The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity\; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group M. [provided by RefSeq, Jul 2008].
Fouquet, Pawlikowska, Caburet, Guigon, Mäkinen, Tanner, Hietala, Urbanska, Bellutti, Legois, Bessieres, Gougeon, Benachi, Livera, Rosselli, Veitia, Misrahi: "A homozygousFANCMmutation underlies a familial case of non-syndromic primary ovarian insufficiency." in: eLife, Vol. 6, (2018) (PubMed).
Kasak, Punab, Nagirnaja, Grigorova, Minajeva, Lopes, Punab, Aston, Carvalho, Laasik, Smith, Conrad, Laan: "Bi-allelic Recessive Loss-of-Function Variants in FANCM Cause Non-obstructive Azoospermia." in: American journal of human genetics, Vol. 103, Issue 2, pp. 200-212, (2018) (PubMed).
Barroso, Pita, Arias, Menendez, Zamora, Blanco, Benitez, Ribas: "The Fanconi anemia family of genes and its correlation with breast cancer susceptibility and breast cancer features." in: Breast cancer research and treatment, Vol. 118, Issue 3, pp. 655-60, (2009) (PubMed).
Aliases for FANCM 抗体
Fanconi anemia complementation group M (FANCM) 抗体 hypothetical protein (PGTG_17854) 抗体 Fanconi anemia, complementation group M (Fancm) 抗体 AI427100 抗体 C730036B14Rik 抗体 D12Ertd364e 抗体 FAAP250 抗体 KIAA1596 抗体