ZNF41 gene

zinc finger protein 41

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

From NCBI Gene:

This gene encodes a protein that contains KRAB-A and KRAB-B domains multiple zinc finger DNA binding motifs and finger linking regions characteristic of the Kruppel family. An initial study suggested that this gene may be associated with X-linked mental retardation, but a later study has called this finding into question (PMID:23871722).[provided by RefSeq, Apr 2016]

From UniProt:

May be involved in transcriptional regulation.

From UniProt:

A chromosomal aberration involving ZNF41 has been found in a patient with severe mental retardation. Translocation t(X;7)(p11.3;q11.21).

Cytogenetic Location: Xp11.3, which is the short (p) arm of the X chromosome at position 11.3

Molecular Location: base pairs 47,444,691 to 47,483,671 on the X chromosome (Homo sapiens Annotation Release 108, GRCh38.p7) (NCBI)

Cytogenetic Location: Xp11.3, which is the short (p) arm of the X chromosome at position 11.3