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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM04861 Resource Report Resource Website |
Coriell Cat# GM04861, RRID:CVCL_1I67 | Homo sapiens (Human) | Huntington's disease | Part of: Venezuelan Huntington disease kindreds subcollection. | Finite cell line | Male | Coriell | GM04861 | CLO:CLO_0025796, Coriell:GM04861, Wikidata:Q54838730 |
CVCL_1I67 | 2026-07-25 04:33:03 | 0 | ||||
|
GM04866 Resource Report Resource Website |
Coriell Cat# GM04866, RRID:CVCL_1I70 | Homo sapiens (Human) | Huntington's disease | Part of: Venezuelan Huntington disease kindreds subcollection. | Transformed cell line | Male | GM04866A, GM04866B | Coriell | GM04866 | CLO:CLO_0025788, Coriell:GM04866, Wikidata:Q54838735 |
CVCL_1I70 | 2026-07-25 04:33:03 | 0 | |||
|
GM04876 Resource Report Resource Website |
RRID:CVCL_V571 | Homo sapiens (Human) | Huntington's disease | Part of: Venezuelan Huntington disease kindreds subcollection. | Transformed cell line | Female | GM04876A | CLO:CLO_0025763, Coriell:GM04876, Wikidata:Q54838739 |
CVCL_V571 | 2026-07-25 04:33:03 | 0 | |||||
|
GM04938 Resource Report Resource Website |
RRID:CVCL_8A07 | Homo sapiens (Human) | Tourette syndrome | Population: Caucasian. | Transformed cell line | Female | CLO:CLO_0025578, Coriell:GM04938, Wikidata:Q54838775 |
CVCL_8A07 | 2026-07-25 04:33:04 | 0 | ||||||
|
GM04914 Resource Report Resource Website |
RRID:CVCL_2Z53 | Homo sapiens (Human) | Krabbe disease | Population: Caucasian; Greek. | PMID:3926002 | Finite cell line | Sex unspecified | GM 4914 | CLO:CLO_0025607, Coriell:GM04914, Wikidata:Q54838759 |
CVCL_2Z53 | 2026-07-25 04:33:04 | 0 | ||||
|
GM04926 Resource Report Resource Website |
RRID:CVCL_X312 | Homo sapiens (Human) | Fragile X syndrome | Population: Caucasian. | Finite cell line | Male | CLO:CLO_0025603, Coriell:GM04926, Wikidata:Q54838763 |
CVCL_X312 | 2026-07-25 04:33:04 | 0 | ||||||
|
GM04859 Resource Report Resource Website |
RRID:CVCL_1I65 | Homo sapiens (Human) | Part of: Venezuelan Huntington disease kindreds subcollection. | Finite cell line | Male | CLO:CLO_0025783, Coriell:GM04859, Wikidata:Q54838728 |
CVCL_1I65 | 2026-07-25 04:33:03 | 0 | |||||||
|
GM04901 Resource Report Resource Website |
Coriell Cat# GM04901, RRID:CVCL_JL90 | Homo sapiens (Human) | Glucocorticoid resistance | Population: Caucasian; Dutch. | Finite cell line | Male | Coriell | GM04901 | CLO:CLO_0025591, Coriell:GM04901, Wikidata:Q54838751 |
CVCL_JL90 | 2026-07-25 04:33:04 | 0 | ||||
|
GM04852 Resource Report Resource Website |
Coriell Cat# GM04852, RRID:CVCL_1I58 | Homo sapiens (Human) | Huntington's disease | Part of: Venezuelan Huntington disease kindreds subcollection. | Transformed cell line | Male | GM04852A | Coriell | GM04852 | CLO:CLO_0018185, Coriell:GM04852, Wikidata:Q54838719 |
CVCL_1I58 | 2026-07-25 04:33:03 | 0 | |||
|
GM04916 Resource Report Resource Website |
RRID:CVCL_AT06 | Homo sapiens (Human) | Multiple sulfatase deficiency disease | Transformed cell line | Male | CLO:CLO_0025605, Coriell:GM04916, Wikidata:Q54838761 |
CVCL_AT06 | 2026-07-25 04:33:04 | 0 | |||||||
|
GM04887 Resource Report Resource Website |
RRID:CVCL_V574 | Homo sapiens (Human) | Huntington's disease | Part of: Venezuelan Huntington disease kindreds subcollection. | PMID:6230415 | Finite cell line | Female | GM 4887 | CLO:CLO_0025777, Coriell:GM04887, Wikidata:Q54838742 |
CVCL_V574 | 2026-07-25 04:33:03 | 0 | ||||
|
GM04867 Resource Report Resource Website |
RRID:CVCL_1I71 | Homo sapiens (Human) | Huntington's disease | Part of: Venezuelan Huntington disease kindreds subcollection. | PMID:6230415 | Finite cell line | Male | GM 4867 | CLO:CLO_0025785, Coriell:GM04867, Wikidata:Q54838736 |
CVCL_1I71 | 2026-07-25 04:33:03 | 0 | ||||
|
GM04912 Resource Report Resource Website |
RRID:CVCL_F601 | Homo sapiens (Human) | Glycogen storage disease type II | Population: African American. |
PMID:1652892 PMID:2112341 PMID:10189220 PMID:25488666 |
Finite cell line | Male | GM 4912, GM 04912 | CLO:CLO_0025608, Coriell:GM04912, Wikidata:Q54838757 |
CVCL_F601 | 2026-07-25 04:33:04 | 0 | ||||
|
GM04846 Resource Report Resource Website |
Coriell Cat# GM04846, RRID:CVCL_1I55 | Homo sapiens (Human) | Huntington's disease | Part of: Venezuelan Huntington disease kindreds subcollection. | Transformed cell line | Male | GM04846A, GM04846C | Coriell | GM04846 | CLO:CLO_0018173, Coriell:GM04846, Wikidata:Q54838716 |
CVCL_1I55 | 2026-07-25 04:33:03 | 0 | |||
|
GM04937 Resource Report Resource Website |
RRID:CVCL_8A06 | Homo sapiens (Human) | Tourette syndrome | Population: Caucasian. | Finite cell line | Female | CLO:CLO_0025577, Coriell:GM04937, Wikidata:Q54838774 |
CVCL_8A06 | 2026-07-25 04:33:04 | 0 | ||||||
|
GM04928 Resource Report Resource Website |
Coriell Cat# GM04928, RRID:CVCL_V478 | Homo sapiens (Human) | Down syndrome |
PMID:6661932 PMID:8643543 |
Finite cell line | Male | GM 4928, GM04928A, GM 4928A | Coriell | GM04928 | CLO:CLO_0025601, Coriell:GM04928, Wikidata:Q54838765 |
CVCL_V478 | 2026-07-25 04:33:04 | 0 | |||
|
GM04863 Resource Report Resource Website |
RRID:CVCL_4N45 | Homo sapiens (Human) | Population: Jewish; Ashkenazi. | PMID:19815695 | Finite cell line | Male | GM 4863 | CLO:CLO_0025793, Coriell:GM04863, Wikidata:Q54838732 |
CVCL_4N45 | 2026-07-25 04:33:03 | 0 | |||||
|
GM04932 Resource Report Resource Website |
Coriell Cat# GM04932, RRID:CVCL_N034 | Homo sapiens (Human) | Adrenoleukodystrophy | Population: Pacific., Part of: Human variation panel. | Finite cell line | Male | GM17386 | Coriell | GM04932 | CLO:CLO_0012164, CLO:CLO_0025574, Coriell:GM04932, Coriell:GM17386, Wikidata:Q54838770 |
CVCL_N034 | 2026-07-25 04:33:04 | 0 | |||
|
GM04849 Resource Report Resource Website |
RRID:CVCL_1I57 | Homo sapiens (Human) | Huntington's disease | Part of: Venezuelan Huntington disease kindreds subcollection. | Finite cell line | Female | CLO:CLO_0018176, Coriell:GM04849, Wikidata:Q54838718 |
CVCL_1I57 | 2026-07-25 04:33:03 | 0 | ||||||
|
GM04894 Resource Report Resource Website |
RRID:CVCL_1I74 | Homo sapiens (Human) | Huntington's disease | Population: Caucasian. | Transformed cell line | Male | CLO:CLO_0025768, Coriell:GM04894, Wikidata:Q54838744 |
CVCL_1I74 | 2026-07-25 04:33:03 | 0 |
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