abnormal urine color Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any alteration from the usual straw-coloration of the urine (Mammalian Phenotype Ontology, MP_0003619)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003619
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13 gene mutations causing the abnormal urine color phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGA aspartylglucosaminidase
APRT adenine phosphoribosyltransferase
AQP2 aquaporin 2 (collecting duct)
CHRNA3 cholinergic receptor, nicotinic, alpha 3 (neuronal)
CYS1 cystin 1
HGD homogentisate 1,2-dioxygenase
HMBS hydroxymethylbilane synthase
PDSS2 prenyl (decaprenyl) diphosphate synthase, subunit 2
TTC7A tetratricopeptide repeat domain 7A
UOX urate oxidase, pseudogene
UROS uroporphyrinogen III synthase
VAMP8 vesicle-associated membrane protein 8
XPNPEP1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble