SPG11, SPG11 vesicle trafficking associated, spatacsin

SPG11, SPG11 vesicle trafficking associated, spatacsin

• The protein encoded by this gene is a potential transmembrane protein that is phosphorylated upon DNA damage. Defects in this gene are a cause of spastic paraplegia type 11 (SPG11). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]

• Gene Synonyms (spatacsin, SPG11, spatacsin vesicle trafficking associated, amyotrophic lateral sclerosis 5, colorectal carcinoma-associated protein, spastic paraplegia 11 (autosomal recessive), spastic paraplegia 11 protein, ALS5, CMT2X, KIAA1840,)
• NCBI Gene ID: 80208
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q96JI7
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

SPG11 vesicle trafficking associated, spatacsin interacts with:

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.