ASCL1 Chromosome 12

Achaete-scute family bHLH transcription factor 1
1 variant 1 Health Risk

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What This Gene Does
This gene encodes a member of the basic helix-loop-helix (BHLH) family of transcription factors. The protein activates transcription by binding to the E box (5'-CANNTG-3'). Dimerization with other BHLH proteins is required for efficient DNA binding. This protein plays a role in the neuronal commitment and differentiation and in the generation of olfactory and autonomic neurons. Mutations in this gene may contribute to the congenital central hypoventilation syndrome (CCHS) phenotype in rare cases. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
Basic helix-loop-helix proteins
Locus Type
gene with protein product
Location
12q23.2
Ensembl
ENSG00000139352
Associated Conditions (1)
ASCL1-related disorder
Key Variants
All Variants (1)
RSID Category Clinical Significance Conditions
RS3832799 Health Risk Conflicting classifications of pathogenicity ASCL1-related disorder, ASCL1-related disorder
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