abnormal pillar cell morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the supporting cells that form the inner and outer walls of the tunnel in the organ of Corti (Mammalian Phenotype Ontology, MP_0003825)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003825
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Genes

15 gene mutations causing the abnormal pillar cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADGRV1 adhesion G protein-coupled receptor V1
ATP2B2 ATPase, Ca++ transporting, plasma membrane 2
CDKN1B cyclin-dependent kinase inhibitor 1B (p27, Kip1)
CYS1 cystin 1
ESPN espin
FGF20 fibroblast growth factor 20
FGFR3 fibroblast growth factor receptor 3
GATA3 GATA binding protein 3
PAX8 paired box 8
PCDH15 protocadherin-related 15
POU4F3 POU class 4 homeobox 3
SOD1 superoxide dismutase 1, soluble
SPRY2 sprouty homolog 2 (Drosophila)
SRRM4 serine/arginine repetitive matrix 4
THRB thyroid hormone receptor, beta