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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
GM00806
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00806, RRID:CVCL_CX43 Homo sapiens (Human) Galactosialidosis PMID:8910459 Finite cell line Female GM-806, GM 806 Coriell GM00806 Coriell:GM00806,
Wikidata:Q54836465
CVCL_CX43 Cellosaurus 2026-10-10 05:25:15 0
GM00898
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_CX65 Homo sapiens (Human) Niemann-Pick disease, type A Finite cell line Sex unspecified GM-898 Coriell:GM00898,
Wikidata:Q54836518
CVCL_CX65 Cellosaurus 2026-10-10 05:25:17 0
GM00891
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_JE19 Homo sapiens (Human) Transformed cell line Sex unspecified GM-891 Coriell:GM00891,
Wikidata:Q54836513
CVCL_JE19 Cellosaurus 2026-10-10 05:25:17 0
GM00885
 
Resource Report
Resource Website
RRID:CVCL_2H09 Homo sapiens (Human) Homocystinuria Population: Caucasian. Finite cell line Male GM0885, GM-885 CLO:CLO_0029611,
Coriell:GM00885,
Wikidata:Q54836508
CVCL_2H09 Cellosaurus 2026-10-10 05:25:16 0
GM00863
 
Resource Report
Resource Website
RRID:CVCL_7303 Homo sapiens (Human) Wolman disease PMID:6782865 Finite cell line Female GM-863, GM 0863 CLO:CLO_0003517,
CLO:CLO_0029632,
CLDB:cl1484,
Coriell:GM00863,
Wikidata:Q54836485
CVCL_7303 Cellosaurus 2026-10-10 05:25:16 0
GM00901
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00901, RRID:CVCL_CX32 Homo sapiens (Human) Hunter syndrome Finite cell line Male GM-901 Coriell GM00901 Coriell:GM00901,
Wikidata:Q54836519
CVCL_CX32 Cellosaurus 2026-10-10 05:25:17 0
GM00804
 
Resource Report
Resource Website
RRID:CVCL_H175 Homo sapiens (Human) Nephropathic cystinosis Finite cell line Male GM-804 CLO:CLO_0029644,
Coriell:GM00804,
Wikidata:Q54836463
CVCL_H175 Cellosaurus 2026-10-10 05:25:15 0
GM00898
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00898, RRID:CVCL_CX65 Homo sapiens (Human) Niemann-Pick disease, type A Finite cell line Sex unspecified GM-898 Coriell GM00898 Coriell:GM00898,
Wikidata:Q54836518
CVCL_CX65 Cellosaurus 2026-10-10 05:25:17 0
GM00897
 
Resource Report
Resource Website
RRID:CVCL_H137 Homo sapiens (Human) Cystic fibrosis Population: Caucasian. Transformed cell line Male GM-897 CLO:CLO_0029580,
Coriell:GM00897,
Wikidata:Q54836517
CVCL_H137 Cellosaurus 2026-10-10 05:25:17 0
GM00845
 
Resource Report
Resource Website
RRID:CVCL_V782 Homo sapiens (Human) Karyotypic information: 46,XX,t(2;8)(2pter->2q37::8q13->8qter;8pter->8q13::2q37->2qter)mat (Coriell=GM00845)., Population: Caucasian. PMID:648194 Finite cell line Female GM-845 CLO:CLO_0029652,
Coriell:GM00845,
Wikidata:Q54836470
CVCL_V782 Cellosaurus 2026-10-10 05:25:16 0
GM00805
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_JD85 Homo sapiens (Human) Finite cell line Male GM-805 Coriell:GM00805,
Wikidata:Q54836464
CVCL_JD85 Cellosaurus 2026-10-10 05:25:15 0
GM00904
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00904, RRID:CVCL_CX39 Homo sapiens (Human) Farber lipogranulomatosis Finite cell line Female GM-904 Coriell GM00904 Coriell:GM00904,
Wikidata:Q54836522
CVCL_CX39 Cellosaurus 2026-10-10 05:25:17 0
GM00860
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00860, RRID:CVCL_X238 Homo sapiens (Human) PMID:6661932
PMID:23665875
Finite cell line Female GM-860, GM 860 Coriell GM00860 CLO:CLO_0029629,
Coriell:GM00860,
Wikidata:Q54836481
CVCL_X238 Cellosaurus 2026-10-10 05:25:16 0
GM00857
 
Resource Report
Resource Website
Coriell Cat# GM00857, RRID:CVCL_X237 Homo sapiens (Human) Turner syndrome PMID:6661932
PMID:21949351
PMID:23665875
Finite cell line Female GM-857, GM 857, GM00857A, TS3 fibroblast Coriell GM00857 CLO:CLO_0029630,
Coriell:GM00857,
Wikidata:Q54836480
CVCL_X237 Cellosaurus 2026-10-10 05:25:16 0
GM00862
 
Resource Report
Resource Website
RRID:CVCL_4D19 Homo sapiens (Human) Hunter syndrome Population: Puerto Rican. Finite cell line Male GM-862 CLO:CLO_0029635,
Coriell:GM00862,
Wikidata:Q54836484
CVCL_4D19 Cellosaurus 2026-10-10 05:25:16 0
GM00869
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00869, RRID:CVCL_JC76 Homo sapiens (Human) Renal agenesis Finite cell line Female GM-869 Coriell GM00869 Coriell:GM00869,
Wikidata:Q54836492
CVCL_JC76 Cellosaurus 2026-10-10 05:25:16 0
GM00854
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00854, RRID:CVCL_CX48 Homo sapiens (Human) Krabbe disease Finite cell line Female GM-854 Coriell GM00854 Coriell:GM00854,
Wikidata:Q54836477
CVCL_CX48 Cellosaurus 2026-10-10 05:25:16 0
GM00844
 
Resource Report
Resource Website
RRID:CVCL_4E24 Homo sapiens (Human) Sea-blue histiocyte syndrome Population: Caucasian. Finite cell line Male GM-844 CLO:CLO_0029649,
Coriell:GM00844,
Wikidata:Q54836469
CVCL_4E24 Cellosaurus 2026-10-10 05:25:15 0
GM00806
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_CX43 Homo sapiens (Human) Galactosialidosis PMID:8910459 Finite cell line Female GM-806, GM 806 Coriell:GM00806,
Wikidata:Q54836465
CVCL_CX43 Cellosaurus 2026-10-10 05:25:15 0
GM00868
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00868, RRID:CVCL_JD86 Homo sapiens (Human) 46,XY gonadal dysgenesis Finite cell line Sex ambiguous GM-868 Coriell GM00868 Coriell:GM00868,
Wikidata:Q54836491
CVCL_JD86 Cellosaurus 2026-10-10 05:25:16 0

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