ENSG00000147180


Homo sapiens

Features
Gene ID: ENSG00000147180
  
Biological name :ZNF711
  
Synonyms : Q9Y462 / zinc finger protein 711 / ZNF711
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: X
Strand: 1
Band: q21.1
Gene start: 85244032
Gene end: 85273362
  
Corresponding Affymetrix probe sets: 207781_s_at (Human Genome U133 Plus 2.0 Array)   228988_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000276123
Ensembl peptide - ENSP00000353922
Ensembl peptide - ENSP00000362260
NCBI entrez gene - 7552     See in Manteia.
OMIM - 314990
RefSeq - XM_017029809
RefSeq - NM_021998
RefSeq - XM_017029806
RefSeq - XM_017029807
RefSeq - XM_017029808
RefSeq - XM_005262186
RefSeq - XM_005262187
RefSeq - XM_005262188
RefSeq - XM_005262189
RefSeq - XM_011531019
RefSeq - XM_011531020
RefSeq - XM_011531021
RefSeq - XM_011531022
RefSeq - XM_011531023
RefSeq - XM_011531024
RefSeq - XM_011531025
RefSeq - XM_011531026
RefSeq - XM_017029803
RefSeq - XM_017029804
RefSeq - XM_017029805
RefSeq Peptide - NP_068838
RefSeq Peptide - NP_001317503
swissprot - Q9Y462
Ensembl - ENSG00000147180
  
Related genetic diseases (OMIM): 300803 - Mental retardation, X-linked 97, 300803

This gene has been taged as a transcription factor by TFT
See expression report in BioGPS
See gene description in Wikigenes
See gene description in GeneCards
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 znf711ENSDARG00000071868Danio rerio
 ZNF711ENSGALG00000006929Gallus gallus
 Zfp711ENSMUSG00000025529Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
ZFX / P17010 / zinc finger protein, X-linkedENSG0000000588958
ZFY / P08048 / zinc finger protein, Y-linkedENSG0000006764653
Q9UID6 / ZNF639 / zinc finger protein 639ENSG0000012186411


Protein motifs (from Interpro)
Interpro ID Name
 IPR006794  Transcriptional activator, Zfx / Zfy domain
 IPR013087  Zinc finger C2H2-type
 IPR036236  Zinc finger C2H2 superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006351 transcription, DNA-templated IEA
 biological_processGO:0006355 regulation of transcription, DNA-templated IEA
 biological_processGO:0006357 regulation of transcription by RNA polymerase II IEA
 biological_processGO:0045893 positive regulation of transcription, DNA-templated IMP
 cellular_componentGO:0005634 nucleus IDA
 cellular_componentGO:0070062 extracellular exosome HDA
 molecular_functionGO:0000981 RNA polymerase II transcription factor activity, sequence-specific DNA binding ISM
 molecular_functionGO:0003676 nucleic acid binding IEA
 molecular_functionGO:0003677 DNA binding IEA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0043565 sequence-specific DNA binding IDA
 molecular_functionGO:0046872 metal ion binding IEA


Pathways (from Reactome)
Pathway description
Generic Transcription Pathway


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0001249 Mental retardation 
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 HP:0001417 X-linked inheritance "A mode of inheritance that is observed for traits related to a gene encoded on the X chromosome." [HPO:curators]
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 HP:0002342 Mental retardation, moderate "Moderate mental retardation is defined as an intelligence quotient (IQ) in the range of 35-49." [HPO:curators]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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