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Cellosaurus LUMCi008-B (CVCL_WR62)

[Text version]

Cell line name LUMCi008-B
Synonyms 152-3; LUMC0152iHD03
Accession CVCL_WR62
Resource Identification Initiative To cite this cell line use: LUMCi008-B (RRID:CVCL_WR62)
Comments From: Leiden University Medical Center; Leiden; Netherlands.
Derived from sampling site: Skin.
Sequence variations Heterozygous for HTT p.Gln18[46]; has 46 CAG repeats in one of the 2 alleles (PubMed=31326748).
Disease Huntington's disease (NCIt: C82342)
Huntington disease (ORDO: Orphanet_399)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_WR61 ! LUMCi008-A
CVCL_WR63 ! LUMCi008-C
Sex of cell Female
Age at sampling 49Y
Category Induced pluripotent stem cell

PubMed=31326748; DOI=10.1016/j.scr.2019.101498
van der Graaf L.M., Gardiner S.L., Tok M., Brands T., Boogaard M.W., Pepers B.A., Eussen B., de Klein A., Aziz N.A., Freund C., Buijsen R.A.M., van Roon-Mom W.M.C.
Generation of 5 induced pluripotent stem cell lines, LUMCi007-A and B and LUMCi008-A, B and C, from 2 patients with Huntington disease.
Stem Cell Res. 39:101498-101498(2019)

Cell line databases/resources hPSCreg; LUMCi008-B
Other Wikidata; Q95983453
Entry history
Entry creation05-Jul-2019
Last entry update02-Jul-2020
Version number4