Article · Wikipedia archive · Last revised Jun 22, 2026

CMTX2

Charcot-Marie-Tooth neuropathy, X-linked 2 (recessive) is a protein that in humans is encoded by the CMTX2 gene. Its cytogenetic location is Xp22.2. It is associated with a variant of Charcot-Marie-Tooth disease.

Last revised
Jun 22, 2026
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≈ 1 min
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Citations
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Wikipedia ↗
CMTX2
Identifiers
AliasesCMTX2, Charcot-Marie-Tooth neuropathy, X-linked 2 (recessive)
External IDsGeneCards: CMTX2; OMA:CMTX2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez

1253

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Ensembl

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UniProt

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RefSeq (mRNA)

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RefSeq (protein)

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Location (UCSC)n/an/a
PubMed search1n/a
Wikidata
View/Edit Human

Charcot-Marie-Tooth neuropathy, X-linked 2 (recessive) is a protein that in humans is encoded by the CMTX2 gene.2 Its cytogenetic location is Xp22.2.3 It is associated with a variant of Charcot-Marie-Tooth disease.2

References

References

  1. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  2. "Entrez Gene: Charcot-Marie-Tooth neuropathy, X-linked 2 (recessive)". Retrieved 2014-02-23.
  3. "CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 2; CMTX2". Online Mendelian Inheritance in Man. Retrieved 2024-10-17.
Further reading

Further reading