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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM01018 Resource Report Resource Website |
RRID:CVCL_M980 | Homo sapiens (Human) | Metachromatic leukodystrophy | Population: Puerto Rican., Part of: Human variation panel. | PMID:7313555 | Transformed cell line | Female | GM-1018, GM 1018, GM01018A, GM17072 | CLO:CLO_0014601, CLO:CLO_0029492, BioSample:SAMN00803563, Coriell:GM01018, Coriell:GM17072, Wikidata:Q54836604 |
CVCL_M980 | 2026-07-25 04:32:11 | 0 | ||||
|
GM01118 Resource Report Resource Website |
Coriell Cat# GM01118, RRID:CVCL_4D80 | Homo sapiens (Human) | Supernumerary circular chromosome | Karyotypic information: 46,XX,r(18) [39]; 45,XX,-18 [11] (Coriell=GM01118)., Population: Mexican. | Finite cell line | Female | GM-1118 | Coriell | GM01118 | CLO:CLO_0030174, BioSample:SAMN00803638, Coriell:GM01118, Wikidata:Q54836651 |
CVCL_4D80 | 2026-07-25 04:32:12 | 0 | |||
|
GM01053 Resource Report Resource Website |
Coriell Cat# GM01053, RRID:CVCL_V531 | Homo sapiens (Human) | Hurler syndrome | Population: Caucasian. | Finite cell line | Male | GM-1053, GM01053A | Coriell | GM01053 | CLO:CLO_0030370, BioSample:SAMN00803592, Coriell:GM01053, Wikidata:Q54836622 |
CVCL_V531 | 2026-07-25 04:32:12 | 0 | |||
|
GM00989 Resource Report Resource Website |
RRID:CVCL_CV39 | Homo sapiens (Human) | Progeria | PMID:7253718 | Finite cell line | Male | GM-989, GM00989B, AG00989, AG-989, AG00989B, AG0989B | CLO:CLO_0029474, CLO:CLO_0036917, Coriell:AG00989, Coriell:GM00989, Wikidata:Q54836584 |
CVCL_CV39 | 2026-07-25 04:32:11 | 0 | |||||
|
GM01059 Resource Report Resource Website |
Coriell Cat# GM01059, RRID:CVCL_X079 | Homo sapiens (Human) | Population: Caucasian. |
PMID:6617268 PMID:6661932 PMID:23665875 |
Finite cell line | Female | GM-1059, GM 1059, GM01059A | Coriell | GM01059 | CLO:CLO_0030365, BioSample:SAMN00803600, Coriell:GM01059, Wikidata:Q54836626 |
CVCL_X079 | 2026-07-25 04:32:12 | 0 | |||
|
GM01085 Resource Report Resource Website |
Coriell Cat# GM01085, RRID:CVCL_V038 | Homo sapiens (Human) | Huntington's disease | Population: Caucasian. |
PMID:6220707 PMID:6458814 |
Finite cell line | Male | GM-1085, GM 1085 | Coriell | GM01085 | CLO:CLO_0030193, BioSample:SAMN00803614, Coriell:GM01085, Wikidata:Q54836637 |
CVCL_V038 | 2026-07-25 04:32:12 | 0 | ||
|
GM00994 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM00994, RRID:CVCL_CX40 | Homo sapiens (Human) | Finite cell line | Female | GM-994 | Coriell | GM00994 | Coriell:GM00994, Wikidata:Q54836586 |
CVCL_CX40 | 2026-07-25 04:32:11 | 0 | |||||
|
GM01032 Resource Report Resource Website |
RRID:CVCL_M981 | Homo sapiens (Human) | Hurler-Scheie syndrome | Population: Indo Pakistani., Part of: Human variation panel. | Transformed cell line | Female | GM-1032, GM01032A, GM17021 | CLO:CLO_0014695, CLO:CLO_0030374, BioSample:SAMN00803585, Coriell:GM01032, Coriell:GM17021, Wikidata:Q54836616 |
CVCL_M981 | 2026-07-25 04:32:11 | 0 | |||||
|
GM01101 Resource Report Resource Website |
Coriell Cat# GM01101, RRID:CVCL_0P87 | Homo sapiens (Human) | Karyotypic information: 46,XY,(4qter->4p16::12p11->12pter;12qter->12p11::4p16->4pter) (Coriell=GM01101)., Population: Caucasian. | Finite cell line | Male | GM-1101 | Coriell | GM01101 | CLO:CLO_0030188, BioSample:SAMN00803630, Coriell:GM01101, Wikidata:Q54836646 |
CVCL_0P87 | 2026-07-25 04:32:12 | 0 | ||||
|
GM01061 Resource Report Resource Website |
Coriell Cat# GM01061, RRID:CVCL_V036 | Homo sapiens (Human) | Huntington's disease | Population: Caucasian. |
PMID:2973075 PMID:6220707 PMID:6458814 |
Finite cell line | Male | GM-1061, GM 1061, GM1061, GM01061A | Coriell | GM01061 | CLO:CLO_0030368, BioSample:SAMN00803602, Coriell:GM01061, Wikidata:Q54836627 |
CVCL_V036 | 2026-07-25 04:32:11 | 0 | ||
|
GM01024 Resource Report Resource Website |
RRID:CVCL_V792 | Homo sapiens (Human) | Fucosidosis |
PMID:2803224 PMID:3265056 PMID:8399358 |
Transformed cell line | Male | GM-1024, GM 1024, GM1024 | CLO:CLO_0029489, BioSample:SAMN00803571, Coriell:GM01024, Wikidata:Q54836609 |
CVCL_V792 | 2026-07-25 04:32:11 | 0 | |||||
|
GM01082 Resource Report Resource Website |
RRID:CVCL_GS53 | Homo sapiens (Human) | Erythropoietic porphyria | Population: Caucasian. | Finite cell line | Male | GM-1082, GM01082A | CLO:CLO_0030364, BioSample:SAMN00803610, Coriell:GM01082, Wikidata:Q54836633 |
CVCL_GS53 | 2026-07-25 04:32:12 | 0 | |||||
|
GM01057 Resource Report Resource Website 1+ mentions |
RRID:CVCL_H964 | Homo sapiens (Human) | Menkes disease | Population: Caucasian. | PMID:7438975 | Finite cell line | Male | GM-1057 | CLO:CLO_0030350, BioSample:SAMN00803596, Coriell:GM01057, Wikidata:Q54836624 |
CVCL_H964 | 2026-07-25 04:32:11 | 1 | ||||
|
GM01068 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM01068, RRID:CVCL_CX37 | Homo sapiens (Human) | Fabry disease | Finite cell line | Male | GM-1068 | Coriell | GM01068 | Coriell:GM01068, Wikidata:Q54836630 |
CVCL_CX37 | 2026-07-25 04:32:11 | 0 | ||||
|
GM01034 Resource Report Resource Website |
RRID:CVCL_1V11 | Homo sapiens (Human) | Hurler syndrome | Transformed cell line | Female | GM-1034, GM01034A | CLO:CLO_0030373, BioSample:SAMN00803586, Coriell:GM01034, Wikidata:Q54836617 |
CVCL_1V11 | 2026-07-25 04:32:11 | 0 | ||||||
|
GM01016 Resource Report Resource Website |
Coriell Cat# GM01016, RRID:CVCL_6B40 | Homo sapiens (Human) | Transformed cell line | Male | GM-1016 | Coriell | GM01016 | CLO:CLO_0029497, BioSample:SAMN00803559, Coriell:GM01016, Wikidata:Q54836602 |
CVCL_6B40 | 2026-07-25 04:32:11 | 0 | |||||
|
GM01053 Resource Report Resource Website |
RRID:CVCL_V531 | Homo sapiens (Human) | Hurler syndrome | Population: Caucasian. | Finite cell line | Male | GM-1053, GM01053A | CLO:CLO_0030370, BioSample:SAMN00803592, Coriell:GM01053, Wikidata:Q54836622 |
CVCL_V531 | 2026-07-25 04:32:11 | 0 | |||||
|
GM01061 Resource Report Resource Website |
RRID:CVCL_V036 | Homo sapiens (Human) | Huntington's disease | Population: Caucasian. |
PMID:2973075 PMID:6220707 PMID:6458814 |
Finite cell line | Male | GM-1061, GM 1061, GM1061, GM01061A | CLO:CLO_0030368, BioSample:SAMN00803602, Coriell:GM01061, Wikidata:Q54836627 |
CVCL_V036 | 2026-07-25 04:32:11 | 0 | ||||
|
GM01125 Resource Report Resource Website |
Coriell Cat# GM01125, RRID:CVCL_DF15 | Homo sapiens (Human) | Macular dystrophy, retinal, 1 | Finite cell line | Female | GM-1125 | Coriell | GM01125 | CLO:CLO_0030166, BioSample:SAMN00803642, Coriell:GM01125, Wikidata:Q54836654 |
CVCL_DF15 | 2026-07-25 04:32:12 | 0 | ||||
|
GM01208 Resource Report Resource Website |
RRID:CVCL_M982 | Homo sapiens (Human) | Population: Latino or Hispanic; Dominican., Part of: Human variation panel. | Finite cell line | Male | GM-1208, GM17350 | CLO:CLO_0013724, CLO:CLO_0030252, BioSample:SAMN00803714, Coriell:GM01208, Coriell:GM17350, Wikidata:Q54836703 |
CVCL_M982 | 2026-07-25 04:32:14 | 0 |
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