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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.

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95,747 Results - per page

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GM03870
 
Resource Report
Resource Website 		RRID:CVCL_1H75 Homo sapiens (Human) Population: Caucasian. Finite cell line Female GM03870A CLO:CLO_0016028,
BioSample:SAMN00808582,
Coriell:GM03870,
Wikidata:Q54838289		 CVCL_1H75 2026-07-25 04:32:52 0
GM03863
 
Resource Report
Resource Website 		RRID:CVCL_1H68 Homo sapiens (Human) Huntington's disease Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease., Population: Caucasian. Transformed cell line Female CLO:CLO_0015734,
BioSample:SAMN00808575,
Coriell:GM03863,
Wikidata:Q54838282		 CVCL_1H68 2026-07-25 04:32:52 0
GM03836
 
Resource Report
Resource Website 		Coriell Cat# GM03836, RRID:CVCL_AK87 Homo sapiens (Human) Retinitis pigmentosa Population: Caucasian. PMID:6726265 Transformed cell line Female GM 3836 Coriell GM03836 CLO:CLO_0015642,
BioSample:SAMN00808560,
Coriell:GM03836,
Wikidata:Q54838264		 CVCL_AK87 2026-07-25 04:32:52 0
GM03866
 
Resource Report
Resource Website 		Coriell Cat# GM03866, RRID:CVCL_1H71 Homo sapiens (Human) Huntington's disease Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease., Population: Caucasian. Finite cell line Female Coriell GM03866 CLO:CLO_0015710,
BioSample:SAMN00808578,
Coriell:GM03866,
Wikidata:Q54838285		 CVCL_1H71 2026-07-25 04:32:52 0
GM03869
 
Resource Report
Resource Website 		Coriell Cat# GM03869, RRID:CVCL_1H74 Homo sapiens (Human) Huntington's disease Population: Caucasian. Transformed cell line Female Coriell GM03869 CLO:CLO_0016026,
BioSample:SAMN00808581,
Coriell:GM03869,
Wikidata:Q54838288		 CVCL_1H74 2026-07-25 04:32:52 0
GM03850
 
Resource Report
Resource Website 		Coriell Cat# GM03850, RRID:CVCL_AM66 Homo sapiens (Human) Ehlers-Danlos syndrome Population: Caucasian. PMID:7094393 Finite cell line Female GM3850 Coriell GM03850 CLO:CLO_0015631,
BioSample:SAMN00808564,
Coriell:GM03850,
Wikidata:Q54838268		 CVCL_AM66 2026-07-25 04:32:52 0
GM03882
 
Resource Report
Resource Website 		RRID:CVCL_2S97 Homo sapiens (Human) Karyotypic information: 46,XX,t(3;10)(3pter->3q25::10p15->10pter;10qter->10p15::3q25->3qter) (Coriell=GM03882)., Population: Caucasian. Finite cell line Female CLO:CLO_0016041,
BioSample:SAMN00808589,
Coriell:GM03882,
Wikidata:Q54838297		 CVCL_2S97 2026-07-25 04:32:53 0
GM03861
 
Resource Report
Resource Website 		Coriell Cat# GM03861, RRID:CVCL_1H66 Homo sapiens (Human) Population: Caucasian. Transformed cell line Female Coriell GM03861 CLO:CLO_0015730,
BioSample:SAMN00808573,
Coriell:GM03861,
Wikidata:Q54838280		 CVCL_1H66 2026-07-25 04:32:52 0
GM03847
 
Resource Report
Resource Website 		Coriell Cat# GM03847, RRID:CVCL_2S96 Homo sapiens (Human) Karyotypic information: 46,XX,t(11;22)(11pter->11q23::22q11.2->22qter;22pter->22q11.2::11q23->11qter)mat (Coriell=GM03847)., Population: Caucasian. PMID:10577914 Finite cell line Female Coriell GM03847 CLO:CLO_0015633,
BioSample:SAMN00808563,
Coriell:GM03847,
Wikidata:Q54838267		 CVCL_2S96 2026-07-25 04:32:52 0
GM03865
 
Resource Report
Resource Website 		RRID:CVCL_1H70 Homo sapiens (Human) Huntington's disease Population: Caucasian. Transformed cell line Female CLO:CLO_0015737,
BioSample:SAMN00808577,
Coriell:GM03865,
Wikidata:Q54838284		 CVCL_1H70 2026-07-25 04:32:52 0
GM03851
 
Resource Report
Resource Website 		RRID:CVCL_GY19 Homo sapiens (Human) Leber congenital amaurosis Population: Caucasian. Transformed cell line Female CLO:CLO_0015629,
BioSample:SAMN00808565,
Coriell:GM03851,
Wikidata:Q54838269		 CVCL_GY19 2026-07-25 04:32:52 0
GM03837
 
Resource Report
Resource Website 		RRID:CVCL_AK88 Homo sapiens (Human) Retinitis pigmentosa Population: Caucasian. Finite cell line Female CLO:CLO_0015639,
BioSample:SAMN00808561,
Coriell:GM03837,
Wikidata:Q54838265		 CVCL_AK88 2026-07-25 04:32:52 0
GM03886
 
Resource Report
Resource Website 		Coriell Cat# GM03886, RRID:CVCL_2S98 Homo sapiens (Human) Karyotypic information: 46,XX,t(4;9)(4pter->4q33::9q12->9qter;9pter->9q12::4q33->4qter) (Coriell=GM03886)., Population: Caucasian. Finite cell line Female Coriell GM03886 CLO:CLO_0016012,
BioSample:SAMN00808592,
Coriell:GM03886,
Wikidata:Q54838300		 CVCL_2S98 2026-07-25 04:32:53 0
GM03838
 
Resource Report
Resource Website 		Coriell Cat# GM03838, RRID:CVCL_AK89 Homo sapiens (Human) Retinitis pigmentosa Population: Caucasian. Transformed cell line Female Coriell GM03838 CLO:CLO_0015636,
BioSample:SAMN00808562,
Coriell:GM03838,
Wikidata:Q54838266		 CVCL_AK89 2026-07-25 04:32:52 0
GM03861
 
Resource Report
Resource Website 		RRID:CVCL_1H66 Homo sapiens (Human) Population: Caucasian. Transformed cell line Female CLO:CLO_0015730,
BioSample:SAMN00808573,
Coriell:GM03861,
Wikidata:Q54838280		 CVCL_1H66 2026-07-25 04:32:52 0
GM03911
 
Resource Report
Resource Website 		Coriell Cat# GM03911, RRID:CVCL_AK95 Homo sapiens (Human) Retinitis pigmentosa Population: Caucasian. PMID:6726265 Transformed cell line Female GM 3911, GM03911A Coriell GM03911 CLO:CLO_0016123,
Coriell:GM03911,
Wikidata:Q54838318		 CVCL_AK95 2026-07-25 04:32:53 0
GM03887
 
Resource Report
Resource Website 		RRID:CVCL_X113 Homo sapiens (Human) PMID:6617268
PMID:6661932
PMID:23665875 		Transformed cell line Female GM 3887 CLO:CLO_0016009,
BioSample:SAMN00808593,
Coriell:GM03887,
Wikidata:Q54838301		 CVCL_X113 2026-07-25 04:32:53 0
GM03867
 
Resource Report
Resource Website 		Coriell Cat# GM03867, RRID:CVCL_1H72 Homo sapiens (Human) Huntington's disease Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease., Population: Caucasian. Transformed cell line Female Coriell GM03867 CLO:CLO_0015709,
BioSample:SAMN00808579,
Coriell:GM03867,
Wikidata:Q54838286		 CVCL_1H72 2026-07-25 04:32:52 0
GM03838
 
Resource Report
Resource Website 		RRID:CVCL_AK89 Homo sapiens (Human) Retinitis pigmentosa Population: Caucasian. Transformed cell line Female CLO:CLO_0015636,
BioSample:SAMN00808562,
Coriell:GM03838,
Wikidata:Q54838266		 CVCL_AK89 2026-07-25 04:32:52 0
GM03871
 
Resource Report
Resource Website 		Coriell Cat# GM03871, RRID:CVCL_1H76 Homo sapiens (Human) Population: Caucasian. Transformed cell line Female Coriell GM03871 CLO:CLO_0016030,
BioSample:SAMN00808583,
Coriell:GM03871,
Wikidata:Q54838290		 CVCL_1H76 2026-07-25 04:32:52 0

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