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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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256,031 Results - per page

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GM03940
 
Resource Report
Resource Website 		Coriell Cat# GM03940, RRID:CVCL_CY31 Homo sapiens (Human) Familial adenomatous polyposis Donor information: At sampling donor was not affected with familial adenomatous polyposis but at risk for disease., Population: Caucasian. Finite cell line Male Coriell GM03940 CLO:CLO_0016105,
Coriell:GM03940,
Wikidata:Q54838334		 CVCL_CY31 2026-09-12 05:32:35 0
GM03959
 
Resource Report
Resource Website
Possibly Discontinued 		Coriell Cat# GM03959, RRID:CVCL_UR84 Homo sapiens (Human) Friedreich ataxia Transformed cell line Male GM03959A Coriell GM03959 Coriell:GM03959,
Wikidata:Q93586590		 CVCL_UR84 2026-09-12 05:32:35 0
GM04026
 
Resource Report
Resource Website
1+ mentions 		RRID:CVCL_AX77 Homo sapiens (Human) Fragile X syndrome Population: Caucasian. Finite cell line Male CLO:CLO_0016230,
Coriell:GM04026,
Wikidata:Q54838375		 CVCL_AX77 2026-09-12 05:32:36 1
GM04023
 
Resource Report
Resource Website 		RRID:CVCL_1H82 Homo sapiens (Human) Huntington's disease Donor information: At sampling donor was not affected with Huntington disease but at 50% risk for disease., Population: Caucasian. Transformed cell line Female CLO:CLO_0016248,
Coriell:GM04023,
Wikidata:Q54838372		 CVCL_1H82 2026-09-12 05:32:36 0
GM04024
 
Resource Report
Resource Website 		RRID:CVCL_1N27 Homo sapiens (Human) Fragile X syndrome Population: African American. Finite cell line Male GM04024B CLO:CLO_0016245,
Coriell:GM04024,
Wikidata:Q54838373		 CVCL_1N27 2026-09-12 05:32:36 0
GM04139
 
Resource Report
Resource Website 		Coriell Cat# GM04139, RRID:CVCL_2T01 Homo sapiens (Human) Karyotypic information: 46,XX,t(2;13)(2pter->2q31::13q32->13qter;13pter->13q32::2q31->2qter) (Coriell=GM04139)., Population: Caucasian. Finite cell line Female Coriell GM04139 CLO:CLO_0016199,
Coriell:GM04139,
Wikidata:Q54838395		 CVCL_2T01 2026-09-12 05:32:36 0
GM04017
 
Resource Report
Resource Website 		RRID:CVCL_1H79 Homo sapiens (Human) Huntington's disease Population: Caucasian. Transformed cell line Female CLO:CLO_0016239,
Coriell:GM04017,
Wikidata:Q54838367		 CVCL_1H79 2026-09-12 05:32:36 0
GM03923
 
Resource Report
Resource Website 		RRID:CVCL_X116 Homo sapiens (Human) Karyotypic information: 46,X,del(X)(q13;q22) (PubMed=10377420)., Population: Caucasian; English. PMID:6617268
PMID:6661932
PMID:10377420
PMID:23665875 		Finite cell line Female GM 3923, GM3923 CLO:CLO_0016127,
Coriell:GM03923,
Wikidata:Q54838327		 CVCL_X116 2026-09-12 05:32:35 0
GM04081
 
Resource Report
Resource Website 		Coriell Cat# GM04081, RRID:CVCL_0R01 Homo sapiens (Human) Primary carnitine deficiency Population: Caucasian. Finite cell line Male Coriell GM04081 CLO:CLO_0016224,
Coriell:GM04081,
Wikidata:Q54838384		 CVCL_0R01 2026-09-12 05:32:36 0
GM04100
 
Resource Report
Resource Website 		RRID:CVCL_5M90 Homo sapiens (Human) Duchenne muscular dystrophy Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:6726265
PMID:21354051
PMID:23665875 		Transformed cell line Male RB 4100 CLO:CLO_0016212,
Coriell:GM04100,
Wikidata:Q54838387		 CVCL_5M90 2026-09-12 05:32:36 0
GM03931
 
Resource Report
Resource Website 		Coriell Cat# GM03931, RRID:CVCL_9S52 Homo sapiens (Human) Limb-girdle muscular dystrophy type 2A Population: Caucasian. Transformed cell line Male GM03931B Coriell GM03931 CLO:CLO_0016134,
Coriell:GM03931,
Wikidata:Q54838330		 CVCL_9S52 2026-09-12 05:32:35 0
GM03946
 
Resource Report
Resource Website 		RRID:CVCL_CY37 Homo sapiens (Human) Familial adenomatous polyposis Population: Caucasian. Finite cell line Female CLO:CLO_0016111,
Coriell:GM03946,
Wikidata:Q54838341		 CVCL_CY37 2026-09-12 05:32:35 0
GM04053
 
Resource Report
Resource Website 		Coriell Cat# GM04053, RRID:CVCL_V240 Ovis aries (Sheep) Finite cell line Female Coriell GM04053 CLO:CLO_0016220,
Coriell:GM04053,
Wikidata:Q54838380		 CVCL_V240 2026-09-12 05:32:36 0
GM04033
 
Resource Report
Resource Website 		RRID:CVCL_7405 Homo sapiens (Human) Dystrophia myotonica 1 Population: Caucasian. Finite cell line Male DMPK CTG1000, DMPK CTG(1000) CLO:CLO_0016231,
Coriell:GM04033,
Wikidata:Q54838376		 CVCL_7405 2026-09-12 05:32:36 0
GM03942
 
Resource Report
Resource Website 		RRID:CVCL_CY33 Homo sapiens (Human) Familial adenomatous polyposis Donor information: At sampling donor was not affected with familial adenomatous polyposis but at significant risk for disease., Population: Caucasian. Finite cell line Female CLO:CLO_0016107,
Coriell:GM03942,
Wikidata:Q54838337		 CVCL_CY33 2026-09-12 05:32:35 0
GM04111
 
Resource Report
Resource Website 		RRID:CVCL_X302 Homo sapiens (Human) Karyotypic information: 46,XX,t(4;5)(4pter->4q31.1::5p15->5pter;5qter->5p15::4q31.1->4qter),del(21)(qter->p11) (Coriell=GM04111)., Population: Caucasian. PMID:6661932 Finite cell line Female GM 4111 CLO:CLO_0016201,
Coriell:GM04111,
Wikidata:Q54838390		 CVCL_X302 2026-09-12 05:32:36 0
GM03997
 
Resource Report
Resource Website 		Coriell Cat# GM03997, RRID:CVCL_5M88 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM03997 CLO:CLO_0016075,
Coriell:GM03997,
Wikidata:Q54838363		 CVCL_5M88 2026-09-12 05:32:35 0
GM03999
 
Resource Report
Resource Website 		Coriell Cat# GM03999, RRID:CVCL_X117 Homo sapiens (Human) Population: African American. PMID:6617268
PMID:6661932
PMID:23665875 		Finite cell line Female GM 3999 Coriell GM03999 CLO:CLO_0016070,
Coriell:GM03999,
Wikidata:Q54838365		 CVCL_X117 2026-09-12 05:32:36 0
GM04125
 
Resource Report
Resource Website 		Coriell Cat# GM04125, RRID:CVCL_1Q58 Homo sapiens (Human) Karyotypic information: 46,XY,t(15;18)(15pter->15q15::18p11.3->18pter;18qter->18p11.3::15q15->15qter) (Coriell=GM04125)., Population: Caucasian. Finite cell line Male Coriell GM04125 CLO:CLO_0016208,
Coriell:GM04125,
Wikidata:Q54838391		 CVCL_1Q58 2026-09-12 05:32:36 0
GM03928
 
Resource Report
Resource Website 		Coriell Cat# GM03928, RRID:CVCL_N013 Homo sapiens (Human) Dystrophia myotonica 1 Population: Caucasian., Part of: Human variation panel. Transformed cell line Female GM18013 Coriell GM03928 CLO:CLO_0016014,
CLO:CLO_0016138,
Coriell:GM03928,
Coriell:GM18013,
Wikidata:Q54838328		 CVCL_N013 2026-09-12 05:32:35 0

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