Myotubularin is a protein that in humans is encoded by the MTM1 gene.[5]

MTM1
Identifiers
AliasesMTM1, CNM, MTMX, XLMTM, Myotubularin 1, myotubularin, CNMX
External IDsOMIM: 300415; MGI: 1099452; HomoloGene: 37279; GeneCards: MTM1; OMA:MTM1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000252
NM_001376906
NM_001376907
NM_001376908

RefSeq (protein)

NP_000243
NP_001363835
NP_001363836
NP_001363837

Location (UCSC)Chr X: 150.57 – 150.67 MbChr X: 70.25 – 70.36 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

This gene is a member of a gene family that encodes lipid phosphatases. Myotubularin is required for muscle cell differentiation and mutations in this gene have been identified as being responsible for X-linked myotubular myopathy.[5]

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000171100Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000031337Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ a b "Entrez Gene: MTM1 myotubularin 1".

Further reading

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