abnormal otic capsule morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the cartilage or bony capsule surrounding the inner ear mechanism (Mammalian Phenotype Ontology, MP_0000039)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000039
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Genes

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

Symbol Name
CHRD chordin
DLX5 distal-less homeobox 5
DUSP6 dual specificity phosphatase 6
FGF10 fibroblast growth factor 10
FGFR2 fibroblast growth factor receptor 2
GBX2 gastrulation brain homeobox 2
GLI3 GLI family zinc finger 3
HOXA1 homeobox A1
HOXA2 homeobox A2
IGF1 insulin-like growth factor 1 (somatomedin C)
MAFB v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog B
PHEX phosphate regulating endopeptidase homolog, X-linked
PRRX1 paired related homeobox 1
SIX1 SIX homeobox 1
TBX1 T-box 1
TNFRSF11B tumor necrosis factor receptor superfamily, member 11b