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- NCIT_C102797 IAO_0000115 "Human DNM2 wild-type allele is located in the vicinity of 19p13.2 and is approximately 118 kb in length. This allele, which encodes dynamin-2 protein, is involved in both microtubule polymerization and GTPase activity. Mutation of the gene is associated with centronuclear myopathy type 1 and Charcot-Marie-Tooth disease types dominant intermediate B and 2M axonal." @default.
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- NCIT_C102797 NCIT_P106 "Gene or Genome" @default.
- NCIT_C102797 NCIT_P108 "DNM2 wt Allele" @default.
- NCIT_C102797 NCIT_P207 "C3540809" @default.
- NCIT_C102797 NCIT_P321 "1785" @default.
- NCIT_C102797 NCIT_P98 "Somatic mutation of the DNM2 gene may be associated with early T-cell precursor acute lymphoblastic leukemia. (Nature. 2012; 481:157-163.)" @default.
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- NCIT_C102797 hasExactSynonym "CMT2M" @default.
- NCIT_C102797 hasExactSynonym "CMTDI1" @default.
- NCIT_C102797 hasExactSynonym "CMTDIB" @default.
- NCIT_C102797 hasExactSynonym "DI-CMTB" @default.
- NCIT_C102797 hasExactSynonym "DNM2 wt Allele" @default.
- NCIT_C102797 hasExactSynonym "DYN2" @default.
- NCIT_C102797 hasExactSynonym "DYNII" @default.
- NCIT_C102797 hasExactSynonym "Dynamin 2 wt Allele" @default.
- NCIT_C102797 type Class @default.
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- NCIT_C102797 label "DNM2 wt Allele" @default.
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