albuminuria Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Increased concentration of albumin in the urine. (Human Phenotype Ontology, HP_0012592)
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Genes

33 genes associated with the disease albuminuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
ADAM23 ADAM metallopeptidase domain 23
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
AGTR2 angiotensin II receptor, type 2
CCL5 chemokine (C-C motif) ligand 5
CCSER1 coiled-coil serine-rich protein 1
CDKAL1 CDK5 regulatory subunit associated protein 1-like 1
CLEC1B C-type lectin domain family 1, member B
CUBN cubilin (intrinsic factor-cobalamin receptor)
DECR1 2,4-dienoyl CoA reductase 1, mitochondrial
DISC1 disrupted in schizophrenia 1
DOK5 docking protein 5
DPP4 dipeptidyl-peptidase 4
EFHC1 EF-hand domain (C-terminal) containing 1
EIF3A eukaryotic translation initiation factor 3, subunit A
FGD4 FYVE, RhoGEF and PH domain containing 4
GLI3 GLI family zinc finger 3
HS6ST3 heparan sulfate 6-O-sulfotransferase 3
MALRD1 MAM and LDL receptor class A domain containing 1
MICU3 mitochondrial calcium uptake family, member 3
MREG melanoregulin
NPAS3 neuronal PAS domain protein 3
NPHS2 nephrosis 2, idiopathic, steroid-resistant (podocin)
NPPA natriuretic peptide A
PTPRK protein tyrosine phosphatase, receptor type, K
RAD54B RAD54 homolog B (S. cerevisiae)
RPH3A rabphilin 3A
SELP selectin P (granule membrane protein 140kDa, antigen CD62)
SLC35F3 solute carrier family 35, member F3
SLC35F4 solute carrier family 35, member F4
SMIM23 small integral membrane protein 23
SPAG16 sperm associated antigen 16
SSBP2 single-stranded DNA binding protein 2