Cellosaurus UM38-2 PGD (CVCL_B839)
Cell line name | UM38-2 PGD |
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Synonyms | UM38-2-PGD; UM38-2PGD |
Accession | CVCL_B839 |
Resource Identification Initiative | To cite this cell line use: UM38-2 PGD (RRID:CVCL_B839) |
Comments | From: University of Michigan; Ann Arbor; USA. Registration: NIH Human Embryonic Stem Cell Registry; NIHhESC-12-0155. Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358. Cell type: Embryonic stem cell; CL=CL_0002322. |
Sequence variations |
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Disease | Familial hypertrophic cardiomyopathy type 4 (NCIt: C133725) Rare familial disorder with hypertrophic cardiomyopathy (ORDO: Orphanet_99739) |
Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
Sex of cell | Sex unspecified |
Age at sampling | Blastocyst stage |
Category | Embryonic stem cell |
Web pages | https://www.mstemcell.org/purchase-stem-cell-lines/ http://www.ur.umich.edu/update/archives/120614/stemcell |
Cross-references | |
Cell line databases/resources | NIHhESC; NIHhESC-12-0155 |
Encyclopedic resources | Wikidata; Q54991041 |
Entry history | |
Entry creation | 06-Jun-2012 |
Last entry update | 19-Dec-2024 |
Version number | 20 |