abnormal urine cytology Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An anomalous finding in the examination of the urine for cells. (Human Phenotype Ontology, HP_0012614)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012614
Similar Terms
Downloads & Tools

Genes

65 genes associated with the abnormal urine cytology 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
ACVRL1 activin A receptor type II-like 1
ADAMTS13 ADAM metallopeptidase with thrombospondin type 1 motif, 13
AGGF1 angiogenic factor with G patch and FHA domains 1
AGXT alanine-glyoxylate aminotransferase
AMMECR1 Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1
APOA1 apolipoprotein A-I
APRT adenine phosphoribosyltransferase
CARD9 caspase recruitment domain family, member 9
CD2AP CD2-associated protein
CFH complement factor H
CFHR5 complement factor H-related 5
CLCN5 chloride channel, voltage-sensitive 5
CLDN16 claudin 16
CLDN19 claudin 19
CLEC7A C-type lectin domain family 7, member A
COL3A1 collagen, type III, alpha 1
COL4A1 collagen, type IV, alpha 1
COL4A3 collagen, type IV, alpha 3 (Goodpasture antigen)
COL4A4 collagen, type IV, alpha 4
COL4A5 collagen, type IV, alpha 5
CTLA4 cytotoxic T-lymphocyte-associated protein 4
CTNS cystinosin, lysosomal cystine transporter
DIS3L2 DIS3 like 3'-5' exoribonuclease 2
DNASE1L3 deoxyribonuclease I-like 3
ENG endoglin
FAN1 FANCD2/FANCI-associated nuclease 1
FGA fibrinogen alpha chain
FN1 fibronectin 1
GATA3 GATA binding protein 3
GBA glucosidase, beta, acid
GDF2 growth differentiation factor 2
GLA galactosidase, alpha
H19 H19, imprinted maternally expressed transcript (non-protein coding)
HBB hemoglobin, beta
HLA-DPB1 major histocompatibility complex, class II, DP beta 1
HMOX1 heme oxygenase 1
HPRT1 hypoxanthine phosphoribosyltransferase 1
IL17F interleukin 17F
IL17RA interleukin 17 receptor A
KCNE5 potassium channel, voltage gated subfamily E regulatory beta subunit 5
LAMB2 laminin, beta 2 (laminin S)
LMNB2 lamin B2
LMX1B LIM homeobox transcription factor 1, beta
LPIN2 lipin 2
LYZ lysozyme
MMACHC methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
MYH9 myosin, heavy chain 9, non-muscle
MYO1E myosin IE
OCRL oculocerebrorenal syndrome of Lowe
POU6F2 POU class 6 homeobox 2
PRTN3 proteinase 3
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
SCARB2 scavenger receptor class B, member 2
SLC37A4 solute carrier family 37 (glucose-6-phosphate transporter), member 4
SLITRK6 SLIT and NTRK-like family, member 6
SMAD4 SMAD family member 4
STAT1 signal transducer and activator of transcription 1, 91kDa
TRAF3IP2 TRAF3 interacting protein 2
TREX1 three prime repair exonuclease 1
TSC1 tuberous sclerosis 1
TSC2 tuberous sclerosis 2
UMPS uridine monophosphate synthetase
WT1 Wilms tumor 1
YAP1 Yes-associated protein 1