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Cellosaurus UM38-2 PGD (CVCL_B839)

[Text version]
Cell line name UM38-2 PGD
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
  • Mutation; HGNC; HGNC:7551; MYBPC3; Unexplicit; Not described; Zygosity=Unspecified (NIHhESC=NIHhESC-12-0155).
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 creation06-Jun-2012
Last entry update19-Dec-2024
Version number20