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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM00023 Resource Report Resource Website |
RRID:CVCL_7268 | Homo sapiens (Human) | Population: Caucasian. |
PMID:19896956 PMID:26184184 |
Finite cell line | Female | GM0023, GM-23, GM00023A | CLO:CLO_0025190, Coriell:GM00023, Wikidata:Q54835979 |
CVCL_7268 | 2026-08-29 04:27:14 | 0 | |||||
|
GloResponse NF-kappaB-RE-luc2P HEK293 Resource Report Resource Website |
RRID:CVCL_LB61 | Homo sapiens (Human) | Characteristics: The luciferase reporter gene is under the control of a minimal TATA promoter with multiple copies of the NF-kappaB response element. | Transformed cell line | Female | GloResponse NF-kB-RE-luc2P HEK293, GloResponse NF-KB-RE-luc2P HEK293 | Wikidata:Q54835948 | cvcl_0045 | CVCL_LB61 | 2026-08-29 04:27:14 | 0 | |||||
|
GM00111 Resource Report Resource Website |
Coriell Cat# GM00111, RRID:CVCL_1F01 | Homo sapiens (Human) | Glycogen storage disease type III | Population: Caucasian. | Finite cell line | Female | GM-111 | Coriell | GM00111 | CLO:CLO_0025823, Coriell:GM00111, Wikidata:Q54836044 |
CVCL_1F01 | 2026-08-29 04:27:16 | 0 | |||
|
GM00043 Resource Report Resource Website |
Coriell Cat# GM00043, RRID:CVCL_7273 | Homo sapiens (Human) | Population: African American. |
PMID:694721 PMID:7779715 PMID:19896956 PMID:30567591 |
Finite cell line | Female | GM0043, GM-43, GM43, GM00043A, GM00043B | Coriell | GM00043 | CLO:CLO_0025173, Coriell:GM00043, GEO:GSM3124654, Wikidata:Q54836000 |
CVCL_7273 | 2026-08-29 04:27:15 | 0 | |||
|
GM00135 Resource Report Resource Website |
RRID:CVCL_R904 | Homo sapiens (Human) | Lesch-Nyhan syndrome | Population: African American. | Finite cell line | Female | GM-135, GM 135, GM135, GM00135A | CLO:CLO_0003509, CLO:CLO_0025832, CLDB:cl1476, Coriell:GM00135, Wikidata:Q54836057 |
CVCL_R904 | 2026-08-29 04:27:16 | 0 | |||||
|
GM00088 Resource Report Resource Website |
Coriell Cat# GM00088, RRID:CVCL_X224 | Homo sapiens (Human) | Turner syndrome | Karyotypic information: 46,X,i(X)(p11.21) (PubMed=10377420)., Population: Caucasian. |
PMID:4780774 PMID:6661932 PMID:10377420 PMID:23665875 |
Finite cell line | Female | GM-88, GM-0088, GM0088, GM 88 | Coriell | GM00088 | CLO:CLO_0025156, Coriell:GM00088, Wikidata:Q54836029 |
CVCL_X224 | 2026-08-29 04:27:16 | 0 | ||
|
GM00082 Resource Report Resource Website |
JCRB Cat# KURB1026, RRID:CVCL_L495 | Homo sapiens (Human) | Xeroderma pigmentosum, complementation group A | Population: Caucasian. |
PMID:1372102 PMID:1702221 PMID:9671271 |
Finite cell line | Female | GM-82, GM82 | JCRB | KURB1026 | CLO:CLO_0025151, Coriell:GM00082, JCRB:KURB1026, Wikidata:Q54836023 |
CVCL_L495 | 2026-08-29 04:27:15 | 0 | ||
|
GM00057 Resource Report Resource Website |
Coriell Cat# GM00057, RRID:CVCL_2N23 | Homo sapiens (Human) | Propionic acidemia | Population: Caucasian. | PMID:5101292 | Finite cell line | Female | GM-57, GM00057A, GM0057A | Coriell | GM00057 | CLO:CLO_0025161, Coriell:GM00057, Wikidata:Q54836008 |
CVCL_2N23 | 2026-08-29 04:27:15 | 0 | ||
|
GM00059 Resource Report Resource Website |
RRID:CVCL_0P14 | Homo sapiens (Human) | Canavan disease |
PMID:19815695 PMID:33304759 |
Finite cell line | Female | GM-59, GM00059A, CD#59 | CLO:CLO_0025162, Coriell:GM00059, Wikidata:Q54836009 |
CVCL_0P14 | 2026-08-29 04:27:15 | 0 | |||||
|
GM00097 Resource Report Resource Website |
Coriell Cat# GM00097, RRID:CVCL_V747 | Homo sapiens (Human) | Simpson Golabi Behmel syndrome type 1 | Karyotypic information: 46,X,t(X;1)(q26;q21) (PubMed=10377420)., Population: Caucasian. |
PMID:1679663 PMID:2498246 PMID:4139001 PMID:10377420 |
Finite cell line | Female | GM-97, GM0097, GM 0097, GM00097A | Coriell | GM00097 | CLO:CLO_0025819, Coriell:GM00097, Wikidata:Q54836039 |
CVCL_V747 | 2026-08-29 04:27:16 | 0 | ||
|
GM00089 Resource Report Resource Website |
Coriell Cat# GM00089, RRID:CVCL_F600 | Homo sapiens (Human) | Karyotypic information: 46,X,t(X;19)(q22;q13.3) (PubMed=10377420)., Population: Caucasian. |
PMID:6293786 PMID:10377420 |
Finite cell line | Female | GM-89, GM0089, GM089 | Coriell | GM00089 | CLO:CLO_0025157, Coriell:GM00089, Wikidata:Q54836030 |
CVCL_F600 | 2026-08-29 04:27:16 | 0 | |||
|
GM00118 Resource Report Resource Website |
RRID:CVCL_V749 | Homo sapiens (Human) | Karyotypic information: 46,XX,der(15)(15qter->15p1::Yq11->Yqter)pat (Coriell=GM00118)., Population: Caucasian; Danish. |
PMID:1225503 PMID:6661932 |
Finite cell line | Female | GM-118, GM-0118, GM 118 | CLO:CLO_0025828, Coriell:GM00118, Wikidata:Q54836047 |
CVCL_V749 | 2026-08-29 04:27:16 | 0 | |||||
|
GM00113 Resource Report Resource Website |
RRID:CVCL_9R60 | Homo sapiens (Human) | Mucolipidosis type IIIA | Population: Caucasian. | PMID:16465621 | Finite cell line | Female | GM-113, GM00113A | CLO:CLO_0025825, Coriell:GM00113, Wikidata:Q54836046 |
CVCL_9R60 | 2026-08-29 04:27:16 | 0 | ||||
|
GM00082 Resource Report Resource Website |
Coriell Cat# GM00082, RRID:CVCL_L495 | Homo sapiens (Human) | Xeroderma pigmentosum, complementation group A | Population: Caucasian. |
PMID:1372102 PMID:1702221 PMID:9671271 |
Finite cell line | Female | GM-82, GM82 | Coriell | GM00082 | CLO:CLO_0025151, Coriell:GM00082, JCRB:KURB1026, Wikidata:Q54836023 |
CVCL_L495 | 2026-08-29 04:27:15 | 0 | ||
|
GM00144 Resource Report Resource Website |
Coriell Cat# GM00144, RRID:CVCL_V459 | Homo sapiens (Human) | Down syndrome | Population: Caucasian. |
PMID:4139000 PMID:6661932 PMID:19727395 |
Finite cell line | Female | GM-144, GM-0144, GM 144 | Coriell | GM00144 | CLO:CLO_0025850, Coriell:GM00144, GEO:GSM426280, Wikidata:Q54836063 |
CVCL_V459 | 2026-08-29 04:27:16 | 0 | ||
|
GM00120 Resource Report Resource Website |
RRID:CVCL_4J08 | Homo sapiens (Human) | Population: African; Kenyan. |
PMID:4502820 PMID:6156493 PMID:7803800 |
Finite cell line | Female | GM-120, GM 120 | CLO:CLO_0025831, Coriell:GM00120, Wikidata:Q54836049 |
CVCL_4J08 | 2026-08-29 04:27:16 | 0 | |||||
|
GM00088 Resource Report Resource Website |
RRID:CVCL_X224 | Homo sapiens (Human) | Turner syndrome | Karyotypic information: 46,X,i(X)(p11.21) (PubMed=10377420)., Population: Caucasian. |
PMID:4780774 PMID:6661932 PMID:10377420 PMID:23665875 |
Finite cell line | Female | GM-88, GM-0088, GM0088, GM 88 | CLO:CLO_0025156, Coriell:GM00088, Wikidata:Q54836029 |
CVCL_X224 | 2026-08-29 04:27:16 | 0 | ||||
|
GM00185 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_JD92 | Homo sapiens (Human) | Finite cell line | Female | GM-185 | Coriell:GM00185, Wikidata:Q54836076 |
CVCL_JD92 | 2026-08-29 04:27:17 | 0 | |||||||
|
GM00194 Resource Report Resource Website |
Coriell Cat# GM00194, RRID:CVCL_H961 | Homo sapiens (Human) | Karyotypic information: 46,X,t(X;3)(q28;q21) (Coriell=GM00194)., Population: Caucasian; Finnish. |
PMID:1225501 PMID:2498246 |
Finite cell line | Female | GM-194, GM0194 | Coriell | GM00194 | CLO:CLO_0025667, Coriell:GM00194, Wikidata:Q54836077 |
CVCL_H961 | 2026-08-29 04:27:17 | 0 | |||
|
GM00201 Resource Report Resource Website |
Coriell Cat# GM00201, RRID:CVCL_V460 | Homo sapiens (Human) | Down syndrome |
PMID:1132251 PMID:6293786 PMID:6661932 |
Finite cell line | Female | GM-201, GM-0201, GM 201, GM201, GM00201A, GM 0201A | Coriell | GM00201 | CLO:CLO_0025659, Coriell:GM00201, Wikidata:Q54836088 |
CVCL_V460 | 2026-08-29 04:27:17 | 0 |
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