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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM03827 Resource Report Resource Website |
RRID:CVCL_X057 | Homo sapiens (Human) | Karyotypic information: 46,X,del(X)(pter->q21) (Coriell=GM03827)., Population: African American. |
PMID:6617268 PMID:6661932 |
Finite cell line | Female | GM 3827 | CLO:CLO_0015670, BioSample:SAMN00808553, Coriell:GM03827, Wikidata:Q54838257 |
CVCL_X057 | 2026-07-25 04:32:51 | 0 | |||||
|
GM03823 Resource Report Resource Website |
Coriell Cat# GM03823, RRID:CVCL_AK78 | Homo sapiens (Human) | Retinitis pigmentosa | Population: Caucasian; German. | PMID:6726265 | Transformed cell line | Male | GM 3823, GM03823A | Coriell | GM03823 | CLO:CLO_0015540, BioSample:SAMN00808549, Coriell:GM03823, Wikidata:Q54838253 |
CVCL_AK78 | 2026-07-25 04:32:51 | 0 | ||
|
GM03747 Resource Report Resource Website |
RRID:CVCL_1H62 | Homo sapiens (Human) | Huntington's disease | Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease. | Transformed cell line | Male | CLO:CLO_0015521, BioSample:SAMN00808517, Coriell:GM03747, Wikidata:Q54838216 |
CVCL_1H62 | 2026-07-25 04:32:50 | 0 | ||||||
|
GM03774 Resource Report Resource Website |
Coriell Cat# GM03774, RRID:CVCL_2M99 | Homo sapiens (Human) | Turner syndrome | Population: Caucasian. | PMID:23665875 | Finite cell line | Female | Coriell | GM03774 | CLO:CLO_0015499, BioSample:SAMN00808527, Coriell:GM03774, Wikidata:Q54838229 |
CVCL_2M99 | 2026-07-25 04:32:51 | 0 | |||
|
GM03835 Resource Report Resource Website |
Coriell Cat# GM03835, RRID:CVCL_AK86 | Homo sapiens (Human) | Retinitis pigmentosa | Population: Caucasian. | Finite cell line | Female | Coriell | GM03835 | CLO:CLO_0015668, BioSample:SAMN00808559, Coriell:GM03835, Wikidata:Q54838263 |
CVCL_AK86 | 2026-07-25 04:32:52 | 0 | ||||
|
GM03799 Resource Report Resource Website |
Coriell Cat# GM03799, RRID:CVCL_2S94 | Homo sapiens (Human) | Transformed cell line | Female | Coriell | GM03799 | CLO:CLO_0015547, BioSample:SAMN00808540, Coriell:GM03799, Wikidata:Q54838244 |
CVCL_2S94 | 2026-07-25 04:32:51 | 0 | ||||||
|
GM03813 Resource Report Resource Website 1+ mentions |
RRID:CVCL_F172 | Homo sapiens (Human) | Spinal muscular atrophy type 2 | Population: Caucasian., Problematic cell line: Misclassified. Originally thought to be a SMA type 1 (SMA1) cell line but shown to be from a SMA type 2 (SMA2) (PubMed=28284873).. |
PMID:3941662 PMID:26190808 PMID:26247043 PMID:28284873 |
Finite cell line | Male | GM 3813, SMA1FABE | CLO:CLO_0015532, BioSample:SAMN00808545, Coriell:GM03813, Wikidata:Q54838249 |
CVCL_F172 | 2026-07-25 04:32:51 | 2 | ||||
|
GM03786 Resource Report Resource Website |
Coriell Cat# GM17375, RRID:CVCL_N012 | Homo sapiens (Human) | Karyotypic information: 45,XX,dic(13;14)(13qter->13p11::14p11->14qter) (Coriell=GM03786)., Population: Caucasian; Greek., Part of: Human variation panel. | Finite cell line | Female | GM17375 | Coriell | GM17375 | CLO:CLO_0013696, CLO:CLO_0015567, BioSample:SAMN00808534, Coriell:GM03786, Coriell:GM17375, Wikidata:Q54838238 |
CVCL_N012 | 2026-07-25 04:32:51 | 0 | ||||
|
GM03733 Resource Report Resource Website |
RRID:CVCL_X110 | Homo sapiens (Human) | Karyotypic information: 46,XY,del(7)(pter->q34) (Coriell=GM03733)., Population: Caucasian. |
PMID:6617268 PMID:6661932 |
Finite cell line | Male | GM-3733, GM 3733 | CLO:CLO_0015525, BioSample:SAMN00808514, Coriell:GM03733, Wikidata:Q54838213 |
CVCL_X110 | 2026-07-25 04:32:50 | 0 | |||||
|
GM03782 Resource Report Resource Website |
RRID:CVCL_5M85 | Homo sapiens (Human) | Duchenne muscular dystrophy | Population: Caucasian; Iberian., Part of: Genetic Testing Reference Material (GeT-RM) samples. |
PMID:6726265 PMID:21354051 PMID:23665875 |
Transformed cell line | Male | GM 3782, GM3782 | CLO:CLO_0015601, BioSample:SAMN00808530, Coriell:GM03782, Wikidata:Q54838232 |
CVCL_5M85 | 2026-07-25 04:32:51 | 0 | ||||
|
GM03828 Resource Report Resource Website |
Coriell Cat# GM03828, RRID:CVCL_X058 | Homo sapiens (Human) | Karyotypic information: 46,X,del(X)(pter->q21) (Coriell=GM03828)., Population: African American. |
PMID:6617268 PMID:6661932 |
Finite cell line | Female | GM 3828 | Coriell | GM03828 | CLO:CLO_0015676, BioSample:SAMN00808554, Coriell:GM03828, Wikidata:Q54838258 |
CVCL_X058 | 2026-07-25 04:32:51 | 0 | |||
|
GM03828 Resource Report Resource Website |
RRID:CVCL_X058 | Homo sapiens (Human) | Karyotypic information: 46,X,del(X)(pter->q21) (Coriell=GM03828)., Population: African American. |
PMID:6617268 PMID:6661932 |
Finite cell line | Female | GM 3828 | CLO:CLO_0015676, BioSample:SAMN00808554, Coriell:GM03828, Wikidata:Q54838258 |
CVCL_X058 | 2026-07-25 04:32:51 | 0 | |||||
|
GM03725 Resource Report Resource Website |
RRID:CVCL_7654 | Homo sapiens (Human) | Population: African American., Part of: Human variation panel. | PMID:16260726 | Transformed cell line | Male | GM17103 | CLO:CLO_0014898, CLO:CLO_0015510, BioSample:SAMN00808511, Coriell:GM03725, Coriell:GM17103, GEO:GSM273373, GEO:GSM569500, GEO:GSM596171, GEO:GSM596972, GEO:GSM924613, IPD-IMGT/HLA:15335, Wikidata:Q54838210 |
CVCL_7654 | 2026-07-25 04:32:50 | 0 | |||||
|
GM03746 Resource Report Resource Website |
RRID:CVCL_1H61 | Homo sapiens (Human) | Huntington's disease | Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease. | Transformed cell line | Female | CLO:CLO_0015522, BioSample:SAMN00808516, Coriell:GM03746, Wikidata:Q54838215 |
CVCL_1H61 | 2026-07-25 04:32:50 | 0 | ||||||
|
GM03808 Resource Report Resource Website |
RRID:CVCL_JE12 | Homo sapiens (Human) | WAGR syndrome | Population: Caucasian. | PMID:2559742 | Finite cell line | Male | GM3808, 3808 | CLO:CLO_0015562, BioSample:SAMN00808541, Coriell:GM03808, Wikidata:Q54838245 |
CVCL_JE12 | 2026-07-25 04:32:51 | 0 | ||||
|
GM03809 Resource Report Resource Website |
RRID:CVCL_JE58 | Homo sapiens (Human) | WAGR syndrome | PMID:2570029 | Finite cell line | Female | GM3809 | CLO:CLO_0015559, BioSample:SAMN00808542, Coriell:GM03809, Wikidata:Q54838246 |
CVCL_JE58 | 2026-07-25 04:32:51 | 0 | |||||
|
GM03725 Resource Report Resource Website |
Coriell Cat# GM03725, RRID:CVCL_7654 | Homo sapiens (Human) | Population: African American., Part of: Human variation panel. | PMID:16260726 | Transformed cell line | Male | GM17103 | Coriell | GM03725 | CLO:CLO_0014898, CLO:CLO_0015510, BioSample:SAMN00808511, Coriell:GM03725, Coriell:GM17103, GEO:GSM273373, GEO:GSM569500, GEO:GSM596171, GEO:GSM596972, GEO:GSM924613, IPD-IMGT/HLA:15335, Wikidata:Q54838210 |
CVCL_7654 | 2026-07-25 04:32:50 | 0 | |||
|
GM03831 Resource Report Resource Website |
Coriell Cat# GM03831, RRID:CVCL_AK82 | Homo sapiens (Human) | Retinitis pigmentosa | Population: Caucasian. | Finite cell line | Female | Coriell | GM03831 | CLO:CLO_0015674, BioSample:SAMN00808555, Coriell:GM03831, Wikidata:Q54838259 |
CVCL_AK82 | 2026-07-25 04:32:52 | 0 | ||||
|
GM03876 Resource Report Resource Website |
RRID:CVCL_1N78 | Homo sapiens (Human) | Karyotypic information: 46,XY,t(1;20)(1qter->1p13::20q13.3->20qter;20pter->20q13.3::1p13->1pter) (Coriell=GM03876)., Population: Caucasian. | PMID:2535035 | Finite cell line | Male | GM3876 | CLO:CLO_0016034, BioSample:SAMN00808586, Coriell:GM03876, Wikidata:Q54838293 |
CVCL_1N78 | 2026-07-25 04:32:52 | 0 | |||||
|
GM03911 Resource Report Resource Website |
RRID:CVCL_AK95 | Homo sapiens (Human) | Retinitis pigmentosa | Population: Caucasian. | PMID:6726265 | Transformed cell line | Female | GM 3911, GM03911A | CLO:CLO_0016123, Coriell:GM03911, Wikidata:Q54838318 |
CVCL_AK95 | 2026-07-25 04:32:53 | 0 |
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