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Cellosaurus GM04887 (CVCL_V574)

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Cell line name GM04887
Synonyms GM 4887
Accession CVCL_V574
Resource Identification Initiative To cite this cell line use: GM04887 (RRID:CVCL_V574)
Comments Part of: Venezuelan Huntington disease kindreds subcollection.
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[45] (c.52CAG(45)) (c.52CAG[(40_?)]); ClinVar=VCV000000409; Zygosity=Heterozygous (from child cell line ND38546).
Disease Huntington's disease (NCIt: C82342)
Huntington disease (ORDO: Orphanet_399)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_Y815 (ND38546)
Originate from same individual CVCL_V573 ! GM04886
Sex of cell Female
Age at sampling 48Y
Category Finite cell line
Publications

PubMed=6230415; DOI=10.1016/0022-510x(83)90187-9
Carlota Sumbilla, Joseph Raymond Lakowicz;
Evidence for normal fibroblast cell membranes from individuals with Huntington's disease. A fluorescence probe study.
J. Neurol. Sci. 62:23-40(1983)

CLPUB00447
Richard A. Mulivor, Sharon F. Suchy;
1992/1993 catalog of cell lines. NIGMS human genetic mutant cell repository. 16th edition. October 1992.
(In misc. document) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda; USA (1992)

Cross-references
Cell line collections (Providers) Coriell; GM04887
Cell line databases/resources CLO; CLO_0025777
Encyclopedic resources Wikidata; Q54838742
Entry history
Entry creation16-Apr-2014
Last entry update19-Dec-2024
Version number15