Cellosaurus UM139-2 PGD (CVCL_X366)
| Cell line name | UM139-2 PGD |
|---|---|
| Synonyms | UM139-2-PGD; UM 139-2; UM139-2 |
| Accession | CVCL_X366 |
| Resource Identification Initiative | To cite this cell line use: UM139-2 PGD (RRID:CVCL_X366) |
| Comments | From: University of Michigan; Ann Arbor; USA. Registration: NIH Human Embryonic Stem Cell Registry; NIHhESC-14-0292. Omics: Transcriptomics; RNAseq. Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358. Cell type: Embryonic stem cell; CL=CL_0002322. |
| Disease | Fragile X syndrome (NCIt: C84717) Fragile X syndrome (ORDO: Orphanet_908) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Sex of cell | Male |
| Age at sampling | Blastocyst stage |
| Category | Embryonic stem cell |
| Web pages | Provider; MStem Cell; -; https://www.mstemcell.org/purchase-stem-cell-lines/ |
| Publications | PubMed=30158855; DOI=10.3389/fnmol.2018.00282; PMCID=PMC6104480 |
| Cross-references | |
| Cell line databases/resources | NIHhESC; NIHhESC-14-0292 |
| Encyclopedic resources | Wikidata; Q54991008 |
| Gene expression databases | GEO; GSM3053266
GEO; GSM3053267 |
| Entry history | |
| Entry creation | 17-Jul-2014 |
| Last entry update | 10-Apr-2025 |
| Version number | 12 |