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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM20184 Resource Report Resource Website |
RRID:CVCL_DB95 | Homo sapiens (Human) | Transformed cell line | Male | CLO:CLO_0027948, Coriell:GM20184, Wikidata:Q54850828 |
CVCL_DB95 | 2026-09-05 10:58:47 | 0 | ||||||||
|
GM20019 Resource Report Resource Website |
RRID:CVCL_8A73 | Homo sapiens (Human) | Farber lipogranulomatosis | Finite cell line | Female | CLO:CLO_0028341, Coriell:GM20019, Wikidata:Q54850783 |
CVCL_8A73 | 2026-09-05 10:58:46 | 0 | |||||||
|
GM19999 Resource Report Resource Website |
RRID:CVCL_F105 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Female | CLO:CLO_0028367, Coriell:GM19999, Wikidata:Q54850769 |
CVCL_F105 | 2026-09-05 10:58:46 | 0 | |||||||
|
GM19982 Resource Report Resource Website |
RRID:CVCL_N879 | Homo sapiens (Human) | Population: African ancestry in Southwest USA (ASW)., Part of: International Genome Sample Resource (1000 genomes project) cell lines. | PMID:21397061 | Transformed cell line | Male | CLO:CLO_0028374, Coriell:GM19982, GEO:GSM650213, GEO:GSM1720348, IGSR:NA19982, Wikidata:Q54850764 |
CVCL_N879 | 2026-09-05 10:58:46 | 0 | ||||||
|
GM1T#17 Resource Report Resource Website |
RRID:CVCL_A3YY | Homo sapiens (Human) | Galloway-Mowat syndrome | Population: Asian. | Induced pluripotent stem cell | Female | SKIP:SKIP005471, Wikidata:Q105506957 |
CVCL_A3YY | 2026-09-05 10:58:46 | 0 | ||||||
|
GM20201 Resource Report Resource Website |
Coriell Cat# GM20201, RRID:CVCL_5R05 | Homo sapiens (Human) | Autism spectrum disorder | PMID:23665875 | Transformed cell line | Female | Coriell | GM20201 | CLO:CLO_0027994, Coriell:GM20201, Wikidata:Q54850842 |
CVCL_5R05 | 2026-09-05 10:58:47 | 0 | ||||
|
GM20101 Resource Report Resource Website |
RRID:CVCL_DA81 | Homo sapiens (Human) | Congenital disorder of glycosylation type Ig | Finite cell line | Male | CLO:CLO_0028338, Coriell:GM20101, Wikidata:Q54850802 |
CVCL_DA81 | 2026-09-05 10:58:46 | 0 | |||||||
|
GM19984 Resource Report Resource Website |
Coriell Cat# GM19984, RRID:CVCL_N880 | Homo sapiens (Human) | Population: African ancestry in Southwest USA (ASW)., Part of: International Genome Sample Resource (1000 genomes project) cell lines. | PMID:21397061 | Transformed cell line | Male | Coriell | GM19984 | Coriell:GM19984, GEO:GSM650215, GEO:GSM1720349, IGSR:NA19984, Wikidata:Q54850766 |
CVCL_N880 | 2026-09-05 10:58:46 | 0 | ||||
|
GM20123 iPSC Resource Report Resource Website |
RRID:CVCL_UD94 | Homo sapiens (Human) | Population: Caucasian; Dutch. | PMID:25488666 | Induced pluripotent stem cell | Female | Control 1 | Wikidata:Q93864425 | cvcl_1l21 | CVCL_UD94 | 2026-09-05 10:58:47 | 0 | ||||
|
GM20015 Resource Report Resource Website |
RRID:CVCL_8A69 | Homo sapiens (Human) | Farber lipogranulomatosis | Population: Tunisian. | PMID:34088014 | Finite cell line | Male | CLO:CLO_0028366, Coriell:GM20015, Wikidata:Q54850778 |
CVCL_8A69 | 2026-09-05 10:58:46 | 0 | |||||
|
GM20087 Resource Report Resource Website |
Coriell Cat# GM20087, RRID:CVCL_5T66 | Homo sapiens (Human) | Lennox-Gastaut syndrome | Population: African American. | PMID:23665875 | Transformed cell line | Female | Coriell | GM20087 | CLO:CLO_0028310, Coriell:GM20087, Wikidata:Q54850794 |
CVCL_5T66 | 2026-09-05 10:58:46 | 0 | |||
|
GM20190 Resource Report Resource Website |
RRID:CVCL_GS93 | Homo sapiens (Human) | Deafness, autosomal recessive 49 | Population: Pakistani. | PMID:17186462 | Transformed cell line | Male | CLO:CLO_0027940, Coriell:GM20190, Wikidata:Q54850832 |
CVCL_GS93 | 2026-09-05 10:58:47 | 0 | |||||
|
GM20087 Resource Report Resource Website |
RRID:CVCL_5T66 | Homo sapiens (Human) | Lennox-Gastaut syndrome | Population: African American. | PMID:23665875 | Transformed cell line | Female | CLO:CLO_0028310, Coriell:GM20087, Wikidata:Q54850794 |
CVCL_5T66 | 2026-09-05 10:58:46 | 0 | |||||
|
GM20129 Resource Report Resource Website |
Coriell Cat# GM20129, RRID:CVCL_1A91 | Homo sapiens (Human) | Population: African ancestry in Southwest USA (ASW)., Part of: International Genome Sample Resource (1000 genomes project) cell lines. | PMID:21397061 | Transformed cell line | Female | Coriell | GM20129 | CLO:CLO_0027703, Coriell:GM20129, GEO:GSM650220, IGSR:NA20129, Wikidata:Q54850813 |
CVCL_1A91 | 2026-09-05 10:58:47 | 0 | ||||
|
GM20000 Resource Report Resource Website |
RRID:CVCL_E127 | Homo sapiens (Human) | Cornelia de Lange syndrome | Part of: ENCODE project common cell types; tier 3. | Transformed cell line | Male | CLO:CLO_0028368, EFO:EFO_0005352, Coriell:GM20000, ENCODE:ENCBS223AAA, GEO:GSM1008587, Wikidata:Q54850776 |
CVCL_E127 | 2026-09-05 10:58:46 | 0 | ||||||
|
GM20173 Resource Report Resource Website |
RRID:CVCL_CZ76 | Homo sapiens (Human) | Population: Pakistani. | PMID:17186462 | Transformed cell line | Male | CLO:CLO_0027933, Coriell:GM20173, Wikidata:Q54850819 |
CVCL_CZ76 | 2026-09-05 10:58:47 | 0 | ||||||
|
GM20089 Resource Report Resource Website |
RRID:CVCL_1L16 | Homo sapiens (Human) | Glycogen storage disease type II | PMID:25488666 | Finite cell line | Female | CLO:CLO_0028329, BioSample:SAMN00805674, Coriell:GM20089, Wikidata:Q54850796 |
CVCL_1L16 | 2026-09-05 10:58:46 | 0 | ||||||
|
GM20129 Resource Report Resource Website |
RRID:CVCL_1A91 | Homo sapiens (Human) | Population: African ancestry in Southwest USA (ASW)., Part of: International Genome Sample Resource (1000 genomes project) cell lines. | PMID:21397061 | Transformed cell line | Female | CLO:CLO_0027703, Coriell:GM20129, GEO:GSM650220, IGSR:NA20129, Wikidata:Q54850813 |
CVCL_1A91 | 2026-09-05 10:58:47 | 0 | ||||||
|
GM20022 Resource Report Resource Website |
RRID:CVCL_5R01 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Male | CLO:CLO_0028340, Coriell:GM20022, Wikidata:Q54850784 |
CVCL_5R01 | 2026-09-05 10:58:46 | 0 | |||||||
|
GM20126 Resource Report Resource Website |
RRID:CVCL_N882 | Homo sapiens (Human) | Population: African ancestry in Southwest USA (ASW)., Part of: International Genome Sample Resource (1000 genomes project) cell lines. | PMID:21397061 | Transformed cell line | Male | CLO:CLO_0027708, BioSample:SAMN00007827, Coriell:GM20126, GEO:GSM650217, GEO:GSM1720351, IGSR:NA20126, Wikidata:Q54850809 |
CVCL_N882 | 2026-09-05 10:58:47 | 0 |
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