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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM06812 Resource Report Resource Website |
Coriell Cat# GM06812, RRID:CVCL_8A85 | Homo sapiens (Human) | Ectopia lentis | Population: Caucasian. | Finite cell line | Female | Coriell | GM06812 | CLO:CLO_0036531, Coriell:GM06812, Wikidata:Q54842342 |
CVCL_8A85 | 2026-07-25 04:33:30 | 0 | ||||
|
GM06902 Resource Report Resource Website 1+ mentions |
RRID:CVCL_Y703 | Homo sapiens (Human) | Ornithine carbamoyltransferase deficiency disease | Population: Caucasian. | Finite cell line | Male | GM6902 | CLO:CLO_0036484, Coriell:GM06902, Wikidata:Q54842378 |
CVCL_Y703 | 2026-07-25 04:33:31 | 1 | |||||
|
GM06836 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM06836, RRID:CVCL_UR72 | Homo sapiens (Human) | Isovaleric acidemia | Finite cell line | Female | GM6836 | Coriell | GM06836 | Coriell:GM06836, Wikidata:Q93792463 |
CVCL_UR72 | 2026-07-25 04:33:31 | 0 | ||||
|
GM06870 Resource Report Resource Website |
RRID:CVCL_5N47 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Female | CLO:CLO_0036508, Coriell:GM06870, Wikidata:Q54842357 |
CVCL_5N47 | 2026-07-25 04:33:31 | 0 | |||||||
|
GM06809 Resource Report Resource Website |
RRID:CVCL_2Z58 | Homo sapiens (Human) | Population: Caucasian. | Transformed cell line | Female | CLO:CLO_0036535, Coriell:GM06809, Wikidata:Q54842340 |
CVCL_2Z58 | 2026-07-25 04:33:30 | 0 | |||||||
|
GM06862 Resource Report Resource Website |
RRID:CVCL_7459 | Homo sapiens (Human) | Population: Caucasian., Part of: Human variation panel. | Transformed cell line | Female | GM17266 | CLO:CLO_0013181, CLO:CLO_0036511, Coriell:GM06862, Coriell:GM17266, GEO:GSM569724, GEO:GSM596330, GEO:GSM596752, GEO:GSM924868, Wikidata:Q54842352 |
CVCL_7459 | 2026-07-25 04:33:31 | 0 | ||||||
|
GM06862 Resource Report Resource Website |
Coriell Cat# GM06862, RRID:CVCL_7459 | Homo sapiens (Human) | Population: Caucasian., Part of: Human variation panel. | Transformed cell line | Female | GM17266 | Coriell | GM06862 | CLO:CLO_0013181, CLO:CLO_0036511, Coriell:GM06862, Coriell:GM17266, GEO:GSM569724, GEO:GSM596330, GEO:GSM596752, GEO:GSM924868, Wikidata:Q54842352 |
CVCL_7459 | 2026-07-25 04:33:30 | 0 | ||||
|
GM06855 Resource Report Resource Website |
RRID:CVCL_F297 | Homo sapiens (Human) | Familial adenomatous polyposis | PMID:3374507 | Finite cell line | Male | GM6855 | CLO:CLO_0036519, Coriell:GM06855, Wikidata:Q54842348 |
CVCL_F297 | 2026-07-25 04:33:30 | 0 | |||||
|
GM06830 Resource Report Resource Website |
RRID:CVCL_FA33 | Homo sapiens (Human) | Aniridia | Transformed cell line | Male | CLO:CLO_0036516, Coriell:GM06830, Wikidata:Q54842344 |
CVCL_FA33 | 2026-07-25 04:33:30 | 0 | |||||||
|
GM06876 Resource Report Resource Website |
Coriell Cat# GM06876, RRID:CVCL_GQ67 | Homo sapiens (Human) | Bipolar disorder | Transformed cell line | Female | Coriell | GM06876 | CLO:CLO_0036493, Coriell:GM06876, Wikidata:Q54842361 |
CVCL_GQ67 | 2026-07-25 04:33:32 | 0 | |||||
|
GM06865 Resource Report Resource Website |
Coriell Cat# GM17104, RRID:CVCL_N056 | Homo sapiens (Human) | Population: African American., Part of: Human variation panel. |
PMID:16260726 PMID:33426406 |
Transformed cell line | Male | GM17104 | Coriell | GM17104 | CLO:CLO_0014900, CLO:CLO_0036514, Coriell:GM06865, Coriell:GM17104, GEO:GSM273374, GEO:GSM569501, GEO:GSM596172, GEO:GSM596973, GEO:GSM924614, Wikidata:Q54842355 |
CVCL_N056 | 2026-07-25 04:33:31 | 0 | |||
|
GM06906 Resource Report Resource Website |
RRID:CVCL_AX97 | Homo sapiens (Human) | Population: Caucasian. |
PMID:1672039 PMID:18165276 PMID:25776194 |
Transformed cell line | Male | GM6906, GM06906A | CLO:CLO_0036480, Coriell:GM06906, Wikidata:Q54842382 |
CVCL_AX97 | 2026-07-25 04:33:31 | 0 | |||||
|
GM06813 Resource Report Resource Website |
RRID:CVCL_AD70 | Homo sapiens (Human) | X-linked centronuclear myopathy | Population: Caucasian. | PMID:9305655 | Finite cell line | Male | GM-06813 | CLO:CLO_0036532, Coriell:GM06813, Wikidata:Q54842343 |
CVCL_AD70 | 2026-07-25 04:33:31 | 0 | ||||
|
GM06896 Resource Report Resource Website |
RRID:CVCL_AX93 | Homo sapiens (Human) | PMID:25776194 | Transformed cell line | Female | GM06896A | CLO:CLO_0036482, Coriell:GM06896, Wikidata:Q54842376 |
CVCL_AX93 | 2026-07-25 04:33:32 | 0 | ||||||
|
GM06937 Resource Report Resource Website |
RRID:CVCL_5N51 | Homo sapiens (Human) | Karyotypic information: 46,XX,del(10)(p13->qter) (Coriell=GM06937)., Population: Caucasian. | Finite cell line | Female | CLO:CLO_0036456, Coriell:GM06937, Wikidata:Q54842398 |
CVCL_5N51 | 2026-07-25 04:33:32 | 0 | |||||||
|
GM06935 Resource Report Resource Website |
RRID:CVCL_F594 | Homo sapiens (Human) | Fanconi anemia | Population: Arab. | Transformed cell line | Female | GM06935A | CLO:CLO_0036464, Coriell:GM06935, Wikidata:Q54842396 |
cvcl_f593 | CVCL_F594 | 2026-07-25 04:33:32 | 0 | ||||
|
GM06876 Resource Report Resource Website |
RRID:CVCL_GQ67 | Homo sapiens (Human) | Bipolar disorder | Transformed cell line | Female | CLO:CLO_0036493, Coriell:GM06876, Wikidata:Q54842361 |
CVCL_GQ67 | 2026-07-25 04:33:31 | 0 | |||||||
|
GM06871 Resource Report Resource Website |
RRID:CVCL_5N48 | Homo sapiens (Human) | Karyotypic information: 47,XX,+i(18)(pter->p10::p10->pter) (Coriell=GM06871). | Finite cell line | Female | CLO:CLO_0036505, Coriell:GM06871, Wikidata:Q54842358 |
CVCL_5N48 | 2026-07-25 04:33:31 | 0 | |||||||
|
GM06804 Resource Report Resource Website |
RRID:CVCL_F609 | Homo sapiens (Human) | Lesch-Nyhan syndrome | Population: Caucasian. | Transformed cell line | Male | GM6804, GM 6804, GM06804A, GM06804B | CLO:CLO_0036539, Coriell:GM06804, Wikidata:Q54842335 |
CVCL_F609 | 2026-07-25 04:33:31 | 0 | |||||
|
GM06852 Resource Report Resource Website |
RRID:CVCL_AX86 | Homo sapiens (Human) | Fragile X syndrome | Population: Caucasian. |
PMID:1672039 PMID:25776194 |
Transformed cell line | Male | GM6852, GM06852A | CLO:CLO_0036518, Coriell:GM06852, Wikidata:Q54842346 |
CVCL_AX86 | 2026-07-25 04:33:30 | 0 |
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