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256,031 Results - per page

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Name Proper Citation Organism Disease Comments Defining Citation Category Sex Synonyms Vendor Catalog Number Cross References Hierarchy Originate from Same Individual ID Authority Record Last Update Mentions Count
GM00477
 
Resource Report
Resource Website
RRID:CVCL_H131 Homo sapiens (Human) PMID:6661932 Finite cell line Female GM-477, GM 0477 CLO:CLO_0025964,
Coriell:GM00477,
Wikidata:Q54836251
CVCL_H131 Cellosaurus 2026-10-10 05:25:09 0
GM00474
 
Resource Report
Resource Website
Coriell Cat# GM00474, RRID:CVCL_H130 Homo sapiens (Human) Finite cell line Male GM-474 Coriell GM00474 CLO:CLO_0025965,
Coriell:GM00474,
Wikidata:Q54836250
CVCL_H130 Cellosaurus 2026-10-10 05:25:09 0
GM00392
 
Resource Report
Resource Website
RRID:CVCL_V769 Homo sapiens (Human) Karyotypic information: 45,XX,der(13;22)(13qter->13q10::22q10->22qter) (Coriell=GM00392)., Population: Caucasian. PMID:1058758 Finite cell line Female GM-392 CLO:CLO_0026295,
Coriell:GM00392,
Wikidata:Q54836198
CVCL_V769 Cellosaurus 2026-10-10 05:25:08 0
GM00467
 
Resource Report
Resource Website
RRID:CVCL_J105 Homo sapiens (Human) Lesch-Nyhan syndrome PMID:6286839 Transformed cell line Female GM-467, GM 0467, GM0467, GM00467A CLO:CLO_0025976,
Coriell:GM00467,
Wikidata:Q54836242
CVCL_J105 Cellosaurus 2026-10-10 05:25:09 0
GM00403
 
Resource Report
Resource Website
RRID:CVCL_2N25 Homo sapiens (Human) Population: Caucasian. Finite cell line Female GM-403 CLO:CLO_0026294,
Coriell:GM00403,
Wikidata:Q54836199
CVCL_2N25 Cellosaurus 2026-10-10 05:25:08 0
GM00391
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00391, RRID:CVCL_JD74 Homo sapiens (Human) Fanconi anemia Finite cell line Female GM-391 Coriell GM00391 Coriell:GM00391,
Wikidata:Q54836197
CVCL_JD74 Cellosaurus 2026-10-10 05:25:08 0
GM00473
 
Resource Report
Resource Website
Coriell Cat# GM00473, RRID:CVCL_7287 Homo sapiens (Human) Finite cell line Male GM-473 Coriell GM00473 CLO:CLO_0025968,
Coriell:GM00473,
Wikidata:Q54836249
CVCL_7287 Cellosaurus 2026-10-10 05:25:09 0
GM00380
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM00380, RRID:CVCL_V768 Homo sapiens (Human) Karyotypic information: 46,XX,t(4;11)(4pter->4q23::11q11->11qter;11pter->11q11::4q23->4qter) (Coriell=GM00380)., Population: Caucasian. PMID:1149495 Finite cell line Female GM-380 Coriell GM00380 CLO:CLO_0026293,
Coriell:GM00380,
Wikidata:Q54836195
CVCL_V768 Cellosaurus 2026-10-10 05:25:08 1
GM00415
 
Resource Report
Resource Website
Coriell Cat# GM00415, RRID:CVCL_V529 Homo sapiens (Human) Hurler syndrome Population: Caucasian. PMID:8328452
PMID:30052969
Finite cell line Male GM-415, GM 00415 Coriell GM00415 CLO:CLO_0026126,
Coriell:GM00415,
Wikidata:Q54836208
CVCL_V529 Cellosaurus 2026-10-10 05:25:08 0
GM00392
 
Resource Report
Resource Website
Coriell Cat# GM00392, RRID:CVCL_V769 Homo sapiens (Human) Karyotypic information: 45,XX,der(13;22)(13qter->13q10::22q10->22qter) (Coriell=GM00392)., Population: Caucasian. PMID:1058758 Finite cell line Female GM-392 Coriell GM00392 CLO:CLO_0026295,
Coriell:GM00392,
Wikidata:Q54836198
CVCL_V769 Cellosaurus 2026-10-10 05:25:08 0
GM00407
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00407, RRID:CVCL_V428 Homo sapiens (Human) PMID:180603 Finite cell line GM-407, GM 407 Coriell GM00407 Coriell:GM00407,
Wikidata:Q54836202
CVCL_V428 Cellosaurus 2026-10-10 05:25:08 0
GM00432
 
Resource Report
Resource Website
RRID:CVCL_CV38 Homo sapiens (Human) Gout Population: Caucasian. Finite cell line Male GM-432 CLO:CLO_0026110,
Coriell:GM00432,
Wikidata:Q54836216
CVCL_CV38 Cellosaurus 2026-10-10 05:25:09 0
GM00378
 
Resource Report
Resource Website
RRID:CVCL_Y983 Homo sapiens (Human) Nephropathic cystinosis Population: Caucasian. PMID:28649545 Finite cell line Female GM0378, GM-378 CLO:CLO_0026290,
Coriell:GM00378,
Wikidata:Q54836193
CVCL_Y983 Cellosaurus 2026-10-10 05:25:08 0
GM00451
 
Resource Report
Resource Website
RRID:CVCL_X052 Homo sapiens (Human) Karyotypic information: 46,XY,inv(9)(pter->p13::q13->p13::q13->qter) (Coriell=GM00451)., Population: Caucasian. PMID:6617268 Finite cell line Male GM-451, GM 451 CLO:CLO_0026108,
Coriell:GM00451,
Wikidata:Q54836237
CVCL_X052 Cellosaurus 2026-10-10 05:25:09 0
GM00467
 
Resource Report
Resource Website
Coriell Cat# GM00467, RRID:CVCL_J105 Homo sapiens (Human) Lesch-Nyhan syndrome PMID:6286839 Transformed cell line Female GM-467, GM 0467, GM0467, GM00467A Coriell GM00467 CLO:CLO_0025976,
Coriell:GM00467,
Wikidata:Q54836242
CVCL_J105 Cellosaurus 2026-10-10 05:25:09 0
GM00470
 
Resource Report
Resource Website
Coriell Cat# GM00470, RRID:CVCL_M921 Homo sapiens (Human) Sandhoff disease Population: Mexican., Part of: Human variation panel. PMID:817596
PMID:3017984
Finite cell line Female GM-470, GM 470, GM17062 Coriell GM00470 CLO:CLO_0014561,
CLO:CLO_0025971,
Coriell:GM00470,
Coriell:GM17062,
Wikidata:Q54836246
CVCL_M921 Cellosaurus 2026-10-10 05:25:09 0
GM00486
 
Resource Report
Resource Website
RRID:CVCL_4N04 Homo sapiens (Human) Hyperlipoproteinemia, type IIa Population: Caucasian. Finite cell line Female GM-486, GM00486A, GM00486C CLO:CLO_0025957,
Coriell:GM00486,
Wikidata:Q54836256
CVCL_4N04 Cellosaurus 2026-10-10 05:25:10 0
GM00469
 
Resource Report
Resource Website
RRID:CVCL_7285 Homo sapiens (Human) Adenosine deaminase deficiency Population: Caucasian. PMID:1346349
PMID:2567118
PMID:7380831
Finite cell line Male GM 0469, GM-469, GM 469 CLO:CLO_0003511,
CLO:CLO_0025974,
CLDB:cl1478,
Coriell:GM00469,
Wikidata:Q54836244
CVCL_7285 Cellosaurus 2026-10-10 05:25:09 0
GM00474
 
Resource Report
Resource Website
RRID:CVCL_H130 Homo sapiens (Human) Finite cell line Male GM-474 CLO:CLO_0025965,
Coriell:GM00474,
Wikidata:Q54836250
CVCL_H130 Cellosaurus 2026-10-10 05:25:09 0
GM00446
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00446, RRID:CVCL_JD81 Homo sapiens (Human) Finite cell line Male GM-446 Coriell GM00446 Coriell:GM00446,
Wikidata:Q54836232
CVCL_JD81 Cellosaurus 2026-10-10 05:25:09 0

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