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Cellosaurus WG1656 (CVCL_RG06)

[Text version]
Cell line name WG1656
Accession CVCL_RG06
Resource Identification Initiative To cite this cell line use: WG1656 (RRID:CVCL_RG06)
Comments From: Montreal Children's Hospital cell repository; Montreal; Canada.
Population: Caucasian.
Omics: Variations; SNP array analysis.
Miscellaneous: Cell line no longer available.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Transcobalamin II deficiency (NCIt: C142806)
Transcobalamin deficiency (ORDO: Orphanet_859)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 4Y
Category Finite cell line
Publications

PubMed=21418647; DOI=10.1186/gb-2011-12-3-r25; PMCID=PMC3129675
Lisanne Morcos, Bing Ge, Vonda Koka, Kevin C.L. Lam, Dmitry K. Pokholok, Kevin L. Gunderson, Alexandre Montpetit, Dominique J. Verlaan, Tomi Pastinen;
Genome-wide assessment of imprinted expression in human cells.
Genome Biol. 12:R25.1-R25.14(2011)

PubMed=25326100; DOI=10.15252/msb.20145114; PMCID=PMC4299376
Veronique Adoue, Alicia Schiavi, Nicholas Light, Jonas Carlsson Almlof, Per Lundmark, Bing Ge, Tony Kwan, Maxime Caron, Lars Ronnblom, Chuan Wang, Shu-Huang Chen ...Show all 17 authors... , Alison H. Goodall, Francois Cambien, Panos Deloukas, Willem Hendrik Ouwehand, Ann-Christine Syvanen, Tomi Pastinen; Show fewer authors
Allelic expression mapping across cellular lineages to establish impact of non-coding SNPs.
Mol. Syst. Biol. 10:754-754(2014)

Cross-references
Encyclopedic resources Wikidata; Q54993911
Gene expression databases GEO; GSM651134
GEO; GSM651135
GEO; GSM1266920
GEO; GSM1267012
Entry history
Entry creation05-Mar-2018
Last entry update10-Apr-2025
Version number9