CMT2J

MPZ | 2000

Illustration of a DNA double helix overlaid on nerve cells, with text reading ‘Experts in CMT: CMT Genes and Subtypes Database

CMT2J is caused by mutations in the MPZ gene. This gene provides instructions for making myelin protein zero, a crucial structural protein essential for the formation of normal peripheral nerve myelin. Mutations in the MPZ gene disrupt the formation and stability of myelin, leading to slowed nerve signal transmission, although signal transmission is only somewhat slowed in CMT2J.

CMT2J is autosomal dominant, meaning that just one of the gene’s two copies needs a mutation to cause this subtype.

Clinical Features

CMT2J is a late-onset subtype, with symptoms usually beginning in the thirties or later. Nerve conduction studies usually show somewhat slowed conduction velocities and reduced amplitudes, consistent with an axonal form of CMT.

CMT2J symptoms may include:

  • Weakness in the feet and lower legs
  • Muscle atrophy
  • Foot drop
  • steppage-style walking pattern
  • Foot deformities, including high arches and hammertoes (clawed toes)
  • Reduced sensation
  • Muscle cramping
  • Reduced or absent reflexes
  • Enlarged peripheral nerves (hypertrophic nerves)
  • Clawing of the fingers
  • Spinal curvature, including scoliosis or kyphoscoliosis
  • Abnormal pupil responses, including pupils that remain dilated or respond poorly to light
  • Significant hearing loss
  • Additional symptoms not listed here

Disease Course

CMT2J shows wide variability in severity and progression. Some individuals remain mildly affected, while others develop a more severe disease. Progression is generally slow, and life expectancy is not reduced.

Clinical Basics

Subtype
CMT2J

Classification
CMT2

Neuropathy Type
Axonal

Inheritance Pattern
Autosomal Dominant

Genetic Context

HGNC-Approved Gene Symbol
MPZ

Gene Full Name
Myelin Protein Zero

HGNC Gene Alias(es)
P₀

Chromosome
1q23.3

Zygosity of Responsible Variant
Heterozygous

Mitochondrial Involvement
No

ClinVar Pathogenic Variants

View CMT2J ClinVar Variants

More Info

Research Opportunity

CMT Natural History Study

Original Discovery Publication

Publication Title

An Axonal Form of Charcot-Marie-Tooth Disease Showing Distinctive Features in Association with Mutations in the Peripheral Myelin Protein Zero Gene (Thr124Met or Asp75Val)

Authors

Misu, K., Yoshihara, T., Shikama, Y., Awaki, E., Yamamoto, M., Hattori, N., Hirayama, M., Takegami, T., Nakashima, K., & Sobue, G.

Publication Date
December 1, 2000

Updated: February 7, 2026 | By: K. Raymond

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