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LongevityMap Gene

Gene details

HGNC symbol
PIGC 
Aliases
GPI2 
Common name
phosphatidylinositol glycan anchor biosynthesis class C 
Description
This gene encodes an endoplasmic reticulum associated protein that is involved in glycosylphosphatidylinositol (GPI) lipid anchor biosynthesis. The GPI lipid anchor is a glycolipid found on many blood cells and serves to anchor proteins to the cell surface. The encoded protein is one subunit of the GPI N-acetylglucosaminyl (GlcNAc) transferase that transfers GlcNAc to phosphatidylinositol (PI) on the cytoplasmic side of the endoplasmic reticulum. Two alternatively spliced transcripts that encode the same protein have been found for this gene. A pseudogene on chromosome 11 has also been characterized. [provided by RefSeq, Jul 2008]
Cytogenetic Location
1q24.3
UCSC Genome Browser
View 1q24.3 on the UCSC genome browser
OMIM
601730
Ensembl
ENSG00000135845
UniProt/Swiss-Prot
PIGC_HUMAN
Entrez Gene
5279
UniGene
188456
1000 Genomes
1000 Genomes

Homologs in model organisms

Caenorhabditis elegans
T20D3.8
Danio rerio
pigc
Drosophila melanogaster
PIG-C
Mus musculus
Pigc
Rattus norvegicus
Pigc
Schizosaccharomyces pombe
gpi2

Studies (1)

Significant/Non-significant: 0/1

Longevity Association
Non-significant
Population
American (Caucasian and African-American)
Study Design
The baseline levels of sCD14 (soluble form of CD14) were measured in 5888 European-American and black adults aged 65 years and older from the Cardiovascular Health Study. A genome-wide cardiovascular disease candidate gene-centric association with sCD14 was conducted separately in the European-Americans (n=2952) and blacks (n=528). Finally, the ability of sCD14 and its main genetic determinants to predict incident CVD and mortality during follow-up was assessed.
Conclusions
sCD14 was positively correlated with cardio-metabolic risk factors and with subclinical measures of vascular disease, and was also inversely correlated with body mass index (all P<0.001). In European Americans the minor allele at the index SNP rs5744441 was associated with lower sCD14, the C allele of index SNP rs1063412 was associated with lower sCD14. In Blacks the index SNP rs778584 was associated with higher sCD14. In the fully adjusted model, sCD14 was associated with death because of cardiovascular causes (hazard ratio=1.13, P=0.001) and death because of noncardiovascular causes (hazard ratio=1.11, P=0.001). CD14 independently predicts risk mortality in older adults. However, no SNPs were associated with risk of mortality when corrected for multiple hypothesis testing.
Indentifier
rs1063412
Reference