abnormal external auditory canal morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the canal that connects the outer and middle ear (Mammalian Phenotype Ontology, MP_0006033)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006033
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14 gene mutations causing the abnormal external auditory canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CTSV cathepsin V
DLX5 distal-less homeobox 5
ECE1 endothelin converting enzyme 1
EYA1 EYA transcriptional coactivator and phosphatase 1
FBXO11 F-box protein 11
FGFR1 fibroblast growth factor receptor 1
GSC goosecoid homeobox
HOXA2 homeobox A2
IDUA iduronidase, alpha-L-
PAX8 paired box 8
PRKRA protein kinase, interferon-inducible double stranded RNA dependent activator
SFN stratifin
TBX1 T-box 1
TSHZ1 teashirt zinc finger homeobox 1