| Cell line name | TRNDi010-B |
|---|---|
| Synonyms | HT592B |
| Accession | CVCL_XI87 |
| Resource Identification Initiative | To cite this cell line use: TRNDi010-B (RRID:CVCL_XI87) |
| 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) |
| Sex of cell | Female |
| Age at sampling | 16Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line databases/resources | hPSCreg; TRNDi010-B |
| Encyclopedic resources | Wikidata; Q98133604 |
| Entry history | |
| Entry creation | 19-Dec-2019 |
| Last entry update | 05-Oct-2023 |
| Version number | 9 |