Cellosaurus GM25952 (CVCL_IJ32)
| Cell line name | GM25952 |
|---|---|
| Accession | CVCL_IJ32 |
| Resource Identification Initiative | To cite this cell line use: GM25952 (RRID:CVCL_IJ32) |
| Comments | Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. |
| Sequence variations |
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| Disease | Mental retardation, X-linked 102 (NCIt: C129931) X-linked intellectual disability-hypotonia-movement disorder syndrome (ORDO: Orphanet_457260) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Sex of cell | Female |
| Age at sampling | 10Y |
| Category | Finite cell line |
| Cross-references | |
| Cell line collections (Providers) | Coriell; GM25952 |
| Encyclopedic resources | Wikidata; Q54854033 |
| Entry history | |
| Entry creation | 01-Dec-2016 |
| Last entry update | 19-Dec-2024 |
| Version number | 11 |