| Cell line name | HPSI1116i-mebq_1 |
|---|---|
| Synonyms | WTSIi662-A |
| Accession | CVCL_LL91 |
| Resource Identification Initiative | To cite this cell line use: HPSI1116i-mebq_1 (RRID:CVCL_LL91) |
| Comments | From: University College London; London; UK. From: Wellcome Trust Sanger Institute; Hinxton; UK. Derived from sampling site: Skin. |
| Disease | Neuronal ceroid lipofuscinosis type 3 (NCIt: C61258) CLN3 disease (ORDO: Orphanet_228346) |
| Species of origin | Homo sapiens (Human)
(NCBI Taxonomy: 9606)
|
| Originate from same individual | CVCL_LL92 ! HPSI1116i-mebq_7 |
| Sex of cell | Male |
| Age at sampling | 5-9Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections | ECACC; 77650759 |
| Cell line databases/resources | HipSci; HPSI1116i-mebq_1
hPSCreg; WTSIi662-A |
| Biological sample resources | BioSamples; SAMEA104012540 |
| Other | Wikidata; Q54891693 |
| Entry history | |
| Entry creation | 15-Nov-2017 |
| Last entry update | 12-Mar-2020 |
| Version number | 5 |