absent cochlear hair cells Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the sensory epithelial cells of the cochlea; these cells are normally in synaptic contact with the auditory nerve (Mammalian Phenotype Ontology, MP_0004405)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004405
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Genes

19 gene mutations causing the absent cochlear hair cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACAN aggrecan
ATOH1 atonal homolog 1 (Drosophila)
ATP2B2 ATPase, Ca++ transporting, plasma membrane 2
CLRN1 clarin 1
COL11A1 collagen, type XI, alpha 1
CYS1 cystin 1
FGFR1 fibroblast growth factor receptor 1
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
LAMA2 laminin, alpha 2
LOC102723475 putative uncharacterized protein LOC388820
MYO15A myosin XVA
POU4F3 POU class 4 homeobox 3
SLC12A2 solute carrier family 12 (sodium/potassium/chloride transporter), member 2
SLC12A7 solute carrier family 12 (potassium/chloride transporter), member 7
SLC26A4 solute carrier family 26 (anion exchanger), member 4
SOX2 SRY (sex determining region Y)-box 2
SRRM4 serine/arginine repetitive matrix 4
TMPRSS3 transmembrane protease, serine 3
USH1G Usher syndrome 1G (autosomal recessive)