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C9ORF72 gene

C9orf72-SMCR8 complex subunit

Key facts

Official symbol
C9ORF72
Full name
C9ORF72
Chromosome
9
Map location
9p21.2
Organism
Homo sapiens
NCBI Gene ID
203228
Also known as
ALSFTD, DENND9, DENNL72, FTDALS, FTDALS1

Function summary

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].

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Data source: NCBI Gene · alsesAI Gene Library