Homo sapiens FA complementation group M (FANCM), transcript variant 2, - Nucleotide

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TXLNA enhances TBK1 phosphorylation by suppressing PPM1B recruitment. [Biochim Biophys Acta Mol Cell ...]
TXLNA enhances TBK1 phosphorylation by suppressing PPM1B recruitment.
Tian X, Zhang Z, Ding M. Biochim Biophys Acta Mol Cell Res. 2023 Oct; 1870(7):119550. Epub 2023 Jul 26.
FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women. [Eur J Hum Genet. 2023]
FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women.
Figlioli G, Billaud A, Ahearn TU, Antonenkova NN, Becher H, Beckmann MW, Behrens S, Benitez J, Bermisheva M, Blok MJ, et al. Eur J Hum Genet. 2023 May; 31(5):578-587. Epub 2023 Jan 27.
The Nse5/6-like SIMC1-SLF2 complex localizes SMC5/6 to viral replication centers. [Elife. 2022]
The Nse5/6-like SIMC1-SLF2 complex localizes SMC5/6 to viral replication centers.
Oravcová M, Nie M, Zilio N, Maeda S, Jami-Alahmadi Y, Lazzerini-Denchi E, Wohlschlegel JA, Ulrich HD, Otomo T, Boddy MN. Elife. 2022 Nov 14; 11. Epub 2022 Nov 14.

RefSeq alternative splicing
See 19 reference mRNA sequence splice variants for the FANCM gene.
RefSeq protein product
See the reference protein sequence for Fanconi anemia group M protein isoform 2 (NP_001295062.1).

Protein
Protein sequence from Nucleotide coding region
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GenScript latest version of gene cDNA ORF Clone [GenScript latest version of g...]
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Noccaea tymphaea isolate GR2008_A4 internal transcribed spacer 1, partial sequen...
Noccaea tymphaea isolate GR2008_A4 internal transcribed spacer 1, partial sequence; 5.8S ribosomal RNA gene, complete sequence; and internal transcribed spacer 2, partial sequence
gi|893689750|gb|KP163816.1|

Nucleotide

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Nucleotide