abnormal circulating bicarbonate level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description aberrant concentration of inorganic salts that contain the -HCO3 radical in the circulation, which are an important factor in regulating the pH of the blood (Mammalian Phenotype Ontology, MP_0003015)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003015
Similar Terms
Downloads & Tools

Genes

13 gene mutations causing the abnormal circulating bicarbonate level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATP6V1B1 ATPase, H+ transporting, lysosomal 56/58kDa, V1 subunit B1
BSND barttin CLCNK-type chloride channel accessory beta subunit
CA2 carbonic anhydrase II
EDN2 endothelin 2
OXGR1 oxoglutarate (alpha-ketoglutarate) receptor 1
SLC26A4 solute carrier family 26 (anion exchanger), member 4
SLC26A7 solute carrier family 26 (anion exchanger), member 7
SLC4A1 solute carrier family 4 (anion exchanger), member 1 (Diego blood group)
SLC4A4 solute carrier family 4 (sodium bicarbonate cotransporter), member 4
SLC4A5 solute carrier family 4 (sodium bicarbonate cotransporter), member 5
SLC9A8 solute carrier family 9, subfamily A (NHE8, cation proton antiporter 8), member 8
WNK4 WNK lysine deficient protein kinase 4
WWOX WW domain containing oxidoreductase