pale kidney Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description kidney lacks normal reddish coloration; often occurs with a bloodless or reduced vasculature condition (Mammalian Phenotype Ontology, MP_0004969)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004969
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Genes

31 gene mutations causing the pale kidney phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACTN4 actinin, alpha 4
AQP11 aquaporin 11
ARID5B AT rich interactive domain 5B (MRF1-like)
BCL2 B-cell CLL/lymphoma 2
CHD2 chromodomain helicase DNA binding protein 2
COL4A3 collagen, type IV, alpha 3 (Goodpasture antigen)
COL4A4 collagen, type IV, alpha 4
COL4A5 collagen, type IV, alpha 5
FAH fumarylacetoacetate hydrolase (fumarylacetoacetase)
FOXP3 forkhead box P3
GLIS2 GLIS family zinc finger 2
GNE glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
GOLM1 golgi membrane protein 1
HSD17B2 hydroxysteroid (17-beta) dehydrogenase 2
KMT2A lysine (K)-specific methyltransferase 2A
LGMN legumain
LIPA lipase A, lysosomal acid, cholesterol esterase
MYO1E myosin IE
PDSS2 prenyl (decaprenyl) diphosphate synthase, subunit 2
PIK3C2A phosphatidylinositol-4-phosphate 3-kinase, catalytic subunit type 2 alpha
PTGS2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)
RRM2B ribonucleotide reductase M2 B (TP53 inducible)
SGPL1 sphingosine-1-phosphate lyase 1
TIPARP TCDD-inducible poly(ADP-ribose) polymerase
TNS1 tensin 1
TTC7A tetratricopeptide repeat domain 7A
UOX urate oxidase, pseudogene
VEGFA vascular endothelial growth factor A
WWTR1 WW domain containing transcription regulator 1
XDH xanthine dehydrogenase
ZFP36L2 ZFP36 ring finger protein-like 2