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MTMR2

  • MTMR2
  • Protein-coding gene in the species Homo sapiens

    phosphatidylinositol-3-phosphate phosphatase is a protein that in humans is encoded by the MTMR2 gene. This gene is a member of the myotubularin family and encodes a putative

    MTMR2

    MTMR2

    MTMR2

  • GRAM domain
  • Protein domain

    lipids. GRAMD1A; GRAMD1B; GRAMD1C; GRAMD2A; GRAMD2B; GRAMD4; MTM1; MTMR1; MTMR2; NCOA7; NSMAF; OXR1; SBF1; SBF2; TBC1D8; TBC1D8B; TBC1D9; TBC1D9B; WBP2;

    GRAM domain

    GRAM domain

    GRAM_domain

  • SBF2
  • Protein-coding gene in the species Homo sapiens

    et al. (2003). "Mutations in MTMR13, a new pseudophosphatase homologue of MTMR2 and Sbf1, in two families with an autosomal recessive demyelinating form

    SBF2

    SBF2

    SBF2

  • Charcot–Marie–Tooth disease classifications
  • Peripheral nervous system disorders

    GDAP1 8q21.11 Autosomal recessive Allelic with subtype CMTRIA CMT4B1 601382 MTMR2 11q21 Autosomal recessive CMT4B2 604563 SBF2 11p15.4 Autosomal recessive

    Charcot–Marie–Tooth disease classifications

    Charcot–Marie–Tooth_disease_classifications

  • MTMR1
  • Protein-coding gene in the species Homo sapiens

    PMID 11275328. Kim SA, Taylor GS, Torgersen KM, Dixon JE (2002). "Myotubularin and MTMR2, phosphatidylinositol 3-phosphatases mutated in myotubular myopathy and

    MTMR1

    MTMR1

    MTMR1

  • SBF1
  • Protein-coding gene in the species Homo sapiens

    humans is encoded by the SBF1 gene. SBF1 has been shown to interact with MTMR2 and SUV39H1. GRCh38: Ensembl release 89: ENSG00000100241 – Ensembl, May

    SBF1

    SBF1

    SBF1

  • Pseudoenzyme
  • Catalytically deficient enzymes

    conventional phosphatases MTMR13 binds and promotes lipid phosphatase activity of MTMR2 Regulation of protein localisation in a cell STYX acts as a nuclear anchor

    Pseudoenzyme

    Pseudoenzyme

  • Phosphatidylinositol 5-phosphate
  • Concordantly, genetic ablation of the myotubularin-related protein 2 (MTMR2) causes elevation of cellular PtdIns(3,5)P2 and a decrease of PtdIns5P.

    Phosphatidylinositol 5-phosphate

    Phosphatidylinositol_5-phosphate

  • List of human protein-coding genes 5
  • HGNC:27339; Q8NCU8 9991 MTM1 HGNC:7448; Q13496 9992 MTMR1 HGNC:7449; Q13613 9993 MTMR2 HGNC:7450; Q13614 9994 MTMR3 HGNC:7451; Q13615 9995 MTMR4 HGNC:7452; Q9NYA4

    List of human protein-coding genes 5

    List_of_human_protein-coding_genes_5

  • Myotubularin
  • Protein domain

    myotubularin-related proteins have been associated with disease. MTM1; MTMR1; MTMR2; MTMR3; MTMR4; MTMR6; MTMR7; MTMR8; MTMR9; MTMR10; MTMR11; MTMR12; MTMR14;

    Myotubularin

    Myotubularin

    Myotubularin

  • Phosphatidylinositol 3,5-bisphosphate
  • Chemical compound

    turnover involves the myotubularin family of phosphatases. Myotubularin 1 and MTMR2 dephosphorylate the 3-position of PtdIns(3,5)P2; therefore, the product

    Phosphatidylinositol 3,5-bisphosphate

    Phosphatidylinositol 3,5-bisphosphate

    Phosphatidylinositol_3,5-bisphosphate

  • List of OMIM disorder codes
  • disease type 4A; 214400; GDAP1 Charcot–Marie–Tooth disease type 4B1; 601382; MTMR2 Charcot–Marie–Tooth disease type 4B2; 604563; SBF2 Charcot–Marie–Tooth disease

    List of OMIM disorder codes

    List_of_OMIM_disorder_codes

  • BBSome
  • Protein complex involved in cilium biogenesis

    Stuckey, J.A. (Dec 2003) Crystal structure of a phosphoinositide phosphatase, MTMR2: insights into myotubular myopathy and Charcot-Marie-Tooth syndrome. Molecular

    BBSome

    BBSome

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