Cellosaurus FS1 (CVCL_C8X2)
Cell line name | FS1 |
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Accession | CVCL_C8X2 |
Resource Identification Initiative | To cite this cell line use: FS1 (RRID:CVCL_C8X2) |
Comments | Characteristics: Homogenous cell morphology with prominent nucleoli and long cytoplasmic processes. Expresses WT1 and show reversion of the WT1+-KTS isoform ratio. Expresses Sertoli cell markers SOX9, MIC2, AR and INHA. Strongly positive for vimentin, which is expressed in Sertoli cells. Negative for the germ cell marker VASA1 and for the Leydig cell marker LHCGR (Direct_author_submission). Karyotypic information: 46,XY (PubMed=18271004). Transformant: NCBI_TaxID; 1891767; Simian virus 40 (SV40). Omics: Transcriptome analysis by microarray. Miscellaneous: Detailed characteristics from personal communication of Schulz, Birte. Derived from site: In situ; Testis; UBERON=UBERON_0000473. Cell type: Sertoli cell; CL=CL_0000216. |
Sequence variations |
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Disease | Frasier syndrome (NCIt: C122805) Frasier syndrome (ORDO: Orphanet_347) |
Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
Sex of cell | Male |
Age at sampling | 19Y |
Category | Transformed cell line |
Publications | PubMed=18271004; DOI=10.1002/mrd.20889 PubMed=27688058; DOI=10.1007/s00418-016-1503-y PubMed=34153645; DOI=10.1016/j.neo.2021.05.008; PMCID=PMC8233172 PubMed=36899312; DOI=10.1186/s12885-023-10696-7; PMCID=PMC10007848 |
Cross-references | |
Encyclopedic resources | Wikidata; Q123031314 |
Gene expression databases | GEO; GSM5209347
GEO; GSM5209348 GEO; GSM5209349 GEO; GSM5209350 GEO; GSM5209351 GEO; GSM5209352 GEO; GSM5209353 GEO; GSM5209354 |
Entry history | |
Entry creation | 05-Oct-2023 |
Last entry update | 19-Dec-2024 |
Version number | 4 |