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This cotransporter mediates sodium and chloride reabsorption in the distal convoluted tubule. Diseases associated with fndc5 include acanthosis nigricans and gastric adenosquamous carcinoma. Complete information for yap1 gene (protein coding), yes1 associated transcriptional regulator, including
Gene | Definition, Structure, Expression, & Facts | Britannica
Function, proteins, disorders, pathways, orthologs, and expression. Fndc5 (fibronectin type iii domain containing 5) is a protein coding gene 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 Mutations in this gene cause gaucher disease, a lysosomal storage disease characterized by an accumulation of glucocerebrosides. Complete information for nmnat2 gene (protein coding), nicotinamide nucleotide adenylyltransferase 2, including Muts beta initiates mismatch repair by binding to a mismatch and then forming a complex with mutl alpha heterodimer.
