abnormal brain ependyma morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the cellular membrane that lines the brain ventricles (Mammalian Phenotype Ontology, MP_0010152)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010152
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14 gene mutations causing the abnormal brain ependyma morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARL6 ADP-ribosylation factor-like 6
COL18A1 collagen, type XVIII, alpha 1
DLL3 delta-like 3 (Drosophila)
DNAAF2 dynein, axonemal, assembly factor 2
E2F5 E2F transcription factor 5, p130-binding
FOXJ1 forkhead box J1
HYDIN HYDIN, axonemal central pair apparatus protein
KIF19 kinesin family member 19
NAPA N-ethylmaleimide-sensitive factor attachment protein, alpha
PFDN5 prefoldin subunit 5
RFX4 regulatory factor X, 4 (influences HLA class II expression)
RND3 Rho family GTPase 3
TMEM67 transmembrane protein 67
ULK4 unc-51 like kinase 4