Drosophila melanogaster SLY-1 homologous (Slh), transcript variant G, - Nucleotide

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Identification of atlastin genetic modifiers in a model of hereditary spastic paraplegia in Drosophila. [Hum Genet. 2023]
Identification of atlastin genetic modifiers in a model of hereditary spastic paraplegia in Drosophila.
Candia N, Ibacache A, Medina-Yáñez I, Olivares GH, Ramírez M, Vega-Macaya F, Couve A, Sierralta J, Olguín P. Hum Genet. 2023 Aug; 142(8):1303-1315. Epub 2023 Jun 27.
Loss of amyotrophic lateral sclerosis risk factor SCFD1 causes motor dysfunction in Drosophila. [Neurobiol Aging. 2023]
Loss of amyotrophic lateral sclerosis risk factor SCFD1 causes motor dysfunction in Drosophila.
Borg R, Purkiss A, Cacciottolo R, Herrera P, Cauchi RJ. Neurobiol Aging. 2023 Jun; 126:67-76. Epub 2023 Feb 21.
In vivo profiling of the Zucchini proximal proteome in the Drosophila ovary. [Development. 2023]
In vivo profiling of the Zucchini proximal proteome in the Drosophila ovary.
Nguyen TTM, Munkhzul C, Kim J, Kyoung Y, Vianney M, Shin S, Ju S, Pham-Bui HA, Kim J, Kim JS, et al. Development. 2023 Feb 15; 150(4). Epub 2023 Feb 16.

RefSeq alternative splicing
See the other reference mRNA sequence splice variant for the Slh gene (NM_205892.2).
RefSeq protein product
See the reference protein sequence for SLY-1 homologous, isoform G (NP_001137769.2).

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GenScript latest version of gene cDNA ORF Clone [GenScript latest version of g...]
GenScript latest version of gene cDNA ORF Clone

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Nucleotide