Cellosaurus XPCS2BA (CVCL_V272)
| Cell line name | XPCS2BA |
|---|---|
| Synonyms | XP2BA; Xeroderma Pigmentosum/Cockayne Syndrome 2 BAsel; GM13026 |
| Accession | CVCL_V272 |
| Resource Identification Initiative | To cite this cell line use: XPCS2BA (RRID:CVCL_V272) |
| 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 | Xeroderma pigmentosum-Cockayne syndrome complex (NCIt: C156031) Xeroderma pigmentosum-Cockayne syndrome complex (ORDO: Orphanet_220295) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Hierarchy | Children couldn't be retrieved from the API |
| Sex of cell | Male |
| Age at sampling | 36Y |
| Category | Finite cell line |
| Publications | PubMed=8408834; DOI=10.1016/0190-9622(93)70263-s PubMed=9584159; DOI=10.1128/mcb.18.6.3182; PMCID=PMC108900 PubMed=10332046; DOI=10.1093/hmg/8.6.1125 PubMed=16947863; DOI=10.1002/humu.20392 PubMed=18079351; DOI=10.1259/bjr/27072321 PubMed=26184184; DOI=10.3390/ijms160715985; PMCID=PMC4519934 |
| Cross-references | |
| Cell line collections (Providers) | Coriell; GM13026 |
| Cell line databases/resources | CLO; CLO_0013998 |
| Biological sample resources | BioSample; SAMN00802024 |
| Encyclopedic resources | Wikidata; Q54846269 |
| Experimental variables resources | EFO; EFO_0022698 |
| Entry history | |
| Entry creation | 16-Apr-2014 |
| Last entry update | 19-Dec-2024 |
| Version number | 16 |