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This gene encodes one member of the sodium channel alpha subunit gene family Mutations in this gene cause gaucher disease, a lysosomal storage disease characterized by an accumulation of glucocerebrosides. Allelic variants of this gene are associated with seizure disorders and autism spectrum disorder.
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This cotransporter mediates sodium and chloride reabsorption in the distal convoluted tubule. This gene encodes a protein that is instrumental in patterning the early embryo Complete information for yap1 gene (protein coding), yes1 associated transcriptional regulator, including
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Function, proteins, disorders, pathways, orthologs, and expression.
This gene encodes a protein that belongs to the serine protease family This gene encodes one of the two receptors of the vegf This receptor, known as kinase insert domain receptor, is a type iii receptor tyrosine kinase Complete information for nmnat2 gene (protein coding), nicotinamide nucleotide adenylyltransferase 2, including
