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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM27930 Resource Report Resource Website |
RRID:CVCL_A9ZH | Homo sapiens (Human) | Neurodegeneration with brain iron accumulation 5 | Induced pluripotent stem cell | Female | GM27930*B | Coriell:GM27930, Wikidata:Q102113947 |
cvcl_a2sp | CVCL_A9ZH | 2026-07-25 04:38:11 | 0 | |||||
|
GM28012 Resource Report Resource Website |
RRID:CVCL_A2YR | Homo sapiens (Human) | Leigh disease | Finite cell line | Female | Coriell:GM28012, Wikidata:Q105507438 |
CVCL_A2YR | 2026-07-25 04:38:11 | 0 | |||||||
|
GM27910 Resource Report Resource Website |
RRID:CVCL_ZW47 | Homo sapiens (Human) | Cerebral creatine deficiency syndrome 1 | Population: Caucasian; British. | Transformed cell line | Male | Coriell:GM27910, Wikidata:Q102113944 |
CVCL_ZW47 | 2026-07-25 04:38:11 | 0 | ||||||
|
GM28017 Resource Report Resource Website |
RRID:CVCL_A2YV | Homo sapiens (Human) | Population: Caucasian; German. | Finite cell line | Female | Coriell:GM28017, Wikidata:Q105507453 |
CVCL_A2YV | 2026-07-25 04:38:11 | 0 | |||||||
|
GM27864 Resource Report Resource Website |
Coriell Cat# GM27864, RRID:CVCL_ZH99 | Homo sapiens (Human) | Population: Caucasian; Spanish. | Transformed cell line | Male | Coriell | GM27864 | Coriell:GM27864, Wikidata:Q98126634 |
CVCL_ZH99 | 2026-07-25 04:38:10 | 0 | |||||
|
GM27889 Resource Report Resource Website |
Coriell Cat# GM27889, RRID:CVCL_ZW55 | Homo sapiens (Human) | Cerebral creatine deficiency syndrome 1 | Finite cell line | Male | Coriell | GM27889 | Coriell:GM27889, Wikidata:Q102113939 |
CVCL_ZW55 | 2026-07-25 04:38:11 | 0 | |||||
|
GM28095 Resource Report Resource Website |
RRID:CVCL_B0IR | Homo sapiens (Human) | Leigh disease | Population: Caucasian; Austrian. | Finite cell line | Male | Coriell:GM28095, Wikidata:Q108820309 |
CVCL_B0IR | 2026-07-25 04:38:12 | 0 | ||||||
|
GM28026 Resource Report Resource Website |
RRID:CVCL_A5MF | Homo sapiens (Human) | Multicentric carpotarsal osteolysis syndrome | Transformed cell line | Female | Coriell:GM28026, Wikidata:Q107115201 |
CVCL_A5MF | 2026-07-25 04:38:11 | 0 | |||||||
|
GM28032 Resource Report Resource Website |
RRID:CVCL_A5MJ | Homo sapiens (Human) | Population: Caucasian; Polish. | Finite cell line | Female | Coriell:GM28032, Wikidata:Q107115205 |
CVCL_A5MJ | 2026-07-25 04:38:12 | 0 | |||||||
|
GM27899 Resource Report Resource Website |
RRID:CVCL_A2TV | Homo sapiens (Human) | SLC6A1-associated myoclonic-atonic epilepsy | Population: Caucasian. | Finite cell line | Male | Coriell:GM27899, Wikidata:Q105507400 |
CVCL_A2TV | 2026-07-25 04:38:11 | 0 | ||||||
|
GM27936 Resource Report Resource Website |
RRID:CVCL_A2TR | Homo sapiens (Human) | Intellectual developmental disorder, autosomal dominant 9 | Induced pluripotent stem cell | Male | GM27936*B | Coriell:GM27936, Wikidata:Q105507421 |
CVCL_A2TR | 2026-07-25 04:38:11 | 0 | ||||||
|
GM28013 Resource Report Resource Website |
RRID:CVCL_A2YS | Homo sapiens (Human) | Leigh disease | Population: Indian. | Finite cell line | Female | Coriell:GM28013, Wikidata:Q105507442 |
CVCL_A2YS | 2026-07-25 04:38:11 | 0 | ||||||
|
GM27909 Resource Report Resource Website |
RRID:CVCL_ZW46 | Homo sapiens (Human) | Cerebral creatine deficiency syndrome 1 | Population: Caucasian; German. | Finite cell line | Male | Coriell:GM27909, Wikidata:Q102113942 |
CVCL_ZW46 | 2026-07-25 04:38:11 | 0 | ||||||
|
GM28009 Resource Report Resource Website |
Coriell Cat# GM28009, RRID:CVCL_A2YN | Homo sapiens (Human) | Population: Caucasian. | Finite cell line | Female | Coriell | GM28009 | Coriell:GM28009, Wikidata:Q105507428 |
CVCL_A2YN | 2026-07-25 04:38:11 | 0 | |||||
|
GM27873 Resource Report Resource Website |
Coriell Cat# GM27873, RRID:CVCL_A2SS | Homo sapiens (Human) | Population: Caucasian; Spanish (Chilean). | Transformed cell line | Female | Coriell | GM27873 | Coriell:GM27873, Wikidata:Q105507373 |
CVCL_A2SS | 2026-07-25 04:38:10 | 0 | |||||
|
GM28035 Resource Report Resource Website |
Coriell Cat# GM28035, RRID:CVCL_B0I4 | Homo sapiens (Human) | Population: Caucasian. | Finite cell line | Female | Coriell | GM28035 | Coriell:GM28035, Wikidata:Q108820300 |
CVCL_B0I4 | 2026-07-25 04:38:12 | 0 | |||||
|
GM27890 Resource Report Resource Website |
RRID:CVCL_A2TF | Homo sapiens (Human) | Nemaline myopathy 3 | Population: Jewish; Ashkenazi. | Transformed cell line | Female | Coriell:GM27890, Wikidata:Q105507397 |
CVCL_A2TF | 2026-07-25 04:38:11 | 0 | ||||||
|
GM27880 Resource Report Resource Website |
RRID:CVCL_A2TB | Homo sapiens (Human) | Rett syndrome, congenital variant | PMID:37071670 | Induced pluripotent stem cell | Male | GM27880*C, 1123-FOXG1-LOF-Hom#A8 | Coriell:GM27880, Wikidata:Q105507379 |
cvcl_a2ty | CVCL_A2TB | 2026-07-25 04:38:10 | 0 | ||||
|
GM27888 Resource Report Resource Website |
Coriell Cat# GM27888, RRID:CVCL_ZW54 | Homo sapiens (Human) | Cerebral creatine deficiency syndrome 1 | Finite cell line | Male | Coriell | GM27888 | Coriell:GM27888, Wikidata:Q102113938 |
CVCL_ZW54 | 2026-07-25 04:38:11 | 0 | |||||
|
GM28063 Resource Report Resource Website |
RRID:CVCL_B3SE | Homo sapiens (Human) | Leigh disease | Population: Indian. | Finite cell line | Male | Coriell:GM28063, Wikidata:Q110432830 |
CVCL_B3SE | 2026-07-25 04:38:12 | 0 |
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