JKAMP (JNK1/MAPK8 associated membrane protein)

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Gene: JKAMP (JNK1/MAPK8 associated membrane protein) Homo sapiens

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Symbol:

JKAMP

Name:

JNK1/MAPK8 associated membrane protein

RGD ID:

1318960

HGNC Page

HGNC:20184

Description:

Enables ubiquitin protein ligase binding activity. Involved in ERAD pathway. Predicted to be located in endoplasmic reticulum membrane.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

C14orf100; C24orf100; CDA06; HSPC213; HSPC327; JAMP; JNK-associated membrane protein; JNK1-associated membrane protein; Jun N-terminal kinase 1-associated membrane protein; medulloblastoma antigen MU-MB-50.4

RGD Orthologs

Alliance Orthologs

More Info

more info ...

Related Pseudogenes:

JKAMPP1

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	14	59,484,517 - 59,505,410 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	14	59,484,443 - 59,505,410 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	14	59,951,235 - 59,972,128 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	14	59,020,914 - 59,041,834 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	14	59,020,978 - 59,041,182	NCBI
Celera	14	40,000,231 - 40,021,171 (+)	NCBI		Celera
Cytogenetic Map	14	q23.1	NCBI
HuRef	14	40,115,022 - 40,135,955 (+)	NCBI		HuRef
CHM1_1	14	59,889,332 - 59,910,261 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	14	53,691,449 - 53,712,359 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

1,2-dimethylhydrazine (ISO)

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

aflatoxin B1 (EXP)

all-trans-retinoic acid (EXP)

aristolochic acid A (ISO)

arsenite(3-) (EXP)

arsenous acid (ISO)

benzo[a]pyrene diol epoxide I (EXP)

bisphenol A (ISO)

cadmium dichloride (EXP,ISO)

clofibrate (ISO)

copper(II) sulfate (EXP)

cyclosporin A (EXP)

diarsenic trioxide (ISO)

dicrotophos (EXP)

dorsomorphin (EXP)

doxorubicin (EXP)

ethanol (ISO)

fenitrothion (ISO)

finasteride (ISO)

folic acid (ISO)

formaldehyde (EXP)

lead diacetate (ISO)

lipopolysaccharide (EXP)

metformin (ISO)

methyl methanesulfonate (EXP)

ochratoxin A (EXP)

paracetamol (EXP,ISO)

resveratrol (EXP,ISO)

rotenone (EXP)

SB 431542 (EXP)

sulindac (ISO)

temozolomide (EXP)

tetrachloromethane (ISO)

thapsigargin (ISO)

thioacetamide (ISO)

titanium dioxide (ISO)

trichostatin A (EXP)

triphenyl phosphate (EXP)

valproic acid (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

ERAD pathway (IBA,IDA)

response to unfolded protein (IEA)

Cellular Component

endoplasmic reticulum (IEA)

endoplasmic reticulum membrane (IEA)

membrane (IEA)

Molecular Function

protein binding (IPI)

ubiquitin protein ligase binding (IBA,IPI)

References

References - curated

#	Reference Title	Reference Citation
1.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:11042152	PMID:11076863	PMID:11230166	PMID:12477932	PMID:12800201	PMID:14702039	PMID:15489334	PMID:15489336	PMID:16166642	PMID:16381901	PMID:18784250	PMID:19269966
PMID:20379614	PMID:21873635	PMID:23798571	PMID:24453475	PMID:25173965	PMID:28298427	PMID:30021884	PMID:32296183

Genomics

Comparative Map Data

JKAMP
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	14	59,484,517 - 59,505,410 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	14	59,484,443 - 59,505,410 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	14	59,951,235 - 59,972,128 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	14	59,020,914 - 59,041,834 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	14	59,020,978 - 59,041,182	NCBI
Celera	14	40,000,231 - 40,021,171 (+)	NCBI		Celera
Cytogenetic Map	14	q23.1	NCBI
HuRef	14	40,115,022 - 40,135,955 (+)	NCBI		HuRef
CHM1_1	14	59,889,332 - 59,910,261 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	14	53,691,449 - 53,712,359 (+)	NCBI		T2T-CHM13v2.0

Jkamp
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	12	72,132,348 - 72,148,301 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	12	72,132,363 - 72,148,235 (+)	Ensembl		GRCm39 Ensembl
GRCm38	12	72,085,548 - 72,101,527 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	12	72,085,589 - 72,101,461 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	12	73,187,110 - 73,201,848 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	12	73,004,707 - 73,019,445 (+)	NCBI		MGSCv36	mm8
Celera	12	73,197,119 - 73,211,857 (+)	NCBI		Celera
Cytogenetic Map	12	C3	NCBI
cM Map	12	30.2	NCBI

Jkamp
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	6	96,383,976 - 96,397,917 (+)	NCBI		GRCr8
mRatBN7.2	6	90,648,043 - 90,661,985 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	6	90,648,160 - 90,662,501 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	6	91,018,912 - 91,032,859 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	6	91,318,376 - 91,332,323 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	6	90,757,932 - 90,771,879 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	6	94,835,845 - 94,849,784 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	6	94,835,845 - 94,849,784 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	6	104,280,504 - 104,294,443 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	6	94,281,853 - 94,295,840 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	6	94,285,308 - 94,299,859 (+)	NCBI
Celera	6	89,112,919 - 89,126,861 (+)	NCBI		Celera
Cytogenetic Map	6	q24	NCBI

Jkamp
(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_004955466	13,205,424 - 13,225,573 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955466	13,205,424 - 13,225,573 (+)	NCBI	ChiLan1.0	ChiLan1.0

JKAMP
(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	15	60,616,571 - 60,637,288 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	14	59,833,579 - 59,854,431 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	14	40,087,037 - 40,107,897 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	14	58,351,807 - 58,372,653 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	14	58,351,807 - 58,372,653 (+)	Ensembl	panpan1.1		panPan2

JKAMP
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	8	34,686,354 - 34,725,069 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	8	34,699,621 - 34,724,711 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	8	34,446,775 - 34,486,056 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	8	34,921,937 - 34,961,231 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	8	34,921,837 - 34,961,230 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	8	34,539,170 - 34,578,449 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	8	34,608,227 - 34,647,500 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	8	34,975,465 - 35,014,732 (+)	NCBI		UU_Cfam_GSD_1.0

Jkamp
(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_024408640	70,342,621 - 70,352,652 (-)	NCBI		HiC_Itri_2
SpeTri2.0	NW_004936495	3,839,057 - 3,849,062 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

JKAMP
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	1	188,598,501 - 188,624,892 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	1	188,598,456 - 188,617,705 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1

JKAMP
(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	24	36,714,768 - 36,737,601 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	24	36,714,915 - 36,737,799 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666053	24,969,340 - 24,992,036 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Jkamp
(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_004624734	41,610,985 - 41,625,707 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624734	41,610,973 - 41,625,736 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in JKAMP
15 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 14q22.3-23.3(chr14:57041036-67208231)x1	copy number loss	See cases [RCV000051521]	Chr14:57041036..67208231 [GRCh38] Chr14:57507754..67674948 [GRCh37] Chr14:56577507..66744701 [NCBI36] Chr14:14q22.3-23.3	pathogenic
GRCh38/hg38 14q23.1(chr14:58146022-61273619)x1	copy number loss	See cases [RCV000051522]	Chr14:58146022..61273619 [GRCh38] Chr14:58612740..61740337 [GRCh37] Chr14:57682493..60810090 [NCBI36] Chr14:14q23.1	pathogenic
GRCh38/hg38 14q11.2-32.33(chr14:20151149-106855263)x3	copy number gain	See cases [RCV000135543]	Chr14:20151149..106855263 [GRCh38] Chr14:20619308..107263478 [GRCh37] Chr14:19689148..106334523 [NCBI36] Chr14:14q11.2-32.33	pathogenic
GRCh38/hg38 14q23.1-23.2(chr14:57653413-64093528)x1	copy number loss	See cases [RCV000138348]	Chr14:57653413..64093528 [GRCh38] Chr14:58120131..64560246 [GRCh37] Chr14:57189884..63629999 [NCBI36] Chr14:14q23.1-23.2	pathogenic
GRCh38/hg38 14q11.2-32.33(chr14:20043514-106877229)x3	copy number gain	See cases [RCV000143373]	Chr14:20043514..106877229 [GRCh38] Chr14:20511673..107285437 [GRCh37] Chr14:19581513..106356482 [NCBI36] Chr14:14q11.2-32.33	pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19794561-107234280)x3	copy number gain	See cases [RCV000446256]	Chr14:19794561..107234280 [GRCh37] Chr14:14q11.2-32.33	pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:20511673-107285437)	copy number gain	See cases [RCV000512041]	Chr14:20511673..107285437 [GRCh37] Chr14:14q11.2-32.33	pathogenic
GRCh37/hg19 14q23.1(chr14:59527587-60119877)x3	copy number gain	not provided [RCV000683612]	Chr14:59527587..60119877 [GRCh37] Chr14:14q23.1	uncertain significance
GRCh37/hg19 14q11.2-32.33(chr14:19280733-107287663)x3	copy number gain	not provided [RCV000738413]	Chr14:19280733..107287663 [GRCh37] Chr14:14q11.2-32.33	pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19327823-107287663)x3	copy number gain	not provided [RCV000738414]	Chr14:19327823..107287663 [GRCh37] Chr14:14q11.2-32.33	pathogenic
GRCh37/hg19 14q11.1-32.33(chr14:19000422-107289053)x3	copy number gain	not provided [RCV000738412]	Chr14:19000422..107289053 [GRCh37] Chr14:14q11.1-32.33	pathogenic
GRCh37/hg19 14q23.1(chr14:59939135-60006849)x3	copy number gain	not provided [RCV000846465]	Chr14:59939135..60006849 [GRCh37] Chr14:14q23.1	uncertain significance
NM_016475.5(JKAMP):c.920G>C (p.Gly307Ala)	single nucleotide variant	not specified [RCV004292396]	Chr14:59504056 [GRCh38] Chr14:59970774 [GRCh37] Chr14:14q23.1	uncertain significance
GRCh37/hg19 14q22.2-24.3(chr14:54654001-75828024)x3	copy number gain	14q22.2q24.3 duplication [RCV001506967]	Chr14:54654001..75828024 [GRCh37] Chr14:14q22.2-24.3	likely pathogenic
GRCh37/hg19 14q13.3-32.33(chr14:37671058-106985955)x2	copy number gain	See cases [RCV002286356]	Chr14:37671058..106985955 [GRCh37] Chr14:14q13.3-32.33	pathogenic
GRCh37/hg19 14q22.3-23.2(chr14:57804997-63590203)x1	copy number loss	not provided [RCV002472446]	Chr14:57804997..63590203 [GRCh37] Chr14:14q22.3-23.2	likely pathogenic
NM_016475.5(JKAMP):c.926A>G (p.Asn309Ser)	single nucleotide variant	not specified [RCV004107577]	Chr14:59504062 [GRCh38] Chr14:59970780 [GRCh37] Chr14:14q23.1	uncertain significance
NM_016475.5(JKAMP):c.166T>A (p.Tyr56Asn)	single nucleotide variant	not specified [RCV004137366]	Chr14:59487743 [GRCh38] Chr14:59954461 [GRCh37] Chr14:14q23.1	uncertain significance
NM_016475.5(JKAMP):c.610G>A (p.Val204Met)	single nucleotide variant	not specified [RCV004214967]	Chr14:59498878 [GRCh38] Chr14:59965596 [GRCh37] Chr14:14q23.1	uncertain significance
NM_016475.5(JKAMP):c.20C>G (p.Pro7Arg)	single nucleotide variant	not specified [RCV004130374]	Chr14:59486728 [GRCh38] Chr14:59953446 [GRCh37] Chr14:14q23.1	uncertain significance
NM_016475.5(JKAMP):c.275T>C (p.Ile92Thr)	single nucleotide variant	not specified [RCV004243943]	Chr14:59495041 [GRCh38] Chr14:59961759 [GRCh37] Chr14:14q23.1	uncertain significance
NM_001164399.2(CCDC175):c.2342C>A (p.Pro781Gln)	single nucleotide variant	not specified [RCV004199227]	Chr14:59505279 [GRCh38] Chr14:59971997 [GRCh37] Chr14:14q23.1	uncertain significance
NM_016475.5(JKAMP):c.713T>C (p.Ile238Thr)	single nucleotide variant	not specified [RCV004280553]	Chr14:59501263 [GRCh38] Chr14:59967981 [GRCh37] Chr14:14q23.1	uncertain significance
NM_001164399.2(CCDC175):c.2320A>G (p.Ile774Val)	single nucleotide variant	not specified [RCV004337228]	Chr14:59505301 [GRCh38] Chr14:59972019 [GRCh37] Chr14:14q23.1	uncertain significance
NM_016475.5(JKAMP):c.470T>C (p.Val157Ala)	single nucleotide variant	not specified [RCV004342587]	Chr14:59498738 [GRCh38] Chr14:59965456 [GRCh37] Chr14:14q23.1	uncertain significance
GRCh37/hg19 14q22.3-23.2(chr14:55667390-64447598)x1	copy number loss	not provided [RCV003483204]	Chr14:55667390..64447598 [GRCh37] Chr14:14q22.3-23.2	pathogenic
GRCh37/hg19 14q11.2-23.1(chr14:20511673-61826023)x3	copy number gain	not provided [RCV003485022]	Chr14:20511673..61826023 [GRCh37] Chr14:14q11.2-23.1	pathogenic
GRCh37/hg19 14q23.1-32.33(chr14:58894502-107227240)x3	copy number gain	not provided [RCV003485036]	Chr14:58894502..107227240 [GRCh37] Chr14:14q23.1-32.33	pathogenic
GRCh37/hg19 14q22.3-24.1(chr14:57588965-68334517)x3	copy number gain	not provided [RCV003485034]	Chr14:57588965..68334517 [GRCh37] Chr14:14q22.3-24.1	likely pathogenic
NM_016475.5(JKAMP):c.35T>G (p.Leu12Arg)	single nucleotide variant	not specified [RCV004401246]	Chr14:59486743 [GRCh38] Chr14:59953461 [GRCh37] Chr14:14q23.1	uncertain significance
NM_016475.5(JKAMP):c.353G>A (p.Arg118His)	single nucleotide variant	not specified [RCV004401245]	Chr14:59495119 [GRCh38] Chr14:59961837 [GRCh37] Chr14:14q23.1	uncertain significance
NM_016475.5(JKAMP):c.254C>A (p.Ser85Tyr)	single nucleotide variant	not specified [RCV004401244]	Chr14:59495020 [GRCh38] Chr14:59961738 [GRCh37] Chr14:14q23.1	uncertain significance
NM_016475.5(JKAMP):c.895G>A (p.Glu299Lys)	single nucleotide variant	not specified [RCV004401248]	Chr14:59504031 [GRCh38] Chr14:59970749 [GRCh37] Chr14:14q23.1	uncertain significance
NM_016475.5(JKAMP):c.646G>A (p.Ala216Thr)	single nucleotide variant	not specified [RCV004401247]	Chr14:59501196 [GRCh38] Chr14:59967914 [GRCh37] Chr14:14q23.1	uncertain significance
NM_016475.5(JKAMP):c.617A>G (p.Gln206Arg)	single nucleotide variant	not specified [RCV004635758]	Chr14:59498885 [GRCh38] Chr14:59965603 [GRCh37] Chr14:14q23.1	uncertain significance
NM_016475.5(JKAMP):c.352C>T (p.Arg118Cys)	single nucleotide variant	not specified [RCV004635757]	Chr14:59495118 [GRCh38] Chr14:59961836 [GRCh37] Chr14:14q23.1	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	1653
Count of miRNA genes:	689
Interacting mature miRNAs:	787
Transcripts:	ENST00000261247, ENST00000356057, ENST00000425728, ENST00000553156, ENST00000553647, ENST00000553941, ENST00000554271, ENST00000554721, ENST00000554754, ENST00000554795, ENST00000555491, ENST00000556985, ENST00000557560, ENST00000602482
Prediction methods:	Miranda, Rnahybrid, Targetscan
Result types:	miRGate_prediction

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

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

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
407131068	GWAS780044_H	schizophrenia QTL GWAS780044 (human)		0.000003	schizophrenia		14	59498575	59498576	Human

Markers in Region

RH11221

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	14	59,971,921 - 59,972,024	UniSTS	GRCh37
Build 36	14	59,041,674 - 59,041,777	RGD	NCBI36
Celera	14	40,021,011 - 40,021,114	RGD
Cytogenetic Map	14	q23.1	UniSTS
HuRef	14	40,135,795 - 40,135,898	UniSTS
GeneMap99-GB4 RH Map	14	134.21	UniSTS

G20716

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	14	59,971,166 - 59,971,360	UniSTS	GRCh37
Build 36	14	59,040,919 - 59,041,113	RGD	NCBI36
Celera	14	40,020,256 - 40,020,450	RGD
Cytogenetic Map	14	q23.1	UniSTS
HuRef	14	40,135,040 - 40,135,234	UniSTS

A006D06

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	14	59,971,166 - 59,971,360	UniSTS	GRCh37
Build 36	14	59,040,919 - 59,041,113	RGD	NCBI36
Celera	14	40,020,256 - 40,020,450	RGD
Cytogenetic Map	14	q23.1	UniSTS
HuRef	14	40,135,040 - 40,135,234	UniSTS
GeneMap99-GB4 RH Map	14	134.21	UniSTS

G20388

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	14	59,967,451 - 59,967,659	UniSTS	GRCh37
Build 36	14	59,037,204 - 59,037,412	RGD	NCBI36
Celera	14	40,016,523 - 40,016,731	RGD
Cytogenetic Map	14	q23.1	UniSTS
HuRef	14	40,131,304 - 40,131,512	UniSTS

A005P02

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	14	59,967,451 - 59,967,659	UniSTS	GRCh37
Build 36	14	59,037,204 - 59,037,412	RGD	NCBI36
Celera	14	40,016,523 - 40,016,731	RGD
Cytogenetic Map	14	q23.1	UniSTS
HuRef	14	40,131,304 - 40,131,512	UniSTS
GeneMap99-GB4 RH Map	14	134.21	UniSTS

SHGC-24111

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	14	59,971,228 - 59,971,377	UniSTS	GRCh37
Build 36	14	59,040,981 - 59,041,130	RGD	NCBI36
Celera	14	40,020,318 - 40,020,467	RGD
Cytogenetic Map	14	q23.1	UniSTS
HuRef	14	40,135,102 - 40,135,251	UniSTS
Stanford-G3 RH Map	14	1937.0	UniSTS
NCBI RH Map	14	597.7	UniSTS
GeneMap99-G3 RH Map	14	1985.0	UniSTS

D14S828

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	14	59,971,220 - 59,971,395	UniSTS	GRCh37
Build 36	14	59,040,973 - 59,041,148	RGD	NCBI36
Celera	14	40,020,310 - 40,020,485	RGD
Cytogenetic Map	14	q23.1	UniSTS
HuRef	14	40,135,094 - 40,135,269	UniSTS
GeneMap99-GB4 RH Map	14	136.02	UniSTS
Whitehead-RH Map	14	202.9	UniSTS
Whitehead-YAC Contig Map	14		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	2253	4974	1726	2351	6	624	1951	465	2270	7306	6472	53	3734	1	852	1744	1617	175	1

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001098625	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001284201	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001284202	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001284203	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001284204	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_016475	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006720171	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017021366	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024449627	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047431467	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054376204	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054376205	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AA461198	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF151047	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF161445	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF212245	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF529304	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK021683	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK027591	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK056145	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK128628	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK298209	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL121694	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL136696	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL159140	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL162471	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC005198	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC010359	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BU928810	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX161501	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471061	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068264	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CR457163	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CR533510	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DC381037	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HY340214	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000356057 ⟹ ENSP00000348351

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	59,484,443 - 59,505,404 (+)	Ensembl

Ensembl Acc Id:

ENST00000425728 ⟹ ENSP00000389699

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	59,484,503 - 59,504,703 (+)	Ensembl

Ensembl Acc Id:

ENST00000553156

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	59,484,528 - 59,485,968 (+)	Ensembl

Ensembl Acc Id:

ENST00000553647

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	59,500,882 - 59,504,036 (+)	Ensembl

Ensembl Acc Id:

ENST00000553941

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	59,484,569 - 59,504,274 (+)	Ensembl

Ensembl Acc Id:

ENST00000554271 ⟹ ENSP00000450749

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	59,484,545 - 59,504,705 (+)	Ensembl

Ensembl Acc Id:

ENST00000554721

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	59,487,194 - 59,504,703 (+)	Ensembl

Ensembl Acc Id:

ENST00000554754

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	59,484,445 - 59,498,777 (+)	Ensembl

Ensembl Acc Id:

ENST00000554795 ⟹ ENSP00000450813

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	59,484,560 - 59,501,267 (+)	Ensembl

Ensembl Acc Id:

ENST00000555491 ⟹ ENSP00000451723

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	59,484,531 - 59,501,247 (+)	Ensembl

Ensembl Acc Id:

ENST00000556985 ⟹ ENSP00000451076

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	59,484,537 - 59,495,305 (+)	Ensembl

Ensembl Acc Id:

ENST00000557560

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	59,484,492 - 59,495,152 (+)	Ensembl

Ensembl Acc Id:

ENST00000602482

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	59,486,681 - 59,505,410 (+)	Ensembl

Ensembl Acc Id:

ENST00000616435 ⟹ ENSP00000479775

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	59,484,517 - 59,505,410 (+)	Ensembl

RefSeq Acc Id:

NM_001098625 ⟹ NP_001092095

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	59,484,517 - 59,505,410 (+)	NCBI
GRCh37	14	59,951,161 - 59,972,081 (+)	RGD
GRCh37	14	59,951,161 - 59,972,081 (+)	NCBI
Build 36	14	59,020,914 - 59,041,834 (+)	NCBI Archive
Celera	14	40,000,231 - 40,021,171 (+)	RGD
HuRef	14	40,115,022 - 40,135,999 (+)	NCBI
CHM1_1	14	59,889,332 - 59,910,305 (+)	NCBI
T2T-CHM13v2.0	14	53,691,449 - 53,712,359 (+)	NCBI

Sequence:

show sequence

GTGGCCCGGATGTTCGGTGCAGCTGCCAGATCCGCTGATCTAGTGCTTCTCGAAAAAAACCTTC
AGGCGGCCCATGGCATGCCTTGGACTTTATTGTGGGAAGACCCTATTATTTAAAAATGGCTCAA
CTGAAATATATGGAGAATGTGGGGTATGCCCAAGAGGACAGAGAACGAATGCACAGAAATATTG
TCAGCCTTGCACAGAATCTCCTGAACTTTATGATTGGCTCTATCTTGGATTTATGGCAATGCTT
CCTCTGGTTTTACATTGGTTCTTCATTGAATGGTACTCGGGGAAAAAGAGTTCCAGCGCACTTT
TCCAACACATCACTGCATTATTTGAATGCAGCATGGCAGCTATTATCACCTTACTTGTGAGTGA
TCCAGTTGGTGTTCTTTATATTCGTTCATGTCGAGTATTGATGCTTTCTGACTGGTACACGATG
CTTTACAACCCAAGTCCAGATTACGTTACCACAGTACACTGTACTCATGAAGCCGTCTACCCAC
TATATACCATTGTATTTATCTATTACGCATTCTGCTTGGTATTAATGATGCTGCTCCGACCTCT
TCTGGTGAAGAAGATTGCATGTGGGTTAGGGAAATCTGATCGATTTAAAAGTATTTATGCTGCA
CTTTACTTCTTCCCAATTTTAACCGTGCTTCAGGCAGTTGGTGGAGGCCTTTTATATTACGCCT
TCCCATACATTATATTAGTGTTATCTTTGGTTACTCTGGCTGTGTACATGTCTGCTTCTGAAAT
AGAGAACTGCTATGATCTTCTGGTCAGAAAGAAAAGACTTATTGTTCTCTTCAGCCACTGGTTA
CTTCATGCCTATGGAATAATCTCCATTTCCAGAGTGGATAAACTTGAGCAAGATTTGCCCCTTT
TGGCTTTGGTACCTACACCAGCCCTTTTTTACTTGTTCACTGCAAAATTTACCGAACCTTCAAG
GATACTCTCAGAAGGAGCCAATGGACACTGAGTGTAGACATGTGAAATGCCAAAAACCTGAGAA
GTGCTCCTAATAAAAAAGTAAATCAATCTTAACAGTGTATGAGAACTATTCTATCATATATGGG
AACAAGATTGTCAGTATATCTTAATGTTTGGGTTTGTCTTTGTTTTGTTTATGGTTAGACTTAC
AGACTTGGAAAATGCAAAACTCTGTAATACTCTGTTACACAGGGTAATATTATCTGCTACACTG
GAAGGCCGCTAGGAAGCCCTTGCTTCTCTCAACAGTTCAGCTGTTCTTTAGGGCAAAATCATGT
TTCTGTGTACCTAGCAATGTGTTCCCATTTTATTAAGAAAAGCTTTAACACGTGTAATCTGCAG
TCCTTAACAGTGGCGTAATTGTACTTACCTGTTGTGTTTCAGTTTGTTTTTCACCTATAATGAA
TTGTAAAAACAAACATACTTGTGGGGTCTGATAGCAAACATAGAAATGATGTATATTGTTTTTT
GTTATCTATTTATTTTCATCAATACAGTATTTTGATGTATTGCAAAAATAGATAATAATTTATA
TAACAGGTTTTCTGTTTATAGATTGGTTCAAGATTTGTTTGGATTATTGTTCCTGTAAAGAAAA
CAATAATAAAAAGCTTACCTACATAAAATTTCAATGTTTTGACACTTAATTGTTGTTTGGCACA
ATAGTATGGAAGTAATTCAAACTGGTAAATAGTTTCCTCTCATATCTCGGGTATATATACATAC
CATATTTTATTGATCCAGAGATACTTATTTCACTTTGTGACATCTCTGAATTAGGATGCATCTT
ACAACTGATGGCTTATTAGATTTAATGAAATACAGAAGATACACAGAATAAAAAGGGTTTTCCT
GTGGTTGGTTTGTGGTTTGTGATAGGTGTTCTGTGATGTTTATGCTTTGAAGGCCTTAAGACTC
ATGGTTGCAACCATGGAAGCAAAATGAAATTTTTAGCTCTTAACCTAACAACCTGACCATGTTT
ATCCATTTTTATTGTTTAGAAGTTTATTTACTGATACTTGGTGGAGGTTGTGTGAATTAGTTAA
ATTTTAAATGTTTAAGACTTCTATTAACAGCTGCAAAATATGAAAGTAAGTGCACTCACTTTTC
CTGTAGTAGTCTGTCTTTTGAATTCACAGCAGTTGTATCCTTGAGTTACTTTGTTAATGTATTT
TTCTCAGTACATTTAACCACTGGGAAATGAACCCTTGTACGAATGTGTTTCTTCTTCTCTGTAG
GAATAAAAAATAAATATAAAAATTTTATTTGTATTGCACACATTTGGGGGGTTATTAGTGTTCA
TTAAAATTCTGAGTTGCCCAAAGAA

hide sequence

RefSeq Acc Id:

NM_001284201 ⟹ NP_001271130

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	59,484,517 - 59,505,410 (+)	NCBI
HuRef	14	40,115,022 - 40,135,999 (+)	NCBI
CHM1_1	14	59,889,332 - 59,910,305 (+)	NCBI
T2T-CHM13v2.0	14	53,691,449 - 53,712,359 (+)	NCBI

Sequence:

show sequence

GTGGCCCGGATGTTCGGTGCAGCTGCCAGATCCGCTGATCTAGTGCTTCTCGAAAAAAACCTTC
AGGCGGCCCATGGGTGAGTGGTCGCCAAGATCCCGGGAAGCGTTTCTGGTAGTCCCGACTACTT
TCCTACACGGCTGGCCTCGGGCTCGGCTCTTTGTAGGCGGCCTTCGGTTGGCGGCGCAGGCTCG
CCCCTTGACCCCGCCCGCCCTCGGGCCGGGCTCCGCACTCCTGCGGGGTTGGGGTGGTCTGTCC
GCAACGGGCTACTAGGGGAGGCGCGCTGTCTGCGGCGAAATGCCAGGTCTTTGTTGTTTGGTCC
GAAATGTCTCTTCAGTCCCTTAGTTTAATGTCGAGGGAACACTTGCTTGAGGGTTGACTTCGGA
ATTGAAAACGCGGGTGATAGTGCAGAAAAAACAGTAAAGCAGAAGCAAGTTGCTGCATAATTTG
TCTACTGCTTCAACCTCAAACGTAGATTTATAGCGCCCGTCACAAAGGGCAGGACCGCTGCAAA
AAAATGGAATCTTAAAACTTTAGCCATCGTTCGCTAAAGGAAATGAAAGGAGAAATTCAACAGT
CGCTTGGAGCCTGGGTTTTGCTTACTGTCGATATTCAACCAGCATGCCTTGGACTTTATTGTGG
GAAGACCCTATTATTTAAAAATGGCTCAACTGAAATATATGGAGAATGTGGGGTATGCCCAAGA
GGACAGAGAACGAATGCACAGAAATATTGTCAGCCTTGCACAGAATCTCCTGAACTTTATGATT
GGCTCTATCTTGGATTTATGGCAATGCTTCCTCTGGTTTTACATTGGTTCTTCATTGAATGGTA
CTCGGGGAAAAAGAGTTCCAGCGCACTTTTCCAACACATCACTGCATTATTTGAATGCAGCATG
GCAGCTATTATCACCTTACTTGTGAGTGATCCAGTTGGTGTTCTTTATATTCGTTCATGTCGAG
TATTGATGCTTTCTGACTGGTACACGATGCTTTACAACCCAAGTCCAGATTACGTTACCACAGT
ACACTGTACTCATGAAGCCGTCTACCCACTATATACCATTGTATTTATCTATTACGCATTCTGC
TTGGTATTAATGATGCTGCTCCGACCTCTTCTGGTGAAGAAGATTGCATGTGGGTTAGGGAAAT
CTGATCGATTTAAAAGTATTTATGCTGCACTTTACTTCTTCCCAATTTTAACCGTGCTTCAGGC
AGTTGGTGGAGGCCTTTTATATTACGCCTTCCCATACATTATATTAGTGTTATCTTTGGTTACT
CTGGCTGTGTACATGTCTGCTTCTGAAATAGAGAACTGCTATGATCTTCTGGTCAGAAAGAAAA
GACTTATTGTTCTCTTCAGCCACTGGTTACTTCATGCCTATGGAATAATCTCCATTTCCAGAGT
GGATAAACTTGAGCAAGATTTGCCCCTTTTGGCTTTGGTACCTACACCAGCCCTTTTTTACTTG
TTCACTGCAAAATTTACCGAACCTTCAAGGATACTCTCAGAAGGAGCCAATGGACACTGAGTGT
AGACATGTGAAATGCCAAAAACCTGAGAAGTGCTCCTAATAAAAAAGTAAATCAATCTTAACAG
TGTATGAGAACTATTCTATCATATATGGGAACAAGATTGTCAGTATATCTTAATGTTTGGGTTT
GTCTTTGTTTTGTTTATGGTTAGACTTACAGACTTGGAAAATGCAAAACTCTGTAATACTCTGT
TACACAGGGTAATATTATCTGCTACACTGGAAGGCCGCTAGGAAGCCCTTGCTTCTCTCAACAG
TTCAGCTGTTCTTTAGGGCAAAATCATGTTTCTGTGTACCTAGCAATGTGTTCCCATTTTATTA
AGAAAAGCTTTAACACGTGTAATCTGCAGTCCTTAACAGTGGCGTAATTGTACTTACCTGTTGT
GTTTCAGTTTGTTTTTCACCTATAATGAATTGTAAAAACAAACATACTTGTGGGGTCTGATAGC
AAACATAGAAATGATGTATATTGTTTTTTGTTATCTATTTATTTTCATCAATACAGTATTTTGA
TGTATTGCAAAAATAGATAATAATTTATATAACAGGTTTTCTGTTTATAGATTGGTTCAAGATT
TGTTTGGATTATTGTTCCTGTAAAGAAAACAATAATAAAAAGCTTACCTACATAAAATTTCAAT
GTTTTGACACTTAATTGTTGTTTGGCACAATAGTATGGAAGTAATTCAAACTGGTAAATAGTTT
CCTCTCATATCTCGGGTATATATACATACCATATTTTATTGATCCAGAGATACTTATTTCACTT
TGTGACATCTCTGAATTAGGATGCATCTTACAACTGATGGCTTATTAGATTTAATGAAATACAG
AAGATACACAGAATAAAAAGGGTTTTCCTGTGGTTGGTTTGTGGTTTGTGATAGGTGTTCTGTG
ATGTTTATGCTTTGAAGGCCTTAAGACTCATGGTTGCAACCATGGAAGCAAAATGAAATTTTTA
GCTCTTAACCTAACAACCTGACCATGTTTATCCATTTTTATTGTTTAGAAGTTTATTTACTGAT
ACTTGGTGGAGGTTGTGTGAATTAGTTAAATTTTAAATGTTTAAGACTTCTATTAACAGCTGCA
AAATATGAAAGTAAGTGCACTCACTTTTCCTGTAGTAGTCTGTCTTTTGAATTCACAGCAGTTG
TATCCTTGAGTTACTTTGTTAATGTATTTTTCTCAGTACATTTAACCACTGGGAAATGAACCCT
TGTACGAATGTGTTTCTTCTTCTCTGTAGGAATAAAAAATAAATATAAAAATTTTATTTGTATT
GCACACATTTGGGGGGTTATTAGTGTTCATTAAAATTCTGAGTTGCCCAAAGAA

hide sequence

RefSeq Acc Id:

NM_001284202 ⟹ NP_001271131

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	59,484,517 - 59,505,410 (+)	NCBI
HuRef	14	40,115,022 - 40,135,999 (+)	NCBI
CHM1_1	14	59,889,332 - 59,910,305 (+)	NCBI
T2T-CHM13v2.0	14	53,691,449 - 53,712,359 (+)	NCBI

Sequence:

show sequence

GTGGCCCGGATGTTCGGTGCAGCTGCCAGATCCGCTGATCTAGTGCTTCTCGAAAAAAACCTTC
AGGCGGCCCATGGATTTATAGCGCCCGTCACAAAGGGCAGGACCGCTGCAAAAAAATGGAATCT
TAAAACTTTAGCCATCGTTCGCTAAAGGAAATGAAAGGAGAAATTCAACAGTCGCTTGGAGCCT
GGGTTTTGCTTACATGCCTTGGACTTTATTGTGGGAAGACCCTATTATTTAAAAATGGCTCAAC
TGAAATATATGGAGAATGTGGGGTATGCCCAAGAGGACAGAGAACGAATGCACAGAAATATTGT
CAGCCTTGCACAGAATCTCCTGAACTTTATGATTGGCTCTATCTTGGATTTATGGCAATGCTTC
CTCTGGTTTTACATTGGTTCTTCATTGAATGGTACTCGGGGAAAAAGAGTTCCAGCGCACTTTT
CCAACACATCACTGCATTATTTGAATGCAGCATGGCAGCTATTATCACCTTACTTGTGAGTGAT
CCAGTTGGTGTTCTTTATATTCGTTCATGTCGAGTATTGATGCTTTCTGACTGGTACACGATGC
TTTACAACCCAAGTCCAGATTACGTTACCACAGTACACTGTACTCATGAAGCCGTCTACCCACT
ATATACCATTGTATTTATCTATTACGCATTCTGCTTGGTATTAATGATGCTGCTCCGACCTCTT
CTGGTGAAGAAGATTGCATGTGGGTTAGGGAAATCTGATCGATTTAAAAGTATTTATGCTGCAC
TTTACTTCTTCCCAATTTTAACCGTGCTTCAGGCAGTTGGTGGAGGCCTTTTATATTACGCCTT
CCCATACATTATATTAGTGTTATCTTTGGTTACTCTGGCTGTGTACATGTCTGCTTCTGAAATA
GAGAACTGCTATGATCTTCTGGTCAGAAAGAAAAGACTTATTGTTCTCTTCAGCCACTGGTTAC
TTCATGCCTATGGAATAATCTCCATTTCCAGAGTGGATAAACTTGAGCAAGATTTGCCCCTTTT
GGCTTTGGTACCTACACCAGCCCTTTTTTACTTGTTCACTGCAAAATTTACCGAACCTTCAAGG
ATACTCTCAGAAGGAGCCAATGGACACTGAGTGTAGACATGTGAAATGCCAAAAACCTGAGAAG
TGCTCCTAATAAAAAAGTAAATCAATCTTAACAGTGTATGAGAACTATTCTATCATATATGGGA
ACAAGATTGTCAGTATATCTTAATGTTTGGGTTTGTCTTTGTTTTGTTTATGGTTAGACTTACA
GACTTGGAAAATGCAAAACTCTGTAATACTCTGTTACACAGGGTAATATTATCTGCTACACTGG
AAGGCCGCTAGGAAGCCCTTGCTTCTCTCAACAGTTCAGCTGTTCTTTAGGGCAAAATCATGTT
TCTGTGTACCTAGCAATGTGTTCCCATTTTATTAAGAAAAGCTTTAACACGTGTAATCTGCAGT
CCTTAACAGTGGCGTAATTGTACTTACCTGTTGTGTTTCAGTTTGTTTTTCACCTATAATGAAT
TGTAAAAACAAACATACTTGTGGGGTCTGATAGCAAACATAGAAATGATGTATATTGTTTTTTG
TTATCTATTTATTTTCATCAATACAGTATTTTGATGTATTGCAAAAATAGATAATAATTTATAT
AACAGGTTTTCTGTTTATAGATTGGTTCAAGATTTGTTTGGATTATTGTTCCTGTAAAGAAAAC
AATAATAAAAAGCTTACCTACATAAAATTTCAATGTTTTGACACTTAATTGTTGTTTGGCACAA
TAGTATGGAAGTAATTCAAACTGGTAAATAGTTTCCTCTCATATCTCGGGTATATATACATACC
ATATTTTATTGATCCAGAGATACTTATTTCACTTTGTGACATCTCTGAATTAGGATGCATCTTA
CAACTGATGGCTTATTAGATTTAATGAAATACAGAAGATACACAGAATAAAAAGGGTTTTCCTG
TGGTTGGTTTGTGGTTTGTGATAGGTGTTCTGTGATGTTTATGCTTTGAAGGCCTTAAGACTCA
TGGTTGCAACCATGGAAGCAAAATGAAATTTTTAGCTCTTAACCTAACAACCTGACCATGTTTA
TCCATTTTTATTGTTTAGAAGTTTATTTACTGATACTTGGTGGAGGTTGTGTGAATTAGTTAAA
TTTTAAATGTTTAAGACTTCTATTAACAGCTGCAAAATATGAAAGTAAGTGCACTCACTTTTCC
TGTAGTAGTCTGTCTTTTGAATTCACAGCAGTTGTATCCTTGAGTTACTTTGTTAATGTATTTT
TCTCAGTACATTTAACCACTGGGAAATGAACCCTTGTACGAATGTGTTTCTTCTTCTCTGTAGG
AATAAAAAATAAATATAAAAATTTTATTTGTATTGCACACATTTGGGGGGTTATTAGTGTTCAT
TAAAATTCTGAGTTGCCCAAAGAA

hide sequence

RefSeq Acc Id:

NM_001284203 ⟹ NP_001271132

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	59,484,517 - 59,505,410 (+)	NCBI
HuRef	14	40,115,022 - 40,135,999 (+)	NCBI
CHM1_1	14	59,889,332 - 59,910,305 (+)	NCBI
T2T-CHM13v2.0	14	53,691,449 - 53,712,359 (+)	NCBI

Sequence:

show sequence

GTGGCCCGGATGTTCGGTGCAGCTGCCAGATCCGCTGATCTAGTGCTTCTCGAAAAAAACCTTC
AGGCGGCCCATGGATGTTACTATACTGGCATTTGTTTTTAAAAAGCTGTCGATATTCAACCAGC
ATGCCTTGGACTTTATTGTGGGAAGACCCTATTATTTAAAAATGGCTCAACTGAAATATATGGA
GAATGTGGGGTATGCCCAAGAGGACAGAGAACGAATGCACAGAAATATTGTCAGCCTTGCACAG
AATCTCCTGAACTTTATGATTGGCTCTATCTTGGATTTATGGCAATGCTTCCTCTGGTTTTACA
TTGGTTCTTCATTGAATGGTACTCGGGGAAAAAGAGTTCCAGCGCACTTTTCCAACACATCACT
GCATTATTTGAATGCAGCATGGCAGCTATTATCACCTTACTTGTGAGTGATCCAGTTGGTGTTC
TTTATATTCGTTCATGTCGAGTATTGATGCTTTCTGACTGGTACACGATGCTTTACAACCCAAG
TCCAGATTACGTTACCACAGTACACTGTACTCATGAAGCCGTCTACCCACTATATACCATTGTA
TTTATCTATTACGCATTCTGCTTGGTATTAATGATGCTGCTCCGACCTCTTCTGGTGAAGAAGA
TTGCATGTGGGTTAGGGAAATCTGATCGATTTAAAAGTATTTATGCTGCACTTTACTTCTTCCC
AATTTTAACCGTGCTTCAGGCAGTTGGTGGAGGCCTTTTATATTACGCCTTCCCATACATTATA
TTAGTGTTATCTTTGGTTACTCTGGCTGTGTACATGTCTGCTTCTGAAATAGAGAACTGCTATG
ATCTTCTGGTCAGAAAGAAAAGACTTATTGTTCTCTTCAGCCACTGGTTACTTCATGCCTATGG
AATAATCTCCATTTCCAGAGTGGATAAACTTGAGCAAGATTTGCCCCTTTTGGCTTTGGTACCT
ACACCAGCCCTTTTTTACTTGTTCACTGCAAAATTTACCGAACCTTCAAGGATACTCTCAGAAG
GAGCCAATGGACACTGAGTGTAGACATGTGAAATGCCAAAAACCTGAGAAGTGCTCCTAATAAA
AAAGTAAATCAATCTTAACAGTGTATGAGAACTATTCTATCATATATGGGAACAAGATTGTCAG
TATATCTTAATGTTTGGGTTTGTCTTTGTTTTGTTTATGGTTAGACTTACAGACTTGGAAAATG
CAAAACTCTGTAATACTCTGTTACACAGGGTAATATTATCTGCTACACTGGAAGGCCGCTAGGA
AGCCCTTGCTTCTCTCAACAGTTCAGCTGTTCTTTAGGGCAAAATCATGTTTCTGTGTACCTAG
CAATGTGTTCCCATTTTATTAAGAAAAGCTTTAACACGTGTAATCTGCAGTCCTTAACAGTGGC
GTAATTGTACTTACCTGTTGTGTTTCAGTTTGTTTTTCACCTATAATGAATTGTAAAAACAAAC
ATACTTGTGGGGTCTGATAGCAAACATAGAAATGATGTATATTGTTTTTTGTTATCTATTTATT
TTCATCAATACAGTATTTTGATGTATTGCAAAAATAGATAATAATTTATATAACAGGTTTTCTG
TTTATAGATTGGTTCAAGATTTGTTTGGATTATTGTTCCTGTAAAGAAAACAATAATAAAAAGC
TTACCTACATAAAATTTCAATGTTTTGACACTTAATTGTTGTTTGGCACAATAGTATGGAAGTA
ATTCAAACTGGTAAATAGTTTCCTCTCATATCTCGGGTATATATACATACCATATTTTATTGAT
CCAGAGATACTTATTTCACTTTGTGACATCTCTGAATTAGGATGCATCTTACAACTGATGGCTT
ATTAGATTTAATGAAATACAGAAGATACACAGAATAAAAAGGGTTTTCCTGTGGTTGGTTTGTG
GTTTGTGATAGGTGTTCTGTGATGTTTATGCTTTGAAGGCCTTAAGACTCATGGTTGCAACCAT
GGAAGCAAAATGAAATTTTTAGCTCTTAACCTAACAACCTGACCATGTTTATCCATTTTTATTG
TTTAGAAGTTTATTTACTGATACTTGGTGGAGGTTGTGTGAATTAGTTAAATTTTAAATGTTTA
AGACTTCTATTAACAGCTGCAAAATATGAAAGTAAGTGCACTCACTTTTCCTGTAGTAGTCTGT
CTTTTGAATTCACAGCAGTTGTATCCTTGAGTTACTTTGTTAATGTATTTTTCTCAGTACATTT
AACCACTGGGAAATGAACCCTTGTACGAATGTGTTTCTTCTTCTCTGTAGGAATAAAAAATAAA
TATAAAAATTTTATTTGTATTGCACACATTTGGGGGGTTATTAGTGTTCATTAAAATTCTGAGT
TGCCCAAAGAA

hide sequence

RefSeq Acc Id:

NM_001284204 ⟹ NP_001271133

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	59,484,517 - 59,505,410 (+)	NCBI
HuRef	14	40,115,022 - 40,135,999 (+)	NCBI
CHM1_1	14	59,889,332 - 59,910,305 (+)	NCBI
T2T-CHM13v2.0	14	53,691,449 - 53,712,359 (+)	NCBI

Sequence:

show sequence

GTGGCCCGGATGTTCGGTGCAGCTGCCAGATCCGCTGATCTAGTGCTTCTCGAAAAAAACCTTC
AGGCGGCCCATGGCTGTCGATATTCAACCAGCATGCCTTGGACTTTATTGTGGGAAGACCCTAT
TATTTAAAAATGGCTCAACTGAAATATATGGAGAATGTGGGGTATGCCCAAGAGGACAGAGAAC
GAATGCACAGAAATATTGTCAGCCTTGCACAGAATCTCCTGAACTTTATGATTGGCTCTATCTT
GGATTTATGGCAATGCTTCCTCTGGTTTTACATTGGTTCTTCATTGAATGGTACTCGGGGAAAA
AGAGTTCCAGCGCACTTTTCCAACACATCACTGCATTATTTGAATGCAGCATGGCAGCTATTAT
CACCTTACTTGTGAGTGATCCAGTTGGTGTTCTTTATATTCGTTCATGTCGAGTATTGATGCTT
TCTGACTGGTACACGATGCTTTACAACCCAAGTCCAGATTACGTTACCACAGTACACTGTACTC
ATGAAGCCGTCTACCCACTATATACCATTGTATTTATCTATTACGCATTCTGCTTGGTATTAAT
GATGCTGCTCCGACCTCTTCTGGTGAAGAAGATTGCATGTGGGTTAGGGAAATCTGATCGATTT
AAAAGTATTTATGCTGCACTTTACTTCTTCCCAATTTTAACCGTGCTTCAGGCAGTTGGTGGAG
GCCTTTTATAACTGCTATGATCTTCTGGTCAGAAAGAAAAGACTTATTGTTCTCTTCAGCCACT
GGTTACTTCATGCCTATGGAATAATCTCCATTTCCAGAGTGGATAAACTTGAGCAAGATTTGCC
CCTTTTGGCTTTGGTACCTACACCAGCCCTTTTTTACTTGTTCACTGCAAAATTTACCGAACCT
TCAAGGATACTCTCAGAAGGAGCCAATGGACACTGAGTGTAGACATGTGAAATGCCAAAAACCT
GAGAAGTGCTCCTAATAAAAAAGTAAATCAATCTTAACAGTGTATGAGAACTATTCTATCATAT
ATGGGAACAAGATTGTCAGTATATCTTAATGTTTGGGTTTGTCTTTGTTTTGTTTATGGTTAGA
CTTACAGACTTGGAAAATGCAAAACTCTGTAATACTCTGTTACACAGGGTAATATTATCTGCTA
CACTGGAAGGCCGCTAGGAAGCCCTTGCTTCTCTCAACAGTTCAGCTGTTCTTTAGGGCAAAAT
CATGTTTCTGTGTACCTAGCAATGTGTTCCCATTTTATTAAGAAAAGCTTTAACACGTGTAATC
TGCAGTCCTTAACAGTGGCGTAATTGTACTTACCTGTTGTGTTTCAGTTTGTTTTTCACCTATA
ATGAATTGTAAAAACAAACATACTTGTGGGGTCTGATAGCAAACATAGAAATGATGTATATTGT
TTTTTGTTATCTATTTATTTTCATCAATACAGTATTTTGATGTATTGCAAAAATAGATAATAAT
TTATATAACAGGTTTTCTGTTTATAGATTGGTTCAAGATTTGTTTGGATTATTGTTCCTGTAAA
GAAAACAATAATAAAAAGCTTACCTACATAAAATTTCAATGTTTTGACACTTAATTGTTGTTTG
GCACAATAGTATGGAAGTAATTCAAACTGGTAAATAGTTTCCTCTCATATCTCGGGTATATATA
CATACCATATTTTATTGATCCAGAGATACTTATTTCACTTTGTGACATCTCTGAATTAGGATGC
ATCTTACAACTGATGGCTTATTAGATTTAATGAAATACAGAAGATACACAGAATAAAAAGGGTT
TTCCTGTGGTTGGTTTGTGGTTTGTGATAGGTGTTCTGTGATGTTTATGCTTTGAAGGCCTTAA
GACTCATGGTTGCAACCATGGAAGCAAAATGAAATTTTTAGCTCTTAACCTAACAACCTGACCA
TGTTTATCCATTTTTATTGTTTAGAAGTTTATTTACTGATACTTGGTGGAGGTTGTGTGAATTA
GTTAAATTTTAAATGTTTAAGACTTCTATTAACAGCTGCAAAATATGAAAGTAAGTGCACTCAC
TTTTCCTGTAGTAGTCTGTCTTTTGAATTCACAGCAGTTGTATCCTTGAGTTACTTTGTTAATG
TATTTTTCTCAGTACATTTAACCACTGGGAAATGAACCCTTGTACGAATGTGTTTCTTCTTCTC
TGTAGGAATAAAAAATAAATATAAAAATTTTATTTGTATTGCACACATTTGGGGGGTTATTAGT
GTTCATTAAAATTCTGAGTTGCCCAAAGAA

hide sequence

RefSeq Acc Id:

NM_016475 ⟹ NP_057559

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	59,484,517 - 59,505,410 (+)	NCBI
GRCh37	14	59,951,161 - 59,972,081 (+)	RGD
GRCh37	14	59,951,161 - 59,972,081 (+)	NCBI
Build 36	14	59,020,914 - 59,041,834 (+)	NCBI Archive
Celera	14	40,000,231 - 40,021,171 (+)	RGD
HuRef	14	40,115,022 - 40,135,999 (+)	NCBI
CHM1_1	14	59,889,332 - 59,910,305 (+)	NCBI
T2T-CHM13v2.0	14	53,691,449 - 53,712,359 (+)	NCBI

Sequence:

show sequence

GTGGCCCGGATGTTCGGTGCAGCTGCCAGATCCGCTGATCTAGTGCTTCTCGAAAAAAACCTTC
AGGCGGCCCATGGCTGTCGATATTCAACCAGCATGCCTTGGACTTTATTGTGGGAAGACCCTAT
TATTTAAAAATGGCTCAACTGAAATATATGGAGAATGTGGGGTATGCCCAAGAGGACAGAGAAC
GAATGCACAGAAATATTGTCAGCCTTGCACAGAATCTCCTGAACTTTATGATTGGCTCTATCTT
GGATTTATGGCAATGCTTCCTCTGGTTTTACATTGGTTCTTCATTGAATGGTACTCGGGGAAAA
AGAGTTCCAGCGCACTTTTCCAACACATCACTGCATTATTTGAATGCAGCATGGCAGCTATTAT
CACCTTACTTGTGAGTGATCCAGTTGGTGTTCTTTATATTCGTTCATGTCGAGTATTGATGCTT
TCTGACTGGTACACGATGCTTTACAACCCAAGTCCAGATTACGTTACCACAGTACACTGTACTC
ATGAAGCCGTCTACCCACTATATACCATTGTATTTATCTATTACGCATTCTGCTTGGTATTAAT
GATGCTGCTCCGACCTCTTCTGGTGAAGAAGATTGCATGTGGGTTAGGGAAATCTGATCGATTT
AAAAGTATTTATGCTGCACTTTACTTCTTCCCAATTTTAACCGTGCTTCAGGCAGTTGGTGGAG
GCCTTTTATATTACGCCTTCCCATACATTATATTAGTGTTATCTTTGGTTACTCTGGCTGTGTA
CATGTCTGCTTCTGAAATAGAGAACTGCTATGATCTTCTGGTCAGAAAGAAAAGACTTATTGTT
CTCTTCAGCCACTGGTTACTTCATGCCTATGGAATAATCTCCATTTCCAGAGTGGATAAACTTG
AGCAAGATTTGCCCCTTTTGGCTTTGGTACCTACACCAGCCCTTTTTTACTTGTTCACTGCAAA
ATTTACCGAACCTTCAAGGATACTCTCAGAAGGAGCCAATGGACACTGAGTGTAGACATGTGAA
ATGCCAAAAACCTGAGAAGTGCTCCTAATAAAAAAGTAAATCAATCTTAACAGTGTATGAGAAC
TATTCTATCATATATGGGAACAAGATTGTCAGTATATCTTAATGTTTGGGTTTGTCTTTGTTTT
GTTTATGGTTAGACTTACAGACTTGGAAAATGCAAAACTCTGTAATACTCTGTTACACAGGGTA
ATATTATCTGCTACACTGGAAGGCCGCTAGGAAGCCCTTGCTTCTCTCAACAGTTCAGCTGTTC
TTTAGGGCAAAATCATGTTTCTGTGTACCTAGCAATGTGTTCCCATTTTATTAAGAAAAGCTTT
AACACGTGTAATCTGCAGTCCTTAACAGTGGCGTAATTGTACTTACCTGTTGTGTTTCAGTTTG
TTTTTCACCTATAATGAATTGTAAAAACAAACATACTTGTGGGGTCTGATAGCAAACATAGAAA
TGATGTATATTGTTTTTTGTTATCTATTTATTTTCATCAATACAGTATTTTGATGTATTGCAAA
AATAGATAATAATTTATATAACAGGTTTTCTGTTTATAGATTGGTTCAAGATTTGTTTGGATTA
TTGTTCCTGTAAAGAAAACAATAATAAAAAGCTTACCTACATAAAATTTCAATGTTTTGACACT
TAATTGTTGTTTGGCACAATAGTATGGAAGTAATTCAAACTGGTAAATAGTTTCCTCTCATATC
TCGGGTATATATACATACCATATTTTATTGATCCAGAGATACTTATTTCACTTTGTGACATCTC
TGAATTAGGATGCATCTTACAACTGATGGCTTATTAGATTTAATGAAATACAGAAGATACACAG
AATAAAAAGGGTTTTCCTGTGGTTGGTTTGTGGTTTGTGATAGGTGTTCTGTGATGTTTATGCT
TTGAAGGCCTTAAGACTCATGGTTGCAACCATGGAAGCAAAATGAAATTTTTAGCTCTTAACCT
AACAACCTGACCATGTTTATCCATTTTTATTGTTTAGAAGTTTATTTACTGATACTTGGTGGAG
GTTGTGTGAATTAGTTAAATTTTAAATGTTTAAGACTTCTATTAACAGCTGCAAAATATGAAAG
TAAGTGCACTCACTTTTCCTGTAGTAGTCTGTCTTTTGAATTCACAGCAGTTGTATCCTTGAGT
TACTTTGTTAATGTATTTTTCTCAGTACATTTAACCACTGGGAAATGAACCCTTGTACGAATGT
GTTTCTTCTTCTCTGTAGGAATAAAAAATAAATATAAAAATTTTATTTGTATTGCACACATTTG
GGGGGTTATTAGTGTTCATTAAAATTCTGAGTTGCCCAAAGAA

hide sequence

RefSeq Acc Id:

XM_024449627 ⟹ XP_024305395

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	59,484,517 - 59,505,410 (+)	NCBI

Sequence:

show sequence

GCGGAGCCGCCGAGCTCGCTGTGGCCCGGATGTTCGGTGCAGCTGCCAGATCCGCTGATCTAGT
GCTTCTCGAAAAAAACCTTCAGGCGGCCCATGGATTTATAGCGCCCGTCACAAAGGGCAGGACC
GCTGCAAAAAAATGGAATCTTAAAACTTTAGCCATCGTTCGCTAAAGGAAATGAAAGGAGAAAT
TCAACAGTCGCTTGGAGCCTGGGTTTTGCTTACTGTCGATATTCAACCAGCATGCCTTGGACTT
TATTGTGGGAAGACCCTATTATTTAAAAATGGCTCAACTGAAATATATGGAGAATGTGGGGTAT
GCCCAAGAGGACAGAGAACGAATGCACAGAAATATTGTCAGCCTTGCACAGAATCTCCTGAACT
TTATGATTGGCTCTATCTTGGATTTATGGCAATGCTTCCTCTGGTTTTACATTGGTTCTTCATT
GAATGGTACTCGGGGAAAAAGAGTTCCAGCGCACTTTTCCAACACATCACTGCATTATTTGAAT
GCAGCATGGCAGCTATTATCACCTTACTTGTGAGTGATCCAGTTGGTGTTCTTTATATTCGTTC
ATGTCGAGTATTGATGCTTTCTGACTGGTACACGATGCTTTACAACCCAAGTCCAGATTACGTT
ACCACAGTACACTGTACTCATGAAGCCGTCTACCCACTATATACCATTGTATTTATCTATTACG
CATTCTGCTTGGTATTAATGATGCTGCTCCGACCTCTTCTGGTGAAGAAGATTGCATGTGGGTT
AGGGAAATCTGATCGATTTAAAAGTATTTATGCTGCACTTTACTTCTTCCCAATTTTAACCGTG
CTTCAGGCAGTTGGTGGAGGCCTTTTATATTACGCCTTCCCATACATTATATTAGTGTTATCTT
TGGTTACTCTGGCTGTGTACATGTCTGCTTCTGAAATAGAGAACTGCTATGATCTTCTGGTCAG
AAAGAAAAGACTTATTGTTCTCTTCAGCCACTGGTTACTTCATGCCTATGGAATAATCTCCATT
TCCAGAGTGGATAAACTTGAGCAAGATTTGCCCCTTTTGGCTTTGGTACCTACACCAGCCCTTT
TTTACTTGTTCACTGCAAAATTTACCGAACCTTCAAGGATACTCTCAGAAGGAGCCAATGGACA
CTGAGTGTAGACATGTGAAATGCCAAAAACCTGAGAAGTGCTCCTAATAAAAAAGTAAATCAAT
CTTAACAGTGTATGAGAACTATTCTATCATATATGGGAACAAGATTGTCAGTATATCTTAATGT
TTGGGTTTGTCTTTGTTTTGTTTATGGTTAGACTTACAGACTTGGAAAATGCAAAACTCTGTAA
TACTCTGTTACACAGGGTAATATTATCTGCTACACTGGAAGGCCGCTAGGAAGCCCTTGCTTCT
CTCAACAGTTCAGCTGTTCTTTAGGGCAAAATCATGTTTCTGTGTACCTAGCAATGTGTTCCCA
TTTTATTAAGAAAAGCTTTAACACGTGTAATCTGCAGTCCTTAACAGTGGCGTAATTGTACTTA
CCTGTTGTGTTTCAGTTTGTTTTTCACCTATAATGAATTGTAAAAACAAACATACTTGTGGGGT
CTGATAGCAAACATAGAAATGATGTATATTGTTTTTTGTTATCTATTTATTTTCATCAATACAG
TATTTTGATGTATTGCAAAAATAGATAATAATTTATATAACAGGTTTTCTGTTTATAGATTGGT
TCAAGATTTGTTTGGATTATTGTTCCTGTAAAGAAAACAATAATAAAAAGCTTACCTACATAAA
ATTTCAATGTTTTGACACTTAATTGTTGTTTGGCACAATAGTATGGAAGTAATTCAAACTGGTA
AATAGTTTCCTCTCATATCTCGGGTATATATACATACCATATTTTATTGATCCAGAGATACTTA
TTTCACTTTGTGACATCTCTGAATTAGGATGCATCTTACAACTGATGGCTTATTAGATTTAATG
AAATACAGAAGATACACAGAATAAAAAGGGTTTTCCTGTGGTTGGTTTGTGGTTTGTGATAGGT
GTTCTGTGATGTTTATGCTTTGAAGGCCTTAAGACTCATGGTTGCAACCATGGAAGCAAAATGA
AATTTTTAGCTCTTAACCTAACAACCTGACCATGTTTATCCATTTTTATTGTTTAGAAGTTTAT
TTACTGATACTTGGTGGAGGTTGTGTGAATTAGTTAAATTTTAAATGTTTAAGACTTCTATTAA
CAGCTGCAAAATATGAAAGTAAGTGCACTCACTTTTCCTGTAGTAGTCTGTCTTTTGAATTCAC
AGCAGTTGTATCCTTGAGTTACTTTGTTAATGTATTTTTCTCAGTACATTTAACCACTGGGAAA
TGAACCCTTGTACGAATGTGTTTCTTCTTCTCTGTAGGAATAAAAAATAAATATAAAAATTTTA

hide sequence

RefSeq Acc Id:

XM_047431467 ⟹ XP_047287423

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	59,484,517 - 59,505,410 (+)	NCBI

RefSeq Acc Id:

XM_054376204 ⟹ XP_054232179

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	53,691,449 - 53,712,359 (+)	NCBI

RefSeq Acc Id:

XM_054376205 ⟹ XP_054232180

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	53,691,449 - 53,712,359 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_001092095	(Get FASTA)	NCBI Sequence Viewer
	NP_001271130	(Get FASTA)	NCBI Sequence Viewer
	NP_001271131	(Get FASTA)	NCBI Sequence Viewer
	NP_001271132	(Get FASTA)	NCBI Sequence Viewer
	NP_001271133	(Get FASTA)	NCBI Sequence Viewer
	NP_057559	(Get FASTA)	NCBI Sequence Viewer
	XP_024305395	(Get FASTA)	NCBI Sequence Viewer
	XP_047287423	(Get FASTA)	NCBI Sequence Viewer
	XP_054232179	(Get FASTA)	NCBI Sequence Viewer
	XP_054232180	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAF29005	(Get FASTA)	NCBI Sequence Viewer
	AAF36133	(Get FASTA)	NCBI Sequence Viewer
	AAG41781	(Get FASTA)	NCBI Sequence Viewer
	AAH05198	(Get FASTA)	NCBI Sequence Viewer
	AAH10359	(Get FASTA)	NCBI Sequence Viewer
	AAP85636	(Get FASTA)	NCBI Sequence Viewer
	BAB13874	(Get FASTA)	NCBI Sequence Viewer
	BAB55216	(Get FASTA)	NCBI Sequence Viewer
	BAG51634	(Get FASTA)	NCBI Sequence Viewer
	BAG60479	(Get FASTA)	NCBI Sequence Viewer
	CAB66631	(Get FASTA)	NCBI Sequence Viewer
	CAD61945	(Get FASTA)	NCBI Sequence Viewer
	CAG33444	(Get FASTA)	NCBI Sequence Viewer
	CAG38541	(Get FASTA)	NCBI Sequence Viewer
	EAW80753	(Get FASTA)	NCBI Sequence Viewer
	EAW80754	(Get FASTA)	NCBI Sequence Viewer
	EAW80755	(Get FASTA)	NCBI Sequence Viewer
	EAW80756	(Get FASTA)	NCBI Sequence Viewer
	EAW80757	(Get FASTA)	NCBI Sequence Viewer
	EAW80758	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000348351
	ENSP00000348351.5
	ENSP00000389699
	ENSP00000389699.2
	ENSP00000450749
	ENSP00000450749.1
	ENSP00000450813.1
	ENSP00000451076.1
	ENSP00000451723.1
	ENSP00000479775
	ENSP00000479775.2
GenBank Protein	Q9P055	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_057559 ⟸ NM_016475
- Peptide Label:	isoform 1
- UniProtKB:	Q9HAH5 (UniProtKB/Swiss-Prot), Q9H2W0 (UniProtKB/Swiss-Prot), Q9H0Q6 (UniProtKB/Swiss-Prot), Q86SY6 (UniProtKB/Swiss-Prot), Q7Z5D4 (UniProtKB/Swiss-Prot), Q6IAJ2 (UniProtKB/Swiss-Prot), Q6FIB6 (UniProtKB/Swiss-Prot), B4DP67 (UniProtKB/Swiss-Prot), Q9P0R3 (UniProtKB/Swiss-Prot), Q9P055 (UniProtKB/Swiss-Prot), B3KPC2 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAVDIQPACLGLYCGKTLLFKNGSTEIYGECGVCPRGQRTNAQKYCQPCTESPELYDWLYLGFM AMLPLVLHWFFIEWYSGKKSSSALFQHITALFECSMAAIITLLVSDPVGVLYIRSCRVLMLSDW YTMLYNPSPDYVTTVHCTHEAVYPLYTIVFIYYAFCLVLMMLLRPLLVKKIACGLGKSDRFKSI YAALYFFPILTVLQAVGGGLLYYAFPYIILVLSLVTLAVYMSASEIENCYDLLVRKKRLIVLFS HWLLHAYGIISISRVDKLEQDLPLLALVPTPALFYLFTAKFTEPSRILSEGANGH hide sequence

RefSeq Acc Id:	NP_001092095 ⟸ NM_001098625
- Peptide Label:	isoform 2
- UniProtKB:	B3KPC2 (UniProtKB/TrEMBL)
- Sequence:	show sequence MACLGLYCGKTLLFKNGSTEIYGECGVCPRGQRTNAQKYCQPCTESPELYDWLYLGFMAMLPLV LHWFFIEWYSGKKSSSALFQHITALFECSMAAIITLLVSDPVGVLYIRSCRVLMLSDWYTMLYN PSPDYVTTVHCTHEAVYPLYTIVFIYYAFCLVLMMLLRPLLVKKIACGLGKSDRFKSIYAALYF FPILTVLQAVGGGLLYYAFPYIILVLSLVTLAVYMSASEIENCYDLLVRKKRLIVLFSHWLLHA YGIISISRVDKLEQDLPLLALVPTPALFYLFTAKFTEPSRILSEGANGH hide sequence

RefSeq Acc Id:	NP_001271130 ⟸ NM_001284201
- Peptide Label:	isoform 3
- UniProtKB:	B3KPC2 (UniProtKB/TrEMBL), G3V2M4 (UniProtKB/TrEMBL)
- Sequence:	show sequence MKGEIQQSLGAWVLLTVDIQPACLGLYCGKTLLFKNGSTEIYGECGVCPRGQRTNAQKYCQPCT ESPELYDWLYLGFMAMLPLVLHWFFIEWYSGKKSSSALFQHITALFECSMAAIITLLVSDPVGV LYIRSCRVLMLSDWYTMLYNPSPDYVTTVHCTHEAVYPLYTIVFIYYAFCLVLMMLLRPLLVKK IACGLGKSDRFKSIYAALYFFPILTVLQAVGGGLLYYAFPYIILVLSLVTLAVYMSASEIENCY DLLVRKKRLIVLFSHWLLHAYGIISISRVDKLEQDLPLLALVPTPALFYLFTAKFTEPSRILSE GANGH hide sequence

RefSeq Acc Id:	NP_001271131 ⟸ NM_001284202
- Peptide Label:	isoform 4 precursor
- UniProtKB:	B3KPC2 (UniProtKB/TrEMBL)
- Sequence:	show sequence MKGEIQQSLGAWVLLTCLGLYCGKTLLFKNGSTEIYGECGVCPRGQRTNAQKYCQPCTESPELY DWLYLGFMAMLPLVLHWFFIEWYSGKKSSSALFQHITALFECSMAAIITLLVSDPVGVLYIRSC RVLMLSDWYTMLYNPSPDYVTTVHCTHEAVYPLYTIVFIYYAFCLVLMMLLRPLLVKKIACGLG KSDRFKSIYAALYFFPILTVLQAVGGGLLYYAFPYIILVLSLVTLAVYMSASEIENCYDLLVRK KRLIVLFSHWLLHAYGIISISRVDKLEQDLPLLALVPTPALFYLFTAKFTEPSRILSEGANGH hide sequence

RefSeq Acc Id:

NP_001271132 ⟸ NM_001284203

- Peptide Label:

isoform 5

- Sequence:

show sequence

MAMLPLVLHWFFIEWYSGKKSSSALFQHITALFECSMAAIITLLVSDPVGVLYIRSCRVLMLSD
WYTMLYNPSPDYVTTVHCTHEAVYPLYTIVFIYYAFCLVLMMLLRPLLVKKIACGLGKSDRFKS
IYAALYFFPILTVLQAVGGGLLYYAFPYIILVLSLVTLAVYMSASEIENCYDLLVRKKRLIVLF
SHWLLHAYGIISISRVDKLEQDLPLLALVPTPALFYLFTAKFTEPSRILSEGANGH

hide sequence

RefSeq Acc Id:	NP_001271133 ⟸ NM_001284204
- Peptide Label:	isoform 6
- UniProtKB:	G3V2R2 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAVDIQPACLGLYCGKTLLFKNGSTEIYGECGVCPRGQRTNAQKYCQPCTESPELYDWLYLGFM AMLPLVLHWFFIEWYSGKKSSSALFQHITALFECSMAAIITLLVSDPVGVLYIRSCRVLMLSDW YTMLYNPSPDYVTTVHCTHEAVYPLYTIVFIYYAFCLVLMMLLRPLLVKKIACGLGKSDRFKSI YAALYFFPILTVLQAVGGGLL hide sequence

RefSeq Acc Id:	XP_024305395 ⟸ XM_024449627
- Peptide Label:	isoform X1
- UniProtKB:	G3V2M4 (UniProtKB/TrEMBL), B3KPC2 (UniProtKB/TrEMBL)
- Sequence:	show sequence MKGEIQQSLGAWVLLTVDIQPACLGLYCGKTLLFKNGSTEIYGECGVCPRGQRTNAQKYCQPCT ESPELYDWLYLGFMAMLPLVLHWFFIEWYSGKKSSSALFQHITALFECSMAAIITLLVSDPVGV LYIRSCRVLMLSDWYTMLYNPSPDYVTTVHCTHEAVYPLYTIVFIYYAFCLVLMMLLRPLLVKK IACGLGKSDRFKSIYAALYFFPILTVLQAVGGGLLYYAFPYIILVLSLVTLAVYMSASEIENCY DLLVRKKRLIVLFSHWLLHAYGIISISRVDKLEQDLPLLALVPTPALFYLFTAKFTEPSRILSE GANGH hide sequence

Ensembl Acc Id:

ENSP00000451723 ⟸ ENST00000555491

Ensembl Acc Id:

ENSP00000451076 ⟸ ENST00000556985

Ensembl Acc Id:

ENSP00000389699 ⟸ ENST00000425728

Ensembl Acc Id:

ENSP00000479775 ⟸ ENST00000616435

Ensembl Acc Id:

ENSP00000348351 ⟸ ENST00000356057

Ensembl Acc Id:

ENSP00000450813 ⟸ ENST00000554795

Ensembl Acc Id:

ENSP00000450749 ⟸ ENST00000554271

RefSeq Acc Id:	XP_047287423 ⟸ XM_047431467
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054232179 ⟸ XM_054376204
- Peptide Label:	isoform X1
- UniProtKB:	G3V2M4 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054232180 ⟸ XM_054376205
- Peptide Label:	isoform X2

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q9P055-F1-model_v2	AlphaFold	Q9P055	1-311	view protein structure

Promoters

RGD ID:

6791448

Promoter ID:

HG_KWN:19495

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

ENST00000356057, NM_001098625, NM_016475, OTTHUMT00000072254, OTTHUMT00000072257, OTTHUMT00000072258, UC001XEG.2, UC001XEI.2

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	14	59,019,311 - 59,020,942 (+)	MPROMDB

RGD ID:

6852024

Promoter ID:

EP73818

Type:

initiation region

Name:

HS_C14ORF100

Description:

Chromosome 14 open reading frame 100.

SO ACC ID:

SO:0000170

Source:

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

Experiment Methods:

NEDO full length human cDNA sequencing project.; Oligo-capping

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	14	59,020,985 - 59,021,045	EPD

RGD ID:

7227757

Promoter ID:

EPDNEW_H19624

Type:

initiation region

Name:

JKAMP_1

Description:

JNK1/MAPK8-associated membrane protein

SO ACC ID:

SO:0000170

Source:

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

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	59,484,517 - 59,484,577	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:20184	AgrOrtholog
COSMIC	JKAMP	COSMIC
Ensembl Genes	ENSG00000050130	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000356057	ENTREZGENE
	ENST00000356057.9	UniProtKB/Swiss-Prot
	ENST00000425728	ENTREZGENE
	ENST00000425728.6	UniProtKB/Swiss-Prot
	ENST00000554271	ENTREZGENE
	ENST00000554271.5	UniProtKB/TrEMBL
	ENST00000554795.1	UniProtKB/TrEMBL
	ENST00000555491.5	UniProtKB/TrEMBL
	ENST00000556985.5	UniProtKB/TrEMBL
	ENST00000602482	ENTREZGENE
	ENST00000616435	ENTREZGENE
	ENST00000616435.5	UniProtKB/Swiss-Prot
GTEx	ENSG00000050130	GTEx
HGNC ID	HGNC:20184	ENTREZGENE
Human Proteome Map	JKAMP	Human Proteome Map
InterPro	JAMP	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:51528	UniProtKB/Swiss-Prot
NCBI Gene	51528	ENTREZGENE
OMIM	611176	OMIM
PANTHER	JNK1/MAPK8-ASSOCIATED MEMBRANE PROTEIN	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	PTHR12740	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	JAMP	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA165479069	PharmGKB
UniProt	B3KPC2	ENTREZGENE, UniProtKB/TrEMBL
	B4DP67	ENTREZGENE
	G3V2M4	ENTREZGENE, UniProtKB/TrEMBL
	G3V2R2	ENTREZGENE, UniProtKB/TrEMBL
	G3V372_HUMAN	UniProtKB/TrEMBL
	G3V4D0_HUMAN	UniProtKB/TrEMBL
	JKAMP_HUMAN	UniProtKB/Swiss-Prot
	Q6FIB6	ENTREZGENE
	Q6IAJ2	ENTREZGENE
	Q7Z5D4	ENTREZGENE
	Q86SY6	ENTREZGENE
	Q9H0Q6	ENTREZGENE
	Q9H2W0	ENTREZGENE
	Q9HAH5	ENTREZGENE
	Q9P055	ENTREZGENE
	Q9P0R3	ENTREZGENE
UniProt Secondary	B4DP67	UniProtKB/Swiss-Prot
	Q6FIB6	UniProtKB/Swiss-Prot
	Q6IAJ2	UniProtKB/Swiss-Prot
	Q7Z5D4	UniProtKB/Swiss-Prot
	Q86SY6	UniProtKB/Swiss-Prot
	Q9H0Q6	UniProtKB/Swiss-Prot
	Q9H2W0	UniProtKB/Swiss-Prot
	Q9HAH5	UniProtKB/Swiss-Prot
	Q9P0R3	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2017-09-26	JKAMP	JNK1/MAPK8 associated membrane protein		JNK1/MAPK8-associated membrane protein	Symbol and/or name change	5135510	APPROVED
2011-07-27	JKAMP	JNK1/MAPK8-associated membrane protein	C14orf100	chromosome 14 open reading frame 100	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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