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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM01466 Resource Report Resource Website |
Coriell Cat# GM01466, RRID:CVCL_AA16 | Homo sapiens (Human) | Familial dysautonomia | Transformed cell line | Male | GM-1466, GM01466A | Coriell | GM01466 | CLO:CLO_0031431, BioSample:SAMN00806862, Coriell:GM01466, Wikidata:Q54836851 |
CVCL_AA16 | 2026-07-25 04:32:17 | 0 | ||||
|
GM01491 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_JD87 | Homo sapiens (Human) | 46,XY gonadal dysgenesis | Finite cell line | Sex ambiguous | GM-1491 | Coriell:GM01491, Wikidata:Q54836867 |
CVCL_JD87 | 2026-07-25 04:32:17 | 0 | ||||||
|
GM01524 Resource Report Resource Website |
Coriell Cat# GM01524, RRID:CVCL_X249 | Homo sapiens (Human) | Developmental delay | Karyotypic information: 46,XY,der(5)(5pter->5q33::6q15->6q25::5q33->5qter)mat (Coriell=GM01524)., Population: African American. |
PMID:6661932 PMID:9150358 PMID:11687795 |
Finite cell line | Male | GM-1524, GM 1524, GM1524 | Coriell | GM01524 | CLO:CLO_0031474, BioSample:SAMN00806890, Coriell:GM01524, GEO:GSM796, Wikidata:Q54836881 |
CVCL_X249 | 2026-07-25 04:32:18 | 0 | ||
|
GM01509 Resource Report Resource Website |
Coriell Cat# GM01509, RRID:CVCL_1F07 | Homo sapiens (Human) | Xeroderma pigmentosum | Population: Caucasian. | Finite cell line | Female | GM-1509 | Coriell | GM01509 | CLO:CLO_0031448, BioSample:SAMN00806884, Coriell:GM01509, Wikidata:Q54836878 |
CVCL_1F07 | 2026-07-25 04:32:18 | 0 | |||
|
GM01530 Resource Report Resource Website |
RRID:CVCL_V213 | Homo sapiens (Human) | Cystic fibrosis | Transformed cell line | Male | GM-1530 | CLO:CLO_0031471, Coriell:GM01530, Wikidata:Q54836886 |
CVCL_V213 | 2026-07-25 04:32:20 | 0 | ||||||
|
GM01566 Resource Report Resource Website |
RRID:CVCL_GY17 | Homo sapiens (Human) | Cystathioninuria | Karyotypic information: 47,XX,+12 [66%]; 46,XX,-10,+12 [30%]; 45,XX,-10 [4%] (Coriell=GM01566)., Population: Caucasian. | Transformed cell line | Female | GM-1566 | CLO:CLO_0031450, BioSample:SAMN00806919, Coriell:GM01566, Wikidata:Q54836914 |
CVCL_GY17 | 2026-07-25 04:32:19 | 0 | |||||
|
GM01486 Resource Report Resource Website |
Coriell Cat# GM01486, RRID:CVCL_H973 | Homo sapiens (Human) | Maturity-onset diabetes of the young | Population: Caucasian. | Finite cell line | Male | GM-1486 | Coriell | GM01486 | CLO:CLO_0031432, BioSample:SAMN00806868, Coriell:GM01486, Wikidata:Q54836854 |
CVCL_H973 | 2026-07-25 04:32:17 | 0 | |||
|
GM01568 Resource Report Resource Website |
RRID:CVCL_1K52 | Homo sapiens (Human) | Transformed cell line | Male | GM-1568 | CLO:CLO_0031452, BioSample:SAMN00806923, Coriell:GM01568, Wikidata:Q54836916 |
CVCL_1K52 | 2026-07-25 04:32:19 | 0 | |||||||
|
GM01461 Resource Report Resource Website |
RRID:CVCL_EJ28 | Homo sapiens (Human) | Transformed cell line | Female | GM-1461 | CLO:CLO_0030873, BioSample:SAMN00803910, Coriell:GM01461, Wikidata:Q54836846 |
CVCL_EJ28 | 2026-07-25 04:32:17 | 0 | |||||||
|
GM01553 Resource Report Resource Website |
Coriell Cat# GM01553, RRID:CVCL_2Z62 | Homo sapiens (Human) | Nevoid basal cell carcinoma syndrome | Population: Caucasian. | Transformed cell line | Male | GM-1553 | Coriell | GM01553 | CLO:CLO_0031484, BioSample:SAMN00806908, Coriell:GM01553, Wikidata:Q54836896 |
CVCL_2Z62 | 2026-07-25 04:32:19 | 0 | |||
|
GM01529 Resource Report Resource Website |
Coriell Cat# GM01529, RRID:CVCL_2H20 | Homo sapiens (Human) | Population: Caucasian. | PMID:8528202 | Transformed cell line | Female | GM-1529 | Coriell | GM01529 | CLO:CLO_0031470, Coriell:GM01529, Wikidata:Q54836885 |
CVCL_2H20 | 2026-07-25 04:32:18 | 0 | |||
|
GM01589 Resource Report Resource Website |
RRID:CVCL_9Q88 | Homo sapiens (Human) | Population: Caucasian. | PMID:16465621 | Finite cell line | Male | GM-1589 | CLO:CLO_0031544, BioSample:SAMN00806949, Coriell:GM01589, Wikidata:Q54836932 |
CVCL_9Q88 | 2026-07-25 04:32:19 | 0 | |||||
|
GM01625 Resource Report Resource Website |
RRID:CVCL_4J36 | Homo sapiens (Human) | Acute intermittent porphyria | Population: Caucasian. | Finite cell line | Male | GM-1625 | CLO:CLO_0031495, BioSample:SAMN00806987, Coriell:GM01625, Wikidata:Q54836961 |
CVCL_4J36 | 2026-07-25 04:32:20 | 0 | |||||
|
GM01580 Resource Report Resource Website |
RRID:CVCL_0P97 | Homo sapiens (Human) | Karyotypic information: 46,XX,t(10;21)(10pter->10q26::21q21->21qter;21pter->21q21::10q26->10qter) (Coriell=GM01580)., Population: African American. | Finite cell line | Female | GM-1580 | CLO:CLO_0031461, BioSample:SAMN00806937, Coriell:GM01580, Wikidata:Q54836924 |
CVCL_0P97 | 2026-07-25 04:32:21 | 0 | ||||||
|
GM01633 Resource Report Resource Website |
RRID:CVCL_9Z54 | Homo sapiens (Human) | Neurofibromatosis type 1 | Population: Caucasian. | Finite cell line | Male | GM-1633 | CLO:CLO_0031498, BioSample:SAMN00806999, Coriell:GM01633, Wikidata:Q54836968 |
CVCL_9Z54 | 2026-07-25 04:32:20 | 0 | |||||
|
GM01601 Resource Report Resource Website |
RRID:CVCL_AK19 | Homo sapiens (Human) | Population: Caucasian. | Finite cell line | Female | GM-1601 | CLO:CLO_0031554, BioSample:SAMN00806959, Coriell:GM01601, Wikidata:Q54836937 |
CVCL_AK19 | 2026-07-25 04:32:21 | 0 | ||||||
|
GM01637 Resource Report Resource Website |
Coriell Cat# GM01637, RRID:CVCL_5L41 | Homo sapiens (Human) | Tuberous sclerosis 1 | Population: African American. | Finite cell line | Female | GM-1637 | Coriell | GM01637 | CLO:CLO_0031520, BioSample:SAMN00807007, Coriell:GM01637, Wikidata:Q54836972 |
CVCL_5L41 | 2026-07-25 04:32:20 | 0 | |||
|
GM01611 Resource Report Resource Website |
Coriell Cat# GM01611, RRID:CVCL_1D24 | Homo sapiens (Human) | Wolfram syndrome | Population: Caucasian. | Finite cell line | Female | GM-1611 | Coriell | GM01611 | CLO:CLO_0031558, BioSample:SAMN00806973, Coriell:GM01611, Wikidata:Q54836947 |
CVCL_1D24 | 2026-07-25 04:32:20 | 0 | |||
|
GM01643 Resource Report Resource Website |
RRID:CVCL_5L43 | Homo sapiens (Human) | Tuberous sclerosis 1 | Population: African American. | Finite cell line | Male | GM-1643 | CLO:CLO_0031524, BioSample:SAMN00807015, Coriell:GM01643, Wikidata:Q54836976 |
CVCL_5L43 | 2026-07-25 04:32:20 | 0 | |||||
|
GM01628 Resource Report Resource Website |
Coriell Cat# GM01628, RRID:CVCL_DS07 | Homo sapiens (Human) | 46,XY sex reversal 1 | Population: Caucasian. | Finite cell line | Sex ambiguous | GM-1628 | Coriell | GM01628 | CLO:CLO_0031490, BioSample:SAMN00806989, Coriell:GM01628, Wikidata:Q54836962 |
CVCL_DS07 | 2026-07-25 04:32:22 | 0 |
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