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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.

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