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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM04022 Resource Report Resource Website |
RRID:CVCL_1H81 | Homo sapiens (Human) | Huntington's disease | Donor information: At sampling donor was not affected with Huntington disease but at 50% risk for disease., Population: Caucasian. | PMID:25928884 | Finite cell line | Female | CLO:CLO_0016242, Coriell:GM04022, Wikidata:Q54838369 |
CVCL_1H81 | 2026-07-25 04:32:54 | 0 | |||||
|
GM03986 Resource Report Resource Website |
RRID:CVCL_F111 | Homo sapiens (Human) | Dystrophia myotonica 1 | Population: Caucasian. | PMID:23680132 | Transformed cell line | Male | GM03986A | CLO:CLO_0016057, Coriell:GM03986, Wikidata:Q54838355 |
CVCL_F111 | 2026-07-25 04:32:54 | 0 | ||||
|
GM04012 Resource Report Resource Website |
RRID:CVCL_2S99 | Homo sapiens (Human) | Karyotypic information: 46,XX,t(2;5)(2qter->2p25::5q33->5qter;5pter->5q33::2p25->2pter) (Coriell=GM04012)., Population: Caucasian. | Finite cell line | Female | CLO:CLO_0016069, Coriell:GM04012, Wikidata:Q54838366 |
CVCL_2S99 | 2026-07-25 04:32:54 | 0 | |||||||
|
GM04017 Resource Report Resource Website |
Coriell Cat# GM04017, RRID:CVCL_1H79 | Homo sapiens (Human) | Huntington's disease | Population: Caucasian. | Transformed cell line | Female | Coriell | GM04017 | CLO:CLO_0016239, Coriell:GM04017, Wikidata:Q54838367 |
CVCL_1H79 | 2026-07-25 04:32:54 | 0 | ||||
|
GM03999 Resource Report Resource Website |
RRID:CVCL_X117 | Homo sapiens (Human) | Population: African American. |
PMID:6617268 PMID:6661932 PMID:23665875 |
Finite cell line | Female | GM 3999 | CLO:CLO_0016070, Coriell:GM03999, Wikidata:Q54838365 |
CVCL_X117 | 2026-07-25 04:32:54 | 0 | |||||
|
GM03923 Resource Report Resource Website |
Coriell Cat# GM03923, RRID:CVCL_X116 | Homo sapiens (Human) | Karyotypic information: 46,X,del(X)(q13;q22) (PubMed=10377420)., Population: Caucasian; English. |
PMID:6617268 PMID:6661932 PMID:10377420 PMID:23665875 |
Finite cell line | Female | GM 3923, GM3923 | Coriell | GM03923 | CLO:CLO_0016127, Coriell:GM03923, Wikidata:Q54838327 |
CVCL_X116 | 2026-07-25 04:32:53 | 0 | |||
|
GM04126 Resource Report Resource Website |
Coriell Cat# GM04126, RRID:CVCL_V820 | Homo sapiens (Human) | Wolf-Hirschhorn syndrome | Population: Caucasian. |
PMID:6617268 PMID:6661932 PMID:23665875 |
Finite cell line | Male | GM 4126 | Coriell | GM04126 | CLO:CLO_0016204, Coriell:GM04126, Wikidata:Q54838392 |
CVCL_V820 | 2026-07-25 04:32:55 | 0 | ||
|
GM04106 Resource Report Resource Website |
Coriell Cat# GM04106, RRID:CVCL_9Q94 | Homo sapiens (Human) | LEOPARD syndrome | Population: Caucasian. | Transformed cell line | Male | Coriell | GM04106 | CLO:CLO_0016209, Coriell:GM04106, Wikidata:Q54838388 |
CVCL_9Q94 | 2026-07-25 04:32:55 | 0 | ||||
|
GM03991 Resource Report Resource Website |
RRID:CVCL_X126 | Homo sapiens (Human) | Dystrophia myotonica 1 | Population: Caucasian. | Finite cell line | Female | CLO:CLO_0016072, Coriell:GM03991, Wikidata:Q54838362 |
CVCL_X126 | 2026-07-25 04:32:54 | 0 | ||||||
|
GM04078 Resource Report Resource Website 1+ mentions |
RRID:CVCL_T820 | Homo sapiens (Human) | Friedreich ataxia | Caution: Indicated by Coriell to have 420 and 541 GAA repeats., Population: Caucasian. |
PMID:27002638 PMID:28444186 PMID:29125828 |
Finite cell line | Male | GM-4078, F4078, 4078 | CLO:CLO_0016228, ChEMBL-Cells:CHEMBL4802059, Coriell:GM04078, GEO:GSM2794424, PubChem_Cell_line:CVCL_T820, Wikidata:Q54838382 |
CVCL_T820 | 2026-07-25 04:32:54 | 1 | ||||
|
GM03949 Resource Report Resource Website |
RRID:CVCL_L947 | Homo sapiens (Human) | Familial adenomatous polyposis | Population: Caucasian. | Transformed cell line | Female | CLO:CLO_0016082, Coriell:GM03949, Wikidata:Q54838344 |
CVCL_L947 | 2026-07-25 04:32:54 | 0 | ||||||
|
GM04106 Resource Report Resource Website |
RRID:CVCL_9Q94 | Homo sapiens (Human) | LEOPARD syndrome | Population: Caucasian. | Transformed cell line | Male | CLO:CLO_0016209, Coriell:GM04106, Wikidata:Q54838388 |
CVCL_9Q94 | 2026-07-25 04:32:55 | 0 | ||||||
|
GM04125 Resource Report Resource Website |
RRID:CVCL_1Q58 | Homo sapiens (Human) | Karyotypic information: 46,XY,t(15;18)(15pter->15q15::18p11.3->18pter;18qter->18p11.3::15q15->15qter) (Coriell=GM04125)., Population: Caucasian. | Finite cell line | Male | CLO:CLO_0016208, Coriell:GM04125, Wikidata:Q54838391 |
CVCL_1Q58 | 2026-07-25 04:32:55 | 0 | |||||||
|
GM03959 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_UR84 | Homo sapiens (Human) | Friedreich ataxia | Transformed cell line | Male | GM03959A | Coriell:GM03959, Wikidata:Q93586590 |
CVCL_UR84 | 2026-07-25 04:32:54 | 0 | ||||||
|
GM03998 Resource Report Resource Website |
Coriell Cat# GM03998, RRID:CVCL_IZ39 | Homo sapiens (Human) | Hyperlipoproteinemia, type I | Population: Caucasian. | Finite cell line | Male | Coriell | GM03998 | CLO:CLO_0016074, Coriell:GM03998, Wikidata:Q54838364 |
CVCL_IZ39 | 2026-07-25 04:32:54 | 0 | ||||
|
GM04099 Resource Report Resource Website |
RRID:CVCL_5M89 | Homo sapiens (Human) | Part of: Genetic Testing Reference Material (GeT-RM) samples. |
PMID:21354051 PMID:23665875 |
Transformed cell line | Female | CLO:CLO_0016211, Coriell:GM04099, Wikidata:Q54838386 |
CVCL_5M89 | 2026-07-25 04:32:55 | 0 | ||||||
|
GM04045 Resource Report Resource Website |
RRID:CVCL_X118 | Homo sapiens (Human) | Karyotypic information: 46,XY,t(2;4)(2pter->2q14::4q31.3->4qter;4pter->4q31.1::2q14->2qter) (Coriell=GM04045)., Population: Caucasian; Greek. |
PMID:6617268 PMID:6661932 |
Finite cell line | Male | GM-4045, GM 4045, GM04045B, GM 4045 B | CLO:CLO_0016233, Coriell:GM04045, Wikidata:Q54838379 |
CVCL_X118 | 2026-07-25 04:32:54 | 0 | |||||
|
GM04195 Resource Report Resource Website |
RRID:CVCL_1H90 | Homo sapiens (Human) | Huntington's disease | Population: Caucasian. | PMID:6316146 | Transformed cell line | Female | CLO:CLO_0015923, Coriell:GM04195, Wikidata:Q54838408 |
CVCL_1H90 | 2026-07-25 04:32:55 | 0 | |||||
|
GM04199 Resource Report Resource Website |
RRID:CVCL_1H94 | Homo sapiens (Human) | Huntington's disease | Population: Caucasian. | PMID:6316146 | Transformed cell line | Female | GM04199B | CLO:CLO_0019498, Coriell:GM04199, Wikidata:Q54838412 |
CVCL_1H94 | 2026-07-25 04:32:55 | 0 | ||||
|
GM04204 Resource Report Resource Website |
Coriell Cat# GM04204, RRID:CVCL_M948 | Homo sapiens (Human) | Population: Caucasian. |
PMID:6316146 PMID:25928884 |
Finite cell line | Male | Coriell | GM04204 | CLO:CLO_0019494, Coriell:GM04204, Wikidata:Q54838420 |
CVCL_M948 | 2026-07-25 04:32:56 | 0 |
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