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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
HH0027 Resource Report Resource Website |
ECACC Cat# 89030625, RRID:CVCL_8W77 | Homo sapiens (Human) | Karyotypic information: 47,XX,inv dup(15)(q11.2) (ECACC=89030625)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 89030625 | ECACC:89030625, Wikidata:Q54887363 |
CVCL_8W77 | 2026-02-07 08:16:47 | 0 | |||||
|
HH0004 Resource Report Resource Website |
ECACC Cat# 910430171, RRID:CVCL_8W59 | Homo sapiens (Human) | Karyotypic information: 46,Y,Xp- (ECACC=910430171)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC | 910430171 | ECACC:910430171, Wikidata:Q54887343 |
CVCL_8W59 | 2026-02-07 08:16:46 | 0 | |||||
|
HH0005 Resource Report Resource Website |
ECACC Cat# 89030635, RRID:CVCL_8W60 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 89030635 | ECACC:89030635, Wikidata:Q54887344 |
CVCL_8W60 | 2026-02-07 08:16:36 | 0 | |||||
|
HH0025 Resource Report Resource Website |
ECACC Cat# 89030628, RRID:CVCL_8W76 | Homo sapiens (Human) | Karyotypic information: 46,XX,-18,+i(18q); 47,XX,-18,+i(18q)+i(18p) (ECACC=89030628)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 89030628 | ECACC:89030628, Wikidata:Q54887362 |
CVCL_8W76 | 2026-02-07 08:16:35 | 0 | |||||
|
HH0117 Resource Report Resource Website |
ECACC Cat# 89042115, RRID:CVCL_8X14 | Homo sapiens (Human) | Karyotypic information: 46,XX,t(2;9)(p11.2;p13) (ECACC=89042115)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 89042115 | ECACC:89042115, Wikidata:Q54887407 |
CVCL_8X14 | 2026-02-07 08:16:49 | 0 | |||||
|
HH0094 Resource Report Resource Website |
ECACC Cat# 89061910, RRID:CVCL_8X00 | Homo sapiens (Human) | Karyotypic information: 47,XX,+i(12p) (ECACC=89061910)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 89061910 | ECACC:89061910, Wikidata:Q54887387 |
CVCL_8X00 | 2026-02-07 08:16:36 | 0 | |||||
|
HH0106 Resource Report Resource Website |
ECACC Cat# 89041151, RRID:CVCL_8X08 | Homo sapiens (Human) | Karyotypic information: 46,X,dup(Xq) (ECACC=89041151)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 89041151 | ECACC:89041151, Wikidata:Q54887396 |
CVCL_8X08 | 2026-02-07 08:16:49 | 0 | |||||
|
HH0092 Resource Report Resource Website |
ECACC Cat# 89041120, RRID:CVCL_8W98 | Homo sapiens (Human) | Karyotypic information: 46,X,inv(X)(p11;q28) (ECACC=89041120)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 89041120 | ECACC:89041120, Wikidata:Q54887385 |
CVCL_8W98 | 2026-02-07 08:16:48 | 0 | |||||
|
HH0134 Resource Report Resource Website |
ECACC Cat# 89061429, RRID:CVCL_8X27 | Homo sapiens (Human) | Fragile X syndrome | Population: Caucasian., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Sex unspecified | ECACC | 89061429 | ECACC:89061429, Wikidata:Q54887420 |
CVCL_8X27 | 2026-02-07 08:16:39 | 0 | ||||
|
HH0055 Resource Report Resource Website |
ECACC Cat# 89022424, RRID:CVCL_8W87 | Homo sapiens (Human) | Karyotypic information: 46,XY,t(3;5;12)(q12;q11;p11),t(6;17)(p21;q21) (ECACC=89022424)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 89022424 | ECACC:89022424, Wikidata:Q54887374 |
CVCL_8W87 | 2026-02-07 08:16:37 | 0 | |||||
|
HH0059 Resource Report Resource Website |
ECACC Cat# 89022840, RRID:CVCL_8W90 | Homo sapiens (Human) | Karyotypic information: 46,XY,18p- (ECACC=89022840)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 89022840 | ECACC:89022840, Wikidata:Q54887377 |
CVCL_8W90 | 2026-02-07 08:16:37 | 0 | |||||
|
HH0066 Resource Report Resource Website |
ECACC Cat# 89030279, RRID:CVCL_8W93 | Homo sapiens (Human) | Ring chromosome 22 syndrome | Karyotypic information: 46,XY,r(22) (ECACC=89030279)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 89030279 | ECACC:89030279, Wikidata:Q54887380 |
CVCL_8W93 | 2026-02-07 08:16:37 | 0 | ||||
|
HH0056 Resource Report Resource Website |
ECACC Cat# 89022837, RRID:CVCL_8W88 | Homo sapiens (Human) | Karyotypic information: 47,XY,+i(Xq) (ECACC=89022837)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 89022837 | ECACC:89022837, Wikidata:Q54887375 |
CVCL_8W88 | 2026-02-07 08:16:35 | 0 | |||||
|
HH0073 Resource Report Resource Website |
ECACC Cat# 89030287, RRID:CVCL_8W95 | Homo sapiens (Human) | Karyotypic information: 46,XY; 46,XY,5p- (ECACC=89030287)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 89030287 | ECACC:89030287, Wikidata:Q54887382 |
CVCL_8W95 | 2026-02-07 08:16:48 | 0 | |||||
|
HH0108 Resource Report Resource Website |
ECACC Cat# 89041153, RRID:CVCL_8X10 | Homo sapiens (Human) | Karyotypic information: 46,XX,t(1;14)(q21;q32) (ECACC=89041153)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 89041153 | ECACC:89041153, Wikidata:Q54887399 |
CVCL_8X10 | 2026-02-07 08:16:36 | 0 | |||||
|
HH0123 Resource Report Resource Website |
ECACC Cat# 89042126, RRID:CVCL_8X19 | Homo sapiens (Human) | Karyotypic information: 47,XY,+f (ECACC=89042126)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC | 89042126 | ECACC:89042126, Wikidata:Q54887412 |
CVCL_8X19 | 2026-02-07 08:16:37 | 0 | |||||
|
HH0102 Resource Report Resource Website |
ECACC Cat# 89041144, RRID:CVCL_8X04 | Homo sapiens (Human) | Karyotypic information: 48,XX,+i(Yq)+i(Yq) (ECACC=89041144)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 89041144 | ECACC:89041144, Wikidata:Q54887392 |
CVCL_8X04 | 2026-02-07 08:16:36 | 0 | |||||
|
HH0039 Resource Report Resource Website |
ECACC Cat# 89030274, RRID:CVCL_8W82 | Homo sapiens (Human) | Population: Caucasian., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 89030274 | ECACC:89030274, Wikidata:Q54887369 |
CVCL_8W82 | 2026-02-07 08:16:35 | 0 | |||||
|
HH0095 Resource Report Resource Website |
ECACC Cat# 89041125, RRID:CVCL_8X01 | Homo sapiens (Human) | Karyotypic information: 46,XY; 46,XY,inv(21) (ECACC=89041125)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC | 89041125 | ECACC:89041125, Wikidata:Q54887388 |
CVCL_8X01 | 2026-02-07 08:16:49 | 0 | |||||
|
HH0061 Resource Report Resource Website |
ECACC Cat# 89030272, RRID:CVCL_8W91 | Homo sapiens (Human) | Karyotypic information: 46,XX,dir ins(2;18)(q2.1;q11.2 q21.3) (ECACC=89030272)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 89030272 | ECACC:89030272, Wikidata:Q54887378 |
CVCL_8W91 | 2026-02-07 08:16:36 | 0 |
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