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_RT64
Organism: Homo sapiens (Human)
Disease: Congenital disorder of deglycosylation
Category: Finite cell line
Comments: Population: Caucasian; German.
Proper citation: RRID:CVCL_RT64 Copy
https://web.expasy.org/cellosaurus/CVCL_XC54
Organism: Homo sapiens (Human)
Disease: Nemaline myopathy 3
Category: Finite cell line
Comments: Population: Caucasian; English/German/Irish.
Proper citation: RRID:CVCL_XC54 Copy
https://web.expasy.org/cellosaurus/CVCL_RT87
Organism: Homo sapiens (Human)
Category: Finite cell line
Proper citation: RRID:CVCL_RT87 Copy
https://web.expasy.org/cellosaurus/CVCL_RT69
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian; German/Polish.
Proper citation: RRID:CVCL_RT69 Copy
https://web.expasy.org/cellosaurus/CVCL_VH43
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Indian.
Proper citation: RRID:CVCL_VH43 Copy
https://web.expasy.org/cellosaurus/CVCL_RT91
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian; German.
Proper citation: RRID:CVCL_RT91 Copy
https://web.expasy.org/cellosaurus/CVCL_VI95
Organism: Homo sapiens (Human)
Disease: Pitt-Hopkins syndrome
Category: Finite cell line
Comments: Population: Caucasian and Native North American.
Proper citation: RRID:CVCL_VI95 Copy
https://web.expasy.org/cellosaurus/CVCL_RT85
Organism: Homo sapiens (Human)
Disease: Congenital disorder of deglycosylation
Category: Finite cell line
Comments: Population: Caucasian; German.
Proper citation: RRID:CVCL_RT85 Copy
https://web.expasy.org/cellosaurus/CVCL_RT89
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_RT89 Copy
https://web.expasy.org/cellosaurus/CVCL_YN35
Organism: Homo sapiens (Human)
Disease: Congenital disorder of glycosylation type Ia
Category: Finite cell line
Proper citation: RRID:CVCL_YN35 Copy
https://web.expasy.org/cellosaurus/CVCL_A2QG
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM27265, RRID:CVCL_A2QG Copy
https://web.expasy.org/cellosaurus/CVCL_YN32
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian; Dutch.
Proper citation: RRID:CVCL_YN32 Copy
https://web.expasy.org/cellosaurus/CVCL_VV69
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian; Mennonite.
Proper citation: RRID:CVCL_VV69 Copy
https://web.expasy.org/cellosaurus/CVCL_A2QA
Organism: Homo sapiens (Human)
Disease: Pitt-Hopkins syndrome
Category: Finite cell line
Proper citation: RRID:CVCL_A2QA Copy
https://web.expasy.org/cellosaurus/CVCL_ZG17
Organism: Homo sapiens (Human)
Disease: Merosin-deficient congenital muscular dystrophy type 1A
Category: Finite cell line
Proper citation: RRID:CVCL_ZG17 Copy
https://web.expasy.org/cellosaurus/CVCL_ZG17
Organism: Homo sapiens (Human)
Disease: Merosin-deficient congenital muscular dystrophy type 1A
Category: Finite cell line
Proper citation: Coriell Cat# GM27195, RRID:CVCL_ZG17 Copy
https://web.expasy.org/cellosaurus/CVCL_XC47
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Native North American; Alaskan.
Proper citation: Coriell Cat# GM27409, RRID:CVCL_XC47 Copy
https://web.expasy.org/cellosaurus/CVCL_XC47
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Native North American; Alaskan.
Proper citation: RRID:CVCL_XC47 Copy
https://web.expasy.org/cellosaurus/CVCL_YE51
Organism: Homo sapiens (Human)
Disease: Rett syndrome, congenital variant
Category: Finite cell line
Comments: Population: Caucasian; French.
Proper citation: RRID:CVCL_YE51 Copy
https://web.expasy.org/cellosaurus/CVCL_YE56
Organism: Homo sapiens (Human)
Disease: Schinzel-Giedion midface-retraction syndrome
Category: Finite cell line
Proper citation: RRID:CVCL_YE56 Copy
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