HMGCLL1 (3-hydroxymethyl-3-methylglutaryl-CoA lyase-like 1) is a protein-coding gene. Diseases associated with HMGCLL1 include hmg coa lyase deficiency, and optic atrophy, and among its related super-pathways are Branched-chain amino acid catabolism. GO annotations related to this gene include hydroxymethylglutaryl-CoA lyase activity and metal ion binding. An important paralog of this gene is HMGCL.
Pathway
leucine degradation I.
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