abnormal urine glucose level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any change in the amount of glucose in the urine (Mammalian Phenotype Ontology, MP_0001758)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001758
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Genes

20 gene mutations causing the abnormal urine glucose level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AQP7 aquaporin 7
ASIP agouti signaling protein
CDK4 cyclin-dependent kinase 4
CLCN5 chloride channel, voltage-sensitive 5
CRH corticotropin releasing hormone
DNAJC3 DnaJ (Hsp40) homolog, subfamily C, member 3
GCK glucokinase (hexokinase 4)
GDF15 growth differentiation factor 15
HNF1A HNF1 homeobox A
INS insulin
INSR insulin receptor
LEP leptin
LEPR leptin receptor
MAF v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog
MAFA v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog A
NEUROG3 neurogenin 3
SCARB2 scavenger receptor class B, member 2
SIM1 single-minded family bHLH transcription factor 1
SLC5A1 solute carrier family 5 (sodium/glucose cotransporter), member 1
SLC5A2 solute carrier family 5 (sodium/glucose cotransporter), member 2