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Cellosaurus HHW693 (CVCL_5U05)

[Text version]
Cell line name HHW693
Synonyms HHW 693; GM14190
Accession CVCL_5U05
Resource Identification Initiative To cite this cell line use: HHW693 (RRID:CVCL_5U05)
Comments Group: Human/rodent somatic cell hybrid.
Characteristics: Hybrid for chromosome 4 mapping.
Anecdotal: Was used to identify HTT, the Huntington disease causing gene.
Species of origin Cricetulus griseus (Chinese hamster) (Cricetulus barabensis griseus) (NCBI Taxonomy: 10029)
Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_5U04 (HHW661)
Category Hybrid cell line
Publications

PubMed=2945430
Wasmuth J.J., Carlock L.R., Smith B., Immken L.L.
A cell hybrid and recombinant DNA library that facilitate identification of polymorphic loci in the vicinity of the Huntington disease gene.
Am. J. Hum. Genet. 39:397-403(1986)

PubMed=2884625; DOI=10.1093/nar/15.11.4617
Overhauser J., McMahon J., Wasmuth J.J.
Identification of 28 DNA fragments that detect RFLPs in 13 distinct physical regions of the short arm of chromosome 5.
Nucleic Acids Res. 15:4617-4627(1987)

PubMed=2557612; DOI=10.1073/pnas.86.24.10011
Doggett N.A., Cheng J.-F., Smith C.L., Cantor C.R.
The Huntington disease locus is most likely within 325 kilobases of the chromosome 4p telomere.
Proc. Natl. Acad. Sci. U.S.A. 86:10011-10014(1989)

Cross-references
Cell line collections (Providers) Coriell; GM14190
Cell line databases/resources CLO; CLO_0034318
Encyclopedic resources Wikidata; Q54889483
Entry history
Entry creation23-Feb-2016
Last entry update29-Jun-2023
Version number9