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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM00801 Resource Report Resource Website |
RRID:CVCL_1B69 | Homo sapiens (Human) | Fucosidosis | PMID:4074382 | Finite cell line | Male | GM-801, GM 801, GM801 | CLO:CLO_0028848, Coriell:GM00801, Wikidata:Q54836460 |
CVCL_1B69 | 2026-08-15 04:28:52 | 0 | |||||
|
GM00740 Resource Report Resource Website |
Coriell Cat# GM00740, RRID:CVCL_9W77 | Homo sapiens (Human) | Rhizomelic chondrodysplasia punctata | Population: Caucasian. | Finite cell line | Female | GM-740 | Coriell | GM00740 | CLO:CLO_0028820, Coriell:GM00740, Wikidata:Q54836434 |
CVCL_9W77 | 2026-08-15 04:28:52 | 0 | |||
|
GM00731 Resource Report Resource Website |
RRID:CVCL_7301 | Homo sapiens (Human) | Population: Caucasian. |
PMID:3860870 PMID:15450399 |
Finite cell line | Male | GM0731, GM 0731, GM-731, GM 731, GM00731A, GM0731A, GM 0731A | CLO:CLO_0028816, Coriell:GM00731, Wikidata:Q54836423 |
CVCL_7301 | 2026-08-15 04:28:52 | 0 | |||||
|
GM00737 Resource Report Resource Website |
RRID:CVCL_0L94 | Homo sapiens (Human) | Mucopolysaccharidosis type IIIB | Population: Caucasian. | Finite cell line | Male | GM-737 | CLO:CLO_0028814, Coriell:GM00737, Wikidata:Q54836431 |
CVCL_0L94 | 2026-08-15 04:28:52 | 0 | |||||
|
GM00705 Resource Report Resource Website |
RRID:CVCL_0P86 | Homo sapiens (Human) | Karyotypic information: 46,X,t(X;9)(q13.1;p24) (PubMed=10377420)., Population: Caucasian. |
PMID:113895 PMID:559490 PMID:1056018 PMID:2338345 PMID:8268921 PMID:10377420 PMID:23665875 |
Finite cell line | Female | GM-705, GM0705, GM00705A, GM0705A, GMO 705, AnLy | CLO:CLO_0028893, Coriell:GM00705, Wikidata:Q54836399 |
CVCL_0P86 | 2026-08-15 04:28:51 | 0 | |||||
|
GM00726 Resource Report Resource Website |
RRID:CVCL_M979 | Homo sapiens (Human) | Population: Korean., Part of: Human variation panel. |
PMID:3863481 PMID:7301938 PMID:19896956 PMID:30567591 |
Finite cell line | Female | GM0726, GM-726, GM726, GM00726A, GM0726A, GM17081 | CLO:CLO_0014483, CLO:CLO_0028791, Coriell:GM00726, Coriell:GM17081, GEO:GSM3124683, Wikidata:Q54836419 |
CVCL_M979 | 2026-08-15 04:28:52 | 0 | |||||
|
GM00718 Resource Report Resource Website |
RRID:CVCL_H135 | Homo sapiens (Human) | Ataxia telangiectasia syndrome | PMID:761484 | Transformed cell line | Male | GM-718, GM00718A | CLO:CLO_0028798, Coriell:GM00718, Wikidata:Q54836412 |
CVCL_H135 | 2026-08-15 04:28:51 | 0 | |||||
|
GM00690 Resource Report Resource Website |
Coriell Cat# GM00690, RRID:CVCL_W657 | Homo sapiens (Human) | Hunter syndrome | Population: Caucasian. | Finite cell line | Male | GM-690 | Coriell | GM00690 | CLO:CLO_0028910, Coriell:GM00690, Wikidata:Q54836390 |
CVCL_W657 | 2026-08-15 04:28:51 | 0 | |||
|
GM00734 Resource Report Resource Website 1+ mentions |
RRID:CVCL_X236 | Homo sapiens (Human) | Trisomy 18 | Karyotypic information: 47,XX,+18 (Coriell=GM00734). | PMID:6661932 | Finite cell line | Female | GM-734, GM 734 | CLO:CLO_0028817, Coriell:GM00734, Wikidata:Q54836427 |
CVCL_X236 | 2026-08-15 04:28:52 | 1 | ||||
|
GM00724 Resource Report Resource Website |
Coriell Cat# GM00724, RRID:CVCL_2H00 | Homo sapiens (Human) | Homocystinuria | Population: Caucasian. | Finite cell line | Male | GM0724, GM-724 | Coriell | GM00724 | CLO:CLO_0028793, Coriell:GM00724, Wikidata:Q54836417 |
CVCL_2H00 | 2026-08-15 04:28:52 | 0 | |||
|
GM00799 Resource Report Resource Website |
RRID:CVCL_1V09 | Homo sapiens (Human) | Population: Caucasian. | Finite cell line | Female | GM-799 | CLO:CLO_0028846, Coriell:GM00799, Wikidata:Q54836458 |
CVCL_1V09 | 2026-08-15 04:28:52 | 0 | ||||||
|
GM00694 Resource Report Resource Website |
RRID:CVCL_DN45 | Homo sapiens (Human) | Hypercholesterolemia, familial, 4 | Population: Lebanese. | Finite cell line | Female | GM-694 | CLO:CLO_0028914, Coriell:GM00694, Wikidata:Q54836393 |
CVCL_DN45 | 2026-08-15 04:28:51 | 0 | |||||
|
GM00705 Resource Report Resource Website |
Coriell Cat# GM00705, RRID:CVCL_0P86 | Homo sapiens (Human) | Karyotypic information: 46,X,t(X;9)(q13.1;p24) (PubMed=10377420)., Population: Caucasian. |
PMID:113895 PMID:559490 PMID:1056018 PMID:2338345 PMID:8268921 PMID:10377420 PMID:23665875 |
Finite cell line | Female | GM-705, GM0705, GM00705A, GM0705A, GMO 705, AnLy | Coriell | GM00705 | CLO:CLO_0028893, Coriell:GM00705, Wikidata:Q54836399 |
CVCL_0P86 | 2026-08-15 04:28:51 | 0 | |||
|
GM00719 Resource Report Resource Website |
Coriell Cat# GM00719, RRID:CVCL_7300 | Homo sapiens (Human) | Ataxia telangiectasia syndrome |
PMID:761484 PMID:2805228 PMID:16166284 |
Transformed cell line | Female | GM-719, GM719, GM00719A | Coriell | GM00719 | CLO:CLO_0028797, EFO:EFO_0004922, Coriell:GM00719, Wikidata:Q54836413 |
CVCL_7300 | 2026-08-15 04:28:51 | 0 | |||
|
GM00760 Resource Report Resource Website |
RRID:CVCL_W236 | Homo sapiens (Human) | Nephropathic cystinosis | Population: Caucasian. |
PMID:9792862 PMID:28649545 |
Finite cell line | Male | GM0760, GM-760, GM 760, GM760 | CLO:CLO_0028827, Coriell:GM00760, Wikidata:Q54836447 |
CVCL_W236 | 2026-08-15 04:28:52 | 0 | ||||
|
GM00768 Resource Report Resource Website |
RRID:CVCL_H138 | Homo sapiens (Human) | Cystic fibrosis | Population: Caucasian. | Finite cell line | Male | GM-768 | CLO:CLO_0028826, Coriell:GM00768, Wikidata:Q54836448 |
CVCL_H138 | 2026-08-15 04:28:52 | 0 | |||||
|
GM00695 Resource Report Resource Website |
RRID:CVCL_CX57 | Homo sapiens (Human) | Population: Lebanese. | Finite cell line | Male | GM-695, GM00695A | CLO:CLO_0028937, Coriell:GM00695, Wikidata:Q54836394 |
CVCL_CX57 | 2026-08-15 04:28:51 | 0 | ||||||
|
GM00744 Resource Report Resource Website |
RRID:CVCL_DD65 | Homo sapiens (Human) | Osteogenesis imperfecta | Population: Caucasian. | PMID:6689020 | Finite cell line | Female | GM-744, IMR-744 | CLO:CLO_0028825, Coriell:GM00744, Wikidata:Q54836437 |
CVCL_DD65 | 2026-08-15 04:28:52 | 0 | ||||
|
GM00692 Resource Report Resource Website |
Coriell Cat# GM00692, RRID:CVCL_X235 | Homo sapiens (Human) | Intellectual developmental disorder | Population: Caucasian. |
PMID:6661932 PMID:23665875 |
Finite cell line | Male | GM-692, GM-0692, GM 692 | Coriell | GM00692 | CLO:CLO_0028912, Coriell:GM00692, Wikidata:Q54836391 |
CVCL_X235 | 2026-08-15 04:28:51 | 0 | ||
|
GM00693 Resource Report Resource Website |
RRID:CVCL_V461 | Homo sapiens (Human) | Karyotypic information: 46,XX,t(2;21)(2pter->2q37::21q21->21qter;21pter->21q21::2q37->2qter) (Coriell=GM00693)., Population: Caucasian. | Finite cell line | Female | GM-693 | CLO:CLO_0028913, Coriell:GM00693, Wikidata:Q54836392 |
CVCL_V461 | 2026-08-15 04:28:51 | 0 |
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