abnormal circulating ammonia level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description aberrant amount of ammonia or its compounds in blood, formed in the body during organic decomposition (Mammalian Phenotype Ontology, MP_0005308)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005308
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13 gene mutations causing the abnormal circulating ammonia level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARG1 arginase 1
ASL argininosuccinate lyase
ASS1 argininosuccinate synthase 1
BTD biotinidase
CA5A carbonic anhydrase VA, mitochondrial
CPS1 carbamoyl-phosphate synthase 1, mitochondrial
HNF1A HNF1 homeobox A
NAGS N-acetylglutamate synthase
OAT ornithine aminotransferase
OTC ornithine carbamoyltransferase
PCK1 phosphoenolpyruvate carboxykinase 1 (soluble)
SLC22A5 solute carrier family 22 (organic cation/carnitine transporter), member 5
SLC7A7 solute carrier family 7 (amino acid transporter light chain, y+L system), member 7