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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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GM02256
 
Resource Report
Resource Website 		RRID:CVCL_4N22 Homo sapiens (Human) Autosomal recessive torsion dystonia 2 Transformed cell line Female GM-2256 CLO:CLO_0032158,
Coriell:GM02256,
Wikidata:Q54837396		 CVCL_4N22 Cellosaurus 2026-09-26 06:48:54 0
GM02242
 
Resource Report
Resource Website 		RRID:CVCL_GZ40 Homo sapiens (Human) Adrenal gland hyperplasia III Population: Caucasian. Transformed cell line Female GM-2242 CLO:CLO_0032239,
BioSample:SAMN00807624,
Coriell:GM02242,
Wikidata:Q54837387		 CVCL_GZ40 Cellosaurus 2026-09-26 06:48:54 0
GM02316
 
Resource Report
Resource Website 		RRID:CVCL_8A66 Homo sapiens (Human) Population: Caucasian; Irish. PMID:21418647
PMID:24555846
PMID:25326100 		Finite cell line Male GM-2316 CLO:CLO_0032169,
BioSample:SAMN00807689,
Coriell:GM02316,
GEO:GSM651150,
GEO:GSM651151,
GEO:GSM1257697,
GEO:GSM1266972,
GEO:GSM1267051,
GEO:GSM1288439,
GEO:GSM1314047,
Wikidata:Q54837424		 CVCL_8A66 Cellosaurus 2026-09-26 06:48:54 0
GM02207
 
Resource Report
Resource Website
Possibly Discontinued 		RRID:CVCL_JB90 Homo sapiens (Human) Ehlers-Danlos syndrome, type IV Finite cell line Female GM-2207 Coriell:GM02207,
Wikidata:Q54837372		 CVCL_JB90 Cellosaurus 2026-09-26 06:48:53 0
GM02266
 
Resource Report
Resource Website 		Coriell Cat# GM02266, RRID:CVCL_BT13 Homo sapiens (Human) Beta thalassemia Transformed cell line Female GM-2266, GM02266A Coriell GM02266 CLO:CLO_0032119,
BioSample:SAMN00807642,
Coriell:GM02266,
Wikidata:Q54837398		 CVCL_BT13 Cellosaurus 2026-09-26 06:48:54 0
GM02290
 
Resource Report
Resource Website 		RRID:CVCL_7356 Homo sapiens (Human) Lesch-Nyhan syndrome Population: Caucasian. PMID:477417
PMID:6087472 		Finite cell line Male GM-2290, GM 2290 GM02290A CLO:CLO_0003523,
CLO:CLO_0032129,
CLDB:cl1490,
BioSample:SAMN00807654,
Coriell:GM02290,
Wikidata:Q54837406		 CVCL_7356 Cellosaurus 2026-09-26 06:48:54 0
GM02267
 
Resource Report
Resource Website 		RRID:CVCL_BT14 Homo sapiens (Human) Beta thalassemia PMID:6196781 Transformed cell line Female GM-2267 CLO:CLO_0032120,
BioSample:SAMN00807644,
Coriell:GM02267,
Wikidata:Q54837399		 CVCL_BT14 Cellosaurus 2026-09-26 06:48:54 0
GM02292
 
Resource Report
Resource Website 		Coriell Cat# GM02292, RRID:CVCL_D868 Homo sapiens (Human) Lesch-Nyhan syndrome Population: Caucasian. PMID:477417
PMID:2762303 		Transformed cell line Male GM-2292, GM 2292, GM2292A, GM02292B Coriell GM02292 CLO:CLO_0032131,
BioSample:SAMN00807658,
Coriell:GM02292,
Wikidata:Q54837408		 CVCL_D868 Cellosaurus 2026-09-26 06:48:54 0
GM02264
 
Resource Report
Resource Website 		RRID:CVCL_1U20 Homo sapiens (Human) Autosomal dominant torsion dystonia 1 Transformed cell line Female GM-2264 CLO:CLO_0032161,
BioSample:SAMN00807640,
Coriell:GM02264,
Wikidata:Q54837397		 CVCL_1U20 Cellosaurus 2026-09-26 06:48:54 0
GM02300
 
Resource Report
Resource Website 		Coriell Cat# GM02300, RRID:CVCL_IL09 Homo sapiens (Human) Androgen insensitivity syndrome Population: African American. Finite cell line Sex ambiguous GM-2300, GM02300A Coriell GM02300 CLO:CLO_0032203,
BioSample:SAMN00807669,
Coriell:GM02300,
Wikidata:Q54837414		 CVCL_IL09 Cellosaurus 2026-09-26 06:48:54 0
GM02324
 
Resource Report
Resource Website 		RRID:CVCL_X261 Homo sapiens (Human) Karyotypic information: 46,XX,9qh+,t(16;22)(16qter->16p13.11::22q11.21->22qter;22pter->22q11.21::16p13.11->16pter) (Coriell=GM02324)., Population: Caucasian. PMID:2714795 Transformed cell line Female GM-2324, GM2324, GM02324A CLO:CLO_0032172,
BioSample:SAMN00807693,
Coriell:GM02324,
Wikidata:Q54837426		 CVCL_X261 Cellosaurus 2026-09-26 06:48:54 0
GM02211
 
Resource Report
Resource Website
Possibly Discontinued 		RRID:CVCL_JB67 Homo sapiens (Human) Wolman disease PMID:6782865 Finite cell line Male GM-2211, GM 2211, GM2211 Coriell:GM02211,
Wikidata:Q54837374		 CVCL_JB67 Cellosaurus 2026-09-26 06:48:54 0
GM02255
 
Resource Report
Resource Website 		RRID:CVCL_4N21 Homo sapiens (Human) Autosomal recessive torsion dystonia 2 Finite cell line Female GM-2255 CLO:CLO_0032157,
Coriell:GM02255,
Wikidata:Q54837395		 CVCL_4N21 Cellosaurus 2026-09-26 06:48:54 0
GM02264
 
Resource Report
Resource Website 		Coriell Cat# GM02264, RRID:CVCL_1U20 Homo sapiens (Human) Autosomal dominant torsion dystonia 1 Transformed cell line Female GM-2264 Coriell GM02264 CLO:CLO_0032161,
BioSample:SAMN00807640,
Coriell:GM02264,
Wikidata:Q54837397		 CVCL_1U20 Cellosaurus 2026-09-26 06:48:54 0
GM02273
 
Resource Report
Resource Website 		RRID:CVCL_9Q90 Homo sapiens (Human) I-cell disease Population: Caucasian. PMID:16465621 Finite cell line Male GM-2273, GM02273F, GM02273G CLO:CLO_0032126,
BioSample:SAMN00807650,
Coriell:GM02273,
Wikidata:Q54837402		 CVCL_9Q90 Cellosaurus 2026-09-26 06:48:54 0
GM02228
 
Resource Report
Resource Website 		Coriell Cat# GM02228, RRID:CVCL_U949 Homo sapiens (Human) Alkaptonuria Population: Caucasian. Finite cell line Male GM2228, GM-2228 Coriell GM02228 CLO:CLO_0032242,
BioSample:SAMN00807614,
Coriell:GM02228,
Wikidata:Q54837382		 CVCL_U949 Cellosaurus 2026-09-26 06:48:54 0
GM02426
 
Resource Report
Resource Website 		RRID:CVCL_2S82 Homo sapiens (Human) Karyotypic information: 46,XY,t(5;6)(5qter->5p15::6p21->6pter;6qter->6p21::5p15->5pter) (Coriell=GM02426)., Population: Caucasian. Finite cell line Male CLO:CLO_0033093,
BioSample:SAMN00807759,
Coriell:GM02426,
Wikidata:Q54837479		 CVCL_2S82 Cellosaurus 2026-09-26 06:48:55 0
GM02380
 
Resource Report
Resource Website 		RRID:CVCL_H181 Homo sapiens (Human) PMID:6617268 Finite cell line Female GM 2380 CLO:CLO_0033104,
Coriell:GM02380,
Wikidata:Q54837466		 CVCL_H181 Cellosaurus 2026-09-26 06:48:55 0
GM02365
 
Resource Report
Resource Website 		RRID:CVCL_1R62 Homo sapiens (Human) Coffin-Lowry syndrome Population: Caucasian. PMID:23665875 Finite cell line Male GM02365A CLO:CLO_0033101,
BioSample:SAMN00807737,
Coriell:GM02365,
Wikidata:Q54837463		 CVCL_1R62 Cellosaurus 2026-09-26 06:48:55 0
GM02422
 
Resource Report
Resource Website 		Coriell Cat# GM02422, RRID:CVCL_H183 Homo sapiens (Human) Trisomy 18 PMID:6661932 Finite cell line Female GM 2422 Coriell GM02422 CLO:CLO_0033089,
BioSample:SAMN00807755,
Coriell:GM02422,
Wikidata:Q54837476		 CVCL_H183 Cellosaurus 2026-09-26 06:48:55 0

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