Cellosaurus TAF12 (CVCL_A7MS)
Cell line name | TAF12 | |||
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Synonyms | TAF-12 | |||
Accession | CVCL_A7MS | |||
Resource Identification Initiative | To cite this cell line use: TAF12 (RRID:CVCL_A7MS) | |||
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 18 syndrome (NCIt: C175706) Ring chromosome 18 syndrome (ORDO: Orphanet_1442) | |||
Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) | |||
Hierarchy | Children:
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Sex of cell | Male | |||
Age at sampling | 3Y | |||
Category | Finite cell line | |||
Publications | PubMed=33212351; DOI=10.1016/j.scr.2020.102076 PubMed=33619287; DOI=10.1038/s41598-021-83399-3; PMCID=PMC7900208 | |||
Cross-references | ||||
Encyclopedic resources | Wikidata; Q107117010 | |||
Entry history | ||||
Entry creation | 20-May-2021 | |||
Last entry update | 29-Jun-2023 | |||
Version number | 5 |