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Cellosaurus HG1626 (CVCL_WX55)

[Text version]
Cell line name HG1626
Accession CVCL_WX55
Resource Identification Initiative To cite this cell line use: HG1626 (RRID:CVCL_WX55)
Comments Population: Japanese.
Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
Donor information: From Bloom Syndrome Registry patient 93(YoYa) (BSR93).
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
Disease Bloom syndrome (NCIt: C2903)
Bloom syndrome (ORDO: Orphanet_125)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_W042 ! BS2KA
CVCL_2869 ! BSL2KA
Sex of cell Male
Category Transformed cell line
Publications

PubMed=6705251; DOI=10.1111/j.1399-0004.1984.tb00480.x
German J.L. 3rd, Bloom D., Passarge E.
Bloom's syndrome. XI. Progress report for 1983.
Clin. Genet. 25:166-174(1984)

PubMed=7585968; DOI=10.1016/0092-8674(95)90105-1
Ellis N.A., Groden J., Ye T.-Z., Straughen J.E., Lennon D.J., Ciocci S., Proytcheva M., German J.L. 3rd
The Bloom's syndrome gene product is homologous to RecQ helicases.
Cell 83:655-666(1995)

PubMed=17407155; DOI=10.1002/humu.20501
German J.L. 3rd, Sanz M.M., Ciocci S., Ye T.-Z., Ellis N.A.
Syndrome-causing mutations of the BLM gene in persons in the Bloom's Syndrome Registry.
Hum. Mutat. 28:743-753(2007)

Cross-references
Encyclopedic resources Wikidata; Q94192547
Entry history
Entry creation06-Sep-2019
Last entry update19-Dec-2024
Version number8