KEGG   VARIANT: 4099v1
Entry
4099v1                      Variant                                
Name
MAG mutation
Type
Loss of function
Gene
MAG  myelin associated glycoprotein [KO:K06771]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 159460
Network
nt06546  IgSF CAM signaling
Disease
H00266  Hereditary spastic paraplegia
Reference
  Authors
Lossos A, Elazar N, Lerer I, Schueler-Furman O, Fellig Y, Glick B, Zimmerman BE, Azulay H, Dotan S, Goldberg S, Gomori JM, Ponger P, Newman JP, Marreed H, Steck AJ, Schaeren-Wiemers N, Mor N, Harel M, Geiger T, Eshed-Eisenbach Y, Meiner V, Peles E
  Title
Myelin-associated glycoprotein gene mutation causes Pelizaeus-Merzbacher disease-like disorder.
  Journal
Brain 138:2521-36 (2015)
DOI:10.1093/brain/awv204
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