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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM50174 Resource Report Resource Website |
RRID:CVCL_AB26 | Homo sapiens (Human) | Cri du chat syndrome | Transformed cell line | Female | JL362 | CLO:CLO_0015009, Coriell:GM50174, Wikidata:Q54854246 |
CVCL_AB26 | 2026-07-25 04:38:15 | 0 | ||||||
|
GM50113 Resource Report Resource Website |
Coriell Cat# GM50113, RRID:CVCL_0F90 | Homo sapiens (Human) | Deletion 18q syndrome |
PMID:8488839 PMID:23665875 |
Transformed cell line | Female | JL143 | Coriell | GM50113 | CLO:CLO_0014755, Coriell:GM50113, Wikidata:Q54854201 |
CVCL_0F90 | 2026-07-25 04:38:14 | 0 | |||
|
GM50147 Resource Report Resource Website |
Coriell Cat# GM50147, RRID:CVCL_5T50 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Female | JL273 | Coriell | GM50147 | CLO:CLO_0014683, Coriell:GM50147, Wikidata:Q54854221 |
CVCL_5T50 | 2026-07-25 04:38:15 | 0 | ||||
|
GM50129 Resource Report Resource Website |
Coriell Cat# GM50129, RRID:CVCL_2U67 | Homo sapiens (Human) | Transformed cell line | Female | JL240 | Coriell | GM50129 | CLO:CLO_0014674, Coriell:GM50129, Wikidata:Q54854214 |
CVCL_2U67 | 2026-07-25 04:38:14 | 0 | |||||
|
GM50175 Resource Report Resource Website |
Coriell Cat# GM50175, RRID:CVCL_5L33 | Homo sapiens (Human) | Deletion 18q syndrome | PMID:23665875 | Transformed cell line | Male | JL366 | Coriell | GM50175 | CLO:CLO_0015010, Coriell:GM50175, Wikidata:Q54854247 |
CVCL_5L33 | 2026-07-25 04:38:15 | 0 | |||
|
GM50118 Resource Report Resource Website |
Coriell Cat# GM50118, RRID:CVCL_0F98 | Homo sapiens (Human) | Deletion 18q syndrome |
PMID:8488839 PMID:23665875 |
Transformed cell line | Male | JL172 | Coriell | GM50118 | CLO:CLO_0014758, Coriell:GM50118, Wikidata:Q54854205 |
CVCL_0F98 | 2026-07-25 04:38:14 | 0 | |||
|
GM50173 Resource Report Resource Website |
RRID:CVCL_0G63 | Homo sapiens (Human) | Transformed cell line | Female | JL361 | CLO:CLO_0015008, Coriell:GM50173, Wikidata:Q54854245 |
CVCL_0G63 | 2026-07-25 04:38:15 | 0 | |||||||
|
GM50164 Resource Report Resource Website |
Coriell Cat# GM50164, RRID:CVCL_5L29 | Homo sapiens (Human) | Deletion 18q syndrome | PMID:23665875 | Transformed cell line | Female | JL325 | Coriell | GM50164 | CLO:CLO_0014721, Coriell:GM50164, Wikidata:Q54854236 |
CVCL_5L29 | 2026-07-25 04:38:15 | 0 | |||
|
GM50150 Resource Report Resource Website |
RRID:CVCL_5T52 | Homo sapiens (Human) | Holoprosencephaly | PMID:23665875 | Transformed cell line | Female | JL278 | CLO:CLO_0014715, Coriell:GM50150, Wikidata:Q54854224 |
CVCL_5T52 | 2026-07-25 04:38:15 | 0 | |||||
|
GM50139 Resource Report Resource Website |
Coriell Cat# GM50139, RRID:CVCL_0G55 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Female | JL259 | Coriell | GM50139 | CLO:CLO_0014675, Coriell:GM50139, Wikidata:Q54854216 |
CVCL_0G55 | 2026-07-25 04:38:14 | 0 | ||||
|
GM50122 Resource Report Resource Website |
RRID:CVCL_0F92 | Homo sapiens (Human) | Deletion 18q syndrome |
PMID:8488839 PMID:23665875 |
Transformed cell line | Male | JL184 | CLO:CLO_0014752, Coriell:GM50122, Wikidata:Q54854208 |
CVCL_0F92 | 2026-07-25 04:38:14 | 0 | |||||
|
GM50116 Resource Report Resource Website |
RRID:CVCL_0F96 | Homo sapiens (Human) | Deletion 18q syndrome |
PMID:8488839 PMID:23665875 |
Transformed cell line | Male | JL156 | CLO:CLO_0014761, Coriell:GM50116, Wikidata:Q54854204 |
CVCL_0F96 | 2026-07-25 04:38:14 | 0 | |||||
|
GM50175 Resource Report Resource Website |
RRID:CVCL_5L33 | Homo sapiens (Human) | Deletion 18q syndrome | PMID:23665875 | Transformed cell line | Male | JL366 | CLO:CLO_0015010, Coriell:GM50175, Wikidata:Q54854247 |
CVCL_5L33 | 2026-07-25 04:38:15 | 0 | |||||
|
GM50171 Resource Report Resource Website |
Coriell Cat# GM50171, RRID:CVCL_AB25 | Homo sapiens (Human) | Cri du chat syndrome | Transformed cell line | Male | JL347 | Coriell | GM50171 | CLO:CLO_0015026, Coriell:GM50171, Wikidata:Q54854243 |
CVCL_AB25 | 2026-07-25 04:38:15 | 0 | ||||
|
GM50152 Resource Report Resource Website |
RRID:CVCL_5L26 | Homo sapiens (Human) | Deletion 18p syndrome | PMID:23665875 | Transformed cell line | Female | JL280 | CLO:CLO_0014709, Coriell:GM50152, Wikidata:Q54854225 |
CVCL_5L26 | 2026-07-25 04:38:15 | 0 | |||||
|
GM50128 Resource Report Resource Website |
Coriell Cat# GM50128, RRID:CVCL_2U66 | Homo sapiens (Human) | Transformed cell line | Male | JL237 | Coriell | GM50128 | CLO:CLO_0014672, Coriell:GM50128, Wikidata:Q54854213 |
CVCL_2U66 | 2026-07-25 04:38:14 | 0 | |||||
|
GM50172 Resource Report Resource Website |
Coriell Cat# GM50172, RRID:CVCL_5L32 | Homo sapiens (Human) | Deletion 18q syndrome | PMID:23665875 | Transformed cell line | Female | JL351 | Coriell | GM50172 | CLO:CLO_0015028, Coriell:GM50172, Wikidata:Q54854244 |
CVCL_5L32 | 2026-07-25 04:38:15 | 0 | |||
|
GM50148 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_5T51 | Homo sapiens (Human) | Deletion 18p syndrome | PMID:23665875 | Transformed cell line | Female | Coriell:GM50148, Wikidata:Q54854222 |
CVCL_5T51 | 2026-07-25 04:38:15 | 0 | ||||||
|
GM50114 Resource Report Resource Website |
Coriell Cat# GM50114, RRID:CVCL_5T46 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Male | Coriell | GM50114 | Coriell:GM50114, Wikidata:Q54854202 |
CVCL_5T46 | 2026-07-25 04:38:14 | 0 | |||||
|
GM50124 Resource Report Resource Website |
RRID:CVCL_1U16 | Homo sapiens (Human) | Deletion 18q syndrome | PMID:23665875 | Transformed cell line | Male | JL208 | CLO:CLO_0014753, Coriell:GM50124, Wikidata:Q54854209 |
CVCL_1U16 | 2026-07-25 04:38:14 | 0 |
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