Searching the RRID Resource Information Network
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Cellosaurus is database indexing available cell lines from various collections: American Type Culture Collection (ATCC), Bioresource Collection and Research Center, Taiwan (BCRC), Banco de Células do Rio de Janeiro (BCRJ), CellBank Australia (CBA), Collection of Cell Lines in Veterinary Medicine (CCLV), Cell Lines Service (CLS), Coriell, Drosophila Genomics Resource Center (DGRC), Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH (DSMZ), European Bank for induced pluripotent Stem Cells (EBiSC), European Collection of Authenticated Cell Cultures (ECACC), Interlab Cell Line Collection (ICLC), Institute for Fermentation Osaka (IFO), Istituto Zooprofilattico Sperimentale della Lombardia e dell'Emilia Romagna (IZSLER) biobank, Japanese Collection of Research Bioresources (JCRB) Cell Bank, Kunming Cell Bank of Type Culture Collection (KCB), Korean Cell Line Bank (KCLB), Millipore, National Cell Bank of Iran (NCBI_Iran), National Cancer Institute - Developmental Therapeutics Program (NCI-DTP), NINDS Human Cell and Data Repository (NHCDR), NIH AIDS Reagent Program (NIH-ARP), NISES, RIKEN Bioresource Center Cell Bank (RCB), Royan Stem Cell Bank (RSCB), Tick Cell Biobank (TCB), Tohoku University cell line catalog (TKG), and Ximbio.
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_X055
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM03121, RRID:CVCL_X055 Copy
https://web.expasy.org/cellosaurus/CVCL_H189
Organism: Homo sapiens (Human)
Disease: Klinefelter syndrome
Category: Finite cell line
Comments: Karyotypic information: 47,XXY (Coriell=GM03102)., Population: Caucasian.
Proper citation: Coriell Cat# GM03102, RRID:CVCL_H189 Copy
https://web.expasy.org/cellosaurus/CVCL_F064
Organism: Homo sapiens (Human)
Disease: Lesch-Nyhan syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_F064 Copy
https://web.expasy.org/cellosaurus/CVCL_4N38
Organism: Homo sapiens (Human)
Disease: Hyperlipoproteinemia, type IIa
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_4N38 Copy
https://web.expasy.org/cellosaurus/CVCL_4Z83
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian; Sardinian.
Proper citation: RRID:CVCL_4Z83 Copy
https://web.expasy.org/cellosaurus/CVCL_JE49
Organism: Homo sapiens (Human)
Disease: WAGR syndrome
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_JE49 Copy
https://web.expasy.org/cellosaurus/CVCL_CW74
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_CW74 Copy
https://web.expasy.org/cellosaurus/CVCL_F065
Organism: Homo sapiens (Human)
Disease: Lesch-Nyhan syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM03117, RRID:CVCL_F065 Copy
https://web.expasy.org/cellosaurus/CVCL_JM08
Organism: Homo sapiens (Human)
Disease: Anetoderma
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_JM08 Copy
https://web.expasy.org/cellosaurus/CVCL_X429
Organism: Homo sapiens (Human)
Disease: X-linked ichthyosis
Category: Finite cell line
Comments: Population: Caucasian; Sardinian.
Proper citation: Coriell Cat# GM03035, RRID:CVCL_X429 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_V745
Organism: Homo sapiens (Human)
Disease: Lesch-Nyhan syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_V745 Copy
https://web.expasy.org/cellosaurus/CVCL_CW73
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM03074, RRID:CVCL_CW73 Copy
https://web.expasy.org/cellosaurus/CVCL_X276
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XY,rec(3)(qter->p25::q21->qter)pat (Coriell=GM03039)., Population: Caucasian.
Proper citation: RRID:CVCL_X276 Copy
https://web.expasy.org/cellosaurus/CVCL_X102
Organism: Homo sapiens (Human)
Disease: Tetralogy of Fallot
Category: Finite cell line
Comments: Karyotypic information: 46,XX,der(1)(pter->p13.1::q21.1->p13.1::q21.1->q42.3) (Coriell=GM03126)., Population: African American.
Proper citation: RRID:CVCL_X102 Copy
https://web.expasy.org/cellosaurus/CVCL_CW75
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_CW75 Copy
https://web.expasy.org/cellosaurus/CVCL_7371
Organism: Homo sapiens (Human)
Disease: Smith-Lemli-Opitz syndrome
Category: Finite cell line
Comments: Karyotypic information: 45,XY,der(13;14)(13qter->13q10::14q10->14qter) (Coriell=GM03044)., Population: Caucasian.
Proper citation: Coriell Cat# GM03044, RRID:CVCL_7371 Copy
https://web.expasy.org/cellosaurus/CVCL_X279
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Puerto Rican.
Proper citation: Coriell Cat# GM03089, RRID:CVCL_X279 Copy
https://web.expasy.org/cellosaurus/CVCL_H190
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(9;17)(9qter->9p22::17p11->17pter;17qter->17p11::9p22->9pter)mat (Coriell=GM03100)., Population: Caucasian.
Proper citation: RRID:CVCL_H190 Copy
https://web.expasy.org/cellosaurus/CVCL_CW72
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM03073, RRID:CVCL_CW72 Copy
https://web.expasy.org/cellosaurus/CVCL_X054
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 45,X,-Y,inv(9)(p11;q13) [13]; 46,XY,inv(9)(p11;q13) [7] (Coriell=GM03120).
Proper citation: Coriell Cat# GM03120, RRID:CVCL_X054 Copy
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