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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM27336 Resource Report Resource Website |
RRID:CVCL_XC51 | Homo sapiens (Human) | Transformed cell line | Female | Coriell:GM27336, Wikidata:Q93933169 |
CVCL_XC51 | 2026-07-25 04:38:02 | 0 | ||||||||
|
GM27250 Resource Report Resource Website |
RRID:CVCL_VV58 | Homo sapiens (Human) | Population: Caucasian; French and Chinese. | Transformed cell line | Female | Coriell:GM27250, Wikidata:Q93933125 |
CVCL_VV58 | 2026-07-25 04:38:01 | 0 | |||||||
|
GM27226 Resource Report Resource Website |
RRID:CVCL_YN35 | Homo sapiens (Human) | Congenital disorder of glycosylation type Ia | Finite cell line | Male | Coriell:GM27226, Wikidata:Q93933090 |
CVCL_YN35 | 2026-07-25 04:38:01 | 0 | |||||||
|
GM27265 Resource Report Resource Website |
Coriell Cat# GM27265, RRID:CVCL_A2QG | Homo sapiens (Human) | Population: Caucasian. | Finite cell line | Male | Coriell | GM27265 | Coriell:GM27265, Wikidata:Q105507119 |
CVCL_A2QG | 2026-07-25 04:38:01 | 0 | |||||
|
GM27318 Resource Report Resource Website |
Coriell Cat# GM27318, RRID:CVCL_A1UL | Homo sapiens (Human) | Rett syndrome, congenital variant | Population: Caucasian; German. | Transformed cell line | Male | Coriell | GM27318 | Coriell:GM27318, Wikidata:Q105507128 |
CVCL_A1UL | 2026-07-25 04:38:01 | 0 | ||||
|
GM27379 Resource Report Resource Website |
RRID:CVCL_A1UW | Homo sapiens (Human) | Rett syndrome, congenital variant | Population: Caucasian; Dutch. | Transformed cell line | Male | Coriell:GM27379, Wikidata:Q105507168 |
CVCL_A1UW | 2026-07-25 04:38:02 | 0 | ||||||
|
GM27291 Resource Report Resource Website |
RRID:CVCL_VV62 | Homo sapiens (Human) | Vici syndrome | Population: Jewish; Ashkenazi. | PMID:35700637 | Induced pluripotent stem cell | Male | GM27291*B, CIMRi001-A | BioSamples:SAMEA10457755, Coriell:GM27291, hPSCreg:CIMRi001-A, Wikidata:Q93933153 |
cvcl_lh34 | CVCL_VV62 | 2026-07-25 04:38:01 | 0 | |||
|
GM27326 Resource Report Resource Website |
Coriell Cat# GM27326, RRID:CVCL_YN41 | Homo sapiens (Human) | Transformed cell line | Female | Coriell | GM27326 | Coriell:GM27326, Wikidata:Q93933161 |
CVCL_YN41 | 2026-07-25 04:38:02 | 0 | ||||||
|
GM27206 Resource Report Resource Website |
RRID:CVCL_YN32 | Homo sapiens (Human) | Population: Caucasian; Dutch. | Finite cell line | Female | Coriell:GM27206, Wikidata:Q93933081 |
CVCL_YN32 | 2026-07-25 04:38:01 | 0 | |||||||
|
GM27249 Resource Report Resource Website |
RRID:CVCL_VV57 | Homo sapiens (Human) | Population: Caucasian; French. | Transformed cell line | Male | Coriell:GM27249, Wikidata:Q93933123 |
CVCL_VV57 | 2026-07-25 04:38:01 | 0 | |||||||
|
GM27381 Resource Report Resource Website |
RRID:CVCL_XC50 | Homo sapiens (Human) | Congenital disorder of deglycosylation | Population: Caucasian. | Induced pluripotent stem cell | Male | GM27381*B | Coriell:GM27381, Wikidata:Q93933196 |
cvcl_bx28 | CVCL_XC50 | 2026-07-25 04:38:02 | 0 | ||||
|
GM27288 Resource Report Resource Website |
RRID:CVCL_YN37 | Homo sapiens (Human) | Developmental and epileptic encephalopathy 25 | Population: Caucasian. | Transformed cell line | Female | Coriell:GM27288, Wikidata:Q93933148 |
CVCL_YN37 | 2026-07-25 04:38:01 | 0 | ||||||
|
GM27324 Resource Report Resource Website |
RRID:CVCL_A1UR | Homo sapiens (Human) | Population: Caucasian. | Transformed cell line | Male | Coriell:GM27324, Wikidata:Q105507153 |
CVCL_A1UR | 2026-07-25 04:38:02 | 0 | |||||||
|
GM27376 Resource Report Resource Website |
RRID:CVCL_A1UV | Homo sapiens (Human) | Population: Caucasian; British. | Transformed cell line | Male | Coriell:GM27376, Wikidata:Q105507164 |
CVCL_A1UV | 2026-07-25 04:38:02 | 0 | |||||||
|
GM27267 Resource Report Resource Website |
RRID:CVCL_VV61 | Homo sapiens (Human) | Rett syndrome, congenital variant | Transformed cell line | Female | Coriell:GM27267, Wikidata:Q93933142 |
CVCL_VV61 | 2026-07-25 04:38:01 | 0 | |||||||
|
GM27315 Resource Report Resource Website |
RRID:CVCL_A1UJ | Homo sapiens (Human) | Rett syndrome, congenital variant | Population: Southeast Asian; Thai and Chinese. | Transformed cell line | Female | Coriell:GM27315, Wikidata:Q105507125 |
CVCL_A1UJ | 2026-07-25 04:38:01 | 0 | ||||||
|
GM27337 Resource Report Resource Website |
Coriell Cat# GM27337, RRID:CVCL_VV64 | Homo sapiens (Human) | Transformed cell line | Male | Coriell | GM27337 | Coriell:GM27337, Wikidata:Q93933173 |
CVCL_VV64 | 2026-07-25 04:38:02 | 0 | ||||||
|
GM27371 Resource Report Resource Website |
RRID:CVCL_VV69 | Homo sapiens (Human) | Population: Caucasian; Mennonite. | Finite cell line | Male | Coriell:GM27371, Wikidata:Q93933194 |
CVCL_VV69 | 2026-07-25 04:38:02 | 0 | |||||||
|
GM27260 Resource Report Resource Website |
Coriell Cat# GM27260, RRID:CVCL_A2QC | Homo sapiens (Human) | Rett syndrome, congenital variant | Population: Caucasian. | Transformed cell line | Male | Coriell | GM27260 | Coriell:GM27260, Wikidata:Q105507105 |
CVCL_A2QC | 2026-07-25 04:38:01 | 0 | ||||
|
GM27241 Resource Report Resource Website |
RRID:CVCL_UT83 | Homo sapiens (Human) | Rett syndrome, congenital variant | Population: Caucasian. | Transformed cell line | Male | Coriell:GM27241, Wikidata:Q93933100 |
CVCL_UT83 | 2026-07-25 04:38:01 | 0 |
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