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Cellosaurus HG1742 (CVCL_WX89)

[Text version]
Cell line name HG1742
Accession CVCL_WX89
Resource Identification Initiative To cite this cell line use: HG1742 (RRID:CVCL_WX89)
Comments Population: Jewish; Ashkenazi/Sephardic.
Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
Donor information: From Bloom Syndrome Registry patient 107(MyAsa) (BSR107).
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; HGNC:1058; BLM; Simple; p.Tyr736Leufs*5 (c.2207_2212delATCTGAinsTAGATTC) (2281del6ins7) (BLMAsh); ClinVar=VCV000005454; Zygosity=Homozygous (PubMed=17407155).
Disease Bloom syndrome (NCIt: C2903)
Bloom syndrome (ORDO: Orphanet_125)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_U708 ! GM16859
CVCL_WX72 ! HG2654
Sex of cell Female
Age at sampling >40Y
Category Transformed cell line
Publications

PubMed=2647324; DOI=10.1111/j.1399-0004.1989.tb02905.x
German J.L. 3rd, Passarge E.
Bloom's syndrome. XII. Report from the Registry for 1987.
Clin. Genet. 35:57-69(1989)

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; Q94192558
Entry history
Entry creation06-Sep-2019
Last entry update19-Dec-2024
Version number9