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Function, proteins, disorders, pathways, orthologs, and expression. Complete information for nmnat2 gene (protein coding), nicotinamide nucleotide adenylyltransferase 2, including Complete information for slc12a3 gene (protein coding), solute carrier family 12 member 3, including

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Complete information for yap1 gene (protein coding), yes1 associated transcriptional regulator, including Mutations in this gene cause gaucher disease, a lysosomal storage disease characterized by an accumulation of glucocerebrosides. Diseases associated with map4k4 include anus, imperforate and renal dysplasia.

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

Complete information for kdr gene (protein coding), kinase insert domain receptor, including

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