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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_8T85
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 46,XY,del(11)(p14.1) (ECACC=92042901)., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_8T85 Copy
https://web.expasy.org/cellosaurus/CVCL_8T85
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 46,XY,del(11)(p14.1) (ECACC=92042901)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92042901, RRID:CVCL_8T85 Copy
https://web.expasy.org/cellosaurus/CVCL_8U20
Organism: Homo sapiens (Human)
Disease: Campomelic dysplasia
Category: Transformed cell line
Comments: Karyotypic information: 46,XY,inv(17)(q11.2;q24.3->q25.1) (ECACC=93092205)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection.
Proper citation: RRID:CVCL_8U20 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_JD86
Organism: Homo sapiens (Human)
Disease: 46,XY gonadal dysgenesis
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_JD86 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_JD86
Organism: Homo sapiens (Human)
Disease: 46,XY gonadal dysgenesis
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM00868, RRID:CVCL_JD86 Copy
https://web.expasy.org/cellosaurus/CVCL_JC90
Organism: Homo sapiens (Human)
Disease: Androgen insensitivity syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,XY; but phenotypically female (Coriell=GM01404)., Population: African American.
Proper citation: Coriell Cat# GM01404, RRID:CVCL_JC90 Copy
https://web.expasy.org/cellosaurus/CVCL_JC90
Organism: Homo sapiens (Human)
Disease: Androgen insensitivity syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,XY; but phenotypically female (Coriell=GM01404)., Population: African American.
Proper citation: RRID:CVCL_JC90 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_JD87
Organism: Homo sapiens (Human)
Disease: 46,XY gonadal dysgenesis
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_JD87 Copy
https://web.expasy.org/cellosaurus/CVCL_DS07
Organism: Homo sapiens (Human)
Disease: 46,XY sex reversal 1
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM01628, RRID:CVCL_DS07 Copy
https://web.expasy.org/cellosaurus/CVCL_X252
Organism: Homo sapiens (Human)
Disease: Gonadal dysgenesis
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_X252 Copy
https://web.expasy.org/cellosaurus/CVCL_JC91
Organism: Homo sapiens (Human)
Disease: Androgen insensitivity syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM01721, RRID:CVCL_JC91 Copy
https://web.expasy.org/cellosaurus/CVCL_JC91
Organism: Homo sapiens (Human)
Disease: Androgen insensitivity syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_JC91 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_JD89
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM01862, RRID:CVCL_JD89 Copy
https://web.expasy.org/cellosaurus/CVCL_5M70
Organism: Homo sapiens (Human)
Disease: XX male
Category: Finite cell line
Comments: Karyotypic information: 46,XX (Coriell=GM01889)., Population: Caucasian.
Proper citation: Coriell Cat# GM01889, RRID:CVCL_5M70 Copy
https://web.expasy.org/cellosaurus/CVCL_DS11
Organism: Homo sapiens (Human)
Disease: 46,XY sex reversal 1
Category: Finite cell line
Comments: Population: African American.
Proper citation: Coriell Cat# GM03368, RRID:CVCL_DS11 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_DS12
Organism: Homo sapiens (Human)
Disease: 46,XY sex reversal 1
Category: Finite cell line
Comments: Population: African American.
Proper citation: Coriell Cat# GM03368-A, RRID:CVCL_DS12 Copy
https://web.expasy.org/cellosaurus/CVCL_UR79
Organism: Homo sapiens (Human)
Disease: 17-beta-hydroxysteroid dehydrogenase 3 deficiency
Category: Finite cell line
Comments: Population: Arab.
Proper citation: Coriell Cat# GM03547, RRID:CVCL_UR79 Copy
https://web.expasy.org/cellosaurus/CVCL_X107
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,X,del(Y)(pter->q11) [42]; 45,X [8] (Coriell=GM03595)., Population: Caucasian.
Proper citation: RRID:CVCL_X107 Copy
https://web.expasy.org/cellosaurus/CVCL_X107
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,X,del(Y)(pter->q11) [42]; 45,X [8] (Coriell=GM03595)., Population: Caucasian.
Proper citation: Coriell Cat# GM03595, RRID:CVCL_X107 Copy
https://web.expasy.org/cellosaurus/CVCL_X307
Organism: Homo sapiens (Human)
Disease: Trisomy 16
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_X307 Copy
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Data set from Kravitz, Owen and Kretizer's 2012 paper "Optogenetic identification of striatal projection neuron subtypes during in vivo recordings."
