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Gene: ARMH4 (armadillo like helical domain containing 4) Homo sapiens

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Symbol:

ARMH4

Name:

armadillo like helical domain containing 4

RGD ID:

1351933

HGNC Page

HGNC:19846

Description:

Predicted to enable TORC2 complex binding activity. Involved in regulation of inflammatory response. Located in membrane.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

armadillo-like helical domain containing 4; armadillo-like helical domain-containing protein 4; c14_5376; C14orf37; chromosome 14 open reading frame 37; hypothetical protein LOC145407; uncharacterized protein C14orf37; upstream of mTORC2; UT2

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	14	58,000,761 - 58,152,213 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	14	57,999,735 - 58,298,139 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	14	58,467,479 - 58,618,931 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	14	57,540,561 - 57,688,600 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	14	57,540,560 - 57,688,600	NCBI
Celera	14	38,520,760 - 38,668,792 (-)	NCBI		Celera
Cytogenetic Map	14	q23.1	NCBI
HuRef	14	38,636,789 - 38,784,667 (-)	NCBI		HuRef
CHM1_1	14	58,409,339 - 58,557,390 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	14	52,207,688 - 52,359,170 (-)	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

1,1,1-trichloro-2,2-bis(4-hydroxyphenyl)ethane (ISO)

17beta-estradiol (EXP)

2,2',4,4'-Tetrabromodiphenyl ether (EXP)

2,4-dibromophenyl 2,4,5-tribromophenyl ether (ISO)

3',5'-cyclic AMP (ISO)

6-propyl-2-thiouracil (ISO)

acrylamide (ISO)

aristolochic acid A (EXP)

benzo[a]pyrene (EXP)

bisphenol A (EXP,ISO)

bisphenol F (EXP)

butanal (EXP)

cadmium dichloride (ISO)

copper atom (ISO)

copper(0) (ISO)

diquat (ISO)

dorsomorphin (EXP)

doxorubicin (EXP)

endosulfan (ISO)

entinostat (EXP)

epoxiconazole (ISO)

fenvalerate (ISO)

fulvestrant (EXP)

genistein (ISO)

gentamycin (ISO)

lipopolysaccharide (EXP)

methoxychlor (ISO)

methylmercury chloride (EXP)

p-chloromercuribenzoic acid (EXP)

panobinostat (EXP)

paracetamol (ISO)

paraquat (ISO)

phenylmercury acetate (EXP)

propanal (EXP)

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

SB 431542 (EXP)

sodium arsenite (EXP)

sunitinib (EXP)

temozolomide (EXP)

trichostatin A (EXP)

urethane (EXP)

valproic acid (EXP)

vorinostat (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

regulation of inflammatory response (IDA)

regulation of TORC2 signaling (IEA,ISS)

Cellular Component

membrane (IDA,IEA)

Molecular Function

protein binding (IPI)

TORC2 complex binding (IEA,ISS)

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:12477932	PMID:15489334	PMID:16344560	PMID:20379614	PMID:24378760	PMID:24925725	PMID:25418727	PMID:26927669	PMID:28514442	PMID:29117863	PMID:29507755	PMID:30021884
PMID:33961781	PMID:36649229

Genomics

Comparative Map Data

ARMH4
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	14	58,000,761 - 58,152,213 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	14	57,999,735 - 58,298,139 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	14	58,467,479 - 58,618,931 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	14	57,540,561 - 57,688,600 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	14	57,540,560 - 57,688,600	NCBI
Celera	14	38,520,760 - 38,668,792 (-)	NCBI		Celera
Cytogenetic Map	14	q23.1	NCBI
HuRef	14	38,636,789 - 38,784,667 (-)	NCBI		HuRef
CHM1_1	14	58,409,339 - 58,557,390 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	14	52,207,688 - 52,359,170 (-)	NCBI		T2T-CHM13v2.0

Armh4
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	14	49,919,017 - 50,020,843 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	14	49,913,409 - 50,020,840 (-)	Ensembl		GRCm39 Ensembl
GRCm38	14	49,681,560 - 49,783,480 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	14	49,675,952 - 49,783,383 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	14	50,301,694 - 50,403,042 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	14	48,603,511 - 48,705,279 (-)	NCBI		MGSCv36	mm8
Celera	14	45,883,049 - 46,001,900 (-)	NCBI		Celera
Cytogenetic Map	14	C1	NCBI
cM Map	14	25.78	NCBI

Armh4
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	15	25,455,478 - 25,556,569 (-)	NCBI		GRCr8
mRatBN7.2	15	22,975,895 - 23,076,986 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	15	22,975,895 - 23,076,949 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	15	25,753,156 - 25,854,222 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	15	26,714,490 - 26,815,560 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	15	24,961,684 - 25,062,756 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	15	26,586,359 - 26,687,412 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	15	26,587,179 - 26,678,420 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	15	30,512,209 - 30,613,262 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	15	25,680,073 - 25,781,128 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	15	25,696,592 - 25,796,832 (-)	NCBI
Celera	15	23,343,119 - 23,443,765 (-)	NCBI		Celera
Cytogenetic Map	15	p14	NCBI

Armh4
(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	11,777,693 - 11,880,257 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955466	11,771,258 - 11,889,444 (-)	NCBI	ChiLan1.0	ChiLan1.0

ARMH4
(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	59,120,298 - 59,276,345 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	14	58,336,812 - 58,492,972 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	14	38,600,338 - 38,746,397 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	14	56,870,406 - 57,003,380 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	14	56,870,406 - 57,003,380 (-)	Ensembl	panpan1.1		panPan2

ARMH4
(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	33,411,953 - 33,575,083 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	8	33,412,665 - 33,551,054 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	8	33,174,352 - 33,336,785 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	8	33,651,725 - 33,816,624 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	8	33,651,740 - 33,782,102 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	8	33,267,316 - 33,429,880 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	8	33,332,566 - 33,497,069 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	8	33,707,637 - 33,872,149 (-)	NCBI		UU_Cfam_GSD_1.0

Armh4
(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	71,623,762 - 71,738,159 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936495	2,456,147 - 2,558,354 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936495	2,452,971 - 2,567,862 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

ARMH4
(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	187,103,809 - 187,259,015 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	1	187,118,498 - 187,259,069 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	1	208,103,943 - 208,170,315 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

ARMH4
(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	35,195,374 - 35,344,585 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	24	35,196,061 - 35,344,708 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666053	23,428,549 - 23,584,010 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Armh4
(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_004624884	3,034,414 - 3,223,161 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624884	3,027,799 - 3,225,859 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in ARMH4
17 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
NM_001001872.2(C14orf37):c.2090-6612G>T	single nucleotide variant	Lung cancer [RCV000098955]	Chr14:58018762 [GRCh38] Chr14:58485480 [GRCh37] Chr14:14q23.1	uncertain significance
NM_001001872.2(C14orf37):c.2090-15848T>A	single nucleotide variant	Lung cancer [RCV000098956]	Chr14:58027998 [GRCh38] Chr14:58494716 [GRCh37] Chr14:14q23.1	uncertain significance
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
GRCh38/hg38 14q22.3-23.1(chr14:57121531-58028799)x1	copy number loss	See cases [RCV000143401]	Chr14:57121531..58028799 [GRCh38] Chr14:57588249..58495517 [GRCh37] Chr14:56658002..57565270 [NCBI36] Chr14:14q22.3-23.1	uncertain significance
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(chr14:58598190-58733421)x3	copy number gain	not provided [RCV000512697]	Chr14:58598190..58733421 [GRCh37] Chr14:14q23.1	likely benign
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 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 14q23.1(chr14:58483217-58561961)x3	copy number gain	not provided [RCV000751029]	Chr14:58483217..58561961 [GRCh37] Chr14:14q23.1	benign
GRCh37/hg19 14q22.3-23.1(chr14:56605398-59404256)x1	copy number loss	not provided [RCV001006637]	Chr14:56605398..59404256 [GRCh37] Chr14:14q22.3-23.1	pathogenic
GRCh37/hg19 14q23.1(chr14:58412701-58474350)x1	copy number loss	not provided [RCV001259674]	Chr14:58412701..58474350 [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_001001872.4(ARMH4):c.1624C>G (p.Gln542Glu)	single nucleotide variant	not provided [RCV003393444]	Chr14:58131719 [GRCh38] Chr14:58598437 [GRCh37] Chr14:14q23.1	likely benign
GRCh37/hg19 14q22.3-23.1(chr14:57675327-59806898)x1	copy number loss	not provided [RCV003326901]	Chr14:57675327..59806898 [GRCh37] Chr14:14q22.3-23.1	uncertain significance
NM_001001872.4(ARMH4):c.57C>T (p.Phe19=)	single nucleotide variant	not provided [RCV003393445]	Chr14:58139302 [GRCh38] Chr14:58606020 [GRCh37] Chr14:14q23.1	likely benign
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 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_001001872.4(ARMH4):c.1127C>T (p.Thr376Met)	single nucleotide variant	not specified [RCV004418059]	Chr14:58138232 [GRCh38] Chr14:58604950 [GRCh37] Chr14:14q23.1	likely benign
NM_001001872.4(ARMH4):c.960G>C (p.Glu320Asp)	single nucleotide variant	not specified [RCV004418066]	Chr14:58138399 [GRCh38] Chr14:58605117 [GRCh37] Chr14:14q23.1	uncertain significance
NM_001001872.4(ARMH4):c.1453C>A (p.Leu485Ile)	single nucleotide variant	not specified [RCV004418060]	Chr14:58133258 [GRCh38] Chr14:58599976 [GRCh37] Chr14:14q23.1	uncertain significance
NM_001001872.4(ARMH4):c.788A>G (p.Asp263Gly)	single nucleotide variant	not specified [RCV004418065]	Chr14:58138571 [GRCh38] Chr14:58605289 [GRCh37] Chr14:14q23.1	uncertain significance
NM_001001872.4(ARMH4):c.1868A>G (p.Asp623Gly)	single nucleotide variant	not specified [RCV004418064]	Chr14:58096945 [GRCh38] Chr14:58563663 [GRCh37] Chr14:14q23.1	uncertain significance
NM_001001872.4(ARMH4):c.1456G>A (p.Glu486Lys)	single nucleotide variant	not specified [RCV004418061]	Chr14:58133255 [GRCh38] Chr14:58599973 [GRCh37] Chr14:14q23.1	uncertain significance
NM_001001872.4(ARMH4):c.1667T>A (p.Val556Asp)	single nucleotide variant	not specified [RCV004418062]	Chr14:58131676 [GRCh38] Chr14:58598394 [GRCh37] Chr14:14q23.1	uncertain significance
NM_001001872.4(ARMH4):c.1684A>G (p.Thr562Ala)	single nucleotide variant	not specified [RCV004418063]	Chr14:58131659 [GRCh38] Chr14:58598377 [GRCh37] Chr14:14q23.1	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	1974
Count of miRNA genes:	1050
Interacting mature miRNAs:	1270
Transcripts:	ENST00000267485, ENST00000334342, ENST00000554218, ENST00000555101, ENST00000556788, ENST00000557175
Prediction methods:	Microtar, Miranda, Rnahybrid, Targetscan
Result types:	miRGate_prediction

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

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

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
406961043	GWAS610019_H	gut microbiome measurement, taxonomic microbiome measurement QTL GWAS610019 (human)		9e-10	gut microbiome measurement, taxonomic microbiome measurement		14	58060100	58060101	Human
597428137	GWAS1524211_H	depressive symptom measurement, stressful life event measurement QTL GWAS1524211 (human)		0.000002	depressive symptom measurement, stressful life event measurement		14	58047955	58047956	Human
407147889	GWAS796865_H	lupus nephritis QTL GWAS796865 (human)		0.000002	lupus nephritis		14	58092523	58092524	Human
597217280	GWAS1313354_H	body height QTL GWAS1313354 (human)		1e-17	body height (VT:0001253)	body height (CMO:0000106)	14	58102161	58102162	Human
597095544	GWAS1191618_H	dementia, Alzheimer's disease neuropathologic change QTL GWAS1191618 (human)		0.000002	dementia, Alzheimer's disease neuropathologic change		14	58109602	58109603	Human

Markers in Region

SHGC-81588

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	14	58,531,039 - 58,531,314	UniSTS	GRCh37
Build 36	14	57,600,792 - 57,601,067	RGD	NCBI36
Celera	14	38,580,991 - 38,581,266	RGD
Cytogenetic Map	14	q23.1	UniSTS
HuRef	14	38,696,912 - 38,697,187	UniSTS
TNG Radiation Hybrid Map	14	17993.0	UniSTS

SHGC-81560

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	14	58,530,826 - 58,531,162	UniSTS	GRCh37
Build 36	14	57,600,579 - 57,600,915	RGD	NCBI36
Celera	14	38,580,778 - 38,581,114	RGD
Cytogenetic Map	14	q23.1	UniSTS
HuRef	14	38,696,699 - 38,697,035	UniSTS
TNG Radiation Hybrid Map	14	18003.0	UniSTS

SHGC-36423

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	14	58,467,849 - 58,467,928	UniSTS	GRCh37
Build 36	14	57,537,602 - 57,537,681	RGD	NCBI36
Celera	14	38,517,801 - 38,517,880	RGD
Cytogenetic Map	14	q23.1	UniSTS
HuRef	14	38,633,847 - 38,633,926	UniSTS

RH69498

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	14	58,470,230 - 58,470,432	UniSTS	GRCh37
Build 36	14	57,539,983 - 57,540,185	RGD	NCBI36
Celera	14	38,520,182 - 38,520,384	RGD
Cytogenetic Map	14	q23.1	UniSTS
HuRef	14	38,636,211 - 38,636,413	UniSTS
GeneMap99-GB4 RH Map	14	132.18	UniSTS

RH44675

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	14	58,563,484 - 58,563,618	UniSTS	GRCh37
Build 36	14	57,633,237 - 57,633,371	RGD	NCBI36
Celera	14	38,613,440 - 38,613,574	RGD
Cytogenetic Map	14	q23.1	UniSTS
HuRef	14	38,729,227 - 38,729,361	UniSTS
GeneMap99-GB4 RH Map	14	132.18	UniSTS

G35522

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	14	58,570,012 - 58,570,177	UniSTS	GRCh37
Build 36	14	57,639,765 - 57,639,930	RGD	NCBI36
Celera	14	38,619,968 - 38,620,133	RGD
Cytogenetic Map	14	q23.1	UniSTS
HuRef	14	38,735,754 - 38,735,919	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	2422	2787	2238	4974	1711	2326	5	610	1242	450	2270	6582	5776	52	3733	1	851	1740	1606	174	1

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001001872	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001320173	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AK292513	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK292605	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK294599	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL049838	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL121579	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC013707	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC031314	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC062772	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC146861	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX161411	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX161448	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX649130	(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
	DA126898	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000267485 ⟹ ENSP00000267485

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	58,000,761 - 58,152,213 (-)	Ensembl

Ensembl Acc Id:

ENST00000334342

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	58,116,124 - 58,152,183 (-)	Ensembl

Ensembl Acc Id:

ENST00000554218

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	58,139,101 - 58,298,139 (-)	Ensembl

Ensembl Acc Id:

ENST00000555101 ⟹ ENSP00000477692

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	58,131,207 - 58,133,131 (-)	Ensembl

Ensembl Acc Id:

ENST00000556788

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	57,999,735 - 58,004,024 (-)	Ensembl

Ensembl Acc Id:

ENST00000557175

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	58,116,116 - 58,139,241 (-)	Ensembl

RefSeq Acc Id:

NM_001001872 ⟹ NP_001001872

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	58,000,761 - 58,152,213 (-)	NCBI
GRCh37	14	58,470,808 - 58,618,847 (-)	RGD
Build 36	14	57,540,561 - 57,688,600 (-)	NCBI Archive
Celera	14	38,520,760 - 38,668,792 (-)	RGD
HuRef	14	38,636,789 - 38,784,667 (-)	RGD
CHM1_1	14	58,409,305 - 58,557,500 (-)	NCBI
T2T-CHM13v2.0	14	52,207,688 - 52,359,170 (-)	NCBI

Sequence:

show sequence

CTCCCCCTAGCGTCCCAGACAGCGGAGGGAGTCGCCGCCGCTACCGCCGCCGCCGCCGCAGGGC
CCGCCGCTGGGATGCCGAGCGCCCGCGCCGCCGCTGCCTCTGTCCTCCGCGCGCTGCTCAGCTG
AAGGCGCACAGGATTCAATTACTGGACTTGTCAACTCTGCCAGTGTACGTGCCATTTCTCTTCC
ACTATGAGAGGACCGATTGTATTGCACATTTGTCTGGCTTTCTGTAGCCTTCTGCTTTTCAGCG
TTGCCACACAATGTCTGGCCTTCCCCAAAATAGAAAGGAGGAGGGAGATAGCACATGTTCATGC
GGAAAAAGGGCAGTCCGATAAGATGAACACCGATGACCTAGAAAATAGCTCTGTTACCTCAAAG
CAGACTCCCCAACTGGTGGTCTCTGAAGATCCAATGATGATGTCAGCAGTACCATCGGCAACAT
CATTAAATAAAGCATTCTCGATTAACAAAGAAACCCAGCCTGGACAAGCTGGGCTCATGCAAAC
AGAACGCCCTGGTGTTTCCACACCTACTGAGTCAGGTGTCCCCTCAGCTGAAGAAGTATTTGGT
TCCAGCCAGCCAGAGAGAATATCTCCTGAAAGTGGACTTGCCAAGGCCATGTTAACCATTGCTA
TCACTGCGACTCCTTCTCTGACTGTTGATGAAAAGGAGGAACTCCTTACAAGCACTAACTTTCA
GCCCATTGTAGAAGAGATCACAGAAACCACAAAAGGTTTTCTGAAGTATATGGATAATCAATCA
TTTGCAACTGAAAGTCAGGAAGGAGTTGGTTTGGGACATTCACCTTCATCCTATGTGAATACTA
AGGAAATGCTAACCACCAATCCAAAGACTGAGAAATTTGAAGCAGACACAGACCACAGGACAAC
TTCTTTTCCTGGTGCTGAGTCCACAGCAGGCAGTGAGCCTGGAAGCCTCACCCCTGATAAGGAG
AAGCCTTCGCAGATGACAGCTGATAACACCCAGGCTGCTGCCACCAAGCAACCACTCGAAACTT
CCGAGTACACCCTGAGTGTTGAGCCAGAAACTGATAGTCTGCTGGGAGCCCCAGAAGTCACAGT
GAGTGTCAGCACAGCTGTTCCAGCTGCCTCTGCCTTAAGTGATGAGTGGGATGACACCAAATTA
GAGAGTGTAAGCCGGATAAGGACCCCCAAGCTTGGAGACAATGAAGAGACTCAGGTGAGAACGG
AGATGTCTCAGACAGCACAAGTAAGCCATGAGGGTATGGAAGGAGGCCAGCCTTGGACAGAGGC
TGCACAGGTGGCTCTGGGGCTGCCTGAAGGGGAAACACACACGGGCACAGCCCTGCTAATAGCG
CATGGGAATGAGAGATCACCTGCTTTCACTGATCAAAGTTCCTTTACCCCCACAAGTCTGATGG
AAGACATGAAAGTTTCCATTGTGAACTTGCTCCAAAGTACGGGAGACTTCACGGAATCCACCAA
GGAAAACGATGCCCTGTTTTTCTTAGAAACCACTGTTTCTGTCTCTGTATATGAGTCTGAGGCA
GACCAACTGTTGGGAAATACAATGAAAGACATCATCACTCAAGAGATGACAACAGCTGTTCAAG
AGCCAGATGCCACTTTATCCATGGTGACACAAGAGCAGGTTGCTACCCTCGAGCTTATCAGAGA
CAGTGGCAAGACTGAGGAAGAAAAGGAGGACCCCTCTCCTGTGTCTGACGTTCCTGGTGTTACT
CAGCTGTCAAGAAGATGGGAGCCTCTGGCCACTACAATTTCAACTACAGTCGTCCCTTTGTCTT
TTGAAGTTACTCCCACTGTGGAAGAACAAATGGACACAGTCACAGGGCCAAATGAGGAGTTCAC
ACCAGTTCTGGGATCTCCAGTGACACCTCCTGGAATAATGGTGGGGGAACCCAGCATTTCCCCT
GCACTTCCTGCTTTGGAGGCATCCTCTGAGAGAAGAACTGTTGTTCCATCTATTACTCGTGTTA
ATACAGCTGCCTCATATGGCCTGGACCAACTTGAATCTGAAGAGGGACAAGAAGATGAGGATGA
AGAGGATGAAGAAGATGAAGATGAAGAAGAGGAAGATGAGGAAGAAGATGAGGAAGATAAAGAT
GCAGACTCGCTGGATGAGGGCTTGGATGGTGACACTGAGCTGCCAGGTTTTACCCTCCCTGGTA
TCACATCCCAGGAACCAGGCTTAGAGGAGGGAAACATGGACCTGTTGGAGGGAGCTACCTACCA
GGTGCCAGATGCCCTCGAGTGGGAACAGCAGAATCAAGGCCTGGTGAGAAGCTGGATGGAAAAA
TTAAAAGACAAGGCTGGTTACATGTCTGGGATGCTGGTGCCTGTAGGGGTTGGGATAGCTGGAG
CCTTGTTCATCTTGGGAGCCCTCTACAGCATTAAGGTTATGAATCGCCGAAGGAGAAATGGCTT
CAAAAGGCATAAAAGAAAGCAGAGAGAATTCAACAGCATGCAAGATCGAGTAATGCTCTTAGCC
GACAGCTCTGAAGATGAATTTTGAATTGGACTGGGTTTTAATTGGGATATTCAACGATGCTACT
ATTCTAATTTTTATTTTGGAGCAGAAAAAAAAAAAGAACAACCTGCCACATTGCTGCTATCAGG
CCGTTAGTCCTAGTGTCTGCTGGGTGCTGGGTAGTAGATTTTTCTTGTACTGAGCAGAAATGGC
ATGTTGTATACTAAACGTATCATGCAGTATTTGGTTTTATTCTGTAGTGAATTTTCCACAACCG
TGGGCTACAACTCATAAATATGCAACATATATGTTTTTCAGTAGGAGTTGCTACATTAGGCAGA
GTAAATATTTTGTAGTTTTCCACAGTGTCTTTTCCTTGGTTTGAATTACCTGCATTGAGAATAA
TGATTGTTGCCACCAAGGCATGCTTGACTCTGAGATATAAATCTTAACAAAGAATAACTTCTCA
AGATATACTCTACCTACTTGAAACCACAGGGTTGTGGGCCATGGTACATACTGCATTTGCATCA
AACTAGCAGTAACTCAGAATGAAATCATTTTCATTAAGAAGCTCTCTCAGCATATTAGGATTAT
ATGTAGATTTGTATGTATTTTGCATTATGTACTTCAGTCTCCTAGTTTTATTATTCTCACCTTC
CGTTTTATTCTTGGCGAGGAAAAAAATGCACTAGAAATAATACATTAAACTGACTCTTAGTCTT
AATGTACGTTTGCTGTCTTAAATAGTGTGATTGAGTCCAACAGACTCAATCATACATGTCATAC
ATGTTTATGATTAAGAGATATTCTTTTTGTGTGCTAGTTGATTTTGCCGAGAAAAAATGAAGAA
GAATTCAAGAATGAGATGAGGGTAGGTAAGCTCTCAGAGCATTTCTGTCTGCCATTTGGTTCTA
TGCTTATGTGGCTGCTAATGTGACTAATTCAGAGTGTTGTATTTCCACATCTGTGGACTCCACC
ATGGAAAAGGTGGGCTACCATTGGTCCTTATATGGCTTTATTAGAAAAATAGACATTCTATCGT
TTGTCTGCCCAGTGGCCAGAGTCCTGGTGAACAACAGAGCTCATGGGAAACCAGCCTCTCTCAG
GGCACCCCGCTATGAGGATATTGAAATATGTTCAATCATTTCTCATCTCCCTTGGAATGTAATT
CCCTGCCCTATACAAAATAGGATATTCCAATGCGCTATTTGAATCTAGGGATTGAGGATTTGTA
GTTGAGTTTTGGGGTAAAGGCTTGGCTCATTGCCATGGAAGAATAAAAGTTATTTATTAATAGT
GCTGTCACTGTGGAGTACTTGTTGGTGTTTATTAGAAGTTGTCTACTATGTTCAAGAAAAGTTG
CACAGTTATTCCTCAGAGCTACTATGTGAGGTAGGACATATGTTTTTATTCTCCCATTTGACTG
AAGATGGAACTGAAGCAGAGAAGTGAAATGATTTTCCAAAGTTGTACCCAGAGAGAATCAGCGT
GAGAACCCACTTGGACCCAGCCATGCACCCTTATCTTCAGTTCAGTAACCTTTTCATAGACTTT
GGTGGAAGCAGTGACATTTCAGGGTCCTTCTTTAAAACAAAGGTTCTAAGGGAATAGCAGGGAA
TAGCTGCCTGGTCAAGGAACGTTTGATGTGAATTTCCATCTTTGTTAAATGAATGATGCCTTTC
TAATTTCTCTCTTACTCACACACAAGTTCTTTCCTTCCCCATCTCAGTTATCAGTTATTTCCTT
TACAGTCATACATTTGAGTATCACCTCTATGGAACTAATAAACCTTCCTAGAATCCGTTTTTGA
ATAATGTCTGGCTCACAAGAACATTTTCATCAAATAATTTTAACTCTTTTTGCCAAGAGATGTA
AGCAAATATGTGAAACTGATCAAGAGAAGTGAAAAGCTCTGTACAGTCAAATAGAAGTTAGCAA
CTGGCAAATTAGCTCAAGGTCAGATTTTAAAAATAGAATTCAGAATCATGACACTCAGAAGTGA
TTTGTAATTTCACGAGTAGAGACATCCTGATATTGCATAAGGGATGTTTTCCTTTTCTAAGAGC
AGCCCTTTGCTGTAAGTGTTTCTAAGGTTGGGAGTAAGTGAGCATGGTGTGGCATTACTGTCTT
TGTATTCTTGACAAACTATTTGTTGAGAATACGTCGTAGGCCACTTAACTGAGTAGCACATGGG
TGATACTAGTGGCCATTATTGCCTTGGGCTACTCAATCTATAGTCTTAACTAAACCATGGCTAA
TAGGTTGAATCTTCAAACTGTAGTGTAATAAATTCCCAAATAACAGACCCATATTTTCATTTCT
CAGAGGTCCGTGAGGATGACATGTATGTGAATTTTGGCTTAACACAGTATCTCTGTGGTCCTTT
TTGGGACACATGATTTCTTAAAGGAAAAGATTATACTTAGAGTACATTTCTGTACAAACCCATT
TAAACATCTGGATTGAGTGGAAGGTCGGTGGATGGTACAAATGACATGTTTATTTTGGCCATTT
TCCTTGCTGCTGGTGGCTGTGGAATAATGATTTTCAGTGGTTGGCTTAGATTATTAAGAGGATC
AGAAAAGGTTGTCATATTTTAAACAAAACCTGGGATTAGAGATGCTGCTACGAGATGGAAGTGC
TGGCCAGTGGTTATATAGTGGTCCAGTTGAGAAGTAGTAAATCAGGCACTTGTAGGTTTACCCA
AAATAAGTGACAAGTATGCTTATATTTGCACAATTAAAATAGAAAGTCAACTTTTTATTCAAAC
AACTAGGCTTAAAACATTTAACAGTGAAACAAATAAAGCTGTCTGGAAAGGAGGGCTGATTCCT
GCAGCTTCAGTTGTGAACACCATCCCCACTGGACTGAGTTTACCCAGCCAGAACTGCCAGCATC
CCACCGCAGGGGCAGGAACTAGGTCTTCTTCTCGGAGGGAGAGGCAGTGTTTCCAGAATTTGCA
GGCTCATAAAAATCACCTGGGACACTTGTGAAACATACAGATCTCAAGGCCTTGCCCCAGACCT
GATGAGTTAGAATCTCCAGGGAAGGAGCTTGGGGTATTCATGCCCCAGCAAGCTTGGGAACACA
GCTAGGAGGGATCTATCTAGAGAACCACTTCCTTATGATAGAGACAAGGTCATTTAAAGTCACA
ATGAGATACCACCTCACACCTATTGGGATGGCTATTATTCAATAAAACAAAATATAACAATTGT
TTCTGAGGATGTGGAGAAATTGGAATCCTTGTATACTGTGGGTGGGAATGTAAAATGGATAGCC
ACTGTGGAAAACAGTATGAAGATTCCTCAAAAAATTAAGATAGAACTACTATATAATCCAACTA
TCCCACTTCTGGGCATATATCCAAAAGAATAGAAATCAGGATCTTGAAGAAGTATCTGTACGCC
TGTGTTCATTGCTTATGCTTATAAGCATATTATTCACAATAAGCTTATAAGTATTATTCACAAT
AGCCAAGATATGGAAATTGCATTGATAGATATGCAAATATCTATCAATAGATGAATGGATAAAG
AAAATGTGGTATATACATACAGTAGAATATTATTCAGCCATAGGAAATAAGGAAATTCTGTCAT
TGTGACAATATGGATATACATGGAGAACATTATGCTAAGTGAAATAAACTAGTGACAGAAGGAC
AAATGCATGATTGCACTTCTTTGAGGTATCCAAAATAATCAAACTCATAAGGGCAGAGGCAAAA
TGGTGCTTGCCACGGGCTGGGCAAAGTTAAAGGTGGGGAGATGTTGATTAATTATGTTTCAGTT
ATGCAAGATGAATAAGTTCTAGAGCTCTGCTGTATAACATAGTGCCTATAGTTAACAATATCGT
ACTGTGCAGTTAAAAATTTGTTAAGAGGGCCGGGTGTGGTGGCTCACGCCTGTAATCCCAGCAC
TTTGGGAGGCCAAGGTGGGCAGATCATGAGGTCAGGAGATAGAAACCATCCTGGCTAACATGGT
GAAACCCCATCTCTACTAAAAATACAAAAAA

hide sequence

RefSeq Acc Id:

NM_001320173 ⟹ NP_001307102

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	58,116,086 - 58,152,213 (-)	NCBI
CHM1_1	14	58,521,406 - 58,557,500 (-)	NCBI
T2T-CHM13v2.0	14	52,323,040 - 52,359,170 (-)	NCBI

Sequence:

show sequence

CTCCCCCTAGCGTCCCAGACAGCGGAGGGAGTCGCCGCCGCTACCGCCGCCGCCGCCGCAGGGC
CCGCCGCTGGGATGCCGAGCGCCCGCGCCGCCGCTGCCTCTGTCCTCCGCGCGCTGCTCAGCTG
AAGGCGCACAGGATTCAATTACTGGACTTGTCAACTCTGCCAGTGTACGTGCCATTTCTCTTCC
ACTATGAGAGGACCGATTGTATTGCACATTTGTCTGGCTTTCTGTAGCCTTCTGCTTTTCAGCG
TTGCCACACAATGTCTGGCCTTCCCCAAAATAGAAAGGAGGAGGGAGATAGCACATGTTCATGC
GGAAAAAGGGCAGTCCGATAAGATGAACACCGATGACCTAGAAAATAGCTCTGTTACCTCAAAG
CAGACTCCCCAACTGGTGGTCTCTGAAGATCCAATGATGATGTCAGCAGTACCATCGGCAACAT
CATTAAATAAAGCATTCTCGATTAACAAAGAAACCCAGCCTGGACAAGCTGGGCTCATGCAAAC
AGAACGCCCTGGTGTTTCCACACCTACTGAGTCAGGTGTCCCCTCAGCTGAAGAAGTATTTGGT
TCCAGCCAGCCAGAGAGAATATCTCCTGAAAGTGGACTTGCCAAGGCCATGTTAACCATTGCTA
TCACTGCGACTCCTTCTCTGACTGTTGATGAAAAGGAGGAACTCCTTACAAGCACTAACTTTCA
GCCCATTGTAGAAGAGATCACAGAAACCACAAAAGGTTTTCTGAAGTATATGGATAATCAATCA
TTTGCAACTGAAAGTCAGGAAGGAGTTGGTTTGGGACATTCACCTTCATCCTATGTGAATACTA
AGGAAATGCTAACCACCAATCCAAAGACTGAGAAATTTGAAGCAGACACAGACCACAGGACAAC
TTCTTTTCCTGGTGCTGAGTCCACAGCAGGCAGTGAGCCTGGAAGCCTCACCCCTGATAAGGAG
AAGCCTTCGCAGATGACAGCTGATAACACCCAGGCTGCTGCCACCAAGCAACCACTCGAAACTT
CCGAGTACACCCTGAGTGTTGAGCCAGAAACTGATAGTCTGCTGGGAGCCCCAGAAGTCACAGT
GAGTGTCAGCACAGCTGTTCCAGCTGCCTCTGCCTTAAGTGATGAGTGGGATGACACCAAATTA
GAGAGTGTAAGCCGGATAAGGACCCCCAAGCTTGGAGACAATGAAGAGACTCAGGTGAGAACGG
AGATGTCTCAGACAGCACAAGTAAGCCATGAGGGTATGGAAGGAGGCCAGCCTTGGACAGAGGC
TGCACAGGTGGCTCTGGGGCTGCCTGAAGGGGAAACACACACGGGCACAGCCCTGCTAATAGCG
CATGGGAATGAGAGATCACCTGCTTTCACTGATCAAAGTTCCTTTACCCCCACAAGTCTGATGG
AAGACATGAAAGTTTCCATTGTGAACTTGCTCCAAAGTACGGGAGACTTCACGGAATCCACCAA
GGAAAACGATGCCCTGTTTTTCTTAGAAACCACTGTTTCTGTCTCTGTATATGAGTCTGAGGCA
GACCAACTGTTGGGAAATACAATGAAAGACATCATCACTCAAGAGATGACAACAGCTGTTCAAG
AGCCAGATGCCACTTTATCCATGGTGACACAAGAGCAGGTTGCTACCCTCGAGCTTATCAGAGA
CAGTGGCAAGACTGAGGAAGAAAAGGAGGACCCCTCTCCTGTGTCTGACGTTCCTGGTGTTACT
CAGCTGTCAAGAAGATGGGAGCCTCTGGCCACTACAATTTCAACTACAGTCGTCCCTTTGTCTT
TTGAAGTTACTCCCACTGTGGAAGAACAAATGGACACAGTCACAGGGCCAAATGAGGAGTTCAC
ACCAGTTCTGGGATCTCCAGTGACACCTCCTGGAATAATGGTGGGGGAACCCAGCATTTCCCCT
GCACTTCCTGCTTTGGAGGCATCCTCTGAGAGAAGAACTGTTGTTCCATCTATTACTCGTGTTA
ATACAGCTGCCTCATATGGCCTGGACCAACTTGAATCTGAAGAGACGGGGTTTCACCATGTTGC
CCAGGCTCGTCTCAAACTCCTGGGCTTAAGAAGTCTGCCTGCCTCGGCCTCCCAAAGTGTTGGA
ATTACAAGTGTGAACTCCTGCACCCAGCCAAGAAAATATTTAAACAGCTGCCTGAAATGGAAAT
TGAATCCAAAACATTTTGCCACTGGTGTTTGAAGTGGACTATCTTGTCTCAAGCCTTTTTATTT
TCTCATGAATGTACCTTCTAAATATTGTTAAGGCTACAATGGAGGAAATTTTAAATTATTATAT
TTACTATTTTACAGTGAGTGGAAAATTTGAAATTTAGTAAAAAGTTTTCAAGAAATTTTTATAG
ATTAATAATGGAGTTTAAAAAGTCATGGCGATGAGGCATTTAACAAGGAGAGAACTGAATAAAT
TAACAGACATGTTTAA

hide sequence

Protein Sequences


Protein RefSeqs	NP_001001872	(Get FASTA)	NCBI Sequence Viewer
	NP_001307102	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH62772	(Get FASTA)	NCBI Sequence Viewer
	AAI46862	(Get FASTA)	NCBI Sequence Viewer
	BAF85202	(Get FASTA)	NCBI Sequence Viewer
	BAF85294	(Get FASTA)	NCBI Sequence Viewer
	BAG57786	(Get FASTA)	NCBI Sequence Viewer
	CAD61887	(Get FASTA)	NCBI Sequence Viewer
	CAD61913	(Get FASTA)	NCBI Sequence Viewer
	EAW80712	(Get FASTA)	NCBI Sequence Viewer
	EAW80713	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000267485
	ENSP00000267485.7
	ENSP00000477692.1
GenBank Protein	Q86TY3	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_001001872 ⟸ NM_001001872
- Peptide Label:	isoform 1 precursor
- UniProtKB:	Q86TY3 (UniProtKB/Swiss-Prot), Q6P5Q1 (UniProtKB/Swiss-Prot), A8K8Z8 (UniProtKB/Swiss-Prot), Q86TY1 (UniProtKB/Swiss-Prot), A8K990 (UniProtKB/TrEMBL)
- Sequence:	show sequence MRGPIVLHICLAFCSLLLFSVATQCLAFPKIERRREIAHVHAEKGQSDKMNTDDLENSSVTSKQ TPQLVVSEDPMMMSAVPSATSLNKAFSINKETQPGQAGLMQTERPGVSTPTESGVPSAEEVFGS SQPERISPESGLAKAMLTIAITATPSLTVDEKEELLTSTNFQPIVEEITETTKGFLKYMDNQSF ATESQEGVGLGHSPSSYVNTKEMLTTNPKTEKFEADTDHRTTSFPGAESTAGSEPGSLTPDKEK PSQMTADNTQAAATKQPLETSEYTLSVEPETDSLLGAPEVTVSVSTAVPAASALSDEWDDTKLE SVSRIRTPKLGDNEETQVRTEMSQTAQVSHEGMEGGQPWTEAAQVALGLPEGETHTGTALLIAH GNERSPAFTDQSSFTPTSLMEDMKVSIVNLLQSTGDFTESTKENDALFFLETTVSVSVYESEAD QLLGNTMKDIITQEMTTAVQEPDATLSMVTQEQVATLELIRDSGKTEEEKEDPSPVSDVPGVTQ LSRRWEPLATTISTTVVPLSFEVTPTVEEQMDTVTGPNEEFTPVLGSPVTPPGIMVGEPSISPA LPALEASSERRTVVPSITRVNTAASYGLDQLESEEGQEDEDEEDEEDEDEEEEDEEEDEEDKDA DSLDEGLDGDTELPGFTLPGITSQEPGLEEGNMDLLEGATYQVPDALEWEQQNQGLVRSWMEKL KDKAGYMSGMLVPVGVGIAGALFILGALYSIKVMNRRRRNGFKRHKRKQREFNSMQDRVMLLAD SSEDEF hide sequence

RefSeq Acc Id:	NP_001307102 ⟸ NM_001320173
- Peptide Label:	isoform 2 precursor
- UniProtKB:	Q86TY3 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MRGPIVLHICLAFCSLLLFSVATQCLAFPKIERRREIAHVHAEKGQSDKMNTDDLENSSVTSKQ TPQLVVSEDPMMMSAVPSATSLNKAFSINKETQPGQAGLMQTERPGVSTPTESGVPSAEEVFGS SQPERISPESGLAKAMLTIAITATPSLTVDEKEELLTSTNFQPIVEEITETTKGFLKYMDNQSF ATESQEGVGLGHSPSSYVNTKEMLTTNPKTEKFEADTDHRTTSFPGAESTAGSEPGSLTPDKEK PSQMTADNTQAAATKQPLETSEYTLSVEPETDSLLGAPEVTVSVSTAVPAASALSDEWDDTKLE SVSRIRTPKLGDNEETQVRTEMSQTAQVSHEGMEGGQPWTEAAQVALGLPEGETHTGTALLIAH GNERSPAFTDQSSFTPTSLMEDMKVSIVNLLQSTGDFTESTKENDALFFLETTVSVSVYESEAD QLLGNTMKDIITQEMTTAVQEPDATLSMVTQEQVATLELIRDSGKTEEEKEDPSPVSDVPGVTQ LSRRWEPLATTISTTVVPLSFEVTPTVEEQMDTVTGPNEEFTPVLGSPVTPPGIMVGEPSISPA LPALEASSERRTVVPSITRVNTAASYGLDQLESEETGFHHVAQARLKLLGLRSLPASASQSVGI TSVNSCTQPRKYLNSCLKWKLNPKHFATGV hide sequence

Ensembl Acc Id:

ENSP00000477692 ⟸ ENST00000555101

Ensembl Acc Id:

ENSP00000267485 ⟸ ENST00000267485

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q86TY3-F1-model_v2	AlphaFold	Q86TY3	1-774	view protein structure

Promoters

RGD ID:

7227725

Promoter ID:

EPDNEW_H19608

Type:

initiation region

Name:

C14orf37_1

Description:

chromosome 14 open reading frame 37

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	58,152,197 - 58,152,257	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:19846	AgrOrtholog
COSMIC	ARMH4	COSMIC
Ensembl Genes	ENSG00000139971	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000267485	ENTREZGENE
	ENST00000267485.7	UniProtKB/Swiss-Prot
	ENST00000334342	ENTREZGENE
	ENST00000555101.1	UniProtKB/TrEMBL
GTEx	ENSG00000139971	GTEx
HGNC ID	HGNC:19846	ENTREZGENE
Human Proteome Map	ARMH4	Human Proteome Map
InterPro	ARMH4	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:145407	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene	145407	ENTREZGENE
PANTHER	ARMADILLO-LIKE HELICAL DOMAIN-CONTAINING PROTEIN 4	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	PTHR21585	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	DUF4696	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA134941886	PharmGKB
UniProt	A0A087WT98_HUMAN	UniProtKB/TrEMBL
	A8K8Z8	ENTREZGENE
	A8K990	ENTREZGENE, UniProtKB/TrEMBL
	ARMD4_HUMAN	UniProtKB/Swiss-Prot
	B2RUU6_HUMAN	UniProtKB/TrEMBL
	Q6P5Q1	ENTREZGENE
	Q86TY1	ENTREZGENE
	Q86TY3	ENTREZGENE
UniProt Secondary	A8K8Z8	UniProtKB/Swiss-Prot
	Q6P5Q1	UniProtKB/Swiss-Prot
	Q86TY1	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2019-02-26	ARMH4	armadillo like helical domain containing 4		armadillo-like helical domain containing 4	Symbol and/or name change	5135510	APPROVED
2018-02-06	ARMH4	armadillo-like helical domain containing 4	C14orf37	chromosome 14 open reading frame 37	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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