WDR37 gene

WD repeat domain 37

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

From NCBI Gene:

This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. [provided by RefSeq, Jul 2008]

From NCBI Gene:

  • NEUROOCULOCARDIOGENITOURINARY SYNDROME

From UniProt:

Neurooculocardiogenitourinary syndrome (NOCGUS): An autosomal dominant multisystem disorder characterized by significant neurological impairment with structural brain defects and seizures, poor feeding, poor postnatal growth, ocular anomalies, dysmorphic facial features, and variable skeletal, cardiac and genitourinary defects. Death in infancy may occur. [MIM:618652]

Cytogenetic Location: 10p15.3, which is the short (p) arm of chromosome 10 at position 15.3

Molecular Location: base pairs 1,056,385 to 1,132,372 on chromosome 10 (Homo sapiens Updated Annotation Release 109.20200522, GRCh38.p13) (NCBI)

Cytogenetic Location: 10p15.3, which is the short (p) arm of chromosome 10 at position 15.3
  • NOCGUS