| Cell line name | KCL017 |
|---|---|
| Synonyms | KCL-017; VHL4; KCL017_VHL4; KCLe013-A |
| Accession | CVCL_A250 |
| Resource Identification Initiative | To cite this cell line use: KCL017 (RRID:CVCL_A250) |
| Comments | From: King's College London; London; United Kingdom. Registration: NIH Human Embryonic Stem Cell Registry; NIHhESC-13-0217. Registration: UK Stem Cell Bank (UKSCB); Steering comm. appl. SCSC10-34. Donor information: Embryo is sibling to those giving rise to KCL015 (Cellosaurus=CVCL_A248) and KCL016 (Cellosaurus=CVCL_A249). Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358. Cell type: Embryonic stem cell; CL=CL_0002322. |
| 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 | Male |
| Age at sampling | Blastocyst stage |
| Category | Embryonic stem cell |
| Publications | PubMed=27345980; DOI=10.1016/j.scr.2016.01.013 |
| Cross-references | |
| Cell line databases/resources | hPSCreg; KCLe013-A
ISCR; 1871 NIHhESC; NIHhESC-13-0217 SKIP; SKIP002361 |
| Encyclopedic resources | Wikidata; Q54899664 |
| Entry history | |
| Entry creation | 06-Jun-2012 |
| Last entry update | 29-Jun-2023 |
| Version number | 22 |