hydronephrosis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000519
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Genes

78 gene mutations causing the hydronephrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
ADAMTS1 ADAM metallopeptidase with thrombospondin type 1 motif, 1
AGA aspartylglucosaminidase
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
AGTR2 angiotensin II receptor, type 2
APRT adenine phosphoribosyltransferase
AQP2 aquaporin 2 (collecting duct)
ATP6V0A4 ATPase, H+ transporting, lysosomal V0 subunit a4
AVPR2 arginine vasopressin receptor 2
BMP4 bone morphogenetic protein 4
BMP5 bone morphogenetic protein 5
BMPR2 bone morphogenetic protein receptor, type II (serine/threonine kinase)
BSND barttin CLCNK-type chloride channel accessory beta subunit
CCDC39 coiled-coil domain containing 39
CHRM3 cholinergic receptor, muscarinic 3
CHRNA3 cholinergic receptor, nicotinic, alpha 3 (neuronal)
CLDN4 claudin 4
CLEC6A C-type lectin domain family 6, member A
CNTRL centriolin
CRIM1 cysteine rich transmembrane BMP regulator 1 (chordin-like)
CXCR4 chemokine (C-X-C motif) receptor 4
DACT1 dishevelled-binding antagonist of beta-catenin 1
DCN decorin
DLG1 discs, large homolog 1 (Drosophila)
DNAH11 dynein, axonemal, heavy chain 11
DNAH5 dynein, axonemal, heavy chain 5
DNM2 dynamin 2
DYM dymeclin
FAIM2 Fas apoptotic inhibitory molecule 2
FOXC1 forkhead box C1
FOXD2 forkhead box D2
FSTL1 follistatin-like 1
GATA2 GATA binding protein 2
GNE glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
GPC3 glypican 3
HIVEP3 human immunodeficiency virus type I enhancer binding protein 3
HOXA13 homeobox A13
HSPA4L heat shock 70kDa protein 4-like
HTR3A 5-hydroxytryptamine (serotonin) receptor 3A, ionotropic
ID2 inhibitor of DNA binding 2, dominant negative helix-loop-helix protein
IMPA2 inositol(myo)-1(or 4)-monophosphatase 2
INS insulin
KCNJ1 potassium channel, inwardly rectifying subfamily J, member 1
LAMC1 laminin, gamma 1 (formerly LAMB2)
LGMN legumain
LRP2 low density lipoprotein receptor-related protein 2
LZTS2 leucine zipper, putative tumor suppressor 2
MET MET proto-oncogene, receptor tyrosine kinase
MYH11 myosin, heavy chain 11, smooth muscle
NDST1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1
NEDD4L neural precursor cell expressed, developmentally down-regulated 4-like, E3 ubiquitin protein ligase
NEU1 sialidase 1 (lysosomal sialidase)
NFIA nuclear factor I/A
PAX2 paired box 2
PDGFRA platelet-derived growth factor receptor, alpha polypeptide
PORCN porcupine homolog (Drosophila)
PSAP prosaposin
REN renin
RET ret proto-oncogene
ROBO1 roundabout, axon guidance receptor, homolog 1 (Drosophila)
SCARB2 scavenger receptor class B, member 2
SESTD1 SEC14 and spectrin domains 1
SGSH N-sulfoglucosamine sulfohydrolase
SLC12A1 solute carrier family 12 (sodium/potassium/chloride transporter), member 1
SLC2A9 solute carrier family 2 (facilitated glucose transporter), member 9
SLC7A9 solute carrier family 7 (amino acid transporter light chain, bo,+ system), member 9
SPTB spectrin, beta, erythrocytic
TGFB2 transforming growth factor, beta 2
TIMP3 TIMP metallopeptidase inhibitor 3
TSHZ3 teashirt zinc finger homeobox 3
UMOD uromodulin
UOX urate oxidase, pseudogene
UPK2 uroplakin 2
UPK3A uroplakin 3A
VAMP8 vesicle-associated membrane protein 8
WWTR1 WW domain containing transcription regulator 1
XYLT2 xylosyltransferase II
ZBTB14 zinc finger and BTB domain containing 14