ZNF81 gene

zinc finger protein 81

The information on this page was automatically extracted from online scientific databases.

From NCBI Gene:

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]

From UniProt:

May be involved in transcriptional regulation.

From NCBI Gene:

  • Mental retardation, X-linked 45

From UniProt:

A chromosomal aberration involving ZNF81 is found in a severe mental retardation patient. Translocation t(X;9)(p11.23;q34.3).

Cytogenetic Location: Xp11.23, which is the short (p) arm of the X chromosome at position 11.23

Molecular Location: base pairs 47,836,864 to 47,925,626 on the X chromosome (Homo sapiens Annotation Release 108, GRCh38.p7) (NCBI)

Cytogenetic Location: Xp11.23, which is the short (p) arm of the X chromosome at position 11.23
  • dJ54B20.6
  • HFZ20
  • MRX45