Cellosaurus HPS2896 (CVCL_A3WQ)
| Cell line name | HPS2896 |
|---|---|
| Accession | CVCL_A3WQ |
| Resource Identification Initiative | To cite this cell line use: HPS2896 (RRID:CVCL_A3WQ) |
| 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_A3WR ! HPS2897 CVCL_A3WS ! HPS2898 CVCL_A3WT ! HPS2899 |
| Sex of cell | Male |
| Age at sampling | 20-29Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | RCB; HPS2896 |
| Encyclopedic resources | Wikidata; Q105508982 |
| Entry history | |
| Entry creation | 12-Jan-2021 |
| Last entry update | 19-Dec-2024 |
| Version number | 5 |