Cellosaurus WG1663 (CVCL_QZ32)
| Cell line name | WG1663 |
|---|---|
| Accession | CVCL_QZ32 |
| Resource Identification Initiative | To cite this cell line use: WG1663 (RRID:CVCL_QZ32) |
| Comments | From: Montreal Children's Hospital cell repository; Montreal; Canada. Miscellaneous: Cell line no longer available. Misspelling: WB1663; PubMed=1627355. Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. |
| Disease | Homocystinuria-megaloblastic anemia, cblE complementation type (NCIt: C142173) Methylcobalamin deficiency type cblE (ORDO: Orphanet_2169) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Category | Finite cell line |
| Publications | PubMed=1627355; DOI=10.1016/0885-4505(92)90032-T |
| Cross-references | |
| Encyclopedic resources | Wikidata; Q54993914 |
| Entry history | |
| Entry creation | 05-Mar-2018 |
| Last entry update | 29-Jun-2023 |
| Version number | 7 |