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Cellosaurus GM03102 (CVCL_H189)

[Text version]
Cell line name GM03102
Accession CVCL_H189
Resource Identification Initiative To cite this cell line use: GM03102 (RRID:CVCL_H189)
Comments Population: Caucasian.
Karyotypic information: 47,XXY (Coriell=GM03102).
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Klinefelter syndrome (NCIt: C34752)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_A9Y6 (KAUSTi008-A)CVCL_A9Y7 (KAUSTi008-B)CVCL_A9Y8 (KAUSTi008-C)
CVCL_A9Y9 (KAUSTi008-D)CVCL_A9YA (KAUSTi008-E)CVCL_A9YB (KAUSTi008-F)
CVCL_A9YF (KAUSTi008-G)
Originate from same individual CVCL_H188 ! GM03091
Sex of cell Male
Age at sampling 18FW
Category Finite cell line
Publications

CLPUB00447
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=33333453; DOI=10.1016/j.scr.2020.102119
Fiacco E., Alowaysi M., Astro V., Adamo A.
Generation of an iPSC cohort of isogenic iPSC lines (46-XY and 47-XXY) from a non-mosaic Klinefelter syndrome patient (47-XXY) (KAUSTi008-A, KAUSTi008-B, KAUSTi008-C, KAUSTi008-D, KAUSTi008-E, KAUSTi008-F, KAUSTi008-G).
Stem Cell Res. 50:102119-102119(2021)

Cross-references
Cell line collections (Providers) Coriell; GM03102
Cell line databases/resources CLO; CLO_0013479
Biological sample resources BioSample; SAMN00808250
Encyclopedic resources Wikidata; Q54837874
Entry history
Entry creation11-Feb-2013
Last entry update29-Jun-2023
Version number12