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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM06230 Resource Report Resource Website |
Coriell Cat# GM06230, RRID:CVCL_5N41 | Homo sapiens (Human) | Population: Asian. | PMID:23665875 | Finite cell line | Female | Coriell | GM06230 | CLO:CLO_0023095, Coriell:GM06230, Wikidata:Q54842234 |
CVCL_5N41 | 2026-08-01 05:05:07 | 0 | ||||
|
GM06370 Resource Report Resource Website |
RRID:CVCL_1J33 | Homo sapiens (Human) | Part of: Venezuelan Huntington disease kindreds subcollection. | Transformed cell line | Female | CLO:CLO_0023090, Coriell:GM06370, Wikidata:Q54842268 |
CVCL_1J33 | 2026-08-01 05:05:01 | 0 | |||||||
|
GM06327 Resource Report Resource Website |
RRID:CVCL_9X01 | Homo sapiens (Human) | Maroteaux-Lamy syndrome | Population: Caucasian. | Finite cell line | Female | CLO:CLO_0023062, Coriell:GM06327, Wikidata:Q54842255 |
CVCL_9X01 | 2026-08-01 05:05:03 | 0 | ||||||
|
GM06325 Resource Report Resource Website |
RRID:CVCL_N051 | Homo sapiens (Human) | Population: Caucasian; Portuguese., Part of: Human variation panel. | Finite cell line | Female | GM17093 | CLO:CLO_0014520, CLO:CLO_0023061, Coriell:GM06325, Coriell:GM17093, Wikidata:Q54842253 |
CVCL_N051 | 2026-08-01 05:05:08 | 0 | ||||||
|
GM06275 Resource Report Resource Website |
Coriell Cat# GM06275, RRID:CVCL_F670 | Homo sapiens (Human) | PMID:10577914 | Transformed cell line | Female | GM6275, GM06275A | Coriell | GM06275 | CLO:CLO_0023113, Coriell:GM06275, Wikidata:Q54842244 |
CVCL_F670 | 2026-08-01 05:05:00 | 0 | ||||
|
GM06333 Resource Report Resource Website |
RRID:CVCL_W048 | Homo sapiens (Human) | Trichothiodystrophy 4, nonphotosensitive | Population: Moroccan. | Finite cell line | Female | CLO:CLO_0023073, Coriell:GM06333, Wikidata:Q54842261 |
CVCL_W048 | 2026-08-01 05:05:03 | 0 | ||||||
|
GM06330 Resource Report Resource Website |
RRID:CVCL_CY54 | Homo sapiens (Human) | Gyrate atrophy | Population: Caucasian; Italian. | Finite cell line | Female | GM6330 | CLO:CLO_0023078, Coriell:GM06330, Wikidata:Q54842258 |
CVCL_CY54 | 2026-08-01 05:05:03 | 0 | |||||
|
GM06274 Resource Report Resource Website |
Coriell Cat# GM06274, RRID:CVCL_V046 | Homo sapiens (Human) | Huntington's disease | Population: Caucasian. | PMID:7847674 | Finite cell line | Female | Coriell | GM06274 | CLO:CLO_0023114, Coriell:GM06274, Wikidata:Q54842242 |
CVCL_V046 | 2026-08-01 05:05:03 | 0 | |||
|
GM06228 Resource Report Resource Website |
Coriell Cat# GM06228, RRID:CVCL_2T20 | Homo sapiens (Human) |
PMID:10577914 PMID:23665875 |
Transformed cell line | Female | Coriell | GM06228 | CLO:CLO_0023094, Coriell:GM06228, Wikidata:Q54842232 |
CVCL_2T20 | 2026-08-01 05:05:03 | 0 | |||||
|
GM06231 Resource Report Resource Website |
RRID:CVCL_N050 | Homo sapiens (Human) | Peroxisome biogenesis disorder 8A | Population: Africans north of the Sahara., Part of: Human variation panel. | PMID:9922452 | Finite cell line | Female | GM6231, GM17380, PBD061 | CLO:CLO_0012204, CLO:CLO_0023106, Coriell:GM06231, Coriell:GM17380, Wikidata:Q54842235 |
CVCL_N050 | 2026-08-01 05:05:00 | 0 | ||||
|
GM06274 Resource Report Resource Website |
RRID:CVCL_V046 | Homo sapiens (Human) | Huntington's disease | Population: Caucasian. | PMID:7847674 | Finite cell line | Female | CLO:CLO_0023114, Coriell:GM06274, Wikidata:Q54842242 |
CVCL_V046 | 2026-08-01 05:05:00 | 0 | |||||
|
GM06314 Resource Report Resource Website |
RRID:CVCL_H157 | Homo sapiens (Human) | Glycogen storage disease type II | Population: Caucasian; Italian., Part of: Human variation panel. |
PMID:1652892 PMID:2112341 |
Transformed cell line | Female | GM 6314, GM06314A, GM17323 | CLO:CLO_0013649, CLO:CLO_0023128, Coriell:GM06314, Coriell:GM17323, Wikidata:Q54842246 |
CVCL_H157 | 2026-08-01 05:05:00 | 0 | ||||
|
GM06229 Resource Report Resource Website |
RRID:CVCL_F669 | Homo sapiens (Human) | PMID:10577914 | Transformed cell line | Female | GM6229, GM06229A, GM06229B | CLO:CLO_0023093, Coriell:GM06229, Wikidata:Q54842233 |
CVCL_F669 | 2026-08-01 05:05:07 | 0 | ||||||
|
GM06256 Resource Report Resource Website |
Coriell Cat# GM06256, RRID:CVCL_4F54 | Homo sapiens (Human) | Zellweger syndrome | Karyotypic information: 46,XX,inv(9)(pter->p11::q21->p11::q21->qter)pat (Coriell=GM06256)., Population: Caucasian. | Finite cell line | Female | Coriell | GM06256 | CLO:CLO_0023109, Coriell:GM06256, Wikidata:Q54842238 |
CVCL_4F54 | 2026-08-01 05:05:08 | 0 | ||||
|
GM06221 Resource Report Resource Website |
Coriell Cat# GM06221, RRID:CVCL_GS73 | Homo sapiens (Human) | Erythropoietic protoporphyria | Population: Caucasian. | Transformed cell line | Female | Coriell | GM06221 | CLO:CLO_0023146, Coriell:GM06221, Wikidata:Q54842222 |
CVCL_GS73 | 2026-08-01 05:05:03 | 0 | ||||
|
GM06256 Resource Report Resource Website |
RRID:CVCL_4F54 | Homo sapiens (Human) | Zellweger syndrome | Karyotypic information: 46,XX,inv(9)(pter->p11::q21->p11::q21->qter)pat (Coriell=GM06256)., Population: Caucasian. | Finite cell line | Female | CLO:CLO_0023109, Coriell:GM06256, Wikidata:Q54842238 |
CVCL_4F54 | 2026-08-01 05:05:03 | 0 | ||||||
|
GM06230 Resource Report Resource Website |
RRID:CVCL_5N41 | Homo sapiens (Human) | Population: Asian. | PMID:23665875 | Finite cell line | Female | CLO:CLO_0023095, Coriell:GM06230, Wikidata:Q54842234 |
CVCL_5N41 | 2026-08-01 05:05:03 | 0 | ||||||
|
GM06363 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_UT27 | Homo sapiens (Human) | Part of: Venezuelan Huntington disease kindreds subcollection. | Finite cell line | Female | GM06363Z | Coriell:GM06363, Wikidata:Q93791840 |
CVCL_UT27 | 2026-08-01 05:05:09 | 0 | ||||||
|
GM06375 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_US79 | Homo sapiens (Human) | Part of: Venezuelan Huntington disease kindreds subcollection. | Finite cell line | Female | GM06375Z | Coriell:GM06375, Wikidata:Q93791861 |
CVCL_US79 | 2026-08-01 05:05:09 | 0 | ||||||
|
GM06248 Resource Report Resource Website |
RRID:CVCL_5U21 | Homo sapiens (Human) | Analbuminemia | Population: Native North American; Salish. |
PMID:3353369 PMID:23665875 |
Finite cell line | Female | GM6248 | CLO:CLO_0023108, Coriell:GM06248, Wikidata:Q54842237 |
CVCL_5U21 | 2026-08-01 05:05:00 | 0 |
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