Homo sapiens cardiolipin synthase 1 (CRLS1), transcript variant 3, mRN - Nucleotide

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Mitochondrial and metabolic remodelling in human skin fibroblasts in response to glucose availability. [FEBS J. 2022]
Mitochondrial and metabolic remodelling in human skin fibroblasts in response to glucose availability.
Pinho SA, Costa CF, Deus CM, Pinho SLC, Miranda-Santos I, Afonso G, Bagshaw O, Stuart JA, Oliveira PJ, Cunha-Oliveira T. FEBS J. 2022 Sep; 289(17):5198-5217. Epub 2022 Mar 7.
Deleterious variants in CRLS1 lead to cardiolipin deficiency and cause an autosomal recessive multi-system mitochondrial disease. [Hum Mol Genet. 2022]
Deleterious variants in CRLS1 lead to cardiolipin deficiency and cause an autosomal recessive multi-system mitochondrial disease.
Lee RG, Balasubramaniam S, Stentenbach M, Kralj T, McCubbin T, Padman B, Smith J, Riley LG, Priyadarshi A, Peng L, et al. Hum Mol Genet. 2022 Oct 28; 31(21):3597-3612.
Integrative oncogene-dependency mapping identifies RIT1 vulnerabilities and synergies in lung cancer. [Nat Commun. 2021]
Integrative oncogene-dependency mapping identifies RIT1 vulnerabilities and synergies in lung cancer.
Vichas A, Riley AK, Nkinsi NT, Kamlapurkar S, Parrish PCR, Lo A, Duke F, Chen J, Fung I, Watson J, et al. Nat Commun. 2021 Aug 9; 12(1):4789. Epub 2021 Aug 9.

RefSeq alternative splicing
See 14 reference mRNA sequence splice variants for the CRLS1 gene.
RefSeq protein product
See the reference protein sequence for cardiolipin synthase (CMP-forming) isoform 3 (NP_001310490.1).

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Protein sequence from Nucleotide coding region
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Nucleotide