C9ORF72 Chromosome 9

C9orf72-SMCR8 complex subunit
1 variant 1 Health Risk

Upload your DNA to see your personal genotypes for variants in C9ORF72.

What This Gene Does
The protein encoded by this gene plays an important role in the regulation of endosomal trafficking, and has been shown to interact with Rab proteins that are involved in autophagy and endocytic transport. Expansion of a GGGGCC repeat from 2-22 copies to 700-1600 copies in the intronic sequence between alternate 5' exons in transcripts from this gene is associated with 9p-linked ALS (amyotrophic lateral sclerosis) and FTD (frontotemporal dementia) (PMID: 21944778, 21944779). Studies suggest that hexanucleotide expansions could result in the selective stabilization of repeat-containing pre-mRNA, and the accumulation of insoluble dipeptide repeat protein aggregates that could be pathogenic in FTD-ALS patients (PMID: 23393093). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2016]
Gene Info
Gene Group
"DENN domain containing|SWC tripartite complex"
Locus Type
gene with protein product
Location
9p21.2
Ensembl
ENSG00000147894
Associated Conditions (1)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 1
Key Variants
All Variants (1)
RSID Category Clinical Significance Conditions
RS143561967 Health Risk Pathogenic Frontotemporal dementia and/or amyotrophic lateral sclerosis 1, Frontotemporal dementia and/or amyotrophic lateral sclerosis 1
Sign Up to Analyze Your DNA Log In