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]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| BHLHA9-20-RE | 20 (40 μL) | 200 μL |  |
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| BHLHA9-20-OR | 20 (40 μL) | 200 μL |  |
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| BHLHA9-20-GO | 20 (40 μL) | 200 μL |  |
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| BHLHA9-20-GR | 20 (40 μL) | 200 μL |  |
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| BHLHA9-20-AQ | 20 (40 μL) | 200 μL |  |
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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 Symbol : BHLHA9
Gene Name : Basic helix-loop-helix family member a9
Chromosome : CHR 17: 127,056,3-127,127,0
Locus : 17p13.3
Alt. Genes : EBI3
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