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Cellosaurus INCABRi001-A (CVCL_LK61)

[Text version]
Cell line name INCABRi001-A
Synonyms PMF6.1; INCABRi001-A1
Accession CVCL_LK61
Resource Identification Initiative To cite this cell line use: INCABRi001-A (RRID:CVCL_LK61)
Comments From: Instituto Nacional de Cancer (INCA); Rio de Janeiro; Brazil.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; 18318; ASXL1; Simple; p.Arg693Ter (c.2077C>T); ClinVar=VCV000620281; Zygosity=Unspecified (PubMed=29034885).
  • Mutation; HGNC; 1455; CALR; Simple; p.Leu367Thrfs*46 (c.1092_1143del52); ClinVar=VCV000097006; Zygosity=Unspecified (PubMed=29034885).
Disease Adult acute myeloid leukemia (NCIt: C9154)
Primary myelofibrosis (NCIt: C2862)
Acute myeloid leukemia (ORDO: Orphanet_519)
Primary myelofibrosis (ORDO: Orphanet_824)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 61Y
Category Induced pluripotent stem cell
Publications

PubMed=29034885; DOI=10.1016/j.scr.2017.08.006
Gomez Limia C.E., Devalle S., Reis M., Sochacki J., Carneiro M., Madeiro da Costa R., D'Andrea M., Padilha T., Zalcberg I.R., Solza C., Daumas A., Rehen S.K., Monte-Mor B., Bonamino M.H.
Generation and characterization of a human induced pluripotent stem (iPS) cell line derived from an acute myeloid leukemia patient evolving from primary myelofibrosis carrying the CALR 52 bp deletion and the ASXL1 p.R693X mutation.
Stem Cell Res. 24:16-20(2017)

Cross-references
Cell line databases/resources hPSCreg; INCABRi001-A
Encyclopedic resources Wikidata; Q54897706
Entry history
Entry creation15-Nov-2017
Last entry update29-Jun-2023
Version number10