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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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GM04326
 
Resource Report
Resource Website 		RRID:CVCL_0Q83 Homo sapiens (Human) Citrullinemia type I Population: Caucasian. Finite cell line Female GM4326 CLO:CLO_0019535,
Coriell:GM04326,
Wikidata:Q54838484		 CVCL_0Q83 Cellosaurus 2026-09-26 06:49:15 0
GM04426
 
Resource Report
Resource Website 		RRID:CVCL_9Y79 Homo sapiens (Human) Albright's hereditary osteodystrophy Transformed cell line Male CLO:CLO_0019681,
Coriell:GM04426,
Wikidata:Q54838523		 CVCL_9Y79 Cellosaurus 2026-09-26 06:49:16 0
GM04426
 
Resource Report
Resource Website 		Coriell Cat# GM04426, RRID:CVCL_9Y79 Homo sapiens (Human) Albright's hereditary osteodystrophy Transformed cell line Male Coriell GM04426 CLO:CLO_0019681,
Coriell:GM04426,
Wikidata:Q54838523		 CVCL_9Y79 Cellosaurus 2026-09-26 06:49:16 0
GM04504
 
Resource Report
Resource Website 		RRID:CVCL_7411 Homo sapiens (Human) Donor information: Established from monozygotic twin of GM04503 (Cellosaurus=CVCL_7410)., Part of: ENCODE project common cell types; tier 3. PMID:30567591 Finite cell line Female GM04504A, HF23 CLO:CLO_0018812,
Coriell:GM04504,
ENCODE:ENCBS016ENC,
ENCODE:ENCBS388KHM,
GEO:GSM3124652,
Wikidata:Q54838544		 CVCL_7411 Cellosaurus 2026-09-26 06:49:17 0
GM04516
 
Resource Report
Resource Website 		Coriell Cat# GM04516, RRID:CVCL_AW70 Homo sapiens (Human) Sideroblastic anemia Population: Caucasian. Finite cell line Female Coriell GM04516 CLO:CLO_0018850,
Coriell:GM04516,
Wikidata:Q54838554		 CVCL_AW70 Cellosaurus 2026-09-26 06:49:17 0
GM04428
 
Resource Report
Resource Website 		Coriell Cat# GM17067, RRID:CVCL_N018 Homo sapiens (Human) Albright's hereditary osteodystrophy Population: Mexican., Part of: Human variation panel. Transformed cell line Male GM17067 Coriell GM17067 CLO:CLO_0014566,
CLO:CLO_0019689,
Coriell:GM04428,
Coriell:GM17067,
Wikidata:Q54838525		 CVCL_N018 Cellosaurus 2026-09-26 06:49:16 0
GM04589
 
Resource Report
Resource Website 		RRID:CVCL_AA25 Homo sapiens (Human) Familial dysautonomia Population: Caucasian. PMID:29762696
PMID:30905397 		Finite cell line Male CLO:CLO_0018883,
Coriell:GM04589,
GEO:GSM3592405,
GEO:GSM3592411,
Wikidata:Q54838577		 CVCL_AA25 Cellosaurus 2026-09-26 06:49:17 0
GM04514
 
Resource Report
Resource Website 		RRID:CVCL_X308 Homo sapiens (Human) Population: Caucasian. PMID:6661932 Finite cell line Female GM 4514 CLO:CLO_0018832,
Coriell:GM04514,
Wikidata:Q54838552		 CVCL_X308 Cellosaurus 2026-09-26 06:49:17 0
GM04601
 
Resource Report
Resource Website 		RRID:CVCL_Y793 Homo sapiens (Human) Dystrophia myotonica 1 Population: Caucasian. Finite cell line Female CLO:CLO_0018919,
Coriell:GM04601,
Wikidata:Q54838587		 CVCL_Y793 Cellosaurus 2026-09-26 06:49:18 0
GM04516
 
Resource Report
Resource Website 		RRID:CVCL_AW70 Homo sapiens (Human) Sideroblastic anemia Population: Caucasian. Finite cell line Female CLO:CLO_0018850,
Coriell:GM04516,
Wikidata:Q54838554		 CVCL_AW70 Cellosaurus 2026-09-26 06:49:17 0
GM04505
 
Resource Report
Resource Website 		Coriell Cat# GM04505, RRID:CVCL_7412 Homo sapiens (Human) Donor information: Established from monozygotic twin of GM04506 (Cellosaurus=CVCL_7413)., Population: Caucasian. PMID:30567591 Finite cell line Female GM04505A, HF24 Coriell GM04505 CLO:CLO_0018816,
Coriell:GM04505,
GEO:GSM3124650,
Wikidata:Q54838545		 CVCL_7412 Cellosaurus 2026-09-26 06:49:17 0
GM04476
 
Resource Report
Resource Website 		Coriell Cat# GM04476, RRID:CVCL_V339 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Male Coriell GM04476 CLO:CLO_0019665,
Coriell:GM04476,
Wikidata:Q54838530		 CVCL_V339 Cellosaurus 2026-09-26 06:49:16 0
GM04599
 
Resource Report
Resource Website
Possibly Discontinued 		Coriell Cat# GM04599, RRID:CVCL_0L60 Homo sapiens (Human) Population: African American. Finite cell line Male GM04599A Coriell GM04599 Coriell:GM04599,
Wikidata:Q54838586		 CVCL_0L60 Cellosaurus 2026-09-26 06:49:18 0
GM04535
 
Resource Report
Resource Website 		Coriell Cat# GM17053, RRID:CVCL_N019 Homo sapiens (Human) Phosphoglycerate kinase 1 deficiency Population: Japanese., Part of: Human variation panel. Transformed cell line Male GM17053 Coriell GM17053 CLO:CLO_0014663,
CLO:CLO_0018864,
Coriell:GM04535,
Coriell:GM17053,
Wikidata:Q54838561		 CVCL_N019 Cellosaurus 2026-09-26 06:49:17 0
GM04593
 
Resource Report
Resource Website 		RRID:CVCL_DB60 Homo sapiens (Human) Population: Caucasian. Finite cell line Male CLO:CLO_0018889,
Coriell:GM04593,
Wikidata:Q54838579		 CVCL_DB60 Cellosaurus 2026-09-26 06:49:17 0
GM04496
 
Resource Report
Resource Website 		Coriell Cat# GM04496, RRID:CVCL_9R20 Homo sapiens (Human) Adrenoleukodystrophy PMID:1634904
PMID:21721033 		Finite cell line Male GM 4496 Coriell GM04496 CLO:CLO_0019670,
Coriell:GM04496,
Wikidata:Q54838539		 CVCL_9R20 Cellosaurus 2026-09-26 06:49:17 0
GM04603
 
Resource Report
Resource Website 		Coriell Cat# GM04603, RRID:CVCL_Y795 Homo sapiens (Human) Population: Caucasian. Finite cell line Male Coriell GM04603 CLO:CLO_0018909,
Coriell:GM04603,
Wikidata:Q54838589		 CVCL_Y795 Cellosaurus 2026-09-26 06:49:18 0
GM04592
 
Resource Report
Resource Website
1+ mentions 		RRID:CVCL_V473 Homo sapiens (Human) Down syndrome Population: Caucasian. PMID:6661932
PMID:23665875 		Finite cell line Female GM 4592, GM04592A CLO:CLO_0018882,
Coriell:GM04592,
Wikidata:Q54838578		 CVCL_V473 Cellosaurus 2026-09-26 06:49:17 1
GM04595
 
Resource Report
Resource Website 		RRID:CVCL_GY22 Homo sapiens (Human) Charcot-Marie-Tooth neuropathy X type 1 Population: Caucasian. Finite cell line Female CLO:CLO_0018887,
Coriell:GM04595,
Wikidata:Q54838581		 CVCL_GY22 Cellosaurus 2026-09-26 06:49:18 0
GM04535
 
Resource Report
Resource Website 		RRID:CVCL_N019 Homo sapiens (Human) Phosphoglycerate kinase 1 deficiency Population: Japanese., Part of: Human variation panel. Transformed cell line Male GM17053 CLO:CLO_0014663,
CLO:CLO_0018864,
Coriell:GM04535,
Coriell:GM17053,
Wikidata:Q54838561		 CVCL_N019 Cellosaurus 2026-09-26 06:49:17 0

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