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pmp22 gene
Pathology:
- mutations in seen in Charcot-Marie-Tooth neuropathy, type 1a & Dejerine-Sottas syndrome
Laboratory:
- PMS2 gene deletion, duplication & mutation analysis
Related
peripheral myelin protein 22; PMP-22; growth arrest-specific protein 3; GAS-3 (PMP22, GAS3)
General
unclassified gene
Properties
TEMPLATE-FOR: messenger RNA
TEMPLATE-FOR: peripheral myelin protein 22
LOCUS: human chromosome-17 P11.2
MOTIF: transcription factor binding site
transcriptional start site
exon
intron
transcriptional termination site
Database Correlations
OMIM 159440