abnormal type i vestibular cell Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly in the flask-shaped sensory cells of the maculae and cristae of the vestibular labyrinth of the inner ear, which are normally enclosed in calyx endings of afferent neurons; afferent and efferent nerve fibers of the vestibular nerve synapse with them; from the apical end of each cell a bundle of stereocilia and a kinocilium extend into the otolithic membrane of the maculae or the cupula of the cristae (Mammalian Phenotype Ontology, MP_0004428)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004428
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Genes

4 gene mutations causing the abnormal type i vestibular cell phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BDNF brain-derived neurotrophic factor
CACNG2 calcium channel, voltage-dependent, gamma subunit 2
GRXCR1 glutaredoxin, cysteine rich 1
NTRK2 neurotrophic tyrosine kinase, receptor, type 2