CMTX2

Genetic element in the species Homo sapiens From Wikipedia, the free encyclopedia

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]

AliasesCMTX2, Charcot-Marie-Tooth neuropathy, X-linked 2 (recessive)
External IDsGeneCards: CMTX2; OMA:CMTX2 - orthologs
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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 (protein)

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Location (UCSC)n/an/a
PubMed search[1]n/a
Wikidata
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