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SPTBN5 (Spectrin Beta, Non-Erythrocytic 5) is a Protein Coding gene. Diseases associated with SPTBN5 include Epileptic Encephalopathy, Early Infantile, 5 and Spinocerebellar Ataxia 5. Among its related pathways are RET signaling and Signaling by GPCR. Gene Ontology (GO) annotations related to this gene include actin binding and kinesin binding. An important paralog of this gene is DST. [GeneCards]
beta V spectrin; beta-V spectrin; BSPECV; HU HUSPECV; HUBSPECV; HUSPECV; spectrin beta chain, brain 4; spectrin beta chain, non-erythrocytic 5; spectrin beta, non-erythrocytic 5; spectrin, beta, non-erythrocytic 5; spectrin, non-erythroid beta chain 4; SPTBN5
100 µL
100 µL