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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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  • References:pmid:23665875 (facet)

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GM50125
 
Resource Report
Resource Website 		Coriell Cat# GM50125, RRID:CVCL_0F94 Homo sapiens (Human) Deletion 18q syndrome PMID:8488839
PMID:23665875 		Transformed cell line Female JL209 Coriell GM50125 CLO:CLO_0014669,
Coriell:GM50125,
Wikidata:Q54854210		 CVCL_0F94 2026-09-19 05:33:10 0
GM50167
 
Resource Report
Resource Website 		Coriell Cat# GM50167, RRID:CVCL_0G61 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Female JL333 Coriell GM50167 CLO:CLO_0015017,
Coriell:GM50167,
Wikidata:Q54854240		 CVCL_0G61 2026-09-19 05:33:11 0
GM50167
 
Resource Report
Resource Website 		RRID:CVCL_0G61 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Female JL333 CLO:CLO_0015017,
Coriell:GM50167,
Wikidata:Q54854240		 CVCL_0G61 2026-09-19 05:33:11 0
GM50145
 
Resource Report
Resource Website 		RRID:CVCL_5L25 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male JL268 CLO:CLO_0014679,
Coriell:GM50145,
Wikidata:Q54854219		 CVCL_5L25 2026-09-19 05:33:10 0
GM50126
 
Resource Report
Resource Website 		Coriell Cat# GM50126, RRID:CVCL_0G80 Homo sapiens (Human) Holoprosencephaly PMID:7485158
PMID:23665875 		Transformed cell line Female JL219 Coriell GM50126 CLO:CLO_0014670,
Coriell:GM50126,
Wikidata:Q54854211		 CVCL_0G80 2026-09-19 05:33:10 0
GM50153
 
Resource Report
Resource Website 		Coriell Cat# GM50153, RRID:CVCL_5L27 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Female JL284 Coriell GM50153 CLO:CLO_0014710,
Coriell:GM50153,
Wikidata:Q54854226		 CVCL_5L27 2026-09-19 05:33:11 0
GM50120
 
Resource Report
Resource Website 		Coriell Cat# GM50120, RRID:CVCL_0F88 Homo sapiens (Human) Deletion 18q syndrome PMID:8488839
PMID:23665875 		Transformed cell line Female JL181 Coriell GM50120 CLO:CLO_0014750,
Coriell:GM50120,
Wikidata:Q54854206		 CVCL_0F88 2026-09-19 05:33:10 0
GM50166
 
Resource Report
Resource Website 		RRID:CVCL_5T54 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Male Coriell:GM50166,
Wikidata:Q54854239		 CVCL_5T54 2026-09-19 05:33:11 0
GM50147
 
Resource Report
Resource Website 		RRID:CVCL_5T50 Homo sapiens (Human) PMID:23665875 Transformed cell line Female JL273 CLO:CLO_0014683,
Coriell:GM50147,
Wikidata:Q54854221		 CVCL_5T50 2026-09-19 05:33:10 0
GM50176
 
Resource Report
Resource Website 		Coriell Cat# GM50176, RRID:CVCL_5L34 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male JL369 Coriell GM50176 CLO:CLO_0015011,
Coriell:GM50176,
Wikidata:Q54854248		 CVCL_5L34 2026-09-19 05:33:11 0
GM50163
 
Resource Report
Resource Website 		Coriell Cat# GM50163, RRID:CVCL_0H56 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Female JL317 Coriell GM50163 CLO:CLO_0014722,
Coriell:GM50163,
Wikidata:Q54854235		 CVCL_0H56 2026-09-19 05:33:11 0
GM50113
 
Resource Report
Resource Website 		RRID:CVCL_0F90 Homo sapiens (Human) Deletion 18q syndrome PMID:8488839
PMID:23665875 		Transformed cell line Female JL143 CLO:CLO_0014755,
Coriell:GM50113,
Wikidata:Q54854201		 CVCL_0F90 2026-09-19 05:33:10 0
GM50118
 
Resource Report
Resource Website 		RRID:CVCL_0F98 Homo sapiens (Human) Deletion 18q syndrome PMID:8488839
PMID:23665875 		Transformed cell line Male JL172 CLO:CLO_0014758,
Coriell:GM50118,
Wikidata:Q54854205		 CVCL_0F98 2026-09-19 05:33:10 0
GM50193
 
Resource Report
Resource Website 		Coriell Cat# GM50193, RRID:CVCL_5L36 Homo sapiens (Human) Deletion 18p syndrome PMID:23665875 Transformed cell line Female JL451 Coriell GM50193 CLO:CLO_0014989,
Coriell:GM50193,
Wikidata:Q54854256		 CVCL_5L36 2026-09-19 05:33:12 0
GM50204
 
Resource Report
Resource Website 		RRID:CVCL_5T57 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Male Coriell:GM50204,
Wikidata:Q54854258		 CVCL_5T57 2026-09-19 05:33:12 0
GM50275
 
Resource Report
Resource Website 		Coriell Cat# GM50275, RRID:CVCL_5T61 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM50275 Coriell:GM50275,
Wikidata:Q54854262		 CVCL_5T61 2026-09-19 05:33:12 0
GM50204
 
Resource Report
Resource Website 		Coriell Cat# GM50204, RRID:CVCL_5T57 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Male Coriell GM50204 Coriell:GM50204,
Wikidata:Q54854258		 CVCL_5T57 2026-09-19 05:33:12 0
GM50323
 
Resource Report
Resource Website 		RRID:CVCL_1U18 Homo sapiens (Human) PMID:23665875 Transformed cell line Female JL92 CLO:CLO_0012520,
Coriell:GM50323,
Wikidata:Q54854269		 CVCL_1U18 2026-09-19 05:33:12 0
GM50178
 
Resource Report
Resource Website 		RRID:CVCL_0G67 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Female JL378 CLO:CLO_0014986,
Coriell:GM50178,
Wikidata:Q54854249		 CVCL_0G67 2026-09-19 05:33:11 0
GM50324
 
Resource Report
Resource Website 		Coriell Cat# GM50324, RRID:CVCL_5T64 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM50324 Coriell:GM50324,
Wikidata:Q54854270		 CVCL_5T64 2026-09-19 05:33:12 0

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