abnormal vestibular hair cell number Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description abnormal number of cells in the sensory epithelium of the maculae and cristae of the membranous labyrinth of the internal ear (Mammalian Phenotype Ontology, MP_0004326)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004326
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Genes

16 gene mutations causing the abnormal vestibular hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATF2 activating transcription factor 2
ATOH1 atonal homolog 1 (Drosophila)
ATP2B2 ATPase, Ca++ transporting, plasma membrane 2
EYA1 EYA transcriptional coactivator and phosphatase 1
GFI1 growth factor independent 1 transcription repressor
HES1 hes family bHLH transcription factor 1
HES5 hes family bHLH transcription factor 5
HMX2 H6 family homeobox 2
HMX3 H6 family homeobox 3
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
LAMA2 laminin, alpha 2
MYO6 myosin VI
POU4F3 POU class 4 homeobox 3
SLC26A4 solute carrier family 26 (anion exchanger), member 4
SOX2 SRY (sex determining region Y)-box 2
SRRM4 serine/arginine repetitive matrix 4