abnormal auditory cortex morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly in the region of the cerebral cortex that receives the auditory radiation from the medial geniculate body, a thalamic cell group receiving auditory input from the cochlear nuclei in the rhombencephalon and is responsible for processing of auditory (sound) information (Mammalian Phenotype Ontology, MP_0004631)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004631
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5 gene mutations causing the abnormal auditory cortex morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARHGAP33 Rho GTPase activating protein 33
ATP2B2 ATPase, Ca++ transporting, plasma membrane 2
CHRM1 cholinergic receptor, muscarinic 1
SPTBN4 spectrin, beta, non-erythrocytic 4
TUBA1A tubulin, alpha 1a