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Cellosaurus CS83iCTR33-n2 (CVCL_ZC84)

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Cell line name CS83iCTR33-n2
Synonyms CS83iCTR33n2
Accession CVCL_ZC84
Resource Identification Initiative To cite this cell line use: CS83iCTR33-n2 (RRID:CVCL_ZC84)
Comments From: Cedars-Sinai Medical Center iPSC Core Facility; Los Angeles; USA.
Population: Caucasian.
Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:4851; HTT; Repeat_expansion; p.Gln18[33] (c.52CAG(33)) (c.52CAG[(27_35)]); ClinVar=VCV000031915; Zygosity=Heterozygous (from parent cell line).
Disease Huntington's disease (NCIt: C82342)
Huntington disease (ORDO: Orphanet_399)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_W557 (GM02183)
Sex of cell Female
Age at sampling 21Y
Category Induced pluripotent stem cell
Publications

PubMed=25740845; DOI=10.1093/hmg/ddv080; PMCID=PMC4424959
Virginia B. Mattis, Colton Tom, Sergey Akimov, Jasmine Saeedian, Michael E. Ostergaard, Amber L. Southwell, Crystal N. Doty, Loren Ornelas, Anais Sahabian, Lindsay Lenaeus, Berhan Mandefro ...Show all 16 authors... , Dhruv Sareen, Jamshid Arjomand, Michael Reuben Hayden, Christopher A. Ross, Clive N. Svendsen; Show fewer authors
HD iPSC-derived neural progenitors accumulate in culture and are susceptible to BDNF withdrawal due to glutamate toxicity.
Hum. Mol. Genet. 24:3257-3271(2015)

Cross-references
Encyclopedic resources Wikidata; Q98125773
Entry history
Entry creation02-Jul-2020
Last entry update19-Dec-2024
Version number9