abnormal glomerular capsule space morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the luminal region between the glomerular capsule visceral and parietal layers, into which filtrate enters after passing through the filtration barrier from the glomerular capillaries (Mammalian Phenotype Ontology, MP_0011499)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011499
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21 gene mutations causing the abnormal glomerular capsule space morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
BCL2 B-cell CLL/lymphoma 2
BDKRB2 bradykinin receptor B2
BICC1 BicC family RNA binding protein 1
CRIM1 cysteine rich transmembrane BMP regulator 1 (chordin-like)
DCN decorin
FRAS1 Fraser extracellular matrix complex subunit 1
GLIS2 GLIS family zinc finger 2
GLIS3 GLIS family zinc finger 3
GNE glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
INVS inversin
MXI1 MAX interactor 1, dimerization protein
NPHS1 nephrosis 1, congenital, Finnish type (nephrin)
PKD2 polycystic kidney disease 2 (autosomal dominant)
PKHD1 polycystic kidney and hepatic disease 1 (autosomal recessive)
RRM2B ribonucleotide reductase M2 B (TP53 inducible)
SCTR secretin receptor
TNS1 tensin 1
UOX urate oxidase, pseudogene
WT1 Wilms tumor 1
WWTR1 WW domain containing transcription regulator 1