Cellosaurus WG1656 (CVCL_RG06)
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: 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 PubMed=25326100; DOI=10.15252/msb.20145114; PMCID=PMC4299376 |
Cross-references | |
Encyclopedic resources | Wikidata; Q54993911 |
Gene expression databases | GEO; GSM651134
GEO; GSM651135 GEO; GSM1266920 GEO; GSM1267012 |
Entry history | |
Entry creation | 05-Mar-2018 |
Last entry update | 29-Jun-2023 |
Version number | 8 |