RecName: Full=Mitochondrial 2-oxodicarboxylate carrier; Short=ODC; Alt - Protein

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Correction: Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy-like disease. [Genet Med. 2019]
Correction: Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy-like disease.
Boczonadi V, King MS, Smith AC, Olahova M, Bansagi B, Roos A, Eyassu F, Borchers C, Ramesh V, Lochmüller H, et al. Genet Med. 2019 Sep; 21(9):2163-2164.
Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy-like disease. [Genet Med. 2018]
Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy-like disease.
Boczonadi V, King MS, Smith AC, Olahova M, Bansagi B, Roos A, Eyassu F, Borchers C, Ramesh V, Lochmüller H, et al. Genet Med. 2018 Oct; 20(10):1224-1235. Epub 2018 Mar 8.
Identification of a Novel 14q13.3 Deletion Involving the SLC25A21 Gene Associated with Familial Synpolydactyly. [Mol Syndromol. 2012]
Identification of a Novel 14q13.3 Deletion Involving the SLC25A21 Gene Associated with Familial Synpolydactyly.
Meyertholen K, Ravnan JB, Matalon R. Mol Syndromol. 2012 Jun; 3(1):25-9. Epub 2012 Jun 13.

RefSeq protein isoforms
See 8 reference sequence protein isoforms for the SLC25A21 gene.

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MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF) [MODBASE, Database of Comparat...]
MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF)
Transcript/Protein Information [PANTHER Classification System]
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Protein