Cellosaurus CS32iSMA-n3 (CVCL_IW30)
| Cell line name | CS32iSMA-n3 |
|---|---|
| Synonyms | CS32iSMA-nxx |
| Accession | CVCL_IW30 |
| Resource Identification Initiative | To cite this cell line use: CS32iSMA-n3 (RRID:CVCL_IW30) |
| Comments | From: Cedars-Sinai Medical Center iPSC Core Facility; Los Angeles; USA. Population: Caucasian. Omics: Chromatin accessibility by ATAC-seq. Omics: Transcriptome analysis by RNAseq. Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. |
| Sequence variations |
|
| Disease | Werdnig-Hoffmann disease (NCIt: C98670) Proximal spinal muscular atrophy type 1 (ORDO: Orphanet_83330) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Hierarchy | Parent: CVCL_Y965 (GM00232) |
| Sex of cell | Male |
| Age at sampling | 7M |
| Category | Induced pluripotent stem cell |
| Web pages | https://biomanufacturing.cedars-sinai.org/product/cs32isma-nxx/ |
| Cross-references | |
| Cell line databases/resources | CLO; CLO_0037507
LINCS_LDP; LSC-1009 |
| Encyclopedic resources | Wikidata; Q54814549 |
| Entry history | |
| Entry creation | 03-Mar-2017 |
| Last entry update | 19-Dec-2024 |
| Version number | 16 |