delayed kidney development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description late onset of the induction and/or differentiation of the kidney (Mammalian Phenotype Ontology, MP_0000528)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000528
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Genes

17 gene mutations causing the delayed kidney development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BCL2 B-cell CLL/lymphoma 2
CBS cystathionine-beta-synthase
CTNNBIP1 catenin, beta interacting protein 1
FOXD1 forkhead box D1
FRAS1 Fraser extracellular matrix complex subunit 1
GNAS GNAS complex locus
IGF2BP1 insulin-like growth factor 2 mRNA binding protein 1
NF1 neurofibromin 1
PBX1 pre-B-cell leukemia homeobox 1
PEX5 peroxisomal biogenesis factor 5
POU3F3 POU class 3 homeobox 3
PTRH2 peptidyl-tRNA hydrolase 2
RSPO2 R-spondin 2
TCF21 transcription factor 21
WNT11 wingless-type MMTV integration site family, member 11
WNT4 wingless-type MMTV integration site family, member 4
WNT9B wingless-type MMTV integration site family, member 9B