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Gene: ZNF267 (zinc finger protein 267) Homo sapiens

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Symbol:

ZNF267

Name:

zinc finger protein 267

RGD ID:

1343571

HGNC Page

HGNC:13060

Description:

Predicted to enable transcription cis-regulatory region binding activity. Predicted to be involved in negative regulation of transcription by RNA polymerase II. Predicted to be active in nucleus.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

HZF2; zinc finger (C2H2); zinc finger protein 2; zinc finger protein HZF2

RGD Orthologs

Alliance Orthologs

More Info

more info ...

Related Pseudogenes:

LOC100419781

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	16	31,873,807 - 31,917,357 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	16	31,873,783 - 31,918,055 (+)	Ensembl		GRCh38.p14 Ensembl	hg38	GRCh38
GRCh37	16	31,885,128 - 31,928,678 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	16	31,792,655 - 31,836,128 (+)	NCBI	Build 36	Build 36	hg18	NCBI36
Build 34	16	31,792,660 - 31,836,127	NCBI
Celera	16	28,380,251 - 28,423,800 (-)	NCBI		Celera
Cytogenetic Map	16	p11.2	NCBI
HuRef	16	29,445,530 - 29,489,069 (+)	NCBI		HuRef
CHM1_1	16	33,203,771 - 33,247,293 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	16	32,261,274 - 32,304,813 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

Arsenic Poisoning (EXP)

hepatocellular carcinoma (IAGP)

melanoma (IAGP)

multiple sclerosis (EXP)

skin disease (EXP)

urinary bladder cancer (IAGP)

uterine corpus endometrial carcinoma (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

1,2-dimethylhydrazine (ISO)

17beta-estradiol (EXP)

2-hydroxypropanoic acid (EXP)

3-isobutyl-1-methyl-7H-xanthine (EXP)

acrylamide (EXP)

aflatoxin B1 (EXP)

aflatoxin M1 (EXP)

all-trans-retinoic acid (EXP)

arsane (EXP,ISO)

arsenic atom (EXP,ISO)

benzo[a]pyrene (EXP)

bisphenol A (ISO)

bisphenol F (EXP)

cadmium dichloride (EXP)

caffeine (EXP)

chromium(6+) (EXP)

copper(II) sulfate (EXP)

cyclosporin A (EXP)

dexamethasone (EXP)

Dibutyl phosphate (EXP)

dicrotophos (EXP)

formaldehyde (EXP)

FR900359 (EXP)

gentamycin (ISO)

GSK-J4 (EXP)

indometacin (EXP)

lipopolysaccharide (ISO)

manganese atom (EXP)

manganese(0) (EXP)

manganese(II) chloride (EXP)

methylseleninic acid (EXP)

nickel atom (EXP)

okadaic acid (EXP)

paracetamol (EXP)

perfluorooctane-1-sulfonic acid (EXP)

phenobarbital (ISO)

rac-lactic acid (EXP)

silicon dioxide (EXP)

silver atom (ISO)

silver(0) (ISO)

sodium arsenite (EXP,ISO)

succimer (ISO)

sunitinib (EXP)

tamibarotene (EXP)

thioacetamide (ISO)

thiram (EXP)

triphenyl phosphate (EXP,ISO)

valproic acid (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

negative regulation of transcription by RNA polymerase II (IBA)

regulation of DNA-templated transcription (IEA)

Cellular Component

cytoplasm (IEA)

nucleus (IBA,IEA)

Molecular Function

transcription cis-regulatory region binding (IBA)

Phenotype Annotations Click to see Annotation Detail View

Human Phenotype

Hepatocellular carcinoma (IAGP)

Melanoma (IAGP)

References

References - curated

#	Reference Title	Reference Citation
1.	GOAs Human GO annotations	GOA_HUMAN data from the GO Consortium
2.	ClinVar Automated Import and Annotation Pipeline	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:7865130	PMID:11121585	PMID:12477932	PMID:14702039	PMID:15489334	PMID:15592455	PMID:15814297	PMID:16054593	PMID:16344560	PMID:17081983	PMID:18029348	PMID:18461144
PMID:19274049	PMID:21840307	PMID:21873635	PMID:21988832	PMID:22076166	PMID:23602568	PMID:28514442	PMID:31391242	PMID:32807901	PMID:33961781	PMID:34732716	PMID:35271311
PMID:35563538	PMID:36138187	PMID:36691044	PMID:37372979

Genomics

Comparative Map Data

ZNF267
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	16	31,873,807 - 31,917,357 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	16	31,873,783 - 31,918,055 (+)	Ensembl		GRCh38.p14 Ensembl	hg38	GRCh38
GRCh37	16	31,885,128 - 31,928,678 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	16	31,792,655 - 31,836,128 (+)	NCBI	Build 36	Build 36	hg18	NCBI36
Build 34	16	31,792,660 - 31,836,127	NCBI
Celera	16	28,380,251 - 28,423,800 (-)	NCBI		Celera
Cytogenetic Map	16	p11.2	NCBI
HuRef	16	29,445,530 - 29,489,069 (+)	NCBI		HuRef
CHM1_1	16	33,203,771 - 33,247,293 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	16	32,261,274 - 32,304,813 (+)	NCBI		T2T-CHM13v2.0

Zfp267
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	3	36,205,233 - 36,224,491 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	3	36,205,166 - 36,224,491 (+)	Ensembl		GRCm39 Ensembl		GRCm39
GRCm38	3	36,151,080 - 36,170,341 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	3	36,151,017 - 36,170,342 (+)	Ensembl		GRCm38.p6 Ensembl	mm10	GRCm38
MGSCv37	3	36,050,002 - 36,069,263 (+)	NCBI	MGSCv37	MGSCv37	mm9	NCBIm37
MGSCv36	3	36,342,566 - 36,361,891 (+)	NCBI		MGSCv36	mm8
Celera	3	36,033,417 - 36,052,679 (+)	NCBI		Celera
Cytogenetic Map	3	B	NCBI
cM Map	3	17.41	NCBI

Zfp267
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	2	120,945,434 - 120,964,039 (+)	NCBI	GRCr8	GRCr8		GRCr8
GRCr8 Ensembl	2	120,945,434 - 120,964,032 (+)	Ensembl				GRCr8
mRatBN7.2	2	119,017,280 - 119,035,885 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	2	119,017,285 - 119,031,900 (+)	Ensembl				mRatBN7.2
Dahl_SR_JrHsd	2	120,203,286 - 120,221,920 (+)	NCBI
Lyon_Normotensive	2	120,268,156 - 120,286,790 (+)	NCBI
Lyon_Hypertensive	2	120,133,031 - 120,151,667 (+)	NCBI
F344_StmMcwi	2	119,959,368 - 119,978,006 (+)	NCBI
Rnor_6.0	2	122,855,036 - 122,873,696 (+)	NCBI	Rnor_6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	2	122,865,100 - 122,869,616 (+)	Ensembl		Rnor_6.0 Ensembl	rn6	Rnor6.0
Rnor_5.0	2	142,480,922 - 142,499,556 (+)	NCBI	Rnor_5.0	Rnor_5.0	rn5
RGSC_v3.4	2	122,650,827 - 122,655,890 (+)	NCBI	RGSC_v3.4	RGSC_v3.4	rn4
Celera	2	113,977,669 - 113,996,320 (+)	NCBI		Celera
Cytogenetic Map	2	q25	NCBI

ZNF267
(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	18	35,204,096 - 35,248,638 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	16	40,124,941 - 40,169,383 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	16	22,924,355 - 22,968,670 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	16	32,336,772 - 32,380,262 (+)	NCBI	PanPan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	16	32,336,675 - 32,380,262 (+)	Ensembl		PanPan1.1 Ensembl	panPan2	panpan1.1

ZNF267
(Chlorocebus sabaeus - green monkey)

Green Monkey Assembly	Chr	Position (strand)	Source	Genome Browsers
Green Monkey Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
mChlSab1.0.hap1	5	28,792,969 - 28,935,893 (+)	NCBI		mChlSab1.0.hap1
Vero_WHO_p1.0	NW_023666068	870,321 - 915,381 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0
ChlSab1.1	5	28,517,588 - 28,561,125 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	5	28,517,720 - 28,561,117 (+)	Ensembl		ChlSab1.1 Ensembl	chlSab2	Vervet-AGM

Variants

Variants in ZNF267
53 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
NM_003414.5(ZNF267):c.1026C>T (p.Ile342=)	single nucleotide variant	Malignant melanoma [RCV000063027]	Chr16:31915275 [GRCh38] Chr16:31926596 [GRCh37] Chr16:31834097 [NCBI36] Chr16:16p11.2	not provided
GRCh38/hg38 16p11.2-11.1(chr16:30691912-36160463)x3	copy number gain	See cases [RCV000133811]	Chr16:16p11.2-11.1	pathogenic
GRCh38/hg38 16p11.2(chr16:31894396-33495702)x1	copy number loss	See cases [RCV000136426]	Chr16:16p11.2	benign
GRCh38/hg38 16p12.2-11.2(chr16:23752047-31943755)x3	copy number gain	Developmental delay AND/OR other significant developmental or morphological phenotypes [RCV000141141]	Chr16:16p12.2-11.2	pathogenic
GRCh37/hg19 16p11.2(chr16:31154186-31926800)x3	copy number gain	Breast ductal adenocarcinoma [RCV000207245]	Chr16:31154186..31926800 [GRCh37] Chr16:16p11.2	uncertain significance
GRCh37/hg19 16p13.3-11.2(chr16:1279324-31926800)x3	copy number gain	Breast ductal adenocarcinoma [RCV000207053]	Chr16:1279324..31926800 [GRCh37] Chr16:16p13.3-11.2	uncertain significance
GRCh37/hg19 16p13.3-q24.3(chr16:69193-90274381)x3	copy number gain	Developmental delay AND/OR other significant developmental or morphological phenotypes [RCV000446684]	Chr16:16p13.3-q24.3	pathogenic
maternal UPD(16p)	complex	Hemimegalencephaly [RCV000494707]	Chr16:1280042..33710558 [GRCh37] Chr16:16p13.3-11.2	pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062)	copy number gain	Polydactyly [RCV000511296]	Chr16:16p13.3-q24.3	pathogenic
NM_003414.6(ZNF267):c.1138T>A (p.Tyr380Asn)	single nucleotide variant	not specified [RCV004300477]	Chr16:31915387 [GRCh38] Chr16:31926708 [GRCh37] Chr16:16p11.2	uncertain significance
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062)x3	copy number gain	Ventricular septal defect [RCV000512138]	Chr16:16p13.3-q24.3	pathogenic
NM_003414.6(ZNF267):c.1457A>G (p.His486Arg)	single nucleotide variant	not specified [RCV004314778]	Chr16:31915706 [GRCh38] Chr16:31927027 [GRCh37] Chr16:16p11.2	uncertain significance
GRCh37/hg19 16p11.2(chr16:28826162-29043901)x1	copy number loss	See cases [RCV000448084]	Chr16:16p11.2	likely pathogenic
GRCh37/hg19 16p13.2-q24.3(chr16:9273328-89548493)x3	copy number gain	See cases [RCV000511622]	Chr16:16p13.2-q24.3	uncertain significance
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90274695)x3	copy number gain	not provided [RCV000738918]	Chr16:88165..90274695 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:61451-90294632)x3	copy number gain	not provided [RCV000738915]	Chr16:61451..90294632 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16p11.2(chr16:30738551-34194635)x3	copy number gain	not provided [RCV000739123]	Chr16:30738551..34194635 [GRCh37] Chr16:16p11.2	benign
NM_003414.6(ZNF267):c.347G>C (p.Arg116Thr)	single nucleotide variant	not specified [RCV004317760]	Chr16:31914596 [GRCh38] Chr16:31925917 [GRCh37] Chr16:16p11.2	uncertain significance
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90163275)x3	copy number gain	not provided [RCV000738917]	Chr16:88165..90163275 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
NM_003414.6(ZNF267):c.1186A>G (p.Ile396Val)	single nucleotide variant	not specified [RCV004293240]	Chr16:31915435 [GRCh38] Chr16:31926756 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.2182A>G (p.Arg728Gly)	single nucleotide variant	not specified [RCV004300962]	Chr16:31916431 [GRCh38] Chr16:31927752 [GRCh37] Chr16:16p11.2	uncertain significance
GRCh37/hg19 16p13.3-11.2(chr16:5805001-34230001)	copy number gain	Microcephaly [RCV001252948]	Chr16:16p13.3-11.2	pathogenic
NM_003414.6(ZNF267):c.1591T>C (p.Cys531Arg)	single nucleotide variant	not specified [RCV005523580]	Chr16:31915840 [GRCh38] Chr16:31927161 [GRCh37] Chr16:16p11.2	uncertain significance
GRCh37/hg19 16p11.2(chr16:30350747-31905898)x3	copy number gain	not provided [RCV001258619]	Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.168G>T (p.Leu56Phe)	single nucleotide variant	Hepatocellular carcinoma [RCV006103858]	Chr16:31885198 [GRCh38] Chr16:31896519 [GRCh37] Chr16:16p11.2	evidence_only
NM_003414.6(ZNF267):c.244A>G (p.Asn82Asp)	single nucleotide variant	not specified [RCV006674053]	Chr16:31914493 [GRCh38] Chr16:31925814 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.131-9A>G	single nucleotide variant	Hepatocellular carcinoma [RCV006103856]	Chr16:31885152 [GRCh38] Chr16:31896473 [GRCh37] Chr16:16p11.2	evidence_only
NM_003414.6(ZNF267):c.1868G>A (p.Arg623Gln)	single nucleotide variant	Malignant tumor of urinary bladder [RCV006103862]	Chr16:31916117 [GRCh38] Chr16:31927438 [GRCh37] Chr16:16p11.2	evidence_only
NM_003414.6(ZNF267):c.524T>A (p.Leu175His)	single nucleotide variant	not specified [RCV004147752]	Chr16:31914773 [GRCh38] Chr16:31926094 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1382A>G (p.Glu461Gly)	single nucleotide variant	not specified [RCV004234348]	Chr16:31915631 [GRCh38] Chr16:31926952 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.998A>G (p.His333Arg)	single nucleotide variant	not specified [RCV004080618]	Chr16:31915247 [GRCh38] Chr16:31926568 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1676A>G (p.Tyr559Cys)	single nucleotide variant	not specified [RCV004174241]	Chr16:31915925 [GRCh38] Chr16:31927246 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.761T>A (p.Leu254His)	single nucleotide variant	not specified [RCV004186668]	Chr16:31915010 [GRCh38] Chr16:31926331 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1124C>A (p.Thr375Asn)	single nucleotide variant	not specified [RCV004206992]	Chr16:31915373 [GRCh38] Chr16:31926694 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.140T>G (p.Val47Gly)	single nucleotide variant	not specified [RCV004112541]	Chr16:31885170 [GRCh38] Chr16:31896491 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.941T>C (p.Ile314Thr)	single nucleotide variant	not specified [RCV004125566]	Chr16:31915190 [GRCh38] Chr16:31926511 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.502G>A (p.Val168Ile)	single nucleotide variant	not specified [RCV004157260]	Chr16:31914751 [GRCh38] Chr16:31926072 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1867C>T (p.Arg623Trp)	single nucleotide variant	not specified [RCV004204268]	Chr16:31916116 [GRCh38] Chr16:31927437 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.2154T>G (p.Cys718Trp)	single nucleotide variant	not specified [RCV004108443]	Chr16:31916403 [GRCh38] Chr16:31927724 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.2035C>T (p.Arg679Trp)	single nucleotide variant	not specified [RCV004081971]	Chr16:31916284 [GRCh38] Chr16:31927605 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1423C>T (p.Arg475Cys)	single nucleotide variant	not specified [RCV004226222]	Chr16:31915672 [GRCh38] Chr16:31926993 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.763C>G (p.Gln255Glu)	single nucleotide variant	not specified [RCV004180512]	Chr16:31915012 [GRCh38] Chr16:31926333 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.2195T>C (p.Ile732Thr)	single nucleotide variant	not specified [RCV005523576]	Chr16:31916444 [GRCh38] Chr16:31927765 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.204G>C (p.Glu68Asp)	single nucleotide variant	not specified [RCV004274765]	Chr16:31885234 [GRCh38] Chr16:31896555 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1661G>A (p.Gly554Asp)	single nucleotide variant	not specified [RCV005523578]	Chr16:31915910 [GRCh38] Chr16:31927231 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.4-166C>T	single nucleotide variant	Uterine corpus endometrial carcinoma [RCV006103854]	Chr16:31884332 [GRCh38] Chr16:31895653 [GRCh37] Chr16:16p11.2	evidence_only
NM_003414.6(ZNF267):c.1508G>A (p.Arg503His)	single nucleotide variant	not specified [RCV006350025]	Chr16:31915757 [GRCh38] Chr16:31927078 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1507C>T (p.Arg503Cys)	single nucleotide variant	not specified [RCV005523582]	Chr16:31915756 [GRCh38] Chr16:31927077 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1197G>T (p.Gln399His)	single nucleotide variant	Melanoma [RCV006103861]	Chr16:31915446 [GRCh38] Chr16:31926767 [GRCh37] Chr16:16p11.2	evidence_only
NM_003414.6(ZNF267):c.1898A>T (p.Lys633Ile)	single nucleotide variant	not specified [RCV005523577]	Chr16:31916147 [GRCh38] Chr16:31927468 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.149C>T (p.Pro50Leu)	single nucleotide variant	not specified [RCV004366110]	Chr16:31885179 [GRCh38] Chr16:31896500 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.770T>C (p.Met257Thr)	single nucleotide variant	not specified [RCV004338270]	Chr16:31915019 [GRCh38] Chr16:31926340 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.264G>C (p.Glu88Asp)	single nucleotide variant	not specified [RCV004363985]	Chr16:31914513 [GRCh38] Chr16:31925834 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.852A>G (p.Gln284=)	single nucleotide variant	not provided [RCV003426686]	Chr16:31915101 [GRCh38] Chr16:31926422 [GRCh37] Chr16:16p11.2	likely benign
NM_003414.6(ZNF267):c.1376C>T (p.Thr459Ile)	single nucleotide variant	not specified [RCV004494122]	Chr16:31915625 [GRCh38] Chr16:31926946 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.23A>C (p.Asp8Ala)	single nucleotide variant	not specified [RCV004494123]	Chr16:31884517 [GRCh38] Chr16:31895838 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.402T>A (p.Phe134Leu)	single nucleotide variant	not specified [RCV004494124]	Chr16:31914651 [GRCh38] Chr16:31925972 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.646T>C (p.Tyr216His)	single nucleotide variant	not specified [RCV004494126]	Chr16:31914895 [GRCh38] Chr16:31926216 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.656A>G (p.Asn219Ser)	single nucleotide variant	not specified [RCV004494127]	Chr16:31914905 [GRCh38] Chr16:31926226 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.659A>C (p.Asn220Thr)	single nucleotide variant	not specified [RCV004494128]	Chr16:31914908 [GRCh38] Chr16:31926229 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.689G>A (p.Ser230Asn)	single nucleotide variant	not specified [RCV004494130]	Chr16:31914938 [GRCh38] Chr16:31926259 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.679C>G (p.Gln227Glu)	single nucleotide variant	not specified [RCV004494129]	Chr16:31914928 [GRCh38] Chr16:31926249 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.209C>T (p.Thr70Ile)	single nucleotide variant	not specified [RCV004688312]	Chr16:31885239 [GRCh38] Chr16:31896560 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1277A>G (p.His426Arg)	single nucleotide variant	not specified [RCV004891163]	Chr16:31915526 [GRCh38] Chr16:31926847 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1339C>T (p.Arg447Cys)	single nucleotide variant	not specified [RCV004891164]	Chr16:31915588 [GRCh38] Chr16:31926909 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1247C>T (p.Ala416Val)	single nucleotide variant	not specified [RCV004891165]	Chr16:31915496 [GRCh38] Chr16:31926817 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1121A>C (p.Asp374Ala)	single nucleotide variant	not specified [RCV004891167]	Chr16:31915370 [GRCh38] Chr16:31926691 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.2210G>A (p.Ser737Asn)	single nucleotide variant	not specified [RCV004891168]	Chr16:31916459 [GRCh38] Chr16:31927780 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.548T>C (p.Ile183Thr)	single nucleotide variant	not specified [RCV004891169]	Chr16:31914797 [GRCh38] Chr16:31926118 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1498G>A (p.Val500Ile)	single nucleotide variant	not specified [RCV004891170]	Chr16:31915747 [GRCh38] Chr16:31927068 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1406G>A (p.Cys469Tyr)	single nucleotide variant	not specified [RCV004891171]	Chr16:31915655 [GRCh38] Chr16:31926976 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.2096A>G (p.Tyr699Cys)	single nucleotide variant	not specified [RCV005523579]	Chr16:31916345 [GRCh38] Chr16:31927666 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1259G>A (p.Ser420Asn)	single nucleotide variant	not specified [RCV005523581]	Chr16:31915508 [GRCh38] Chr16:31926829 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1336A>G (p.Asn446Asp)	single nucleotide variant	not specified [RCV005787512]	Chr16:31915585 [GRCh38] Chr16:31926906 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1708C>G (p.His570Asp)	single nucleotide variant	not specified [RCV005779235]	Chr16:31915957 [GRCh38] Chr16:31927278 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1925A>G (p.Asn642Ser)	single nucleotide variant	not specified [RCV005787514]	Chr16:31916174 [GRCh38] Chr16:31927495 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1187T>C (p.Ile396Thr)	single nucleotide variant	not specified [RCV005787515]	Chr16:31915436 [GRCh38] Chr16:31926757 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.297A>G (p.Ile99Met)	single nucleotide variant	not specified [RCV005787521]	Chr16:31914546 [GRCh38] Chr16:31925867 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.919T>C (p.Ser307Pro)	single nucleotide variant	not specified [RCV005787511]	Chr16:31915168 [GRCh38] Chr16:31926489 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.2036G>A (p.Arg679Gln)	single nucleotide variant	not specified [RCV005779236]	Chr16:31916285 [GRCh38] Chr16:31927606 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1754T>C (p.Phe585Ser)	single nucleotide variant	not specified [RCV005787516]	Chr16:31916003 [GRCh38] Chr16:31927324 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1099C>T (p.Leu367Phe)	single nucleotide variant	not specified [RCV005787518]	Chr16:31915348 [GRCh38] Chr16:31926669 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1565G>A (p.Cys522Tyr)	single nucleotide variant	not specified [RCV005779239]	Chr16:31915814 [GRCh38] Chr16:31927135 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1121A>G (p.Asp374Gly)	single nucleotide variant	not specified [RCV004215130]	Chr16:31915370 [GRCh38] Chr16:31926691 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.2141G>C (p.Arg714Thr)	single nucleotide variant	not specified [RCV004120404]	Chr16:31916390 [GRCh38] Chr16:31927711 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1036G>A (p.Glu346Lys)	single nucleotide variant	not specified [RCV004207393]	Chr16:31915285 [GRCh38] Chr16:31926606 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1033A>G (p.Thr345Ala)	single nucleotide variant	not specified [RCV004168109]	Chr16:31915282 [GRCh38] Chr16:31926603 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1723C>A (p.Pro575Thr)	single nucleotide variant	not specified [RCV004209147]	Chr16:31915972 [GRCh38] Chr16:31927293 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.856C>G (p.Gln286Glu)	single nucleotide variant	not specified [RCV006350024]	Chr16:31915105 [GRCh38] Chr16:31926426 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1199G>A (p.Arg400Lys)	single nucleotide variant	not specified [RCV006350026]	Chr16:31915448 [GRCh38] Chr16:31926769 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.868A>G (p.Ile290Val)	single nucleotide variant	not specified [RCV006669258]	Chr16:31915117 [GRCh38] Chr16:31926438 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.535G>A (p.Glu179Lys)	single nucleotide variant	not specified [RCV006350021]	Chr16:31914784 [GRCh38] Chr16:31926105 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1118T>C (p.Ile373Thr)	single nucleotide variant	not specified [RCV006350022]	Chr16:31915367 [GRCh38] Chr16:31926688 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1340G>A (p.Arg447His)	single nucleotide variant	not specified [RCV006350023]	Chr16:31915589 [GRCh38] Chr16:31926910 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.130+1G>A	single nucleotide variant	Malignant tumor of urinary bladder [RCV006103855]	Chr16:31884625 [GRCh38] Chr16:31895946 [GRCh37] Chr16:16p11.2	evidence_only
NM_003414.6(ZNF267):c.1968A>C (p.Gly656=)	single nucleotide variant	not provided [RCV004810319]	Chr16:31916217 [GRCh38] Chr16:31927538 [GRCh37] Chr16:16p11.2	likely benign
NM_003414.6(ZNF267):c.31G>A (p.Val11Ile)	single nucleotide variant	not specified [RCV005302927]	Chr16:31884525 [GRCh38] Chr16:31895846 [GRCh37] Chr16:16p11.2	likely benign
NM_003414.6(ZNF267):c.136G>C (p.Val46Leu)	single nucleotide variant	not specified [RCV005302928]	Chr16:31885166 [GRCh38] Chr16:31896487 [GRCh37] Chr16:16p11.2	likely benign
NM_003414.6(ZNF267):c.1953G>C (p.Gln651His)	single nucleotide variant	not specified [RCV005302929]	Chr16:31916202 [GRCh38] Chr16:31927523 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1576G>A (p.Ala526Thr)	single nucleotide variant	not specified [RCV005302930]	Chr16:31915825 [GRCh38] Chr16:31927146 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1252C>T (p.Arg418Cys)	single nucleotide variant	not specified [RCV005302931]	Chr16:31915501 [GRCh38] Chr16:31926822 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1160A>G (p.Lys387Arg)	single nucleotide variant	not specified [RCV005779238]	Chr16:31915409 [GRCh38] Chr16:31926730 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1859T>C (p.Ile620Thr)	single nucleotide variant	not specified [RCV005787517]	Chr16:31916108 [GRCh38] Chr16:31927429 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.90G>C (p.Gln30His)	single nucleotide variant	not specified [RCV005787522]	Chr16:31884584 [GRCh38] Chr16:31895905 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1135C>G (p.Leu379Val)	single nucleotide variant	not specified [RCV005787513]	Chr16:31915384 [GRCh38] Chr16:31926705 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.360G>C (p.Glu120Asp)	single nucleotide variant	not specified [RCV005787520]	Chr16:31914609 [GRCh38] Chr16:31925930 [GRCh37] Chr16:16p11.2	uncertain significance
NM_003414.6(ZNF267):c.1435C>T (p.Leu479Phe)	single nucleotide variant	not specified [RCV005787523]	Chr16:31915684 [GRCh38] Chr16:31927005 [GRCh37] Chr16:16p11.2	uncertain significance

miRNA Target Status (No longer updated)

Predicted Target Of

	Summary Value
Count of predictions:	834
Count of miRNA genes:	464
Interacting mature miRNAs:	494
Transcripts:	ENST00000300870, ENST00000394846, ENST00000561814, ENST00000562971, ENST00000566541, ENST00000575471
Prediction methods:	Microtar, Miranda, Rnahybrid
Result types:	miRGate_prediction

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

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

QTLs in Region (GRCh38)

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
628749420	GWAS2657649_H	acylcarnitine measurement QTL GWAS2657649 (human)		0.000004	blood protein amount (VT:0005416)		16	31885987	31885988	Human

Markers in Region

RH70917

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	16	31,927,821 - 31,927,950	UniSTS	GRCh37
Build 36	16	31,835,322 - 31,835,451	RGD	NCBI36
Celera	16	28,380,928 - 28,381,057	RGD
Cytogenetic Map	16	p11.2	UniSTS
HuRef	16	29,488,261 - 29,488,390	UniSTS

RH104437

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	16	31,927,838 - 31,928,020	UniSTS	GRCh37
Build 36	16	31,835,339 - 31,835,521	RGD	NCBI36
Celera	16	28,380,858 - 28,381,040	RGD
Cytogenetic Map	16	p11.2	UniSTS
HuRef	16	29,488,278 - 29,488,460	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	4973	1726	2351	6	624	1951	465	2269	7306	6472	53	3734	1	852	1744	1617	174	1

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001265588	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_003414	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_049749	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AA570774	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC034105	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF220492	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AI636367	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK096390	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK292573	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL832123	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC036367	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC127088	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC127089	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471192	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068262	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA657367	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB091947	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB484386	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KF456187	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	X78925	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000300870 ⟹ ENSP00000300870

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	31,873,807 - 31,917,357 (+)	Ensembl

Ensembl Acc Id:

ENST00000394846 ⟹ ENSP00000461286

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	31,873,788 - 31,914,725 (+)	Ensembl

Ensembl Acc Id:

ENST00000561814 ⟹ ENSP00000454369

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	31,873,833 - 31,914,527 (+)	Ensembl

Ensembl Acc Id:

ENST00000562971 ⟹ ENSP00000455493

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	31,874,066 - 31,914,620 (+)	Ensembl

Ensembl Acc Id:

ENST00000566541 ⟹ ENSP00000454753

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	31,873,831 - 31,914,558 (+)	Ensembl

Ensembl Acc Id:

ENST00000575471

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	31,911,854 - 31,916,852 (+)	Ensembl

Ensembl Acc Id:

ENST00000854651 ⟹ ENSP00000524710

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	31,873,788 - 31,918,055 (+)	Ensembl

Ensembl Acc Id:

ENST00000996528 ⟹ ENSP00000666345

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	31,873,788 - 31,917,304 (+)	Ensembl

Ensembl Acc Id:

ENST00001061766 ⟹ ENSP00000731572

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	31,873,783 - 31,917,307 (+)	Ensembl

Ensembl Acc Id:

ENST00001119649 ⟹ ENSP00000789454

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	31,873,788 - 31,897,134 (+)	Ensembl

Ensembl Acc Id:

ENST00001132469 ⟹ ENSP00000805439

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	31,873,788 - 31,918,055 (+)	Ensembl

RefSeq Acc Id:

NM_001265588 ⟹ NP_001252517

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	31,873,807 - 31,917,357 (+)	NCBI
GRCh37	16	31,885,079 - 31,928,629 (+)	NCBI
HuRef	16	29,445,530 - 29,489,069 (+)	NCBI
CHM1_1	16	33,203,771 - 33,247,293 (+)	NCBI
T2T-CHM13v2.0	16	32,261,274 - 32,304,813 (+)	NCBI

Sequence:

show sequence

AGTTAGAGCTCGGGTCTCCTCGCCACAGCTCCGAGTCTTTCGTTCTGGGAGGCCCAGGCGGCTT
CGCGTTCTGAGAATAAACAGAACCTCTGTTGCTCTGCGACTTGCAGGCACTGGGAGATTCGTAG
CTAAGACGCCAGGGCATCCCGGAAGCTGGGAAATGGGCCCTGTATAGCCACCCTCTATCCAGTC
TTTTCCTGTTCCTGAATTTCAGAACTGTCTGGGATGACTCAAGATGCCCACAGTGGCCATGTCT
CCTGGAGTGTTTAGTGACTGTCAGCCCCAGGTCACCTCCTGTTAGAGGACCGCCCAAGGGACTG
TTGACATTCAGGGATGTGGCCGTAGAATTCTCTTTGGAGGAGTGGGAACACCTGGAACCAGCTC
AGAAGAATTTGTATCAGGATGTGATGTTAGAAAACTACAGAAACCTGGTCTCTCTGGGTCTTGT
TGTCTCTAAGCCGGACCTGATCACCTTTTTGGAACAAAGGAAAGAGCCTTGGAATGTGAAGAGT
GAGGAGACAGTAGCCATCCAGCCAGATGTGTTTTCGCATTATAACAAGGACCTGTTGACAGAGC
ACTGCACAGAAGCTTCATTCCAAAAAGTGATATCGAGGAGACATGGGAGCTGTGATCTTGAGAA
TTTACATTTAAGAAAAAGGTGGAAAAGGGAGGAGTGTGAAGGGCACAATGGATGTTATGATGAA
AAGACTTTTAAATATGATCAATTTGATGAATCCTCTGTTGAAAGTTTGTTTCACCAGCAAATAC
TTTCTTCTTGTGCCAAAAGCTATAACTTTGATCAATATAGGAAGGTCTTTACTCATTCATCATT
GCTTAATCAACAAGAGGAAATAGATATTTGGGGAAAACATCACATATATGATAAAACTTCAGTG
TTATTTAGGCAGGTCTCTACTCTAAATAGTTACCGAAATGTTTTTATTGGAGAGAAAAATTATC
ATTGCAATAATTCTGAAAAAACCTTGAACCAAAGCTCAAGCCCTAAAAATCATCAGGAAAATTA
TTTTCTAGAAAAACAATACAAATGTAAAGAATTTGAGGAAGTCTTTCTTCAGAGTATGCATGGG
CAAGAGAAACAAGAACAGTCTTACAAATGTAATAAATGTGTAGAAGTTTGTACCCAGTCATTAA
AACATATTCAACATCAGACCATCCATATCAGAGAAAACTCATATAGCTATAACAAATATGATAA
AGATCTTAGTCAGTCATCAAATCTTAGAAAGCAGATAATCCATAATGAAGAGAAACCATACAAA
TGTGAAAAATGTGGGGATAGCTTAAACCATAGTTTGCACCTTACTCAACATCAGATCATTCCTA
CCGAAGAGAAACCCTGTAAATGGAAAGAATGTGGCAAGGTCTTTAACCTTAACTGTAGTTTATA
CCTTACTAAACAGCAGCAAATTGATACTGGAGAAAACCTTTACAAATGTAAAGCATGTAGCAAA
TCTTTTACTCGTTCCTCCAATCTTATTGTGCATCAGAGAATTCACACTGGAGAGAAACCATACA
AATGTAAAGAATGTGGCAAAGCCTTTCGCTGTAGTTCATACCTTACTAAACATAAGCGAATTCA
TACTGGAGAGAAACCTTATAAATGTAAAGAATGTGGAAAAGCTTTTAACCGTAGTTCATGCCTT
ACTCAACATCAGACAACTCATACAGGAGAAAAACTTTACAAATGTAAAGTATGTAGCAAATCTT
ATGCTCGTTCTTCAAATCTTATTATGCATCAGAGAGTTCATACTGGAGAGAAGCCTTATAAATG
TAAAGAATGTGGCAAAGTCTTTAGCCGTAGTTCTTGCCTTACTCAACATCGGAAAATTCATACT
GGAGAAAATCTTTACAAATGCAAAGTATGTGCTAAACCTTTTACTTGTTTCTCAAATCTTATTG
TGCATGAGAGAATTCATACTGGAGAGAAACCCTATAAATGTAAAGAATGTGGCAAAGCCTTTCC
TTATAGTTCACACCTTATTCGACATCATCGAATTCATACTGGAGAAAAACCATACAAATGTAAA
GCATGTAGCAAATCTTTTAGTGACTCCTCAGGTCTTACTGTGCATCGGCGAACTCATACTGGAG
AGAAACCCTATACATGTAAAGAATGTGGCAAAGCCTTTAGTTATAGTTCAGATGTTATTCAGCA
TCGGAGAATTCATACTGGCCAGAGACCCTACAAATGTGAAGAATGTGGCAAAGCCTTCAACTAT
AGGTCATACCTCACTACACATCAGAGAAGTCATACTGGAGAGAGACCCTACAAATGTGAAGAAT
GTGGCAAAGCCTTCAACTCTAGGTCATACCTCACTACACATCGGAGAAGACATACTGGAGAGAG
ACCCTACAAATGTGATGAATGTGGTAAAGCCTTCAGCTATAGGTCATACCTCACTACACATCGG
AGAAGTCATAGTGGAGAGAGACCCTACAAATGTGAAGAATGTGGCAAAGCCTTTAACTCTAGGT
CATACCTCATTGCACATCAGAGAAGTCATACTAGAGAAAAACTTTAAAAATGTAAAACATGGAG
CAGATTTTTTACTTGTTACCCATGTCTTATTGTGCATCAGATAATTTATATGGGAGTGAAACCC
TACAAATGTTAAGAATGTGGCATAACCTTTAACTATTTTCAAGCCTTACACAATAGCAGAGAAT
ATAAACTGAAAAAATCCATACAAATATTAAAAATGTGGCAAATTATTTTAAACTGTGCTCAACC
CTTACTCAAGATAATCCATACTAGAGAAACACTATAGATGTAAAAATGTGAAAAGTTTTATTCA
AAATATCAAACTTATGAGTCACCTAGGGGTTCATAGAAAAAGGAAGTTTGCAGATGCAATAAAT
GTGAGGAAGTATTTAATAAAAAATGAAGTCTAAATGTGTCAGAGAATTTATGTGAGAAAGGACT
AAAGCACAGACACTTTCAGCCTTTATACTAAATAAGAGTATTTTTTGTACAGAATAATCTAAAG
GCAAAATAATTAGATAATTTATTTGCTTATATGTTTTAAAGTAGCAAGAACATTGATGTTTTGA
CAGGTATATTTCATAGATACTTCATTTGTATTTACAGTATTTGAGGTTTTTGGAAAGCAAATAT
TATTTATATAATTCAGCTTTCAAATCTGTTGCTGCTTTTCCTTAATCCGTGGTGTTCATGTGAA
AATATGTGTTCTGTTTTTTTTTCTGCATCAGAACAATGTGAGGTCATTCTACGTTAATATCATT
AATATCAGCATTTTTCATGGAAGTTTAATGCCAAATGTAAAACACATGAAAATTTTTAAAAATA
TGCTCTTTGTGTTTGAATAAAGTAGTAATGCATGTAAACATATACGTGTTTAGAGCTCTTTTCT
ATATTAAAGTAAGAGGGATATTCTGAA

hide sequence

RefSeq Acc Id:

NM_003414 ⟹ NP_003405

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	31,873,807 - 31,917,357 (+)	NCBI
GRCh37	16	31,885,079 - 31,928,629 (+)	NCBI
Build 36	16	31,792,655 - 31,836,128 (+)	NCBI Archive
Celera	16	28,380,251 - 28,423,800 (-)	RGD
HuRef	16	29,445,530 - 29,489,069 (+)	NCBI
CHM1_1	16	33,203,771 - 33,247,293 (+)	NCBI
T2T-CHM13v2.0	16	32,261,274 - 32,304,813 (+)	NCBI

Sequence:

show sequence

AGTTAGAGCTCGGGTCTCCTCGCCACAGCTCCGAGTCTTTCGTTCTGGGAGGCCCAGGCGGCTT
CGCGTTCTGAGAATAAACAGAACCTCTGTTGCTCTGCGACTTGCAGGCACTGGGAGATTCGTAG
CTAAGACGCCAGGGCATCCCGGAAGCTGGGAAATGGGACTGTTGACATTCAGGGATGTGGCCGT
AGAATTCTCTTTGGAGGAGTGGGAACACCTGGAACCAGCTCAGAAGAATTTGTATCAGGATGTG
ATGTTAGAAAACTACAGAAACCTGGTCTCTCTGGGTCTTGTTGTCTCTAAGCCGGACCTGATCA
CCTTTTTGGAACAAAGGAAAGAGCCTTGGAATGTGAAGAGTGAGGAGACAGTAGCCATCCAGCC
AGATGTGTTTTCGCATTATAACAAGGACCTGTTGACAGAGCACTGCACAGAAGCTTCATTCCAA
AAAGTGATATCGAGGAGACATGGGAGCTGTGATCTTGAGAATTTACATTTAAGAAAAAGGTGGA
AAAGGGAGGAGTGTGAAGGGCACAATGGATGTTATGATGAAAAGACTTTTAAATATGATCAATT
TGATGAATCCTCTGTTGAAAGTTTGTTTCACCAGCAAATACTTTCTTCTTGTGCCAAAAGCTAT
AACTTTGATCAATATAGGAAGGTCTTTACTCATTCATCATTGCTTAATCAACAAGAGGAAATAG
ATATTTGGGGAAAACATCACATATATGATAAAACTTCAGTGTTATTTAGGCAGGTCTCTACTCT
AAATAGTTACCGAAATGTTTTTATTGGAGAGAAAAATTATCATTGCAATAATTCTGAAAAAACC
TTGAACCAAAGCTCAAGCCCTAAAAATCATCAGGAAAATTATTTTCTAGAAAAACAATACAAAT
GTAAAGAATTTGAGGAAGTCTTTCTTCAGAGTATGCATGGGCAAGAGAAACAAGAACAGTCTTA
CAAATGTAATAAATGTGTAGAAGTTTGTACCCAGTCATTAAAACATATTCAACATCAGACCATC
CATATCAGAGAAAACTCATATAGCTATAACAAATATGATAAAGATCTTAGTCAGTCATCAAATC
TTAGAAAGCAGATAATCCATAATGAAGAGAAACCATACAAATGTGAAAAATGTGGGGATAGCTT
AAACCATAGTTTGCACCTTACTCAACATCAGATCATTCCTACCGAAGAGAAACCCTGTAAATGG
AAAGAATGTGGCAAGGTCTTTAACCTTAACTGTAGTTTATACCTTACTAAACAGCAGCAAATTG
ATACTGGAGAAAACCTTTACAAATGTAAAGCATGTAGCAAATCTTTTACTCGTTCCTCCAATCT
TATTGTGCATCAGAGAATTCACACTGGAGAGAAACCATACAAATGTAAAGAATGTGGCAAAGCC
TTTCGCTGTAGTTCATACCTTACTAAACATAAGCGAATTCATACTGGAGAGAAACCTTATAAAT
GTAAAGAATGTGGAAAAGCTTTTAACCGTAGTTCATGCCTTACTCAACATCAGACAACTCATAC
AGGAGAAAAACTTTACAAATGTAAAGTATGTAGCAAATCTTATGCTCGTTCTTCAAATCTTATT
ATGCATCAGAGAGTTCATACTGGAGAGAAGCCTTATAAATGTAAAGAATGTGGCAAAGTCTTTA
GCCGTAGTTCTTGCCTTACTCAACATCGGAAAATTCATACTGGAGAAAATCTTTACAAATGCAA
AGTATGTGCTAAACCTTTTACTTGTTTCTCAAATCTTATTGTGCATGAGAGAATTCATACTGGA
GAGAAACCCTATAAATGTAAAGAATGTGGCAAAGCCTTTCCTTATAGTTCACACCTTATTCGAC
ATCATCGAATTCATACTGGAGAAAAACCATACAAATGTAAAGCATGTAGCAAATCTTTTAGTGA
CTCCTCAGGTCTTACTGTGCATCGGCGAACTCATACTGGAGAGAAACCCTATACATGTAAAGAA
TGTGGCAAAGCCTTTAGTTATAGTTCAGATGTTATTCAGCATCGGAGAATTCATACTGGCCAGA
GACCCTACAAATGTGAAGAATGTGGCAAAGCCTTCAACTATAGGTCATACCTCACTACACATCA
GAGAAGTCATACTGGAGAGAGACCCTACAAATGTGAAGAATGTGGCAAAGCCTTCAACTCTAGG
TCATACCTCACTACACATCGGAGAAGACATACTGGAGAGAGACCCTACAAATGTGATGAATGTG
GTAAAGCCTTCAGCTATAGGTCATACCTCACTACACATCGGAGAAGTCATAGTGGAGAGAGACC
CTACAAATGTGAAGAATGTGGCAAAGCCTTTAACTCTAGGTCATACCTCATTGCACATCAGAGA
AGTCATACTAGAGAAAAACTTTAAAAATGTAAAACATGGAGCAGATTTTTTACTTGTTACCCAT
GTCTTATTGTGCATCAGATAATTTATATGGGAGTGAAACCCTACAAATGTTAAGAATGTGGCAT
AACCTTTAACTATTTTCAAGCCTTACACAATAGCAGAGAATATAAACTGAAAAAATCCATACAA
ATATTAAAAATGTGGCAAATTATTTTAAACTGTGCTCAACCCTTACTCAAGATAATCCATACTA
GAGAAACACTATAGATGTAAAAATGTGAAAAGTTTTATTCAAAATATCAAACTTATGAGTCACC
TAGGGGTTCATAGAAAAAGGAAGTTTGCAGATGCAATAAATGTGAGGAAGTATTTAATAAAAAA
TGAAGTCTAAATGTGTCAGAGAATTTATGTGAGAAAGGACTAAAGCACAGACACTTTCAGCCTT
TATACTAAATAAGAGTATTTTTTGTACAGAATAATCTAAAGGCAAAATAATTAGATAATTTATT
TGCTTATATGTTTTAAAGTAGCAAGAACATTGATGTTTTGACAGGTATATTTCATAGATACTTC
ATTTGTATTTACAGTATTTGAGGTTTTTGGAAAGCAAATATTATTTATATAATTCAGCTTTCAA
ATCTGTTGCTGCTTTTCCTTAATCCGTGGTGTTCATGTGAAAATATGTGTTCTGTTTTTTTTTC
TGCATCAGAACAATGTGAGGTCATTCTACGTTAATATCATTAATATCAGCATTTTTCATGGAAG
TTTAATGCCAAATGTAAAACACATGAAAATTTTTAAAAATATGCTCTTTGTGTTTGAATAAAGT
AGTAATGCATGTAAACATATACGTGTTTAGAGCTCTTTTCTATATTAAAGTAAGAGGGATATTC
TGAA

hide sequence

RefSeq Acc Id:

NR_049749

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	31,873,807 - 31,917,357 (+)	NCBI
GRCh37	16	31,885,079 - 31,928,629 (+)	NCBI
HuRef	16	29,445,530 - 29,489,069 (+)	NCBI
CHM1_1	16	33,203,771 - 33,247,293 (+)	NCBI
T2T-CHM13v2.0	16	32,261,274 - 32,304,813 (+)	NCBI

Sequence:

show sequence

AGTTAGAGCTCGGGTCTCCTCGCCACAGCTCCGAGTCTTTCGTTCTGGGAGGCCCAGGCGGCTT
CGCGTTCTGAGAATAAACAGAACCTCTGTTGCTCTGCGACTTGCAGGCACTGGGAGATTCGTAG
CTAAGACGCCAGGGCATCCCGGAAGCTGGGAAATGGGACTGTTGACATTCAGGGATGTGGCCGT
AGAATTCTCTTTGGAGGAGTGGGAACACCTGGAACCAGCTCAGAAGAATTTGTATCAGGATGTG
ATGTTAGAAAACTACAGAAACCTGGTCTCTCTGGGTCTTGTTGTCTCTAAGCCGGACCTGATCA
CCTTTTTGGAACAAAGGAAAGAGCCTTGGAATGTGAAGAGTGAGGAGACAGTAGCCATCCAGCC
AGGACATTGAAGTTCCCTGTTATTGCATTTCGTTTTCTCACCACAGATGTGTTTTCGCATTATA
ACAAGGACCTGTTGACAGAGCACTGCACAGAAGCTTCATTCCAAAAAGTGATATCGAGGAGACA
TGGGAGCTGTGATCTTGAGAATTTACATTTAAGAAAAAGGTGGAAAAGGGAGGAGTGTGAAGGG
CACAATGGATGTTATGATGAAAAGACTTTTAAATATGATCAATTTGATGAATCCTCTGTTGAAA
GTTTGTTTCACCAGCAAATACTTTCTTCTTGTGCCAAAAGCTATAACTTTGATCAATATAGGAA
GGTCTTTACTCATTCATCATTGCTTAATCAACAAGAGGAAATAGATATTTGGGGAAAACATCAC
ATATATGATAAAACTTCAGTGTTATTTAGGCAGGTCTCTACTCTAAATAGTTACCGAAATGTTT
TTATTGGAGAGAAAAATTATCATTGCAATAATTCTGAAAAAACCTTGAACCAAAGCTCAAGCCC
TAAAAATCATCAGGAAAATTATTTTCTAGAAAAACAATACAAATGTAAAGAATTTGAGGAAGTC
TTTCTTCAGAGTATGCATGGGCAAGAGAAACAAGAACAGTCTTACAAATGTAATAAATGTGTAG
AAGTTTGTACCCAGTCATTAAAACATATTCAACATCAGACCATCCATATCAGAGAAAACTCATA
TAGCTATAACAAATATGATAAAGATCTTAGTCAGTCATCAAATCTTAGAAAGCAGATAATCCAT
AATGAAGAGAAACCATACAAATGTGAAAAATGTGGGGATAGCTTAAACCATAGTTTGCACCTTA
CTCAACATCAGATCATTCCTACCGAAGAGAAACCCTGTAAATGGAAAGAATGTGGCAAGGTCTT
TAACCTTAACTGTAGTTTATACCTTACTAAACAGCAGCAAATTGATACTGGAGAAAACCTTTAC
AAATGTAAAGCATGTAGCAAATCTTTTACTCGTTCCTCCAATCTTATTGTGCATCAGAGAATTC
ACACTGGAGAGAAACCATACAAATGTAAAGAATGTGGCAAAGCCTTTCGCTGTAGTTCATACCT
TACTAAACATAAGCGAATTCATACTGGAGAGAAACCTTATAAATGTAAAGAATGTGGAAAAGCT
TTTAACCGTAGTTCATGCCTTACTCAACATCAGACAACTCATACAGGAGAAAAACTTTACAAAT
GTAAAGTATGTAGCAAATCTTATGCTCGTTCTTCAAATCTTATTATGCATCAGAGAGTTCATAC
TGGAGAGAAGCCTTATAAATGTAAAGAATGTGGCAAAGTCTTTAGCCGTAGTTCTTGCCTTACT
CAACATCGGAAAATTCATACTGGAGAAAATCTTTACAAATGCAAAGTATGTGCTAAACCTTTTA
CTTGTTTCTCAAATCTTATTGTGCATGAGAGAATTCATACTGGAGAGAAACCCTATAAATGTAA
AGAATGTGGCAAAGCCTTTCCTTATAGTTCACACCTTATTCGACATCATCGAATTCATACTGGA
GAAAAACCATACAAATGTAAAGCATGTAGCAAATCTTTTAGTGACTCCTCAGGTCTTACTGTGC
ATCGGCGAACTCATACTGGAGAGAAACCCTATACATGTAAAGAATGTGGCAAAGCCTTTAGTTA
TAGTTCAGATGTTATTCAGCATCGGAGAATTCATACTGGCCAGAGACCCTACAAATGTGAAGAA
TGTGGCAAAGCCTTCAACTATAGGTCATACCTCACTACACATCAGAGAAGTCATACTGGAGAGA
GACCCTACAAATGTGAAGAATGTGGCAAAGCCTTCAACTCTAGGTCATACCTCACTACACATCG
GAGAAGACATACTGGAGAGAGACCCTACAAATGTGATGAATGTGGTAAAGCCTTCAGCTATAGG
TCATACCTCACTACACATCGGAGAAGTCATAGTGGAGAGAGACCCTACAAATGTGAAGAATGTG
GCAAAGCCTTTAACTCTAGGTCATACCTCATTGCACATCAGAGAAGTCATACTAGAGAAAAACT
TTAAAAATGTAAAACATGGAGCAGATTTTTTACTTGTTACCCATGTCTTATTGTGCATCAGATA
ATTTATATGGGAGTGAAACCCTACAAATGTTAAGAATGTGGCATAACCTTTAACTATTTTCAAG
CCTTACACAATAGCAGAGAATATAAACTGAAAAAATCCATACAAATATTAAAAATGTGGCAAAT
TATTTTAAACTGTGCTCAACCCTTACTCAAGATAATCCATACTAGAGAAACACTATAGATGTAA
AAATGTGAAAAGTTTTATTCAAAATATCAAACTTATGAGTCACCTAGGGGTTCATAGAAAAAGG
AAGTTTGCAGATGCAATAAATGTGAGGAAGTATTTAATAAAAAATGAAGTCTAAATGTGTCAGA
GAATTTATGTGAGAAAGGACTAAAGCACAGACACTTTCAGCCTTTATACTAAATAAGAGTATTT
TTTGTACAGAATAATCTAAAGGCAAAATAATTAGATAATTTATTTGCTTATATGTTTTAAAGTA
GCAAGAACATTGATGTTTTGACAGGTATATTTCATAGATACTTCATTTGTATTTACAGTATTTG
AGGTTTTTGGAAAGCAAATATTATTTATATAATTCAGCTTTCAAATCTGTTGCTGCTTTTCCTT
AATCCGTGGTGTTCATGTGAAAATATGTGTTCTGTTTTTTTTTCTGCATCAGAACAATGTGAGG
TCATTCTACGTTAATATCATTAATATCAGCATTTTTCATGGAAGTTTAATGCCAAATGTAAAAC
ACATGAAAATTTTTAAAAATATGCTCTTTGTGTTTGAATAAAGTAGTAATGCATGTAAACATAT
ACGTGTTTAGAGCTCTTTTCTATATTAAAGTAAGAGGGATATTCTGAA

hide sequence

Protein Sequences


Protein RefSeqs	NP_001252517	(Get FASTA)	NCBI Sequence Viewer
	NP_003405	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAF73867	(Get FASTA)	NCBI Sequence Viewer
	AAH36367	(Get FASTA)	NCBI Sequence Viewer
	AAI27089	(Get FASTA)	NCBI Sequence Viewer
	AAI27090	(Get FASTA)	NCBI Sequence Viewer
	BAF85262	(Get FASTA)	NCBI Sequence Viewer
	BAG53279	(Get FASTA)	NCBI Sequence Viewer
	CAA55525	(Get FASTA)	NCBI Sequence Viewer
	EAW52106	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000300870
	ENSP00000300870.10
GenBank Protein	Q14586	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_003405 ⟸ NM_003414
- Peptide Label:	isoform 1
- UniProtKB:	Q8NE41 (UniProtKB/Swiss-Prot), Q14586 (UniProtKB/Swiss-Prot), A0JNZ9 (UniProtKB/Swiss-Prot), Q9NRJ0 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MGLLTFRDVAVEFSLEEWEHLEPAQKNLYQDVMLENYRNLVSLGLVVSKPDLITFLEQRKEPWN VKSEETVAIQPDVFSHYNKDLLTEHCTEASFQKVISRRHGSCDLENLHLRKRWKREECEGHNGC YDEKTFKYDQFDESSVESLFHQQILSSCAKSYNFDQYRKVFTHSSLLNQQEEIDIWGKHHIYDK TSVLFRQVSTLNSYRNVFIGEKNYHCNNSEKTLNQSSSPKNHQENYFLEKQYKCKEFEEVFLQS MHGQEKQEQSYKCNKCVEVCTQSLKHIQHQTIHIRENSYSYNKYDKDLSQSSNLRKQIIHNEEK PYKCEKCGDSLNHSLHLTQHQIIPTEEKPYKWKECGKVFNLNCSLYLTKQQQIDTGENLYKCKA CSKSFTRSSNLIVHQRIHTGEKPYKCKECGKAFRCSSYLTKHKRIHTGEKPYKCKECGKAFNRS SCLTQHQTTHTGEKLYKCKVCSKSYARSSNLIMHQRVHTGEKPYKCKECGKVFSRSSCLTQHRK IHTGENLYKCKVCAKPFTCFSNLIVHERIHTGEKPYKCKECGKAFPYSSHLIRHHRIHTGEKPY KCKACSKSFSDSSGLTVHRRTHTGEKPYTCKECGKAFSYSSDVIQHRRIHTGQRPYKCEECGKA FNYRSYLTTHQRSHTGERPYKCEECGKAFNSRSYLTTHRRRHTGERPYKCDECGKAFSYRSYLT THRRSHSGERPYKCEECGKAFNSRSYLIAHQRSHTREKL hide sequence

RefSeq Acc Id:

NP_001252517 ⟸ NM_001265588

- Peptide Label:

isoform 2

- Sequence:

show sequence

MLENYRNLVSLGLVVSKPDLITFLEQRKEPWNVKSEETVAIQPDVFSHYNKDLLTEHCTEASFQ
KVISRRHGSCDLENLHLRKRWKREECEGHNGCYDEKTFKYDQFDESSVESLFHQQILSSCAKSY
NFDQYRKVFTHSSLLNQQEEIDIWGKHHIYDKTSVLFRQVSTLNSYRNVFIGEKNYHCNNSEKT
LNQSSSPKNHQENYFLEKQYKCKEFEEVFLQSMHGQEKQEQSYKCNKCVEVCTQSLKHIQHQTI
HIRENSYSYNKYDKDLSQSSNLRKQIIHNEEKPYKCEKCGDSLNHSLHLTQHQIIPTEEKPYKW
KECGKVFNLNCSLYLTKQQQIDTGENLYKCKACSKSFTRSSNLIVHQRIHTGEKPYKCKECGKA
FRCSSYLTKHKRIHTGEKPYKCKECGKAFNRSSCLTQHQTTHTGEKLYKCKVCSKSYARSSNLI
MHQRVHTGEKPYKCKECGKVFSRSSCLTQHRKIHTGENLYKCKVCAKPFTCFSNLIVHERIHTG
EKPYKCKECGKAFPYSSHLIRHHRIHTGEKPYKCKACSKSFSDSSGLTVHRRTHTGEKPYTCKE
CGKAFSYSSDVIQHRRIHTGQRPYKCEECGKAFNYRSYLTTHQRSHTGERPYKCEECGKAFNSR
SYLTTHRRRHTGERPYKCDECGKAFSYRSYLTTHRRSHSGERPYKCEECGKAFNSRSYLIAHQR
SHTREKL

hide sequence

Ensembl Acc Id:

ENSP00000454369 ⟸ ENST00000561814

Ensembl Acc Id:

ENSP00000455493 ⟸ ENST00000562971

Ensembl Acc Id:

ENSP00000300870 ⟸ ENST00000300870

Ensembl Acc Id:

ENSP00000461286 ⟸ ENST00000394846

Ensembl Acc Id:

ENSP00000454753 ⟸ ENST00000566541

Ensembl Acc Id:

ENSP00000524710 ⟸ ENST00000854651

Ensembl Acc Id:

ENSP00000805439 ⟸ ENST00001132469

Ensembl Acc Id:

ENSP00000731572 ⟸ ENST00001061766

Ensembl Acc Id:

ENSP00000666345 ⟸ ENST00000996528

Ensembl Acc Id:

ENSP00000789454 ⟸ ENST00001119649

Protein Domains

KRAB

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q14586-F1-model_v2	AlphaFold	Q14586	1-743	view protein structure

Promoters

RGD ID:

6793632

Promoter ID:

HG_KWN:23648

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

NM_003414

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	16	31,792,454 - 31,792,954 (+)	MPROMDB

RGD ID:

7232117

Promoter ID:

EPDNEW_H21803

Type:

initiation region

Name:

ZNF267_1

Description:

zinc finger protein 267

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	16	31,873,811 - 31,873,871	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:13060	AgrOrtholog
COSMIC	ZNF267	COSMIC
Ensembl Genes	ENSG00000185947	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000300870	ENTREZGENE
	ENST00000300870.15	UniProtKB/Swiss-Prot
Gene3D-CATH	6.10.140.140	UniProtKB/Swiss-Prot
	Classic Zinc Finger	UniProtKB/Swiss-Prot
GTEx	ENSG00000185947	GTEx
HGNC ID	HGNC:13060	ENTREZGENE
Human Proteome Map	ZNF267	Human Proteome Map
InterPro	KRAB	UniProtKB/Swiss-Prot
	KRAB_dom_sf	UniProtKB/Swiss-Prot
	Znf_C2H2_sf	UniProtKB/Swiss-Prot
	Znf_C2H2_type	UniProtKB/Swiss-Prot
KEGG Report	hsa:10308	UniProtKB/Swiss-Prot
NCBI Gene	10308	ENTREZGENE
OMIM	604752	OMIM
PANTHER	KRAB AND ZINC FINGER DOMAIN-CONTAINING	UniProtKB/Swiss-Prot
	ZINC FINGER PROTEIN 737-LIKE-RELATED	UniProtKB/Swiss-Prot
Pfam	KRAB	UniProtKB/Swiss-Prot
	zf-C2H2	UniProtKB/Swiss-Prot
PharmGKB	PA37638	PharmGKB
PROSITE	KRAB	UniProtKB/Swiss-Prot
	ZINC_FINGER_C2H2_1	UniProtKB/Swiss-Prot
	ZINC_FINGER_C2H2_2	UniProtKB/Swiss-Prot
SMART	KRAB	UniProtKB/Swiss-Prot
	ZnF_C2H2	UniProtKB/Swiss-Prot
Superfamily-SCOP	SSF109640	UniProtKB/Swiss-Prot
	SSF57667	UniProtKB/Swiss-Prot
UniProt	A0ACI8QVC5_HUMAN	UniProtKB/TrEMBL
	A0JNZ9	ENTREZGENE
	H3BMG2_HUMAN	UniProtKB/TrEMBL
	H3BNA3_HUMAN	UniProtKB/TrEMBL
	H3BPW2_HUMAN	UniProtKB/TrEMBL
	I3L4I6_HUMAN	UniProtKB/TrEMBL
	Q14586	ENTREZGENE
	Q8NE41	ENTREZGENE
	Q9NRJ0	ENTREZGENE
	ZN267_HUMAN	UniProtKB/Swiss-Prot
UniProt Secondary	A0JNZ9	UniProtKB/Swiss-Prot
	Q8NE41	UniProtKB/Swiss-Prot
	Q9NRJ0	UniProtKB/Swiss-Prot

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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Imported Disease Annotations - CTD

Imported Human Phenotype Annotations - ClinVar

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Imported Disease Annotations - ClinVar

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