abnormal carbon dioxide level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomalous concentration of CO2 in the blood, alveoli or other tissues resulting in the increased pressure of this component of body gases (Mammalian Phenotype Ontology, MP_0003860)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003860
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8 gene mutations causing the abnormal carbon dioxide level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACSS1 acyl-CoA synthetase short-chain family member 1
BCKDK branched chain ketoacid dehydrogenase kinase
EDN1 endothelin 1
EDN2 endothelin 2
EDNRB endothelin receptor type B
HIF1AN hypoxia inducible factor 1, alpha subunit inhibitor
RYR1 ryanodine receptor 1 (skeletal)
SOD2 superoxide dismutase 2, mitochondrial