SPTBN2 (Entrez ID: 6712)

Entrez Gene ID 6712
Official Gene Symbol SPTBN2 (GeneCards)
Full name spectrin beta, non-erythrocytic 2
Location 11q13.2
Other ids Vega : OTTHUMG00000167262
MIM : 604985
HGNC : HGNC:11276
Ensembl : ENSG00000173898
Other names SCA5, SCAR14, GTRAP41
Summary Spectrins are principle components of a cell's membrane-cytoskeleton and are composed of two alpha and two beta spectrin subunits. The protein encoded by this gene (SPTBN2), is called spectrin beta non-erythrocytic 2 or beta-III spectrin. It is related to, but distinct from, the beta-II spectrin gene which is also known as spectrin beta non-erythrocytic 1 (SPTBN1). SPTBN2 regulates the glutamate signaling pathway by stabilizing the glutamate transporter EAAT4 at the surface of the plasma membrane. Mutations in this gene cause a form of spinocerebellar ataxia, SCA5, that is characterized by neurodegeneration, progressive locomotor incoordination, dysarthria, and uncoordinated eye movements. [provided by RefSeq, Dec 2009]

Variants

Found 3 variants in this database.