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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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GM09789
 
Resource Report
Resource Website 		RRID:CVCL_AA94 Homo sapiens (Human) Familial dysautonomia Population: Jewish; Ashkenazi. Transformed cell line Male CLO:CLO_0030462,
Coriell:GM09789,
Wikidata:Q54844058		 CVCL_AA94 2026-08-01 05:05:51 0
GM09793
 
Resource Report
Resource Website 		RRID:CVCL_AA98 Homo sapiens (Human) Population: Jewish; Ashkenazi. Transformed cell line Male GM09793A CLO:CLO_0030466,
Coriell:GM09793,
Wikidata:Q54844062		 CVCL_AA98 2026-08-01 05:05:52 0
GM09822
 
Resource Report
Resource Website 		Coriell Cat# GM09822, RRID:CVCL_GT53 Homo sapiens (Human) Transformed cell line Female Coriell GM09822 CLO:CLO_0030659,
Coriell:GM09822,
Wikidata:Q54844077		 CVCL_GT53 2026-08-01 05:05:52 0
GM09832
 
Resource Report
Resource Website 		Coriell Cat# GM09832, RRID:CVCL_GT54 Homo sapiens (Human) Hereditary hemorrhagic telangiectasia Transformed cell line Female Coriell GM09832 CLO:CLO_0030636,
Coriell:GM09832,
Wikidata:Q54844085		 CVCL_GT54 2026-08-01 05:05:52 0
GM09763
 
Resource Report
Resource Website 		RRID:CVCL_AL90 Homo sapiens (Human) Retinitis pigmentosa Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection. PMID:10391211 Transformed cell line Male CLO:CLO_0030544,
Coriell:GM09763,
Wikidata:Q54844029		 CVCL_AL90 2026-08-01 05:05:50 0
GM09768
 
Resource Report
Resource Website 		RRID:CVCL_AL94 Homo sapiens (Human) Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection. Transformed cell line Male CLO:CLO_0030539,
Coriell:GM09768,
Wikidata:Q54844034		 CVCL_AL94 2026-08-01 05:05:51 0
GM09783
 
Resource Report
Resource Website 		RRID:CVCL_AM08 Homo sapiens (Human) Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection. Transformed cell line Female CLO:CLO_0030497,
Coriell:GM09783,
Wikidata:Q54844051		 CVCL_AM08 2026-08-01 05:05:51 0
GM09814
 
Resource Report
Resource Website 		Coriell Cat# GM09814, RRID:CVCL_DB69 Homo sapiens (Human) Transformed cell line Male Coriell GM09814 CLO:CLO_0030673,
Coriell:GM09814,
Wikidata:Q54844072		 CVCL_DB69 2026-08-01 05:05:52 0
GM09779
 
Resource Report
Resource Website 		RRID:CVCL_AM04 Homo sapiens (Human) Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection. Transformed cell line Male CLO:CLO_0030494,
Coriell:GM09779,
Wikidata:Q54844047		 CVCL_AM04 2026-08-01 05:05:51 0
GM09795
 
Resource Report
Resource Website 		RRID:CVCL_AB00 Homo sapiens (Human) Population: Jewish; Ashkenazi. Transformed cell line Female CLO:CLO_0030468,
Coriell:GM09795,
Wikidata:Q54844064		 CVCL_AB00 2026-08-01 05:05:51 0
GM09814
 
Resource Report
Resource Website 		RRID:CVCL_DB69 Homo sapiens (Human) Transformed cell line Male CLO:CLO_0030673,
Coriell:GM09814,
Wikidata:Q54844072		 CVCL_DB69 2026-08-01 05:05:52 0
GM09822
 
Resource Report
Resource Website 		RRID:CVCL_GT53 Homo sapiens (Human) Transformed cell line Female CLO:CLO_0030659,
Coriell:GM09822,
Wikidata:Q54844077		 CVCL_GT53 2026-08-01 05:05:52 0
GM09812
 
Resource Report
Resource Website 		RRID:CVCL_6G79 Homo sapiens (Human) Seckel syndrome Population: Jewish. PMID:19896956 Finite cell line Female CLO:CLO_0030457,
Coriell:GM09812,
Wikidata:Q54844071		 CVCL_6G79 2026-08-01 05:05:52 0
GM09764
 
Resource Report
Resource Website 		Coriell Cat# GM17366, RRID:CVCL_N118 Homo sapiens (Human) Population: Jewish; Ashkenazi., Part of: Human variation panel. Transformed cell line Female GM09764A, GM17366 Coriell GM17366 CLO:CLO_0013709,
CLO:CLO_0030543,
Coriell:GM09764,
Coriell:GM17366,
Wikidata:Q54844030		 CVCL_N118 2026-08-01 05:05:50 0
GM09771
 
Resource Report
Resource Website 		Coriell Cat# GM09771, RRID:CVCL_N119 Homo sapiens (Human) Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:20889555
PMID:29959025 		Transformed cell line Female GM17289 Coriell GM09771 CLO:CLO_0013077,
CLO:CLO_0030524,
Coriell:GM09771,
Coriell:GM17289,
GEO:GSM569759,
GEO:GSM596353,
GEO:GSM596771,
GEO:GSM924891,
Wikidata:Q54844038		 CVCL_N119 2026-08-01 05:05:51 0
GM09788
 
Resource Report
Resource Website 		RRID:CVCL_AA93 Homo sapiens (Human) Population: Jewish; Ashkenazi. Transformed cell line Female GM09788B CLO:CLO_0030489,
Coriell:GM09788,
Wikidata:Q54844057		 CVCL_AA93 2026-08-01 05:05:51 0
GM09816
 
Resource Report
Resource Website 		Coriell Cat# GM09816, RRID:CVCL_X474 Homo sapiens (Human) Population: Caucasian. Finite cell line Female Coriell GM09816 CLO:CLO_0030665,
Coriell:GM09816,
Wikidata:Q54844074		 CVCL_X474 2026-08-01 05:05:52 0
GM09762
 
Resource Report
Resource Website 		Coriell Cat# GM09762, RRID:CVCL_AL89 Homo sapiens (Human) Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection. Transformed cell line Male Coriell GM09762 CLO:CLO_0030545,
Coriell:GM09762,
Wikidata:Q54844028		 CVCL_AL89 2026-08-01 05:05:50 0
GM09833
 
Resource Report
Resource Website 		RRID:CVCL_2Z77 Homo sapiens (Human) Nevoid basal cell carcinoma syndrome Karyotypic information: 46,XX,ins(5;15)(5pter->5q23.2::15q23->15q26.1::5q23.2->5qter;15pter->15q23::15q26.1->15qter) (Coriell=GM09833)., Population: Caucasian; Irish. Transformed cell line Female CLO:CLO_0030633,
Coriell:GM09833,
Wikidata:Q54844086		 CVCL_2Z77 2026-08-01 05:05:52 0
GM09784
 
Resource Report
Resource Website 		Coriell Cat# GM09784, RRID:CVCL_AM09 Homo sapiens (Human) Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection. Transformed cell line Male Coriell GM09784 CLO:CLO_0030496,
Coriell:GM09784,
Wikidata:Q54844052		 CVCL_AM09 2026-08-01 05:05:51 0

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