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.
| Name | Proper Citation | Organism | Disease |
Comments |
Defining Citation | Category | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
DD3084 Resource Report Resource Website |
RRID:CVCL_9M17 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC:98032001, Wikidata:Q54830552 |
CVCL_9M17 | 2026-09-05 10:52:16 | 0 | |||||||
|
DD3115 Resource Report Resource Website |
RRID:CVCL_9M35 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC:98042011, Wikidata:Q54830574 |
CVCL_9M35 | 2026-09-05 10:52:17 | 0 | ||||||
|
DD3136 Resource Report Resource Website |
ECACC Cat# 98050506, RRID:CVCL_9M46 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 98050506 | ECACC:98050506, Wikidata:Q54830588 |
CVCL_9M46 | 2026-09-05 10:52:17 | 0 | ||||
|
DD3102 Resource Report Resource Website |
RRID:CVCL_9M31 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC:98041501, Wikidata:Q54830568 |
CVCL_9M31 | 2026-09-05 10:52:17 | 0 | ||||||
|
DD3105 Resource Report Resource Website |
ECACC Cat# 98041711, RRID:CVCL_9M32 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 98041711 | ECACC:98041711, Wikidata:Q54830569 |
CVCL_9M32 | 2026-09-05 10:52:17 | 0 | ||||
|
DD3075 Resource Report Resource Website |
ECACC Cat# 98031010, RRID:CVCL_9M10 | Homo sapiens (Human) | Karyotypic information: 46,XX,der(14;18)?(q10:q10) (ECACC=98031010)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 98031010 | ECACC:98031010, Wikidata:Q54830545 |
CVCL_9M10 | 2026-09-05 10:52:16 | 0 | |||||
|
DD3168 Resource Report Resource Website |
RRID:CVCL_9M50 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC:98061112, Wikidata:Q54830594 |
CVCL_9M50 | 2026-09-05 10:52:17 | 0 | |||||||
|
DD3129 Resource Report Resource Website |
ECACC Cat# 98050115, RRID:CVCL_9M40 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 98050115 | ECACC:98050115, Wikidata:Q54830582 |
CVCL_9M40 | 2026-09-05 10:52:17 | 0 | |||||
|
DD3126 Resource Report Resource Website |
ECACC Cat# 980427186, RRID:CVCL_9M37 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 980427186 | ECACC:980427186, Wikidata:Q54830579 |
CVCL_9M37 | 2026-09-05 10:52:17 | 0 | |||||
|
DD3131 Resource Report Resource Website |
ECACC Cat# 98050117, RRID:CVCL_9M42 | Homo sapiens (Human) | Type 1 diabetes mellitus | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 98050117 | ECACC:98050117, Wikidata:Q54830584 |
CVCL_9M42 | 2026-09-05 10:52:17 | 0 | ||||
|
DD3106 Resource Report Resource Website |
ECACC Cat# 98041712, RRID:CVCL_9M33 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 98041712 | ECACC:98041712, Wikidata:Q54830570 |
CVCL_9M33 | 2026-09-05 10:52:17 | 0 | ||||
|
DD3115 Resource Report Resource Website |
ECACC Cat# 98042011, RRID:CVCL_9M35 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 98042011 | ECACC:98042011, Wikidata:Q54830574 |
CVCL_9M35 | 2026-09-05 10:52:17 | 0 | ||||
|
DD3113 Resource Report Resource Website |
RRID:CVCL_9M34 | Homo sapiens (Human) | Karyotypic information: 46,XX,del(22)(q13) (ECACC=98042009)., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC:98042009, Wikidata:Q54830573 |
CVCL_9M34 | 2026-09-05 10:52:17 | 0 | |||||||
|
DD3082 Resource Report Resource Website |
RRID:CVCL_9M15 | Homo sapiens (Human) | Congenital eyelid ptosis | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC:98031908, Wikidata:Q54830550 |
CVCL_9M15 | 2026-09-05 10:52:16 | 0 | ||||||
|
DD3072 Resource Report Resource Website |
RRID:CVCL_9M08 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC:98031002, Wikidata:Q54830543 |
CVCL_9M08 | 2026-09-05 10:52:16 | 0 | |||||||
|
DD3078 Resource Report Resource Website |
ECACC Cat# 98031013, RRID:CVCL_9M13 | Homo sapiens (Human) | Nevus of Ito | Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 98031013 | ECACC:98031013, Wikidata:Q54830548 |
CVCL_9M13 | 2026-09-05 10:52:16 | 0 | ||||
|
DD3083 Resource Report Resource Website |
ECACC Cat# 98031909, RRID:CVCL_9M16 | Homo sapiens (Human) | Congenital eyelid ptosis | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 98031909 | ECACC:98031909, Wikidata:Q54830551 |
CVCL_9M16 | 2026-09-05 10:52:16 | 0 | ||||
|
DD3084 Resource Report Resource Website |
ECACC Cat# 98032001, RRID:CVCL_9M17 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 98032001 | ECACC:98032001, Wikidata:Q54830552 |
CVCL_9M17 | 2026-09-05 10:52:16 | 0 | |||||
|
DD3134 Resource Report Resource Website |
RRID:CVCL_9M45 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC:98050504, Wikidata:Q54830587 |
CVCL_9M45 | 2026-09-05 10:52:17 | 0 | ||||||
|
DD3120 Resource Report Resource Website |
ECACC Cat# 98042302, RRID:CVCL_9N77 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 98042302 | ECACC:98042302, Wikidata:Q54830577 |
CVCL_9N77 | 2026-09-05 10:52:17 | 0 |
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