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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
HH0313 Resource Report Resource Website |
ECACC Cat# 93021718, RRID:CVCL_8X45 | Homo sapiens (Human) | Karyotypic information: 46,XX,-15,+(15),t(15;Y)(p12;q12) (ECACC=93021718)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 93021718 | ECACC:93021718, Wikidata:Q54887439 |
CVCL_8X45 | 2026-08-15 04:39:24 | 0 | |||||
|
HH0279 Resource Report Resource Website |
ECACC Cat# 89061903, RRID:CVCL_8X32 | Homo sapiens (Human) | Thanatophoric dysplasia | Karyotypic information: 46,XX,inv(1)(q25;q32) (ECACC=89061903)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 89061903 | ECACC:89061903, Wikidata:Q54887426 |
CVCL_8X32 | 2026-08-15 04:39:24 | 0 | ||||
|
HH0370 Resource Report Resource Website |
ECACC Cat# 97092508, RRID:CVCL_8X62 | Homo sapiens (Human) | Karyotypic information: 46,X,der(X),t(X;17)(p22.1;q23)mat (ECACC=97092508)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 97092508 | ECACC:97092508, Wikidata:Q54887463 |
CVCL_8X62 | 2026-08-15 04:39:25 | 0 | |||||
|
HH0305 Resource Report Resource Website |
ECACC Cat# 92090701, RRID:CVCL_8X39 | Homo sapiens (Human) | Karyotypic information: 46,XX,t(1;5)(p32;q35)mat (ECACC=92090701)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 92090701 | ECACC:92090701, Wikidata:Q54887433 |
CVCL_8X39 | 2026-08-15 04:39:24 | 0 | |||||
|
HH0334 Resource Report Resource Website |
ECACC Cat# 93120814, RRID:CVCL_8X56 | Homo sapiens (Human) | Congenital adrenal gland hypoplasia | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 93120814 | ECACC:93120814, Wikidata:Q54887456 |
CVCL_8X56 | 2026-08-15 04:39:25 | 0 | ||||
|
HH0314 Resource Report Resource Website |
ECACC Cat# 93040109, RRID:CVCL_8X46 | Homo sapiens (Human) | Karyotypic information: 46,XX,del(4)(p15.2->pter) (ECACC=93040109)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 93040109 | ECACC:93040109, Wikidata:Q54887440 |
CVCL_8X46 | 2026-08-15 04:39:24 | 0 | |||||
|
HH0312 Resource Report Resource Website |
ECACC Cat# 93021717, RRID:CVCL_8X44 | Homo sapiens (Human) | Karyotypic information: 46,XX,t(4;6)(q35;q15) (ECACC=93021717)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 93021717 | ECACC:93021717, Wikidata:Q54887438 |
CVCL_8X44 | 2026-08-15 04:39:24 | 0 | |||||
|
HH0378 Resource Report Resource Website |
ECACC Cat# 01042409, RRID:CVCL_8X65 | Homo sapiens (Human) | Intellectual developmental disorder | Population: Caucasian., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 01042409 | ECACC:01042409, Wikidata:Q54887466 |
CVCL_8X65 | 2026-08-15 04:39:25 | 0 | ||||
|
HH0302 Resource Report Resource Website |
ECACC Cat# 890306072, RRID:CVCL_8X37 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Sex unspecified | ECACC | 890306072 | ECACC:890306072, Wikidata:Q54887431 |
CVCL_8X37 | 2026-08-15 04:39:23 | 0 | |||||
|
HH0299 Resource Report Resource Website |
ECACC Cat# 89022802, RRID:CVCL_8X35 | Homo sapiens (Human) | 47,XYY syndrome | Karyotypic information: 47,XYY (ECACC=89022802)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC | 89022802 | ECACC:89022802, Wikidata:Q54887429 |
CVCL_8X35 | 2026-08-15 04:39:24 | 0 | ||||
|
HH0375 Resource Report Resource Website |
ECACC Cat# 98022709, RRID:CVCL_8X63 | Homo sapiens (Human) | Karyotypic information: 46,XX,inv(12)(q15;q24.1)mat (ECACC=98022709)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 98022709 | ECACC:98022709, Wikidata:Q54887464 |
CVCL_8X63 | 2026-08-15 04:39:24 | 0 | |||||
|
HPSI1213i-xuja_2 Resource Report Resource Website |
ECACC Cat# 77650087, RRID:CVCL_AI23 | Homo sapiens (Human) | Population: Caucasian; British., From: Wellcome Trust Sanger Institute; Hinxton; United Kingdom., From: Cambridge BioResource; Cambridge; United Kingdom. | PMID:28489815 | Induced pluripotent stem cell | Female | WTSIi083-A | ECACC | 77650087 | ArrayExpress:E-MTAB-4057, BioSamples:SAMEA2494988, EBiSC:WTSIi083-A, ECACC:66540198, ECACC:77650087, HipSci:HPSI1213i-xuja_2, hPSCreg:WTSIi083-A, SKIP:SKIP002701, Wikidata:Q54891734 |
CVCL_AI23 | 2026-08-15 04:40:55 | 0 | |||
|
HPSI1116i-zies_2 Resource Report Resource Website |
ECACC Cat# 77650784, RRID:CVCL_LL99 | Homo sapiens (Human) | Retinitis pigmentosa | Population: Caucasian., From: Wellcome Trust Sanger Institute; Hinxton; United Kingdom., From: University College London; London; United Kingdom. | Induced pluripotent stem cell | Female | WTSIi693-A | ECACC | 77650784 | BioSamples:SAMEA104236993, ECACC:77650784, HipSci:HPSI1116i-zies_2, hPSCreg:WTSIi693-A, Wikidata:Q54891704 |
CVCL_LL99 | 2026-08-15 04:40:54 | 0 | |||
|
HPSI1213i-pahc_4 Resource Report Resource Website |
ECACC Cat# 77650046, RRID:CVCL_AI21 | Homo sapiens (Human) | Population: Caucasian; British., From: Wellcome Trust Sanger Institute; Hinxton; United Kingdom., From: Cambridge BioResource; Cambridge; United Kingdom. | PMID:28489815 | Induced pluripotent stem cell | Female | WTSIi001-A | ECACC | 77650046 | ArrayExpress:E-MTAB-4057, BioSamples:SAMEA2547633, ECACC:77650046, HipSci:HPSI1213i-pahc_4, hPSCreg:WTSIi001-A, SKIP:SKIP002514, Wikidata:Q54891726 |
CVCL_AI21 | 2026-08-15 04:40:56 | 0 | |||
|
HPSI1213i-hehd_1 Resource Report Resource Website |
ECACC Cat# 77650555, RRID:CVCL_AI17 | Homo sapiens (Human) | Population: Caucasian; British., From: Wellcome Trust Sanger Institute; Hinxton; United Kingdom., From: Cambridge BioResource; Cambridge; United Kingdom. | PMID:28489815 | Induced pluripotent stem cell | Female | WTSIi003-B, WTSIi346-A | ECACC | 77650555 | ArrayExpress:E-MTAB-4057, BioSamples:SAMEA2518338, ECACC:77650555, HipSci:HPSI1213i-hehd_1, hPSCreg:WTSIi003-B, Wikidata:Q54891717 |
CVCL_AI17 | 2026-08-15 04:40:56 | 0 | |||
|
HPSI1116i-yiek_6 Resource Report Resource Website |
ECACC Cat# 77650838, RRID:CVCL_WJ68 | Homo sapiens (Human) | Neuronal ceroid lipofuscinosis type 3 | Population: Caucasian; Romani., From: Wellcome Trust Sanger Institute; Hinxton; United Kingdom., From: University College London; London; United Kingdom. | Induced pluripotent stem cell | Male | ECACC | 77650838 | BioSamples:SAMEA104132897, ECACC:77650838, HipSci:HPSI1116i-yiek_6, Wikidata:Q94236759 |
CVCL_WJ68 | 2026-08-15 04:40:57 | 0 | ||||
|
HPSI1116i-zehh_4 Resource Report Resource Website |
ECACC Cat# 77650824, RRID:CVCL_YU08 | Homo sapiens (Human) | Nervous system disorder | Donor information: Donor is said to be suffering from a 'rare genetic neurological disorder'., Population: Caucasian; British., From: Cambridge BioResource; Cambridge; United Kingdom. | Induced pluripotent stem cell | Female | ECACC | 77650824 | BioSamples:SAMEA104134253, ECACC:77650824, HipSci:HPSI1016i-zehh_4, Wikidata:Q94236773 |
CVCL_YU08 | 2026-08-15 04:40:57 | 0 | ||||
|
HPSI1213i-foqj_2 Resource Report Resource Website |
ECACC Cat# 77650101, RRID:CVCL_AI16 | Homo sapiens (Human) | From: Wellcome Trust Sanger Institute; Hinxton; United Kingdom., From: Cambridge BioResource; Cambridge; United Kingdom. |
PMID:28489815 PMID:30784590 |
Induced pluripotent stem cell | Female | WTSIi297-B, WTSIi298-A | ECACC | 77650101 | BioSamples:SAMEA2399194, ECACC:77650101, HipSci:HPSI1213i-foqj_2, hPSCreg:WTSIi297-B, Wikidata:Q54891715 |
CVCL_AI16 | 2026-08-15 04:40:56 | 0 | |||
|
HPSI1116i-zehh_3 Resource Report Resource Website |
ECACC Cat# 77650823, RRID:CVCL_YU07 | Homo sapiens (Human) | Nervous system disorder | Donor information: Donor is said to be suffering from a 'rare genetic neurological disorder'., Population: Caucasian; British., From: Cambridge BioResource; Cambridge; United Kingdom. | Induced pluripotent stem cell | Female | ECACC | 77650823 | BioSamples:SAMEA104134252, ECACC:77650823, HipSci:HPSI1016i-zehh_3, Wikidata:Q94236770 |
CVCL_YU07 | 2026-08-15 04:40:55 | 0 | ||||
|
HPSI1213i-babk_2 Resource Report Resource Website 1+ mentions |
ECACC Cat# 66540098, RRID:CVCL_AI14 | Homo sapiens (Human) | Population: Caucasian; British., From: Wellcome Trust Sanger Institute; Hinxton; United Kingdom., From: Cambridge BioResource; Cambridge; United Kingdom. | PMID:28489815 | Induced pluripotent stem cell | Female | WTSIi028-A | ECACC | 66540098 | ArrayExpress:E-MTAB-4057, BioSamples:SAMEA2459959, EBiSC:WTSIi028-A, ECACC:66540098, ECACC:77650032, HipSci:HPSI1213i-babk_2, hPSCreg:WTSIi028-A, SKIP:SKIP002558, Wikidata:Q54891711 |
CVCL_AI14 | 2026-08-15 04:40:54 | 1 |
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