abnormal oligodendrocyte physiology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any functional anomaly of the neuroglia of the central nervous system that form the insulating myelin sheath of axons in the CNS (Mammalian Phenotype Ontology, MP_0008917)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008917
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9 gene mutations causing the abnormal oligodendrocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CNTF ciliary neurotrophic factor
GFAP glial fibrillary acidic protein
GJC2 gap junction protein, gamma 2, 47kDa
KIF14 kinesin family member 14
MAN2C1 mannosidase, alpha, class 2C, member 1
NFASC neurofascin
S1PR5 sphingosine-1-phosphate receptor 5
TENM4 teneurin transmembrane protein 4
TNFRSF21 tumor necrosis factor receptor superfamily, member 21