Homo sapiens partial mRNA for aldo-keto reductase family 1, member D1 - Nucleotide

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Recurrent AKR1D1 c.580-13T>A Variant: A Cause of Δ(4)-3-Oxosteroid-5β-Reductase Deficiency. [J Mol Diagn. 2023]
Recurrent AKR1D1 c.580-13T>A Variant: A Cause of Δ(4)-3-Oxosteroid-5β-Reductase Deficiency.
Zhao J, Qiu YL, Wang L, Li ZD, Xie XB, Lu Y, Setchell KDR, Cheng Y, Xing QH, Wang JS. J Mol Diagn. 2023 Apr; 25(4):227-233. Epub 2023 Feb 4.
Pediatric Genetic Cholestatic Liver Disease Overview. [GeneReviews(®). 1993]
Pediatric Genetic Cholestatic Liver Disease Overview.
Amendola M, Squires JE. GeneReviews(®). 1993-2024. 2022 Sep 15 [updated 2023 May 25]
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome. [Cell. 2021]
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
Huttlin EL, Bruckner RJ, Navarrete-Perea J, Cannon JR, Baltier K, Gebreab F, Gygi MP, Thornock A, Zarraga G, Tam S, et al. Cell. 2021 May 27; 184(11):3022-3040.e28. Epub 2021 May 6.

RefSeq alternative splicing
See 8 reference mRNA sequence splice variants for the AKR1D1 gene.

Homo sapiens putative G-protein-coupled receptor FKSG78 (FKSG78) mRNA, complete ...
Homo sapiens putative G-protein-coupled receptor FKSG78 (FKSG78) mRNA, complete cds
gi|13517959|gb|AF345566.1|

Nucleotide
175809[uid] (1)
Taxonomy
Fusarium sambucinum
Fusarium sambucinum

Genome

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Nucleotide