solute carrier family 25 member 44 isoform X1 [Homo sapiens]

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Genome Evolutionary Dynamics Meets Functional Genomics: A Case Story on the Identification of SLC25A44. [Int J Mol Sci. 2021]
Genome Evolutionary Dynamics Meets Functional Genomics: A Case Story on the Identification of SLC25A44.
Darbani B. Int J Mol Sci. 2021 May 26; 22(11). Epub 2021 May 26.
The GBA-370Rec Parkinson's disease risk haplotype harbors a potentially pathogenic variant in the mitochondrial gene SLC25A44. [Mol Genet Metab. 2021]
The GBA-370Rec Parkinson's disease risk haplotype harbors a potentially pathogenic variant in the mitochondrial gene SLC25A44.
Goldstein O, Gana-Weisz M, Attar R, Bar-Shira A, Lederkremer M, Shiner T, Thaler A, Mirelman A, Giladi N, Orr-Urtreger A. Mol Genet Metab. 2021 May; 133(1):109-112. Epub 2021 Mar 18.
Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage. [Am J Hum Genet. 2014]
Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage.
Woo D, Falcone GJ, Devan WJ, Brown WM, Biffi A, Howard TD, Anderson CD, Brouwers HB, Valant V, Battey TW, et al. Am J Hum Genet. 2014 Apr 3; 94(4):511-21. Epub 2014 Mar 20.

RefSeq mRNA
See reference mRNA sequence for the SLC25A44 gene (XM_011510180.2).
RefSeq protein isoforms
See 22 reference sequence protein isoforms for the SLC25A44 gene.

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