The Human Ageing Genomic Resources are at risk. Please support our work at JustGiving.

LongevityMap Gene

Gene details

HGNC symbol
WDR13 
Aliases
MG21 
Common name
WD repeat domain 13 
Description
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. A similar protein in mouse is thought to be a negative regulator of the pancreatic beta cell proliferation. Mice lacking this gene exhibit increased pancreatic islet mass and higher serum insulin levels, and are mildly obese. [provided by RefSeq, Nov 2016]
Cytogenetic Location
Xp11.23
UCSC Genome Browser
View Xp11.23 on the UCSC genome browser
OMIM
300512
Ensembl
ENSG00000101940
UniProt/Swiss-Prot
WDR13_HUMAN
Entrez Gene
64743
UniGene
521973
1000 Genomes
1000 Genomes

Homologs in model organisms

Danio rerio
wdr13
Mus musculus
Wdr13
Rattus norvegicus
Wdr13

Studies (1)

Significant/Non-significant: 0/1

Longevity Association
Non-significant
Population
Italian (Northern) and Japanese
Study Design
AGTR1 was sequenced in 173 Italian centenarians (99-106 y, mean 100.9 ± 1.7 y, 83% female) and 376 younger controls (49-78 y, mean 65.9 ± 9.1 y, 43 % females). The results were then verified in 589 Japanese cases (99-115 y, mean 104.5 ± 3 y, 84% femal) and 422 controls (69-72 y, mean 70.1 ± 0.9 y, 52 % female).
Conclusions
rs422858, rs275653 were significantly associated with extreme longevity (P = 0.004). Other SNPs were not associated with longevity.
Indentifier
rs2272656
Reference