ZNF81
Summary: This gene encodes a protein that likely functions as a transcription factor. The protein contains an N-terminal KRAB domain and several C2H2-type zinc finger motifs. Mutations in this gene cause an X-linked form of intellectual disability (MRX45). Microduplication of a region of chromosome X including this gene has also been associated with other forms of intellectual disability. [provided by RefSeq, Jul 2017].
Name | OMIM ID | Ensembl ID | HGNC ID | PHARMGKB ID | Map Location |
---|---|---|---|---|---|
zinc finger protein 81 | MIM:314998 | Ensembl:ENSG00000197779 | HGNC:HGNC:13156 | PA37730 | Xp11.23 |
GO terms in ZNF81
Term Type | Evidence Type | GO Term ID | GO Des. |
---|---|---|---|
CC | IEA | GO:0005634 | nucleus |
BP | IEA | GO:0006351 | transcription, DNA-templated |
BP | IEA | GO:0006357 | regulation of transcription by RNA polymerase II |
MF | ISA | GO:0000981 | RNA polymerase II transcription factor activity, sequence-specific DNA binding |
MF | IEA | GO:0003677 | DNA binding |
MF | IEA | GO:0046872 | metal ion binding |
Gene expression in normal tissue: ZNF81
Gene-model tissue-cancer distribution: Bubble Plot
Gene-drug pathway distribution
Pathways in ZNF81
Database | Pathway ID | Pathway Des. |
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Gene in drug-gene network: Network Plot
Gene-drug targets distribution
Gene Structure: PDB
Models in ZNF81