Cellosaurus TAF6 (CVCL_A9Q2)
Cell line name | TAF6 | ||||
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Synonyms | TAF-6 | ||||
Accession | CVCL_A9Q2 | ||||
Resource Identification Initiative | To cite this cell line use: TAF6 (RRID:CVCL_A9Q2) | ||||
Comments | Population: Caucasian. Omics: Array-based CGH. Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. | ||||
Disease | Developmental delay (NCIt: C116942) Ring chromosome 13 syndrome (NCIt: C179703) Ring chromosome 13 syndrome (ORDO: Orphanet_96176) | ||||
Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) | ||||
Hierarchy | Children:
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Sex of cell | Male | ||||
Age at sampling | 17Y | ||||
Category | Finite cell line | ||||
Publications | PubMed=30500678; DOI=10.1016/j.scr.2018.11.009 PubMed=33619287; DOI=10.1038/s41598-021-83399-3; PMCID=PMC7900208 | ||||
Cross-references | |||||
Encyclopedic resources | Wikidata; Q102114968 | ||||
Entry history | |||||
Entry creation | 29-Oct-2020 | ||||
Last entry update | 29-Jun-2023 | ||||
Version number | 7 |