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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
GM02217
 
Resource Report
Resource Website
RRID:CVCL_1U19 Homo sapiens (Human) Autosomal dominant torsion dystonia 1 Transformed cell line Male GM-2217 CLO:CLO_0032248,
BioSample:SAMN00807612,
Coriell:GM02217,
Wikidata:Q54837378
CVCL_1U19 Cellosaurus 2026-09-26 06:48:54 0
GM02270
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_UR70 Homo sapiens (Human) Population: Caucasian. Finite cell line Male GM2270, GM02270A, GM2270A Coriell:GM02270,
Wikidata:Q93576868
CVCL_UR70 Cellosaurus 2026-09-26 06:48:54 0
GM02294
 
Resource Report
Resource Website
RRID:CVCL_CZ84 Homo sapiens (Human) Adenosine deaminase deficiency Population: African American. PMID:2567118 Transformed cell line Male GM 2294 CLO:CLO_0032206,
BioSample:SAMN00807662,
Coriell:GM02294,
Wikidata:Q54837410
CVCL_CZ84 Cellosaurus 2026-09-26 06:48:54 0
GM02274
 
Resource Report
Resource Website
RRID:CVCL_CX30 Homo sapiens (Human) Population: Caucasian. PMID:16465621 Finite cell line Female GM-2274 CLO:CLO_0032128,
BioSample:SAMN00807652,
Coriell:GM02274,
Wikidata:Q54837405
CVCL_CX30 Cellosaurus 2026-09-26 06:48:54 0
GM02209
 
Resource Report
Resource Website
RRID:CVCL_CZ04 Homo sapiens (Human) Population: Caucasian. PMID:7438795 Finite cell line Female GM2209 CLO:CLO_0032261,
BioSample:SAMN00807606,
Coriell:GM02209,
Wikidata:Q54837373
CVCL_CZ04 Cellosaurus 2026-09-26 06:48:54 0
GM02291
 
Resource Report
Resource Website
RRID:CVCL_7357 Homo sapiens (Human) Lesch-Nyhan syndrome Population: Caucasian. PMID:477417 Finite cell line Male GM-2291 CLO:CLO_0003524,
CLO:CLO_0032130,
CLDB:cl1491,
BioSample:SAMN00807656,
Coriell:GM02291,
Wikidata:Q54837407
CVCL_7357 Cellosaurus 2026-09-26 06:48:54 0
GM02226
 
Resource Report
Resource Website
RRID:CVCL_R906 Homo sapiens (Human) PMID:21335555 Finite cell line Female GM-2226, GM 2226, GM2226 CLO:CLO_0032251,
Coriell:GM02226,
Wikidata:Q54837380
CVCL_R906 Cellosaurus 2026-09-26 06:48:54 0
GM02206
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_L969 Homo sapiens (Human) Ehlers-Danlos syndrome Population: Caucasian. PMID:6617268
PMID:23665875
PMID:25326100
Finite cell line Female GM-2206 GM 2206, GM01514 CLO:CLO_0032262,
BioSample:SAMN00807604,
Coriell:GM01514,
Coriell:GM02206,
GEO:GSM1266977,
Wikidata:Q54837370
CVCL_L969 Cellosaurus 2026-09-26 06:48:53 0
GM02256
 
Resource Report
Resource Website
RRID:CVCL_4N22 Homo sapiens (Human) Autosomal recessive torsion dystonia 2 Transformed cell line Female GM-2256 CLO:CLO_0032158,
Coriell:GM02256,
Wikidata:Q54837396
CVCL_4N22 Cellosaurus 2026-09-26 06:48:54 0
GM02242
 
Resource Report
Resource Website
RRID:CVCL_GZ40 Homo sapiens (Human) Adrenal gland hyperplasia III Population: Caucasian. Transformed cell line Female GM-2242 CLO:CLO_0032239,
BioSample:SAMN00807624,
Coriell:GM02242,
Wikidata:Q54837387
CVCL_GZ40 Cellosaurus 2026-09-26 06:48:54 0
GM02316
 
Resource Report
Resource Website
RRID:CVCL_8A66 Homo sapiens (Human) Population: Caucasian; Irish. PMID:21418647
PMID:24555846
PMID:25326100
Finite cell line Male GM-2316 CLO:CLO_0032169,
BioSample:SAMN00807689,
Coriell:GM02316,
GEO:GSM651150,
GEO:GSM651151,
GEO:GSM1257697,
GEO:GSM1266972,
GEO:GSM1267051,
GEO:GSM1288439,
GEO:GSM1314047,
Wikidata:Q54837424
CVCL_8A66 Cellosaurus 2026-09-26 06:48:54 0
GM02207
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_JB90 Homo sapiens (Human) Ehlers-Danlos syndrome, type IV Finite cell line Female GM-2207 Coriell:GM02207,
Wikidata:Q54837372
CVCL_JB90 Cellosaurus 2026-09-26 06:48:53 0
GM02266
 
Resource Report
Resource Website
Coriell Cat# GM02266, RRID:CVCL_BT13 Homo sapiens (Human) Beta thalassemia Transformed cell line Female GM-2266, GM02266A Coriell GM02266 CLO:CLO_0032119,
BioSample:SAMN00807642,
Coriell:GM02266,
Wikidata:Q54837398
CVCL_BT13 Cellosaurus 2026-09-26 06:48:54 0
GM02290
 
Resource Report
Resource Website
RRID:CVCL_7356 Homo sapiens (Human) Lesch-Nyhan syndrome Population: Caucasian. PMID:477417
PMID:6087472
Finite cell line Male GM-2290, GM 2290 GM02290A CLO:CLO_0003523,
CLO:CLO_0032129,
CLDB:cl1490,
BioSample:SAMN00807654,
Coriell:GM02290,
Wikidata:Q54837406
CVCL_7356 Cellosaurus 2026-09-26 06:48:54 0
GM02267
 
Resource Report
Resource Website
RRID:CVCL_BT14 Homo sapiens (Human) Beta thalassemia PMID:6196781 Transformed cell line Female GM-2267 CLO:CLO_0032120,
BioSample:SAMN00807644,
Coriell:GM02267,
Wikidata:Q54837399
CVCL_BT14 Cellosaurus 2026-09-26 06:48:54 0
GM02292
 
Resource Report
Resource Website
Coriell Cat# GM02292, RRID:CVCL_D868 Homo sapiens (Human) Lesch-Nyhan syndrome Population: Caucasian. PMID:477417
PMID:2762303
Transformed cell line Male GM-2292, GM 2292, GM2292A, GM02292B Coriell GM02292 CLO:CLO_0032131,
BioSample:SAMN00807658,
Coriell:GM02292,
Wikidata:Q54837408
CVCL_D868 Cellosaurus 2026-09-26 06:48:54 0
GM02264
 
Resource Report
Resource Website
RRID:CVCL_1U20 Homo sapiens (Human) Autosomal dominant torsion dystonia 1 Transformed cell line Female GM-2264 CLO:CLO_0032161,
BioSample:SAMN00807640,
Coriell:GM02264,
Wikidata:Q54837397
CVCL_1U20 Cellosaurus 2026-09-26 06:48:54 0
GM02300
 
Resource Report
Resource Website
Coriell Cat# GM02300, RRID:CVCL_IL09 Homo sapiens (Human) Androgen insensitivity syndrome Population: African American. Finite cell line Sex ambiguous GM-2300, GM02300A Coriell GM02300 CLO:CLO_0032203,
BioSample:SAMN00807669,
Coriell:GM02300,
Wikidata:Q54837414
CVCL_IL09 Cellosaurus 2026-09-26 06:48:54 0
GM02324
 
Resource Report
Resource Website
RRID:CVCL_X261 Homo sapiens (Human) Karyotypic information: 46,XX,9qh+,t(16;22)(16qter->16p13.11::22q11.21->22qter;22pter->22q11.21::16p13.11->16pter) (Coriell=GM02324)., Population: Caucasian. PMID:2714795 Transformed cell line Female GM-2324, GM2324, GM02324A CLO:CLO_0032172,
BioSample:SAMN00807693,
Coriell:GM02324,
Wikidata:Q54837426
CVCL_X261 Cellosaurus 2026-09-26 06:48:54 0
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 Cellosaurus 2026-09-26 06:48:54 0

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