abnormal oligodendrocyte morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the neuroglia of the central nervous system that form the insulating myelin sheath of axons in the CNS (Mammalian Phenotype Ontology, MP_0000953)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000953
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33 gene mutations causing the abnormal oligodendrocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ASPA aspartoacylase
EIF2B5 eukaryotic translation initiation factor 2B, subunit 5 epsilon, 82kDa
ERBB2 erb-b2 receptor tyrosine kinase 2
GALC galactosylceramidase
GFAP glial fibrillary acidic protein
GJC2 gap junction protein, gamma 2, 47kDa
GPR17 G protein-coupled receptor 17
IL1B interleukin 1, beta
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
KLK6 kallikrein-related peptidase 6
MAG myelin associated glycoprotein
MBP myelin basic protein
MGAT5B mannosyl (alpha-1,6-)-glycoprotein beta-1,6-N-acetyl-glucosaminyltransferase, isozyme B
MMP12 matrix metallopeptidase 12
MMP9 matrix metallopeptidase 9
NKX2-2 NK2 homeobox 2
NOS2 nitric oxide synthase 2, inducible
NRG1 neuregulin 1
OLIG1 oligodendrocyte transcription factor 1
PDGFRA platelet-derived growth factor receptor, alpha polypeptide
PLP1 proteolipid protein 1
PLXNA1 plexin A1
PRKAB1 protein kinase, AMP-activated, beta 1 non-catalytic subunit
PTPRC protein tyrosine phosphatase, receptor type, C
PTPRZ1 protein tyrosine phosphatase, receptor-type, Z polypeptide 1
QKI QKI, KH domain containing, RNA binding
SOX10 SRY (sex determining region Y)-box 10
TENM4 teneurin transmembrane protein 4
TERT telomerase reverse transcriptase
TNFRSF21 tumor necrosis factor receptor superfamily, member 21
TYROBP TYRO protein tyrosine kinase binding protein
ZNF24 zinc finger protein 24
ZNF365 zinc finger protein 365