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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
DD3026 Resource Report Resource Website |
ECACC Cat# 97121509, RRID:CVCL_9N69 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 97121509 | ECACC:97121509, Wikidata:Q54830521 |
CVCL_9N69 | 2026-08-15 04:26:58 | 0 | |||||
|
DD3024 Resource Report Resource Website |
RRID:CVCL_9N67 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC:97121507, Wikidata:Q54830519 |
CVCL_9N67 | 2026-08-15 04:26:59 | 0 | |||||||
|
DD2982 Resource Report Resource Website |
ECACC Cat# 97092514, RRID:CVCL_9L80 | Homo sapiens (Human) | Autism spectrum disorder | Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 97092514 | ECACC:97092514, Wikidata:Q54830497 |
CVCL_9L80 | 2026-08-15 04:26:58 | 0 | ||||
|
DD2989 Resource Report Resource Website |
RRID:CVCL_9L81 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC:97100915, Wikidata:Q54830501 |
CVCL_9L81 | 2026-08-15 04:26:58 | 0 | ||||||
|
DD3062 Resource Report Resource Website |
RRID:CVCL_9M03 | Homo sapiens (Human) | Leigh disease | Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC:98022304, Wikidata:Q54830538 |
CVCL_9M03 | 2026-08-15 04:26:59 | 0 | ||||||
|
DD2997 Resource Report Resource Website |
RRID:CVCL_9L85 | Homo sapiens (Human) | Karyotypic information: 46,XY,inv(7)(p12.2;p21.3)pat (ECACC=97102401)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC:97102401, Wikidata:Q54830506 |
CVCL_9L85 | 2026-08-15 04:26:58 | 0 | |||||||
|
DD3047 Resource Report Resource Website |
ECACC Cat# 98012701, RRID:CVCL_9M01 | Homo sapiens (Human) | Karyotypic information: 47,XXX (ECACC=98012701)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 98012701 | ECACC:98012701, Wikidata:Q54830536 |
CVCL_9M01 | 2026-08-15 04:26:59 | 0 | |||||
|
DD2987 Resource Report Resource Website |
RRID:CVCL_AR40 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC:97100307, Wikidata:Q54830500 |
CVCL_AR40 | 2026-08-15 04:26:58 | 0 | |||||||
|
DD3011 Resource Report Resource Website |
ECACC Cat# 97112202, RRID:CVCL_9L90 | Homo sapiens (Human) | Karyotypic information: 46,XX,t(9;20)(p24.1;p11.2?3) (ECACC=97112202)., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 97112202 | ECACC:97112202, Wikidata:Q54830514 |
CVCL_9L90 | 2026-08-15 04:26:59 | 0 | |||||
|
DD3013 Resource Report Resource Website |
RRID:CVCL_9L92 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC:97112204, Wikidata:Q54830516 |
CVCL_9L92 | 2026-08-15 04:26:59 | 0 | |||||||
|
DD2977 Resource Report Resource Website |
ECACC Cat# 97091131, RRID:CVCL_9L79 | Homo sapiens (Human) | Autism spectrum disorder | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 97091131 | ECACC:97091131, Wikidata:Q54830496 |
CVCL_9L79 | 2026-08-15 04:26:58 | 0 | ||||
|
DD2955 Resource Report Resource Website |
RRID:CVCL_9L73 | Homo sapiens (Human) | Hypogonadism | Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC:97072713, Wikidata:Q54830489 |
CVCL_9L73 | 2026-08-15 04:26:58 | 0 | ||||||
|
DD3069 Resource Report Resource Website |
ECACC Cat# 98030602, RRID:CVCL_9M06 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 98030602 | ECACC:98030602, Wikidata:Q54830541 |
CVCL_9M06 | 2026-08-15 04:26:59 | 0 | |||||
|
DD2992 Resource Report Resource Website |
ECACC Cat# 97101303, RRID:CVCL_9L82 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC | 97101303 | ECACC:97101303, Wikidata:Q54830502 |
CVCL_9L82 | 2026-08-15 04:26:58 | 0 | |||||
|
DD3028 Resource Report Resource Website |
ECACC Cat# 97122203, RRID:CVCL_9N71 | Homo sapiens (Human) | Developmental delay | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 97122203 | ECACC:97122203, Wikidata:Q54830526 |
CVCL_9N71 | 2026-08-15 04:26:59 | 0 | ||||
|
DD2998 Resource Report Resource Website |
ECACC Cat# 97102402, RRID:CVCL_AR42 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 97102402 | ECACC:97102402, Wikidata:Q54830507 |
CVCL_AR42 | 2026-08-15 04:26:58 | 0 | |||||
|
DD3027 Resource Report Resource Website |
ECACC Cat# 97121905, RRID:CVCL_9N70 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 97121905 | ECACC:97121905, Wikidata:Q54830522 |
CVCL_9N70 | 2026-08-15 04:26:58 | 0 | |||||
|
DD2996 Resource Report Resource Website |
RRID:CVCL_9L84 | Homo sapiens (Human) | Karyotypic information: 46,XY.ish 22q11.2(cH748X2) (ECACC=97102306)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC:97102306, Wikidata:Q54830505 |
CVCL_9L84 | 2026-08-15 04:26:58 | 0 | |||||||
|
DD3044 Resource Report Resource Website |
ECACC Cat# 98011910, RRID:CVCL_9N73 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 98011910 | ECACC:98011910, Wikidata:Q54830534 |
CVCL_9N73 | 2026-08-15 04:26:59 | 0 | |||||
|
DD3006 Resource Report Resource Website |
RRID:CVCL_9L88 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC:97110614, Wikidata:Q54830512 |
CVCL_9L88 | 2026-08-15 04:26:58 | 0 |
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