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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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95,747 Results - per page

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GM09752
 
Resource Report
Resource Website 		RRID:CVCL_AA90 Homo sapiens (Human) Transformed cell line Female CLO:CLO_0030382,
Coriell:GM09752,
Wikidata:Q54844006		 CVCL_AA90 2026-08-08 05:01:28 0
GM09704
 
Resource Report
Resource Website 		RRID:CVCL_9S94 Homo sapiens (Human) Karyotypic information: 46,XX,rec(6)(pter->p12::q26->q16::p12->qter)pat (Coriell=GM09704). Finite cell line Female CLO:CLO_0026597,
Coriell:GM09704,
Wikidata:Q54843963		 CVCL_9S94 2026-08-08 05:01:28 0
GM09706
 
Resource Report
Resource Website 		RRID:CVCL_4D99 Homo sapiens (Human) Supernumerary circular chromosome PMID:23665875 Transformed cell line Female CLO:CLO_0026351,
Coriell:GM09706,
Wikidata:Q54843972		 CVCL_4D99 2026-08-08 05:01:28 0
GM09741
 
Resource Report
Resource Website 		RRID:CVCL_7496 Homo sapiens (Human) Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection. Transformed cell line Female GM09741A CLO:CLO_0030405,
Coriell:GM09741,
Wikidata:Q54843997		 CVCL_7496 2026-08-08 05:01:28 0
GM09707
 
Resource Report
Resource Website 		RRID:CVCL_AA87 Homo sapiens (Human) Population: Jewish; Ashkenazi. Transformed cell line Female CLO:CLO_0026350,
Coriell:GM09707,
Wikidata:Q54843973		 CVCL_AA87 2026-08-08 05:01:28 0
GM09721
 
Resource Report
Resource Website 		Coriell Cat# GM09721, RRID:CVCL_AU81 Homo sapiens (Human) Population: Caucasian; Acadian. Transformed cell line Female Coriell GM09721 CLO:CLO_0026360,
Coriell:GM09721,
Wikidata:Q54843980		 CVCL_AU81 2026-08-08 05:01:28 0
GM09742
 
Resource Report
Resource Website 		RRID:CVCL_4I02 Homo sapiens (Human) Bipolar disorder Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection. Transformed cell line Female GM09742A CLO:CLO_0030402,
Coriell:GM09742,
Wikidata:Q54843998		 CVCL_4I02 2026-08-08 05:01:28 0
GM09690
 
Resource Report
Resource Website 		Coriell Cat# GM09690, RRID:CVCL_9Z96 Homo sapiens (Human) Neurofibromatosis type 1 Population: Caucasian. Transformed cell line Female GM09690A Coriell GM09690 CLO:CLO_0026573,
Coriell:GM09690,
Wikidata:Q54843957		 CVCL_9Z96 2026-08-08 05:01:27 0
GM09772
 
Resource Report
Resource Website 		RRID:CVCL_AL97 Homo sapiens (Human) Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection. Transformed cell line Female GM09772A CLO:CLO_0030523,
Coriell:GM09772,
Wikidata:Q54844039		 CVCL_AL97 2026-08-08 05:01:29 0
GM09816
 
Resource Report
Resource Website 		RRID:CVCL_X474 Homo sapiens (Human) Population: Caucasian. Finite cell line Female CLO:CLO_0030665,
Coriell:GM09816,
Wikidata:Q54844074		 CVCL_X474 2026-08-08 05:01:30 0
GM09824
 
Resource Report
Resource Website 		RRID:CVCL_2N13 Homo sapiens (Human) PMID:23665875 Finite cell line Female CLO:CLO_0030660,
Coriell:GM09824,
Wikidata:Q54844078		 CVCL_2N13 2026-08-08 05:01:30 0
GM09850
 
Resource Report
Resource Website 		RRID:CVCL_GT56 Homo sapiens (Human) Hereditary hemorrhagic telangiectasia Transformed cell line Female CLO:CLO_0030629,
Coriell:GM09850,
Wikidata:Q54844090		 CVCL_GT56 2026-08-08 05:01:30 0
GM09811
 
Resource Report
Resource Website 		RRID:CVCL_IN25 Homo sapiens (Human) Neonatal hemochromatosis Population: Caucasian; Portuguese. PMID:2916654 Finite cell line Female GM 09811 CLO:CLO_0030458,
Coriell:GM09811,
Wikidata:Q54844066		 CVCL_IN25 2026-08-08 05:01:29 0
GM09773
 
Resource Report
Resource Website 		RRID:CVCL_AL98 Homo sapiens (Human) Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection. Transformed cell line Female CLO:CLO_0030526,
Coriell:GM09773,
Wikidata:Q54844040		 CVCL_AL98 2026-08-08 05:01:29 0
GM09771
 
Resource Report
Resource Website 		Coriell Cat# GM17289, 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 GM17289 CLO:CLO_0013077,
CLO:CLO_0030524,
Coriell:GM09771,
Coriell:GM17289,
GEO:GSM569759,
GEO:GSM596353,
GEO:GSM596771,
GEO:GSM924891,
Wikidata:Q54844038		 CVCL_N119 2026-08-08 05:01:29 0
GM09764
 
Resource Report
Resource Website 		RRID:CVCL_N118 Homo sapiens (Human) Population: Jewish; Ashkenazi., Part of: Human variation panel. Transformed cell line Female GM09764A, GM17366 CLO:CLO_0013709,
CLO:CLO_0030543,
Coriell:GM09764,
Coriell:GM17366,
Wikidata:Q54844030		 CVCL_N118 2026-08-08 05:01:29 0
GM09783
 
Resource Report
Resource Website 		Coriell Cat# GM09783, RRID:CVCL_AM08 Homo sapiens (Human) Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection. Transformed cell line Female Coriell GM09783 CLO:CLO_0030497,
Coriell:GM09783,
Wikidata:Q54844051		 CVCL_AM08 2026-08-08 05:01:29 0
GM09775
 
Resource Report
Resource Website 		RRID:CVCL_AM00 Homo sapiens (Human) Retinitis pigmentosa Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection. Transformed cell line Female CLO:CLO_0030520,
Coriell:GM09775,
Wikidata:Q54844042		 CVCL_AM00 2026-08-08 05:01:29 0
GM09792
 
Resource Report
Resource Website 		RRID:CVCL_AA97 Homo sapiens (Human) Familial dysautonomia Population: Jewish; Ashkenazi. Transformed cell line Female CLO:CLO_0030463,
Coriell:GM09792,
Wikidata:Q54844061		 CVCL_AA97 2026-08-08 05:01:29 0
GM09774
 
Resource Report
Resource Website 		RRID:CVCL_AL99 Homo sapiens (Human) Retinitis pigmentosa Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection. Transformed cell line Female CLO:CLO_0030525,
Coriell:GM09774,
Wikidata:Q54844041		 CVCL_AL99 2026-08-08 05:01:29 0

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