RecName: Full=Mitochondrial adenyl nucleotide antiporter SLC25A24; Alt - Protein

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Prenatal diagnosis of SLC25A24 Fontaine progeroid syndrome: description of the fetal phenotype, genotype and detection of parental mosaicism. [Birth Defects Res. 2024]
Prenatal diagnosis of SLC25A24 Fontaine progeroid syndrome: description of the fetal phenotype, genotype and detection of parental mosaicism.
Pannier E, Sekri A, Roux N, Vasiljevic A, El Khattabi L, Chatron N, Grotto S, Menzella D, Grangé G, Thébault F, et al. Birth Defects Res. 2024 Jul; 116(7):e2380.
SLC25A24 Fontaine Progeroid Syndrome. [GeneReviews(®). 1993]
SLC25A24 Fontaine Progeroid Syndrome.
Velasco D, Olney AH, Starr L. GeneReviews(®). 1993-2024. 2022 Jun 9
SLC25A24 gene methylation and gray matter volume in females with and without conduct disorder: an exploratory epigenetic neuroimaging study. [Transl Psychiatry. 2021]
SLC25A24 gene methylation and gray matter volume in females with and without conduct disorder: an exploratory epigenetic neuroimaging study.
Farrow E, Chiocchetti AG, Rogers JC, Pauli R, Raschle NM, Gonzalez-Madruga K, Smaragdi A, Martinelli A, Kohls G, Stadler C, et al. Transl Psychiatry. 2021 Sep 24; 11(1):492. Epub 2021 Sep 24.

RefSeq genomic sequence
See the genomic reference sequence for the SLC25A24 gene (NG_032752.1).
RefSeq protein isoforms
See 2 reference sequence protein isoforms for the SLC25A24 gene.

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Q6NUK1 [Domain Mapping of Disease Mut...]
Q6NUK1
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
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reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

RecName: Full=Mitochondrial adenyl nucleotide antiporter SLC25A24; AltName: Full...
RecName: Full=Mitochondrial adenyl nucleotide antiporter SLC25A24; AltName: Full=Mitochondrial ATP-Mg/Pi carrier protein 1; AltName: Full=Mitochondrial Ca(2+)-dependent solute carrier protein 1; AltName: Full=Short calcium-binding mitochondrial carrier protein 1; Short=SCaMC-1; AltName: Full=Solute carrier family 25 member 24
gi|167016554|sp|Q6NUK1.2|SCMC1_HUMA

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