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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
DD2799 Resource Report Resource Website |
RRID:CVCL_9L11 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC:96112908, Wikidata:Q54830406 |
CVCL_9L11 | 2026-08-15 04:26:55 | 0 | ||||||
|
DD2826 Resource Report Resource Website |
ECACC Cat# 97010804, RRID:CVCL_AR26 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 97010804 | ECACC:97010804, Wikidata:Q54830417 |
CVCL_AR26 | 2026-08-15 04:26:56 | 0 | |||||
|
DD2801 Resource Report Resource Website |
ECACC Cat# 96112923, RRID:CVCL_9L13 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 96112923 | ECACC:96112923, Wikidata:Q54830408 |
CVCL_9L13 | 2026-08-15 04:26:56 | 0 | ||||
|
DD2793 Resource Report Resource Website |
ECACC Cat# 96112321, RRID:CVCL_9L08 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 96112321 | ECACC:96112321, Wikidata:Q54830403 |
CVCL_9L08 | 2026-08-15 04:26:55 | 0 | ||||
|
DD2857 Resource Report Resource Website |
ECACC Cat# 97022604, RRID:CVCL_AR34 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 97022604 | ECACC:97022604, Wikidata:Q54830435 |
CVCL_AR34 | 2026-08-15 04:26:56 | 0 | |||||
|
DD2932 Resource Report Resource Website |
RRID:CVCL_9L64 | Homo sapiens (Human) | Rieger syndrome | Karyotypic information: 46,XY,der(2),t(2;7)mat (ECACC=97070310)., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC:97070310, Wikidata:Q54830476 |
CVCL_9L64 | 2026-08-15 04:26:57 | 0 | ||||||
|
DD2897 Resource Report Resource Website |
RRID:CVCL_9L49 | Homo sapiens (Human) | Karyotypic information: 46,XX,der(5,7)t(4;5;7)(q31:p13;q13:q21)mat (ECACC=97043013)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC:97043013, Wikidata:Q54830459 |
CVCL_9L49 | 2026-08-15 04:26:57 | 0 | |||||||
|
DD2922 Resource Report Resource Website |
ECACC Cat# 97061002, RRID:CVCL_9L58 | Homo sapiens (Human) | Karyotypic information: 46,XX,del(5)(p1?3.3;p14.2)pat (ECACC=97061002)., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 97061002 | ECACC:97061002, Wikidata:Q54830469 |
CVCL_9L58 | 2026-08-15 04:26:57 | 0 | |||||
|
DD2885 Resource Report Resource Website |
RRID:CVCL_9L45 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC:97041801, Wikidata:Q54830454 |
CVCL_9L45 | 2026-08-15 04:26:57 | 0 | ||||||
|
DD2875 Resource Report Resource Website |
ECACC Cat# 97040128, RRID:CVCL_AR35 | Homo sapiens (Human) | X-linked centronuclear myopathy | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 97040128 | ECACC:97040128, Wikidata:Q54830448 |
CVCL_AR35 | 2026-08-15 04:26:56 | 0 | ||||
|
DD2949 Resource Report Resource Website |
RRID:CVCL_9L71 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC:97072204, Wikidata:Q54830487 |
CVCL_9L71 | 2026-08-15 04:26:57 | 0 | |||||||
|
DD2872 Resource Report Resource Website |
ECACC Cat# 97032502, RRID:CVCL_9L38 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 97032502 | ECACC:97032502, Wikidata:Q54830446 |
CVCL_9L38 | 2026-08-15 04:26:57 | 0 | ||||
|
DD2918 Resource Report Resource Website |
RRID:CVCL_9L56 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC:97053006, Wikidata:Q54830466 |
CVCL_9L56 | 2026-08-15 04:26:57 | 0 | ||||||
|
DD2920 Resource Report Resource Website |
ECACC Cat# 97060901, RRID:CVCL_9Q36 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Sex ambiguous | ECACC | 97060901 | ECACC:97060901, Wikidata:Q54830468 |
CVCL_9Q36 | 2026-08-15 04:26:57 | 0 | |||||
|
DD2919 Resource Report Resource Website |
ECACC Cat# 97060207, RRID:CVCL_9L57 | Homo sapiens (Human) | Karyotypic information: 47,XX,+mar pat (ECACC=97060207)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 97060207 | ECACC:97060207, Wikidata:Q54830467 |
CVCL_9L57 | 2026-08-15 04:26:57 | 0 | |||||
|
DD2904 Resource Report Resource Website |
RRID:CVCL_9L52 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC:97051109, Wikidata:Q54830462 |
CVCL_9L52 | 2026-08-15 04:26:57 | 0 | ||||||
|
DD2875 Resource Report Resource Website |
RRID:CVCL_AR35 | Homo sapiens (Human) | X-linked centronuclear myopathy | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC:97040128, Wikidata:Q54830448 |
CVCL_AR35 | 2026-08-15 04:26:57 | 0 | ||||||
|
DD2923 Resource Report Resource Website |
ECACC Cat# 97061003, RRID:CVCL_9L59 | Homo sapiens (Human) | Karyotypic information: 46,XY,del(10)(qter->p15.1); de novo (ECACC=97061003)., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 97061003 | ECACC:97061003, Wikidata:Q54830470 |
CVCL_9L59 | 2026-08-15 04:26:57 | 0 | |||||
|
DD2947 Resource Report Resource Website |
ECACC Cat# 97072101, RRID:CVCL_9L70 | Homo sapiens (Human) | Karyotypic information: 46,XX,t(4;5)(p12;q13.1)mat (ECACC=97072101)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 97072101 | ECACC:97072101, Wikidata:Q54830486 |
CVCL_9L70 | 2026-08-15 04:26:57 | 0 | |||||
|
DD2941 Resource Report Resource Website |
RRID:CVCL_9L67 | Homo sapiens (Human) | Karyotypic information: 46,XY,dup(11)(p15.1;p15.3) (ECACC=97071615)., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC:97071615, Wikidata:Q54830483 |
CVCL_9L67 | 2026-08-15 04:26:58 | 0 |
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