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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM02039 Resource Report Resource Website |
RRID:CVCL_CW69 | Homo sapiens (Human) | Schizophrenia | Population: Caucasian. | Finite cell line | Male | GM-2039 | CLO:CLO_0032555, BioSample:SAMN00807420, Coriell:GM02039, Wikidata:Q54837258 |
CVCL_CW69 | 2026-07-25 04:32:28 | 0 | |||||
|
GM02085 Resource Report Resource Website |
RRID:CVCL_U703 | Homo sapiens (Human) | Bloom syndrome | Donor information: From Bloom Syndrome Registry patient 53(StAs) (BSR53)., Population: Jewish; Ashkenazi. |
PMID:436333 PMID:908169 |
Finite cell line | Female | GM-2085 | CLO:CLO_0032511, BioSample:SAMN00807472, Coriell:GM02085, GEO:GSM1316975, GEO:GSM1317012, Wikidata:Q54837293 |
CVCL_U703 | 2026-07-25 04:32:28 | 0 | ||||
|
GM02079 Resource Report Resource Website |
RRID:CVCL_1H41 | Homo sapiens (Human) | Huntington's disease | Population: Caucasian. | PMID:6220707 | Finite cell line | Female | GM-2079, GM 2079, GM02079A | CLO:CLO_0032509, BioSample:SAMN00807468, Coriell:GM02079, Wikidata:Q54837291 |
CVCL_1H41 | 2026-07-25 04:32:28 | 0 | ||||
|
GM02064 Resource Report Resource Website |
RRID:CVCL_M994 | Homo sapiens (Human) | Hereditary persistence of fetal hemoglobin | Population: Africans south of the Sahara., Part of: Human variation panel. |
PMID:6196781 PMID:7313555 |
Transformed cell line | Male | GM-2064, GM 2064, GM2064, GM02064A, GM17342 | CLO:CLO_0013747, CLO:CLO_0032529, BioSample:SAMN00807450, Coriell:GM02064, Coriell:GM17342, Wikidata:Q54837281 |
CVCL_M994 | 2026-07-25 04:32:29 | 0 | ||||
|
GM02110 Resource Report Resource Website Discontinued |
Coriell Cat# GM02110, RRID:CVCL_L962 | Homo sapiens (Human) | Hyperlipoproteinemia, type IIa | Transformed cell line | Male | GM-2110, GM02110A, GM01450, GM-1450 | Coriell | GM02110 | CLO:CLO_0031830, BioSample:SAMN00807494, Coriell:GM01450, Coriell:GM02110, Wikidata:Q54837305 |
CVCL_L962 | 2026-07-25 04:32:30 | 0 | ||||
|
GM02014 Resource Report Resource Website |
RRID:CVCL_M990 | Homo sapiens (Human) | Population: Arab., Part of: Human variation panel. | PMID:16465621 | Finite cell line | Female | GM-2014, GM02014A, GM17041, GM17331 | CLO:CLO_0013611, CLO:CLO_0014625, CLO:CLO_0032307, BioSample:SAMN00807388, Coriell:GM02014, Coriell:GM17041, Coriell:GM17331, Wikidata:Q54837238 |
CVCL_M990 | 2026-07-25 04:32:27 | 0 | |||||
|
GM02055 Resource Report Resource Website |
RRID:CVCL_H177 | Homo sapiens (Human) | PMID:6617268 | Finite cell line | Female | GM-2055, GM 2055 | CLO:CLO_0032535, Coriell:GM02055, Wikidata:Q54837274 |
CVCL_H177 | 2026-07-25 04:32:28 | 0 | ||||||
|
GM02013 Resource Report Resource Website |
RRID:CVCL_W640 | Homo sapiens (Human) | I-cell disease | Population: Arab. | PMID:16465621 | Finite cell line | Male | GM-2013, GM02013B, GM02013D | CLO:CLO_0032309, BioSample:SAMN00807386, Coriell:GM02013, Wikidata:Q54837237 |
CVCL_W640 | 2026-07-25 04:32:28 | 0 | ||||
|
GM02075 Resource Report Resource Website 1+ mentions |
RRID:CVCL_CW70 | Homo sapiens (Human) | Chediak-Higashi syndrome | Population: Caucasian. |
PMID:8896560 PMID:36259166 |
Finite cell line | Female | GM-2075, GM02075A | CLO:CLO_0032513, BioSample:SAMN00807462, Coriell:GM02075, Wikidata:Q54837288 |
CVCL_CW70 | 2026-07-25 04:32:28 | 1 | ||||
|
GM02025 Resource Report Resource Website |
RRID:CVCL_V825 | Homo sapiens (Human) | Population: Caucasian. |
PMID:6617268 PMID:6661932 PMID:23665875 |
Finite cell line | Male | GM-2025, GM 2025, GM2025 | CLO:CLO_0032577, BioSample:SAMN00807400, Coriell:GM02025, Wikidata:Q54837244 |
CVCL_V825 | 2026-07-25 04:32:27 | 0 | |||||
|
GM02011 Resource Report Resource Website |
RRID:CVCL_V030 | Homo sapiens (Human) | Argininemia | Transformed cell line | Female | GM2011, GM-2011, GM02011A | CLO:CLO_0032312, BioSample:SAMN00807384, Coriell:GM02011, Wikidata:Q54837236 |
CVCL_V030 | 2026-07-25 04:32:27 | 0 | ||||||
|
GM02109 Resource Report Resource Website |
RRID:CVCL_W621 | Homo sapiens (Human) | Wolman disease | Population: African American. | PMID:6782865 | Finite cell line | Male | GM-2109, GM 2109, GM02109B | CLO:CLO_0031819, BioSample:SAMN00807492, Coriell:GM02109, Wikidata:Q54837304 |
CVCL_W621 | 2026-07-25 04:32:29 | 0 | ||||
|
GM02098 Resource Report Resource Website |
RRID:CVCL_2Z72 | Homo sapiens (Human) | Nevoid basal cell carcinoma syndrome | Characteristics: Hypersensitive to cell killing by ionizing radiation (Coriell=GM02098)., Population: Caucasian. |
PMID:2897722 PMID:6442144 |
Finite cell line | Male | GM-2098, GM 2098, GM2098, GM02098A | CLO:CLO_0031824, BioSample:SAMN00807486, Coriell:GM02098, Wikidata:Q54837301 |
CVCL_2Z72 | 2026-07-25 04:32:29 | 0 | ||||
|
GM02093 Resource Report Resource Website |
Coriell Cat# GM02093, RRID:CVCL_6B42 | Homo sapiens (Human) | Metachromatic leukodystrophy | Population: Caucasian. | Finite cell line | Male | GM-2093, GM02093B | Coriell | GM02093 | CLO:CLO_0031828, BioSample:SAMN00807478, Coriell:GM02093, Wikidata:Q54837297 |
CVCL_6B42 | 2026-07-25 04:32:28 | 0 | |||
|
GM02078 Resource Report Resource Website |
Coriell Cat# GM02078, RRID:CVCL_1H40 | 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. | Transformed cell line | Female | GM-2078 | Coriell | GM02078 | CLO:CLO_0032515, BioSample:SAMN00807466, Coriell:GM02078, Wikidata:Q54837290 |
CVCL_1H40 | 2026-07-25 04:32:29 | 0 | |||
|
GM02068 Resource Report Resource Website |
Coriell Cat# GM02068, RRID:CVCL_1N60 | Homo sapiens (Human) | Karyotypic information: 46,XX,t(6;7)(6pter->6q27::7q22->7qter;7pter->7q22::6q27->6qter) (Coriell=GM02068)., Population: Caucasian. | Finite cell line | Female | GM-2068 | Coriell | GM02068 | CLO:CLO_0032518, BioSample:SAMN00807458, Coriell:GM02068, Wikidata:Q54837285 |
CVCL_1N60 | 2026-07-25 04:32:29 | 0 | ||||
|
GM02094 Resource Report Resource Website |
Coriell Cat# GM02094, RRID:CVCL_1Y44 | Homo sapiens (Human) | Sandhoff disease | Population: Caucasian. | PMID:3017984 | Finite cell line | Male | GM-2094, GM 2094, GM2094A | Coriell | GM02094 | CLO:CLO_0031827, BioSample:SAMN00807480, Coriell:GM02094, Wikidata:Q54837298 |
CVCL_1Y44 | 2026-07-25 04:32:29 | 0 | ||
|
GM02053 Resource Report Resource Website |
RRID:CVCL_F593 | Homo sapiens (Human) | Fanconi anemia | Population: Arab. |
PMID:761484 PMID:3030788 |
Finite cell line | Female | GM-2053, GM2053 | CLO:CLO_0032537, BioSample:SAMN00807436, Coriell:GM02053, Wikidata:Q54837272 |
CVCL_F593 | 2026-07-25 04:32:28 | 0 | ||||
|
GM02078 Resource Report Resource Website |
RRID:CVCL_1H40 | 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. | Transformed cell line | Female | GM-2078 | CLO:CLO_0032515, BioSample:SAMN00807466, Coriell:GM02078, Wikidata:Q54837290 |
CVCL_1H40 | 2026-07-25 04:32:28 | 0 | |||||
|
GM02103 Resource Report Resource Website |
Coriell Cat# GM02103, RRID:CVCL_X260 | Homo sapiens (Human) | Karyotypic information: 46,X,t(X;Y)(q11;q11) (PubMed=10377420)., Population: Caucasian. |
PMID:6661932 PMID:10377420 |
Finite cell line | Female | GM-2103, GM 2103, GM2103 | Coriell | GM02103 | CLO:CLO_0031820, BioSample:SAMN00807490, Coriell:GM02103, Wikidata:Q54837303 |
CVCL_X260 | 2026-07-25 04:32:29 | 0 |
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