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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
Cri du Chat Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM00071, RRID:CVCL_4150 | Homo sapiens (Human) | Cri du chat syndrome | Population: Caucasian. |
PMID:1001031 PMID:6661932 PMID:6988327 |
Finite cell line | Female | GM00071, GM-0071, GM-71, GM 71, GM71 | Coriell | GM00071 | CLO:CLO_0002611, CLO:CLO_0025165, CLDB:cl910, ATCC:CCL-90, BioSample:SAMN03471291, Coriell:GM00071, ECACC:90102533, KCB:KCB 94023YJ, Wikidata:Q54814486 |
CVCL_4150 | 2026-09-05 10:46:50 | 0 | ||
|
CS267BE Resource Report Resource Website |
Coriell Cat# GM11551, RRID:CVCL_EG47 | Homo sapiens (Human) | Cockayne syndrome type B | Population: Caucasian. | PMID:12060391 | Finite cell line | Female | Cockayne Syndrome 267 BEthesda, GM11551 | Coriell | GM11551 | CLO:CLO_0021057, Coriell:GM11551, Wikidata:Q54845152 |
CVCL_EG47 | 2026-09-05 10:46:52 | 0 | ||
|
CS1USAU Resource Report Resource Website |
RRID:CVCL_ZP65 | Homo sapiens (Human) | Xeroderma pigmentosum-Cockayne syndrome complex |
PMID:23623389 PMID:30165384 |
Finite cell line | Male | Wikidata:Q98125733 | CVCL_ZP65 | 2026-09-05 10:46:51 | 0 | ||||||
|
CS1BI Resource Report Resource Website |
RRID:CVCL_ZQ18 | Homo sapiens (Human) | Cockayne syndrome | PMID:18079351 | Finite cell line | Sex unspecified | Cockayne Syndrome 1 BIrmingham | Wikidata:Q98125725 | CVCL_ZQ18 | 2026-09-05 10:46:51 | 0 | |||||
|
CS1BR Resource Report Resource Website |
RRID:CVCL_ZN61 | Homo sapiens (Human) | Cockayne syndrome type A |
PMID:18079351 PMID:29572252 |
Finite cell line | Sex unspecified | Cockayne Syndrome 1 BRighton | Wikidata:Q98125728 | CVCL_ZN61 | 2026-09-05 10:46:51 | 0 | |||||
|
CS1MO Resource Report Resource Website |
JCRB Cat# KURB1885, RRID:CVCL_ZP14 | Homo sapiens (Human) | Cockayne syndrome type B | Population: Japanese. | PMID:9777763 | Finite cell line | Female | Cockayne Syndrome 1 MOriguchi | JCRB | KURB1885 | JCRB:KURB1885, JCRB:KURB1886, Wikidata:Q98125731 |
CVCL_ZP14 | 2026-09-05 10:46:51 | 0 | ||
|
CS1MO Resource Report Resource Website |
JCRB Cat# KURB1886, RRID:CVCL_ZP14 | Homo sapiens (Human) | Cockayne syndrome type B | Population: Japanese. | PMID:9777763 | Finite cell line | Female | Cockayne Syndrome 1 MOriguchi | JCRB | KURB1886 | JCRB:KURB1885, JCRB:KURB1886, Wikidata:Q98125731 |
CVCL_ZP14 | 2026-09-05 10:46:51 | 0 | ||
|
CS1YOF Resource Report Resource Website |
RRID:CVCL_B5LT | Homo sapiens (Human) | Population: Japanese. | PMID:6481688 | Finite cell line | Male | Cockayne Syndrome 1 YOkohama Father | JCRB:KURB1957, Wikidata:Q111733139 |
CVCL_B5LT | 2026-09-05 10:46:51 | 0 | |||||
|
CS1ATM Resource Report Resource Website |
RRID:CVCL_B5LX | Homo sapiens (Human) | Cockayne syndrome | Population: Japanese. | PMID:6481688 | Finite cell line | Female | JCRB:KURB1921, Wikidata:Q111733137 |
CVCL_B5LX | 2026-09-05 10:46:51 | 0 | |||||
|
CS1OS Resource Report Resource Website |
RRID:CVCL_M678 | Homo sapiens (Human) | Cockayne syndrome type A | Population: Japanese. |
PMID:7151298 PMID:9777763 |
Finite cell line | Male | Cockayne Syndrome 1 OSaka | JCRB:KURB1906, Wikidata:Q54814531 |
CVCL_M678 | 2026-09-05 10:46:51 | 0 | ||||
|
CS1YO Resource Report Resource Website |
JCRB Cat# KURB1955, RRID:CVCL_B5LS | Homo sapiens (Human) | Cockayne syndrome | Population: Japanese. | PMID:6481688 | Finite cell line | Male | Cockayne Syndrome 1 YOkohama | JCRB | KURB1955 | JCRB:KURB1955, Wikidata:Q111733138 |
CVCL_B5LS | 2026-09-05 10:46:51 | 0 | ||
|
CS210BE Resource Report Resource Website |
Coriell Cat# GM17536, RRID:CVCL_EG51 | Homo sapiens (Human) | Cockayne syndrome | Population: Pakistani. | PMID:27543334 | Finite cell line | Male | Cockayne Syndrome 210 BEthesda, GM17536 | Coriell | GM17536 | CLO:CLO_0013056, Coriell:GM17536, Wikidata:Q54848961 |
CVCL_EG51 | 2026-09-05 10:46:52 | 0 | ||
|
CS1MO Resource Report Resource Website |
RRID:CVCL_ZP14 | Homo sapiens (Human) | Cockayne syndrome type B | Population: Japanese. | PMID:9777763 | Finite cell line | Female | Cockayne Syndrome 1 MOriguchi | JCRB:KURB1885, JCRB:KURB1886, Wikidata:Q98125731 |
CVCL_ZP14 | 2026-09-05 10:46:51 | 0 | ||||
|
CS15PV Resource Report Resource Website |
RRID:CVCL_ZS00 | Homo sapiens (Human) | Cockayne syndrome type A | Population: Moroccan. | PMID:29572252 | Finite cell line | Male | Cockayne Syndrome 15 PaVia | Wikidata:Q98125722 | CVCL_ZS00 | 2026-09-05 10:46:51 | 0 | ||||
|
CS1ATM Resource Report Resource Website |
JCRB Cat# KURB1921, RRID:CVCL_B5LX | Homo sapiens (Human) | Cockayne syndrome | Population: Japanese. | PMID:6481688 | Finite cell line | Female | JCRB | KURB1921 | JCRB:KURB1921, Wikidata:Q111733137 |
CVCL_B5LX | 2026-09-05 10:46:51 | 0 | |||
|
CS2BE Resource Report Resource Website |
RRID:CVCL_7314 | Homo sapiens (Human) | Cockayne syndrome type B | Population: Caucasian. |
PMID:157803 PMID:431551 PMID:6096450 PMID:6622549 PMID:7301938 PMID:7471106 PMID:9443879 PMID:9777763 PMID:12665480 |
Finite cell line | Male | Cockayne Syndrome 2 BEthesda, CS5HO, GM01098, GM-1098, GM 1098, GM1098, GM 1098B, GM01098B | CLO:CLO_0030186, BioSample:SAMN00803626, Coriell:GM01098, JCRB:KURB1916, Wikidata:Q54836644 |
CVCL_7314 | 2026-09-05 10:46:52 | 0 | ||||
|
CS1TAN Resource Report Resource Website |
RRID:CVCL_ZN59 | Homo sapiens (Human) | Cockayne syndrome type B | Population: Turkish. |
PMID:8834235 PMID:9443879 PMID:10767341 |
Finite cell line | Male | Cockayne Syndrome 1 Turkey ANkara | Wikidata:Q98125732 | CVCL_ZN59 | 2026-09-05 10:46:51 | 0 | ||||
|
CS1BO Resource Report Resource Website |
RRID:CVCL_ZQ19 | Homo sapiens (Human) | Cockayne syndrome type B | Population: African American. |
PMID:8834235 PMID:9443879 PMID:18079351 |
Finite cell line | Female | Cockayne Syndrome 1 BOston | Wikidata:Q98125727 | CVCL_ZQ19 | 2026-09-05 10:46:51 | 0 | ||||
|
CS2BR Resource Report Resource Website |
RRID:CVCL_ZN62 | Homo sapiens (Human) | Cockayne syndrome type B |
PMID:8834235 PMID:18079351 |
Finite cell line | Sex unspecified | Cockayne Syndrome 2 BRighton | Wikidata:Q98125741 | CVCL_ZN62 | 2026-09-05 10:46:52 | 0 | |||||
|
CS2AW Resource Report Resource Website |
RRID:CVCL_2879 | Homo sapiens (Human) | Cockayne syndrome type A | Population: Japanese. |
PMID:12655141 PMID:22466610 |
Finite cell line | Female | BioSample:SAMN03471618, JCRB:JCRB0310, JCRB:KURB1889, Wikidata:Q54814538 |
CVCL_2879 | 2026-09-05 10:46:52 | 0 |
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Data set from Kravitz, Owen and Kretizer's 2012 paper "Optogenetic identification of striatal projection neuron subtypes during in vivo recordings."
