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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
XP1MI 2 Resource Report Resource Website |
RRID:CVCL_7351 | Homo sapiens (Human) | Xeroderma pigmentosum, complementation group C | Senescence: Senesces at 24 PDL (PubMed=3003928; PubMed=6492896)., Population: African American. |
PMID:3003928 PMID:6492896 PMID:7389185 PMID:18809580 PMID:23665875 |
Finite cell line | Female | Xeroderma Pigmentosum 1 Miami 2, GM02096, GM-2096, GM 2096, GM2096 | CLO:CLO_0031821, BioSample:SAMN00807484, Coriell:GM02096, Wikidata:Q54837300 |
CVCL_7351 | 2026-09-12 06:04:35 | 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 | ||
|
GM12722 Resource Report Resource Website |
Coriell Cat# GM12722, RRID:CVCL_5P69 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Male | Coriell | GM12722 | CLO:CLO_0022568, Coriell:GM12722, Wikidata:Q54846003 |
CVCL_5P69 | 2026-09-12 05:34:38 | 0 | |||||
|
GM12959 Resource Report Resource Website |
RRID:CVCL_5P71 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Male | CLO:CLO_0022918, Coriell:GM12959, Wikidata:Q54846240 |
CVCL_5P71 | 2026-09-12 05:34:43 | 0 | |||||||
|
GM13164 Resource Report Resource Website |
Coriell Cat# GM13164, RRID:CVCL_4W21 | Homo sapiens (Human) | Rubinstein-Taybi syndrome | Population: African American. | PMID:23665875 | Transformed cell line | Female | Coriell | GM13164 | CLO:CLO_0013645, BioSample:SAMN00802155, Coriell:GM13164, Wikidata:Q54846354 |
CVCL_4W21 | 2026-09-12 05:34:46 | 0 | |||
|
GM13166 Resource Report Resource Website |
Coriell Cat# GM13166, RRID:CVCL_2Q71 | Homo sapiens (Human) | Turner syndrome | PMID:23665875 | Transformed cell line | Female | Coriell | GM13166 | CLO:CLO_0013643, Coriell:GM13166, Wikidata:Q54846355 |
CVCL_2Q71 | 2026-09-12 05:34:46 | 0 | ||||
|
GM13164 Resource Report Resource Website |
RRID:CVCL_4W21 | Homo sapiens (Human) | Rubinstein-Taybi syndrome | Population: African American. | PMID:23665875 | Transformed cell line | Female | CLO:CLO_0013645, BioSample:SAMN00802155, Coriell:GM13164, Wikidata:Q54846354 |
CVCL_4W21 | 2026-09-12 05:34:46 | 0 | |||||
|
GM13277 Resource Report Resource Website |
RRID:CVCL_5P73 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Female | CLO:CLO_0013290, BioSample:SAMN00802246, Coriell:GM13277, Wikidata:Q54846416 |
CVCL_5P73 | 2026-09-12 05:34:47 | 0 | |||||||
|
GM13284 Resource Report Resource Website |
Coriell Cat# GM13284, RRID:CVCL_2U25 | Homo sapiens (Human) | Population: Caucasian. | PMID:23665875 | Finite cell line | Male | Coriell | GM13284 | CLO:CLO_0013286, BioSample:SAMN00802254, Coriell:GM13284, Wikidata:Q54846420 |
CVCL_2U25 | 2026-09-12 05:34:47 | 0 | ||||
|
GM13330 Resource Report Resource Website |
Coriell Cat# GM13330, RRID:CVCL_2U26 | Homo sapiens (Human) | Population: Caucasian. |
PMID:11687795 PMID:23665875 |
Finite cell line | Male | Coriell | GM13330 | CLO:CLO_0013247, BioSample:SAMN00802309, Coriell:GM13330, GEO:GSM809, Wikidata:Q54846466 |
CVCL_2U26 | 2026-09-12 05:34:48 | 0 | ||||
|
GM13451 Resource Report Resource Website |
RRID:CVCL_5P80 | Homo sapiens (Human) | Holoprosencephaly | PMID:23665875 | Finite cell line | Male | Coriell:GM13451, Wikidata:Q54846537 |
CVCL_5P80 | 2026-09-12 05:34:50 | 0 | ||||||
|
GM13321 Resource Report Resource Website |
Coriell Cat# GM13321, RRID:CVCL_N207 | Homo sapiens (Human) | Population: African American., Part of: Human variation panel. |
PMID:16260726 PMID:23665875 |
Transformed cell line | Male | GM17174 | Coriell | GM13321 | CLO:CLO_0013224, CLO:CLO_0014034, BioSample:SAMN00802297, Coriell:GM13321, Coriell:GM17174, GEO:GSM569746, GEO:GSM596238, GEO:GSM597033, GEO:GSM924684, Wikidata:Q54846458 |
CVCL_N207 | 2026-09-12 05:34:48 | 0 | |||
|
GM13451 Resource Report Resource Website |
Coriell Cat# GM13451, RRID:CVCL_5P80 | Homo sapiens (Human) | Holoprosencephaly | PMID:23665875 | Finite cell line | Male | Coriell | GM13451 | Coriell:GM13451, Wikidata:Q54846537 |
CVCL_5P80 | 2026-09-12 05:34:50 | 0 | ||||
|
GM13323 Resource Report Resource Website |
Coriell Cat# GM13323, RRID:CVCL_2N04 | Homo sapiens (Human) | Turner syndrome | Donor information: Established from monozygotic twin of GM13324 (Cellosaurus=CVCL_2N05). | PMID:23665875 | Transformed cell line | Female | Coriell | GM13323 | CLO:CLO_0013275, Coriell:GM13323, Wikidata:Q54846460 |
CVCL_2N04 | 2026-09-12 05:34:48 | 0 | |||
|
GM13324 Resource Report Resource Website |
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 | CLO:CLO_0013274, Coriell:GM13324, Wikidata:Q54846461 |
CVCL_2N05 | 2026-09-12 05:34:48 | 0 | |||||
|
GM13410 Resource Report Resource Website |
RRID:CVCL_2U27 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Sex ambiguous | CLO:CLO_0012856, BioSample:SAMN00802346, Coriell:GM13410, Wikidata:Q54846508 |
CVCL_2U27 | 2026-09-12 05:34:49 | 0 |
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