CCNQ, cyclin Q

CCNQ, cyclin Q

• Mutations in this gene have been shown to cause an X-linked dominant STAR syndrome that typically manifests syndactyly, telecanthus and anogenital and renal malformations. The protein encoded by this gene contains a cyclin-box-fold domain which suggests it may have a role in controlling nuclear cell division cycles. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Oct 2008]

• Gene Synonyms (cyclin-Q, CDK10-activating cyclin, cyclin M, cyclin-related protein FAM58A, family with sequence similarity 58 member A, CycM, FAM58A,)
• NCBI Gene ID: 92002
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q8N1B3
• 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.

cyclin Q interacts with:

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.