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Cellosaurus GM01657 (CVCL_2Z68)

[Text version]
Cell line name GM01657
Synonyms GM-1657
Accession CVCL_2Z68
Resource Identification Initiative To cite this cell line use: GM01657 (RRID:CVCL_2Z68)
Comments Population: Caucasian.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Nevoid basal cell carcinoma syndrome (NCIt: C2892)
Gorlin syndrome (ORDO: Orphanet_377)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_2Z67 ! GM01656
CVCL_2Z69 ! GM01658
Sex of cell Male
Age at sampling 53Y
Category Finite cell line
Publications

DOI=10.5962/bhl.title.4090
Coriell L.L., Greene A.E.
The human genetic mutant cell repository: list of genetic variants, chromosomal aberrations and normal cell cultures submitted to the repository. 4th edition. October 1977.
(In misc. document) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda; USA (1977)

CLPUB00447
Mulivor R.A., Suchy S.F.
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; GM01657
Cell line databases/resources CLO; CLO_0030945
Biological sample resources BioSample; SAMN00807037
Encyclopedic resources Wikidata; Q54836989
Entry history
Entry creation22-Sep-2015
Last entry update29-Jun-2023
Version number9