Cellosaurus HPS2895 (CVCL_A3WP)
Cell line name | HPS2895 |
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Accession | CVCL_A3WP |
Resource Identification Initiative | To cite this cell line use: HPS2895 (RRID:CVCL_A3WP) |
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_A3WQ ! HPS2896 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; HPS2895 |
Encyclopedic resources | Wikidata; Q105508978 |
Entry history | |
Entry creation | 12-Jan-2021 |
Last entry update | 19-Dec-2024 |
Version number | 5 |