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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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GM04865
 
Resource Report
Resource Website 		RRID:CVCL_1I69 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Male CLO:CLO_0025789,
Coriell:GM04865,
Wikidata:Q54838734		 CVCL_1I69 2026-08-01 05:04:41 0
GM04855
 
Resource Report
Resource Website 		RRID:CVCL_1I61 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. PMID:25928884 Finite cell line Male CLO:CLO_0018188,
Coriell:GM04855,
Wikidata:Q54838722		 CVCL_1I61 2026-08-01 05:04:42 0
GM04927
 
Resource Report
Resource Website 		RRID:CVCL_V477 Homo sapiens (Human) Down syndrome PMID:6661932 Transformed cell line Male GM 4927, GM04927C, GM04927D CLO:CLO_0025600,
Coriell:GM04927,
Wikidata:Q54838764		 CVCL_V477 2026-08-01 05:04:40 0
GM04852
 
Resource Report
Resource Website 		RRID:CVCL_1I58 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Male GM04852A CLO:CLO_0018185,
Coriell:GM04852,
Wikidata:Q54838719		 CVCL_1I58 2026-08-01 05:04:41 0
GM04896
 
Resource Report
Resource Website 		RRID:CVCL_AA36 Homo sapiens (Human) Population: Caucasian. Transformed cell line Female CLO:CLO_0025771,
Coriell:GM04896,
Wikidata:Q54838746		 CVCL_AA36 2026-08-01 05:04:41 0
GM04903
 
Resource Report
Resource Website 		RRID:CVCL_9R23 Homo sapiens (Human) Population: Caucasian. Finite cell line Female CLO:CLO_0025593,
Coriell:GM04903,
Wikidata:Q54838753		 CVCL_9R23 2026-08-01 05:04:42 0
GM04915
 
Resource Report
Resource Website 		RRID:CVCL_1I75 Homo sapiens (Human) Huntington's disease Population: Caucasian. Transformed cell line Male GM04915B CLO:CLO_0025604,
Coriell:GM04915,
Wikidata:Q54838760		 CVCL_1I75 2026-08-01 05:04:44 0
GM04938
 
Resource Report
Resource Website 		Coriell Cat# GM04938, RRID:CVCL_8A07 Homo sapiens (Human) Tourette syndrome Population: Caucasian. Transformed cell line Female Coriell GM04938 CLO:CLO_0025578,
Coriell:GM04938,
Wikidata:Q54838775		 CVCL_8A07 2026-08-01 05:04:41 0
GM04934
 
Resource Report
Resource Website 		Coriell Cat# GM04934, RRID:CVCL_9R26 Homo sapiens (Human) Adrenoleukodystrophy Population: Caucasian. PMID:1634904 Finite cell line Male GM 4934 Coriell GM04934 CLO:CLO_0025576,
Coriell:GM04934,
Wikidata:Q54838772		 CVCL_9R26 2026-08-01 05:04:42 0
GM04867
 
Resource Report
Resource Website 		Coriell Cat# GM04867, RRID:CVCL_1I71 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. PMID:6230415 Finite cell line Male GM 4867 Coriell GM04867 CLO:CLO_0025785,
Coriell:GM04867,
Wikidata:Q54838736		 CVCL_1I71 2026-08-01 05:04:43 0
GM04932
 
Resource Report
Resource Website 		RRID:CVCL_N034 Homo sapiens (Human) Adrenoleukodystrophy Population: Pacific., Part of: Human variation panel. Finite cell line Male GM17386 CLO:CLO_0012164,
CLO:CLO_0025574,
Coriell:GM04932,
Coriell:GM17386,
Wikidata:Q54838770		 CVCL_N034 2026-08-01 05:04:42 0
GM04914
 
Resource Report
Resource Website 		Coriell Cat# GM04914, RRID:CVCL_2Z53 Homo sapiens (Human) Krabbe disease Population: Caucasian; Greek. PMID:3926002 Finite cell line Sex unspecified GM 4914 Coriell GM04914 CLO:CLO_0025607,
Coriell:GM04914,
Wikidata:Q54838759		 CVCL_2Z53 2026-08-01 05:04:40 0
GM04864
 
Resource Report
Resource Website 		RRID:CVCL_1I68 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Male GM04864A CLO:CLO_0025792,
Coriell:GM04864,
Wikidata:Q54838733		 CVCL_1I68 2026-08-01 05:04:39 0
GM04858
 
Resource Report
Resource Website 		RRID:CVCL_1I64 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Male GM04858A, GM04858B CLO:CLO_0025784,
Coriell:GM04858,
Wikidata:Q54838727		 CVCL_1I64 2026-08-01 05:04:43 0
GM04930
 
Resource Report
Resource Website 		Coriell Cat# GM04930, RRID:CVCL_BT16 Homo sapiens (Human) Beta thalassemia Population: African American. Finite cell line Male Coriell GM04930 CLO:CLO_0025599,
Coriell:GM04930,
Wikidata:Q54838766		 CVCL_BT16 2026-08-01 05:04:42 0
GM04854
 
Resource Report
Resource Website 		RRID:CVCL_1I60 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Male GM04854B CLO:CLO_0018187,
Coriell:GM04854,
Wikidata:Q54838721		 CVCL_1I60 2026-08-01 05:04:39 0
GM04904
 
Resource Report
Resource Website 		Coriell Cat# GM04904, RRID:CVCL_9R24 Homo sapiens (Human) Adrenoleukodystrophy Population: Caucasian. PMID:1634904 Finite cell line Male GM 4904, GM04904B Coriell GM04904 CLO:CLO_0025594,
Coriell:GM04904,
Wikidata:Q54838754		 CVCL_9R24 2026-08-01 05:04:42 0
GM04926
 
Resource Report
Resource Website 		Coriell Cat# GM04926, RRID:CVCL_X312 Homo sapiens (Human) Fragile X syndrome Population: Caucasian. Finite cell line Male Coriell GM04926 CLO:CLO_0025603,
Coriell:GM04926,
Wikidata:Q54838763		 CVCL_X312 2026-08-01 05:04:42 0
GM04899
 
Resource Report
Resource Website 		RRID:CVCL_AA39 Homo sapiens (Human) Familial dysautonomia Population: Caucasian. PMID:29762696
PMID:30905397 		Finite cell line Female CLO:CLO_0025597,
Coriell:GM04899,
GEO:GSM3592408,
GEO:GSM3592414,
Wikidata:Q54838749		 CVCL_AA39 2026-08-01 05:04:41 0
GM04895
 
Resource Report
Resource Website 		RRID:CVCL_AA35 Homo sapiens (Human) Population: Caucasian. Finite cell line Female CLO:CLO_0025765,
Coriell:GM04895,
Wikidata:Q54838745		 CVCL_AA35 2026-08-01 05:04:43 0

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