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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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1,669 Results - per page

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GM13940
 
Resource Report
Resource Website 		RRID:CVCL_5Q16 Homo sapiens (Human) PMID:23665875 Transformed cell line Female CLO:CLO_0034026,
BioSample:SAMN00802748,
Coriell:GM13940,
Wikidata:Q54846931		 CVCL_5Q16 2026-09-05 10:57:24 0
GM14043
 
Resource Report
Resource Website 		RRID:CVCL_5Q32 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM14043,
Wikidata:Q54846998		 CVCL_5Q32 2026-09-05 10:57:26 0
GM14033
 
Resource Report
Resource Website 		Coriell Cat# GM14033, RRID:CVCL_5Q31 Homo sapiens (Human) Williams syndrome PMID:23665875 Transformed cell line Female Coriell GM14033 CLO:CLO_0033867,
Coriell:GM14033,
Wikidata:Q54846995		 CVCL_5Q31 2026-09-05 10:57:26 0
GM14033
 
Resource Report
Resource Website 		RRID:CVCL_5Q31 Homo sapiens (Human) Williams syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0033867,
Coriell:GM14033,
Wikidata:Q54846995		 CVCL_5Q31 2026-09-05 10:57:26 0
GM14126
 
Resource Report
Resource Website 		RRID:CVCL_W002 Homo sapiens (Human) Cri du chat syndrome PMID:8004090
PMID:23665875 		Transformed cell line Female JL135 CLO:CLO_0034407,
Coriell:GM14126,
Wikidata:Q54847069		 CVCL_W002 2026-09-05 10:57:27 0
GM14116
 
Resource Report
Resource Website 		Coriell Cat# GM14116, RRID:CVCL_V992 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Male JL27 Coriell GM14116 CLO:CLO_0034419,
Coriell:GM14116,
Wikidata:Q54847059		 CVCL_V992 2026-09-05 10:57:27 0
GM14126
 
Resource Report
Resource Website 		Coriell Cat# GM14126, RRID:CVCL_W002 Homo sapiens (Human) Cri du chat syndrome PMID:8004090
PMID:23665875 		Transformed cell line Female JL135 Coriell GM14126 CLO:CLO_0034407,
Coriell:GM14126,
Wikidata:Q54847069		 CVCL_W002 2026-09-05 10:57:27 0
GM14129
 
Resource Report
Resource Website 		Coriell Cat# GM14129, RRID:CVCL_W005 Homo sapiens (Human) Cri du chat syndrome PMID:8004090
PMID:23665875 		Transformed cell line Male JL139 Coriell GM14129 CLO:CLO_0034390,
Coriell:GM14129,
Wikidata:Q54847073		 CVCL_W005 2026-09-05 10:57:27 0
GM14123
 
Resource Report
Resource Website 		RRID:CVCL_V999 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Female JL70 CLO:CLO_0034432,
Coriell:GM14123,
Wikidata:Q54847066		 CVCL_V999 2026-09-05 10:57:27 0
GM14128
 
Resource Report
Resource Website 		RRID:CVCL_W004 Homo sapiens (Human) Cri du chat syndrome PMID:8004090
PMID:23665875 		Transformed cell line Female JL138 CLO:CLO_0034397,
Coriell:GM14128,
Wikidata:Q54847072		 CVCL_W004 2026-09-05 10:57:27 0
GM14116
 
Resource Report
Resource Website 		RRID:CVCL_V992 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Male JL27 CLO:CLO_0034419,
Coriell:GM14116,
Wikidata:Q54847059		 CVCL_V992 2026-09-05 10:57:27 0
GM14106
 
Resource Report
Resource Website 		Coriell Cat# GM14106, RRID:CVCL_5Q35 Homo sapiens (Human) Hypogonadotropic hypogonadism with anosmia PMID:23665875 Transformed cell line Male Coriell GM14106 CLO:CLO_0034055,
Coriell:GM14106,
Wikidata:Q54847046		 CVCL_5Q35 2026-09-05 10:57:27 0
GM14120
 
Resource Report
Resource Website 		RRID:CVCL_V996 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Female JL54 CLO:CLO_0034427,
Coriell:GM14120,
Wikidata:Q54847063		 CVCL_V996 2026-09-05 10:57:27 0
GM14164
 
Resource Report
Resource Website 		RRID:CVCL_5M47 Homo sapiens (Human) Tetralogy of Fallot PMID:23665875 Transformed cell line Female CLO:CLO_0034357,
Coriell:GM14164,
Wikidata:Q54847088		 CVCL_5M47 2026-09-05 10:57:28 0
GM14131
 
Resource Report
Resource Website 		RRID:CVCL_W007 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Female JL142 CLO:CLO_0034401,
Coriell:GM14131,
Wikidata:Q54847075		 CVCL_W007 2026-09-05 10:57:27 0
GM14127
 
Resource Report
Resource Website 		RRID:CVCL_W003 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Female JL136 CLO:CLO_0034395,
Coriell:GM14127,
Wikidata:Q54847071		 CVCL_W003 2026-09-05 10:57:27 0
GM14123
 
Resource Report
Resource Website 		Coriell Cat# GM14123, RRID:CVCL_V999 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Female JL70 Coriell GM14123 CLO:CLO_0034432,
Coriell:GM14123,
Wikidata:Q54847066		 CVCL_V999 2026-09-05 10:57:27 0
GM14120
 
Resource Report
Resource Website 		Coriell Cat# GM14120, RRID:CVCL_V996 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Female JL54 Coriell GM14120 CLO:CLO_0034427,
Coriell:GM14120,
Wikidata:Q54847063		 CVCL_V996 2026-09-05 10:57:27 0
GM14117
 
Resource Report
Resource Website 		RRID:CVCL_V993 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Male JL30 CLO:CLO_0034422,
Coriell:GM14117,
Wikidata:Q54847060		 CVCL_V993 2026-09-05 10:57:27 0
GM14230
 
Resource Report
Resource Website 		Coriell Cat# GM14230, RRID:CVCL_5Q44 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Line 1110 Coriell GM14230 CLO:CLO_0034263,
Coriell:GM14230,
Wikidata:Q54847111		 CVCL_5Q44 2026-09-05 10:57:28 0

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