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Cellosaurus GM03265 (CVCL_9Q84)

[Text version]
Cell line name GM03265
Synonyms GM 03265; GM3265; Lowe 3265
Accession CVCL_9Q84
Resource Identification Initiative To cite this cell line use: GM03265 (RRID:CVCL_9Q84)
Comments Population: Caucasian.
Donor information: At sampling donor was not affected with oculocerebrorenal syndrome but has a 50% risk.
Derived from site: In situ; Fetus; UBERON=UBERON_0000323.
Cell type: Fibroblast; CL=CL_0000057.
Disease Oculocerebrorenal syndrome (NCIt: C84940)
Oculocerebrorenal syndrome of Lowe (ORDO: Orphanet_534)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 17FW
Category Finite cell line

Coriell L.L., Greene A.E., Mulivor R.A.
The human genetic mutant cell repository: list of genetic variants, chromosomal aberrations and normal cell cultures submitted to the repository. 7th edition. October 1980.
(In) Institute for Medical Research (Camden, N.J.) NIH 80-2011; pp.1-254; National Institutes of Health; Bethesda (1980)

Mulivor R.A., Suchy S.F.
1992/1993 catalog of cell lines. NIGMS human genetic mutant cell repository. 16th edition. October 1992.
(In) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda (1992)

PubMed=19700499; DOI=10.1093/hmg/ddp407
Coon B.G., Mukherjee D., Hanna C.B., Riese D.J. II, Lowe M., Aguilar R.C.
Lowe syndrome patient fibroblasts display Ocrl1-specific cell migration defects that cannot be rescued by the homologous Inpp5b phosphatase.
Hum. Mol. Genet. 18:4478-4491(2009)

Cell line collections (Providers) Coriell; GM03265
Cell line databases/resources CLO; CLO_0016705
Biological sample resources BioSample; SAMN00808329
Encyclopedic resources Wikidata; Q54837980
Entry history
Entry creation23-Feb-2016
Last entry update29-Jun-2023
Version number11