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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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GM10526
 
Resource Report
Resource Website 		Coriell Cat# GM10526, RRID:CVCL_AM42 Homo sapiens (Human) Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection. Transformed cell line Male Coriell GM10526 CLO:CLO_0024265,
BioSample:SAMN00800063,
Coriell:GM10526,
Wikidata:Q54844524		 CVCL_AM42 2026-08-15 04:31:06 0
GM10568
 
Resource Report
Resource Website 		Coriell Cat# GM10568, RRID:CVCL_5P20 Homo sapiens (Human) Dyggve-Melchior-Clausen syndrome Population: Pakistani. Finite cell line Male Coriell GM10568 CLO:CLO_0024287,
BioSample:SAMN00800093,
Coriell:GM10568,
Wikidata:Q54844546		 CVCL_5P20 2026-08-15 04:31:07 0
GM10537
 
Resource Report
Resource Website 		Coriell Cat# GM10537, RRID:CVCL_AM52 Homo sapiens (Human) Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection. Transformed cell line Female Coriell GM10537 CLO:CLO_0024298,
BioSample:SAMN00800081,
Coriell:GM10537,
Wikidata:Q54844534		 CVCL_AM52 2026-08-15 04:31:06 0
GM10641
 
Resource Report
Resource Website 		RRID:CVCL_N151 Homo sapiens (Human) Sjogren-Larsson syndrome Population: South American (Andes)., Part of: Human variation panel. Finite cell line Female GM17305 CLO:CLO_0013314,
CLO:CLO_0024560,
BioSample:SAMN00800124,
Coriell:GM10641,
Coriell:GM17305,
Wikidata:Q54844568		 CVCL_N151 2026-08-15 04:31:07 0
GM10531
 
Resource Report
Resource Website 		Coriell Cat# GM10531, RRID:CVCL_AM46 Homo sapiens (Human) Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection. Transformed cell line Male Coriell GM10531 CLO:CLO_0024259,
BioSample:SAMN00800071,
Coriell:GM10531,
Wikidata:Q54844528		 CVCL_AM46 2026-08-15 04:31:06 0
GM10559
 
Resource Report
Resource Website 		Coriell Cat# GM10559, RRID:CVCL_0Q12 Homo sapiens (Human) Marfan syndrome Transformed cell line Female Coriell GM10559 CLO:CLO_0024291,
BioSample:SAMN00800087,
Coriell:GM10559,
Wikidata:Q54844543		 CVCL_0Q12 2026-08-15 04:31:07 0
GM10565
 
Resource Report
Resource Website 		RRID:CVCL_5P19 Homo sapiens (Human) Hypogonadotropic hypogonadism with anosmia PMID:23665875 Transformed cell line Male CLO:CLO_0024289,
BioSample:SAMN00800089,
Coriell:GM10565,
Wikidata:Q54844544		 CVCL_5P19 2026-08-15 04:31:07 0
GM10540
 
Resource Report
Resource Website 		Coriell Cat# GM10540, RRID:CVCL_7502 Homo sapiens (Human) Population: Pacific., Part of: Yale-Stanford Collection from NIGMS Human Genetic Cell Repository., Part of: Human variation panel. PMID:14583597 Transformed cell line Male GM17388, JK965 Coriell GM10540 CLO:CLO_0012179,
CLO:CLO_0024297,
Coriell:GM10540,
Coriell:GM17388,
Wikidata:Q54844537		 CVCL_7502 2026-08-15 04:31:06 0
GM10679
 
Resource Report
Resource Website 		Coriell Cat# GM10679, RRID:CVCL_9S97 Homo sapiens (Human) Karyotypic information: 47,XY,+i(12)(pter->p10::p10->pter) [37]; 46,XY [13] (Coriell=GM10679)., Population: Caucasian. Finite cell line Male Coriell GM10679 CLO:CLO_0024618,
BioSample:SAMN00800148,
Coriell:GM10679,
Wikidata:Q54844587		 CVCL_9S97 2026-08-15 04:31:08 0
GM10720
 
Resource Report
Resource Website 		Coriell Cat# GM10720, RRID:CVCL_1Y47 Homo sapiens (Human) Sandhoff disease Transformed cell line Female Coriell GM10720 CLO:CLO_0023706,
BioSample:SAMN00800180,
Coriell:GM10720,
Wikidata:Q54844623		 CVCL_1Y47 2026-08-15 04:31:09 0
GM10681
 
Resource Report
Resource Website 		RRID:CVCL_AD72 Homo sapiens (Human) Transformed cell line Female CLO:CLO_0024613,
BioSample:SAMN00800152,
Coriell:GM10681,
Wikidata:Q54844589		 CVCL_AD72 2026-08-15 04:31:08 0
GM10720
 
Resource Report
Resource Website 		RRID:CVCL_1Y47 Homo sapiens (Human) Sandhoff disease Transformed cell line Female CLO:CLO_0023706,
BioSample:SAMN00800180,
Coriell:GM10720,
Wikidata:Q54844623		 CVCL_1Y47 2026-08-15 04:31:09 0
GM10659
 
Resource Report
Resource Website 		Coriell Cat# GM10659, RRID:CVCL_1R98 Homo sapiens (Human) Characteristics: Hybrid for chromosomes 15 and 17 mapping (PubMed=9441767)., Group: Human/rodent somatic cell hybrid. PMID:3130306
PMID:9441767 		Hybrid cell line P12.3B6 Coriell GM10659 CLO:CLO_0024584,
Coriell:GM10659,
Wikidata:Q54844576		 cvcl_f739 CVCL_1R98 2026-08-15 04:31:07 0
GM10647
 
Resource Report
Resource Website 		Coriell Cat# GM10647, RRID:CVCL_N152 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:1897572
PMID:20889555
PMID:29959025 		Transformed cell line Male GM17295 Coriell GM10647 CLO:CLO_0013127,
CLO:CLO_0024575,
BioSample:SAMN00800128,
Coriell:GM10647,
Coriell:GM17295,
GEO:GSM569743,
GEO:GSM596359,
GEO:GSM596816,
GEO:GSM924897,
Wikidata:Q54844570		 CVCL_N152 2026-08-15 04:31:07 0
GM10657
 
Resource Report
Resource Website 		RRID:CVCL_1R97 Homo sapiens (Human) Characteristics: Hybrid for chromosome 17 mapping (PubMed=9441767)., Group: Human/rodent somatic cell hybrid. PMID:3130306
PMID:9441767 		Hybrid cell line JW-4 CLO:CLO_0024582,
Coriell:GM10657,
Wikidata:Q54844575		 cvcl_f739 CVCL_1R97 2026-08-15 04:31:07 0
GM10649
 
Resource Report
Resource Website
Possibly Discontinued 		Coriell Cat# GM10649, RRID:CVCL_UR80 Homo sapiens (Human) Osteochondrodysplasia PMID:1897572 Finite cell line Female Coriell GM10649 Coriell:GM10649,
Wikidata:Q93810070		 CVCL_UR80 2026-08-15 04:31:07 0
GM10648
 
Resource Report
Resource Website 		RRID:CVCL_DB76 Homo sapiens (Human) PMID:1897572 Transformed cell line Female CLO:CLO_0024574,
BioSample:SAMN00800130,
Coriell:GM10648,
Wikidata:Q54844571		 CVCL_DB76 2026-08-15 04:31:07 0
GM10710
 
Resource Report
Resource Website 		Coriell Cat# GM10710, RRID:CVCL_AD73 Homo sapiens (Human) Transformed cell line Female Coriell GM10710 CLO:CLO_0023729,
BioSample:SAMN00800170,
Coriell:GM10710,
Wikidata:Q54844614		 CVCL_AD73 2026-08-15 04:31:08 0
GM10691
 
Resource Report
Resource Website 		RRID:CVCL_V053 Homo sapiens (Human) Marfan syndrome Transformed cell line Male GM10691A CLO:CLO_0024622,
BioSample:SAMN00800158,
Coriell:GM10691,
Wikidata:Q54844592		 CVCL_V053 2026-08-15 04:31:08 0
GM10718
 
Resource Report
Resource Website 		Coriell Cat# GM10718, RRID:CVCL_1Y45 Homo sapiens (Human) Sandhoff disease Transformed cell line Male Coriell GM10718 CLO:CLO_0023711,
BioSample:SAMN00800176,
Coriell:GM10718,
Wikidata:Q54844621		 CVCL_1Y45 2026-08-15 04:31:09 0

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