fag

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Related to FANCG: fancy, FANCC, FANCA

fag

Brit (esp formerly) a young public school boy who performs menial chores for an older boy or prefect
References in periodicals archive ?
In >80% of black patients with FA, a homozygous seven base-pair deletion mutation in the FANCG gene (NM_004629.1 g.35077270_35077264del p.Tyr213Lysfs) [2] has been confirmed as the cause of the disease.
The aims of the present study were firstly, to describe the physical phenotype of affected Afrikaner patients with confirmed founder FANCA mutations, and secondly, to compare this phenotype with the physical phenotype in black South African patients with FA caused by the homozygous FANCG deletion mutations described by Feben et al.
The FANCG gene maps to chromosome 9p13, is 6kb in length comprising 14 exons and encoding a 2.5kb mRNA transcript.
(a) Gene Mean (b) SD ARHGDIB 123 472 33 871 BCL2 1024 362 CDC20 19 17 CNN2 14 593 6402 FANCG 594 163 FCGR3A 51 890 44 651 GMFG 21 422 5695 IFNG 163 80 IL1B 4998 2444 IL8 250 170 LGALS9 56 60 MMP16 <10 1 PMS2L3 243 95 PTGS2 879 361 RAG1 14 5 SLC31A2 2516 751 TIMP2 8934 2203 TNF 287 75 TPBG 14 7 (a) Distribution of TA measurement for all genes evaluated.
The FANCG Fanconi anemia protein interacts with CYP2E1: possible role in protection against oxidative DNA damage.
The genetics of FANCC and FANCG in familial pancreatic cancer.