Homo sapiens Protein: ZNF81
Summary
InnateDB Protein IDBP-62081.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol ZNF81
Protein Name zinc finger protein 81
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000366153
InnateDB Gene IDBG-62079 (ZNF81)
Protein Structure
UniProt Annotation
Function May be involved in transcriptional regulation.
Subcellular Localization Nucleus {ECO:0000305}.
Disease Associations Mental retardation, X-linked 45 (MRX45) [MIM:300498]: A disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. Intellectual deficiency is the only primary symptom of non- syndromic X-linked mental retardation, while syndromic mental retardation presents with associated physical, neurological and/or psychiatric manifestations. {ECO:0000269PubMed:15121780}. Note=The disease is caused by mutations affecting the gene represented in this entry.Note=A chromosomal aberration involving ZNF81 is found in a severe mental retardation patient. Translocation t(X;9)(p11.23;q34.3).
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0003676 nucleic acid binding
GO:0003677 DNA binding
GO:0003700 sequence-specific DNA binding transcription factor activity
GO:0046872 metal ion binding
Biological Process
GO:0006351 transcription, DNA-templated
GO:0006355 regulation of transcription, DNA-templated
Cellular Component
GO:0005622 intracellular
GO:0005634 nucleus
Protein Structure and Domains
PDB ID
InterPro IPR001909 Krueppel-associated box
IPR007087 Zinc finger, C2H2
IPR015880 Zinc finger, C2H2-like
PFAM PF01352
PF00096
PRINTS
PIRSF
SMART SM00349
SM00355
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P51508
PhosphoSite PhosphoSite-P51508
TrEMBL
UniProt Splice Variant
Entrez Gene 347344
UniGene Hs.114246
RefSeq
HUGO HGNC:13156
OMIM 314998
CCDS CCDS43933
HPRD
IMGT
EMBL AL022578 AL591394 AY487248 X68011 Z98304
GenPept AAS17752 CAA48148 CAI39462 CAI42739 CAI42943