RAB39B, RAB39B, member RAS oncogene family

RAB39B, RAB39B, member RAS oncogene family

• This gene encodes a member of the Rab family of proteins. Rab proteins are small GTPases that are involved in vesicular trafficking. Mutations in this gene are associated with X-linked cognitive disability. [provided by RefSeq, Aug 2013]

• Gene Synonyms (BGMR, MRX72, WSMN, WSN, ras-related protein Rab-39B, Waisman syndrome, Waisman syndrome (basal ganglion disorder with mental retardation),)
• NCBI Gene ID: 116442
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q96DA2
• 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.

RAB39B, member RAS oncogene family interacts with:

• C9orf72-SMCR8 complex subunit
  WASP homolog associated with actin, golgi membranes and microtubules

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.