CMTX2

CMTX2
Identifiers
Aliases	CMTX2, Charcot-Marie-Tooth neuropathy, X-linked 2 (recessive)
External IDs	GeneCards: CMTX2
Orthologs
Databases	NCBI: entry
	1253
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	n; a
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	Wikidata
View/Edit Human

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.

References

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

This article on a gene on the human X chromosome and/or its associated protein is a stub. You can help Wikipedia by adding missing information.

[1] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[entrez-2] 1 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.