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Cellosaurus ICGi002-B (CVCL_YK91)

[Text version]
Cell line name ICGi002-B
Synonyms DMD1_4
Accession CVCL_YK91
Resource Identification Initiative To cite this cell line use: ICGi002-B (RRID:CVCL_YK91)
Comments From: The Federal Research Center Institute of Cytology and Genetics; Novosibirsk; Russia.
Population: Caucasian.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; 2928; DMD; Simple; c.2950-1G>C; Zygosity=Hemizygous; Note=Splice acceptor mutation (PubMed=32777771).
Disease Duchenne muscular dystrophy (NCIt: C75482)
Duchenne muscular dystrophy (ORDO: Orphanet_98896)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_YK90 ! ICGi002-A
CVCL_YK92 ! ICGi002-C
Sex of cell Male
Age at sampling 10Y
Category Induced pluripotent stem cell
Publications

PubMed=32777771; DOI=10.1016/j.scr.2020.101941
Valetdinova K.R., Maretina M.A., Vyatkin Y.V., Perepelkina M.P., Egorova A.A., Baranov V.S., Kiselev A.V., Gershovich P.M., Zakian S.M.
Generation of three Duchenne muscular dystrophy patient-derived induced pluripotent stem cell (iPSC) lines ICGi002-A, ICGi002-B and ICGi002-C.
Stem Cell Res. 48:101941-101941(2020)

Cross-references
Cell line databases/resources hPSCreg; ICGi002-B
SKIP; SKIP005818
Biological sample resources BioSamples; SAMEA6351049
Encyclopedic resources Wikidata; Q94313401
Entry history
Entry creation19-Dec-2019
Last entry update29-Jun-2023
Version number8