Searching the RRID Resource Information Network
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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.
| Name | Proper Citation | Organism | Disease |
Comments |
Defining Citation | Category | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
BT0001 Resource Report Resource Website |
RRID:CVCL_8T85 | Homo sapiens (Human) | Karyotypic information: 46,XY,del(11)(p14.1) (ECACC=92042901)., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Sex ambiguous | ECACC:92042901, Wikidata:Q54798478 |
CVCL_8T85 | 2026-09-03 06:25:34 | 0 | |||||||
|
BT0001 Resource Report Resource Website |
ECACC Cat# 92042901, RRID:CVCL_8T85 | Homo sapiens (Human) | Karyotypic information: 46,XY,del(11)(p14.1) (ECACC=92042901)., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Sex ambiguous | ECACC | 92042901 | ECACC:92042901, Wikidata:Q54798478 |
CVCL_8T85 | 2026-09-03 06:25:33 | 0 | |||||
|
GM20486 Resource Report Resource Website |
RRID:CVCL_IM22 | Homo sapiens (Human) | Karyotypic information: Chimera 46,XX/46,XY., Population: Chinese; Taiwan. | PMID:15966046 | Finite cell line | Sex ambiguous | CLO:CLO_0029537, Coriell:GM20486, Wikidata:Q54851046 |
CVCL_IM22 | 2026-09-03 06:36:41 | 0 | ||||||
|
GM20486 Resource Report Resource Website |
Coriell Cat# GM20486, RRID:CVCL_IM22 | Homo sapiens (Human) | Karyotypic information: Chimera 46,XX/46,XY., Population: Chinese; Taiwan. | PMID:15966046 | Finite cell line | Sex ambiguous | Coriell | GM20486 | CLO:CLO_0029537, Coriell:GM20486, Wikidata:Q54851046 |
CVCL_IM22 | 2026-09-03 06:36:41 | 0 | ||||
|
GM21894 Resource Report Resource Website |
Coriell Cat# GM21894, RRID:CVCL_HL17 | Homo sapiens (Human) | Campomelic dysplasia | Finite cell line | Sex ambiguous | Coriell | GM21894 | Coriell:GM21894, Wikidata:Q54852215 |
CVCL_HL17 | 2026-09-03 06:37:02 | 0 | |||||
|
GM27840 Resource Report Resource Website |
RRID:CVCL_A2SE | Homo sapiens (Human) | Population: Indian; Tamil. | Transformed cell line | Sex ambiguous | Coriell:GM27840, Wikidata:Q105507330 |
CVCL_A2SE | 2026-09-03 06:37:43 | 0 | |||||||
|
GM27840 Resource Report Resource Website |
Coriell Cat# GM27840, RRID:CVCL_A2SE | Homo sapiens (Human) | Population: Indian; Tamil. | Transformed cell line | Sex ambiguous | Coriell | GM27840 | Coriell:GM27840, Wikidata:Q105507330 |
CVCL_A2SE | 2026-09-03 06:37:43 | 0 | |||||
|
KCL008 Resource Report Resource Website |
RRID:CVCL_A243 | Homo sapiens (Human) | Huntington's disease | From: King's College London; London; United Kingdom. | PMID:20178004 | Embryonic stem cell | Sex ambiguous | KCL008(HD2), KCL-008, HD-2, KCL008-HD2, KCL008_HD2, KCLe007-A | hPSCreg:KCLe007-A, SKIP:SKIP002336, Wikidata:Q27570645 |
CVCL_A243 | 2026-09-03 06:44:58 | 0 | ||||
|
MK-37c Resource Report Resource Website Possibly Discontinued |
JCRB Cat# KURB2732, RRID:CVCL_LC40 | Homo sapiens (Human) | Turner syndrome | Finite cell line | Sex ambiguous | JCRB | KURB2732 | JCRB:JCRB3045, JCRB:KURB2732, Wikidata:Q54905800 |
CVCL_LC40 | 2026-09-03 06:46:45 | 0 | |||||
|
MK-37b Resource Report Resource Website |
JCRB Cat# KURB2731, RRID:CVCL_B3MD | Homo sapiens (Human) | Turner syndrome | Finite cell line | Sex ambiguous | JCRB | KURB2731 | JCRB:JCRB3069, JCRB:KURB2731, Wikidata:Q110433040 |
CVCL_B3MD | 2026-09-03 06:46:45 | 0 | |||||
|
MK-37a Resource Report Resource Website |
JCRB Cat# KURB2730, RRID:CVCL_B3ME | Homo sapiens (Human) | Turner syndrome | Finite cell line | Sex ambiguous | JCRB | KURB2730 | JCRB:KURB2730, Wikidata:Q110433038 |
CVCL_B3ME | 2026-09-03 06:46:45 | 0 | |||||
|
MK-37c Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_LC40 | Homo sapiens (Human) | Turner syndrome | Finite cell line | Sex ambiguous | JCRB:JCRB3045, JCRB:KURB2732, Wikidata:Q54905800 |
CVCL_LC40 | 2026-09-03 06:46:45 | 0 | |||||||
|
HH0244 Resource Report Resource Website |
ECACC Cat# 89042114, RRID:CVCL_8X30 | Homo sapiens (Human) | Population: Asian., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Sex ambiguous | ECACC | 89042114 | ECACC:89042114, Wikidata:Q54887424 |
CVCL_8X30 | 2026-09-03 06:41:08 | 0 | |||||
|
HH0273 Resource Report Resource Website |
ECACC Cat# 89061426, RRID:CVCL_8X31 | Homo sapiens (Human) | Population: Caucasian., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Sex ambiguous | ECACC | 89061426 | ECACC:89061426, Wikidata:Q54887425 |
CVCL_8X31 | 2026-09-03 06:41:08 | 0 | |||||
|
GM01404 Resource Report Resource Website |
Coriell Cat# GM01404, RRID:CVCL_JC90 | Homo sapiens (Human) | Androgen insensitivity syndrome | Karyotypic information: 46,XY; but phenotypically female (Coriell=GM01404)., Population: African American. | Finite cell line | Sex ambiguous | GM-1404 | Coriell | GM01404 | CLO:CLO_0030807, BioSample:SAMN00803860, Coriell:GM01404, Wikidata:Q54836806 |
CVCL_JC90 | 2026-09-03 06:33:10 | 0 | |||
|
GM01404 Resource Report Resource Website |
RRID:CVCL_JC90 | Homo sapiens (Human) | Androgen insensitivity syndrome | Karyotypic information: 46,XY; but phenotypically female (Coriell=GM01404)., Population: African American. | Finite cell line | Sex ambiguous | GM-1404 | CLO:CLO_0030807, BioSample:SAMN00803860, Coriell:GM01404, Wikidata:Q54836806 |
CVCL_JC90 | 2026-09-03 06:33:10 | 0 | |||||
|
GM01491 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_JD87 | Homo sapiens (Human) | 46,XY gonadal dysgenesis | Finite cell line | Sex ambiguous | GM-1491 | Coriell:GM01491, Wikidata:Q54836867 |
CVCL_JD87 | 2026-09-03 06:33:11 | 0 | ||||||
|
GM01628 Resource Report Resource Website |
Coriell Cat# GM01628, RRID:CVCL_DS07 | Homo sapiens (Human) | 46,XY sex reversal 1 | Population: Caucasian. | Finite cell line | Sex ambiguous | GM-1628 | Coriell | GM01628 | CLO:CLO_0031490, BioSample:SAMN00806989, Coriell:GM01628, Wikidata:Q54836962 |
CVCL_DS07 | 2026-09-03 06:33:12 | 0 | |||
|
GM01709 Resource Report Resource Website |
RRID:CVCL_X252 | Homo sapiens (Human) | Gonadal dysgenesis | Population: Caucasian. |
PMID:6661932 PMID:23665875 |
Finite cell line | Sex ambiguous | GM-1709, GM 1709 | CLO:CLO_0030969, BioSample:SAMN00807097, Coriell:GM01709, Wikidata:Q54837028 |
CVCL_X252 | 2026-09-03 06:33:14 | 0 | ||||
|
GM01721 Resource Report Resource Website |
Coriell Cat# GM01721, RRID:CVCL_JC91 | Homo sapiens (Human) | Androgen insensitivity syndrome | Population: Caucasian. | Finite cell line | Sex ambiguous | GM-1721 | Coriell | GM01721 | CLO:CLO_0030979, BioSample:SAMN00807111, Coriell:GM01721, Wikidata:Q54837035 |
CVCL_JC91 | 2026-09-03 06:33:14 | 0 |
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