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Cellosaurus KCL016 (CVCL_A249)

[Text version]

Cell line name KCL016
Synonyms KCL-016; VHL3; KCL016_VHL3; KCLe012-A
Accession CVCL_A249
Resource Identification Initiative To cite this cell line use: KCL016 (RRID:CVCL_A249)
Comments From: King's College London; London; United Kingdom.
Registration: NIH Human Embryonic Stem Cell Registry; NIHhESC-13-0216.
Registration: UK Stem Cell Bank (UKSCB); Steering comm. appl. SCSC10-35.
Miscellaneous: Sibling to KCL015 (CVCL_A248) and KCL017 (CVCL_A250).
Sequence variations
  • Mutation; HGNC; 12687; VHL; Simple; c.676+3A>T; Zygosity=Heterozygous (PubMed=27345783).
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 Female
Age at sampling Blastocyst stage
Category Embryonic stem cell
Web pages https://www.kcl.ac.uk/lsm/research/divisions/wh/groups/medicine/hescell.aspx
https://grants.nih.gov/stem_cells/registry/current.htm?id=656
Publications

PubMed=27345783; DOI=10.1016/j.scr.2015.12.003
Miere C., Hewitson H., Wood V., Kadeva N., Cornwell G., Codognotto S., Stephenson E., Ilic D.
Generation of KCL016 research grade human embryonic stem cell line carrying a mutation in VHL gene.
Stem Cell Res. 16:37-39(2016)

Cross-references
Cell line databases/resources hPSCreg; KCLe012-A
ISCR; 1870
SKIP; SKIP002360
Encyclopedic resources Wikidata; Q54899663
Entry history
Entry creation06-Jun-2012
Last entry update16-Dec-2021
Version number21