ZM90630Homo sapiens (Human)Transformed cell line

AI Summary

No AI-generated summary available for this cell line.

Basic Information

Database IDCVCL_VI21
SpeciesHomo sapiens (Human)
Tissue SourcePeripheral blood[UBERON:UBERON_0000178]

Disease Information

DiseaseWerner syndrome

DepMap Information

Known Sequence Variations

TypeGene/ProteinDescriptionZygosityNoteSource
MutationSimpleWRNp.Lys1046fs*14 (c.3139-1G>C) (IVS25-1G>C)HeterozygousSplice acceptor mutationPubMed=10606667

Publications

WRN helicase expression in Werner syndrome cell lines.";

Monnat R.J. Jr.

Nucleic Acids Res. 28:648-654(2000).

Mismatch repair in extracts of Werner syndrome cell lines.";

Bennett S.E., Umar A., Oshima J., Monnat R.J. Jr., Kunkel T.A.

Cancer Res. 57:2956-2960(1997).