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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM13262 Resource Report Resource Website |
RRID:CVCL_BW64 | Homo sapiens (Human) | D-bifunctional protein deficiency | Population: Caucasian. | Finite cell line | Female | CLO:CLO_0013116, BioSample:SAMN00802222, Coriell:GM13262, Wikidata:Q54846404 |
CVCL_BW64 | 2026-08-01 05:07:03 | 0 | ||||||
|
GM13269 Resource Report Resource Website |
RRID:CVCL_4F68 | Homo sapiens (Human) | Zellweger syndrome | Population: Caucasian. | Finite cell line | Male | CLO:CLO_0013105, BioSample:SAMN00802236, Coriell:GM13269, Wikidata:Q54846411 |
CVCL_4F68 | 2026-08-01 05:07:03 | 0 | ||||||
|
GM13305 Resource Report Resource Website |
Coriell Cat# GM13305, RRID:CVCL_1K71 | Homo sapiens (Human) | Transformed cell line | Female | Coriell | GM13305 | BioSample:SAMN00802277, Coriell:GM13305, Wikidata:Q54846445 |
CVCL_1K71 | 2026-08-01 05:07:02 | 0 | ||||||
|
GM13269 Resource Report Resource Website |
Coriell Cat# GM13269, RRID:CVCL_4F68 | Homo sapiens (Human) | Zellweger syndrome | Population: Caucasian. | Finite cell line | Male | Coriell | GM13269 | CLO:CLO_0013105, BioSample:SAMN00802236, Coriell:GM13269, Wikidata:Q54846411 |
CVCL_4F68 | 2026-08-01 05:07:01 | 0 | ||||
|
GM13252 Resource Report Resource Website |
RRID:CVCL_V141 | Homo sapiens (Human) | Von Hippel-Lindau syndrome | PMID:8493574 | Transformed cell line | Male | CLO:CLO_0013084, BioSample:SAMN00802212, Coriell:GM13252, Wikidata:Q54846398 |
CVCL_V141 | 2026-08-01 05:07:03 | 0 | ||||||
|
GM13251 Resource Report Resource Website |
Coriell Cat# GM13251, RRID:CVCL_V140 | Homo sapiens (Human) | Von Hippel-Lindau syndrome | Transformed cell line | Male | Coriell | GM13251 | CLO:CLO_0013085, Coriell:GM13251, Wikidata:Q54846397 |
CVCL_V140 | 2026-08-01 05:07:06 | 0 | |||||
|
GM13280 Resource Report Resource Website |
Coriell Cat# GM13280, RRID:CVCL_GT65 | Homo sapiens (Human) | Hereditary hemorrhagic telangiectasia | Population: Caucasian. | Finite cell line | Male | Coriell | GM13280 | CLO:CLO_0013282, BioSample:SAMN00802250, Coriell:GM13280, Wikidata:Q54846418 |
CVCL_GT65 | 2026-08-01 05:07:01 | 0 | ||||
|
GM13255 Resource Report Resource Website |
Coriell Cat# GM13255, RRID:CVCL_V143 | Homo sapiens (Human) | Von Hippel-Lindau syndrome | Transformed cell line | Male | Coriell | GM13255 | CLO:CLO_0013088, BioSample:SAMN00802216, Coriell:GM13255, Wikidata:Q54846400 |
CVCL_V143 | 2026-08-01 05:07:01 | 0 | |||||
|
GM13312 Resource Report Resource Website |
RRID:CVCL_4F08 | Homo sapiens (Human) | Ellis-Van Creveld syndrome | Population: Caucasian; Amish. | Transformed cell line | Male | CLO:CLO_0013216, BioSample:SAMN00802289, Coriell:GM13312, Wikidata:Q54846452 |
CVCL_4F08 | 2026-08-01 05:07:04 | 0 | ||||||
|
GM13265 Resource Report Resource Website |
RRID:CVCL_BW67 | Homo sapiens (Human) | D-bifunctional protein deficiency | Population: Caucasian. | Finite cell line | Male | CLO:CLO_0013129, BioSample:SAMN00802228, Coriell:GM13265, Wikidata:Q54846407 |
CVCL_BW67 | 2026-08-01 05:07:01 | 0 | ||||||
|
GM13341 Resource Report Resource Website |
Coriell Cat# GM13341, RRID:CVCL_1S70 | Homo sapiens (Human) | Characteristics: Hybrid for chromosome 3 mapping (PubMed=9441767)., Group: Human/rodent somatic cell hybrid. |
PMID:7713507 PMID:9441767 |
Hybrid cell line | GL5, GL-5 | Coriell | GM13341 | CLO:CLO_0012884, Coriell:GM13341, Wikidata:Q54846472 |
cvcl_v817 | CVCL_1S70 | 2026-08-01 05:07:05 | 0 | |||
|
GM13449 Resource Report Resource Website |
RRID:CVCL_1K77 | Homo sapiens (Human) | Glycogen storage disease type II | Transformed cell line | Male | Coriell:GM13449, Wikidata:Q54846535 |
CVCL_1K77 | 2026-08-01 05:07:10 | 0 | |||||||
|
GM13339 Resource Report Resource Website |
Coriell Cat# GM13339, RRID:CVCL_1S68 | Homo sapiens (Human) | Characteristics: Hybrid for chromosomes 3 and X mapping (PubMed=9441767)., Group: Human/rodent somatic cell hybrid. |
PMID:7713507 PMID:9441767 |
Hybrid cell line | G1A10, G1A-10 | Coriell | GM13339 | CLO:CLO_0012887, Coriell:GM13339, Wikidata:Q54846470 |
CVCL_1S68 | 2026-08-01 05:07:08 | 0 | ||||
|
GM13419 Resource Report Resource Website |
RRID:CVCL_1N85 | Homo sapiens (Human) | Beckwith-Wiedemann syndrome | PMID:23665875 | Transformed cell line | Male | CLO:CLO_0012646, BioSample:SAMN00802356, Coriell:GM13419, Wikidata:Q54846515 |
CVCL_1N85 | 2026-08-01 05:07:06 | 0 | ||||||
|
GM13314 Resource Report Resource Website |
RRID:CVCL_4F10 | Homo sapiens (Human) | Ellis-Van Creveld syndrome | Population: Caucasian; Amish. | Transformed cell line | Female | CLO:CLO_0013218, BioSample:SAMN00802293, Coriell:GM13314, Wikidata:Q54846454 |
CVCL_4F10 | 2026-08-01 05:07:02 | 0 | ||||||
|
GM13412 Resource Report Resource Website |
Coriell Cat# GM13412, RRID:CVCL_1S72 | Cricetulus griseus (Chinese hamster) | Group: Human/rodent somatic cell hybrid. | PMID:2045096 | Hybrid cell line | 1HL35-5, 1HL35 subclone 5 | Coriell | GM13412 | CLO:CLO_0012655, Coriell:GM13412, Wikidata:Q54846510 |
cvcl_1n51 | CVCL_1S72 | 2026-08-01 05:07:09 | 0 | |||
|
GM13343 Resource Report Resource Website |
Coriell Cat# GM13343, RRID:CVCL_GS85 | Homo sapiens (Human) | Pancreatic lipase deficiency | PMID:11393534 | Transformed cell line | Male | Coriell | GM13343 | CLO:CLO_0012899, BioSample:SAMN00802318, Coriell:GM13343, Wikidata:Q54846474 |
CVCL_GS85 | 2026-08-01 05:07:03 | 0 | ||||
|
GM13324 Resource Report Resource Website |
Coriell Cat# GM13324, RRID:CVCL_2N05 | Homo sapiens (Human) | Turner syndrome | Donor information: Established from monozygotic twin of GM13323 (Cellosaurus=CVCL_2N04). | PMID:23665875 | Transformed cell line | Female | Coriell | GM13324 | CLO:CLO_0013274, Coriell:GM13324, Wikidata:Q54846461 |
CVCL_2N05 | 2026-08-01 05:07:08 | 0 | |||
|
GM13446 Resource Report Resource Website |
Coriell Cat# GM13446, RRID:CVCL_DE53 | Cricetulus griseus (Chinese hamster) | Group: Human/rodent somatic cell hybrid. | PMID:1559705 | Hybrid cell line | 640-5A | Coriell | GM13446 | CLO:CLO_0012181, Coriell:GM13446, Wikidata:Q54846533 |
CVCL_DE53 | 2026-08-01 05:07:10 | 0 | ||||
|
GM13436 Resource Report Resource Website |
RRID:CVCL_5P77 | Homo sapiens (Human) | Pelizaeus-Merzbacher disease | Transformed cell line | Male | CLO:CLO_0012664, BioSample:SAMN00802374, Coriell:GM13436, Wikidata:Q54846527 |
CVCL_5P77 | 2026-08-01 05:07:04 | 0 |
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