abnormal urine ammonia level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any change in the amount of ammonia in urine (Mammalian Phenotype Ontology, MP_0011734)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011734
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3 gene mutations causing the abnormal urine ammonia level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
RHCG Rh family, C glycoprotein
SLC26A4 solute carrier family 26 (anion exchanger), member 4
UMOD uromodulin