BHLHA9, basic helix-loop-helix family member a9

BHLHA9, basic helix-loop-helix family member a9

• This gene is a member of the basic helix-loop-helix family. The encoded protein is a transcription factor involved in limb development. Mutations in this gene have been associated with mesoaxial synostotic syndactyly Malik-Percin type (MSSD). Copy number variation of a locus containing this gene has been linked to a form of split-hand/foot malformation with long bone deficiency (SHFLD3). [provided by RefSeq, Mar 2015]

• Gene Synonyms (BHLHF42, CCSPD, class A basic helix-loop-helix protein 9, Fingerin, class F basic helix-loop-helix factor 42, class II basic helix-loop-helix protein,)
• NCBI Gene ID: 727857
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q7RTU4
• 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.

basic helix-loop-helix family member a9 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.