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Cellosaurus UM217-1 PGD (CVCL_A2HS)

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Cell line name UM217-1 PGD
Accession CVCL_A2HS
Resource Identification Initiative To cite this cell line use: UM217-1 PGD (RRID:CVCL_A2HS)
Comments From: University of Michigan; Ann Arbor; USA.
Registration: NIH Human Embryonic Stem Cell Registry; NIHhESC-21-0485.
Donor information: Embryo is sibling to that giving rise to UM217-2 PGD (Cellosaurus=CVCL_C3F4).
Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358.
Cell type: Embryonic stem cell; CL=CL_0002322.
Disease Frontotemporal dementia and/or amyotrophic lateral sclerosis 1 (NCIt: C168756)
Frontotemporal dementia with motor neuron disease (ORDO: Orphanet_275872)
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 Provider; MStem Cell; -; https://www.mstemcell.org/purchase-stem-cell-lines/
Cross-references
Cell line databases/resources NIHhESC; NIHhESC-21-0485
Encyclopedic resources Wikidata; Q105511338
Entry history
Entry creation12-Jan-2021
Last entry update10-Apr-2025
Version number7