abnormal renal glomerular capsule morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the expanded beginning of a nephron that contains the glomerulus (Mammalian Phenotype Ontology, MP_0002828)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002828
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Genes

81 gene mutations causing the abnormal renal glomerular capsule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
ACTN4 actinin, alpha 4
ADIPOQ adiponectin, C1Q and collagen domain containing
AMPD2 adenosine monophosphate deaminase 2
APRT adenine phosphoribosyltransferase
ARHGDIA Rho GDP dissociation inhibitor (GDI) alpha
BCL2 B-cell CLL/lymphoma 2
BDKRB2 bradykinin receptor B2
BICC1 BicC family RNA binding protein 1
BMP7 bone morphogenetic protein 7
C1GALT1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1
CCNI cyclin I
CCR2 chemokine (C-C motif) receptor 2
CD151 CD151 molecule (Raph blood group)
CD2AP CD2-associated protein
CD55 CD55 molecule, decay accelerating factor for complement (Cromer blood group)
COL18A1 collagen, type XVIII, alpha 1
COL4A3 collagen, type IV, alpha 3 (Goodpasture antigen)
COL4A5 collagen, type IV, alpha 5
CPB2 carboxypeptidase B2 (plasma)
CRIM1 cysteine rich transmembrane BMP regulator 1 (chordin-like)
DCN decorin
DDR1 discoidin domain receptor tyrosine kinase 1
FAM20C family with sequence similarity 20, member C
FAS Fas cell surface death receptor
FAT1 FAT atypical cadherin 1
FBLN1 fibulin 1
FOXC2 forkhead box C2
FRAS1 Fraser extracellular matrix complex subunit 1
GDNF glial cell derived neurotrophic factor
GLIS2 GLIS family zinc finger 2
GLIS3 GLIS family zinc finger 3
GNE glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
GOLM1 golgi membrane protein 1
GRM1 glutamate receptor, metabotropic 1
GSTK1 glutathione S-transferase kappa 1
HPRT1 hypoxanthine phosphoribosyltransferase 1
INPP5E inositol polyphosphate-5-phosphatase, 72 kDa
INVS inversin
ITGA1 integrin, alpha 1
ITGA3 integrin, alpha 3 (antigen CD49C, alpha 3 subunit of VLA-3 receptor)
LAMA5 laminin, alpha 5
LAMB2 laminin, beta 2 (laminin S)
LAMC1 laminin, gamma 1 (formerly LAMB2)
LEP leptin
LMX1B LIM homeobox transcription factor 1, beta
MAFB v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog B
MAS1 MAS1 proto-oncogene, G protein-coupled receptor
MKS1 Meckel syndrome, type 1
MPV17 MpV17 mitochondrial inner membrane protein
MXI1 MAX interactor 1, dimerization protein
MYH9 myosin, heavy chain 9, non-muscle
MYO1E myosin IE
NAGLU N-acetylglucosaminidase, alpha
NOS3 nitric oxide synthase 3 (endothelial cell)
NOTCH2 notch 2
NPHP3 nephronophthisis 3 (adolescent)
NPHS1 nephrosis 1, congenital, Finnish type (nephrin)
NPHS2 nephrosis 2, idiopathic, steroid-resistant (podocin)
PDGFRB platelet-derived growth factor receptor, beta polypeptide
PDSS2 prenyl (decaprenyl) diphosphate synthase, subunit 2
PEX13 peroxisomal biogenesis factor 13
PIK3C2A phosphatidylinositol-4-phosphate 3-kinase, catalytic subunit type 2 alpha
PKD2 polycystic kidney disease 2 (autosomal dominant)
PKHD1 polycystic kidney and hepatic disease 1 (autosomal recessive)
PODXL podocalyxin-like
PPT1 palmitoyl-protein thioesterase 1
PTGIS prostaglandin I2 (prostacyclin) synthase
PTPRO protein tyrosine phosphatase, receptor type, O
RASGRP1 RAS guanyl releasing protein 1 (calcium and DAG-regulated)
RET ret proto-oncogene
RRM2B ribonucleotide reductase M2 B (TP53 inducible)
SCTR secretin receptor
SYK spleen tyrosine kinase
TAL1 T-cell acute lymphocytic leukemia 1
TCF21 transcription factor 21
TNS1 tensin 1
UMOD uromodulin
UOX urate oxidase, pseudogene
WT1 Wilms tumor 1
WWTR1 WW domain containing transcription regulator 1