renal tubular acidosis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A renal tubular transport disease characterized by excess levels of acid in the blood, due to a failure of the kidneys to appropriately acidify the urine. (Human Disease Ontology, DOID_14219)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000525
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Genes

8 gene mutations causing the renal tubular acidosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CA2 carbonic anhydrase II
FOXI1 forkhead box I1
RHCG Rh family, C glycoprotein
SLC12A7 solute carrier family 12 (potassium/chloride transporter), member 7
SLC26A7 solute carrier family 26 (anion exchanger), member 7
SLC4A4 solute carrier family 4 (sodium bicarbonate cotransporter), member 4
SLC4A5 solute carrier family 4 (sodium bicarbonate cotransporter), member 5
SLC9A3 solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3