Searching the RRID Resource Information Network
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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM04395 Resource Report Resource Website |
RRID:CVCL_GS64 | Homo sapiens (Human) | Adenosine deaminase deficiency | Population: Caucasian. | Finite cell line | Male | CLO:CLO_0019703, Coriell:GM04395, Wikidata:Q54838512 |
CVCL_GS64 | 2026-07-25 04:32:58 | 0 | ||||||
|
GM04288 Resource Report Resource Website |
RRID:CVCL_Y860 | Homo sapiens (Human) | Huntington's disease | Part of: Venezuelan Huntington disease kindreds subcollection. | Transformed cell line | Male | CLO:CLO_0019640, Coriell:GM04288, Wikidata:Q54838470 |
CVCL_Y860 | 2026-07-25 04:32:57 | 0 | ||||||
|
GM04272 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_V236 | Pongo abelii (Sumatran orangutan) | Group: Non-human primate cell line. | Finite cell line | Male | GM4272 | Coriell:GM04272, Wikidata:Q54838458 |
CVCL_V236 | 2026-07-25 04:32:57 | 0 | ||||||
|
GM04305 Resource Report Resource Website |
RRID:CVCL_IJ33 | Homo sapiens (Human) | Galactosialidosis | Transformed cell line | Female | CLO:CLO_0019629, Coriell:GM04305, Wikidata:Q54838474 |
CVCL_IJ33 | 2026-07-25 04:32:57 | 0 | |||||||
|
GM04408 Resource Report Resource Website |
RRID:CVCL_7408 | Homo sapiens (Human) | Bloom syndrome | Caution: Coriell has p.Cys1055fs*23 (c.3159delT) (3233delT) as the second mutation for this cell line., Donor information: From Bloom Syndrome Registry patient 87(AlFra) (BSR87)., Population: Caucasian; English and Jewish; Ashkenazi., Part of: Genetic Testing Reference Material (GeT-RM) samples. |
PMID:2805228 PMID:6330733 PMID:6667451 PMID:6705251 PMID:17407155 PMID:19815695 |
Transformed cell line | Male | GM4408, GM-4408, GM 4408, GM04408A, HG1440 | BTO:BTO_0005028, CLO:CLO_0019706, Coriell:GM04408, Wikidata:Q54838515 |
CVCL_7408 | 2026-07-25 04:32:58 | 0 | ||||
|
GM04319 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM04319, RRID:CVCL_AX24 | Homo sapiens (Human) | Spinocerebellar ataxia | Finite cell line | Male | Coriell | GM04319 | CLO:CLO_0019527, Coriell:GM04319, Wikidata:Q54838480 |
CVCL_AX24 | 2026-07-25 04:32:57 | 0 | |||||
|
GM04329 Resource Report Resource Website |
RRID:CVCL_2Z44 | Homo sapiens (Human) | Campomelic dysplasia | Population: Caucasian. | Finite cell line | Female | CLO:CLO_0019571, Coriell:GM04329, Wikidata:Q54838486 |
CVCL_2Z44 | 2026-07-25 04:32:57 | 0 | ||||||
|
GM04315 Resource Report Resource Website |
RRID:CVCL_5M92 | Homo sapiens (Human) | Population: African American., Part of: Genetic Testing Reference Material (GeT-RM) samples. |
PMID:21354051 PMID:23665875 |
Finite cell line | Female | CLO:CLO_0019552, Coriell:GM04315, Wikidata:Q54838479 |
CVCL_5M92 | 2026-07-25 04:32:57 | 0 | ||||||
|
GM04347 Resource Report Resource Website |
Coriell Cat# GM04347, RRID:CVCL_4D84 | Homo sapiens (Human) | Transformed cell line | Female | Coriell | GM04347 | CLO:CLO_0019567, Coriell:GM04347, Wikidata:Q54838497 |
CVCL_4D84 | 2026-07-25 04:32:57 | 0 | ||||||
|
GM04326 Resource Report Resource Website |
RRID:CVCL_0Q83 | Homo sapiens (Human) | Citrullinemia type I | Population: Caucasian. | Finite cell line | Female | GM4326 | CLO:CLO_0019535, Coriell:GM04326, Wikidata:Q54838484 |
CVCL_0Q83 | 2026-07-25 04:32:57 | 0 | |||||
|
GM04426 Resource Report Resource Website |
RRID:CVCL_9Y79 | Homo sapiens (Human) | Albright's hereditary osteodystrophy | Transformed cell line | Male | CLO:CLO_0019681, Coriell:GM04426, Wikidata:Q54838523 |
CVCL_9Y79 | 2026-07-25 04:32:58 | 0 | |||||||
|
GM04426 Resource Report Resource Website |
Coriell Cat# GM04426, RRID:CVCL_9Y79 | Homo sapiens (Human) | Albright's hereditary osteodystrophy | Transformed cell line | Male | Coriell | GM04426 | CLO:CLO_0019681, Coriell:GM04426, Wikidata:Q54838523 |
CVCL_9Y79 | 2026-07-25 04:32:58 | 0 | |||||
|
GM04504 Resource Report Resource Website |
RRID:CVCL_7411 | Homo sapiens (Human) | Donor information: Established from monozygotic twin of GM04503 (Cellosaurus=CVCL_7410)., Part of: ENCODE project common cell types; tier 3. | PMID:30567591 | Finite cell line | Female | GM04504A, HF23 | CLO:CLO_0018812, Coriell:GM04504, ENCODE:ENCBS016ENC, ENCODE:ENCBS388KHM, GEO:GSM3124652, Wikidata:Q54838544 |
CVCL_7411 | 2026-07-25 04:32:59 | 0 | |||||
|
GM04516 Resource Report Resource Website |
Coriell Cat# GM04516, RRID:CVCL_AW70 | Homo sapiens (Human) | Sideroblastic anemia | Population: Caucasian. | Finite cell line | Female | Coriell | GM04516 | CLO:CLO_0018850, Coriell:GM04516, Wikidata:Q54838554 |
CVCL_AW70 | 2026-07-25 04:32:59 | 0 | ||||
|
GM04428 Resource Report Resource Website |
Coriell Cat# GM17067, RRID:CVCL_N018 | Homo sapiens (Human) | Albright's hereditary osteodystrophy | Population: Mexican., Part of: Human variation panel. | Transformed cell line | Male | GM17067 | Coriell | GM17067 | CLO:CLO_0014566, CLO:CLO_0019689, Coriell:GM04428, Coriell:GM17067, Wikidata:Q54838525 |
CVCL_N018 | 2026-07-25 04:32:58 | 0 | |||
|
GM04589 Resource Report Resource Website |
RRID:CVCL_AA25 | Homo sapiens (Human) | Familial dysautonomia | Population: Caucasian. |
PMID:29762696 PMID:30905397 |
Finite cell line | Male | CLO:CLO_0018883, Coriell:GM04589, GEO:GSM3592405, GEO:GSM3592411, Wikidata:Q54838577 |
CVCL_AA25 | 2026-07-25 04:32:59 | 0 | |||||
|
GM04514 Resource Report Resource Website |
RRID:CVCL_X308 | Homo sapiens (Human) | Population: Caucasian. | PMID:6661932 | Finite cell line | Female | GM 4514 | CLO:CLO_0018832, Coriell:GM04514, Wikidata:Q54838552 |
CVCL_X308 | 2026-07-25 04:32:59 | 0 | |||||
|
GM04601 Resource Report Resource Website |
RRID:CVCL_Y793 | Homo sapiens (Human) | Dystrophia myotonica 1 | Population: Caucasian. | Finite cell line | Female | CLO:CLO_0018919, Coriell:GM04601, Wikidata:Q54838587 |
CVCL_Y793 | 2026-07-25 04:32:59 | 0 | ||||||
|
GM04516 Resource Report Resource Website |
RRID:CVCL_AW70 | Homo sapiens (Human) | Sideroblastic anemia | Population: Caucasian. | Finite cell line | Female | CLO:CLO_0018850, Coriell:GM04516, Wikidata:Q54838554 |
CVCL_AW70 | 2026-07-25 04:32:59 | 0 | ||||||
|
GM04505 Resource Report Resource Website |
Coriell Cat# GM04505, RRID:CVCL_7412 | Homo sapiens (Human) | Donor information: Established from monozygotic twin of GM04506 (Cellosaurus=CVCL_7413)., Population: Caucasian. | PMID:30567591 | Finite cell line | Female | GM04505A, HF24 | Coriell | GM04505 | CLO:CLO_0018816, Coriell:GM04505, GEO:GSM3124650, Wikidata:Q54838545 |
CVCL_7412 | 2026-07-25 04:32:59 | 0 |
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