CELL SEARCH SYSTEM
  3.II. RCB-CRL : Genetic Mutants  
Cell No. Cell name General characteristics
  GMC0001     B0082     Human B cell line derived from Werner syndrome patient and transformed by Epstein-Barr Virus. The same patient as GMC0002.  
  GMC0002     A0082     Human primary adherent cells derived from Werner syndrome patient's skin. The same patient as GMC0001.  
  GMC0003     B0006     Human B cell line derived from Werner syndrome patient and transformed by Epstein-Barr Virus.  
  GMC0004     A0065     Human primary adherent cells derived from Werner syndrome (questionable) patient's skin.  
  GMC0005     B0031     Human B cell line derived from Werner syndrome patient and transformed by Epstein-Barr Virus. The same patient as GMC0012.  
  GMC0006     WS2RGB     Accelerated aging in vitro, Werner's syndrome  
  GMC0007     WS3RGB     Accelerated aging in vitro, Werner's syndrome.  
  GMC0009     WS6RGB     Werner's syndrome fibroblast  
  GMC0010     UN7RGB     Questionable Werner's syndrome-like. Life span in vitro was over 60 PDL.  
  GMC0012     A0031     Human primary adherent cells derived from Werner syndrome patient's skin. The same patient as GMC0005.  
  GMC0013     B0096     Human B cell line derived from Werner syndrome patient and transformed by Epstein-Barr Virus.  
  GMC0014     A0042     Human primary adherent cells derived from Werner syndrome (questionable) patient's skin. The same patient as GMC0015.  
  GMC0015     B0042     Human B cell line derived from Werner syndrome (questionable) patient and transformed by Epstein-Barr Virus. The same patient as GMC0014.  
  GMC0016     B0022     Human B cell line derived from Werner syndrome patient and transformed by Epstein-Barr Virus.  
  GMC0017     B0055     Human B cell line derived from Werner syndrome patient and transformed by Epstein-Barr Virus.The same patient as GMC0022.  
  GMC0019     B0090     Human B cell line derived from Werner syndrome (questionable) patient and transformed by Epstein-Barr Virus.  
  GMC0020     B0072     Human B cell line derived from Werner syndrome (questionable) patient and transformed by Epstein-Barr Virus. The same patient as GMC0024.  
  GMC0021     A0022     Human primary adherent cells derived from Werner syndrome patient's skin. The same patient as GMC0016.  
  GMC0022     A0055     Human primary adherent cells derived from Werner syndrome patient's skin. The same patient as GMC00017.  
  GMC0023     B0036     Human B cell line derived from Werner syndrome patient and transformed by Epstein-Barr Virus.  
  GMC0024     A0072     Human primary adherent cells derived from Werner syndrome (questionable) patient's skin. The same patient as GMC0020.  
  GMC0025     B0010     Human B cell line derived from Werner syndrome (questionable) patient and transformed by Epstein-Barr Virus. The same patient as GMC0027.  
  GMC0026     B0076     Human B cell line derived from Werner syndrome patient and transformed by Epstein-Barr Virus.  
  GMC0027     A0010     Human primary adherent cells derived from Werner syndrome (questionable) patient's skin. The same patient as GMC0025.  
  GMC0028     A0058     Human primary adherent cells derived from Werner syndrome patient's skin. The same patient as GMC0029.  
  GMC0029     B0058     Human B cell line derived from Werner syndrome patient and transformed by Epstein-Barr Virus. he same patient as GMC0028.  
  GMC0030     B0050     Human B cell line derived from Werner syndrome patient and transformed by Epstein-Barr Virus. The same patient as GMC0031.  
  GMC0031     A0050     Human primary adherent cells derived from Werner syndrome patient's skin. The same patient as GMC0030.  
  GMC0032     B0078     Human B cell line derived from Werner syndrome (questionable) patient and transformed by Epstein-Barr Virus.  
  GMC0033     B0086     Human B cell line derived from Werner syndrome patient and transformed by Epstein-Barr Virus.  
  GMC0034     B0045     Human B cell line derived from Werner syndrome patient and transformed by Epstein-Barr Virus.  
  GMC0035     B0026     Human B cell line derived from Werner syndrome patient and transformed by Epstein-Barr Virus. The same patient as GMC0036.  
  GMC0036     A0026     Human primary adherent cells derived from Werner syndrome patient's skin. The same patient as GMC00035.  
  GMC0037     A0001     Human primary adherent cells derived from Werner syndrome (questionable) patient's skin. The same patient as GMC0038.  
  RCB0252     W-V     SV40-transformed Werner's syndrome fibroblast  
  RCB0266     CLA1RGB     Pseudo congenital lactic acidosis.  
  RCB0388     NCU-F1     Ehlers-Danlos syndrome  
  RCB0389     NCU-F2     Morquio syndrome  
  RCB0390     NCU-F3     Wilson's disease  
  RCB0391     NCU-F4     Wilson's disease  
  RCB0393     NCU-F6     Citrullinemia  
  RCB0394     NCU-F7     Citrullinemia  
  RCB0395     NCU-F8     Wilson's disease  
  RCB0397     NCU-F10     Cockayne's syndrome  
  RCB0407     WS2TKB     Werner's syndrome  
  RCB0409     WS1TKB     Werner's syndrome, the same patient as RCB0433 WS1TKB2.  
  RCB0410     MEN1RGB     Fibroblasts from multiple endocrine neoplasia  
  RCB0421     MEN2RGB     Fibroblasts from multiple endocrine neoplasia  
  RCB0433     WS1TKB2     Werner's syndrome, the same patient as RCB0409 WS1TKB.  
  RCB0492     OTCD1TKB     OTC(-), X-linked, dominant (XD)  
  RCB0520     WR216     APRT(-) EB transformed B cell line  
  RCB0546     AT-PDH1TKB     Pyruvate dehydrogenase deficiency fibroblasts.  
  RCB0697     GM2-1TKB     Tay-Sachs' disease  
  RCB0783     FCP-S1M     Skin fibroblasts from a familial colon polyposis patient.  
  RCB0784     FCP-S2H     Skin fibroblasts from a familial colon polyposis patient at Hiroshima.  
  RCB0785     FCP-S3H     Skin fibroblasts from a familial colon polyposis patient at Hiroshima.  
  RCB0786     FCP-S4H     Skin fibroblasts from a familial colon polyposis patient at Hiroshima.  
  RCB0787     FCP-S5H     Skin fibroblasts from a familial colon polyposis patient at Hiroshima.  
  RCB0788     FCP-S6H     Skin fibroblasts from a familial colon polyposis patient at Hiroshima.  
  RCB1026     GM95     Glucosylceramide synthetase-deficient B16 melanoma mutant.  
  RCB1382     CF1TKB     Japanese cystic fibrosis fibroblast.  
  RCB1560     PWS-Yamaguchi     Prader-Willi syndrome with obesity. del(15) was found in lymphocytes of the patient.  
  RCB1561     RML-Yoshi     Severe insulin-resistance by uncleaved insulin proreceptor. G->T mutation in interconnecting region.  
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