kidney cortex cysts Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000522
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Genes

29 gene mutations causing the kidney cortex cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AQP11 aquaporin 11
BCL2 B-cell CLL/lymphoma 2
BDKRB2 bradykinin receptor B2
BICC1 BicC family RNA binding protein 1
CDKN2C cyclin-dependent kinase inhibitor 2C (p18, inhibits CDK4)
CHRNA3 cholinergic receptor, nicotinic, alpha 3 (neuronal)
CRIM1 cysteine rich transmembrane BMP regulator 1 (chordin-like)
CYS1 cystin 1
GDNF glial cell derived neurotrophic factor
GLIS2 GLIS family zinc finger 2
GLIS3 GLIS family zinc finger 3
GPC3 glypican 3
INPP5E inositol polyphosphate-5-phosphatase, 72 kDa
INVS inversin
MAFB v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog B
MKS1 Meckel syndrome, type 1
NEK1 NIMA-related kinase 1
NEK8 NIMA-related kinase 8
NPHS1 nephrosis 1, congenital, Finnish type (nephrin)
OVOL1 ovo-like zinc finger 1
PKD1 polycystic kidney disease 1 (autosomal dominant)
PKD2 polycystic kidney disease 2 (autosomal dominant)
PTGS2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)
SLC2A9 solute carrier family 2 (facilitated glucose transporter), member 9
TNS1 tensin 1
UOX urate oxidase, pseudogene
VHL von Hippel-Lindau tumor suppressor, E3 ubiquitin protein ligase
WT1 Wilms tumor 1
WWTR1 WW domain containing transcription regulator 1