crystalluria Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description excretion of crystalline material in the urine (Mammalian Phenotype Ontology, MP_0009645)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009645
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Genes

10 gene mutations causing the crystalluria phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGXT alanine-glyoxylate aminotransferase
ALMS1 Alstrom syndrome protein 1
APRT adenine phosphoribosyltransferase
SLC3A1 solute carrier family 3 (amino acid transporter heavy chain), member 1
SLC7A9 solute carrier family 7 (amino acid transporter light chain, bo,+ system), member 9
SPP1 secreted phosphoprotein 1
TMEM27 transmembrane protein 27
UMOD uromodulin
UOX urate oxidase, pseudogene
XDH xanthine dehydrogenase