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BHLHA9


Official Full Name
basic helix-loop-helix family member a9
Organism
Homo sapiens
Gene ID
727857
Background
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]
Synonyms
CCSPD; BHLHF42

Cat.No. Product Name Price
SHH246558 shRNA set against Human BHLHA9 (NM_001164405.1) Inquiry
SHH246562 shRNA set against Mouse BHLHA9 (NM_177182.4) Inquiry
SHW013839 shRNA set against Danio rerio BHLHA9 (NM_001202415) Inquiry
Cat.No. Product Name Price
CDFH001795 Human BHLHA9 cDNA Clone(NM_001164405.1) Inquiry
CDCB175314 Danio rerio BHLHA9 ORF Clone (NM_001202415) Inquiry
CDCB190553 Rabbit BHLHA9 ORF clone (XM_002719057.1) Inquiry
CDCR034538 Human BHLHA9 ORF clone (NM_001164405.1) Inquiry
CDCR034540 Mouse Bhlha9 ORF clone (NM_177182.4) Inquiry
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