abnormal tympanic ring morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the bony ring at the ear canal to which the tympanic membrane is attached (Mammalian Phenotype Ontology, MP_0000030)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000030
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Genes

31 gene mutations causing the abnormal tympanic ring morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BMPER BMP binding endothelial regulator
CHRD chordin
DLX5 distal-less homeobox 5
ECE1 endothelin converting enzyme 1
EDNRA endothelin receptor type A
EFNB1 ephrin-B1
EYA1 EYA transcriptional coactivator and phosphatase 1
FBLN1 fibulin 1
FGF9 fibroblast growth factor 9
FGFR1 fibroblast growth factor receptor 1
FOXC2 forkhead box C2
FOXI3 forkhead box I3
GAS1 growth arrest-specific 1
GJA1 gap junction protein, alpha 1, 43kDa
GLI2 GLI family zinc finger 2
GSC goosecoid homeobox
HAND2 heart and neural crest derivatives expressed 2
HOXA1 homeobox A1
HOXA2 homeobox A2
NABP2 nucleic acid binding protein 2
NKX3-2 NK3 homeobox 2
OSR2 odd-skipped related transciption factor 2
PAX9 paired box 9
PITX1 paired-like homeodomain 1
PRRX1 paired related homeobox 1
RSPO2 R-spondin 2
TBX1 T-box 1
TCOF1 Treacher Collins-Franceschetti syndrome 1
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
TSHZ1 teashirt zinc finger homeobox 1
WDR19 WD repeat domain 19