NCIt definition : Human FEV wild-type allele is located in the vicinity of 2q35 and is approximately
5 kb in length. This allele, which encodes protein FEV, may be involved in the negative
regulation of transcription. Variation in the FEV gene may be associated with susceptibility
to sudden infant death syndrome. A complex chromosomal translocation t(2;21;22)(q23;q22;q12)
that fuses this gene and the EWSR1 gene is associated with Ewing sarcoma.;
NCIt note : A chromosomal translocation involving the FEV gene and the FUS gene may be associated
with Ewing sarcoma. (COSMIC);