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 | |
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 |
Cross-references | |
Cell line databases/resources | hPSCreg; KCLe012-A
ISCR; 1870 SKIP; SKIP002360 |
Encyclopedic resources | Wikidata; Q54899663 |
Entry history | |
Entry creation | 06-Jun-2012 |
Last entry update | 16-Dec-2021 |
Version number | 21 |