FANCE

FANCE

Fanconi anemia, complementation group E, also known as FANCE, is a human gene.cite web | title = Entrez Gene: FANCE Fanconi anemia, complementation group E| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=2178| accessdate = ]

PBB_Summary
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summary_text = The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, and FANCL. 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 E.cite web | title = Entrez Gene: FANCE Fanconi anemia, complementation group E| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=2178| accessdate = ]

References

Further reading

PBB_Further_reading
citations =
*cite journal | author=Joenje H, Lo ten Foe JR, Oostra AB, "et al." |title=Classification of Fanconi anemia patients by complementation analysis: evidence for a fifth genetic subtype. |journal=Blood |volume=86 |issue= 6 |pages= 2156–60 |year= 1995 |pmid= 7662964 |doi=
*cite journal | author=Wegner RD, Henrichs I, Joenje H, Schroeder-Kurth T |title=Fanconi anemia complementation group E: clinical and cytogenetic data of the first patient. |journal=Clin. Genet. |volume=50 |issue= 6 |pages= 479–82 |year= 1997 |pmid= 9147877 |doi=
*cite journal | author=Joenje H, Oostra AB, Wijker M, "et al." |title=Evidence for at least eight Fanconi anemia genes. |journal=Am. J. Hum. Genet. |volume=61 |issue= 4 |pages= 940–4 |year= 1997 |pmid= 9382107 |doi=
*cite journal | author=Waisfisz Q, Saar K, Morgan NV, "et al." |title=The Fanconi anemia group E gene, FANCE, maps to chromosome 6p. |journal=Am. J. Hum. Genet. |volume=64 |issue= 5 |pages= 1400–5 |year= 1999 |pmid= 10205272 |doi=
*cite journal | author=de Winter JP, Léveillé F, van Berkel CG, "et al." |title=Isolation of a cDNA representing the Fanconi anemia complementation group E gene. |journal=Am. J. Hum. Genet. |volume=67 |issue= 5 |pages= 1306–8 |year= 2000 |pmid= 11001585 |doi=
*cite journal | author=Medhurst AL, Huber PA, Waisfisz Q, "et al." |title=Direct interactions of the five known Fanconi anaemia proteins suggest a common functional pathway. |journal=Hum. Mol. Genet. |volume=10 |issue= 4 |pages= 423–9 |year= 2001 |pmid= 11157805 |doi=
*cite journal | author=Pace P, Johnson M, Tan WM, "et al." |title=FANCE: the link between Fanconi anaemia complex assembly and activity. |journal=EMBO J. |volume=21 |issue= 13 |pages= 3414–23 |year= 2002 |pmid= 12093742 |doi= 10.1093/emboj/cdf355
*cite journal | author=Taniguchi T, D'Andrea AD |title=The Fanconi anemia protein, FANCE, promotes the nuclear accumulation of FANCC. |journal=Blood |volume=100 |issue= 7 |pages= 2457–62 |year= 2002 |pmid= 12239156 |doi= 10.1182/blood-2002-03-0860
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Gordon SM, Buchwald M |title=Fanconi anemia protein complex: mapping protein interactions in the yeast 2- and 3-hybrid systems. |journal=Blood |volume=102 |issue= 1 |pages= 136–41 |year= 2003 |pmid= 12649160 |doi= 10.1182/blood-2002-11-3517
*cite journal | author=Meetei AR, Sechi S, Wallisch M, "et al." |title=A multiprotein nuclear complex connects Fanconi anemia and Bloom syndrome. |journal=Mol. Cell. Biol. |volume=23 |issue= 10 |pages= 3417–26 |year= 2003 |pmid= 12724401 |doi=
*cite journal | author=Meetei AR, de Winter JP, Medhurst AL, "et al." |title=A novel ubiquitin ligase is deficient in Fanconi anemia. |journal=Nat. Genet. |volume=35 |issue= 2 |pages= 165–70 |year= 2003 |pmid= 12973351 |doi= 10.1038/ng1241
*cite journal | author=Mungall AJ, Palmer SA, Sims SK, "et al." |title=The DNA sequence and analysis of human chromosome 6. |journal=Nature |volume=425 |issue= 6960 |pages= 805–11 |year= 2003 |pmid= 14574404 |doi= 10.1038/nature02055
*cite journal | author=Hussain S, Wilson JB, Medhurst AL, "et al." |title=Direct interaction of FANCD2 with BRCA2 in DNA damage response pathways. |journal=Hum. Mol. Genet. |volume=13 |issue= 12 |pages= 1241–8 |year= 2004 |pmid= 15115758 |doi= 10.1093/hmg/ddh135
*cite journal | author=Wang X, Andreassen PR, D'Andrea AD |title=Functional interaction of monoubiquitinated FANCD2 and BRCA2/FANCD1 in chromatin. |journal=Mol. Cell. Biol. |volume=24 |issue= 13 |pages= 5850–62 |year= 2004 |pmid= 15199141 |doi= 10.1128/MCB.24.13.5850-5862.2004
*cite journal | author=Léveillé F, Blom E, Medhurst AL, "et al." |title=The Fanconi anemia gene product FANCF is a flexible adaptor protein. |journal=J. Biol. Chem. |volume=279 |issue= 38 |pages= 39421–30 |year= 2004 |pmid= 15262960 |doi= 10.1074/jbc.M407034200
*cite journal | author=Gerhard DS, Wagner L, Feingold EA, "et al." |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504
*cite journal | author=Meetei AR, Levitus M, Xue Y, "et al." |title=X-linked inheritance of Fanconi anemia complementation group B. |journal=Nat. Genet. |volume=36 |issue= 11 |pages= 1219–24 |year= 2004 |pmid= 15502827 |doi= 10.1038/ng1458
*cite journal | author=Meetei AR, Medhurst AL, Ling C, "et al." |title=A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M. |journal=Nat. Genet. |volume=37 |issue= 9 |pages= 958–63 |year= 2005 |pmid= 16116422 |doi= 10.1038/ng1626
*cite journal | author=Gordon SM, Alon N, Buchwald M |title=FANCC, FANCE, and FANCD2 form a ternary complex essential to the integrity of the Fanconi anemia DNA damage response pathway. |journal=J. Biol. Chem. |volume=280 |issue= 43 |pages= 36118–25 |year= 2006 |pmid= 16127171 |doi= 10.1074/jbc.M507758200

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