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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 Record Last Update Mentions Count
GM02211
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_JB67 Homo sapiens (Human) Wolman disease PMID:6782865 Finite cell line Male GM-2211, GM 2211, GM2211 Coriell:GM02211,
Wikidata:Q54837374
CVCL_JB67 2026-07-25 04:32:30 0
GM02255
 
Resource Report
Resource Website
RRID:CVCL_4N21 Homo sapiens (Human) Autosomal recessive torsion dystonia 2 Finite cell line Female GM-2255 CLO:CLO_0032157,
Coriell:GM02255,
Wikidata:Q54837395
CVCL_4N21 2026-07-25 04:32:32 0
GM02264
 
Resource Report
Resource Website
Coriell Cat# GM02264, RRID:CVCL_1U20 Homo sapiens (Human) Autosomal dominant torsion dystonia 1 Transformed cell line Female GM-2264 Coriell GM02264 CLO:CLO_0032161,
BioSample:SAMN00807640,
Coriell:GM02264,
Wikidata:Q54837397
CVCL_1U20 2026-07-25 04:32:31 0
GM02273
 
Resource Report
Resource Website
RRID:CVCL_9Q90 Homo sapiens (Human) I-cell disease Population: Caucasian. PMID:16465621 Finite cell line Male GM-2273, GM02273F, GM02273G CLO:CLO_0032126,
BioSample:SAMN00807650,
Coriell:GM02273,
Wikidata:Q54837402
CVCL_9Q90 2026-07-25 04:32:31 0
GM02228
 
Resource Report
Resource Website
Coriell Cat# GM02228, RRID:CVCL_U949 Homo sapiens (Human) Alkaptonuria Population: Caucasian. Finite cell line Male GM2228, GM-2228 Coriell GM02228 CLO:CLO_0032242,
BioSample:SAMN00807614,
Coriell:GM02228,
Wikidata:Q54837382
CVCL_U949 2026-07-25 04:32:32 0
GM02426
 
Resource Report
Resource Website
RRID:CVCL_2S82 Homo sapiens (Human) Karyotypic information: 46,XY,t(5;6)(5qter->5p15::6p21->6pter;6qter->6p21::5p15->5pter) (Coriell=GM02426)., Population: Caucasian. Finite cell line Male CLO:CLO_0033093,
BioSample:SAMN00807759,
Coriell:GM02426,
Wikidata:Q54837479
CVCL_2S82 2026-07-25 04:32:33 0
GM02380
 
Resource Report
Resource Website
RRID:CVCL_H181 Homo sapiens (Human) PMID:6617268 Finite cell line Female GM 2380 CLO:CLO_0033104,
Coriell:GM02380,
Wikidata:Q54837466
CVCL_H181 2026-07-25 04:32:34 0
GM02365
 
Resource Report
Resource Website
RRID:CVCL_1R62 Homo sapiens (Human) Coffin-Lowry syndrome Population: Caucasian. PMID:23665875 Finite cell line Male GM02365A CLO:CLO_0033101,
BioSample:SAMN00807737,
Coriell:GM02365,
Wikidata:Q54837463
CVCL_1R62 2026-07-25 04:32:32 0
GM02422
 
Resource Report
Resource Website
Coriell Cat# GM02422, RRID:CVCL_H183 Homo sapiens (Human) Trisomy 18 PMID:6661932 Finite cell line Female GM 2422 Coriell GM02422 CLO:CLO_0033089,
BioSample:SAMN00807755,
Coriell:GM02422,
Wikidata:Q54837476
CVCL_H183 2026-07-25 04:32:33 0
GM02336
 
Resource Report
Resource Website
RRID:CVCL_4J51 Homo sapiens (Human) Population: Caucasian. Finite cell line Male GM-2336 CLO:CLO_0033121,
BioSample:SAMN00807715,
Coriell:GM02336,
Wikidata:Q54837437
CVCL_4J51 2026-07-25 04:32:34 0
GM02419
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM02419, RRID:CVCL_UY61 Homo sapiens (Human) Finite cell line Female Coriell GM02419 Coriell:GM02419,
Wikidata:Q93577635
CVCL_UY61 2026-07-25 04:32:33 0
GM02439 GM1-iPSC clone 2
 
Resource Report
Resource Website
RRID:CVCL_VE85 Homo sapiens (Human) GM1 gangliosidosis Population: Turkish. PMID:25925601 Induced pluripotent stem cell Male GM1-iPSC-clone 2 SKIP:SKIP001351,
Wikidata:Q54837492
cvcl_w149 CVCL_VE85 2026-07-25 04:32:33 0
GM02340
 
Resource Report
Resource Website
RRID:CVCL_L749 Homo sapiens (Human) Sickle cell disease PMID:18511599
PMID:20715179
PMID:22905176
Finite cell line Female GM-2340, GM02340B CLO:CLO_0033117,
Coriell:GM02340,
GEO:GSM860991,
GEO:GSM1084803,
Wikidata:Q54837442
CVCL_L749 2026-07-25 04:32:32 0
GM02431
 
Resource Report
Resource Website
Discontinued
Coriell Cat# GM02378, RRID:CVCL_L975 Homo sapiens (Human) Chediak-Higashi syndrome Transformed cell line Male GM02431A, GM02378 Coriell GM02378 CLO:CLO_0033275,
BioSample:SAMN00807765,
Coriell:GM02378,
Coriell:GM02431,
Wikidata:Q54837482
CVCL_L975 2026-07-25 04:32:33 0
GM02408
 
Resource Report
Resource Website
Coriell Cat# GM02408, RRID:CVCL_F267 Homo sapiens (Human) Hyperlipoproteinemia, type IIa Population: Caucasian. Finite cell line Male GM02408A, GM2408A, GM02408C, GM02408D, JD, J.D. Coriell GM02408 CLO:CLO_0003525,
CLO:CLO_0033098,
CLDB:cl1492,
Coriell:GM02408,
Wikidata:Q54837469
CVCL_F267 2026-07-25 04:32:34 0
GM02435
 
Resource Report
Resource Website
Coriell Cat# GM02435, RRID:CVCL_CZ05 Homo sapiens (Human) Population: Caucasian. PMID:2567118 Finite cell line Female GM 2435 Coriell GM02435 CLO:CLO_0033279,
BioSample:SAMN00807773,
Coriell:GM02435,
Wikidata:Q54837487
CVCL_CZ05 2026-07-25 04:32:33 0
GM02440
 
Resource Report
Resource Website
Coriell Cat# GM02440, RRID:CVCL_GR97 Homo sapiens (Human) Type 1 diabetes mellitus Population: Native Central American; Pima. Finite cell line Male Coriell GM02440 CLO:CLO_0033316,
BioSample:SAMN00807777,
Coriell:GM02440,
Wikidata:Q54837494
CVCL_GR97 2026-07-25 04:32:33 0
GM02343
 
Resource Report
Resource Website
RRID:CVCL_AA20 Homo sapiens (Human) Familial dysautonomia Population: Jewish; Ashkenazi. PMID:6458814
PMID:29762696
PMID:30905397
Finite cell line Female GM-2343, GM 2343 CLO:CLO_0033113,
BioSample:SAMN00807723,
Coriell:GM02343,
GEO:GSM3592406,
GEO:GSM3592412,
Wikidata:Q54837445
CVCL_AA20 2026-07-25 04:32:34 0
GM02438
 
Resource Report
Resource Website
RRID:CVCL_IJ35 Homo sapiens (Human) Galactosialidosis PMID:8910459 Finite cell line Female GM02438A, GM02438a CLO:CLO_0033286,
Coriell:GM02438,
Wikidata:Q54837490
CVCL_IJ35 2026-07-25 04:32:33 0
GM02337
 
Resource Report
Resource Website
RRID:CVCL_X090 Homo sapiens (Human) Cri du chat syndrome Karyotypic information: 46,XX,del(5)(qter->p14) (Coriell=GM02337)., Population: Caucasian. PMID:6617268
PMID:6661932
Finite cell line Female GM-2337, GM 2337 CLO:CLO_0033122,
BioSample:SAMN00807717,
Coriell:GM02337,
Wikidata:Q54837438
CVCL_X090 2026-07-25 04:32:32 0

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