decreased cochlear coiling Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description a reduction in cochlear coiling or number of turns; in wild-type mice, the cochlea most commonly exhibits one and three-fourth turns (Mammalian Phenotype Ontology, MP_0003148)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003148
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Genes

15 gene mutations causing the decreased cochlear coiling phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
DLX5 distal-less homeobox 5
EYA1 EYA transcriptional coactivator and phosphatase 1
FGF3 fibroblast growth factor 3
GATA3 GATA binding protein 3
GBX2 gastrulation brain homeobox 2
LMO4 LIM domain only 4
NOG noggin
PAX2 paired box 2
PAX3 paired box 3
POU3F4 POU class 3 homeobox 4
SIX1 SIX homeobox 1
SLC26A4 solute carrier family 26 (anion exchanger), member 4
SOX2 SRY (sex determining region Y)-box 2
VANGL2 VANGL planar cell polarity protein 2
ZEB1 zinc finger E-box binding homeobox 1