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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM04297 Resource Report Resource Website |
Coriell Cat# GM04297, RRID:CVCL_5M91 | Homo sapiens (Human) | Prader-Willi syndrome | PMID:23665875 | Transformed cell line | Female | Coriell | GM04297 | CLO:CLO_0019633, Coriell:GM04297, Wikidata:Q54838472 |
CVCL_5M91 | 2026-09-12 05:32:39 | 0 | ||||
|
GM04375 Resource Report Resource Website |
Coriell Cat# GM04375, RRID:CVCL_W622 | Homo sapiens (Human) | Klinefelter syndrome | Population: Caucasian. |
PMID:6661932 PMID:23665875 |
Finite cell line | Male | GM04375A | Coriell | GM04375 | CLO:CLO_0019338, Coriell:GM04375, Wikidata:Q54838507 |
CVCL_W622 | 2026-09-12 05:32:39 | 0 | ||
|
GM04364 Resource Report Resource Website |
RRID:CVCL_5M95 | Homo sapiens (Human) | Duchenne muscular dystrophy | Population: Caucasian., Part of: Genetic Testing Reference Material (GeT-RM) samples. |
PMID:21354051 PMID:23665875 |
Finite cell line | Male | CLO:CLO_0019314, Coriell:GM04364, Wikidata:Q54838499 |
CVCL_5M95 | 2026-09-12 05:32:39 | 0 | |||||
|
GM00017 Resource Report Resource Website |
RRID:CVCL_X222 | Homo sapiens (Human) | Population: African American. |
PMID:4780773 PMID:6293786 PMID:6661932 PMID:23665875 |
Finite cell line | Male | GM-17, GM-0017, GM0017, GM 17, GM17 | CLO:CLO_0025196, Coriell:GM00017, Wikidata:Q54835975 |
CVCL_X222 | 2026-09-12 05:31:37 | 0 | |||||
|
GM00011 Resource Report Resource Website |
Coriell Cat# GM00011, RRID:CVCL_7267 | Homo sapiens (Human) | Population: African American. |
PMID:694721 PMID:23665875 |
Finite cell line | Male | GM0011, GM-11, GM 11, GM11, GM00011A | Coriell | GM00011 | CLO:CLO_0025204, Coriell:GM00011, GEO:GSM909336, GEO:GSM909337, Wikidata:Q54835971 |
CVCL_7267 | 2026-09-12 05:31:37 | 0 | |||
|
GM00137 Resource Report Resource Website |
RRID:CVCL_X225 | Homo sapiens (Human) | Population: Caucasian. |
PMID:6661932 PMID:23665875 |
Finite cell line | Male | GM-137, GM-0137, GM 137, GM00137B | CLO:CLO_0025846, Coriell:GM00137, Wikidata:Q54836058 |
CVCL_X225 | 2026-09-12 05:31:39 | 0 | |||||
|
GM00072 Resource Report Resource Website |
RRID:CVCL_V746 | Homo sapiens (Human) | Wolf-Hirschhorn syndrome | Population: Caucasian. |
PMID:560288 PMID:6617268 PMID:6661932 PMID:23665875 |
Finite cell line | Male | GM-72, GM-0072, GM 72 | CLO:CLO_0025166, Coriell:GM00072, Wikidata:Q54836016 |
CVCL_V746 | 2026-09-12 05:31:38 | 0 | ||||
|
GM00157 Resource Report Resource Website |
Coriell Cat# GM00157, RRID:CVCL_V753 | Homo sapiens (Human) | 49,XXXXY syndrome | Karyotypic information: 49,XXXXY,t(4;11)(q35;q23).arr(X)x4,(Y)x1 (Coriell=GM00157)., Population: Caucasian. |
PMID:1132249 PMID:1183238 PMID:6661932 PMID:23665875 |
Finite cell line | Male | GM-157, GM-0157, GM 157 | Coriell | GM00157 | CLO:CLO_0025866, Coriell:GM00157, Wikidata:Q54836069 |
CVCL_V753 | 2026-09-12 05:31:39 | 0 | ||
|
GM00496 Resource Report Resource Website |
Coriell Cat# GM00496, RRID:CVCL_X231 | Homo sapiens (Human) | Trisomy 8 |
PMID:694721 PMID:6661932 PMID:23665875 |
Finite cell line | Male | GM-496, GM-0496, GM 496, GM496 | Coriell | GM00496 | CLO:CLO_0025949, Coriell:GM00496, Wikidata:Q54836262 |
CVCL_X231 | 2026-09-12 05:31:44 | 0 | |||
|
GM00501 Resource Report Resource Website |
RRID:CVCL_V774 | Homo sapiens (Human) | Intellectual developmental disorder | Population: Caucasian. |
PMID:1017322 PMID:6661932 PMID:23665875 |
Finite cell line | Male | GM-501, GM-0501, GM 501 | CLO:CLO_0025946, Coriell:GM00501, Wikidata:Q54836267 |
CVCL_V774 | 2026-09-12 05:31:44 | 0 | ||||
|
GM00496 Resource Report Resource Website |
RRID:CVCL_X231 | Homo sapiens (Human) | Trisomy 8 |
PMID:694721 PMID:6661932 PMID:23665875 |
Finite cell line | Male | GM-496, GM-0496, GM 496, GM496 | CLO:CLO_0025949, Coriell:GM00496, Wikidata:Q54836262 |
CVCL_X231 | 2026-09-12 05:31:44 | 0 | |||||
|
GM00657 Resource Report Resource Website |
RRID:CVCL_V780 | Homo sapiens (Human) | Population: Caucasian. |
PMID:477406 PMID:6661932 PMID:23665875 |
Finite cell line | Male | GM-657, GM-0657, GM 657 | CLO:CLO_0028863, Coriell:GM00657, Wikidata:Q54836380 |
CVCL_V780 | 2026-09-12 05:31:46 | 0 | |||||
|
GM00633 Resource Report Resource Website |
RRID:CVCL_H954 | Homo sapiens (Human) | Population: Caucasian. |
PMID:62390 PMID:23665875 |
Transformed cell line | Male | GM-633 | CLO:CLO_0028872, Coriell:GM00633, Wikidata:Q54836357 |
CVCL_H954 | 2026-09-12 05:31:46 | 0 | |||||
|
GM00622 Resource Report Resource Website |
RRID:CVCL_5M64 | Homo sapiens (Human) | Neurofibromatosis type 1 | PMID:23665875 | Finite cell line | Male | GM-622 | CLO:CLO_0028991, Coriell:GM00622, Wikidata:Q54836349 |
CVCL_5M64 | 2026-09-12 05:31:46 | 0 | |||||
|
GM00657 Resource Report Resource Website |
Coriell Cat# GM00657, RRID:CVCL_V780 | Homo sapiens (Human) | Population: Caucasian. |
PMID:477406 PMID:6661932 PMID:23665875 |
Finite cell line | Male | GM-657, GM-0657, GM 657 | Coriell | GM00657 | CLO:CLO_0028863, Coriell:GM00657, Wikidata:Q54836380 |
CVCL_V780 | 2026-09-12 05:31:46 | 0 | |||
|
GM00633 Resource Report Resource Website |
Coriell Cat# GM00633, RRID:CVCL_H954 | Homo sapiens (Human) | Population: Caucasian. |
PMID:62390 PMID:23665875 |
Transformed cell line | Male | GM-633 | Coriell | GM00633 | CLO:CLO_0028872, Coriell:GM00633, Wikidata:Q54836357 |
CVCL_H954 | 2026-09-12 05:31:46 | 0 | |||
|
GM00622 Resource Report Resource Website |
Coriell Cat# GM00622, RRID:CVCL_5M64 | Homo sapiens (Human) | Neurofibromatosis type 1 | PMID:23665875 | Finite cell line | Male | GM-622 | Coriell | GM00622 | CLO:CLO_0028991, Coriell:GM00622, Wikidata:Q54836349 |
CVCL_5M64 | 2026-09-12 05:31:46 | 0 | |||
|
GM00735 Resource Report Resource Website |
Coriell Cat# GM00735, RRID:CVCL_X076 | Homo sapiens (Human) | Isodicentric chromosome | Karyotypic information: 46,X,i(X)(p11) (PubMed=10377420)., Population: Caucasian. |
PMID:6617268 PMID:6661932 PMID:10377420 PMID:23665875 |
Finite cell line | Female | GM-735, GM-0735, GM 735, GM0735 | Coriell | GM00735 | CLO:CLO_0028812, Coriell:GM00735, Wikidata:Q54836428 |
CVCL_X076 | 2026-09-12 05:31:47 | 0 | ||
|
GM00782 Resource Report Resource Website |
RRID:CVCL_4E27 | Homo sapiens (Human) | PMID:23665875 | Finite cell line | Male | GM-782 | CLO:CLO_0028841, Coriell:GM00782, Wikidata:Q54836455 |
CVCL_4E27 | 2026-09-12 05:31:48 | 0 | ||||||
|
GM00692 Resource Report Resource Website |
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 | CLO:CLO_0028912, Coriell:GM00692, Wikidata:Q54836391 |
CVCL_X235 | 2026-09-12 05:31:47 | 0 |
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