absent brain ventricles Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of one or more of the four communicating cavities within the brain that are continuous with the central canal of the spinal cord (Mammalian Phenotype Ontology, MP_0012677)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012677
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Genes

2 gene mutations causing the absent brain ventricles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
SLC25A19 solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19
VCL vinculin