abnormal visual cortex morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the area of the occipital cortex concerned with vision (Mammalian Phenotype Ontology, MP_0000805)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000805
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8 gene mutations causing the abnormal visual cortex morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AP3B1 adaptor-related protein complex 3, beta 1 subunit
ARHGAP33 Rho GTPase activating protein 33
BRAF B-Raf proto-oncogene, serine/threonine kinase
GAD1 glutamate decarboxylase 1 (brain, 67kDa)
LILRB3 leukocyte immunoglobulin-like receptor, subfamily B (with TM and ITIM domains), member 3
PPT1 palmitoyl-protein thioesterase 1
TENM2 teneurin transmembrane protein 2
TUBA1A tubulin, alpha 1a