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Cellosaurus ICGi005-B (CVCL_UF66)

[Text version]

Cell line name ICGi005-B
Synonyms iSMA37
Accession CVCL_UF66
Resource Identification Initiative To cite this cell line use: ICGi005-B (RRID:CVCL_UF66)
Comments From: The Federal Research Center Institute of Cytology and Genetics; Novosibirsk; Russia.
Population: Caucasian.
Derived from sampling site: Skin.
Sequence variations Gene deletion; HGNC; 11117; SMN1; Zygosity=Homozygous (PubMed=30660867).
Disease Werdnig-Hoffmann disease (NCIt: C98670)
Proximal spinal muscular atrophy type 1 (ORDO: Orphanet_83330)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_UF65 ! ICGi005-A
Sex of cell Female
Age at sampling 10Y
Category Induced pluripotent stem cell

Goigoreva E.V., Valetdinova K.R., Ustyantseva E.I., Shevchenko A.I., Medvedev S.P., Mazurok N.A., Maretina M.A., Kuranova M.L., Kiselev A.V., Baranov V.S., Zakyan S.M.
Neural differentiation of patient-specific induced pluripotent stem cells from patients with a hereditary form of spinal muscular atrophy.
Genes and Cells 11:2.70-2.79(2016)

PubMed=30660867; DOI=10.1016/j.scr.2018.101376
Valetdinova K.R., Maretina M.A., Kuranova M.L., Grigor'eva E.V., Minina Y.M., Kizilova E.A., Kiselev A.V., Medvedev S.P., Baranov V.S., Zakian S.M.
Generation of two spinal muscular atrophy (SMA) type I patient-derived induced pluripotent stem cell (iPSC) lines and two SMA type II patient-derived iPSC lines.
Stem Cell Res. 34:101376-101376(2019)

Cell line databases/resources hPSCreg; ICGi005-B
Biological sample resources BioSamples; SAMEA5131663
Encyclopedic resources Wikidata; Q94313409
Entry history
Entry creation13-Nov-2018
Last entry update20-May-2021
Version number7