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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM02434 Resource Report Resource Website |
RRID:CVCL_GS55 | Homo sapiens (Human) | Adenosine deaminase deficiency | Population: Caucasian. | PMID:7380831 | Finite cell line | Male | GM-2434, GM 2434, GM02434A | CLO:CLO_0033277, BioSample:SAMN00807771, Coriell:GM02434, Wikidata:Q54837486 |
CVCL_GS55 | 2026-07-25 04:32:33 | 0 | ||||
|
GM02355 Resource Report Resource Website |
Coriell Cat# GM02355, RRID:CVCL_L945 | Homo sapiens (Human) | Familial adenomatous polyposis | Population: Caucasian. | Finite cell line | Female | GM2355 | Coriell | GM02355 | CLO:CLO_0033110, BioSample:SAMN00807733, Coriell:GM02355, Wikidata:Q54837455 |
CVCL_L945 | 2026-07-25 04:32:32 | 0 | |||
|
GM02442 Resource Report Resource Website |
Coriell Cat# GM02442, RRID:CVCL_GR98 | Homo sapiens (Human) | Type 1 diabetes mellitus | Population: Native Central American; Pima. | Finite cell line | Female | Coriell | GM02442 | CLO:CLO_0033317, BioSample:SAMN00807779, Coriell:GM02442, Wikidata:Q54837496 |
CVCL_GR98 | 2026-07-25 04:32:33 | 0 | ||||
|
GM02363 Resource Report Resource Website |
Coriell Cat# GM02363, RRID:CVCL_AK24 | Homo sapiens (Human) | Fanconi anemia, complementation group A | Finite cell line | Male | GM-2363 | Coriell | GM02363 | CLO:CLO_0033100, Coriell:GM02363, Wikidata:Q54837460 |
CVCL_AK24 | 2026-07-25 04:32:32 | 0 | ||||
|
GM02362 Resource Report Resource Website |
RRID:CVCL_AK23 | Homo sapiens (Human) | Fanconi anemia, complementation group A | Finite cell line | Male | GM-2362, GM02362A | CLO:CLO_0033099, Coriell:GM02362, Wikidata:Q54837459 |
CVCL_AK23 | 2026-07-25 04:32:32 | 0 | ||||||
|
GM02439 GM1-iPSC clone 3 Resource Report Resource Website |
RRID:CVCL_VE86 | Homo sapiens (Human) | GM1 gangliosidosis | Population: Turkish. | PMID:25925601 | Induced pluripotent stem cell | Male | GM1-iPSC-clone 3 | SKIP:SKIP001350, Wikidata:Q54837493 |
cvcl_w149 | CVCL_VE86 | 2026-07-25 04:32:35 | 0 | |||
|
GM02439 Resource Report Resource Website |
RRID:CVCL_W149 | Homo sapiens (Human) | GM1 gangliosidosis | Population: Turkish., From: Montreal Children's Hospital cell repository; Montreal; Canada. | PMID:25925601 | Finite cell line | Male | WG0406, WG406 | CLO:CLO_0033291, Coriell:GM02439, Wikidata:Q54837491 |
CVCL_W149 | 2026-07-25 04:32:33 | 0 | ||||
|
GM02431 Resource Report Resource Website Discontinued |
RRID:CVCL_L975 | Homo sapiens (Human) | Chediak-Higashi syndrome | Transformed cell line | Male | GM02431A, GM02378 | CLO:CLO_0033275, BioSample:SAMN00807765, Coriell:GM02378, Coriell:GM02431, Wikidata:Q54837482 |
CVCL_L975 | 2026-07-25 04:32:35 | 0 | ||||||
|
GM02380 Resource Report Resource Website |
Coriell Cat# GM02380, RRID:CVCL_H181 | Homo sapiens (Human) | PMID:6617268 | Finite cell line | Female | GM 2380 | Coriell | GM02380 | CLO:CLO_0033104, Coriell:GM02380, Wikidata:Q54837466 |
CVCL_H181 | 2026-07-25 04:32:33 | 0 | ||||
|
GM02365 Resource Report Resource Website |
Coriell Cat# GM02365, RRID:CVCL_1R62 | Homo sapiens (Human) | Coffin-Lowry syndrome | Population: Caucasian. | PMID:23665875 | Finite cell line | Male | GM02365A | Coriell | GM02365 | CLO:CLO_0033101, BioSample:SAMN00807737, Coriell:GM02365, Wikidata:Q54837463 |
CVCL_1R62 | 2026-07-25 04:32:32 | 0 | ||
|
GM02425 Resource Report Resource Website |
RRID:CVCL_9R69 | Homo sapiens (Human) | Mucolipidosis type IIIA | Population: Caucasian. | PMID:16465621 | Finite cell line | Male | GM-2425 | CLO:CLO_0033090, BioSample:SAMN00807757, Coriell:GM02425, Wikidata:Q54837477 |
CVCL_9R69 | 2026-07-25 04:32:35 | 0 | ||||
|
GM02419 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_UY61 | Homo sapiens (Human) | Finite cell line | Female | Coriell:GM02419, Wikidata:Q93577635 |
CVCL_UY61 | 2026-07-25 04:32:34 | 0 | ||||||||
|
GM02422 Resource Report Resource Website |
RRID:CVCL_H183 | Homo sapiens (Human) | Trisomy 18 | PMID:6661932 | Finite cell line | Female | GM 2422 | CLO:CLO_0033089, BioSample:SAMN00807755, Coriell:GM02422, Wikidata:Q54837476 |
CVCL_H183 | 2026-07-25 04:32:33 | 0 | |||||
|
GM02346 Resource Report Resource Website |
RRID:CVCL_X091 | Homo sapiens (Human) | Karyotypic information: 46,XY,t(4;16)(4pter->4q35::16q22.1->16qter;16pter->16q22.1::4q35->4qter) (Coriell=GM02346)., Population: Caucasian. |
PMID:2095701 PMID:6617268 PMID:6661932 |
Finite cell line | Male | GM-2346, GM 2346, GM2346 | CLO:CLO_0033112, BioSample:SAMN00807729, Coriell:GM02346, Wikidata:Q54837453 |
CVCL_X091 | 2026-07-25 04:32:32 | 0 | |||||
|
GM02432 Resource Report Resource Website |
Coriell Cat# GM17252, RRID:CVCL_M997 | Homo sapiens (Human) | Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. | PMID:20889555 | Transformed cell line | Female | GM17252 | Coriell | GM17252 | CLO:CLO_0014392, CLO:CLO_0033283, BioSample:SAMN00807767, Coriell:GM02432, Coriell:GM17252, GEO:GSM569642, GEO:GSM596316, GEO:GSM596675, GEO:GSM924854, Wikidata:Q54837483 |
CVCL_M997 | 2026-07-25 04:32:33 | 0 | |||
|
GM02364 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_JD75 | Homo sapiens (Human) | Fanconi anemia | Finite cell line | Male | GM-2364 | Coriell:GM02364, Wikidata:Q54837461 |
CVCL_JD75 | 2026-07-25 04:32:32 | 0 | ||||||
|
GM02340 iPSC clone 6 Resource Report Resource Website |
RRID:CVCL_B5QU | Homo sapiens (Human) | Sickle cell disease | PMID:22905176 | Induced pluripotent stem cell | Female | iPSC clone 6.1 | GEO:GSM861005, GEO:GSM1589943, GEO:GSM1589955, Wikidata:Q111733236 |
cvcl_l749 | CVCL_B5QU | 2026-07-25 04:32:34 | 0 | ||||
|
GM02436 Resource Report Resource Website |
RRID:CVCL_GS56 | Homo sapiens (Human) | Adenosine deaminase deficiency | Population: Caucasian; Swiss. |
PMID:1346349 PMID:1680289 PMID:2567118 PMID:7380831 |
Finite cell line | Female | GM-2436, GM 2436 | CLO:CLO_0033293, BioSample:SAMN00807775, Coriell:GM02436, Wikidata:Q54837488 |
CVCL_GS56 | 2026-07-25 04:32:33 | 0 | ||||
|
GM02430 Resource Report Resource Website |
RRID:CVCL_M996 | Homo sapiens (Human) | Transformed cell line | Female | GM17321 | CLO:CLO_0013646, CLO:CLO_0033274, BioSample:SAMN00807763, Coriell:GM02430, Coriell:GM17321, Wikidata:Q54837481 |
CVCL_M996 | 2026-07-25 04:32:35 | 0 | |||||||
|
GM02437 Resource Report Resource Website |
Coriell Cat# GM02437, RRID:CVCL_5M73 | Homo sapiens (Human) | Dyggve-Melchior-Clausen syndrome | Finite cell line | Female | Coriell | GM02437 | CLO:CLO_0033298, Coriell:GM02437, Wikidata:Q54837489 |
CVCL_5M73 | 2026-07-25 04:32:33 | 0 |
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