| Cell line name | HPS2899 |
|---|---|
| Accession | CVCL_A3WT |
| Resource Identification Initiative | To cite this cell line use: HPS2899 (RRID:CVCL_A3WT) |
| Comments | Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178. |
| Sequence variations |
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| Disease | Congenital myasthenic syndrome 12 (NCIt: C168997) Congenital myasthenic syndromes with glycosylation defect (ORDO: Orphanet_353327) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Originate from same individual | CVCL_UP24 ! HPS2894 CVCL_A3WP ! HPS2895 CVCL_A3WQ ! HPS2896 CVCL_A3WR ! HPS2897 CVCL_A3WS ! HPS2898 |
| Sex of cell | Male |
| Age at sampling | 20-29Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | RCB; HPS2899 |
| Encyclopedic resources | Wikidata; Q105508995 |
| Entry history | |
| Entry creation | 12-Jan-2021 |
| Last entry update | 29-Jun-2023 |
| Version number | 4 |