utricular macular degeneration Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description degeneration or loss of the neuroepithelial sensory receptor in the inferolateral wall of the utricle (Mammalian Phenotype Ontology, MP_0004334)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004334
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7 gene mutations causing the utricular macular degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
HMX3 H6 family homeobox 3
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
MYO6 myosin VI
SLC26A4 solute carrier family 26 (anion exchanger), member 4
SRRM4 serine/arginine repetitive matrix 4