Protein misato homolog 1 is a protein that in humans is encoded by the MSTO1 gene.[5][6]
The MSTO1 gene is 5134 base pairs (located in chromosome 1) and the MSTO1 protein is 570 aminoacids in length. It is located in the outer membrane of the mitochondrion, and is involved in the regulation of mitochondrial distribution and morphology.[7]
^ abcGRCh38: Ensembl release 89: ENSG00000125459 – Ensembl, May 2017
^ abcGRCm38: Ensembl release 89: ENSMUSG00000068922 – Ensembl, May 2017
^"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^Kuryshev VY, Vorobyov E, Zink D, Schmitz J, Rozhdestvensky TS, Munstermann E, Ernst U, Wellenreuther R, Moosmayer P, Bechtel S, Schupp I, Horst J, Korn B, Poustka A, Wiemann S (Jul 2006). "An anthropoid-specific segmental duplication on human chromosome 1q22". Genomics. 88 (2): 143–51. doi:10.1016/j.ygeno.2006.02.002. PMID 16545939.
that in humans is encoded by the MSTO1 gene. The MSTO1 gene is 5134 base pairs (located in chromosome 1) and the MSTO1 protein is 570 aminoacids in length...
dominant (IMMD) CHCHD10 AD 616209 Myopathy, mitochondrial, and ataxia (MMYAT) MSTO1 AR/AD 617675 Mitochondrial myopathy, episodic, with or without optic atrophy...