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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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GM02717
 
Resource Report
Resource Website 		Coriell Cat# GM02717, RRID:CVCL_IL15 Homo sapiens (Human) Karyotypic information: 46,XY (Coriell=GM02717)., Population: Caucasian. Finite cell line Sex ambiguous Coriell GM02717 CLO:CLO_0014861,
BioSample:SAMN00808052,
Coriell:GM02717,
Wikidata:Q54837653		 CVCL_IL15 2026-09-05 10:54:41 0
GM02682
 
Resource Report
Resource Website 		RRID:CVCL_IL11 Homo sapiens (Human) Androgen insensitivity syndrome Population: African American. Finite cell line Sex ambiguous CLO:CLO_0014965,
BioSample:SAMN00808008,
Coriell:GM02682,
Wikidata:Q54837629		 CVCL_IL11 2026-09-05 10:54:40 0
GM02682
 
Resource Report
Resource Website 		Coriell Cat# GM02682, RRID:CVCL_IL11 Homo sapiens (Human) Androgen insensitivity syndrome Population: African American. Finite cell line Sex ambiguous Coriell GM02682 CLO:CLO_0014965,
BioSample:SAMN00808008,
Coriell:GM02682,
Wikidata:Q54837629		 CVCL_IL11 2026-09-05 10:54:40 0
GM02715
 
Resource Report
Resource Website 		Coriell Cat# GM02715, RRID:CVCL_IL13 Homo sapiens (Human) Karyotypic information: 46,XY (Coriell=GM02715)., Population: Caucasian. Finite cell line Sex ambiguous Coriell GM02715 CLO:CLO_0014864,
BioSample:SAMN00808048,
Coriell:GM02715,
Wikidata:Q54837651		 CVCL_IL13 2026-09-05 10:54:41 0
GM02716
 
Resource Report
Resource Website 		RRID:CVCL_IL14 Homo sapiens (Human) Karyotypic information: 46,XY (Coriell=GM02716)., Population: Caucasian. Finite cell line Sex ambiguous CLO:CLO_0014860,
BioSample:SAMN00808050,
Coriell:GM02716,
Wikidata:Q54837652		 CVCL_IL14 2026-09-05 10:54:41 0
GM03368-A
 
Resource Report
Resource Website
Possibly Discontinued 		RRID:CVCL_DS12 Homo sapiens (Human) 46,XY sex reversal 1 Population: African American. Finite cell line Sex ambiguous GM03368A CLO:CLO_0016671,
Coriell:GM03368-A,
Wikidata:Q54838030		 CVCL_DS12 2026-09-05 10:54:50 0
GM03368
 
Resource Report
Resource Website 		RRID:CVCL_DS11 Homo sapiens (Human) 46,XY sex reversal 1 Population: African American. Finite cell line Sex ambiguous GM03368-0 CLO:CLO_0016669,
BioSample:SAMN00808373,
Coriell:GM03368,
Wikidata:Q54838029		 CVCL_DS11 2026-09-05 10:54:50 0
GM03547
 
Resource Report
Resource Website 		RRID:CVCL_UR79 Homo sapiens (Human) 17-beta-hydroxysteroid dehydrogenase 3 deficiency Population: Arab. Finite cell line Sex ambiguous CLO:CLO_0017307,
BioSample:SAMN00808445,
Coriell:GM03547,
Wikidata:Q93584700		 CVCL_UR79 2026-09-05 10:54:52 0
GM01322
 
Resource Report
Resource Website 		Coriell Cat# GM01322, RRID:CVCL_AB28 Homo sapiens (Human) Triploidy syndrome Karyotypic information: 68,XX [1]; 69,XXY [49] (Coriell=GM01322)., Population: African American. PMID:6156493 Finite cell line Sex ambiguous GM-1322, GM 1322 Coriell GM01322 CLO:CLO_0030911,
BioSample:SAMN00803800,
Coriell:GM01322,
Wikidata:Q54836765		 CVCL_AB28 2026-09-05 10:54:19 0
GM01322
 
Resource Report
Resource Website 		RRID:CVCL_AB28 Homo sapiens (Human) Triploidy syndrome Karyotypic information: 68,XX [1]; 69,XXY [49] (Coriell=GM01322)., Population: African American. PMID:6156493 Finite cell line Sex ambiguous GM-1322, GM 1322 CLO:CLO_0030911,
BioSample:SAMN00803800,
Coriell:GM01322,
Wikidata:Q54836765		 CVCL_AB28 2026-09-05 10:54:19 0
GM01491
 
Resource Report
Resource Website
Possibly Discontinued 		Coriell Cat# GM01491, RRID:CVCL_JD87 Homo sapiens (Human) 46,XY gonadal dysgenesis Finite cell line Sex ambiguous GM-1491 Coriell GM01491 Coriell:GM01491,
Wikidata:Q54836867		 CVCL_JD87 2026-09-05 10:54:21 0
GM01628
 
Resource Report
Resource Website 		RRID:CVCL_DS07 Homo sapiens (Human) 46,XY sex reversal 1 Population: Caucasian. Finite cell line Sex ambiguous GM-1628 CLO:CLO_0031490,
BioSample:SAMN00806989,
Coriell:GM01628,
Wikidata:Q54836962		 CVCL_DS07 2026-09-05 10:54:23 0
GM01722
 
Resource Report
Resource Website
Possibly Discontinued 		RRID:CVCL_JC93 Homo sapiens (Human) Androgen insensitivity syndrome Population: Caucasian. Finite cell line Sex ambiguous GM-1722, GM1722 Coriell:GM01722,
Wikidata:Q54837036		 CVCL_JC93 2026-09-05 10:54:25 0
GM01737
 
Resource Report
Resource Website 		Coriell Cat# GM01737, RRID:CVCL_2Z43 Homo sapiens (Human) Campomelic dysplasia Karyotypic information: 46,XY; but phenotypically female (Coriell=GM01737)., Population: Caucasian. Finite cell line Sex ambiguous GM-1737 Coriell GM01737 CLO:CLO_0030995,
BioSample:SAMN00807125,
Coriell:GM01737,
Wikidata:Q54837045		 CVCL_2Z43 2026-09-05 10:54:25 0
GM01722
 
Resource Report
Resource Website
Possibly Discontinued 		Coriell Cat# GM01722, RRID:CVCL_JC93 Homo sapiens (Human) Androgen insensitivity syndrome Population: Caucasian. Finite cell line Sex ambiguous GM-1722, GM1722 Coriell GM01722 Coriell:GM01722,
Wikidata:Q54837036		 CVCL_JC93 2026-09-05 10:54:25 0
GM01737
 
Resource Report
Resource Website 		RRID:CVCL_2Z43 Homo sapiens (Human) Campomelic dysplasia Karyotypic information: 46,XY; but phenotypically female (Coriell=GM01737)., Population: Caucasian. Finite cell line Sex ambiguous GM-1737 CLO:CLO_0030995,
BioSample:SAMN00807125,
Coriell:GM01737,
Wikidata:Q54837045		 CVCL_2Z43 2026-09-05 10:54:25 0
GM01709
 
Resource Report
Resource Website 		Coriell Cat# GM01709, RRID:CVCL_X252 Homo sapiens (Human) Gonadal dysgenesis Population: Caucasian. PMID:6661932
PMID:23665875 		Finite cell line Sex ambiguous GM-1709, GM 1709 Coriell GM01709 CLO:CLO_0030969,
BioSample:SAMN00807097,
Coriell:GM01709,
Wikidata:Q54837028		 CVCL_X252 2026-09-05 10:54:25 0
GM01889
 
Resource Report
Resource Website 		RRID:CVCL_5M70 Homo sapiens (Human) XX male Karyotypic information: 46,XX (Coriell=GM01889)., Population: Caucasian. Finite cell line Sex ambiguous GM-1889 CLO:CLO_0032421,
BioSample:SAMN00807280,
Coriell:GM01889,
Wikidata:Q54837163		 CVCL_5M70 2026-09-05 10:54:28 0
GM01862
 
Resource Report
Resource Website
Possibly Discontinued 		RRID:CVCL_JD89 Homo sapiens (Human) Finite cell line Sex ambiguous GM-1862 Coriell:GM01862,
Wikidata:Q54837135		 CVCL_JD89 2026-09-05 10:54:28 0
GM01865
 
Resource Report
Resource Website
Possibly Discontinued 		RRID:CVCL_DE31 Homo sapiens (Human) Cockayne syndrome PMID:7565859 Finite cell line Sex ambiguous GM-1865, GM1865 Coriell:GM01865,
Wikidata:Q54837141		 CVCL_DE31 2026-09-05 10:54:28 0

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