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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. Complete information for nmnat2 gene (protein coding), nicotinamide nucleotide adenylyltransferase 2, including 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 This gene encodes a protein that is instrumental in patterning the early embryo
