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ALMS1: A gene on chromosome 2p13. Alstrom syndrome is caused by mutation of ALMS1.
The official name of this gene is “Alstrom syndrome 1.†ALMS1 is the gene's official symbol. The ALMS1 gene is also known by other names, listed below.
Complete information for ALMS1 gene (protein-coding), Alstrom syndrome 1
Premature truncation alleles in the ALMS1 gene are a frequent cause of human Alström syndrome. Alström syndrome is a rare disorder characterized by early obesity and ...
View Alms1<Gt(XH152)Byg> allele: origin, molecular description, curated phenotype details and human disease models, gene associations, and references.
Mutations in the human ALMS1 gene cause Alström syndrome (AS), a progressive disease characterized by neurosensory deficits and by metabolic defects including childhood ...