absent brain internal capsule Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the area of white matter in the brain that lies between the lenticular and caudate nuclei, and contains a group of myelinated ascending and descending axonal fiber tracts that connects the cerebral cortex to the brain stem and spinal cord (Mammalian Phenotype Ontology, MP_0008129)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008129
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Genes

5 gene mutations causing the absent brain internal capsule phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CELSR3 cadherin, EGF LAG seven-pass G-type receptor 3
FBXO45 F-box protein 45
FZD3 frizzled class receptor 3
ISLR2 immunoglobulin superfamily containing leucine-rich repeat 2
TTL tubulin tyrosine ligase