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Function, proteins, disorders, pathways, orthologs, and expression. Mutations in this gene cause gaucher disease, a lysosomal storage disease characterized by an accumulation of glucocerebrosides. Lrrk2 (leucine rich repeat kinase 2) is a protein coding gene

Genes - Definition, Function, and Mutations

Diseases associated with lrrk2 include parkinson disease 8, autosomal dominant and parkinson's disease. This receptor, known as kinase insert domain receptor, is a type iii receptor tyrosine kinase This gene encodes a protein that belongs to the serine protease family

Complete information for yap1 gene (protein coding), yes1 associated transcriptional regulator, including

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. This gene encodes one of the two receptors of the vegf