albuminuria Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Increased concentration of albumin in the urine. (Human Phenotype Ontology, HP_0012592)
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40 gene mutations causing the albuminuria 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
ALMS1 Alstrom syndrome protein 1
C1GALT1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1
CD151 CD151 molecule (Raph blood group)
CD55 CD55 molecule, decay accelerating factor for complement (Cromer blood group)
CFH complement factor H
COL4A3 collagen, type IV, alpha 3 (Goodpasture antigen)
COMT catechol-O-methyltransferase
CRIM1 cysteine rich transmembrane BMP regulator 1 (chordin-like)
CXCR3 chemokine (C-X-C motif) receptor 3
ESR1 estrogen receptor 1
FAS Fas cell surface death receptor
GAS6 growth arrest-specific 6
GLIS2 GLIS family zinc finger 2
GNE glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
GRM1 glutamate receptor, metabotropic 1
HPRT1 hypoxanthine phosphoribosyltransferase 1
IFNG interferon, gamma
INS insulin
LAMB2 laminin, beta 2 (laminin S)
LAT linker for activation of T cells
LEP leptin
LEPR leptin receptor
LGMN legumain
LYN LYN proto-oncogene, Src family tyrosine kinase
MAS1 MAS1 proto-oncogene, G protein-coupled receptor
MPV17 MpV17 mitochondrial inner membrane protein
MYH9 myosin, heavy chain 9, non-muscle
MYO1E myosin IE
NOS3 nitric oxide synthase 3 (endothelial cell)
NPHS1 nephrosis 1, congenital, Finnish type (nephrin)
NPHS2 nephrosis 2, idiopathic, steroid-resistant (podocin)
PDGFB platelet-derived growth factor beta polypeptide
PDSS2 prenyl (decaprenyl) diphosphate synthase, subunit 2
SCARB2 scavenger receptor class B, member 2
SMARCAL1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1
STK39 serine threonine kinase 39
TNS2 tensin 2