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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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GM04297
 
Resource Report
Resource Website 		Coriell Cat# GM04297, RRID:CVCL_5M91 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Female Coriell GM04297 CLO:CLO_0019633,
Coriell:GM04297,
Wikidata:Q54838472		 CVCL_5M91 2026-09-12 05:32:39 0
GM04375
 
Resource Report
Resource Website 		Coriell Cat# GM04375, RRID:CVCL_W622 Homo sapiens (Human) Klinefelter syndrome Population: Caucasian. PMID:6661932
PMID:23665875 		Finite cell line Male GM04375A Coriell GM04375 CLO:CLO_0019338,
Coriell:GM04375,
Wikidata:Q54838507		 CVCL_W622 2026-09-12 05:32:39 0
GM04364
 
Resource Report
Resource Website 		RRID:CVCL_5M95 Homo sapiens (Human) Duchenne muscular dystrophy Population: Caucasian., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:21354051
PMID:23665875 		Finite cell line Male CLO:CLO_0019314,
Coriell:GM04364,
Wikidata:Q54838499		 CVCL_5M95 2026-09-12 05:32:39 0
GM04409
 
Resource Report
Resource Website 		Coriell Cat# GM04409, RRID:CVCL_F124 Homo sapiens (Human) Population: Caucasian. PMID:6661932
PMID:23665875 		Finite cell line Male GM-4409, GM 4409 Coriell GM04409 CLO:CLO_0019707,
Coriell:GM04409,
Wikidata:Q54838516		 CVCL_F124 2026-09-12 05:32:40 0
GM04300
 
Resource Report
Resource Website 		Coriell Cat# GM17023, RRID:CVCL_N016 Homo sapiens (Human) Intellectual developmental disorder Population: Indian., Part of: Human variation panel. PMID:23665875 Finite cell line Female GM17023 Coriell GM17023 CLO:CLO_0014707,
CLO:CLO_0019627,
Coriell:GM04300,
Coriell:GM17023,
Wikidata:Q54838473		 CVCL_N016 2026-09-12 05:32:39 0
GM04519
 
Resource Report
Resource Website 		RRID:CVCL_5L50 Homo sapiens (Human) Tuberous sclerosis 2 Population: Caucasian. PMID:23665875 Transformed cell line Female CLO:CLO_0018846,
Coriell:GM04519,
Wikidata:Q54838557		 CVCL_5L50 2026-09-12 05:32:41 0
GM04501
 
Resource Report
Resource Website 		Coriell Cat# GM04501, RRID:CVCL_7409 Homo sapiens (Human) Donor information: Established from monozygotic twin of GM04502 (Cellosaurus=CVCL_F135). PMID:23665875
PMID:30567591 		Finite cell line Male GM04501A, HF20 Coriell GM04501 CLO:CLO_0018819,
Coriell:GM04501,
GEO:GSM3124646,
Wikidata:Q54838541		 CVCL_7409 2026-09-12 05:32:40 0
GM04503
 
Resource Report
Resource Website 		RRID:CVCL_7410 Homo sapiens (Human) Donor information: Established from monozygotic twin of GM04504 (Cellosaurus=CVCL_7411)., Part of: ENCODE project common cell types; tier 3. PMID:23665875
PMID:30567591 		Finite cell line Female GM04503B, GM04503D, HF22 CLO:CLO_0018813,
Coriell:GM04503,
ENCODE:ENCBS015ENC,
ENCODE:ENCBS290AAA,
ENCODE:ENCBS339GFS,
GEO:GSE76836,
GEO:GSM3124651,
Wikidata:Q54838543		 CVCL_7410 2026-09-12 05:32:40 0
GM04592
 
Resource Report
Resource Website
1+ mentions 		Coriell Cat# GM04592, RRID:CVCL_V473 Homo sapiens (Human) Down syndrome Population: Caucasian. PMID:6661932
PMID:23665875 		Finite cell line Female GM 4592, GM04592A Coriell GM04592 CLO:CLO_0018882,
Coriell:GM04592,
Wikidata:Q54838578		 CVCL_V473 2026-09-12 05:32:41 1
GM04503
 
Resource Report
Resource Website 		Coriell Cat# GM04503, RRID:CVCL_7410 Homo sapiens (Human) Donor information: Established from monozygotic twin of GM04504 (Cellosaurus=CVCL_7411)., Part of: ENCODE project common cell types; tier 3. PMID:23665875
PMID:30567591 		Finite cell line Female GM04503B, GM04503D, HF22 Coriell GM04503 CLO:CLO_0018813,
Coriell:GM04503,
ENCODE:ENCBS015ENC,
ENCODE:ENCBS290AAA,
ENCODE:ENCBS339GFS,
GEO:GSE76836,
GEO:GSM3124651,
Wikidata:Q54838543		 CVCL_7410 2026-09-12 05:32:40 0
GM04993
 
Resource Report
Resource Website 		Coriell Cat# GM04993, RRID:CVCL_X314 Homo sapiens (Human) Population: Caucasian. PMID:6661932
PMID:23665875 		Finite cell line Female GM 4993 Coriell GM04993 CLO:CLO_0025652,
Coriell:GM04993,
Wikidata:Q54838797		 CVCL_X314 2026-09-12 05:32:47 0
GM05047
 
Resource Report
Resource Website 		RRID:CVCL_X316 Homo sapiens (Human) PMID:6661932
PMID:23665875 		Transformed cell line Male GM 5047, GM05047A CLO:CLO_0025646,
Coriell:GM05047,
Wikidata:Q54838828		 CVCL_X316 2026-09-12 05:32:47 0
GM04978
 
Resource Report
Resource Website 		RRID:CVCL_5M98 Homo sapiens (Human) Duchenne muscular dystrophy Population: African American., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:21354051
PMID:23665875 		Finite cell line Male GM04978A CLO:CLO_0025654,
Coriell:GM04978,
Wikidata:Q54838790		 CVCL_5M98 2026-09-12 05:32:46 0
GM05011
 
Resource Report
Resource Website 		RRID:CVCL_X135 Homo sapiens (Human) Population: Caucasian. PMID:6661932
PMID:23665875 		Transformed cell line Female GM-5011, GM 5011, GM05011A CLO:CLO_0025669,
Coriell:GM05011,
Wikidata:Q54838810		 CVCL_X135 2026-09-12 05:32:47 0
GM05067
 
Resource Report
Resource Website 		Coriell Cat# GM05067, RRID:CVCL_M939 Homo sapiens (Human) Trisomy 9 Population: Caribbean; Trinidadian. PMID:6661932
PMID:23665875 		Transformed cell line Male GM 5067, GM05067A Coriell GM05067 CLO:CLO_0025332,
Coriell:GM05067,
Wikidata:Q54838841		 CVCL_M939 2026-09-12 05:32:48 0
GM05047
 
Resource Report
Resource Website 		Coriell Cat# GM05047, RRID:CVCL_X316 Homo sapiens (Human) PMID:6661932
PMID:23665875 		Transformed cell line Male GM 5047, GM05047A Coriell GM05047 CLO:CLO_0025646,
Coriell:GM05047,
Wikidata:Q54838828		 CVCL_X316 2026-09-12 05:32:47 0
GM05022
 
Resource Report
Resource Website 		RRID:CVCL_5N03 Homo sapiens (Human) PMID:23665875 Transformed cell line Female CLO:CLO_0025628,
Coriell:GM05022,
Wikidata:Q54838817		 CVCL_5N03 2026-09-12 05:32:47 0
GM05169
 
Resource Report
Resource Website 		RRID:CVCL_L752 Homo sapiens (Human) Duchenne muscular dystrophy PMID:23665875 Finite cell line Male CLO:CLO_0025274,
Coriell:GM05169,
Wikidata:Q54838906		 CVCL_L752 2026-09-12 05:32:49 0
GM05159
 
Resource Report
Resource Website 		RRID:CVCL_5N23 Homo sapiens (Human) Population: Caucasian., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:21354051
PMID:23665875 		Transformed cell line Female CLO:CLO_0025257,
Coriell:GM05159,
Wikidata:Q54838894		 CVCL_5N23 2026-09-12 05:32:49 0
GM05124
 
Resource Report
Resource Website 		RRID:CVCL_5N17 Homo sapiens (Human) Duchenne muscular dystrophy Population: Caucasian., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:6726265
PMID:21354051
PMID:23665875 		Transformed cell line Male RB 5124 CLO:CLO_0025357,
Coriell:GM05124,
Wikidata:Q54838871		 CVCL_5N17 2026-09-12 05:32:48 0

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