Cellosaurus TRNDi010-D (CVCL_B5GI)
Cell line name | TRNDi010-D | ||
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Synonyms | NCATS-CL6103; HT592D | ||
Accession | CVCL_B5GI | ||
Resource Identification Initiative | To cite this cell line use: TRNDi010-D (RRID:CVCL_B5GI) | ||
Comments | From: NIH-NCATS-TRND Branch; Rockville; USA. Population: Caucasian; English. Derived from site: In situ; Arm, skin; UBERON=UBERON_0002427. Cell type: Fibroblast of skin; CL=CL_0002620. | ||
Sequence variations |
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Disease | Congenital disorder of deglycosylation (NCIt: C126746) Alacrimia-choreoathetosis-liver dysfunction syndrome (ORDO: Orphanet_404454) | ||
Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) | ||
Hierarchy | Parent: CVCL_RT93 (GM26612) Children:
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Sex of cell | Female | ||
Age at sampling | 16Y | ||
Category | Induced pluripotent stem cell | ||
Publications | PubMed=34619643; DOI=10.1016/j.scr.2021.102554; PMCID=PMC8647947 | ||
Cross-references | |||
Cell line databases/resources | hPSCreg; TRNDi010-D | ||
Encyclopedic resources | Wikidata; Q110433289 | ||
Entry history | |||
Entry creation | 16-Dec-2021 | ||
Last entry update | 05-Oct-2023 | ||
Version number | 5 |