abnormal blood ph regulation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the function of the buffer systems of the blood in combination with the respiratory and renal systems that control the relative acidity or alkalinity of the blood, as measured by the concentration of the hydrogen ion (Mammalian Phenotype Ontology, MP_0003027)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003027
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8 gene mutations causing the abnormal blood ph regulation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
EDN2 endothelin 2
MUT methylmalonyl CoA mutase
RYR1 ryanodine receptor 1 (skeletal)
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
SLC9A3 solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3
SOD2 superoxide dismutase 2, mitochondrial