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Cellosaurus GM16866 (CVCL_4F75)

[Text version]
Cell line name GM16866
Accession CVCL_4F75
Resource Identification Initiative To cite this cell line use: GM16866 (RRID:CVCL_4F75)
Comments Population: Caucasian.
Derived from site: In situ; Arm, skin; UBERON=UBERON_0002427.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Peroxisome biogenesis disorder 7A (NCIt: C155760)
Peroxisome biogenesis disorder (ORDO: Orphanet_79189)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 14FW
Category Finite cell line
Publications

PubMed=12851857; DOI=10.1086/377004; PMCID=PMC1180364
Matsumoto N., Tamura S., Furuki S., Miyata N., Moser A., Shimozawa N., Moser H.W., Suzuki Y., Kondo N., Fujiki Y.
Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation.
Am. J. Hum. Genet. 73:233-246(2003)

PubMed=16257970; DOI=10.1074/jbc.M510044200
Furuki S., Tamura S., Matsumoto N., Miyata N., Moser A., Moser H.W., Fujiki Y.
Mutations in the peroxin Pex26p responsible for peroxisome biogenesis disorders of complementation group 8 impair its stability, peroxisomal localization, and interaction with the Pex1p x Pex6p complex.
J. Biol. Chem. 281:1317-1323(2006)

Cross-references
Cell line collections (Providers) Coriell; GM16866
Cell line databases/resources CLO; CLO_0018133
Encyclopedic resources Wikidata; Q54848793
Entry history
Entry creation22-Sep-2015
Last entry update29-Jun-2023
Version number9