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117,735 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
GM00882
 
Resource Report
Resource Website
RRID:CVCL_0Q46 Homo sapiens (Human) Fabry disease Population: Caucasian; Italian. PMID:29982630 Finite cell line Male GM-882 CLO:CLO_0029628,
Coriell:GM00882,
Wikidata:Q54836506
CVCL_0Q46 Cellosaurus 2026-09-26 06:48:35 0
GM00804
 
Resource Report
Resource Website
Coriell Cat# GM00804, RRID:CVCL_H175 Homo sapiens (Human) Nephropathic cystinosis Finite cell line Male GM-804 Coriell GM00804 CLO:CLO_0029644,
Coriell:GM00804,
Wikidata:Q54836463
CVCL_H175 Cellosaurus 2026-09-26 06:48:34 0
GM00802
 
Resource Report
Resource Website
Coriell Cat# GM00802, RRID:CVCL_1B70 Homo sapiens (Human) Fucosidosis PMID:4074382 Finite cell line Male GM-802, GM 802, GM802 Coriell GM00802 CLO:CLO_0028847,
Coriell:GM00802,
Wikidata:Q54836461
CVCL_1B70 Cellosaurus 2026-09-26 06:48:34 0
GM00805
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00805, RRID:CVCL_JD85 Homo sapiens (Human) Finite cell line Male GM-805 Coriell GM00805 Coriell:GM00805,
Wikidata:Q54836464
CVCL_JD85 Cellosaurus 2026-09-26 06:48:34 0
GM00813
 
Resource Report
Resource Website
RRID:CVCL_2H04 Homo sapiens (Human) Population: Caucasian. Finite cell line Male GM0813, GM-813 CLO:CLO_0029647,
Coriell:GM00813,
Wikidata:Q54836467
CVCL_2H04 Cellosaurus 2026-09-26 06:48:34 0
GM00811
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_U702 Homo sapiens (Human) Bloom syndrome Donor information: From Bloom Syndrome Registry patient 3(HoCo) (BSR3)., Population: Jewish; Ashkenazi. PMID:436333
PMID:908169
PMID:2878433
Finite cell line Male GM-811, GM0811, GM811, GM 811, GM00811B CLO:CLO_0029646,
Coriell:GM00811,
GEO:GSM1317007,
Wikidata:Q54836466
CVCL_U702 Cellosaurus 2026-09-26 06:48:34 0
GM00803
 
Resource Report
Resource Website
Coriell Cat# GM00803, RRID:CVCL_X077 Homo sapiens (Human) Population: Caucasian. PMID:6617268
PMID:6661932
PMID:23665875
Finite cell line Male GM-803, GM 803 Coriell GM00803 CLO:CLO_0029645,
Coriell:GM00803,
Wikidata:Q54836462
CVCL_X077 Cellosaurus 2026-09-26 06:48:34 0
GM00903
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_CX34 Homo sapiens (Human) Mucopolysaccharidosis type IIIA Finite cell line Male GM-903 Coriell:GM00903,
Wikidata:Q54836521
CVCL_CX34 Cellosaurus 2026-09-26 06:48:36 0
GM00906
 
Resource Report
Resource Website
RRID:CVCL_CW98 Homo sapiens (Human) Population: Caucasian. PMID:28649545 Finite cell line Male GM0906, GM-906 CLO:CLO_0029599,
Coriell:GM00906,
Wikidata:Q54836524
CVCL_CW98 Cellosaurus 2026-09-26 06:48:36 0
GM00847
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM00847, RRID:CVCL_7908 Homo sapiens (Human) Lesch-Nyhan syndrome Characteristics: Cell line positive for alternative lengthening of telomeres (ALT+) (CelloPub=CLPUB00712; PubMed=19935656)., Population: African American. PMID:174085
PMID:191830
PMID:1260760
PMID:3413074
PMID:9175740
PMID:11359895
PMID:12361951
PMID:19935656
PMID:26001292
Transformed cell line Male LN-SV, LNSV, GM-847, GM 847, GM847 Coriell GM00847 CLO:CLO_0029655,
EFO:EFO_0022519,
Coriell:GM00847,
Wikidata:Q54836472
cvcl_f127 CVCL_7908 Cellosaurus 2026-09-26 06:48:35 5
GM00861
 
Resource Report
Resource Website
Coriell Cat# GM00861, RRID:CVCL_4D79 Homo sapiens (Human) Karyotypic information: 46,XY,ins(5;1)(5pter->5q15::1q25->1q32::5q15->5qter;1pter->1q25::1q32->1qter) (Coriell=GM00861)., Population: Caucasian. Finite cell line Male GM-861 Coriell GM00861 CLO:CLO_0029634,
Coriell:GM00861,
Wikidata:Q54836482
CVCL_4D79 Cellosaurus 2026-09-26 06:48:35 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 2026-09-26 06:48:35 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 2026-09-26 06:48:36 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 2026-09-26 06:48:34 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 2026-09-26 06:48:35 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 2026-09-26 06:48:34 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 2026-09-26 06:48:35 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 2026-09-26 06:48:35 0
GM00852
 
Resource Report
Resource Website
RRID:CVCL_8515 Homo sapiens (Human) Gaucher disease Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:6593712
PMID:18691744
PMID:19815695
Finite cell line Male GM-852 CLO:CLO_0029631,
Coriell:GM00852,
Wikidata:Q54836475
CVCL_8515 Cellosaurus 2026-09-26 06:48:35 0
GM00951
 
Resource Report
Resource Website
RRID:CVCL_IL07 Homo sapiens (Human) Scleromyxedema Population: Caucasian. Finite cell line Male GM-951 CLO:CLO_0029519,
Coriell:GM00951,
Wikidata:Q54836559
CVCL_IL07 Cellosaurus 2026-09-26 06:48:36 0

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