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Gene Protein Transcript Promoter Expression GO/PPI PubMed Cross reference

Gene information for SPG11 (Homo sapiens)
(Information is obtained from NCBI Gene database)
Entrez gene ID80208
Official gene symbolSPG11
Full namespastic paraplegia 11 (autosomal recessive)
Aliases,DKFZp762B1512,FLJ21439,KIAA1840,
Gene summaryThe 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]
LocationChromosome: 15   Locus: 15q14
Gene position44955876 - 44854894  Map Viewer
Gene orientationminus
Gene size100983 bp
Gene sequence
OMIM ID610844