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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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GM04203
 
Resource Report
Resource Website 		Coriell Cat# GM04203, RRID:CVCL_1H97 Homo sapiens (Human) Huntington's disease Donor information: At sampling donor was not affected with Huntington disease but at low risk for disease., Population: Caucasian. PMID:6316146 Transformed cell line Female Coriell GM04203 CLO:CLO_0019495,
Coriell:GM04203,
Wikidata:Q54838419		 CVCL_1H97 2026-07-25 04:32:56 0
GM04240
 
Resource Report
Resource Website 		Coriell Cat# GM04240, RRID:CVCL_2T02 Homo sapiens (Human) Karyotypic information: 46,XX,t(4;6)(4pter->4q25::6p25->6pter;6qter->6p25::4q25->4qter) (Coriell=GM04240)., Population: Caucasian. Finite cell line Female Coriell GM04240 CLO:CLO_0019480,
Coriell:GM04240,
Wikidata:Q54838452		 CVCL_2T02 2026-07-25 04:32:56 0
GM04188
 
Resource Report
Resource Website 		Coriell Cat# GM04188, RRID:CVCL_1H83 Homo sapiens (Human) Karyotypic information: 46,XX,t(6;19)(6pter->6q13::19p13.3->19pter;19qter->19p13.3::6q13->6qter) [8]; 46,XX,t(7;22)(7qter->7p15::22q13->22qter;22pter->22q13::7p15>-7pter),del(qter->12)(p13) [4]; 46,XX [38] (Coriell=GM04188)., Population: Caucasian. PMID:6316146 Finite cell line Female Coriell GM04188 CLO:CLO_0015927,
Coriell:GM04188,
Wikidata:Q54838400		 CVCL_1H83 2026-07-25 04:32:55 0
GM04390
 
Resource Report
Resource Website 		Coriell Cat# GM04390, RRID:CVCL_7407 Homo sapiens (Human) Population: Caucasian. PMID:7847674
PMID:8246632
PMID:8650226 		Finite cell line Female GM4390, GM 04390, GM04390A Coriell GM04390 CLO:CLO_0019332,
Coriell:GM04390,
Wikidata:Q54838509		 CVCL_7407 2026-07-25 04:32:58 0
GM04390
 
Resource Report
Resource Website 		RRID:CVCL_7407 Homo sapiens (Human) Population: Caucasian. PMID:7847674
PMID:8246632
PMID:8650226 		Finite cell line Female GM4390, GM 04390, GM04390A CLO:CLO_0019332,
Coriell:GM04390,
Wikidata:Q54838509		 CVCL_7407 2026-07-25 04:32:58 0
GM04338
 
Resource Report
Resource Website 		Coriell Cat# GM04338, RRID:CVCL_0M29 Homo sapiens (Human) Population: Caucasian. Finite cell line Female Coriell GM04338 CLO:CLO_0019579,
Coriell:GM04338,
Wikidata:Q54838492		 CVCL_0M29 2026-07-25 04:32:57 0
GM04282
 
Resource Report
Resource Website 		RRID:CVCL_F113 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection., Part of: Genetic Testing Reference Material (GeT-RM) samples. Transformed cell line Female GM04282A CLO:CLO_0019590,
Coriell:GM04282,
Wikidata:Q54838464		 CVCL_F113 2026-07-25 04:32:57 0
GM04311
 
Resource Report
Resource Website 		RRID:CVCL_AY61 Homo sapiens (Human) Carbamoyl-phosphate synthetase I deficiency Population: Caucasian. Finite cell line Female GM4311 CLO:CLO_0019620,
Coriell:GM04311,
Wikidata:Q54838477		 CVCL_AY61 2026-07-25 04:32:57 0
GM04263
 
Resource Report
Resource Website 		Coriell Cat# GM04263, RRID:CVCL_GT50 Homo sapiens (Human) Hypophosphatasia Population: Caucasian. Finite cell line Female Coriell GM04263 CLO:CLO_0019612,
Coriell:GM04263,
Wikidata:Q54838456		 CVCL_GT50 2026-07-25 04:32:57 0
GM04300
 
Resource Report
Resource Website 		Coriell Cat# GM04300, RRID:CVCL_N016 Homo sapiens (Human) Intellectual developmental disorder Population: Indian., Part of: Human variation panel. PMID:23665875 Finite cell line Female GM17023 Coriell GM04300 CLO:CLO_0014707,
CLO:CLO_0019627,
Coriell:GM04300,
Coriell:GM17023,
Wikidata:Q54838473		 CVCL_N016 2026-07-25 04:32:57 0
GM04300
 
Resource Report
Resource Website 		RRID:CVCL_N016 Homo sapiens (Human) Intellectual developmental disorder Population: Indian., Part of: Human variation panel. PMID:23665875 Finite cell line Female GM17023 CLO:CLO_0014707,
CLO:CLO_0019627,
Coriell:GM04300,
Coriell:GM17023,
Wikidata:Q54838473		 CVCL_N016 2026-07-25 04:32:57 0
GM04370
 
Resource Report
Resource Website 		Coriell Cat# GM04370, RRID:CVCL_X304 Homo sapiens (Human) Intellectual developmental disorder Karyotypic information: 47,XX,+der(22)(22pter->22q11::11q23->11qter)mat (Coriell=GM04370)., Population: Caucasian. PMID:6661932
PMID:10577914 		Finite cell line Female GM 4370, GM04370A Coriell GM04370 CLO:CLO_0019310,
Coriell:GM04370,
Wikidata:Q54838501		 CVCL_X304 2026-07-25 04:32:58 0
GM04340
 
Resource Report
Resource Website 		Coriell Cat# GM04340, RRID:CVCL_N017 Homo sapiens (Human) Zellweger syndrome Population: Caucasian; Iberian., Part of: Human variation panel. Finite cell line Female GM 04340, GM4340, GM04340A, GM17092 Coriell GM04340 CLO:CLO_0014524,
CLO:CLO_0019565,
Coriell:GM04340,
Coriell:GM17092,
Wikidata:Q54838494		 CVCL_N017 2026-07-25 04:32:57 0
GM04289
 
Resource Report
Resource Website
Possibly Discontinued 		RRID:CVCL_US61 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Female GM04289C Coriell:GM04289,
Wikidata:Q93587500		 CVCL_US61 2026-07-25 04:32:57 0
GM04363
 
Resource Report
Resource Website 		RRID:CVCL_5M94 Homo sapiens (Human) Population: Caucasian. Finite cell line Female CLO:CLO_0019311,
Coriell:GM04363,
Wikidata:Q54838498		 CVCL_5M94 2026-07-25 04:32:57 0
GM04411
 
Resource Report
Resource Website 		Coriell Cat# GM04411, RRID:CVCL_9Y77 Homo sapiens (Human) Albright's hereditary osteodystrophy Transformed cell line Female GM04411A Coriell GM04411 CLO:CLO_0019709,
Coriell:GM04411,
Wikidata:Q54838518		 CVCL_9Y77 2026-07-25 04:32:58 0
GM04323
 
Resource Report
Resource Website 		RRID:CVCL_0M25 Homo sapiens (Human) Population: Caucasian. Finite cell line Female CLO:CLO_0019534,
Coriell:GM04323,
Wikidata:Q54838483		 CVCL_0M25 2026-07-25 04:32:57 0
GM04338
 
Resource Report
Resource Website 		RRID:CVCL_0M29 Homo sapiens (Human) Population: Caucasian. Finite cell line Female CLO:CLO_0019579,
Coriell:GM04338,
Wikidata:Q54838492		 CVCL_0M29 2026-07-25 04:32:57 0
GM04311
 
Resource Report
Resource Website 		Coriell Cat# GM04311, RRID:CVCL_AY61 Homo sapiens (Human) Carbamoyl-phosphate synthetase I deficiency Population: Caucasian. Finite cell line Female GM4311 Coriell GM04311 CLO:CLO_0019620,
Coriell:GM04311,
Wikidata:Q54838477		 CVCL_AY61 2026-07-25 04:32:57 0
GM04307
 
Resource Report
Resource Website 		Coriell Cat# GM04307, RRID:CVCL_CZ83 Homo sapiens (Human) Population: Caucasian. Finite cell line Female Coriell GM04307 CLO:CLO_0019625,
Coriell:GM04307,
Wikidata:Q54838476		 CVCL_CZ83 2026-07-25 04:32:57 0

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