abnormal metanephros morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the primordium of the permanent kidney, which develops later than and caudal to the mesonephros, from the mesonephric duct and nephrogenic cord; the metanephros is an endocrine and metabolic organ that filters the blood and excretes the end products of body metabolism in the form of urine (Mammalian Phenotype Ontology, MP_0011364)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011364
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20 gene mutations causing the abnormal metanephros morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BCL2 B-cell CLL/lymphoma 2
CTNNBIP1 catenin, beta interacting protein 1
DLG1 discs, large homolog 1 (Drosophila)
FGFRL1 fibroblast growth factor receptor-like 1
FOXC1 forkhead box C1
FRAS1 Fraser extracellular matrix complex subunit 1
GDF11 growth differentiation factor 11
GREM1 gremlin 1, DAN family BMP antagonist
LAMC1 laminin, gamma 1 (formerly LAMB2)
LGR4 leucine-rich repeat containing G protein-coupled receptor 4
LHX1 LIM homeobox 1
NF1 neurofibromin 1
OSR1 odd-skipped related transciption factor 1
PAX2 paired box 2
PBX1 pre-B-cell leukemia homeobox 1
PLXNB1 plexin B1
RDH10 retinol dehydrogenase 10 (all-trans)
SIX1 SIX homeobox 1
WNT4 wingless-type MMTV integration site family, member 4
WT1 Wilms tumor 1