| 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; UK. 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 | Heterozygous for VHL c.676+3A>T (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 |
| Cross-references | |
| Cell line databases/resources | hPSCreg; KCLe012-A
ISCR; 1870 SKIP; SKIP002360 |
| Other | Wikidata; Q54899663 |
| Entry history | |
| Entry creation | 06-Jun-2012 |
| Last entry updated | 12-Mar-2020 |
| Version number | 19 |