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.
https://web.expasy.org/cellosaurus/CVCL_VJ14
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM25582, RRID:CVCL_VJ14 Copy
https://web.expasy.org/cellosaurus/CVCL_A5NQ
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_A5NQ Copy
https://web.expasy.org/cellosaurus/CVCL_LN99
Organism: Homo sapiens (Human)
Disease: Potocki-Lupski syndrome
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_LN99 Copy
https://web.expasy.org/cellosaurus/CVCL_A5NM
Organism: Homo sapiens (Human)
Disease: Chromosome 16p12.1 deletion syndrome
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_A5NM Copy
https://web.expasy.org/cellosaurus/CVCL_HQ51
Organism: Homo sapiens (Human)
Disease: Pitt-Hopkins syndrome
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_HQ51 Copy
https://web.expasy.org/cellosaurus/CVCL_LP02
Organism: Homo sapiens (Human)
Disease: Potocki-Lupski syndrome
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM25587, RRID:CVCL_LP02 Copy
https://web.expasy.org/cellosaurus/CVCL_EH30
Organism: Homo sapiens (Human)
Disease: Congenital disorder of deglycosylation
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_EH30 Copy
https://web.expasy.org/cellosaurus/CVCL_JF36
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_JF36 Copy
https://web.expasy.org/cellosaurus/CVCL_JF35
Organism: Homo sapiens (Human)
Disease: Potocki-Lupski syndrome
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM25586, RRID:CVCL_JF35 Copy
https://web.expasy.org/cellosaurus/CVCL_VJ23
Organism: Homo sapiens (Human)
Disease: Intellectual developmental disorder, autosomal recessive 34
Category: Finite cell line
Comments: Population: Caucasian; Mennonite.
Proper citation: RRID:CVCL_VJ23 Copy
https://web.expasy.org/cellosaurus/CVCL_A5PA
Organism: Homo sapiens (Human)
Disease: Prader-Willi syndrome
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_A5PA Copy
https://web.expasy.org/cellosaurus/CVCL_A5NP
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM25858, RRID:CVCL_A5NP Copy
https://web.expasy.org/cellosaurus/CVCL_VJ15
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_VJ15 Copy
https://web.expasy.org/cellosaurus/CVCL_JF41
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_JF41 Copy
https://web.expasy.org/cellosaurus/CVCL_A5NR
Organism: Homo sapiens (Human)
Disease: Chromosome 16p12.1 deletion syndrome
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_A5NR Copy
https://web.expasy.org/cellosaurus/CVCL_LP08
Organism: Homo sapiens (Human)
Disease: Potocki-Lupski syndrome
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_LP08 Copy
https://web.expasy.org/cellosaurus/CVCL_A5NU
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian; English/German.
Proper citation: Coriell Cat# GM25886, RRID:CVCL_A5NU Copy
https://web.expasy.org/cellosaurus/CVCL_A5NW
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_A5NW Copy
https://web.expasy.org/cellosaurus/CVCL_EH31
Organism: Homo sapiens (Human)
Disease: Congenital disorder of deglycosylation
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_EH31 Copy
https://web.expasy.org/cellosaurus/CVCL_A5NZ
Organism: Homo sapiens (Human)
Disease: Ornithine carbamoyltransferase deficiency disease
Category: Transformed cell line
Comments: Characteristics: No OTC mutation found., Population: Asian.
Proper citation: Coriell Cat# GM25991, RRID:CVCL_A5NZ Copy
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