Homo sapiens apolipoprotein L domain containing 1 (APOLD1), transcript - Nucleotide

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APOLD1 loss causes endothelial dysfunction involving cell junctions, cytoskeletal architecture, and Weibel-Palade bodies, while disrupting hemostasis. [Haematologica. 2023]
APOLD1 loss causes endothelial dysfunction involving cell junctions, cytoskeletal architecture, and Weibel-Palade bodies, while disrupting hemostasis.
Stritt S, Nurden P, Nurden AT, Schved JF, Bordet JC, Roux M, Alessi MC, Trégouët DA, Mäkinen T, Giansily-Blaizot M. Haematologica. 2023 Mar 1; 108(3):772-784. Epub 2023 Mar 1.
N(6)-Methyladenosine on mRNA facilitates a phase-separated nuclear body that suppresses myeloid leukemic differentiation. [Cancer Cell. 2021]
N(6)-Methyladenosine on mRNA facilitates a phase-separated nuclear body that suppresses myeloid leukemic differentiation.
Cheng Y, Xie W, Pickering BF, Chu KL, Savino AM, Yang X, Luo H, Nguyen DT, Mo S, Barin E, et al. Cancer Cell. 2021 Jul 12; 39(7):958-972.e8. Epub 2021 May 27.
TreeGrafter: phylogenetic tree-based annotation of proteins with Gene Ontology terms and other annotations. [Bioinformatics. 2019]
TreeGrafter: phylogenetic tree-based annotation of proteins with Gene Ontology terms and other annotations.
Tang H, Finn RD, Thomas PD. Bioinformatics. 2019 Feb 1; 35(3):518-520.

RefSeq alternative splicing
See the other reference mRNA sequence splice variant for the APOLD1 gene (NM_001130415.2).
RefSeq protein product
See the reference protein sequence for apolipoprotein L domain-containing protein 1 isoform 2 (NP_110444.3).

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Protein sequence from Nucleotide coding region
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Homo sapiens apolipoprotein L domain containing 1 (APOLD1), transcript variant 2...
Homo sapiens apolipoprotein L domain containing 1 (APOLD1), transcript variant 2, mRNA
gi|1677499276|ref|NM_030817.3|

Nucleotide

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Nucleotide