increased kidney weight Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description greater weight of the organs responsible for urine secretion (Mammalian Phenotype Ontology, MP_0003917)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003917
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Genes

46 gene mutations causing the increased kidney weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADAMTS1 ADAM metallopeptidase with thrombospondin type 1 motif, 1
AGPAT2 1-acylglycerol-3-phosphate O-acyltransferase 2
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
ALMS1 Alstrom syndrome protein 1
ANK1 ankyrin 1, erythrocytic
ANKRD26 ankyrin repeat domain 26
ATP12A ATPase, H+/K+ transporting, nongastric, alpha polypeptide
BCKDK branched chain ketoacid dehydrogenase kinase
CAV1 caveolin 1, caveolae protein, 22kDa
CDKN1A cyclin-dependent kinase inhibitor 1A (p21, Cip1)
CDKN1B cyclin-dependent kinase inhibitor 1B (p27, Kip1)
CXCR2 chemokine (C-X-C motif) receptor 2
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2
CYS1 cystin 1
DFNB31 deafness, autosomal recessive 31
FABP2 fatty acid binding protein 2, intestinal
FAIM2 Fas apoptotic inhibitory molecule 2
G6PC glucose-6-phosphatase, catalytic subunit
GDF15 growth differentiation factor 15
GDNF glial cell derived neurotrophic factor
GSTK1 glutathione S-transferase kappa 1
GSTZ1 glutathione S-transferase zeta 1
HP haptoglobin
INVS inversin
KLF3 Kruppel-like factor 3 (basic)
LEP leptin
LHCGR luteinizing hormone/choriogonadotropin receptor
LRRK2 leucine-rich repeat kinase 2
LYST lysosomal trafficking regulator
MARVELD2 MARVEL domain containing 2
MGP matrix Gla protein
MPV17 MpV17 mitochondrial inner membrane protein
MYO1E myosin IE
NEK8 NIMA-related kinase 8
NPHP3 nephronophthisis 3 (adolescent)
NPHS1 nephrosis 1, congenital, Finnish type (nephrin)
OCA2 oculocutaneous albinism II
PKD1 polycystic kidney disease 1 (autosomal dominant)
PKD2 polycystic kidney disease 2 (autosomal dominant)
PKHD1 polycystic kidney and hepatic disease 1 (autosomal recessive)
PLCB1 phospholipase C, beta 1 (phosphoinositide-specific)
PREP prolyl endopeptidase
RDH16 retinol dehydrogenase 16 (all-trans)
UBE2E2 ubiquitin-conjugating enzyme E2E 2
XYLT2 xylosyltransferase II
ZMPSTE24 zinc metallopeptidase STE24