glomerulopathy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Inflammatory or noninflammatory diseases affecting the glomeruli of the nephron. (Human Phenotype Ontology, HP_0100820)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100820
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Genes

52 genes associated with the glomerulopathy 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
AGPAT2 1-acylglycerol-3-phosphate O-acyltransferase 2
ALMS1 Alstrom syndrome protein 1
AMMECR1 Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1
APOE apolipoprotein E
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin)
C4A complement component 4A (Rodgers blood group)
CAV1 caveolin 1, caveolae protein, 22kDa
COX1
COX2
COX3
CTLA4 cytotoxic T-lymphocyte-associated protein 4
DNASE1L3 deoxyribonuclease I-like 3
FN1 fibronectin 1
FOS FBJ murine osteosarcoma viral oncogene homolog
FOXC2 forkhead box C2
GLA galactosidase, alpha
HLA-B major histocompatibility complex, class I, B
HLA-DPB1 major histocompatibility complex, class II, DP beta 1
IKBKAP inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein
IL10 interleukin 10
IL12RB2 interleukin 12 receptor, beta 2
IL23R interleukin 23 receptor
KCNE5 potassium channel, voltage gated subfamily E regulatory beta subunit 5
LMNA lamin A/C
LMNB2 lamin B2
LMX1B LIM homeobox transcription factor 1, beta
LPIN2 lipin 2
MEFV Mediterranean fever
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
ND1
NOD2 nucleotide-binding oligomerization domain containing 2
OCRL oculocerebrorenal syndrome of Lowe
PRTN3 proteinase 3
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
SMARCAL1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1
STAT4 signal transducer and activator of transcription 4
TLR4 toll-like receptor 4
TRNE
WAS Wiskott-Aldrich syndrome
WIPF1 WAS/WASL interacting protein family, member 1
WT1 Wilms tumor 1