E3 ubiquitin-protein ligase FANCL isoform X10 [Homo sapiens]

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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.
FANCL gene mutations in premature ovarian insufficiency. [Hum Mutat. 2020]
FANCL gene mutations in premature ovarian insufficiency.
Yang Y, Guo T, Liu R, Ke H, Xu W, Zhao S, Qin Y. Hum Mutat. 2020 May; 41(5):1033-1041. Epub 2020 Feb 24.
A founder variant in the South Asian population leads to a high prevalence of FANCL Fanconi anemia cases in India. [Hum Mutat. 2020]
A founder variant in the South Asian population leads to a high prevalence of FANCL Fanconi anemia cases in India.
Donovan FX, Solanki A, Mori M, Chavan N, George M, C SK, Okuno Y, Muramastsu H, Yoshida K, Shimamoto A, et al. Hum Mutat. 2020 Jan; 41(1):122-128. Epub 2019 Sep 26.

RefSeq genomic sequence
See the genomic reference sequence for the FANCL gene (NG_007418.1).
RefSeq mRNA
See reference mRNA sequence for the FANCL gene (XM_011532945.3).
RefSeq protein isoforms
See 28 reference sequence protein isoforms for the FANCL gene.

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Protein