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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Genes

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