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Cellosaurus HG2045 (CVCL_WX99)

[Text version]
Cell line name HG2045
Accession CVCL_WX99
Resource Identification Initiative To cite this cell line use: HG2045 (RRID:CVCL_WX99)
Comments Population: Caucasian.
Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
Donor information: From Bloom Syndrome Registry patient 111(JaKir) (BSR111).
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; HGNC:1058; BLM; Simple; p.Ile770fs (c.2308-117_2555+7420del7811) (Ex11-12fdel); Zygosity=Heterozygous (PubMed=17407155).
  • Mutation; HGNC; HGNC:1058; BLM; Simple; p.Arg899Ter (c.2695C>T); ClinVar=VCV000127491; Zygosity=Heterozygous (PubMed=17407155).
Disease Bloom syndrome (NCIt: C2903)
Bloom syndrome (ORDO: Orphanet_125)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
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; Q94192615
Entry history
Entry creation06-Sep-2019
Last entry update19-Dec-2024
Version number11