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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM01017 Resource Report Resource Website |
RRID:CVCL_6B41 | Homo sapiens (Human) | Metachromatic leukodystrophy | Transformed cell line | Female | GM-1017 | CLO:CLO_0029493, BioSample:SAMN00803561, Coriell:GM01017, Wikidata:Q54836603 |
CVCL_6B41 | 2026-08-15 04:28:55 | 0 | ||||||
|
GM00995 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM00995, RRID:CVCL_CX41 | Homo sapiens (Human) | Finite cell line | Male | GM-995 | Coriell | GM00995 | Coriell:GM00995, Wikidata:Q54836587 |
CVCL_CX41 | 2026-08-15 04:28:55 | 0 | |||||
|
GM00995 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_CX41 | Homo sapiens (Human) | Finite cell line | Male | GM-995 | Coriell:GM00995, Wikidata:Q54836587 |
CVCL_CX41 | 2026-08-15 04:28:55 | 0 | |||||||
|
GM01087 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_JD76 | Homo sapiens (Human) | Finite cell line | Female | GM-1087 | Coriell:GM01087, Wikidata:Q54836638 |
CVCL_JD76 | 2026-08-15 04:28:56 | 0 | |||||||
|
GM01031 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_0R30 | Homo sapiens (Human) | PMID:19815695 | Transformed cell line | Male | GM-1031 | CLO:CLO_0030375, BioSample:SAMN00803583, Coriell:GM01031, Wikidata:Q54836615 |
CVCL_0R30 | 2026-08-15 04:28:56 | 0 | ||||||
|
GM01059 Resource Report Resource Website |
RRID:CVCL_X079 | Homo sapiens (Human) | Population: Caucasian. |
PMID:6617268 PMID:6661932 PMID:23665875 |
Finite cell line | Female | GM-1059, GM 1059, GM01059A | CLO:CLO_0030365, BioSample:SAMN00803600, Coriell:GM01059, Wikidata:Q54836626 |
CVCL_X079 | 2026-08-15 04:28:56 | 0 | |||||
|
GM01028 Resource Report Resource Website |
RRID:CVCL_V431 | Homo sapiens (Human) | Galactosemia | Population: Caucasian. | Transformed cell line | Female | GM-1028, GM01028A | CLO:CLO_0030378, BioSample:SAMN00803577, Coriell:GM01028, Wikidata:Q54836612 |
CVCL_V431 | 2026-08-15 04:28:56 | 0 | |||||
|
GM01012 Resource Report Resource Website |
RRID:CVCL_L744 | Homo sapiens (Human) | Cystic fibrosis | Population: Caucasian. | PMID:20715179 | Finite cell line | Male | GM-1012, GM1012A | CLO:CLO_0029469, BioSample:SAMN00803553, Coriell:GM01012, Wikidata:Q54836599 |
CVCL_L744 | 2026-08-15 04:28:55 | 0 | ||||
|
GM01057 Resource Report Resource Website 1+ mentions |
Coriell Cat# GM01057, RRID:CVCL_H964 | Homo sapiens (Human) | Menkes disease | Population: Caucasian. | PMID:7438975 | Finite cell line | Male | GM-1057 | Coriell | GM01057 | CLO:CLO_0030350, BioSample:SAMN00803596, Coriell:GM01057, Wikidata:Q54836624 |
CVCL_H964 | 2026-08-15 04:28:56 | 1 | ||
|
GM00999 Resource Report Resource Website |
RRID:CVCL_V208 | Homo sapiens (Human) | Cystic fibrosis | Population: Caucasian. | Finite cell line | Female | GM-999, GM00999A | CLO:CLO_0029471, Coriell:GM00999, Wikidata:Q54836594 |
CVCL_V208 | 2026-08-15 04:28:55 | 0 | |||||
|
GM01063 Resource Report Resource Website |
Coriell Cat# GM01063, RRID:CVCL_H139 | Homo sapiens (Human) | Population: African American. |
PMID:62390 PMID:23665875 |
Transformed cell line | Female | GM-1063, GM01063B | Coriell | GM01063 | CLO:CLO_0030367, BioSample:SAMN00803604, Coriell:GM01063, Wikidata:Q54836628 |
CVCL_H139 | 2026-08-15 04:28:56 | 0 | |||
|
GM01122 Resource Report Resource Website |
RRID:CVCL_H970 | Homo sapiens (Human) | Hepatocyte nuclear factor 4-alpha associated monogenic diabetes | Population: Caucasian., Part of: R-W pedigree MODY cell line collection. |
PMID:8945471 PMID:29990710 |
Finite cell line | Female | GM-1122 | CLO:CLO_0030172, Coriell:GM01122, Wikidata:Q54836652 |
CVCL_H970 | 2026-08-15 04:28:56 | 0 | ||||
|
GM01056 Resource Report Resource Website |
Coriell Cat# GM01056, RRID:CVCL_D344 | Homo sapiens (Human) | Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. |
PMID:3495441 PMID:14583597 PMID:16260726 PMID:20889555 PMID:29959025 |
Transformed cell line | Male | GM-1056, GM1056, GM01056A, GM1056-A, GM01056B, GM17211 | Coriell | GM01056 | CLO:CLO_0013890, CLO:CLO_0030349, BioSample:SAMN00803594, Coriell:GM01056, Coriell:GM17211, GEO:GSM569520, GEO:GSM596275, GEO:GSM596636, GEO:GSM924813, Wikidata:Q54836623 |
CVCL_D344 | 2026-08-15 04:28:56 | 0 | |||
|
GM01041 Resource Report Resource Website |
RRID:CVCL_4J19 | Homo sapiens (Human) | Porphyria cutanea tarda | Population: Caucasian. | Finite cell line | Female | GM-1041 | CLO:CLO_0030372, BioSample:SAMN00803588, Coriell:GM01041, Wikidata:Q54836618 |
CVCL_4J19 | 2026-08-15 04:28:56 | 0 | |||||
|
GM01058 Resource Report Resource Website |
RRID:CVCL_H141 | Homo sapiens (Human) | Population: Caucasian. | Finite cell line | Male | GM1058, GM-1058 | CLO:CLO_0030366, BioSample:SAMN00803598, Coriell:GM01058, Wikidata:Q54836625 |
CVCL_H141 | 2026-08-15 04:28:56 | 0 | ||||||
|
GM01018 Resource Report Resource Website |
RRID:CVCL_M980 | Homo sapiens (Human) | Metachromatic leukodystrophy | Population: Puerto Rican., Part of: Human variation panel. | PMID:7313555 | Transformed cell line | Female | GM-1018, GM 1018, GM01018A, GM17072 | CLO:CLO_0014601, CLO:CLO_0029492, BioSample:SAMN00803563, Coriell:GM01018, Coriell:GM17072, Wikidata:Q54836604 |
CVCL_M980 | 2026-08-15 04:28:55 | 0 | ||||
|
GM01118 Resource Report Resource Website |
Coriell Cat# GM01118, RRID:CVCL_4D80 | Homo sapiens (Human) | Supernumerary circular chromosome | Karyotypic information: 46,XX,r(18) [39]; 45,XX,-18 [11] (Coriell=GM01118)., Population: Mexican. | Finite cell line | Female | GM-1118 | Coriell | GM01118 | CLO:CLO_0030174, BioSample:SAMN00803638, Coriell:GM01118, Wikidata:Q54836651 |
CVCL_4D80 | 2026-08-15 04:28:56 | 0 | |||
|
GM01053 Resource Report Resource Website |
Coriell Cat# GM01053, RRID:CVCL_V531 | Homo sapiens (Human) | Hurler syndrome | Population: Caucasian. | Finite cell line | Male | GM-1053, GM01053A | Coriell | GM01053 | CLO:CLO_0030370, BioSample:SAMN00803592, Coriell:GM01053, Wikidata:Q54836622 |
CVCL_V531 | 2026-08-15 04:28:56 | 0 | |||
|
GM00989 Resource Report Resource Website |
RRID:CVCL_CV39 | Homo sapiens (Human) | Progeria | PMID:7253718 | Finite cell line | Male | GM-989, GM00989B, AG00989, AG-989, AG00989B, AG0989B | CLO:CLO_0029474, CLO:CLO_0036917, Coriell:AG00989, Coriell:GM00989, Wikidata:Q54836584 |
CVCL_CV39 | 2026-08-15 04:28:55 | 0 | |||||
|
GM01059 Resource Report Resource Website |
Coriell Cat# GM01059, RRID:CVCL_X079 | Homo sapiens (Human) | Population: Caucasian. |
PMID:6617268 PMID:6661932 PMID:23665875 |
Finite cell line | Female | GM-1059, GM 1059, GM01059A | Coriell | GM01059 | CLO:CLO_0030365, BioSample:SAMN00803600, Coriell:GM01059, Wikidata:Q54836626 |
CVCL_X079 | 2026-08-15 04:28:56 | 0 |
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