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Antibody detects endogenous levels of total SMCR7/MID49.
This gene encodes an outer mitochondrial membrane protein that functions in the regulation of mitochondrial morphology. It can directly recruit the fission mediator dynamin-related protein 1 (Drp1) to the mitochondrial surface. The gene is located within the Smith-Magenis syndrome region on chromosome 17. Alternative splicing results in multiple transcript variants encoding different isoforms.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: mitochondrial dynamic protein MID49; mitochondrial dynamic protein of 49 kDa; mitochondrial dynamic protein of 49 kDa homolog; Mitochondrial dynamics protein MID49; Mitochondrial dynamics protein of 49 kDa; Mitochondrial dynamics protein of 49 kDa homolog; Mitochondrial elongation factor 2; Smith-Magenis syndrome chromosomal region candidate gene 7 protein; Smith-Magenis syndrome chromosomal region candidate gene 7 protein homolog; Smith-Magenis syndrome chromosome region, candidate 7; Smith-Magenis syndrome chromosome region, candidate 7 homolog
Gene Aliases: AI482195; Gm11; MID49; MIEF2; RGD1560728; SMCR7
UniProt ID: (Human) Q96C03, (Mouse) Q5NCS9
Entrez Gene ID: (Human) 125170, (Mouse) 237781, (Rat) 497916
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