abnormal otic vesicle morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the paired sacs of invaginated ectoderm that develop into the membraneous labyrinth of the inner ear (Mammalian Phenotype Ontology, MP_0009806)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009806
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Genes

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

Symbol Name
ALDH1A2 aldehyde dehydrogenase 1 family, member A2
APAF1 apoptotic peptidase activating factor 1
CHD7 chromodomain helicase DNA binding protein 7
CHRD chordin
CSK c-src tyrosine kinase
CSNK2A1 casein kinase 2, alpha 1 polypeptide
DLX5 distal-less homeobox 5
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
GBX2 gastrulation brain homeobox 2
GLI3 GLI family zinc finger 3
GRB2 growth factor receptor-bound protein 2
HESX1 HESX homeobox 1
HOXA1 homeobox A1
LMO4 LIM domain only 4
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
TBX1 T-box 1
TCOF1 Treacher Collins-Franceschetti syndrome 1
VANGL2 VANGL planar cell polarity protein 2