Cellosaurus cell line CRICKi010-A (CVCL

Cross-references
Cell line name	CRICKi010-A
Synonyms	iFCI013 Clone 7; iBK985
Accession	CVCL_C5T2
Resource Identification Initiative	To cite this cell line use: CRICKi010-A (RRID:CVCL_C5T2)
Comments	From: The Francis Crick Institute Limited; London; United Kingdom. Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations	Mutation; HGNC; HGNC:12687; VHL; Simple; p.Phe136Ser (c.407T>C); ClinVar=VCV000496064; Zygosity=Heterozygous (PubMed=39549334).
Disease	Von Hippel-Lindau syndrome (NCIt: C3105) Von Hippel-Lindau disease (ORDO: Orphanet_892)
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell	Male
Age at sampling	23Y
Category	Induced pluripotent stem cell
Publications	PubMed=39549334; DOI=10.1016/j.scr.2024.103611 Devito L.G., Lim E.S.-Y., O'Toole S.M., Shepherd S.T.C., Deng D.-Q., Feng H.-G., Barber T., Drake W.M., Turajlic S., Healy L.E. Generation of two iPSC lines (CRICKi009-A; CRICKi010-A) from patients with type 1 von Hippel-Lindau (VHL) and histopathologically confirmed renal cell carcinoma (RCC). Stem Cell Res. 81:103611-103611(2024)
Cell line databases/resources	hPSCreg; CRICKi010-A
Biological sample resources	BioSamples; SAMEA112239931
Encyclopedic resources	Wikidata; Q116048793
Entry history
Entry creation	15-Dec-2022
Last entry update	10-Apr-2025
Version number	5