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SBF2

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

    Myotubularin-related protein 13 is a protein that in humans is encoded by the SBF2 gene. The family of myotubularin-related proteins includes lipid phosphatases

    SBF2

    SBF2

    SBF2

  • Chromosome 11
  • Human chromosome

    protein 1 SART1: squamous cell carcinoma antigen recognized by T-cells 1 SBF2: SET binding factor 2 SCGB1D2: secretoglobin family 1D member 2 SESN3 encoding

    Chromosome 11

    Chromosome 11

    Chromosome_11

  • GRAM domain
  • Protein domain

    GRAMD2A; GRAMD2B; GRAMD4; MTM1; MTMR1; MTMR2; NCOA7; NSMAF; OXR1; SBF1; SBF2; TBC1D8; TBC1D8B; TBC1D9; TBC1D9B; WBP2; WBP2NL; dJ439F8.1; Doerks T, Strauss

    GRAM domain

    GRAM domain

    GRAM_domain

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

    subtype CMTRIA CMT4B1 601382 MTMR2 11q21 Autosomal recessive CMT4B2 604563 SBF2 11p15.4 Autosomal recessive CMT4B3 615284 SBF1 22q13.33 Autosomal recessive

    Charcot–Marie–Tooth disease classifications

    Charcot–Marie–Tooth_disease_classifications

  • Pleckstrin homology domain
  • Protein domain

    RASA2, RASA3, RASA4, RASAL1, RASGRF1, RGNEF, ROCK1, ROCK2, RTKN, SBF1, SBF2, SCAP2, SGEF, SH2B, SH2B1, SH2B2, SH2B3, SH3BP2, SKAP1, SKAP2, SNTA1, SNTB1

    Pleckstrin homology domain

    Pleckstrin homology domain

    Pleckstrin_homology_domain

  • List of human protein-coding genes 7
  • Q9NPB0 14314 SBDS HGNC:19440; Q9Y3A5 14315 SBF1 HGNC:10542; O95248 14316 SBF2 HGNC:2135; Q86WG5 14317 SBK1 HGNC:17699; Q52WX2 14318 SBK2 HGNC:34416; P0C263

    List of human protein-coding genes 7

    List_of_human_protein-coding_genes_7

  • Myotubularin
  • Protein domain

    MTMR4; MTMR6; MTMR7; MTMR8; MTMR9; MTMR10; MTMR11; MTMR12; MTMR14; SBF1; SBF2; Begley MJ, Taylor GS, Kim SA, Veine DM, Dixon JE, Stuckey JA (December 2003)

    Myotubularin

    Myotubularin

    Myotubularin

  • List of OMIM disorder codes
  • disease type 4B1; 601382; MTMR2 Charcot–Marie–Tooth disease type 4B2; 604563; SBF2 Charcot–Marie–Tooth disease type 4C; 601596; SH3TC2 Charcot–Marie–Tooth disease

    List of OMIM disorder codes

    List_of_OMIM_disorder_codes

  • Mir-19 microRNA precursor family
  • Precursor microRNA family

    to the pro-survival functions: * PTEN tumor suppressor gene * PTEN mRNA * Sbf2 gene * Bcl7a gene * Rnf44 gene In the cell response to stress, the most important

    Mir-19 microRNA precursor family

    Mir-19 microRNA precursor family

    Mir-19_microRNA_precursor_family

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