Cellosaurus GM20951 (CVCL_DB10)
| Cell line name | GM20951 |
|---|---|
| Accession | CVCL_DB10 |
| Resource Identification Initiative | To cite this cell line use: GM20951 (RRID:CVCL_DB10) |
| Comments | Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. |
| Disease | Congenital disorder of glycosylation type Ia (NCIt: C126868) PMM2-CDG (ORDO: Orphanet_79318) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Sex of cell | Male |
| Age at sampling | Age unspecified |
| Category | Finite cell line |
| Cross-references | |
| Cell line collections (Providers) | Coriell; GM20951 |
| Cell line databases/resources | CLO; CLO_0015361 |
| Encyclopedic resources | Wikidata; Q54851491 |
| Entry history | |
| Entry creation | 13-Jul-2016 |
| Last entry update | 29-Jun-2023 |
| Version number | 7 |