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mpz gene
Mutations seen in Charcot-Marie-Tooth neuropathy, type 1b & Dejerine-Sottas syndrome.
Related
myelin P0 protein; myelin protein zero; myelin peripheral protein; MPP (MPZ)
General
unclassified gene
Properties
TEMPLATE-FOR: messenger RNA
TEMPLATE-FOR: myelin P0 protein
LOCUS: human chromosome-1 Q22
MOTIF: transcription factor binding site
transcriptional start site
exon
intron
transcriptional termination site
Database Correlations
OMIM 159440