LongevityMap Gene

Gene details

HGNC symbol
C20orf194 
Aliases
 
Common name
chromosome 20 open reading frame 194 
Description
This gene encodes an uncharacterized protein with a C-terminal coiled-coil region. The gene is located on chromosome 20p13 in a 1.8 Mb region linked to a spinocerebellar ataxia phenotype, but this gene does not appear to be a disease candidate. [provided by RefSeq, Dec 2011]
Cytogenetic Location
20p13
UCSC Genome Browser
View 20p13 on the UCSC genome browser
OMIM
614146
Ensembl
ENSG00000088854
UniProt/Swiss-Prot
CT194_HUMAN
Entrez Gene
25943
UniGene
516853
1000 Genomes
1000 Genomes

Homologs in model organisms

Danio rerio
si:ch211-194c3.5
Mus musculus
uncharacterized_Q7TT
Rattus norvegicus
RGD1565616

Studies (1)

Significant/Non-significant: 1/0

Longevity Association
Significant
Population
American (Caucasian)
Study Design
Genome-wide association study in 801 centenarians and 914 healthy controls
Conclusions
281 SNPs were found to discriminate between cases and controls
Indentifier
rs6115865
Reference