Cellosaurus GM26586 (CVCL_RT73)
| Cell line name | GM26586 |
|---|---|
| Accession | CVCL_RT73 |
| Resource Identification Initiative | To cite this cell line use: GM26586 (RRID:CVCL_RT73) |
| Comments | Derived from site: In situ; Arm, skin; UBERON=UBERON_0002427. Cell type: Fibroblast of skin; CL=CL_0002620. |
| Sequence variations |
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| Disease | Congenital disorder of deglycosylation (NCIt: C126746) Alacrimia-choreoathetosis-liver dysfunction syndrome (ORDO: Orphanet_404454) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Originate from same individual | CVCL_RT72 ! GM26585 |
| Sex of cell | Female |
| Age at sampling | 4Y |
| Category | Finite cell line |
| Cross-references | |
| Cell line collections (Providers) | Coriell; GM26586 |
| Encyclopedic resources | Wikidata; Q54854105 |
| Entry history | |
| Entry creation | 05-Mar-2018 |
| Last entry update | 19-Dec-2024 |
| Version number | 11 |