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- C9orf72 abstract "C9orf72 (chromosome 9 open reading frame 72) is a protein which in humans is encoded by the gene C9orf72.The human C9orf72 gene is located on the short (p) arm of chromosome 9 open reading frame 72, from base pair 27,546,542 to base pair 27,573,863. Its cytogenetic location is at 9p21.2.The protein is found in many regions of the brain, in the cytoplasm of neurons as well as in presynaptic terminals. Disease causing mutations in the gene were first discovered by two independent research teams, led by Rosa Rademakers of Mayo Clinic and Bryan Traynor of the National Institutes of Health, and were first reported in October 2011. The mutations in C9orf72 are significant because it is the first pathogenic mechanism identified to be a genetic link between familial frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS). As of 2012, it is the most common mutation identified that is associated with familial FTD and/or ALS.".
- C9orf72 entrezgene "203228".
- C9orf72 wikiPageID "37692055".
- C9orf72 wikiPageRevisionID "604013351".
- C9orf72 hasPhotoCollection C9orf72.
- C9orf72 subject Category:Genes_on_chromosome_9.
- C9orf72 subject Category:Proteins.
- C9orf72 type Biomolecule.
- C9orf72 type Protein.
- C9orf72 type BiologicalObject.
- C9orf72 comment "C9orf72 (chromosome 9 open reading frame 72) is a protein which in humans is encoded by the gene C9orf72.The human C9orf72 gene is located on the short (p) arm of chromosome 9 open reading frame 72, from base pair 27,546,542 to base pair 27,573,863. Its cytogenetic location is at 9p21.2.The protein is found in many regions of the brain, in the cytoplasm of neurons as well as in presynaptic terminals.".
- C9orf72 label "C9ORF72".
- C9orf72 label "C9orf72".
- C9orf72 sameAs C9ORF72.
- C9orf72 sameAs m.0ndx18k.
- C9orf72 sameAs Q5008447.
- C9orf72 sameAs Q5008447.
- C9orf72 wasDerivedFrom C9orf72?oldid=604013351.
- C9orf72 isPrimaryTopicOf C9orf72.