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Cellosaurus PD20 RV:D2 (CVCL_AK49)

[Text version]
Cell line name PD20 RV:D2
Synonyms PD.20hygro:RV; PD20-wtD2
Accession CVCL_AK49
Resource Identification Initiative To cite this cell line use: PD20 RV:D2 (RRID:CVCL_AK49)
Comments Characteristics: Transfection of wildtype FANCD2 restores the full activity of the protein which is mutated in the parent cell line.
Transfected with: HGNC; 3585; FANCD2.
Transfected with: UniProtKB; P00557; Escherichia coli hygromycin-B 4-O-kinase (hph) (HygR).
Transformant: NCBI_TaxID; 1891767; Simian virus 40 (SV40).
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Fanconi anemia, complementation group D2 (NCIt: C125706)
Fanconi anemia (ORDO: Orphanet_84)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_G042 (GM16633)
Sex of cell Male
Age at sampling 7Y
Category Transformed cell line
Web pages http://www.ohsu.edu/research/fanconi-anemia/celllines.cfm
Publications

PubMed=12361951; DOI=10.1074/jbc.M207937200
Donahue S.L., Campbell C.
A DNA double strand break repair defect in Fanconi anemia fibroblasts.
J. Biol. Chem. 277:46243-46247(2002)

Cross-references
Encyclopedic resources Wikidata; Q54946782
Entry history
Entry creation02-May-2016
Last entry update30-Jan-2024
Version number12