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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Genes

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