Cellosaurus cell line INCABRi001-A (CVCL

Cellosaurus INCABRi001-A (CVCL_LK61)

Cross-references
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; HGNC:18318; ASXL1; Simple; p.Arg693Ter (c.2077C>T); ClinVar=VCV000620281; Zygosity=Unspecified (PubMed=29034885). Mutation; HGNC; 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)
Cell line databases/resources	hPSCreg; INCABRi001-A
Encyclopedic resources	Wikidata; Q54897706
Entry history
Entry creation	15-Nov-2017
Last entry update	19-Dec-2024
Version number	11