proteinuria Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000093
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Genes

115 genes associated with the proteinuria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACSL4 acyl-CoA synthetase long-chain family member 4
ACTN4 actinin, alpha 4
ADAMTS13 ADAM metallopeptidase with thrombospondin type 1 motif, 13
ADCK4 aarF domain containing kinase 4
AMMECR1 Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1
AMN amnion associated transmembrane protein
APOA1 apolipoprotein A-I
APOE apolipoprotein E
ARHGDIA Rho GDP dissociation inhibitor (GDI) alpha
ATP7B ATPase, Cu++ transporting, beta polypeptide
BAZ1B bromodomain adjacent to zinc finger domain, 1B
CD2AP CD2-associated protein
CLCN5 chloride channel, voltage-sensitive 5
CLIP2 CAP-GLY domain containing linker protein 2
COA5 cytochrome c oxidase assembly factor 5
COL4A3 collagen, type IV, alpha 3 (Goodpasture antigen)
COL4A4 collagen, type IV, alpha 4
COL4A5 collagen, type IV, alpha 5
COQ6 coenzyme Q6 monooxygenase
COX1
COX10 COX10 heme A:farnesyltransferase cytochrome c oxidase assembly factor
COX14 COX14 cytochrome c oxidase assembly factor
COX2
COX20 COX20 cytochrome c oxidase assembly factor
COX3
COX6B1 cytochrome c oxidase subunit VIb polypeptide 1 (ubiquitous)
CTLA4 cytotoxic T-lymphocyte-associated protein 4
CTNS cystinosin, lysosomal cystine transporter
CUBN cubilin (intrinsic factor-cobalamin receptor)
DGKE diacylglycerol kinase, epsilon 64kDa
DNASE1L3 deoxyribonuclease I-like 3
EHHADH enoyl-CoA, hydratase/3-hydroxyacyl CoA dehydrogenase
ELN elastin
ERCC6 excision repair cross-complementation group 6
ERCC8 excision repair cross-complementation group 8
FAN1 FANCD2/FANCI-associated nuclease 1
FASTKD2 FAST kinase domains 2
FGA fibrinogen alpha chain
FN1 fibronectin 1
FOXC2 forkhead box C2
G6PC glucose-6-phosphatase, catalytic subunit
GATA3 GATA binding protein 3
GBA glucosidase, beta, acid
GLA galactosidase, alpha
GTF2I general transcription factor IIi
GTF2IRD1 GTF2I repeat domain containing 1
HLA-DPB1 major histocompatibility complex, class II, DP beta 1
HMOX1 heme oxygenase 1
HNF1B HNF1 homeobox B
INF2 inverted formin, FH2 and WH2 domain containing
INSR insulin receptor
ITGA8 integrin, alpha 8
KCNE5 potassium channel, voltage gated subfamily E regulatory beta subunit 5
KIF1B kinesin family member 1B
LAMB2 laminin, beta 2 (laminin S)
LCAT lecithin-cholesterol acyltransferase
LIMK1 LIM domain kinase 1
LMNB2 lamin B2
LMX1B LIM homeobox transcription factor 1, beta
LPIN2 lipin 2
LRP2 low density lipoprotein receptor-related protein 2
LYZ lysozyme
MAFB v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog B
MEFV Mediterranean fever
MMACHC methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
MT-ND4 NADH dehydrogenase, subunit 4 (complex I)
MT-ND5 NADH dehydrogenase, subunit 5 (complex I)
MT-ND6 NADH dehydrogenase, subunit 6 (complex I)
MT-TF tRNA
MT-TH tRNA
MT-TK tRNA
MT-TL1 tRNA
MT-TQ tRNA
MT-TS1 tRNA
MT-TS2 tRNA
MT-TW tRNA
MYH9 myosin, heavy chain 9, non-muscle
MYO1E myosin IE
ND1
NEU1 sialidase 1 (lysosomal sialidase)
NIPBL Nipped-B homolog (Drosophila)
NPHS1 nephrosis 1, congenital, Finnish type (nephrin)
NPHS2 nephrosis 2, idiopathic, steroid-resistant (podocin)
OCRL oculocerebrorenal syndrome of Lowe
OFD1 oral-facial-digital syndrome 1
PAX2 paired box 2
PDSS2 prenyl (decaprenyl) diphosphate synthase, subunit 2
PET100 PET100 homolog (S. cerevisiae)
PEX1 peroxisomal biogenesis factor 1
PLCE1 phospholipase C, epsilon 1
PMM2 phosphomannomutase 2
PRODH proline dehydrogenase (oxidase) 1
PRTN3 proteinase 3
PSTPIP1 proline-serine-threonine phosphatase interacting protein 1
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
PTPRO protein tyrosine phosphatase, receptor type, O
RAB40AL RAB40A, member RAS oncogene family-like
RET ret proto-oncogene
RFC2 replication factor C (activator 1) 2, 40kDa
SARS2 seryl-tRNA synthetase 2, mitochondrial
SCARB2 scavenger receptor class B, member 2
SDHB succinate dehydrogenase complex, subunit B, iron sulfur (Ip)
SDHD succinate dehydrogenase complex, subunit D, integral membrane protein
SLC37A4 solute carrier family 37 (glucose-6-phosphate transporter), member 4
SLITRK6 SLIT and NTRK-like family, member 6
SMARCAL1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1
SNAP29 synaptosomal-associated protein, 29kDa
TACO1 translational activator of mitochondrially encoded cytochrome c oxidase I
TBL2 transducin (beta)-like 2
TREX1 three prime repair exonuclease 1
TRNE
TRPC6 transient receptor potential cation channel, subfamily C, member 6
VHL von Hippel-Lindau tumor suppressor, E3 ubiquitin protein ligase
WDR19 WD repeat domain 19
WT1 Wilms tumor 1