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  2. Mitochondrial DNA - Wikipedia

    en.wikipedia.org/wiki/Mitochondrial_DNA

    Mitochondrial DNA (mtDNA and mDNA) is the DNA located in the mitochondria organelles in a eukaryotic cell that converts chemical energy from food into adenosine triphosphate (ATP). Mitochondrial DNA is a small portion of the DNA contained in a eukaryotic cell; most of the DNA is in the cell nucleus , and, in plants and algae, the DNA also is ...

  3. Human mitochondrial genetics - Wikipedia

    en.wikipedia.org/wiki/Human_mitochondrial_genetics

    Mitochondrial diseases range in severity from asymptomatic to fatal, and are most commonly due to inherited rather than acquired mutations of mitochondrial DNA. A given mitochondrial mutation can cause various diseases depending on the severity of the problem in the mitochondria and the tissue the affected mitochondria are in.

  4. Molecular paleontology - Wikipedia

    en.wikipedia.org/wiki/Molecular_paleontology

    Mitochondrial DNA (mtDNA) is separate from one's nuclear DNA. It is present in organelles called mitochondria in each cell. Unlike nuclear DNA, which is inherited from both parents and rearranged every generation, an exact copy of mitochondrial DNA gets passed down from mother to her sons and daughters. The benefits of performing DNA analysis ...

  5. Sorenson Molecular Genealogy Foundation - Wikipedia

    en.wikipedia.org/wiki/Sorenson_Molecular...

    The Sorenson Database compared mitochondrial DNA from over 76, 000 people in their mitochondrial database to find cousins connected across generations. Users could share their mtDNA results from other commercial labs. The mtDNA test examines three regions of the D-loop of mtDNA: HVR1, HVR2 and HVR3 which is called the Hypervariable region ...

  6. Douglas C. Wallace - Wikipedia

    en.wikipedia.org/wiki/Douglas_C._Wallace

    Wallace is a pioneer in the study of mitochondrial DNA.Wallace and his colleagues introduced human mitochondrial genetics into the field of molecular genetics. [10] In 1975, for the first time ever, Wallace could associate a genetic disorder with the mitochondrial DNA region (resistance to chloramphenicol) [11] and in 1990 he described a mitochondrial DNA mutation as the cause of a particular ...

  7. MT-ND2 - Wikipedia

    en.wikipedia.org/wiki/MT-ND2

    MT-ND2 is located in mitochondrial DNA from base pair 4,470 to 5,511. [5] The MT-ND2 gene produces a 39 kDa protein composed of 347 amino acids. [10] [11] MT-ND2 is one of seven mitochondrial genes encoding subunits of the enzyme NADH dehydrogenase (ubiquinone), together with MT-ND1, MT-ND3, MT-ND4, MT-ND4L, MT-ND5, and MT-ND6.

  8. Cambridge Reference Sequence - Wikipedia

    en.wikipedia.org/wiki/Cambridge_Reference_Sequence

    When mitochondrial DNA sequencing is used for genealogical purposes, the results are often reported as differences from the revised CRS. The CRS is a reference sequence rather than a record of the earliest human mtDNA. A difference between a tested sample and the CRS may have arisen in the lineage of the CRS or in the lineage of the tested sample.

  9. MT-ND4 - Wikipedia

    en.wikipedia.org/wiki/MT-ND4

    The MT-ND4 gene is located in human mitochondrial DNA from base pair 10,760 to 12,137. [5] [11] The MT-ND4 gene produces a 52 kDa protein composed of 459 amino acids.[12] [13] MT-ND4 is one of seven mitochondrial genes encoding subunits of the enzyme NADH dehydrogenase (ubiquinone), together with MT-ND1, MT-ND2, MT-ND3, MT-ND4L, MT-ND5, and MT-ND6.