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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM01619 Resource Report Resource Website |
RRID:CVCL_IN47 | Homo sapiens (Human) | Inosine triphosphatase deficiency | Population: Caucasian. | Transformed cell line | Female | GM-1619 | CLO:CLO_0031563, BioSample:SAMN00806977, Coriell:GM01619, Wikidata:Q54836951 |
CVCL_IN47 | 2026-07-25 04:32:20 | 0 | |||||
|
GM01582 Resource Report Resource Website 1+ mentions Possibly Discontinued Discontinued |
Coriell Cat# GM01582, RRID:CVCL_7323 | Homo sapiens (Human) | Population: Caucasian. |
PMID:12665480 PMID:30567591 |
Finite cell line | Female | GM1582, GM-1582, GM01582A, GM1582A, GM00240, GM0240, GM-240 | Coriell | GM01582 | CLO:CLO_0031462, BioSample:SAMN00806939, Coriell:GM00240, Coriell:GM01582, GEO:GSM3124639, Wikidata:Q54836927 |
CVCL_7323 | 2026-07-25 04:32:21 | 1 | |||
|
GM01635 Resource Report Resource Website |
RRID:CVCL_5L39 | Homo sapiens (Human) | Tuberous sclerosis 1 | Population: African American. | Finite cell line | Male | GM-1635, GM01635B | CLO:CLO_0031508, BioSample:SAMN00807003, Coriell:GM01635, Wikidata:Q54836970 |
CVCL_5L39 | 2026-07-25 04:32:20 | 0 | |||||
|
GM01652 Resource Report Resource Website |
RRID:CVCL_7330 | Homo sapiens (Human) | Population: Caucasian. |
PMID:3111682 PMID:3863481 PMID:6458814 PMID:6726265 PMID:8823375 PMID:25326100 PMID:30567591 |
Finite cell line | Female | GM1652, GM-1652, GM 1652, GM1652A, GM01652B, GM01652C, GMO1652C | CLO:CLO_0030948, BioSample:SAMN00807027, BioSample:SAMN03253066, Coriell:GM01652, GEO:GSM1266914, GEO:GSM3124638, Wikidata:Q54836983 |
CVCL_7330 | 2026-07-25 04:32:22 | 0 | |||||
|
GM01584 Resource Report Resource Website |
Coriell Cat# GM01584, RRID:CVCL_D512 | Homo sapiens (Human) | Hunter syndrome | Population: Caucasian. | Finite cell line | Male | GM-1584 | Coriell | GM01584 | CLO:CLO_0031460, BioSample:SAMN00806943, Coriell:GM01584, Wikidata:Q54836929 |
CVCL_D512 | 2026-07-25 04:32:19 | 0 | |||
|
GM01575 Resource Report Resource Website |
Coriell Cat# GM01575, RRID:CVCL_2Z63 | Homo sapiens (Human) | Nevoid basal cell carcinoma syndrome | Population: Caucasian. |
PMID:2897722 PMID:6442144 |
Finite cell line | Female | GM-1575, GM 1575, GM1575 | Coriell | GM01575 | CLO:CLO_0031455, BioSample:SAMN00806927, Coriell:GM01575, Wikidata:Q54836919 |
CVCL_2Z63 | 2026-07-25 04:32:21 | 0 | ||
|
GM01599 Resource Report Resource Website |
RRID:CVCL_AK17 | Homo sapiens (Human) | Population: Caucasian. | Finite cell line | Male | GM-1599 | CLO:CLO_0031537, BioSample:SAMN00806955, Coriell:GM01599, Wikidata:Q54836935 |
CVCL_AK17 | 2026-07-25 04:32:19 | 0 | ||||||
|
GM01637 Resource Report Resource Website |
RRID:CVCL_5L41 | Homo sapiens (Human) | Tuberous sclerosis 1 | Population: African American. | Finite cell line | Female | GM-1637 | CLO:CLO_0031520, BioSample:SAMN00807007, Coriell:GM01637, Wikidata:Q54836972 |
CVCL_5L41 | 2026-07-25 04:32:22 | 0 | |||||
|
GM01571 Resource Report Resource Website |
Coriell Cat# GM01571, RRID:CVCL_W031 | Homo sapiens (Human) | Hypophosphatasia | Population: African American. |
PMID:1409720 PMID:2705456 PMID:8675582 |
Finite cell line | Male | GM-1571, GM 1571, GM1571 | Coriell | GM01571 | CLO:CLO_0031454, BioSample:SAMN00806925, Coriell:GM01571, Wikidata:Q54836918 |
CVCL_W031 | 2026-07-25 04:32:19 | 0 | ||
|
GM01641 Resource Report Resource Website |
RRID:CVCL_5M69 | Homo sapiens (Human) | Neurofibromatosis type 1 | Population: African American. | PMID:23665875 | Transformed cell line | Female | GM-1641 | CLO:CLO_0031523, BioSample:SAMN00807013, Coriell:GM01641, Wikidata:Q54836975 |
CVCL_5M69 | 2026-07-25 04:32:22 | 0 | ||||
|
GM01578 Resource Report Resource Website |
RRID:CVCL_2Z66 | Homo sapiens (Human) | Nevoid basal cell carcinoma syndrome | Population: Caucasian. | Transformed cell line | Male | GM-1578 | CLO:CLO_0031466, BioSample:SAMN00806933, Coriell:GM01578, Wikidata:Q54836922 |
CVCL_2Z66 | 2026-07-25 04:32:19 | 0 | |||||
|
GM01570 Resource Report Resource Website |
Coriell Cat# GM01570, RRID:CVCL_V809 | Homo sapiens (Human) | Karyotypic information: 6,XY,rec(13)(pter->q22::p11->pter)pat (Coriell=GM01570). |
PMID:446098 PMID:6661932 |
Finite cell line | Male | GM-1570, GM 1570 | Coriell | GM01570 | CLO:CLO_0031453, Coriell:GM01570, Wikidata:Q54836917 |
CVCL_V809 | 2026-07-25 04:32:19 | 0 | |||
|
GM01623 Resource Report Resource Website |
RRID:CVCL_4J34 | Homo sapiens (Human) | Acute intermittent porphyria | Population: Caucasian. | Finite cell line | Male | GM-1623 | CLO:CLO_0031575, BioSample:SAMN00806983, Coriell:GM01623, Wikidata:Q54836958 |
CVCL_4J34 | 2026-07-25 04:32:20 | 0 | |||||
|
GM01586 Resource Report Resource Website |
RRID:CVCL_9Q87 | Homo sapiens (Human) | I-cell disease | Population: Caucasian. | PMID:16465621 | Finite cell line | Male | GM-1586, GM01586C | CLO:CLO_0031463, BioSample:SAMN00806945, Coriell:GM01586, Wikidata:Q54836930 |
CVCL_9Q87 | 2026-07-25 04:32:19 | 0 | ||||
|
GM01579 Resource Report Resource Website |
RRID:CVCL_0P96 | Homo sapiens (Human) | Population: Caucasian. | PMID:23665875 | Finite cell line | Female | GM-1579 | CLO:CLO_0031465, BioSample:SAMN00806935, Coriell:GM01579, Wikidata:Q54836923 |
CVCL_0P96 | 2026-07-25 04:32:19 | 0 | |||||
|
GM01634 Resource Report Resource Website |
Coriell Cat# GM01634, RRID:CVCL_9Z57 | Homo sapiens (Human) | Neurofibromatosis type 1 | Population: Caucasian. | Transformed cell line | Male | GM-1634 | Coriell | GM01634 | CLO:CLO_0031512, BioSample:SAMN00807001, Coriell:GM01634, Wikidata:Q54836969 |
CVCL_9Z57 | 2026-07-25 04:32:20 | 0 | |||
|
GM01600 Resource Report Resource Website |
RRID:CVCL_AK18 | Homo sapiens (Human) | Sitosterolemia | Population: Caucasian. | Finite cell line | Female | GM-1600 | CLO:CLO_0031538, BioSample:SAMN00806957, Coriell:GM01600, Wikidata:Q54836936 |
CVCL_AK18 | 2026-07-25 04:32:19 | 0 | |||||
|
GM01584 Resource Report Resource Website |
RRID:CVCL_D512 | Homo sapiens (Human) | Hunter syndrome | Population: Caucasian. | Finite cell line | Male | GM-1584 | CLO:CLO_0031460, BioSample:SAMN00806943, Coriell:GM01584, Wikidata:Q54836929 |
CVCL_D512 | 2026-07-25 04:32:21 | 0 | |||||
|
GM01581 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_JD78 | Homo sapiens (Human) | Finite cell line | Female | GM-1581 | Coriell:GM01581, Wikidata:Q54836925 |
CVCL_JD78 | 2026-07-25 04:32:19 | 0 | |||||||
|
GM01634 Resource Report Resource Website |
RRID:CVCL_9Z57 | Homo sapiens (Human) | Neurofibromatosis type 1 | Population: Caucasian. | Transformed cell line | Male | GM-1634 | CLO:CLO_0031512, BioSample:SAMN00807001, Coriell:GM01634, Wikidata:Q54836969 |
CVCL_9Z57 | 2026-07-25 04:32:22 | 0 |
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