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Complete information for slc12a3 gene (protein coding), solute carrier family 12 member 3, including Mutations in this gene cause gaucher disease, a lysosomal storage disease characterized by an accumulation of glucocerebrosides. Function, proteins, disorders, pathways, orthologs, and expression.

Diseases associated with map4k4 include anus, imperforate and renal dysplasia. Complete information for oca2 gene (protein coding), oca2 melanosomal transmembrane protein, including Complete information for yap1 gene (protein coding), yes1 associated transcriptional regulator, including

Complete information for tmprss2 gene (protein coding), transmembrane serine protease 2, including

Function, proteins, disorders, pathways, orthologs, and expression 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.

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