abnormal malleus morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the largest of the three auditory ossicles, which resembles a club or hammer (Mammalian Phenotype Ontology, MP_0000029)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000029
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Genes

29 gene mutations causing the abnormal malleus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ANKH ANKH inorganic pyrophosphate transport regulator
CHD7 chromodomain helicase DNA binding protein 7
DLX5 distal-less homeobox 5
ECE1 endothelin converting enzyme 1
EDNRA endothelin receptor type A
EMX2 empty spiracles homeobox 2
EYA1 EYA transcriptional coactivator and phosphatase 1
FGFR1 fibroblast growth factor receptor 1
FGFR3 fibroblast growth factor receptor 3
FOXC2 forkhead box C2
FOXI3 forkhead box I3
GDF6 growth differentiation factor 6
GSC goosecoid homeobox
HAND2 heart and neural crest derivatives expressed 2
HOXA1 homeobox A1
HOXA2 homeobox A2
ISL1 ISL LIM homeobox 1
MSX1 msh homeobox 1
NKX3-2 NK3 homeobox 2
NOG noggin
OTX2 orthodenticle homeobox 2
PBX1 pre-B-cell leukemia homeobox 1
PRRX1 paired related homeobox 1
ROR2 receptor tyrosine kinase-like orphan receptor 2
SIX1 SIX homeobox 1
TBX1 T-box 1
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
TNFRSF11B tumor necrosis factor receptor superfamily, member 11b
TSHZ1 teashirt zinc finger homeobox 1