mitochondrial adenyl nucleotide antiporter SLC25A24 isoform 1 [Homo sa - Protein

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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.
De Novo Mutations in SLC25A24 Cause a Disorder Characterized by Early Aging, Bone Dysplasia, Characteristic Face, and Early Demise. [Am J Hum Genet. 2017]
De Novo Mutations in SLC25A24 Cause a Disorder Characterized by Early Aging, Bone Dysplasia, Characteristic Face, and Early Demise.
Writzl K, Maver A, Kovačič L, Martinez-Valero P, Contreras L, Satrustegui J, Castori M, Faivre L, Lapunzina P, van Kuilenburg ABP, et al. Am J Hum Genet. 2017 Nov 2; 101(5):844-855.

RefSeq genomic sequence
See the genomic reference sequence for the SLC25A24 gene (NG_032752.1).
RefSeq mRNA
See reference mRNA sequence for the SLC25A24 gene (NM_013386.5).
RefSeq protein isoforms
See the other reference sequence protein isoform for the SLC25A24 gene (NP_998816.1).

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NP_037518 [Domain Mapping of Disease Mut...]
NP_037518
Domain Mapping of Disease Mutations
Ensembl [Ensembl]
Ensembl
GlyGen glycoinformatics resource [GlyGen glycoinformatics resou...]
GlyGen glycoinformatics resource
OncoMX cancer biomarker resource [OncoMX cancer biomarker resou...]
OncoMX cancer biomarker resource
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Transcript/Protein Information
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reagents [ExactAntigen/Labome]
reagents
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