impaired branching involved in ureteric bud morphogenesis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description partial or complete failure of the ureteric bud to repeatedly divide into lobules during development of the kidney (Mammalian Phenotype Ontology, MP_0004936)
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37 gene mutations causing the impaired branching involved in ureteric bud morphogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATMIN ATM interactor
BAG6 BCL2-associated athanogene 6
BCL2 B-cell CLL/lymphoma 2
CDH4 cadherin 4, type 1, R-cadherin (retinal)
CTNNBIP1 catenin, beta interacting protein 1
DCHS1 dachsous cadherin-related 1
DLG1 discs, large homolog 1 (Drosophila)
EMX2 empty spiracles homeobox 2
FAT4 FAT atypical cadherin 4
FGF7 fibroblast growth factor 7
FGFRL1 fibroblast growth factor receptor-like 1
FOXD1 forkhead box D1
FRAS1 Fraser extracellular matrix complex subunit 1
GDF11 growth differentiation factor 11
GDNF glial cell derived neurotrophic factor
GFRA1 GDNF family receptor alpha 1
GPC3 glypican 3
GREM1 gremlin 1, DAN family BMP antagonist
HS2ST1 heparan sulfate 2-O-sulfotransferase 1
ILK integrin-linked kinase
ITGA8 integrin, alpha 8
KIF26B kinesin family member 26B
LAMA5 laminin, alpha 5
LGR4 leucine-rich repeat containing G protein-coupled receptor 4
LRP4 low density lipoprotein receptor-related protein 4
MMP14 matrix metallopeptidase 14 (membrane-inserted)
NOTCH2 notch 2
NPNT nephronectin
PARVA parvin, alpha
PAX2 paired box 2
PBX1 pre-B-cell leukemia homeobox 1
RET ret proto-oncogene
SALL1 spalt-like transcription factor 1
SIX2 SIX homeobox 2
TCF21 transcription factor 21
WNT11 wingless-type MMTV integration site family, member 11
WNT9B wingless-type MMTV integration site family, member 9B