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This cotransporter mediates sodium and chloride reabsorption in the distal convoluted tubule. Diseases associated with fndc5 include acanthosis nigricans and gastric adenosquamous carcinoma. Complete information for yap1 gene (protein coding), yes1 associated transcriptional regulator, including
Gene
Function, proteins, disorders, pathways, orthologs, and expression. Fndc5 (fibronectin type iii domain containing 5) is a protein coding gene Lrrk2 (leucine rich repeat kinase 2) is a protein coding gene
Diseases associated with lrrk2 include parkinson disease 8, autosomal dominant and parkinson's disease.
The protein encoded by this gene is part of a complex of proteins that constitute adherens junctions (ajs) Ajs are necessary for the creation and maintenance of epithelial cell layers by regulating cell growth and adhesion between cells. Mutations in this gene cause gaucher disease, a lysosomal storage disease characterized by an accumulation of glucocerebrosides. 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.
Function, proteins, disorders, pathways, orthologs, and expression
