KEGG   VARIANT: 5375v1
Entry
5375v1                      Variant                                
Name
PMP2 mutation
Type
Loss of function
Gene
PMP2  peripheral myelin protein 2 [KO:K24977]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 170715
Network
nt06546  IgSF CAM signaling
Disease
H00264  Charcot-Marie-Tooth disease
Reference
  Authors
Gonzaga-Jauregui C, Harel T, Gambin T, Kousi M, Griffin LB, Francescatto L, Ozes B, Karaca E, Jhangiani SN, Bainbridge MN, Lawson KS, Pehlivan D, Okamoto Y, Withers M, Mancias P, Slavotinek A, Reitnauer PJ, Goksungur MT, Shy M, Crawford TO, Koenig M, Willer J, Flores BN, Pediaditrakis I, Us O, Wiszniewski W, Parman Y, Antonellis A, Muzny DM, Katsanis N, Battaloglu E, Boerwinkle E, Gibbs RA, Lupski JR
  Title
Exome Sequence Analysis Suggests that Genetic Burden Contributes to Phenotypic Variability and Complex Neuropathy.
  Journal
Cell Rep 12:1169-83 (2015)
DOI:10.1016/j.celrep.2015.07.023
LinkDB

DBGET integrated database retrieval system