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Lrrk2 (leucine rich repeat kinase 2) is a protein coding gene The dmd gene is the largest known gene in humans Diseases associated with lrrk2 include parkinson disease 8, autosomal dominant and parkinson's disease.

Complete information for yap1 gene (protein coding), yes1 associated transcriptional regulator, including Complete information for nmnat2 gene (protein coding), nicotinamide nucleotide adenylyltransferase 2, including Function, proteins, disorders, pathways, orthologs, and expression.

The encoded protein is believed to be an integral membrane protein involved in small molecule transport, specifically tyrosine, which is a precursor to melanin synthesis.

Mutations in this gene cause gaucher disease, a lysosomal storage disease characterized by an accumulation of glucocerebrosides.

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