGCCCCCTCCCCAGCGCGCCCCCGGCCGCTCCTCCGC
GCCGCGCTCGTCGGCCATGGCCCGGGAGAACGGCGAGAGCAGCTCCTCCTGGAAAAAGCAAGCT
GAAGACATCAAGAAGATCTTCGAGTTCAAAGAGACCCTCGGAACCGGGGCCTTTTCCGAAGTGG
TTTTAGCTGAAGAGAAGGCAACTGGCAAGCTCTTTGCTGTGAAGTGTATCCCTAAGAAGGCGCT
GAAGGGCAAGGAAAGCAGCATAGAGAATGAGATAGCCGTCCTGAGAAAGATTAAGCATGAAAAT
ATTGTTGCCCTGGAAGACATTTATGAAAGCCCAAATCACCTGTACTTGGTCATGCAGCTGGTGT
CCGGTGGAGAGCTGTTTGACCGGATAGTGGAGAAGGGGTTTTATACAGAGAAGGATGCCAGCAC
TCTGATCCGCCAAGTCTTGGACGCCGTGTACTATCTCCACAGAATGGGCATCGTCCACAGAGAC
CTCAAGCCCGAAAATCTCTTGTACTACAGTCAAGATGAGGAGTCCAAAATAATGATCAGTGACT
TTGGATTGTCAAAAATGGAGGGCAAAGGAGATGTGATGTCCACTGCCTGTGGAACTCCAGGCTA
TGTCGCTCCTGAAGTCCTCGCCCAGAAACCTTACAGCAAAGCCGTTGACTGCTGGTCCATCGGA
GTGATTGCCTACATCTTGCTCTGCGGCTACCCTCCTTTTTATGATGAAAATGACTCCAAGCTCT
TTGAGCAGATCCTCAAGGCGGAATATGAGTTTGACTCTCCCTACTGGGATGACATCTCCGACTC
TGCAAAAGACTTCATTCGGAACCTGATGGAGAAGGACCCGAATAAAAGATACACGTGTGAGCAG
GCAGCTCGGCACCCATGGATCGCTGGTGACACAGCCCTCAACAAAAACATCCACGAGTCCGTCA
GCGCCCAGATCCGGAAAAACTTTGCCAAGAGCAAATGGAGACAAGCATTTAATGCCACGGCCGT
CGTCAGACATATGAGAAAACTACACCTCGGCAGCAGCCTGGACAGTTCAAATGCAAGTGTTTCG
AGCAGCCTCAGTTTGGCCAGCCAAAAAGACTGTGCGTATGTAGCAAAACCAGAATCCCTCAGCT
GACACTGAAGACGAGCCTGGGGTGGAGAGGAGGGAGCCGGCATCTGCCGAGCACCTCCTGTTTG
CCAGGCGCTTTCTATACTTAATCCCATGTCATGCGACCCTAGGACTTTTTTTAACATGTAATCA
CTGGGCTGGGTGCAGTGGCTCACGCCTGTAATCCCAACACTTTGGGAGGCTGAGGCAGGAGGAC
TGTTTGAGTTCAGGAGTTTTAAGACCAGCCTGACCAACATGGTGAAACCCCATCTCTACTAAAA
TATAAAAATTAGCCGGGTGTGGTGGCGAGCACCTGTAATGTCAGCTACTTGGGAGGCTGAGGCA
GGAGAATCACTTGAACCCAGGAAGCGGAGGTTGCAATGAGCTGAGATCACACCACTGCACTCCA
GCCTGGGTGACAGATTGAGACTCCCTCTCAAAAAAAAAAAAGAAAAATCATTGAACACTCGTGG
AACCCTAGGTATTGCTATTTCCATTTACAGTTGAGGAATCCAGGGCTCAAGTCCTCGCAGCCAT
GTCTGTCTGGATAAAGGCCTGGACTCTTTCTCATCTCCATCCTTCCCTCTGATTTACCTCTCAT
TGTACAGTCACTCTTGCGGATTGAGGAAGGGAGAGCAGAGCCTCAGGACAGCCTCCTGCCATTG
ACTTCCATAATGTATATATTTTGGATGCAGACAATGATAATTTGAGCTCATTTATGTGAAGTGC
ATTGACTTTGCAATAAAAGTAATAGTATTTCATTGTC

hide sequence

RefSeq Acc Id:

NM_153498 ⟹ NP_705718

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	12,349,547 - 12,835,545 (+)	NCBI
GRCh37	10	12,391,583 - 12,871,735 (+)	ENTREZGENE
Build 36	10	12,431,589 - 12,911,741 (+)	NCBI Archive
HuRef	10	12,307,786 - 12,784,748 (+)	ENTREZGENE
CHM1_1	10	12,391,496 - 12,877,567 (+)	NCBI
T2T-CHM13v2.0	10	12,360,834 - 12,849,903 (+)	NCBI

Sequence:

show sequence

AGTAGCAGAAAGTGAGGCTGGCAGGCGGCGGCAAAGGAGCCGGCGCGCGGCGGCGGCAGGAAGT
CTGTGCCCGAGAACAGCAGAAATAAGAGCCAGGGAGGGACCGCGGCCGCGGCGGCGGCGGCGAG
AGCGAAAGAGGAAACTGCAGAGGAGGAAGCTGCGCCGCAGCCCGAGCCGCCCGGCATCCCCGCC
GCCTCTGCGCCCGCGCCGCGCCCCCGGCGCCCCCTCCCCAGCGCGCCCCCGGCCGCTCCTCCGC
GCCGCGCTCGTCGGCCATGGCCCGGGAGAACGGCGAGAGCAGCTCCTCCTGGAAAAAGCAAGCT
GAAGACATCAAGAAGATCTTCGAGTTCAAAGAGACCCTCGGAACCGGGGCCTTTTCCGAAGTGG
TTTTAGCTGAAGAGAAGGCAACTGGCAAGCTCTTTGCTGTGAAGTGTATCCCTAAGAAGGCGCT
GAAGGGCAAGGAAAGCAGCATAGAGAATGAGATAGCCGTCCTGAGAAAGATTAAGCATGAAAAT
ATTGTTGCCCTGGAAGACATTTATGAAAGCCCAAATCACCTGTACTTGGTCATGCAGCTGGTGT
CCGGTGGAGAGCTGTTTGACCGGATAGTGGAGAAGGGGTTTTATACAGAGAAGGATGCCAGCAC
TCTGATCCGCCAAGTCTTGGACGCCGTGTACTATCTCCACAGAATGGGCATCGTCCACAGAGAC
CTCAAGCCCGAAAATCTCTTGTACTACAGTCAAGATGAGGAGTCCAAAATAATGATCAGTGACT
TTGGATTGTCAAAAATGGAGGGCAAAGGAGATGTGATGTCCACTGCCTGTGGAACTCCAGGCTA
TGTCGCTCCTGAAGTCCTCGCCCAGAAACCTTACAGCAAAGCCGTTGACTGCTGGTCCATCGGA
GTGATTGCCTACATCTTGCTCTGCGGCTACCCTCCTTTTTATGATGAAAATGACTCCAAGCTCT
TTGAGCAGATCCTCAAGGCGGAATATGAGTTTGACTCTCCCTACTGGGATGACATCTCCGACTC
TGCAAAAGACTTCATTCGGAACCTGATGGAGAAGGACCCGAATAAAAGATACACGTGTGAGCAG
GCAGCTCGGCACCCATGGATCGCTGGTGACACAGCCCTCAACAAAAACATCCACGAGTCCGTCA
GCGCCCAGATCCGGAAAAACTTTGCCAAGAGCAAATGGAGACAAGCATTTAATGCCACGGCCGT
CGTCAGACATATGAGAAAACTACACCTCGGCAGCAGCCTGGACAGTTCAAATGCAAGTGTTTCG
AGCAGCCTCAGTTTGGCCAGCCAAAAAGACTGTCTGGCACCTTCCACGCTCTGTAGTTTCATTT
CTTCTTCGTCGGGGGTCTCAGGAGTTGGAGCCGAGCGGAGACCCAGGCCCACCACTGTGACGGC
AGTGCACTCTGGAAGCAAGTGACTGGCCCTGGAGGTGGGGCCCGGGGTCGGGGCTGGGGAAGGG
GAGCCCCAGGGTCGCCAGAGCCGCGAGCCACTCCAGCGAGACCCCACCTTGCATGGTGCCCCTT
CCTGCATAGGACTGGAAGACCGAAGTTTTTTTATGGCCATATTTTCTACTGCAATTCTGAAGTG
TTCATTTCTCACAAACTGTACTGACTCGAGGGGCGCTGATTTCATAGGATCTGGTGCTGTATAT
ACGAATCTTGCAAAGCTCTAACTGAACGGACCTTCTTATTCCTCTCCCCTAACACCATCGTTTC
CACTCTTCTCAGTGTAGGTAACCGTCTATGGTGTGTTTTTTCATTAATGACAAAAAAAAAAAGG
TTTCAACTGGATTATTTAAATATTGGTAAATATTGTGCATTAGGGTTTGTTTTTCCTTTTAAGA
AGTATGTCCTTTGTATCTCTAAGTTACATGACCTATATCTTTTCCTCTTTAATAGTAGTTTTAT
GTTAACCTTTAAGAGATTTGTTTTTCCTCAAAGGAGAATTTAAAGGTATTTTTTAAAATTCTAA
TAAGAGGATCAGCCGGGTGCAATGACTCATGCCTGTAATCCCAGCACGTTGGGAGGCCAAGTCG
GGCGGATCACAAGGTCAGGAGATCAAGGCCATCCTGGCCAACATGGTGAAACCCCACGTCTACT
AAAAATACAAAAAATTAGCCGGGCGTGGTGGCACACACCTGTAGTCCCGGCTACTCGGGAGGCT
GAGGCAGGAGAATTGCTTGAACCCGGGAGACGGAGGTTGCAGTGAGCTGAGATCGTGCCACTGC
ACTCCAGCCTGGGTGACAGAGCAAGACTCTGTCTCAAAAAAAAAAAAAAAAATTCTAACAAGAG
GATCATGAATCTGTCTCCAAGGCTAAGAGTGCCCTTCACCTCTACTCCTTCTGTTTCTCTCCCC
TTCCCCAGGAGGAGGGGCCCCTCAGTTCTGCGAGGCTCTCTTCTCTGCGGGGGACTTTGGTAGA
GAATCTGCACAGAGCCTTTGCTGGCAACCCATCCAGCAGAACCCACACCCACCAGAGACCCTAG
AGGCCTCTTGCCATCAGCAACCAGAAATAAGCCTGCTCCCCCGAGACGCAGGGCTCAGCTTCAC
AGGCCAGACTTGCTGTGAGTGAGATGCCCACACTGCAGAGATGCAGGACCCTCCCTTGCAAAAG
GAACCAGCTGCCATGTTGCTGAAAGTGGGCCCACACACAACCCTCATTTCTCACGAGAGCTAAC
AGATGAAAGCTCAGCTATGCAGTGTTAAAATTCATCTCTTTCTCTGTGGTTTTTAAAAAAATGC
ATTTCTAATCTTACACTTCACGTGGCCTCCAACACAAAGTTCTTTCTCCACATTTTTACCCTCT
TCTCACATGAATGTTTTCCAAGGGAAGGAAGGGAGGGAAGCAGCCTTGGGAAAGGATCCATTTC
TGGTGGTAAGGAGAGGGGGCCCTGCCAGGCTAATGGGACTTCAGCCACCACAGAGATGACCAAA
GACCACCTCCGCCAGGCCCAGCCAGTGCTTGCAGCCCTCCCATTGGTCAGGGGAGTCTAAAATC
AAAGATACATGGTGGTAGGGTCACCAAACGTCCCATTTGCCCGAGACTGAAGGATTTCTCAGGC
TGTGGACATTTAATGCCAAAACCAGGAATATCCGGGGCAAAGCAGGCTGTGTTGTTCGCCTTTG
TGGAGCCAGGCAGTGTGTGGCCCAGGGAAAGCTGCGTTTCATGGAGGCTTCCAGGAGGCTGCCC
TGTAAAGCCAGGCAGGTGGCTTCAAGTGCCATTCCTGCAAGTGCCCCTGCTTCAGCTCTCAGGC
CCATCCAATGCCTCGAGCCCACGGGGGTGTCCCGGCAGGTCTGCGTCATCACGACCCAGTAACG
CTGCTGGCTGTGTCCTCATGCCCTCTTCCTCTGGCTGGCCAGTCATGGGAAGTCCTGTTGGTTG
AGTCATCTTTGTCACTTCTACACCTTTGAGTATGTACAGGCTGAATGTTGAGTGATGCCCCCCC
ACCCTCTCAATAAACACACACACACACACACACACACACACACACACACACAATGTTATTAGGC
ACAGCAGCTCCATCCTGCTCCCTGAGAATGGCAGTGCAGGCACAGAGAAGAGCAGTTGGGAAGA
CAGGCAGCTGGTCTACCCTGTCCCCGCACACTTCACAGGCACTCCACTGCTTGGCAGGAATTCT
GCATGGCATCTGCCACGCATGCTCACAGGGTGAAAAATCAAGCTGTCACTCTGCAAAATCTAAA
AACCCTGGAAAGGTCTATAAGATGACATTAGACCCAGTTAAGAAGCAAGTGTCACCTGAGTTGG
CCATGCAATGAATGAATATTATAAGCAGTATTGGAGAACTAGGCGGTTGCTTACTAAGAAGTGT
CTTGGAAACATTCGAGTTCATACAGTGCATGACAAAGTAATAGAAGGCTGCAAGCGCTGAAAAT
GCACCCGAATCTGGTACCTAGGATGAGTACATGAATAGTGATGAATAGCCCTTTGTGCTGTGTG
CTATATACAACCATTTGCATTCAGAAAGCAGCATTTGAAGCTGAGTTCCATTACTGGTGATTGA
AGTATTTTCAGGAGCAGATACATGTGGTGCATGTTATATGCACTTAGTTTGAAAGTATCCCTCA
CCCAAAAAGTGCAGAACCTCTGAAAGGTGAGCCGTGGTGCAGGTGCCCCCCTCGCTGTTCGGGT
CAGTTCTTGGCCATGCTTGGCCTGTCACACGCCGGGTCTCAACAACATCGTGCGAGGAGACAGT
GACTGGTTTCAGCCCAAGAGTCAACTGTTGAGCATGACATCAGGAAGCCTGTACTGTCCTGATC
CCACCAGGCTTGGGTTAATTTCCTATTGCTTCAGAGAAAGAGAGGCGCTCTTGTGCTTTTGAGA
GAGCTCTCATGTTAAAAAGAGGTTGTCTTTGCACTGCGCTTGGTATGATTTGTTTTCTTATAAA
ACAGGAAGAGAACCTAGAATGTGCCTTTCGTGAAGGTCTGACAAATGGGGTCTCAGAGTCCTAG
GACCCGCACCAAGGTCAGAGTCCACCTGTAGAGGCTGAGCATTTCTACATGCACCCAGGGTGCT
GGGCTGAGGCTAAGGGTGGACGCGTAGACCCCATCACAGGCTTCCTTCCTGAGCCCAAGTCCCC
CATTTGGTCACTATCCCTTCTCAGAGCAAGTGGATTCTCTTTTCCTCACTTGGAGTATTCAATG
TTGAAGTAGTGGCCTGGAGTGGCCTTTCCCTCAGCTGCCTGTCTGGGCTCCCTGGCTTCCCGGA
TCTTCATCTCATACGTGAGGCAATAGGAGGAGTTTCTATTCATTGAGACAAACAGTGAGCGGGC
ACCAACAGGCCAGCAGCTTGGCCCTTTTCACAGAGGTGGCCTTGGAGTCTGGAGTCTGGGCAGC
TGTCTGCCTCTCTACGGCTCTGCTTCCCAGCGGGCACACGGGTCCGGAGCCTCAGAATGAAGTG
GTGCAGAGGCGCAGGGCACACCTAGGAGAAGCTCAATGACCACCAAAGCCCTTGAGGAGAGACG
GGGTTTGCTGTGTTAGAGAAATGGCAACCCCCAGGACCATGCACGGCTCTGGCAGTGCACAGTG
GCTGATTTTCACCAGTTCCTCCTACCCCTGCCTCTGTCGGAGACTAGAAAACATTCTACCCCTT
CAGGTCTTCTTTTAAAAGAAAAGAGCTATGGCAAAGCGTGCCATACAAAGTTAAAAAAAGGAAG
AGTGGCTTTGCGTTCTTGACCATGGCCACAATTCTGGTCACTTCTAGCATCTGACCTTGAGAAC
GGTGTAGAGTCTCTGAGCCACCGCTGGCCTTTGAGAGAGTCTCACTCTCCAGCTAGCTCTTTGT
GTAGTGTCCAGGGCCCCGGCAGTCAGGATAGAGCGAGCAAAAGAAGATGGACAGTGGACAGGGC
GCAGTGGCTCACGCCTGTAATCCCAGCGCTTTGGGAGAGCGAGGCGGGCAGATCACAAGGTCAA
GAGATCAAGACCATTCTGGCCAACATGGTGAAACCCTGTTTCTACTAAAAATACAAAAATTAGC
TGGGCATGGTGGTGCGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTG
AACCCGGGAGGCAGAGGTTGCAGTGAGCCGAGATCGTGCCACTGCACTCCAGCCTGGGTGACAG
AGCAAGACTCCGTCTCAAAAAAGATGGCCATGCTGGCCAAGGCTGGGCTCATAGGAAATATCTG
TAGTAGGATGAAAGGAATCTGGCCTAGGGAGCCCCGGACTCGGTTTACCTACCCCGTACTCATC
CCACTCATCTGTCTACCCTAGTGTCCATCATGCCCTGGATGAATCGTAGGTGGGAGGGACAGAA
GCCGAGAACACCAGGCACACGGGGTGGGGGGAATGGGGGGAGCCCAGGTGATCCCCTTTGGAAA
GTGGATTGATCCTCTCCCCTGTGGAATGACAGCTTAACCTGATTAACCCACTGGGGCTTGCTAT
TTTATGAGCATTTTTAAACAGAAAGGAAAGATGATATCCCAGTGCAGGTAGACTTTATTTTTGA
AAGCATCGTGGCCCCTCACCTCTCCCTCTCCCCCAGAACCTTGGCCAGAATTGAGTCTTCGCGT
TGGGGAGGCCACGCTGGAACCATTGCTCTAGGGCTGAAGGTGGAAGTAGGGCCACTGCCGCAGC
TTCAGCCAGAGCCCTCGCTGCTTCGCAGAATTTAACAAGCACACGACTGGGATTCCTTTGGATA
TGAGAAAGGAAGGCAAGTGCGGGCAAAGGGAAGCTCCTCCCGTTTTTCATAAACAGAAGTAAGA
TGTCCTCTTTCCCAGGTTTGCACAATCACTTCTGGCAAATTAATTGAAGGTCCTTGAATTCAGC
CAGTGCACGAAACCTTTGCATGTTCTTCTGAAACTGTACTTCTTCCCTATTCTGTCTACCCACA
CTCTGCGAACTTTGCCTTTTCCTTAAACACATTCCAGACCAAACACTGTTCAGTTTGTTAAAAA
AAAAAAAAAAAAAAAAAGATGTATATACCTGTATGTGATCCACCACCCTTTTGAGGGGCACCTG
GTCCTCGGTTGGGGCTGCAGGTGTGCCTGACATTTGCAAAAGATATTCCAGTCTTTCGATGTTC
AGAATTGAAAATGTGGAGATAGAAAAGCTCAAACAGACTCCTAAAAGGAGGGTTTCTTTCCTGA
AGACTCCAAGAAAATGAGTGTGCAGATGAGTTAGCTTGACAACCTCAACTCTGGGGAGCAGGCA
GGCGGTCTGAGGAAGATAAGGGCCCACGCCCCACTCACCTGGCACCTGTTCGGTGGTCCCGGGG
CATCATGGTCTGCAGCTCTGGGCCCCCAGCCCCACTGTGAAGTCAGTCCTGCATGCTGGCCGAG
GCCCGGCCACCTCCCGATGCCTCCAGAGTCAGTGGGAAGGAGTCAGCCCTTCCCAGACTTCCCC
GCCACCTCCAGCAGGAGCAGCTCAGTTTGTGGCTCTGGGAGCTCCGCTTTTGCAAACCCAAAAA
GGCTGTGCATTTGGAAGCCAAACGCTCAGCATGCGGCTGCCGAGTCTGGTTTTGTGGACAAAGC
AAACTGTGGAATGGCTTCTCGGTGTCTGTATAAAGGGACAAACGGTTGCATTCACCCTTTGTAC
TATAACACCGCTTCTGCATTCGCCATATCCGTTTTTTAACCTTTTTGTCTCCGGGGAACTTCTC
ATTCGATTATTATGTCTTCTGATGATTTGCCATGTTATTTTAAAGGTGATTTTATTTTCTTATG
GACAGGAAAAAAGAAAATGAGGAGGAGTTGGTTTTACTCTTAGAGATAAGACTTCAGCAGGGGC
TCAGAAACCCCAAACTCTAGTTAAATTGCTTCTCGGAGGAAAATCTTAATCTAGACAGATTCAG
ATTCCCAGGCTCTCCTGGAAGCCCTGCACTTCAGGGCACAGGGGCCCTGGGACGTGGTTGGCAG
CCAGGCTGCGAGAGAGCTAAAAAGGAACAAGAACATCAGCTCGGATGTTTGTCTCTCAGCCCTG
ACACCTGCCACTCTCCTTCCCGGGGCACTTGGCCCTATCAGAGGGACATGAAATGCTGTCCGAA
TGGTGGCAGAAATGCAGCGACATTGCATGCAGCAGAGTCTTTGCTTCGAAAGATGGGGCGCCAT
GTTTCAGAGAACATTTATCTTAGTCCCACGTTCAGGTGAGAAGACCTCAAAGGTACCCTCTGTC
CAGAATAAACATTGGAACAATCTCTCAATTGGCTTTTGTCACTACACATAATGTAATCTCCCTT
CTTTCAGCTCCCCCAACAGTGAGCATGCTTCCCAAAAAATTACAACATCAAAACCAGGAATGTC
CCCGCATCTACTATTACCAGGCTTGCAATTGGTTCAATTTTCCCATAAAAACATGTTTGTCCAA
AAGAAGGGAAACTGTGAATTTATTCCATGCATGTAATAAACTCTGCAAGAAGTTTAACCCACAT
AGGTTTGCGGCACTGCAAAATTGTTCATGGGTCTATGTAGCAAATGATTCTCTGCCTTGACAAT
CATGTATACATATCAAGATTTCTATCATAATGATAATGAGATTGATGACTTCCTGTTTTCCTCC
AATAAAGACAATTAATCACCTTCA

hide sequence

RefSeq Acc Id:

XM_006717482 ⟹ XP_006717545

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	12,349,547 - 12,835,545 (+)	NCBI

Sequence:

show sequence

GGCGGCAGGGAGGGAGCGGGAGGGAGGCAAGAAAGTAGCAGAAAGTGAGGCTGGCAGGCGGCGG
CAAAGGAGCCGGCGCGCGGCGGCGGCAGGAAGTCTGTGCCCGAGAACAGCAGAAATAAGAGCCA
GGGAGGGACCGCGGCCGCGGCGGCGGCGGCGAGAGCGAAAGAGGAAACTGCAGAGGAGGAAGCT
GCGCCGCAGCCCGAGCCGCCCGGCATCCCCGCCGCCTCTGCGCCCGCGCCGCGCCCCCGGCGCC
CCCTCCCCAGCGCGCCCCCGGCCGCTCCTCCGCGCCGCGCTCGTCGGCCATGGCCCGGGAGAAC
GGCGAGAGCAGCTCCTCCTGGAAAAAGCAAGCTGAAGACATCAAGAAGATCTTCGAGTTCAAAG
AGACCCTCGGAACCGGGGCCTTTTCCGAAGTGGTTTTAGCTGAAGAGAAGGCAACTGGCAAGCT
CTTTGCTGTGAAGTGTATCCCTAAGAAGGCGCTGAAGGGCAAGGAAAGCAGCATAGAGAATGAG
ATAGCCGTCCTGAGAAAGATTAAGCATGAAAATATTGTTGCCCTGGAAGACATTTATGAAAGCC
CAAATCACCTGTACTTGGTCATGCAGCTGGTGTCCGGTGGAGAGCTGTTTGACCGGATAGTGGA
GAAGGGGTTTTATACAGAGAAGGATGCCAGCACTCTGATCCGCCAAGTCTTGGACGCCGTGTAC
TATCTCCACAGAATGGGCATCGTCCACAGAGACCTCAAGCCCGAAAATCTCTTGTACTACAGTC
AAGATGAGGAGTCCAAAATAATGATCAGTGACTTTGGATTGTCAAAAATGGAGGGCAAAGGAGA
TGTGATGTCCACTGCCTGTGGAACTCCAGGCTATGTCGCTCCTGAAGTCCTCGCCCAGAAACCT
TACAGCAAAGCCGTTGACTGCTGGTCCATCGGAGTGATTGCCTACATCTTGCTCTGCGGCTACC
CTCCTTTTTATGATGAAAATGACTCCAAGCTCTTTGAGCAGATCCTCAAGGCGGAATATGAGTT
TGACTCTCCCTACTGGGATGACATCTCCGACTCTGCAAAAGACTTCATTCGGAACCTGATGGAG
AAGGACCCGAATAAAAGATACACGTGTGAGCAGGCAGCTCGGCACCCATGGATCGCTGGTGACA
CAGCCCTCAACAAAAACATCCACGAGTCCGTCAGCGCCCAGATCCGGAAAAACTTTGCCAAGAG
CAAATGGAGACAAGCATTTAATGCCACGGCCGTCGTCAGACATATGAGAAAACTACACCTCGGC
AGCAGCCTGGACAGTTCAAATGTCTGGCACCTTCCACGCTCTGTAGTTTCATTTCTTCTTCGTC
GGGGGTCTCAGGAGTTGGAGCCGAGCGGAGACCCAGGCCCACCACTGTGACGGCAGTGCACTCT
GGAAGCAAGTGACTGGCCCTGGAGGTGGGGCCCGGGGTCGGGGCTGGGGAAGGGGAGCCCCAGG
GTCGCCAGAGCCGCGAGCCACTCCAGCGAGACCCCACCTTGCATGGTGCCCCTTCCTGCATAGG
ACTGGAAGACCGAAGTTTTTTTATGGCCATATTTTCTACTGCAATTCTGAAGTGTTCATTTCTC
ACAAACTGTACTGACTCGAGGGGCGCTGATTTCATAGGATCTGGTGCTGTATATACGAATCTTG
CAAAGCTCTAACTGAACGGACCTTCTTATTCCTCTCCCCTAACACCATCGTTTCCACTCTTCTC
AGTGTAGGTAACCGTCTATGGTGTGTTTTTTCATTAATGACAAAAAAAAAAAGGTTTCAACTGG
ATTATTTAAATATTGGTAAATATTGTGCATTAGGGTTTGTTTTTCCTTTTAAGAAGTATGTCCT
TTGTATCTCTAAGTTACATGACCTATATCTTTTCCTCTTTAATAGTAGTTTTATGTTAACCTTT
AAGAGATTTGTTTTTCCTCAAAGGAGAATTTAAAGGTATTTTTTAAAATTCTAATAAGAGGATC
AGCCGGGTGCAATGACTCATGCCTGTAATCCCAGCACGTTGGGAGGCCAAGTCGGGCGGATCAC
AAGGTCAGGAGATCAAGGCCATCCTGGCCAACATGGTGAAACCCCACGTCTACTAAAAATACAA
AAAATTAGCCGGGCGTGGTGGCACACACCTGTAGTCCCGGCTACTCGGGAGGCTGAGGCAGGAG
AATTGCTTGAACCCGGGAGACGGAGGTTGCAGTGAGCTGAGATCGTGCCACTGCACTCCAGCCT
GGGTGACAGAGCAAGACTCTGTCTCAAAAAAAAAAAAAAAAATTCTAACAAGAGGATCATGAAT
CTGTCTCCAAGGCTAAGAGTGCCCTTCACCTCTACTCCTTCTGTTTCTCTCCCCTTCCCCAGGA
GGAGGGGCCCCTCAGTTCTGCGAGGCTCTCTTCTCTGCGGGGGACTTTGGTAGAGAATCTGCAC
AGAGCCTTTGCTGGCAACCCATCCAGCAGAACCCACACCCACCAGAGACCCTAGAGGCCTCTTG
CCATCAGCAACCAGAAATAAGCCTGCTCCCCCGAGACGCAGGGCTCAGCTTCACAGGCCAGACT
TGCTGTGAGTGAGATGCCCACACTGCAGAGATGCAGGACCCTCCCTTGCAAAAGGAACCAGCTG
CCATGTTGCTGAAAGTGGGCCCACACACAACCCTCATTTCTCACGAGAGCTAACAGATGAAAGC
TCAGCTATGCAGTGTTAAAATTCATCTCTTTCTCTGTGGTTTTTAAAAAAATGCATTTCTAATC
TTACACTTCACGTGGCCTCCAACACAAAGTTCTTTCTCCACATTTTTACCCTCTTCTCACATGA
ATGTTTTCCAAGGGAAGGAAGGGAGGGAAGCAGCCTTGGGAAAGGATCCATTTCTGGTGGTAAG
GAGAGGGGGCCCTGCCAGGCTAATGGGACTTCAGCCACCACAGAGATGACCAAAGACCACCTCC
GCCAGGCCCAGCCAGTGCTTGCAGCCCTCCCATTGGTCAGGGGAGTCTAAAATCAAAGATACAT
GGTGGTAGGGTCACCAAACGTCCCATTTGCCCGAGACTGAAGGATTTCTCAGGCTGTGGACATT
TAATGCCAAAACCAGGAATATCCGGGGCAAAGCAGGCTGTGTTGTTCGCCTTTGTGGAGCCAGG
CAGTGTGTGGCCCAGGGAAAGCTGCGTTTCATGGAGGCTTCCAGGAGGCTGCCCTGTAAAGCCA
GGCAGGTGGCTTCAAGTGCCATTCCTGCAAGTGCCCCTGCTTCAGCTCTCAGGCCCATCCAATG
CCTCGAGCCCACGGGGGTGTCCCGGCAGGTCTGCGTCATCACGACCCAGTAACGCTGCTGGCTG
TGTCCTCATGCCCTCTTCCTCTGGCTGGCCAGTCATGGGAAGTCCTGTTGGTTGAGTCATCTTT
GTCACTTCTACACCTTTGAGTATGTACAGGCTGAATGTTGAGTGATGCCCCCCCACCCTCTCAA
TAAACACACACACACACACACACACACACACACACACACACAATGTTATTAGGCACAGCAGCTC
CATCCTGCTCCCTGAGAATGGCAGTGCAGGCACAGAGAAGAGCAGTTGGGAAGACAGGCAGCTG
GTCTACCCTGTCCCCGCACACTTCACAGGCACTCCACTGCTTGGCAGGAATTCTGCATGGCATC
TGCCACGCATGCTCACAGGGTGAAAAATCAAGCTGTCACTCTGCAAAATCTAAAAACCCTGGAA
AGGTCTATAAGATGACATTAGACCCAGTTAAGAAGCAAGTGTCACCTGAGTTGGCCATGCAATG
AATGAATATTATAAGCAGTATTGGAGAACTAGGCGGTTGCTTACTAAGAAGTGTCTTGGAAACA
TTCGAGTTCATACAGTGCATGACAAAGTAATAGAAGGCTGCAAGCGCTGAAAATGCACCCGAAT
CTGGTACCTAGGATGAGTACATGAATAGTGATGAATAGCCCTTTGTGCTGTGTGCTATATACAA
CCATTTGCATTCAGAAAGCAGCATTTGAAGCTGAGTTCCATTACTGGTGATTGAAGTATTTTCA
GGAGCAGATACATGTGGTGCATGTTATATGCACTTAGTTTGAAAGTATCCCTCACCCAAAAAGT
GCAGAACCTCTGAAAGGTGAGCCGTGGTGCAGGTGCCCCCCTCGCTGTTCGGGTCAGTTCTTGG
CCATGCTTGGCCTGTCACACGCCGGGTCTCAACAACATCGTGCGAGGAGACAGTGACTGGTTTC
AGCCCAAGAGTCAACTGTTGAGCATGACATCAGGAAGCCTGTACTGTCCTGATCCCACCAGGCT
TGGGTTAATTTCCTATTGCTTCAGAGAAAGAGAGGCGCTCTTGTGCTTTTGAGAGAGCTCTCAT
GTTAAAAAGAGGTTGTCTTTGCACTGCGCTTGGTATGATTTGTTTTCTTATAAAACAGGAAGAG
AACCTAGAATGTGCCTTTCGTGAAGGTCTGACAAATGGGGTCTCAGAGTCCTAGGACCCGCACC
AAGGTCAGAGTCCACCTGTAGAGGCTGAGCATTTCTACATGCACCCAGGGTGCTGGGCTGAGGC
TAAGGGTGGACGCGTAGACCCCATCACAGGCTTCCTTCCTGAGCCCAAGTCCCCCATTTGGTCA
CTATCCCTTCTCAGAGCAAGTGGATTCTCTTTTCCTCACTTGGAGTATTCAATGTTGAAGTAGT
GGCCTGGAGTGGCCTTTCCCTCAGCTGCCTGTCTGGGCTCCCTGGCTTCCCGGATCTTCATCTC
ATACGTGAGGCAATAGGAGGAGTTTCTATTCATTGAGACAAACAGTGAGCGGGCACCAACAGGC
CAGCAGCTTGGCCCTTTTCACAGAGGTGGCCTTGGAGTCTGGAGTCTGGGCAGCTGTCTGCCTC
TCTACGGCTCTGCTTCCCAGCGGGCACACGGGTCCGGAGCCTCAGAATGAAGTGGTGCAGAGGC
GCAGGGCACACCTAGGAGAAGCTCAATGACCACCAAAGCCCTTGAGGAGAGACGGGGTTTGCTG
TGTTAGAGAAATGGCAACCCCCAGGACCATGCACGGCTCTGGCAGTGCACAGTGGCTGATTTTC
ACCAGTTCCTCCTACCCCTGCCTCTGTCGGAGACTAGAAAACATTCTACCCCTTCAGGTCTTCT
TTTAAAAGAAAAGAGCTATGGCAAAGCGTGCCATACAAAGTTAAAAAAAGGAAGAGTGGCTTTG
CGTTCTTGACCATGGCCACAATTCTGGTCACTTCTAGCATCTGACCTTGAGAACGGTGTAGAGT
CTCTGAGCCACCGCTGGCCTTTGAGAGAGTCTCACTCTCCAGCTAGCTCTTTGTGTAGTGTCCA
GGGCCCCGGCAGTCAGGATAGAGCGAGCAAAAGAAGATGGACAGTGGACAGGGCGCAGTGGCTC
ACGCCTGTAATCCCAGCGCTTTGGGAGAGCGAGGCGGGCAGATCACAAGGTCAAGAGATCAAGA
CCATTCTGGCCAACATGGTGAAACCCTGTTTCTACTAAAAATACAAAAATTAGCTGGGCATGGT
GGTGCGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAG
GCAGAGGTTGCAGTGAGCCGAGATCGTGCCACTGCACTCCAGCCTGGGTGACAGAGCAAGACTC
CGTCTCAAAAAAGATGGCCATGCTGGCCAAGGCTGGGCTCATAGGAAATATCTGTAGTAGGATG
AAAGGAATCTGGCCTAGGGAGCCCCGGACTCGGTTTACCTACCCCGTACTCATCCCACTCATCT
GTCTACCCTAGTGTCCATCATGCCCTGGATGAATCGTAGGTGGGAGGGACAGAAGCCGAGAACA
CCAGGCACACGGGGTGGGGGGAATGGGGGGAGCCCAGGTGATCCCCTTTGGAAAGTGGATTGAT
CCTCTCCCCTGTGGAATGACAGCTTAACCTGATTAACCCACTGGGGCTTGCTATTTTATGAGCA
TTTTTAAACAGAAAGGAAAGATGATATCCCAGTGCAGGTAGACTTTATTTTTGAAAGCATCGTG
GCCCCTCACCTCTCCCTCTCCCCCAGAACCTTGGCCAGAATTGAGTCTTCGCGTTGGGGAGGCC
ACGCTGGAACCATTGCTCTAGGGCTGAAGGTGGAAGTAGGGCCACTGCCGCAGCTTCAGCCAGA
GCCCTCGCTGCTTCGCAGAATTTAACAAGCACACGACTGGGATTCCTTTGGATATGAGAAAGGA
AGGCAAGTGCGGGCAAAGGGAAGCTCCTCCCGTTTTTCATAAACAGAAGTAAGATGTCCTCTTT
CCCAGGTTTGCACAATCACTTCTGGCAAATTAATTGAAGGTCCTTGAATTCAGCCAGTGCACGA
AACCTTTGCATGTTCTTCTGAAACTGTACTTCTTCCCTATTCTGTCTACCCACACTCTGCGAAC
TTTGCCTTTTCCTTAAACACATTCCAGACCAAACACTGTTCAGTTTGTTAAAAAAAAAAAAAAA
AAAAAAAGATGTATATACCTGTATGTGATCCACCACCCTTTTGAGGGGCACCTGGTCCTCGGTT
GGGGCTGCAGGTGTGCCTGACATTTGCAAAAGATATTCCAGTCTTTCGATGTTCAGAATTGAAA
ATGTGGAGATAGAAAAGCTCAAACAGACTCCTAAAAGGAGGGTTTCTTTCCTGAAGACTCCAAG
AAAATGAGTGTGCAGATGAGTTAGCTTGACAACCTCAACTCTGGGGAGCAGGCAGGCGGTCTGA
GGAAGATAAGGGCCCACGCCCCACTCACCTGGCACCTGTTCGGTGGTCCCGGGGCATCATGGTC
TGCAGCTCTGGGCCCCCAGCCCCACTGTGAAGTCAGTCCTGCATGCTGGCCGAGGCCCGGCCAC
CTCCCGATGCCTCCAGAGTCAGTGGGAAGGAGTCAGCCCTTCCCAGACTTCCCCGCCACCTCCA
GCAGGAGCAGCTCAGTTTGTGGCTCTGGGAGCTCCGCTTTTGCAAACCCAAAAAGGCTGTGCAT
TTGGAAGCCAAACGCTCAGCATGCGGCTGCCGAGTCTGGTTTTGTGGACAAAGCAAACTGTGGA
ATGGCTTCTCGGTGTCTGTATAAAGGGACAAACGGTTGCATTCACCCTTTGTACTATAACACCG
CTTCTGCATTCGCCATATCCGTTTTTTAACCTTTTTGTCTCCGGGGAACTTCTCATTCGATTAT
TATGTCTTCTGATGATTTGCCATGTTATTTTAAAGGTGATTTTATTTTCTTATGGACAGGAAAA
AAGAAAATGAGGAGGAGTTGGTTTTACTCTTAGAGATAAGACTTCAGCAGGGGCTCAGAAACCC
CAAACTCTAGTTAAATTGCTTCTCGGAGGAAAATCTTAATCTAGACAGATTCAGATTCCCAGGC
TCTCCTGGAAGCCCTGCACTTCAGGGCACAGGGGCCCTGGGACGTGGTTGGCAGCCAGGCTGCG
AGAGAGCTAAAAAGGAACAAGAACATCAGCTCGGATGTTTGTCTCTCAGCCCTGACACCTGCCA
CTCTCCTTCCCGGGGCACTTGGCCCTATCAGAGGGACATGAAATGCTGTCCGAATGGTGGCAGA
AATGCAGCGACATTGCATGCAGCAGAGTCTTTGCTTCGAAAGATGGGGCGCCATGTTTCAGAGA
ACATTTATCTTAGTCCCACGTTCAGGTGAGAAGACCTCAAAGGTACCCTCTGTCCAGAATAAAC
ATTGGAACAATCTCTCAATTGGCTTTTGTCACTACACATAATGTAATCTCCCTTCTTTCAGCTC
CCCCAACAGTGAGCATGCTTCCCAAAAAATTACAACATCAAAACCAGGAATGTCCCCGCATCTA
CTATTACCAGGCTTGCAATTGGTTCAATTTTCCCATAAAAACATGTTTGTCCAAAAGAAGGGAA
ACTGTGAATTTATTCCATGCATGTAATAAACTCTGCAAGAAGTTTAACCCACATAGGTTTGCGG
CACTGCAAAATTGTTCATGGGTCTATGTAGCAAATGATTCTCTGCCTTGACAATCATGTATACA
TATCAAGATTTCTATCATAATGATAATGAGATTGATGACTTCCTGTTTTCCTCCAATAAAGACA
ATTAATCACCTTCA

hide sequence

RefSeq Acc Id:

XM_006717483 ⟹ XP_006717546

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	12,349,547 - 12,835,545 (+)	NCBI

Sequence:

show sequence

CAGAAAGTGAGGCTGGCAGGCGGCGGCAAAGGAGCCGGCGCGCGGCGGCGGCAGGAAGTCTGTG
CCCGAGAACAGCAGAAATAAGAGCCAGGGAGGGACCGCGGCCGCGGCGGCGGCGGCGAGAGCGA
AAGAGGAAACTGCAGAGGAGGAAGCTGCGCCGCAGCCCGAGCCGCCCGGCATCCCCGCCGCCTC
TGCGCCCGCGCCGCGCCCCCGGCGCCCCCTCCCCAGCGCGCCCCCGGCCGCTCCTCCGCGCCGC
GCTCGTCGGCCATGGCCCGGGAGAACGGCGAGAGCAGCTCCTCCTGGAAAAAGCAAGCTGAAGA
CATCAAGAAGATCTTCGAGTTCAAAGAGACCCTCGGAACCGGGGCCTTTTCCGAAGTGGTTTTA
GCTGAAGAGAAGGCAACTGGCAAGCTCTTTGCTGTGAAGTGTATCCCTAAGAAGGCGCTGAAGG
GCAAGGAAAGCAGCATAGAGAATGAGATAGCCGTCCTGAGAAAGATTAAGCATGAAAATATTGT
TGCCCTGGAAGACATTTATGAAAGCCCAAATCACCTGTACTTGGTCATGCAGCTGGTGTCCGGT
GGAGAGCTGTTTGACCGGATAGTGGAGAAGGGGTTTTATACAGAGAAGGATGCCAGCACTCTGA
TCCGCCAAGTCTTGGACGCCGTGTACTATCTCCACAGAATGGGCATCGTCCACAGAGACCTCAA
GCCCGAAAATCTCTTGTACTACAGTCAAGATGAGGAGTCCAAAATAATGATCAGTGACTTTGGA
TTGTCAAAAATGGAGGGCAAAGGAGATGTGATGTCCACTGCCTGTGGAACTCCAGGCTATGTCG
CTCCTGAAGTCCTCGCCCAGAAACCTTACAGCAAAGCCGTTGACTGCTGGTCCATCGGAGTGAT
TGCCTACATCTTGCTCTGCGGCTACCCTCCTTTTTATGATGAAAATGACTCCAAGCTCTTTGAG
CAGATCCTCAAGGCGGAATATGAGTTTGACTCTCCCTACTGGGATGACATCTCCGACTCTGCAA
AAGACTTCATTCGGAACCTGATGGAGAAGGACCCGAATAAAAGATACACGTGTGAGCAGGCAGC
TCGGCACCCATGGATCGCTGGTGACACAGCCCTCAACAAAAACATCCACGAGTCCGTCAGCGCC
CAGATCCGGAAAAACTTTGCCAAGAGCAAATGGAGACAAGCATTTAATGCCACGGCCGTCGTCA
GACATATGAGAAAACTACACCTCGGCAGCAGCCTGGACAGTTCAAATGCAAGTGTTTCGAGCAG
CCTCAGTTTGGCCAGCCAAAAAGACTGTGCGTCTGGCACCTTCCACGCTCTGTAGTTTCATTTC
TTCTTCGTCGGGGGTCTCAGGAGTTGGAGCCGAGCGGAGACCCAGGCCCACCACTGTGACGGCA
GTGCACTCTGGAAGCAAGTGACTGGCCCTGGAGGTGGGGCCCGGGGTCGGGGCTGGGGAAGGGG
AGCCCCAGGGTCGCCAGAGCCGCGAGCCACTCCAGCGAGACCCCACCTTGCATGGTGCCCCTTC
CTGCATAGGACTGGAAGACCGAAGTTTTTTTATGGCCATATTTTCTACTGCAATTCTGAAGTGT
TCATTTCTCACAAACTGTACTGACTCGAGGGGCGCTGATTTCATAGGATCTGGTGCTGTATATA
CGAATCTTGCAAAGCTCTAACTGAACGGACCTTCTTATTCCTCTCCCCTAACACCATCGTTTCC
ACTCTTCTCAGTGTAGGTAACCGTCTATGGTGTGTTTTTTCATTAATGACAAAAAAAAAAAGGT
TTCAACTGGATTATTTAAATATTGGTAAATATTGTGCATTAGGGTTTGTTTTTCCTTTTAAGAA
GTATGTCCTTTGTATCTCTAAGTTACATGACCTATATCTTTTCCTCTTTAATAGTAGTTTTATG
TTAACCTTTAA

hide sequence

RefSeq Acc Id:

XM_011519591 ⟹ XP_011517893

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	12,388,982 - 12,835,545 (+)	NCBI

Sequence:

show sequence

CTGACCTCAGGTGATCCGCTGGCCTTGACCTCCCAAAGTGCTGAGATTACACGTGTGAGCCACC
GTGCCCGGCCCAAGCCCTTGTTACTGTCGAATTCTCCCCGAATCAACCTTGAAACTTAACCAGT
TTTCTTGCTTTCAGCTTTTCCCCCAGACTCCAGCTTCTAGATTCTCTGTCTGTCAATAAGAGTG
TCGAGGTTTAGAGCAGAGGCAAAAACTGGTTTACAGCAGAGAAAAAAGCCTTCATCTACGCTGG
TGTGCCTTCTTGGCCCAGGAAATGTTTTTGGCAGTCTGAGTGTTTTGTCTTCTCTGTTGGGGGC
TGTTAAGAGGCACAAGAAAACATACCTGTCTGCTAATTGCAGAGGTTAAAAGGCAAGAGCAAAA
ACACATCGCACCTGACATGCGTTTCAAATTAATAAATTGTTAAAAATGCCTACTTGGGAGACTT
CTGCGGGGCTCAAAGACAGCTCCGTCATTACCTGGGGCTAGAGGCTCCAGCAGTTTTTCAGATA
CTGTGTGGCAATGCGAGGTTTGTCTGCTGTGAAGGGAAAACCATCCCACCGCTTAGGAAGTCGT
GAGATGCAGCACGAATGTGATTTTGTTACCACGCTCCCCTGGAGGCACGTCGTGCTGTTCTAGA
AAGCCTGTCGTTGGAGGAAAACACTTGATGAGCCTGCGGTAAAGGCGTGGCTTGCGATTTCACT
TGGGAAGCACATTGTCGTGTCGTCTGTGTGATTTACATCCCGCAGCTGATGGAGACACCACCAT
ACTCCATGGAAGGTCCTTCCTGTCCGATCTGTCCAAGCGGGGCCTTTTCCGAAGTGGTTTTAGC
TGAAGAGAAGGCAACTGGCAAGCTCTTTGCTGTGAAGTGTATCCCTAAGAAGGCGCTGAAGGGC
AAGGAAAGCAGCATAGAGAATGAGATAGCCGTCCTGAGAAAGATTAAGCATGAAAATATTGTTG
CCCTGGAAGACATTTATGAAAGCCCAAATCACCTGTACTTGGTCATGCAGCTGGTGTCCGGTGG
AGAGCTGTTTGACCGGATAGTGGAGAAGGGGTTTTATACAGAGAAGGATGCCAGCACTCTGATC
CGCCAAGTCTTGGACGCCGTGTACTATCTCCACAGAATGGGCATCGTCCACAGAGACCTCAAGC
CCGAAAATCTCTTGTACTACAGTCAAGATGAGGAGTCCAAAATAATGATCAGTGACTTTGGATT
GTCAAAAATGGAGGGCAAAGGAGATGTGATGTCCACTGCCTGTGGAACTCCAGGCTATGTCGCT
CCTGAAGTCCTCGCCCAGAAACCTTACAGCAAAGCCGTTGACTGCTGGTCCATCGGAGTGATTG
CCTACATCTTGCTCTGCGGCTACCCTCCTTTTTATGATGAAAATGACTCCAAGCTCTTTGAGCA
GATCCTCAAGGCGGAATATGAGTTTGACTCTCCCTACTGGGATGACATCTCCGACTCTGCAAAA
GACTTCATTCGGAACCTGATGGAGAAGGACCCGAATAAAAGATACACGTGTGAGCAGGCAGCTC
GGCACCCATGGATCGCTGGTGACACAGCCCTCAACAAAAACATCCACGAGTCCGTCAGCGCCCA
GATCCGGAAAAACTTTGCCAAGAGCAAATGGAGACAAGCATTTAATGCCACGGCCGTCGTCAGA
CATATGAGAAAACTACACCTCGGCAGCAGCCTGGACAGTTCAAATGCAAGTGTTTCGAGCAGCC
TCAGTTTGGCCAGCCAAAAAGACTGTCTGGCACCTTCCACGCTCTGTAGTTTCATTTCTTCTTC
GTCGGGGGTCTCAGGAGTTGGAGCCGAGCGGAGACCCAGGCCCACCACTGTGACGGCAGTGCAC
TCTGGAAGCAAGTGACTGGCCCTGGAGGTGGGGCCCGGGGTCGGGGCTGGGGAAGGGGAGCCCC
AGGGTCGCCAGAGCCGCGAGCCACTCCAGCGAGACCCCACCTTGCATGGTGCCCCTTCCTGCAT
AGGACTGGAAGACCGAAGTTTTTTTATGGCCATATTTTCTACTGCAATTCTGAAGTGTTCATTT
CTCACAAACTGTACTGACTCGAGGGGCGCTGATTTCATAGGATCTGGTGCTGTATATACGAATC
TTGCAAAGCTCTAACTGAACGGACCTTCTTATTCCTCTCCCCTAACACCATCGTTTCCACTCTT
CTCAGTGTAGGTAACCGTCTATGGTGTGTTTTTTCATTAATGACAAAAAAAAAAAGGTTTCAAC
TGGATTATTTAAATATTGGTAAATATTGTGCATTAGGGTTTGTTTTTCCTTTTAAGAAGTATGT
CCTTTGTATCTCTAAGTTACATGACCTATATCTTTTCCTCTTTAATAGTAGTTTTATGTTAACC
TTTAA

hide sequence

RefSeq Acc Id:

XM_011519592 ⟹ XP_011517894

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	12,664,475 - 12,835,545 (+)	NCBI

Sequence:

show sequence

TAATTTATTGGGGTCCGCAATGATAGCTAGGCAAGTGCTTTGTGTTATTGTTGAATCTGAATGA
ATGACTGGACTCTGGGGCTCAGACAGCCTTCTTGACTCAACCTCCAAGGCAAGCCAGGGCTGCA
GGTGCCAATCTCTAAACCCAATTTAGAGATTGAGTGATGTAAGCAGAGTGATTAGATTTAGCAC
GTGAAAATACAGCATGCCCAGTTACCTCTGAATTTCAGATAAACAACCATGCAATACTTGGGAC
GTACTTAAACTACAAAAGTATTCACCGTTTTGCTACAGTTCAGATGTAACTGTGTGCCATGCAT
TTTCTCTGGCCACTCTTCATATAATCCCATTCCTCCTATTTCTCCAGAAATCTAGGCTCTTCAT
TAACTCTCAAATGAGCTGGACTAAAAGAAAATGTTTATGAGCATGTGATTGATTCCAATTGCAA
ATTAAAACAATTTTTCCAAAAAGGGAAAATCTACGTGATGCCTACTTTTTGTGGGCATATTCTT
TTAGGTAGATCCAATAATGATAATGCCGTGATTTGTAGGATCTTGGTAGTCTCAAGTTAAGCTC
TCTTGGTTTCCTTGGTGGCATAGTTTATTTTCATATGCTGTATGGCTGGTAGTATCTTGCTCAG
ACCACGTAGAAACTATGGCTGACAAATAATTAGACTCTATTCTTTGGAATCAGGTGGAAGGTGA
ATTTAGTATAATCTATTGTTTTAGCTCCTGCAAAACAACTGCATTAACTACTACAAGCTGTAGA
ATTCAAAGGAAAGCTTTACCAGTCTTTGTTAATTATCTTGTTCTCTTTCATCTCAAAAAGAAGA
TAATATTCTTGTTTGTTTTCCACCTTATAAACTTCTTTCGCGGGGAAGACATCACACATTTAGG
AAAATGGTTTCCGTTTTTCCTAACTAAATAAGGTTTCTTGCTGTTTAGCGGCAACAGCCTTTCA
ATATCATTCATTCATTCAGCAAGCATTTATTCAGCAGATCTGTGCTAGGCACCAGGAGCAAACA
AAATGAATAATGTAGTTCTAGCTTTCAAGAGGTTCACAAGAATCTGCGTGTTCTGTGCTTGTCT
TTAAATGGTTCAGCAGTCATTTCAATGAGAGGCTTATGGATTAAGCATGAAAATATTGTTGCCC
TGGAAGACATTTATGAAAGCCCAAATCACCTGTACTTGGTCATGCAGCTGGTGTCCGGTGGAGA
GCTGTTTGACCGGATAGTGGAGAAGGGGTTTTATACAGAGAAGGATGCCAGCACTCTGATCCGC
CAAGTCTTGGACGCCGTGTACTATCTCCACAGAATGGGCATCGTCCACAGAGACCTCAAGCCCG
AAAATCTCTTGTACTACAGTCAAGATGAGGAGTCCAAAATAATGATCAGTGACTTTGGATTGTC
AAAAATGGAGGGCAAAGGAGATGTGATGTCCACTGCCTGTGGAACTCCAGGCTATGTCGCTCCT
GAAGTCCTCGCCCAGAAACCTTACAGCAAAGCCGTTGACTGCTGGTCCATCGGAGTGATTGCCT
ACATCTTGCTCTGCGGCTACCCTCCTTTTTATGATGAAAATGACTCCAAGCTCTTTGAGCAGAT
CCTCAAGGCGGAATATGAGTTTGACTCTCCCTACTGGGATGACATCTCCGACTCTGCAAAAGAC
TTCATTCGGAACCTGATGGAGAAGGACCCGAATAAAAGATACACGTGTGAGCAGGCAGCTCGGC
ACCCATGGATCGCTGGTGACACAGCCCTCAACAAAAACATCCACGAGTCCGTCAGCGCCCAGAT
CCGGAAAAACTTTGCCAAGAGCAAATGGAGACAAGCATTTAATGCCACGGCCGTCGTCAGACAT
ATGAGAAAACTACACCTCGGCAGCAGCCTGGACAGTTCAAATGCAAGTGTTTCGAGCAGCCTCA
GTTTGGCCAGCCAAAAAGACTGTCTGGCACCTTCCACGCTCTGTAGTTTCATTTCTTCTTCGTC
GGGGGTCTCAGGAGTTGGAGCCGAGCGGAGACCCAGGCCCACCACTGTGACGGCAGTGCACTCT
GGAAGCAAGTGACTGGCCCTGGAGGTGGGGCCCGGGGTCGGGGCTGGGGAAGGGGAGCCCCAGG
GTCGCCAGAGCCGCGAGCCACTCCAGCGAGACCCCACCTTGCATGGTGCCCCTTCCTGCATAGG
ACTGGAAGACCGAAGTTTTTTTATGGCCATATTTTCTACTGCAATTCTGAAGTGTTCATTTCTC
ACAAACTGTACTGACTCGAGGGGCGCTGATTTCATAGGATCTGGTGCTGTATATACGAATCTTG
CAAAGCTCTAACTGAACGGACCTTCTTATTCCTCTCCCCTAACACCATCGTTTCCACTCTTCTC
AGTGTAGGTAACCGTCTATGGTGTGTTTTTTCATTAATGACAAAAAAAAAAAGGTTTCAACTGG
ATTATTTAAATATTGGTAAATATTGTGCATTAGGGTTTGTTTTTCCTTTTAAGAAGTATGTCCT
TTGTATCTCTAAGTTACATGACCTATATCTTTTCCTCTTTAATAGTAGTTTTATGTTAACCTTT
AA

hide sequence

RefSeq Acc Id:

XM_011519593 ⟹ XP_011517895

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	12,663,234 - 12,835,545 (+)	NCBI

Sequence:

show sequence

TTATTTTTCTTTTCTTCCAGACACATAGCAGAAACGCAGCAAATGACAATTGCTTGATTGGTTG
ATGGAGAGATATTAATAAAGTGTCTTTCCAGCCACTGTGAAACTGCTATTTGGGATTGTCCTTG
CTGTGTGCAACACTTCTCTGGAACGCTGCAATGGATTAAAAGCAGTTTCTAGTCAGCACTCATG
ATTAAGCATGAAAATATTGTTGCCCTGGAAGACATTTATGAAAGCCCAAATCACCTGTACTTGG
TCATGCAGCTGGTGTCCGGTGGAGAGCTGTTTGACCGGATAGTGGAGAAGGGGTTTTATACAGA
GAAGGATGCCAGCACTCTGATCCGCCAAGTCTTGGACGCCGTGTACTATCTCCACAGAATGGGC
ATCGTCCACAGAGACCTCAAGCCCGAAAATCTCTTGTACTACAGTCAAGATGAGGAGTCCAAAA
TAATGATCAGTGACTTTGGATTGTCAAAAATGGAGGGCAAAGGAGATGTGATGTCCACTGCCTG
TGGAACTCCAGGCTATGTCGCTCCTGAAGTCCTCGCCCAGAAACCTTACAGCAAAGCCGTTGAC
TGCTGGTCCATCGGAGTGATTGCCTACATCTTGCTCTGCGGCTACCCTCCTTTTTATGATGAAA
ATGACTCCAAGCTCTTTGAGCAGATCCTCAAGGCGGAATATGAGTTTGACTCTCCCTACTGGGA
TGACATCTCCGACTCTGCAAAAGACTTCATTCGGAACCTGATGGAGAAGGACCCGAATAAAAGA
TACACGTGTGAGCAGGCAGCTCGGCACCCATGGATCGCTGGTGACACAGCCCTCAACAAAAACA
TCCACGAGTCCGTCAGCGCCCAGATCCGGAAAAACTTTGCCAAGAGCAAATGGAGACAAGCATT
TAATGCCACGGCCGTCGTCAGACATATGAGAAAACTACACCTCGGCAGCAGCCTGGACAGTTCA
AATGCAAGTGTTTCGAGCAGCCTCAGTTTGGCCAGCCAAAAAGACTGTCTGGCACCTTCCACGC
TCTGTAGTTTCATTTCTTCTTCGTCGGGGGTCTCAGGAGTTGGAGCCGAGCGGAGACCCAGGCC
CACCACTGTGACGGCAGTGCACTCTGGAAGCAAGTGACTGGCCCTGGAGGTGGGGCCCGGGGTC
GGGGCTGGGGAAGGGGAGCCCCAGGGTCGCCAGAGCCGCGAGCCACTCCAGCGAGACCCCACCT
TGCATGGTGCCCCTTCCTGCATAGGACTGGAAGACCGAAGTTTTTTTATGGCCATATTTTCTAC
TGCAATTCTGAAGTGTTCATTTCTCACAAACTGTACTGACTCGAGGGGCGCTGATTTCATAGGA
TCTGGTGCTGTATATACGAATCTTGCAAAGCTCTAACTGAACGGACCTTCTTATTCCTCTCCCC
TAACACCATCGTTTCCACTCTTCTCAGTGTAGGTAACCGTCTATGGTGTGTTTTTTCATTAATG
ACAAAAAAAAAAAGGTTTCAACTGGATTATTTAAATATTGGTAAATATTGTGCATTAGGGTTTG
TTTTTCCTTTTAAGAAGTATGTCCTTTGTATCTCTAAGTTACATGACCTATATCTTTTCCTCTT
TAATAGTAGTTTTATGTTAACCTTTAA

hide sequence

RefSeq Acc Id:

XM_011519595 ⟹ XP_011517897

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	12,650,082 - 12,835,545 (+)	NCBI

Sequence:

show sequence

TAAAACCCGCACAGGTGACCTTGGTGACAAAGCCCCTCACAGCAGTCCCTCCTCTACCCTTGGA
GGGGCTGCCGACCACGATTAAGCATGAAAATATTGTTGCCCTGGAAGACATTTATGAAAGCCCA
AATCACCTGTACTTGGTCATGCAGCTGGTGTCCGGTGGAGAGCTGTTTGACCGGATAGTGGAGA
AGGGGTTTTATACAGAGAAGGATGCCAGCACTCTGATCCGCCAAGTCTTGGACGCCGTGTACTA
TCTCCACAGAATGGGCATCGTCCACAGAGACCTCAAGCCCGAAAATCTCTTGTACTACAGTCAA
GATGAGGAGTCCAAAATAATGATCAGTGACTTTGGATTGTCAAAAATGGAGGGCAAAGGAGATG
TGATGTCCACTGCCTGTGGAACTCCAGGCTATGTCGCTCCTGAAGTCCTCGCCCAGAAACCTTA
CAGCAAAGCCGTTGACTGCTGGTCCATCGGAGTGATTGCCTACATCTTGCTCTGCGGCTACCCT
CCTTTTTATGATGAAAATGACTCCAAGCTCTTTGAGCAGATCCTCAAGGCGGAATATGAGTTTG
ACTCTCCCTACTGGGATGACATCTCCGACTCTGCAAAAGACTTCATTCGGAACCTGATGGAGAA
GGACCCGAATAAAAGATACACGTGTGAGCAGGCAGCTCGGCACCCATGGATCGCTGGTGACACA
GCCCTCAACAAAAACATCCACGAGTCCGTCAGCGCCCAGATCCGGAAAAACTTTGCCAAGAGCA
AATGGAGACAAGCATTTAATGCCACGGCCGTCGTCAGACATATGAGAAAACTACACCTCGGCAG
CAGCCTGGACAGTTCAAATGCAAGTGTTTCGAGCAGCCTCAGTTTGGCCAGCCAAAAAGACTGT
CTGGCACCTTCCACGCTCTGTAGTTTCATTTCTTCTTCGTCGGGGGTCTCAGGAGTTGGAGCCG
AGCGGAGACCCAGGCCCACCACTGTGACGGCAGTGCACTCTGGAAGCAAGTGACTGGCCCTGGA
GGTGGGGCCCGGGGTCGGGGCTGGGGAAGGGGAGCCCCAGGGTCGCCAGAGCCGCGAGCCACTC
CAGCGAGACCCCACCTTGCATGGTGCCCCTTCCTGCATAGGACTGGAAGACCGAAGTTTTTTTA
TGGCCATATTTTCTACTGCAATTCTGAAGTGTTCATTTCTCACAAACTGTACTGACTCGAGGGG
CGCTGATTTCATAGGATCTGGTGCTGTATATACGAATCTTGCAAAGCTCTAACTGAACGGACCT
TCTTATTCCTCTCCCCTAACACCATCGTTTCCACTCTTCTCAGTGTAGGTAACCGTCTATGGTG
TGTTTTTTCATTAATGACAAAAAAAAAAAGGTTTCAACTGGATTATTTAAATATTGGTAAATAT
TGTGCATTAGGGTTTGTTTTTCCTTTTAAGAAGTATGTCCTTTGTATCTCTAAGTTACATGACC
TATATCTTTTCCTCTTTAATAGTAGTTTTATGTTAACCTTTAA

hide sequence

RefSeq Acc Id:

XM_047425537 ⟹ XP_047281493

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	12,388,982 - 12,835,545 (+)	NCBI

RefSeq Acc Id:

XM_054366366 ⟹ XP_054222341

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	12,399,027 - 12,849,903 (+)	NCBI

RefSeq Acc Id:

XM_054366367 ⟹ XP_054222342

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	12,360,834 - 12,849,903 (+)	NCBI

RefSeq Acc Id:

XM_054366368 ⟹ XP_054222343

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	12,360,834 - 12,849,903 (+)	NCBI

RefSeq Acc Id:

XM_054366369 ⟹ XP_054222344

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	12,677,492 - 12,849,903 (+)	NCBI

RefSeq Acc Id:

XM_054366370 ⟹ XP_054222345

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	12,676,252 - 12,849,903 (+)	NCBI

RefSeq Acc Id:

XM_054366371 ⟹ XP_054222346

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	12,663,100 - 12,849,903 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_001337961	(Get FASTA)	NCBI Sequence Viewer
	NP_065130	(Get FASTA)	NCBI Sequence Viewer
	NP_705718	(Get FASTA)	NCBI Sequence Viewer
	XP_006717545	(Get FASTA)	NCBI Sequence Viewer
	XP_006717546	(Get FASTA)	NCBI Sequence Viewer
	XP_011517893	(Get FASTA)	NCBI Sequence Viewer
	XP_011517894	(Get FASTA)	NCBI Sequence Viewer
	XP_011517895	(Get FASTA)	NCBI Sequence Viewer
	XP_011517897	(Get FASTA)	NCBI Sequence Viewer
	XP_047281493	(Get FASTA)	NCBI Sequence Viewer
	XP_054222341	(Get FASTA)	NCBI Sequence Viewer
	XP_054222342	(Get FASTA)	NCBI Sequence Viewer
	XP_054222343	(Get FASTA)	NCBI Sequence Viewer
	XP_054222344	(Get FASTA)	NCBI Sequence Viewer
	XP_054222345	(Get FASTA)	NCBI Sequence Viewer
	XP_054222346	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAG00534	(Get FASTA)	NCBI Sequence Viewer
	AAH35745	(Get FASTA)	NCBI Sequence Viewer
	ACA05958	(Get FASTA)	NCBI Sequence Viewer
	ACA05959	(Get FASTA)	NCBI Sequence Viewer
	ACA05960	(Get FASTA)	NCBI Sequence Viewer
	BAC19846	(Get FASTA)	NCBI Sequence Viewer
	BAF82082	(Get FASTA)	NCBI Sequence Viewer
	CBX51344	(Get FASTA)	NCBI Sequence Viewer
	EAW86314	(Get FASTA)	NCBI Sequence Viewer
	EAW86315	(Get FASTA)	NCBI Sequence Viewer
	EAW86316	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000368122
	ENSP00000368122.1
	ENSP00000478874
	ENSP00000478874.1
GenBank Protein	Q8IU85	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_705718 ⟸ NM_153498
- Peptide Label:	isoform 2
- UniProtKB:	B0YIY0 (UniProtKB/Swiss-Prot), Q9HD31 (UniProtKB/Swiss-Prot), Q8IU85 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MARENGESSSSWKKQAEDIKKIFEFKETLGTGAFSEVVLAEEKATGKLFAVKCIPKKALKGKES SIENEIAVLRKIKHENIVALEDIYESPNHLYLVMQLVSGGELFDRIVEKGFYTEKDASTLIRQV LDAVYYLHRMGIVHRDLKPENLLYYSQDEESKIMISDFGLSKMEGKGDVMSTACGTPGYVAPEV LAQKPYSKAVDCWSIGVIAYILLCGYPPFYDENDSKLFEQILKAEYEFDSPYWDDISDSAKDFI RNLMEKDPNKRYTCEQAARHPWIAGDTALNKNIHESVSAQIRKNFAKSKWRQAFNATAVVRHMR KLHLGSSLDSSNASVSSSLSLASQKDCLAPSTLCSFISSSSGVSGVGAERRPRPTTVTAVHSGS K hide sequence

RefSeq Acc Id:	NP_065130 ⟸ NM_020397
- Peptide Label:	isoform 1
- UniProtKB:	Q5SQQ7 (UniProtKB/TrEMBL)
- Sequence:	show sequence MARENGESSSSWKKQAEDIKKIFEFKETLGTGAFSEVVLAEEKATGKLFAVKCIPKKALKGKES SIENEIAVLRKIKHENIVALEDIYESPNHLYLVMQLVSGGELFDRIVEKGFYTEKDASTLIRQV LDAVYYLHRMGIVHRDLKPENLLYYSQDEESKIMISDFGLSKMEGKGDVMSTACGTPGYVAPEV LAQKPYSKAVDCWSIGVIAYILLCGYPPFYDENDSKLFEQILKAEYEFDSPYWDDISDSAKDFI RNLMEKDPNKRYTCEQAARHPWIAGDTALNKNIHESVSAQIRKNFAKSKWRQAFNATAVVRHMR KLHLGSSLDSSNASVSSSLSLASQKDCAYVAKPESLS hide sequence

RefSeq Acc Id:

XP_006717546 ⟸ XM_006717483

- Peptide Label:

isoform X3

- Sequence:

show sequence

MARENGESSSSWKKQAEDIKKIFEFKETLGTGAFSEVVLAEEKATGKLFAVKCIPKKALKGKES
SIENEIAVLRKIKHENIVALEDIYESPNHLYLVMQLVSGGELFDRIVEKGFYTEKDASTLIRQV
LDAVYYLHRMGIVHRDLKPENLLYYSQDEESKIMISDFGLSKMEGKGDVMSTACGTPGYVAPEV
LAQKPYSKAVDCWSIGVIAYILLCGYPPFYDENDSKLFEQILKAEYEFDSPYWDDISDSAKDFI
RNLMEKDPNKRYTCEQAARHPWIAGDTALNKNIHESVSAQIRKNFAKSKWRQAFNATAVVRHMR
KLHLGSSLDSSNASVSSSLSLASQKDCASGTFHAL

hide sequence

RefSeq Acc Id:

XP_006717545 ⟸ XM_006717482

- Peptide Label:

isoform X2

- Sequence:

show sequence

MARENGESSSSWKKQAEDIKKIFEFKETLGTGAFSEVVLAEEKATGKLFAVKCIPKKALKGKES
SIENEIAVLRKIKHENIVALEDIYESPNHLYLVMQLVSGGELFDRIVEKGFYTEKDASTLIRQV
LDAVYYLHRMGIVHRDLKPENLLYYSQDEESKIMISDFGLSKMEGKGDVMSTACGTPGYVAPEV
LAQKPYSKAVDCWSIGVIAYILLCGYPPFYDENDSKLFEQILKAEYEFDSPYWDDISDSAKDFI
RNLMEKDPNKRYTCEQAARHPWIAGDTALNKNIHESVSAQIRKNFAKSKWRQAFNATAVVRHMR
KLHLGSSLDSSNVWHLPRSVVSFLLRRGSQELEPSGDPGPPL

hide sequence

RefSeq Acc Id:

XP_011517893 ⟸ XM_011519591

- Peptide Label:

isoform X1

- Sequence:

show sequence

METPPYSMEGPSCPICPSGAFSEVVLAEEKATGKLFAVKCIPKKALKGKESSIENEIAVLRKIK
HENIVALEDIYESPNHLYLVMQLVSGGELFDRIVEKGFYTEKDASTLIRQVLDAVYYLHRMGIV
HRDLKPENLLYYSQDEESKIMISDFGLSKMEGKGDVMSTACGTPGYVAPEVLAQKPYSKAVDCW
SIGVIAYILLCGYPPFYDENDSKLFEQILKAEYEFDSPYWDDISDSAKDFIRNLMEKDPNKRYT
CEQAARHPWIAGDTALNKNIHESVSAQIRKNFAKSKWRQAFNATAVVRHMRKLHLGSSLDSSNA
SVSSSLSLASQKDCLAPSTLCSFISSSSGVSGVGAERRPRPTTVTAVHSGSK

hide sequence

RefSeq Acc Id:

XP_011517897 ⟸ XM_011519595

- Peptide Label:

isoform X6

- Sequence:

show sequence

MQLVSGGELFDRIVEKGFYTEKDASTLIRQVLDAVYYLHRMGIVHRDLKPENLLYYSQDEESKI
MISDFGLSKMEGKGDVMSTACGTPGYVAPEVLAQKPYSKAVDCWSIGVIAYILLCGYPPFYDEN
DSKLFEQILKAEYEFDSPYWDDISDSAKDFIRNLMEKDPNKRYTCEQAARHPWIAGDTALNKNI
HESVSAQIRKNFAKSKWRQAFNATAVVRHMRKLHLGSSLDSSNASVSSSLSLASQKDCLAPSTL
CSFISSSSGVSGVGAERRPRPTTVTAVHSGSK

hide sequence

RefSeq Acc Id:

XP_011517895 ⟸ XM_011519593

- Peptide Label:

isoform X5

- Sequence:

show sequence

MIKHENIVALEDIYESPNHLYLVMQLVSGGELFDRIVEKGFYTEKDASTLIRQVLDAVYYLHRM
GIVHRDLKPENLLYYSQDEESKIMISDFGLSKMEGKGDVMSTACGTPGYVAPEVLAQKPYSKAV
DCWSIGVIAYILLCGYPPFYDENDSKLFEQILKAEYEFDSPYWDDISDSAKDFIRNLMEKDPNK
RYTCEQAARHPWIAGDTALNKNIHESVSAQIRKNFAKSKWRQAFNATAVVRHMRKLHLGSSLDS
SNASVSSSLSLASQKDCLAPSTLCSFISSSSGVSGVGAERRPRPTTVTAVHSGSK

hide sequence

RefSeq Acc Id:

XP_011517894 ⟸ XM_011519592

- Peptide Label:

isoform X4

- Sequence:

show sequence

MRGLWIKHENIVALEDIYESPNHLYLVMQLVSGGELFDRIVEKGFYTEKDASTLIRQVLDAVYY
LHRMGIVHRDLKPENLLYYSQDEESKIMISDFGLSKMEGKGDVMSTACGTPGYVAPEVLAQKPY
SKAVDCWSIGVIAYILLCGYPPFYDENDSKLFEQILKAEYEFDSPYWDDISDSAKDFIRNLMEK
DPNKRYTCEQAARHPWIAGDTALNKNIHESVSAQIRKNFAKSKWRQAFNATAVVRHMRKLHLGS
SLDSSNASVSSSLSLASQKDCLAPSTLCSFISSSSGVSGVGAERRPRPTTVTAVHSGSK

hide sequence

RefSeq Acc Id:

NP_001337961 ⟸ NM_001351032

- Peptide Label:

isoform 3

- Sequence:

show sequence

MQLVSGGELFDRIVEKGFYTEKDASTLIRQVLDAVYYLHRMGIVHRDLKPENLLYYSQDEESKI
MISDFGLSKMEGKGDVMSTACGTPGYVAPEVLAQKPYSKAVDCWSIGVIAYILLCGYPPFYDEN
DSKLFEQILKAEYEFDSPYWDDISDSAKDFIRNLMEKDPNKRYTCEQAARHPWIAGDTALNKNI
HESVSAQIRKNFAKSKWRQAFNATAVVRHMRKLHLGSSLDSSNASVSSSLSLASQKDCAYVAKP
ESLS

hide sequence

Ensembl Acc Id:

ENSP00000368122 ⟸ ENST00000378845

Ensembl Acc Id:

ENSP00000478861 ⟸ ENST00000615792

Ensembl Acc Id:

ENSP00000478874 ⟸ ENST00000619168

RefSeq Acc Id:	XP_047281493 ⟸ XM_047425537
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_054222343 ⟸ XM_054366368
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054222342 ⟸ XM_054366367
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054222341 ⟸ XM_054366366
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054222346 ⟸ XM_054366371
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_054222345 ⟸ XM_054366370
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054222344 ⟸ XM_054366369
- Peptide Label:	isoform X4

Protein Domains

Protein kinase

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q8IU85-F1-model_v2	AlphaFold	Q8IU85	1-385	view protein structure

Promoters

RGD ID:

7216997

Promoter ID:

EPDNEW_H14244

Type:

initiation region

Name:

CAMK1D_2

Description:

calcium/calmodulin dependent protein kinase ID

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H14245

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	12,349,576 - 12,349,636	EPDNEW

RGD ID:

7216999

Promoter ID:

EPDNEW_H14245

Type:

initiation region

Name:

CAMK1D_1

Description:

calcium/calmodulin dependent protein kinase ID

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H14244

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	12,349,711 - 12,349,771	EPDNEW

RGD ID:

6787435

Promoter ID:

HG_KWN:8610

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:

ENST00000378845, OTTHUMT00000046820, OTTHUMT00000046822

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	10	12,430,826 - 12,431,712 (+)	MPROMDB

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:19341	AgrOrtholog
COSMIC	CAMK1D	COSMIC
Ensembl Genes	ENSG00000183049	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000378845	ENTREZGENE
	ENST00000378845.5	UniProtKB/Swiss-Prot
	ENST00000619168	ENTREZGENE
	ENST00000619168.5	UniProtKB/Swiss-Prot
Gene3D-CATH	Phosphorylase Kinase, domain 1	UniProtKB/Swiss-Prot
	Transferase(Phosphotransferase) domain 1	UniProtKB/Swiss-Prot
GTEx	ENSG00000183049	GTEx
HGNC ID	HGNC:19341	ENTREZGENE
Human Proteome Map	CAMK1D	Human Proteome Map
InterPro	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:57118	UniProtKB/Swiss-Prot
NCBI Gene	57118	ENTREZGENE
OMIM	607957	OMIM
PANTHER	SERINE/THREONINE-PROTEIN KINASE	UniProtKB/Swiss-Prot
Pfam	Pkinase	UniProtKB/Swiss-Prot
PharmGKB	PA134992438	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	B0YIY0	ENTREZGENE
	KCC1D_HUMAN	UniProtKB/Swiss-Prot
	Q5SQQ7	ENTREZGENE, UniProtKB/TrEMBL
	Q8IU85	ENTREZGENE
	Q9HD31	ENTREZGENE
UniProt Secondary	B0YIY0	UniProtKB/Swiss-Prot
	Q9HD31	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2015-12-08	CAMK1D	calcium/calmodulin dependent protein kinase ID	CAMK1D	calcium/calmodulin-dependent protein kinase ID	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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