Homo sapiens solute carrier family 25 member 24 (SLC25A24), transcript - Nucleotide

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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.
MECP2 directly interacts with RNA polymerase II to modulate transcription in human neurons. [Neuron. 2024]
MECP2 directly interacts with RNA polymerase II to modulate transcription in human neurons.
Liu Y, Flamier A, Bell GW, Diao AJ, Whitfield TW, Wang HC, Wu Y, Schulte F, Friesen M, Guo R, et al. Neuron. 2024 Jun 19; 112(12):1943-1958.e10. Epub 2024 May 1.
Antagonistic roles of canonical and Alternative-RPA in disease-associated tandem CAG repeat instability. [Cell. 2023]
Antagonistic roles of canonical and Alternative-RPA in disease-associated tandem CAG repeat instability.
Gall-Duncan T, Luo J, Jurkovic CM, Fischer LA, Fujita K, Deshmukh AL, Harding RJ, Tran S, Mehkary M, Li V, et al. Cell. 2023 Oct 26; 186(22):4898-4919.e25. Epub 2023 Oct 11.

RefSeq alternative splicing
See the other reference mRNA sequence splice variant for the SLC25A24 gene (NM_013386.5).
RefSeq protein product
See the reference protein sequence for mitochondrial adenyl nucleotide antiporter SLC25A24 isoform 2 (NP_998816.1).

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Homo sapiens solute carrier family 25 member 24 (SLC25A24), transcript variant 2...
Homo sapiens solute carrier family 25 member 24 (SLC25A24), transcript variant 2, mRNA; nuclear gene for mitochondrial product
gi|1675008589|ref|NM_213651.3|

Nucleotide

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Nucleotide