abnormal otic vesicle development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the formation of the simple epithelial sac formed from the otic placode that gives rise to the structures of the inner ear (Mammalian Phenotype Ontology, MP_0006030)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006030
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Genes

20 gene mutations causing the abnormal otic vesicle development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APAF1 apoptotic peptidase activating factor 1
CHD7 chromodomain helicase DNA binding protein 7
CSK c-src tyrosine kinase
CSNK2A1 casein kinase 2, alpha 1 polypeptide
EYA1 EYA transcriptional coactivator and phosphatase 1
FBLN1 fibulin 1
FGF3 fibroblast growth factor 3
FGFR2 fibroblast growth factor receptor 2
FOXC2 forkhead box C2
GATA3 GATA binding protein 3
GLI3 GLI family zinc finger 3
GRB2 growth factor receptor-bound protein 2
HOXA1 homeobox A1
LMX1A LIM homeobox transcription factor 1, alpha
MAFB v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog B
PAX3 paired box 3
RDH10 retinol dehydrogenase 10 (all-trans)
SHH sonic hedgehog
SIX1 SIX homeobox 1
VANGL2 VANGL planar cell polarity protein 2