abnormal reissner membrane morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the membrane which separates the cochlear duct from the vestibular canal, i.e. the endolymph of the scala media from the perilymph of the scala vestibuli; the Reissner membrane consists of squamous epithelial cells with microvilli toward the ductus, a basement membrane, and a thin layer of connective tissue toward the scala (Mammalian Phenotype Ontology, MP_0006021)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006021
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11 gene mutations causing the abnormal reissner membrane morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CYS1 cystin 1
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
LOC102723475 putative uncharacterized protein LOC388820
NAGLU N-acetylglucosaminidase, alpha
PHEX phosphate regulating endopeptidase homolog, X-linked
POU3F4 POU class 3 homeobox 4
S1PR2 sphingosine-1-phosphate receptor 2
SLC12A2 solute carrier family 12 (sodium/potassium/chloride transporter), member 2
SLC26A4 solute carrier family 26 (anion exchanger), member 4
SLC4A7 solute carrier family 4, sodium bicarbonate cotransporter, member 7