ID   PGF
AC   CVCL_E806
SY   pGF; GM03107; GM3107
DR   CLO; CLO_0013567
DR   Coriell; GM03107
DR   dbMHC; 49001
DR   ECACC; 94050342
DR   IHW; IHW09318
DR   IPD-IMGT/HLA; 11248
DR   Wikidata; Q54947326
RX   CelloPub=CLPUB00447;
RX   PubMed=6200433;
RX   PubMed=15140828;
RX   PubMed=16440057;
RX   PubMed=16702430;
RX   PubMed=18193213;
RX   PubMed=28360230;
RX   PubMed=29171935;
RX   PubMed=30844424;
CC   Part of: 12th International Histocompatibility Workshop (12IHW) cell line panel.
CC   Population: Caucasian; English.
CC   HLA typing: A*03:01:01:01; B*07:02:01:01; C*07:02:01:03; DPA1*01:03:01:02; DPB1*04:01:01; DQA1*01:02:01:05; DQB1*06:02:01; DRB1*15:01:01; DRB5*01:01:01; DRB6*02:01 (IPD-IMGT/HLA=11248).
CC   HLA typing: A*03:01:01:01; B*07:02:01; C*07:02:01:03; DPA1*01:03:01:02; DPB1*04:01:01:01; DQA1*01:02:01; DQB1*06:02:01; DRB1*15:01:01; DRB5*01:01:01 (PubMed=30844424).
CC   Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
CC   Omics: MHC region genome.
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
CC   Cell type: B-cell; CL=CL_0000236.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   Age unspecified
CA   Transformed cell line
DT   Created: 22-10-12; Last updated: 05-10-23; Version: 19
//
RX   CelloPub=CLPUB00447;
RA   Mulivor R.A., Suchy S.F.;
RT   "1992/1993 catalog of cell lines. NIGMS human genetic mutant cell
RT   repository. 16th edition. October 1992.";
RL   (In) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda (1992).
//
RX   PubMed=6200433; DOI=10.1007/BF00364762;
RA   Brodsky F.M.;
RT   "A matrix approach to human class II histocompatibility antigens:
RT   reactions of four monoclonal antibodies with the products of nine
RT   haplotypes.";
RL   Immunogenetics 19:179-194(1984).
//
RX   PubMed=15140828; DOI=10.1101/gr.2188104;
RA   Stewart C.A., Horton R., Allcock R.J.N., Ashurst J.L., Atrazhev A.M.,
RA   Coggill P., Dunham I., Forbes S., Halls K., Howson J.M.M.,
RA   Humphray S.J., Hunt S., Mungall A.J., Osoegawa K., Palmer S.,
RA   Roberts A.N., Rogers J., Sims S., Wang Y., Wilming L.G., Elliott J.F.,
RA   de Jong P.J., Sawcer S., Todd J.A., Trowsdale J., Beck S.;
RT   "Complete MHC haplotype sequencing for common disease gene mapping.";
RL   Genome Res. 14:1176-1187(2004).
//
RX   PubMed=16440057; DOI=10.1371/journal.pgen.0020009;
RA   Traherne J.A., Horton R., Roberts A.N., Miretti M.M., Hurles M.E.,
RA   Stewart C.A., Ashurst J.L., Atrazhev A.M., Coggill P., Palmer S.,
RA   Almeida-King J., Sims S., Wilming L.G., Rogers J., de Jong P.J.,
RA   Carrington M.N., Elliott J.F., Sawcer S., Todd J.A., Trowsdale J.,
RA   Beck S.;
RT   "Genetic analysis of completely sequenced disease-associated MHC
RT   haplotypes identifies shuffling of segments in recent human history.";
RL   PLoS Genet. 2:E9-E9(2006).
//
RX   PubMed=16702430; DOI=10.1534/genetics.106.057034;
RA   Shiina T., Ota M., Shimizu S., Katsuyama Y., Hashimoto N., Takasu M.,
RA   Anzai T., Kulski J.K., Kikkawa E., Naruse T., Kimura N., Yanagiya K.,
RA   Watanabe A., Hosomichi K., Kohara S., Iwamoto C., Umehara Y.,
RA   Meyer A., Wanner V., Sano K., Macquin C., Ikeo K., Tokunaga K.,
RA   Gojobori T., Inoko H., Bahram S.;
RT   "Rapid evolution of major histocompatibility complex class I genes in
RT   primates generates new disease alleles in humans via hitchhiking
RT   diversity.";
RL   Genetics 173:1555-1570(2006).
//
RX   PubMed=18193213; DOI=10.1007/s00251-007-0262-2;
RA   Horton R., Gibson R., Coggill P., Miretti M.M., Allcock R.J.N.,
RA   Almeida-King J., Forbes S., Gilbert J.G.R., Halls K., Harrow J.L.,
RA   Hart E., Howe K.L., Jackson D.K., Palmer S., Roberts A.N., Sims S.,
RA   Stewart C.A., Traherne J.A., Trevanion S., Wilming L.G., Rogers J.,
RA   de Jong P.J., Elliott J.F., Sawcer S., Todd J.A., Trowsdale J., Beck S.;
RT   "Variation analysis and gene annotation of eight MHC haplotypes: the
RT   MHC Haplotype Project.";
RL   Immunogenetics 60:1-18(2008).
//
RX   PubMed=28360230; DOI=10.1101/gr.213538.116;
RA   Norman P.J., Norberg S.J., Guethlein L.A., Nemat-Gorgani N., Royce T.,
RA   Wroblewski E.E., Dunn T., Mann T., Alicata C., Hollenbach J.A.,
RA   Chang W.-H., Shults Won M., Gunderson K.L., Abi-Rached L., Ronaghi M.,
RA   Parham P.;
RT   "Sequences of 95 human MHC haplotypes reveal extreme coding variation
RT   in genes other than highly polymorphic HLA class I and II.";
RL   Genome Res. 27:813-823(2017).
//
RX   PubMed=29171935; DOI=10.1111/tan.13184;
RA   Turner T.R., Hayhurst J.D., Hayward D.R., Bultitude W.P., Barker D.J.,
RA   Robinson J., Madrigal J.A., Mayor N.P., Marsh S.G.E.;
RT   "Single molecule real-time DNA sequencing of HLA genes at ultra-high
RT   resolution from 126 international HLA and immunogenetics workshop cell
RT   lines.";
RL   HLA 91:88-101(2018).
//
RX   PubMed=30844424; DOI=10.1016/j.humimm.2019.03.001;
RA   Creary L.E., Guerra S.G., Chong W., Brown C.J., Turner T.R.,
RA   Robinson J., Bultitude W.P., Mayor N.P., Marsh S.G.E., Saito K.,
RA   Lam K., Duke J.L., Mosbruger T.L., Ferriola D., Monos D.S., Willis A.,
RA   Askar M., Fischer G.F., Saw C.L., Ragoussis J., Petrek M.,
RA   Serra-Pages C., Juan Otero M., Stavropoulos-Giokas C., Dinou A., Ameen R.,
RA   Al Shemmari S., Spierings E., Gendzekhadze K., Morris G.P., Zhang Q.-H.,
RA   Kashi Z., Hsu S., Gangavarapu S., Mallempati K.C., Yamamoto F.,
RA   Osoegawa K., Vayntrub T., Chang C.-J., Hansen J.A.,
RA   Fernandez-Vina M.A.;
RT   "Next-generation HLA typing of 382 International Histocompatibility
RT   Working Group reference B-lymphoblastoid cell lines: report from the
RT   17th International HLA and Immunogenetics Workshop.";
RL   Hum. Immunol. 80:449-460(2019).
//