Homo sapiens FA complementation group L (FANCL), transcript variant 4, - Nucleotide

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Autosomal recessive systemic microangiopathy associated with FANCL Fanconi anaemia. [J Neurol Neurosurg Psychiatry....]
Autosomal recessive systemic microangiopathy associated with FANCL Fanconi anaemia.
Cousyn L, Demeret S, Philippi A, Bergametti F, Villa C, Morbini P, Riant F, Soulier J, Tournier-Lasserve E, Denier C. J Neurol Neurosurg Psychiatry. 2023 Dec 14; 95(1):98-100. Epub 2023 Dec 14.
Structural and biochemical basis of interdependent FANCI-FANCD2 ubiquitination. [EMBO J. 2023]
Structural and biochemical basis of interdependent FANCI-FANCD2 ubiquitination.
Lemonidis K, Rennie ML, Arkinson C, Chaugule VK, Clarke M, Streetley J, Walden H. EMBO J. 2023 Feb 1; 42(3):e111898. Epub 2022 Nov 17.
Genome-wide CRISPR screens using isogenic cells reveal vulnerabilities conferred by loss of tumor suppressors. [Sci Adv. 2022]
Genome-wide CRISPR screens using isogenic cells reveal vulnerabilities conferred by loss of tumor suppressors.
Feng X, Tang M, Dede M, Su D, Pei G, Jiang D, Wang C, Chen Z, Li M, Nie L, et al. Sci Adv. 2022 May 13; 8(19):eabm6638. Epub 2022 May 13.

RefSeq alternative splicing
See 28 reference mRNA sequence splice variants for the FANCL gene.
RefSeq protein product
See the reference protein sequence for E3 ubiquitin-protein ligase FANCL isoform 3 (NP_001361544.1).

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Nucleotide