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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM03896 Resource Report Resource Website |
Coriell Cat# GM03896, RRID:CVCL_9Z41 | Homo sapiens (Human) | Refsum disease | Population: Caucasian. | Finite cell line | Male | GM3896, GM03896A | Coriell | GM03896 | CLO:CLO_0015985, Coriell:GM03896, Wikidata:Q54838308 |
CVCL_9Z41 | 2026-07-25 04:32:53 | 0 | |||
|
GM03837 Resource Report Resource Website |
RRID:CVCL_AK88 | Homo sapiens (Human) | Retinitis pigmentosa | Population: Caucasian. | Finite cell line | Female | CLO:CLO_0015639, BioSample:SAMN00808561, Coriell:GM03837, Wikidata:Q54838265 |
CVCL_AK88 | 2026-07-25 04:32:52 | 0 | ||||||
|
GM03886 Resource Report Resource Website |
Coriell Cat# GM03886, RRID:CVCL_2S98 | Homo sapiens (Human) | Karyotypic information: 46,XX,t(4;9)(4pter->4q33::9q12->9qter;9pter->9q12::4q33->4qter) (Coriell=GM03886)., Population: Caucasian. | Finite cell line | Female | Coriell | GM03886 | CLO:CLO_0016012, BioSample:SAMN00808592, Coriell:GM03886, Wikidata:Q54838300 |
CVCL_2S98 | 2026-07-25 04:32:53 | 0 | |||||
|
GM03913 Resource Report Resource Website |
Coriell Cat# GM03913, RRID:CVCL_1K35 | Homo sapiens (Human) | Roberts-SC phocomelia syndrome | Karyotypic information: 46,XY [46%]; 47,XY,+7 [54%] (Coriell=GM03913)., Population: Caucasian; French Canadian. | PMID:10655550 | Finite cell line | Male | GM03913A | Coriell | GM03913 | CLO:CLO_0016129, Coriell:GM03913, Wikidata:Q54838320 |
CVCL_1K35 | 2026-07-25 04:32:53 | 0 | ||
|
GM03878 Resource Report Resource Website |
RRID:CVCL_EF95 | Homo sapiens (Human) | Glutathione synthetase deficiency | Population: Caucasian. | PMID:8896573 | Finite cell line | Male | GM 3878, GM03878A | CLO:CLO_0016038, BioSample:SAMN00808588, Coriell:GM03878, Wikidata:Q54838295 |
CVCL_EF95 | 2026-07-25 04:32:52 | 0 | ||||
|
GM03897 Resource Report Resource Website |
Coriell Cat# GM03897, RRID:CVCL_9Z42 | Homo sapiens (Human) | Refsum disease | Population: Caucasian. | Transformed cell line | Male | Coriell | GM03897 | CLO:CLO_0015986, Coriell:GM03897, Wikidata:Q54838309 |
CVCL_9Z42 | 2026-07-25 04:32:53 | 0 | ||||
|
GM03892 Resource Report Resource Website |
RRID:CVCL_W306 | Homo sapiens (Human) | Usher syndrome type 1 | Population: Caucasian. | PMID:6726265 | Transformed cell line | Male | GM 3892, GM03892A | CLO:CLO_0016022, BioSample:SAMN00808597, Coriell:GM03892, Wikidata:Q54838305 |
CVCL_W306 | 2026-07-25 04:32:53 | 0 | ||||
|
GM03838 Resource Report Resource Website |
Coriell Cat# GM03838, RRID:CVCL_AK89 | Homo sapiens (Human) | Retinitis pigmentosa | Population: Caucasian. | Transformed cell line | Female | Coriell | GM03838 | CLO:CLO_0015636, BioSample:SAMN00808562, Coriell:GM03838, Wikidata:Q54838266 |
CVCL_AK89 | 2026-07-25 04:32:52 | 0 | ||||
|
GM03858 Resource Report Resource Website |
RRID:CVCL_DD76 | Homo sapiens (Human) | Hereditary optic atrophy | Population: Jewish. | Finite cell line | Male | CLO:CLO_0015727, BioSample:SAMN00808570, Coriell:GM03858, Wikidata:Q54838274 |
CVCL_DD76 | 2026-07-25 04:32:52 | 0 | ||||||
|
GM03861 Resource Report Resource Website |
RRID:CVCL_1H66 | Homo sapiens (Human) | Population: Caucasian. | Transformed cell line | Female | CLO:CLO_0015730, BioSample:SAMN00808573, Coriell:GM03861, Wikidata:Q54838280 |
CVCL_1H66 | 2026-07-25 04:32:52 | 0 | |||||||
|
GM03911 Resource Report Resource Website |
Coriell Cat# GM03911, RRID:CVCL_AK95 | Homo sapiens (Human) | Retinitis pigmentosa | Population: Caucasian. | PMID:6726265 | Transformed cell line | Female | GM 3911, GM03911A | Coriell | GM03911 | CLO:CLO_0016123, Coriell:GM03911, Wikidata:Q54838318 |
CVCL_AK95 | 2026-07-25 04:32:53 | 0 | ||
|
GM03887 Resource Report Resource Website |
RRID:CVCL_X113 | Homo sapiens (Human) |
PMID:6617268 PMID:6661932 PMID:23665875 |
Transformed cell line | Female | GM 3887 | CLO:CLO_0016009, BioSample:SAMN00808593, Coriell:GM03887, Wikidata:Q54838301 |
CVCL_X113 | 2026-07-25 04:32:53 | 0 | ||||||
|
GM03912 Resource Report Resource Website |
Coriell Cat# GM03912, RRID:CVCL_X114 | Homo sapiens (Human) | Cri du chat syndrome |
PMID:6617268 PMID:6661932 PMID:23665875 |
Finite cell line | Male | GM 3912 | Coriell | GM03912 | CLO:CLO_0016130, Coriell:GM03912, Wikidata:Q54838319 |
CVCL_X114 | 2026-07-25 04:32:53 | 0 | |||
|
GM03867 Resource Report Resource Website |
Coriell Cat# GM03867, RRID:CVCL_1H72 | Homo sapiens (Human) | Huntington's disease | Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease., Population: Caucasian. | Transformed cell line | Female | Coriell | GM03867 | CLO:CLO_0015709, BioSample:SAMN00808579, Coriell:GM03867, Wikidata:Q54838286 |
CVCL_1H72 | 2026-07-25 04:32:52 | 0 | ||||
|
GM03838 Resource Report Resource Website |
RRID:CVCL_AK89 | Homo sapiens (Human) | Retinitis pigmentosa | Population: Caucasian. | Transformed cell line | Female | CLO:CLO_0015636, BioSample:SAMN00808562, Coriell:GM03838, Wikidata:Q54838266 |
CVCL_AK89 | 2026-07-25 04:32:52 | 0 | ||||||
|
GM03871 Resource Report Resource Website |
Coriell Cat# GM03871, RRID:CVCL_1H76 | Homo sapiens (Human) | Population: Caucasian. | Transformed cell line | Female | Coriell | GM03871 | CLO:CLO_0016030, BioSample:SAMN00808583, Coriell:GM03871, Wikidata:Q54838290 |
CVCL_1H76 | 2026-07-25 04:32:52 | 0 | |||||
|
GM03864 Resource Report Resource Website |
RRID:CVCL_1H69 | Homo sapiens (Human) | Huntington's disease | Population: Caucasian. | Finite cell line | Female | GM03864A | CLO:CLO_0015735, BioSample:SAMN00808576, Coriell:GM03864, Wikidata:Q54838283 |
CVCL_1H69 | 2026-07-25 04:32:52 | 0 | |||||
|
GM03893 Resource Report Resource Website |
Coriell Cat# GM03893, RRID:CVCL_AK90 | Homo sapiens (Human) | Retinitis pigmentosa | Population: Caucasian. | Finite cell line | Male | Coriell | GM03893 | CLO:CLO_0016023, BioSample:SAMN00808598, Coriell:GM03893, Wikidata:Q54838306 |
CVCL_AK90 | 2026-07-25 04:32:53 | 0 | ||||
|
GM03891 Resource Report Resource Website |
RRID:CVCL_W305 | Homo sapiens (Human) | Usher syndrome type 1 | Population: Caucasian. | PMID:6726265 | Finite cell line | Male | GM 3891 | CLO:CLO_0016008, BioSample:SAMN00808596, Coriell:GM03891, Wikidata:Q54838304 |
CVCL_W305 | 2026-07-25 04:32:53 | 0 | ||||
|
GM03857 Resource Report Resource Website |
RRID:CVCL_DD75 | Homo sapiens (Human) | Hereditary optic atrophy | Population: Jewish. | Transformed cell line | Male | GM3857, GM03857A | CLO:CLO_0015618, BioSample:SAMN00808569, Coriell:GM03857, Wikidata:Q54838273 |
CVCL_DD75 | 2026-07-25 04:32:52 | 0 |
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