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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
DD2075 Resource Report Resource Website |
RRID:CVCL_9I66 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC:94083108, Wikidata:Q54830099 |
CVCL_9I66 | 2026-08-15 04:26:49 | 0 | |||||||
|
DD2068 Resource Report Resource Website |
RRID:CVCL_9I62 | Homo sapiens (Human) | Trisomy 18 | Karyotypic information: 47,XX,+18 (ECACC=94083002)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC:94083002, Wikidata:Q54830095 |
CVCL_9I62 | 2026-08-15 04:26:46 | 0 | ||||||
|
DD1988 Resource Report Resource Website |
RRID:CVCL_9I28 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC:94071455, Wikidata:Q54830056 |
CVCL_9I28 | 2026-08-15 04:26:48 | 0 | |||||||
|
DD1994 Resource Report Resource Website |
ECACC Cat# 94071515, RRID:CVCL_9I32 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 94071515 | ECACC:94071515, Wikidata:Q54830060 |
CVCL_9I32 | 2026-08-15 04:26:48 | 0 | |||||
|
DD2040 Resource Report Resource Website |
ECACC Cat# 94081111, RRID:CVCL_9I50 | Homo sapiens (Human) | Trisomy 9 | Karyotypic information: 47,XX,+9 (ECACC=94081111)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 94081111 | ECACC:94081111, Wikidata:Q54830080 |
CVCL_9I50 | 2026-08-15 04:26:46 | 0 | ||||
|
DD2036 Resource Report Resource Website |
RRID:CVCL_9I47 | Homo sapiens (Human) | Karyotypic information: 46,XY,dir dup(1)(q32.1;q42.1); de novo (ECACC=94080815)., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC:94080815, Wikidata:Q54830077 |
CVCL_9I47 | 2026-08-15 04:26:46 | 0 | |||||||
|
DD2092 Resource Report Resource Website |
ECACC Cat# 94091613, RRID:CVCL_9I73 | Homo sapiens (Human) | Trisomy 13 | Karyotypic information: 46,XX,+13 (ECACC=94091613)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 94091613 | ECACC:94091613, Wikidata:Q54830106 |
CVCL_9I73 | 2026-08-15 04:26:49 | 0 | ||||
|
DD2133 Resource Report Resource Website |
ECACC Cat# 94111803, RRID:CVCL_9I97 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 94111803 | ECACC:94111803, Wikidata:Q54830130 |
CVCL_9I97 | 2026-08-15 04:26:50 | 0 | |||||
|
DD2156 Resource Report Resource Website |
RRID:CVCL_9J08 | Homo sapiens (Human) | Nevus of Ito | Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC:94121417, Wikidata:Q54830144 |
CVCL_9J08 | 2026-08-15 04:26:51 | 0 | ||||||
|
DD2133 Resource Report Resource Website |
RRID:CVCL_9I97 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC:94111803, Wikidata:Q54830130 |
CVCL_9I97 | 2026-08-15 04:26:47 | 0 | |||||||
|
DD2123 Resource Report Resource Website |
ECACC Cat# 94110706, RRID:CVCL_9I91 | Homo sapiens (Human) | Polysyndactyly | Karyotypic information: 47,XY,+13 (ECACC=94110706)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC | 94110706 | ECACC:94110706, Wikidata:Q54830124 |
CVCL_9I91 | 2026-08-15 04:26:50 | 0 | ||||
|
DD2113 Resource Report Resource Website |
ECACC Cat# 94102710, RRID:CVCL_9I87 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 94102710 | ECACC:94102710, Wikidata:Q54830120 |
CVCL_9I87 | 2026-08-15 04:26:47 | 0 | |||||
|
DD2100 Resource Report Resource Website |
RRID:CVCL_9I78 | Homo sapiens (Human) | Charcot-Marie-Tooth disease | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC:94092904, Wikidata:Q54830111 |
CVCL_9I78 | 2026-08-15 04:26:49 | 0 | ||||||
|
DD2174 Resource Report Resource Website |
ECACC Cat# 95010701, RRID:CVCL_AQ87 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 95010701 | ECACC:95010701, Wikidata:Q54830154 |
CVCL_AQ87 | 2026-08-15 04:26:48 | 0 | |||||
|
DD2205 Resource Report Resource Website |
RRID:CVCL_9J23 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC:95021304, Wikidata:Q54830163 |
CVCL_9J23 | 2026-08-15 04:26:51 | 0 | |||||||
|
DD2145 Resource Report Resource Website |
RRID:CVCL_9J04 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC:94120409, Wikidata:Q54830140 |
CVCL_9J04 | 2026-08-15 04:26:48 | 0 | |||||||
|
DD2135 Resource Report Resource Website |
ECACC Cat# 94112416, RRID:CVCL_9I99 | Homo sapiens (Human) | 47,XYY syndrome | Karyotypic information: 47,XYY (ECACC=94112416)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC | 94112416 | ECACC:94112416, Wikidata:Q54830132 |
CVCL_9I99 | 2026-08-15 04:26:47 | 0 | ||||
|
DD2108 Resource Report Resource Website |
RRID:CVCL_9I82 | Homo sapiens (Human) | Holoprosencephaly | Karyotypic information: 47,XX,+18 (ECACC=94102502)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC:94102502, Wikidata:Q54830115 |
CVCL_9I82 | 2026-08-15 04:26:47 | 0 | ||||||
|
DD2204 Resource Report Resource Website |
ECACC Cat# 95021305, RRID:CVCL_9J22 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 95021305 | ECACC:95021305, Wikidata:Q54830162 |
CVCL_9J22 | 2026-08-15 04:26:48 | 0 | |||||
|
DD2134 Resource Report Resource Website |
ECACC Cat# 94111843, RRID:CVCL_9I98 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Finite cell line | Sex unspecified | ECACC | 94111843 | ECACC:94111843, Wikidata:Q54830131 |
CVCL_9I98 | 2026-08-15 04:26:47 | 0 |
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