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Cellosaurus EUFA426 (CVCL_G069)

[Text version]
Cell line name EUFA426
Accession CVCL_G069
Resource Identification Initiative To cite this cell line use: EUFA426 (RRID:CVCL_G069)
Comments Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; HGNC:3582; FANCA; Simple; p.Val135Cysfs*46 (c.401dupC) (c.401insC); ClinVar=VCV000558097; Zygosity=Heterozygous (PubMed=10094191).
Disease Fanconi anemia, complementation group A (NCIt: C125702)
Fanconi anemia (ORDO: Orphanet_84)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Category Transformed cell line
Publications

PubMed=10094191; DOI=10.1038/sj.ejhg.5200248
Wijker M., Morgan N.V., Herterich S., van Berkel C.G.M., Tipping A.J., Gross H.-J., Gille J.J.P., Pals G., Savino M., Altay C., Mohan S., Dokal I., Cavenagh J.D., Marsh J., van Weel M., Ortega J.J., Schuler D., Samochatova E., Karwacki M.W., Bekassy A.N., Abecasis M., Ebell W., Kwee M.L., de Ravel T.J.L., Mathew C.G.
Heterogeneous spectrum of mutations in the Fanconi anaemia group A gene.
Eur. J. Hum. Genet. 7:52-59(1999)

Cross-references
Encyclopedic resources Wikidata; Q54832914
Entry history
Entry creation11-Feb-2013
Last entry update19-Dec-2024
Version number12