Albuminuria Gene Set

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

26 genes associated with the trait Albuminuria in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Symbol Name Standardized Value
SSBP2 single-stranded DNA binding protein 2 1.47181
CDKAL1 CDK5 regulatory subunit associated protein 1-like 1 1.42272
DPP4 dipeptidyl-peptidase 4 1.37999
EIF3A eukaryotic translation initiation factor 3, subunit A 1.2906
MICU3 mitochondrial calcium uptake family, member 3 1.26816
MREG melanoregulin 1.20852
CUBN cubilin (intrinsic factor-cobalamin receptor) 1.01477
CCSER1 coiled-coil serine-rich protein 1 0.771893
MALRD1 MAM and LDL receptor class A domain containing 1 0.718407
DOK5 docking protein 5 0.668768
DECR1 2,4-dienoyl CoA reductase 1, mitochondrial 0.609535
SPAG16 sperm associated antigen 16 0.571899
NPAS3 neuronal PAS domain protein 3 0.570823
RAD54B RAD54 homolog B (S. cerevisiae) 0.498402
PTPRK protein tyrosine phosphatase, receptor type, K 0.437739
ADAM23 ADAM metallopeptidase domain 23 0.403164
FGD4 FYVE, RhoGEF and PH domain containing 4 0.224716
SLC35F3 solute carrier family 35, member F3 0.207451
EFHC1 EF-hand domain (C-terminal) containing 1 0.112386
RPH3A rabphilin 3A 0.105922
SMIM23 small integral membrane protein 23 0.103467
DISC1 disrupted in schizophrenia 1 0.101514
HS6ST3 heparan sulfate 6-O-sulfotransferase 3 0.101028
GLI3 GLI family zinc finger 3 0.092042
SLC35F4 solute carrier family 35, member F4 0.091165
CLEC1B C-type lectin domain family 1, member B 0.057776