abnormal blood-cerebrospinal fluid barrier function Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the function of the group of barriers and transport systems in the choroid plexus located in the lateral, third, and fourth brain ventricles that controls the entrance of substances into the cerebrospinal fluid from the blood (Mammalian Phenotype Ontology, MP_0006088)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006088
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Genes

2 gene mutations causing the abnormal blood-cerebrospinal fluid barrier function phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCC4 ATP-binding cassette, sub-family C (CFTR/MRP), member 4
ADGRA2 adhesion G protein-coupled receptor A2