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BEAN1

brain expressed associated with NEDD4 1
2 disorders 2 causative 16q21 gene with protein product
HGNC:24160MonarchNCBI Gene 146227ENSG00000166546UniProt Q3B7T3OMIM 612051

Previous symbols: SCA31.

In the knowledge base · computed from kb/ at build time

Disorders

Relationship is the entry's genetic[].relationship_type. untyped means the entry has a genetic record for the gene but does not type it; its free-text association is shown instead.

DisorderRelationshipWhere the gene appears
Autosomal Dominant Cerebellar Ataxia Type III causative
mechanism: SCA31 Repeat-RNA Toxicity
subtype: SCA31
scoped to subtype: SCA31
Spinocerebellar Ataxia Type 31 causative germline
mechanism: BEAN1/TK2 Intronic (TGGAA)n Pentanucleotide Repeat Insertion
Mechanism modules · computed from kb/

Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.