Home  |  Contact

Cellosaurus HPS0164 (CVCL_T929)

[Text version]
Cell line name HPS0164
Synonyms Riken51
Accession CVCL_T929
Resource Identification Initiative To cite this cell line use: HPS0164 (RRID:CVCL_T929)
Comments Population: Japanese.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; 2928; DMD; Unexplicit; Ex48-50del; Zygosity=Hemizygous (PubMed=28439558).
Disease Duchenne muscular dystrophy (NCIt: C75482)
Duchenne muscular dystrophy (ORDO: Orphanet_98896)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 10-19Y
Category Induced pluripotent stem cell
Publications

PubMed=28439558; DOI=10.1126/sciadv.1602814
Zhang Y., Long C.-Z., Li H., McAnally J.R., Baskin K.K., Shelton J.M., Bassel-Duby R., Olson E.N.
CRISPR-Cpf1 correction of muscular dystrophy mutations in human cardiomyocytes and mice.
Sci. Adv. 3:e1602814.1-e1602814.10(2017)

Cross-references
Cell line collections (Providers) RCB; HPS0164
Cell line databases/resources SKIP; SKIP000245
Encyclopedic resources Wikidata; Q54890335
Entry history
Entry creation03-Feb-2014
Last entry update29-Jun-2023
Version number10