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Gene Protein Transcript Promoter Expression GO/PPI PubMed Cross reference

Gene information for SACS (Homo sapiens)
(Information is obtained from NCBI Gene database)
Entrez gene ID26278
Official gene symbolSACS
Full namespastic ataxia of Charlevoix-Saguenay (sacsin)
Aliases,ARSACS,DKFZp686B15167,
Gene summaryThis gene consists of nine exons including a gigantic exon spanning more than 12.8k bp. It encodes the sacsin protein, which includes a UBQ region at the N-terminus, a HEPN domain at the C-terminus and a DnaJ region upstream of the HEPN domain. The gene is highly expressed in the central nervous system, also found in skin, skeletal muscles and at low levels in the pancreas. Mutations in this gene result in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS), a neurodegenerative disorder characterized by early-onset cerebellar ataxia with spasticity and peripheral neuropathy. Alternatively spliced transcript variants encoding different isoforms have been found, but the full-length nature of these variants has not been determined.[provided by RefSeq]
LocationChromosome: 13   Locus: 13q12
Gene position24007841 - 23902965  Map Viewer
Gene orientationminus
Gene size104877 bp
Gene sequence
OMIM ID604490