S12A3 Rabbit Polyclonal Antibody, 100ul Peptide Synthesis Mutations in this gene may

Mutations in this gene may be associated with iron overload in human patients

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This gene has been implicated in numerous human cancers and may act as a metastasis suppressor gene

This gene encodes a nuclear transcription factor that belongs to the NK-linked or NK-like (NKL) subfamily of homeobox genes

S12A3 Rabbit Polyclonal Antibody, 100ul Peptide Synthesis Mutations in this gene mayThis gene encodes a renal thiazide sensitive sodium chloride cotransporter that is important for electrolyte homeostasis. This cotransporter mediates sodium and chloride reabsorption in the distal convoluted tubule. Mutations in this gene cause Gitelman syndrome a disease similar to Bartter's syndrome that is characterized by hypokalemic alkalosis combined with hypomagnesemia low urinary calcium and increased renin activity associated with normal