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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM02029 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_JD98 | Homo sapiens (Human) | Finite cell line | Female | GM-2029 | Coriell:GM02029, Wikidata:Q54837248 |
CVCL_JD98 | 2026-07-25 04:32:28 | 0 | |||||||
|
GM02045 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_CX28 | Homo sapiens (Human) | I-cell disease | Finite cell line | Male | GM-2045 | Coriell:GM02045, Wikidata:Q54837260 |
CVCL_CX28 | 2026-07-25 04:32:28 | 0 | ||||||
|
GM02029 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM02029, RRID:CVCL_JD98 | Homo sapiens (Human) | Finite cell line | Female | GM-2029 | Coriell | GM02029 | Coriell:GM02029, Wikidata:Q54837248 |
CVCL_JD98 | 2026-07-25 04:32:28 | 0 | |||||
|
GM02063 Resource Report Resource Website Possibly Discontinued Possibly Discontinued |
Coriell Cat# GM02063, RRID:CVCL_F127 | Homo sapiens (Human) | Lesch-Nyhan syndrome | Population: African American. | PMID:180603 | Finite cell line | Male | LN, GM-2063, GM 2063, GM-02063, GM00177, GM 177, GM-177, GM177 | Coriell | GM02063 | Coriell:GM00177, Coriell:GM02063, Wikidata:Q54837280 |
CVCL_F127 | 2026-07-25 04:32:28 | 0 | ||
|
GM02145 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM02145, RRID:CVCL_CX29 | Homo sapiens (Human) | Finite cell line | Male | GM-2145 | Coriell | GM02145 | Coriell:GM02145, Wikidata:Q54837319 |
CVCL_CX29 | 2026-07-25 04:32:30 | 0 | |||||
|
GM02144 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM02144, RRID:CVCL_1Y52 | Homo sapiens (Human) | Sandhoff disease | Population: Caucasian. | Finite cell line | Male | GM-2144, GM2144 | Coriell | GM02144 | Coriell:GM02144, Wikidata:Q54837317 |
CVCL_1Y52 | 2026-07-25 04:32:29 | 0 | |||
|
GM02145 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_CX29 | Homo sapiens (Human) | Finite cell line | Male | GM-2145 | Coriell:GM02145, Wikidata:Q54837319 |
CVCL_CX29 | 2026-07-25 04:32:29 | 0 | |||||||
|
GM02206 Resource Report Resource Website Discontinued |
Coriell Cat# GM01514, RRID:CVCL_L969 | Homo sapiens (Human) | Ehlers-Danlos syndrome | Population: Caucasian. |
PMID:6617268 PMID:23665875 PMID:25326100 |
Finite cell line | Female | GM-2206 GM 2206, GM01514 | Coriell | GM01514 | CLO:CLO_0032262, BioSample:SAMN00807604, Coriell:GM01514, Coriell:GM02206, GEO:GSM1266977, Wikidata:Q54837370 |
CVCL_L969 | 2026-07-25 04:32:30 | 0 | ||
|
GM02206 Resource Report Resource Website Discontinued |
Coriell Cat# GM02206, RRID:CVCL_L969 | Homo sapiens (Human) | Ehlers-Danlos syndrome | Population: Caucasian. |
PMID:6617268 PMID:23665875 PMID:25326100 |
Finite cell line | Female | GM-2206 GM 2206, GM01514 | Coriell | GM02206 | CLO:CLO_0032262, BioSample:SAMN00807604, Coriell:GM01514, Coriell:GM02206, GEO:GSM1266977, Wikidata:Q54837370 |
CVCL_L969 | 2026-07-25 04:32:30 | 0 | ||
|
GM02215 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_JB88 | Homo sapiens (Human) | Autosomal dominant torsion dystonia 1 | Finite cell line | Male | GM-2215 | Coriell:GM02215, Wikidata:Q54837377 |
CVCL_JB88 | 2026-07-25 04:32:32 | 0 | ||||||
|
GM02205 Resource Report Resource Website Discontinued |
Coriell Cat# GM02205, RRID:CVCL_L968 | Homo sapiens (Human) | Population: Caucasian. |
PMID:6617268 PMID:23665875 PMID:24555846 PMID:25326100 |
Finite cell line | Male | GM-2205, GM 2205, GM01515 | Coriell | GM02205 | CLO:CLO_0032263, BioSample:SAMN00807602, Coriell:GM01515, Coriell:GM02205, GEO:GSM1266975, GEO:GSM1267054, GEO:GSM1288438, Wikidata:Q54837369 |
CVCL_L968 | 2026-07-25 04:32:30 | 0 | |||
|
GM02211 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM02211, RRID:CVCL_JB67 | Homo sapiens (Human) | Wolman disease | PMID:6782865 | Finite cell line | Male | GM-2211, GM 2211, GM2211 | Coriell | GM02211 | Coriell:GM02211, Wikidata:Q54837374 |
CVCL_JB67 | 2026-07-25 04:32:30 | 0 | |||
|
GM02224 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM02224, RRID:CVCL_CX22 | Homo sapiens (Human) | Lactic acidosis | Finite cell line | Female | GM-2224 | Coriell | GM02224 | Coriell:GM02224, Wikidata:Q54837379 |
CVCL_CX22 | 2026-07-25 04:32:31 | 0 | ||||
|
GM02364 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM02364, RRID:CVCL_JD75 | Homo sapiens (Human) | Fanconi anemia | Finite cell line | Male | GM-2364 | Coriell | GM02364 | Coriell:GM02364, Wikidata:Q54837461 |
CVCL_JD75 | 2026-07-25 04:32:34 | 0 | ||||
|
GM02366 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_U388 | Homo sapiens (Human) | Tay-Sachs disease | Transformed cell line | Male | CLO:CLO_0033102, BioSample:SAMN00807739, Coriell:GM02366, Wikidata:Q54837464 |
CVCL_U388 | 2026-07-25 04:32:34 | 0 | |||||||
|
GM02429 Resource Report Resource Website Discontinued |
RRID:CVCL_L974 | Homo sapiens (Human) | Homocystinuria | Transformed cell line | Female | GM02375 | CLO:CLO_0033094, BioSample:SAMN00807761, Coriell:GM02375, Coriell:GM02429, Wikidata:Q54837480 |
CVCL_L974 | 2026-07-25 04:32:35 | 0 | ||||||
|
GM02412 Resource Report Resource Website Discontinued |
RRID:CVCL_L972 | Homo sapiens (Human) | Galactosemia | Population: Caucasian. | PMID:1766867 | Transformed cell line | Male | GM-2412, GM 2412, GM02412B, GM01027, GM-1027 | CLO:CLO_0033097, BioSample:SAMN00807745, Coriell:GM01027, Coriell:GM02412, Wikidata:Q54837470 |
CVCL_L972 | 2026-07-25 04:32:33 | 0 | ||||
|
GM02407 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_CX54 | Homo sapiens (Human) | Multiple sulfatase deficiency disease | Finite cell line | Female | GM-2407 | Coriell:GM02407, Wikidata:Q54837468 |
CVCL_CX54 | 2026-07-25 04:32:34 | 0 | ||||||
|
GM02429 Resource Report Resource Website Discontinued |
Coriell Cat# GM02375, RRID:CVCL_L974 | Homo sapiens (Human) | Homocystinuria | Transformed cell line | Female | GM02375 | Coriell | GM02375 | CLO:CLO_0033094, BioSample:SAMN00807761, Coriell:GM02375, Coriell:GM02429, Wikidata:Q54837480 |
CVCL_L974 | 2026-07-25 04:32:33 | 0 | ||||
|
GM02431 Resource Report Resource Website Discontinued |
Coriell Cat# GM02431, RRID:CVCL_L975 | Homo sapiens (Human) | Chediak-Higashi syndrome | Transformed cell line | Male | GM02431A, GM02378 | Coriell | GM02431 | CLO:CLO_0033275, BioSample:SAMN00807765, Coriell:GM02378, Coriell:GM02431, Wikidata:Q54837482 |
CVCL_L975 | 2026-07-25 04:32:33 | 0 |
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