Fanconi anemia complementation group G isoform 1, partial [Homo sapien - Protein

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Frequent internuclear bridging in a Fanconi anemia patient with FANCG mutation. [Blood. 2021]
Frequent internuclear bridging in a Fanconi anemia patient with FANCG mutation.
Cochran T, Li W. Blood. 2021 Aug 26; 138(8):738.
Loss of Mitochondrial Localization of Human FANCG Causes Defective FANCJ Helicase. [Mol Cell Biol. 2020]
Loss of Mitochondrial Localization of Human FANCG Causes Defective FANCJ Helicase.
K JCB, Kapoor BS, Mandal K, Ghosh S, Mokhamatam RB, Manna SK, Mukhopadhyay SS. Mol Cell Biol. 2020 Nov 6; 40(23). Epub 2020 Nov 6.
Endocrine profiling in patients with Fanconi anemia, homozygous for a FANCG founder mutation. [Mol Genet Genomic Med. 2020]
Endocrine profiling in patients with Fanconi anemia, homozygous for a FANCG founder mutation.
Dillon B, Feben C, Segal D, du Plessis J, Reynders D, Wainwright R, Poole J, Krause A. Mol Genet Genomic Med. 2020 Aug; 8(8):e1351. Epub 2020 Jun 11.

RefSeq genomic sequence
See the genomic reference sequence for the FANCG gene (NG_007312.1).
RefSeq protein
See the reference protein sequence for Fanconi anemia group G protein (NP_004620.1).

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Fanconi anemia complementation group G isoform 1, partial [Homo sapiens]
Fanconi anemia complementation group G isoform 1, partial [Homo sapiens]
gi|957949356|gb|ALQ33511.1|

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