ZNF267 (zinc finger protein 267) - Rat Genome Database

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Gene: ZNF267 (zinc finger protein 267) Homo sapiens
Analyze
Symbol: ZNF267
Name: zinc finger protein 267
RGD ID: 1343571
HGNC Page HGNC:13060
Description: Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in 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
Mouse
Rat
Bonobo
Green Monkey
Alliance Genes
More Info more info ...
Related Pseudogenes: LOC100419781  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381631,873,807 - 31,917,357 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1631,873,807 - 31,917,357 (+)EnsemblGRCh38hg38GRCh38
GRCh371631,885,128 - 31,928,678 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361631,792,655 - 31,836,128 (+)NCBINCBI36Build 36hg18NCBI36
Build 341631,792,660 - 31,836,127NCBI
Celera1628,380,251 - 28,423,800 (-)NCBICelera
Cytogenetic Map16p11.2NCBI
HuRef1629,445,530 - 29,489,069 (+)NCBIHuRef
CHM1_11633,203,771 - 33,247,293 (+)NCBICHM1_1
T2T-CHM13v2.01632,261,274 - 32,304,813 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
nucleus  (IBA,IEA)

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: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:36691044  


Genomics

Comparative Map Data
ZNF267
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381631,873,807 - 31,917,357 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1631,873,807 - 31,917,357 (+)EnsemblGRCh38hg38GRCh38
GRCh371631,885,128 - 31,928,678 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361631,792,655 - 31,836,128 (+)NCBINCBI36Build 36hg18NCBI36
Build 341631,792,660 - 31,836,127NCBI
Celera1628,380,251 - 28,423,800 (-)NCBICelera
Cytogenetic Map16p11.2NCBI
HuRef1629,445,530 - 29,489,069 (+)NCBIHuRef
CHM1_11633,203,771 - 33,247,293 (+)NCBICHM1_1
T2T-CHM13v2.01632,261,274 - 32,304,813 (+)NCBIT2T-CHM13v2.0
Zfp267
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39336,205,233 - 36,224,491 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl336,205,166 - 36,224,491 (+)EnsemblGRCm39 Ensembl
GRCm38336,151,080 - 36,170,341 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl336,151,017 - 36,170,342 (+)EnsemblGRCm38mm10GRCm38
MGSCv37336,050,002 - 36,069,263 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36336,342,566 - 36,361,891 (+)NCBIMGSCv36mm8
Celera336,033,417 - 36,052,679 (+)NCBICelera
Cytogenetic Map3BNCBI
cM Map317.41NCBI
Zfp267
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr82120,945,434 - 120,964,039 (+)NCBIGRCr8
mRatBN7.22119,017,280 - 119,035,885 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl2119,017,285 - 119,031,900 (+)EnsemblmRatBN7.2 Ensembl
Rnor_6.02122,855,036 - 122,873,696 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl2122,865,100 - 122,869,616 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.02142,480,922 - 142,499,556 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.42122,650,827 - 122,655,890 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera2113,977,669 - 113,996,320 (+)NCBICelera
Cytogenetic Map2q25NCBI
ZNF267
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21835,204,096 - 35,248,638 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11640,124,941 - 40,169,383 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01622,924,355 - 22,968,670 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11632,336,772 - 32,380,262 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1632,336,675 - 32,380,262 (+)Ensemblpanpan1.1panPan2
ZNF267
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1528,517,588 - 28,561,125 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl528,517,720 - 28,561,117 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_023666068870,321 - 915,381 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0

Variants

.
Variants in ZNF267
30 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] Chr16:30691912..36160463 [GRCh38]
Chr16:30703233..35147508 [GRCh37]
Chr16:30610734..35005009 [NCBI36]
Chr16:16p11.2-11.1		 pathogenic
GRCh38/hg38 16p11.2(chr16:31894396-33495702)x1 copy number loss See cases [RCV000136426] Chr16:31894396..33495702 [GRCh38]
Chr16:31905717..33298169 [GRCh37]
Chr16:31813218..33205670 [NCBI36]
Chr16:16p11.2		 benign
GRCh38/hg38 16p12.2-11.2(chr16:23752047-31943755)x3 copy number gain See cases [RCV000141141] Chr16:23752047..31943755 [GRCh38]
Chr16:23763368..31955076 [GRCh37]
Chr16:23670869..31862577 [NCBI36]
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 See cases [RCV000446684] Chr16:69193..90274381 [GRCh37]
Chr16:16p13.3-q24.3		 pathogenic
GRCh37/hg19 16p11.2(chr16:28826162-29043901)x1 copy number loss See cases [RCV000448084] Chr16:28826162..29043901 [GRCh37]
Chr16:16p11.2		 likely pathogenic
GRCh37/hg19 16p13.2-q24.3(chr16:9273328-89548493)x3 copy number gain See cases [RCV000511622] Chr16:9273328..89548493 [GRCh37]
Chr16:16p13.2-q24.3		 uncertain significance
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 See cases [RCV000511296] Chr16:85881..90155062 [GRCh37]
Chr16:16p13.3-q24.3		 pathogenic
NM_003414.6(ZNF267):c.1138T>A (p.Tyr380Asn) single nucleotide variant Inborn genetic diseases [RCV003274798] Chr16:31915387 [GRCh38]
Chr16:31926708 [GRCh37]
Chr16:16p11.2		 uncertain significance
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062)x3 copy number gain See cases [RCV000512138] Chr16:85881..90155062 [GRCh37]
Chr16:16p13.3-q24.3		 pathogenic
NM_003414.6(ZNF267):c.1457A>G (p.His486Arg) single nucleotide variant Inborn genetic diseases [RCV003257336] Chr16:31915706 [GRCh38]
Chr16:31927027 [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
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 Inborn genetic diseases [RCV003268210] Chr16:31914596 [GRCh38]
Chr16:31925917 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_003414.6(ZNF267):c.1186A>G (p.Ile396Val) single nucleotide variant Inborn genetic diseases [RCV003251764] Chr16:31915435 [GRCh38]
Chr16:31926756 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_003414.6(ZNF267):c.2182A>G (p.Arg728Gly) single nucleotide variant Inborn genetic diseases [RCV003242034] 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] Chr16:5805001..34230001 [GRCh37]
Chr16:16p13.3-11.2		 pathogenic
GRCh37/hg19 16p11.2(chr16:30350747-31905898)x3 copy number gain not provided [RCV001258619] Chr16:30350747..31905898 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_003414.6(ZNF267):c.1121A>G (p.Asp374Gly) single nucleotide variant Inborn genetic diseases [RCV002993067] Chr16:31915370 [GRCh38]
Chr16:31926691 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_003414.6(ZNF267):c.524T>A (p.Leu175His) single nucleotide variant Inborn genetic diseases [RCV002865463] Chr16:31914773 [GRCh38]
Chr16:31926094 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_003414.6(ZNF267):c.1382A>G (p.Glu461Gly) single nucleotide variant Inborn genetic diseases [RCV002739753] Chr16:31915631 [GRCh38]
Chr16:31926952 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_003414.6(ZNF267):c.998A>G (p.His333Arg) single nucleotide variant Inborn genetic diseases [RCV002691506] Chr16:31915247 [GRCh38]
Chr16:31926568 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_003414.6(ZNF267):c.1676A>G (p.Tyr559Cys) single nucleotide variant Inborn genetic diseases [RCV002911999] Chr16:31915925 [GRCh38]
Chr16:31927246 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_003414.6(ZNF267):c.761T>A (p.Leu254His) single nucleotide variant Inborn genetic diseases [RCV002951710] Chr16:31915010 [GRCh38]
Chr16:31926331 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_003414.6(ZNF267):c.1124C>A (p.Thr375Asn) single nucleotide variant Inborn genetic diseases [RCV003003678] Chr16:31915373 [GRCh38]
Chr16:31926694 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_003414.6(ZNF267):c.140T>G (p.Val47Gly) single nucleotide variant Inborn genetic diseases [RCV002763397] Chr16:31885170 [GRCh38]
Chr16:31896491 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_003414.6(ZNF267):c.941T>C (p.Ile314Thr) single nucleotide variant Inborn genetic diseases [RCV002804316] Chr16:31915190 [GRCh38]
Chr16:31926511 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_003414.6(ZNF267):c.2141G>C (p.Arg714Thr) single nucleotide variant Inborn genetic diseases [RCV002803162] Chr16:31916390 [GRCh38]
Chr16:31927711 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_003414.6(ZNF267):c.1036G>A (p.Glu346Lys) single nucleotide variant Inborn genetic diseases [RCV003004051] Chr16:31915285 [GRCh38]
Chr16:31926606 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_003414.6(ZNF267):c.502G>A (p.Val168Ile) single nucleotide variant Inborn genetic diseases [RCV002892819] Chr16:31914751 [GRCh38]
Chr16:31926072 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_003414.6(ZNF267):c.1033A>G (p.Thr345Ala) single nucleotide variant Inborn genetic diseases [RCV002915511] Chr16:31915282 [GRCh38]
Chr16:31926603 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_003414.6(ZNF267):c.1867C>T (p.Arg623Trp) single nucleotide variant Inborn genetic diseases [RCV002984651] Chr16:31916116 [GRCh38]
Chr16:31927437 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_003414.6(ZNF267):c.2154T>G (p.Cys718Trp) single nucleotide variant Inborn genetic diseases [RCV002763587] Chr16:31916403 [GRCh38]
Chr16:31927724 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_003414.6(ZNF267):c.1723C>A (p.Pro575Thr) single nucleotide variant Inborn genetic diseases [RCV002674184] Chr16:31915972 [GRCh38]
Chr16:31927293 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_003414.6(ZNF267):c.2035C>T (p.Arg679Trp) single nucleotide variant Inborn genetic diseases [RCV002677405] Chr16:31916284 [GRCh38]
Chr16:31927605 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_003414.6(ZNF267):c.1423C>T (p.Arg475Cys) single nucleotide variant Inborn genetic diseases [RCV002724969] Chr16:31915672 [GRCh38]
Chr16:31926993 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_003414.6(ZNF267):c.763C>G (p.Gln255Glu) single nucleotide variant Inborn genetic diseases [RCV002944931] Chr16:31915012 [GRCh38]
Chr16:31926333 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_003414.6(ZNF267):c.204G>C (p.Glu68Asp) single nucleotide variant Inborn genetic diseases [RCV003216873] Chr16:31885234 [GRCh38]
Chr16:31896555 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_003414.6(ZNF267):c.149C>T (p.Pro50Leu) single nucleotide variant Inborn genetic diseases [RCV003375022] Chr16:31885179 [GRCh38]
Chr16:31896500 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_003414.6(ZNF267):c.770T>C (p.Met257Thr) single nucleotide variant Inborn genetic diseases [RCV003347535] Chr16:31915019 [GRCh38]
Chr16:31926340 [GRCh37]
Chr16:16p11.2		 uncertain significance
NM_003414.6(ZNF267):c.264G>C (p.Glu88Asp) single nucleotide variant Inborn genetic diseases [RCV003374954] 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
miRNA Target Status

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.

Markers in Region
RH70917  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371631,927,821 - 31,927,950UniSTSGRCh37
Build 361631,835,322 - 31,835,451RGDNCBI36
Celera1628,380,928 - 28,381,057RGD
Cytogenetic Map16p11.2UniSTS
HuRef1629,488,261 - 29,488,390UniSTS
RH104437  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371631,927,838 - 31,928,020UniSTSGRCh37
Build 361631,835,339 - 31,835,521RGDNCBI36
Celera1628,380,858 - 28,381,040RGD
Cytogenetic Map16p11.2UniSTS
HuRef1629,488,278 - 29,488,460UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 162 353 136 43 1228 15 528 37 119 75 372 605 36 1 365 99 4 1
Low 2277 2616 1588 579 720 448 3827 2142 3599 343 1088 1008 138 839 2688 2 1
Below cutoff 22 2 2 3 2 1 18 16 1 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

Reference Sequences
RefSeq Acc Id: ENST00000300870   ⟹   ENSP00000300870
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1631,873,807 - 31,917,357 (+)Ensembl
RefSeq Acc Id: ENST00000394846   ⟹   ENSP00000461286
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1631,873,807 - 31,914,725 (+)Ensembl
RefSeq Acc Id: ENST00000561814   ⟹   ENSP00000454369
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1631,873,833 - 31,914,527 (+)Ensembl
RefSeq Acc Id: ENST00000562971   ⟹   ENSP00000455493
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1631,874,066 - 31,914,620 (+)Ensembl
RefSeq Acc Id: ENST00000566541   ⟹   ENSP00000454753
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1631,873,831 - 31,914,558 (+)Ensembl
RefSeq Acc Id: ENST00000575471
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1631,911,854 - 31,916,852 (+)Ensembl
RefSeq Acc Id: NM_001265588   ⟹   NP_001252517
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381631,873,807 - 31,917,357 (+)NCBI
GRCh371631,885,079 - 31,928,629 (+)NCBI
HuRef1629,445,530 - 29,489,069 (+)NCBI
CHM1_11633,203,771 - 33,247,293 (+)NCBI
T2T-CHM13v2.01632,261,274 - 32,304,813 (+)NCBI
Sequence:
RefSeq Acc Id: NM_003414   ⟹   NP_003405
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381631,873,807 - 31,917,357 (+)NCBI
GRCh371631,885,079 - 31,928,629 (+)NCBI
Build 361631,792,655 - 31,836,128 (+)NCBI Archive
Celera1628,380,251 - 28,423,800 (-)RGD
HuRef1629,445,530 - 29,489,069 (+)NCBI
CHM1_11633,203,771 - 33,247,293 (+)NCBI
T2T-CHM13v2.01632,261,274 - 32,304,813 (+)NCBI
Sequence:
RefSeq Acc Id: NR_049749
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381631,873,807 - 31,917,357 (+)NCBI
GRCh371631,885,079 - 31,928,629 (+)NCBI
HuRef1629,445,530 - 29,489,069 (+)NCBI
CHM1_11633,203,771 - 33,247,293 (+)NCBI
T2T-CHM13v2.01632,261,274 - 32,304,813 (+)NCBI
Sequence:
Reference Protein Sequences
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:
RefSeq Acc Id: NP_001252517   ⟸   NM_001265588
- Peptide Label: isoform 2
- Sequence:
RefSeq Acc Id: ENSP00000454369   ⟸   ENST00000561814
RefSeq Acc Id: ENSP00000455493   ⟸   ENST00000562971
RefSeq Acc Id: ENSP00000300870   ⟸   ENST00000300870
RefSeq Acc Id: ENSP00000461286   ⟸   ENST00000394846
RefSeq Acc Id: ENSP00000454753   ⟸   ENST00000566541
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 AssemblyChrPosition (strand)Source
Build 361631,792,454 - 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 AssemblyChrPosition (strand)Source
GRCh381631,873,811 - 31,873,871EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:13060 AgrOrtholog
COSMIC ZNF267 COSMIC
Ensembl Genes ENSG00000185947 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000300870 ENTREZGENE
  ENST00000300870.15 UniProtKB/Swiss-Prot
  ENST00000394846.7 UniProtKB/TrEMBL
  ENST00000561814.1 UniProtKB/TrEMBL
  ENST00000562971.1 UniProtKB/TrEMBL
  ENST00000566541.5 UniProtKB/TrEMBL
Gene3D-CATH 6.10.140.140 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  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, UniProtKB/TrEMBL
  KRAB_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  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 DOMAIN C2H2 ZINC FINGER UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  KRAB DOMAIN-CONTAINING PROTEIN 5-RELATED UniProtKB/TrEMBL
  ZINC FINGER PROTEIN 726 UniProtKB/Swiss-Prot
Pfam KRAB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  zf-C2H2 UniProtKB/Swiss-Prot
PharmGKB PA37638 PharmGKB
PROSITE KRAB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZINC_FINGER_C2H2_1 UniProtKB/Swiss-Prot
  ZINC_FINGER_C2H2_2 UniProtKB/Swiss-Prot
SMART KRAB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZnF_C2H2 UniProtKB/Swiss-Prot
Superfamily-SCOP SSF109640 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF57667 UniProtKB/Swiss-Prot
UniProt 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