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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM26038 Resource Report Resource Website |
RRID:CVCL_HQ53 | Homo sapiens (Human) | Pitt-Hopkins syndrome | Population: Caucasian. | Finite cell line | Male | Coriell:GM26038, Wikidata:Q54854065 |
CVCL_HQ53 | 2026-07-25 04:37:57 | 0 | ||||||
|
GM26156 Resource Report Resource Website |
Coriell Cat# GM26156, RRID:CVCL_A2VW | Homo sapiens (Human) | Central core disease | Population: Caucasian. | Transformed cell line | Female | Coriell | GM26156 | Coriell:GM26156, Wikidata:Q105507030 |
CVCL_A2VW | 2026-07-25 04:37:58 | 0 | ||||
|
GM26131 Resource Report Resource Website |
Coriell Cat# GM26131, RRID:CVCL_A2VM | Homo sapiens (Human) | Population: Korean. | Transformed cell line | Female | Coriell | GM26131 | Coriell:GM26131, Wikidata:Q105507004 |
CVCL_A2VM | 2026-07-25 04:37:58 | 0 | |||||
|
GM26216 Resource Report Resource Website |
RRID:CVCL_A2WH | Homo sapiens (Human) | Pitt-Hopkins syndrome | Transformed cell line | Female | Coriell:GM26216, Wikidata:Q105507070 |
CVCL_A2WH | 2026-07-25 04:37:59 | 0 | |||||||
|
GM26105 Resource Report Resource Website |
Coriell Cat# GM26105, RRID:CVCL_LP11 | Homo sapiens (Human) | Population: Caucasian., Part of: Personal Genome Project (PGP) cell line collection. | Induced pluripotent stem cell | Male | GM26105*C | Coriell | GM26105 | Coriell:GM26105, Wikidata:Q54854080 |
cvcl_1c78 | CVCL_LP11 | 2026-07-25 04:37:58 | 0 | |||
|
GM26116 Resource Report Resource Website |
Coriell Cat# GM26116, RRID:CVCL_A2VH | Homo sapiens (Human) | Population: Caucasian; Lithuanian. | Transformed cell line | Male | Coriell | GM26116 | Coriell:GM26116, Wikidata:Q105506994 |
CVCL_A2VH | 2026-07-25 04:37:58 | 0 | |||||
|
GM26164 Resource Report Resource Website |
RRID:CVCL_A2VY | Homo sapiens (Human) | Population: Caucasian; Italian. | Transformed cell line | Female | Coriell:GM26164, Wikidata:Q105507035 |
CVCL_A2VY | 2026-07-25 04:37:58 | 0 | |||||||
|
GM26154 Resource Report Resource Website |
RRID:CVCL_A2VU | Homo sapiens (Human) | Central core disease | Population: Caucasian. | Transformed cell line | Female | Coriell:GM26154, Wikidata:Q105507024 |
CVCL_A2VU | 2026-07-25 04:37:58 | 0 | ||||||
|
GM26074 Resource Report Resource Website |
RRID:CVCL_HL69 | Homo sapiens (Human) | Tuberous sclerosis | Population: Caucasian; Mennonite. | Finite cell line | Female | Coriell:GM26074, Wikidata:Q54854068 |
CVCL_HL69 | 2026-07-25 04:37:57 | 0 | ||||||
|
GM26036 Resource Report Resource Website |
RRID:CVCL_HK73 | Homo sapiens (Human) | Choroideremia | Transformed cell line | Male | Coriell:GM26036, Wikidata:Q54854063 |
CVCL_HK73 | 2026-07-25 04:37:57 | 0 | |||||||
|
GM26131 Resource Report Resource Website |
RRID:CVCL_A2VM | Homo sapiens (Human) | Population: Korean. | Transformed cell line | Female | Coriell:GM26131, Wikidata:Q105507004 |
CVCL_A2VM | 2026-07-25 04:37:58 | 0 | |||||||
|
GM26098 Resource Report Resource Website |
RRID:CVCL_LH27 | Homo sapiens (Human) | Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1 | Population: Caucasian. | Finite cell line | Female | Coriell:GM26098, Wikidata:Q54854077 |
CVCL_LH27 | 2026-07-25 04:37:58 | 0 | ||||||
|
GM26076 Resource Report Resource Website |
RRID:CVCL_LH23 | Homo sapiens (Human) | Transformed cell line | Female | Coriell:GM26076, Wikidata:Q54854070 |
CVCL_LH23 | 2026-07-25 04:37:57 | 0 | ||||||||
|
GM26113 Resource Report Resource Website |
RRID:CVCL_A2VE | Homo sapiens (Human) | Multiple congenital anomalies-hypotonia-seizures syndrome 1 | Population: Indian. | Finite cell line | Male | Coriell:GM26113, Wikidata:Q105506984 |
CVCL_A2VE | 2026-07-25 04:37:58 | 0 | ||||||
|
GM26046 Resource Report Resource Website |
RRID:CVCL_VP82 | Homo sapiens (Human) | Population: Caucasian; Amish. | Finite cell line | Male | Coriell:GM26046, Wikidata:Q93932339 |
CVCL_VP82 | 2026-07-25 04:37:57 | 0 | |||||||
|
GM26023 Resource Report Resource Website |
RRID:CVCL_A2VA | Homo sapiens (Human) | Pitt-Hopkins syndrome | Population: Caucasian; English. | Finite cell line | Male | Coriell:GM26023, Wikidata:Q105506974 |
CVCL_A2VA | 2026-07-25 04:37:57 | 0 | ||||||
|
GM26198 Resource Report Resource Website |
RRID:CVCL_JF28 | Homo sapiens (Human) | Transformed cell line | Female | Coriell:GM26198, Wikidata:Q54854089 |
CVCL_JF28 | 2026-07-25 04:37:59 | 0 | ||||||||
|
GM26190 Resource Report Resource Website |
RRID:CVCL_LP13 | Homo sapiens (Human) | Transformed cell line | Female | Coriell:GM26190, Wikidata:Q54854086 |
CVCL_LP13 | 2026-07-25 04:37:59 | 0 | ||||||||
|
GM26188 Resource Report Resource Website |
RRID:CVCL_YP67 | Homo sapiens (Human) | Chromosome 15q11-q13 duplication syndrome | Population: Chinese. | Transformed cell line | Female | Coriell:GM26188, Wikidata:Q93932530 |
CVCL_YP67 | 2026-07-25 04:37:58 | 0 | ||||||
|
GM26199 Resource Report Resource Website |
RRID:CVCL_A2WG | Homo sapiens (Human) | Central core disease | Population: Caucasian; Irish. | Transformed cell line | Female | Coriell:GM26199, Wikidata:Q105507067 |
CVCL_A2WG | 2026-07-25 04:37:59 | 0 |
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