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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
GM02217
 
Resource Report
Resource Website
Coriell Cat# GM02217, RRID:CVCL_1U19 Homo sapiens (Human) Autosomal dominant torsion dystonia 1 Transformed cell line Male GM-2217 Coriell GM02217 CLO:CLO_0032248,
BioSample:SAMN00807612,
Coriell:GM02217,
Wikidata:Q54837378
CVCL_1U19 2026-07-25 04:32:32 0
GM02241
 
Resource Report
Resource Website
RRID:CVCL_GZ39 Homo sapiens (Human) Adrenal gland hyperplasia III Population: Caucasian. Finite cell line Female GM-2241 CLO:CLO_0032240,
BioSample:SAMN00807622,
Coriell:GM02241,
Wikidata:Q54837386
CVCL_GZ39 2026-07-25 04:32:31 0
GM02267
 
Resource Report
Resource Website
Coriell Cat# GM02267, RRID:CVCL_BT14 Homo sapiens (Human) Beta thalassemia PMID:6196781 Transformed cell line Female GM-2267 Coriell GM02267 CLO:CLO_0032120,
BioSample:SAMN00807644,
Coriell:GM02267,
Wikidata:Q54837399
CVCL_BT14 2026-07-25 04:32:32 0
GM02314
 
Resource Report
Resource Website
Coriell Cat# GM02314, RRID:CVCL_8A64 Homo sapiens (Human) Farber lipogranulomatosis Population: Caucasian; Irish. PMID:21418647
PMID:25326100
Finite cell line Female GM-2314 Coriell GM02314 CLO:CLO_0032177,
BioSample:SAMN00807685,
Coriell:GM02314,
GEO:GSM651168,
GEO:GSM651169,
GEO:GSM1266974,
GEO:GSM1267053,
Wikidata:Q54837422
CVCL_8A64 2026-07-25 04:32:32 0
GM02327
 
Resource Report
Resource Website
RRID:CVCL_AD65 Homo sapiens (Human) Maple syrup urine disease Population: Caucasian; Mennonite. Finite cell line Female GM2327, GM-2327 CLO:CLO_0032179,
BioSample:SAMN00807697,
Coriell:GM02327,
Wikidata:Q54837428
CVCL_AD65 2026-07-25 04:32:32 0
GM02269
 
Resource Report
Resource Website
RRID:CVCL_H180 Homo sapiens (Human) Finite cell line Male GM-2269 CLO:CLO_0032123,
BioSample:SAMN00807648,
Coriell:GM02269,
Wikidata:Q54837401
CVCL_H180 2026-07-25 04:32:32 0
GM02232
 
Resource Report
Resource Website
RRID:CVCL_BT12 Homo sapiens (Human) Beta thalassemia Population: Caucasian; Greek. Transformed cell line Female GM-2232, GM02232A CLO:CLO_0032243,
BioSample:SAMN00807620,
Coriell:GM02232,
Wikidata:Q54837385
CVCL_BT12 2026-07-25 04:32:31 0
GM02256
 
Resource Report
Resource Website
Coriell Cat# GM02256, RRID:CVCL_4N22 Homo sapiens (Human) Autosomal recessive torsion dystonia 2 Transformed cell line Female GM-2256 Coriell GM02256 CLO:CLO_0032158,
Coriell:GM02256,
Wikidata:Q54837396
CVCL_4N22 2026-07-25 04:32:32 0
GM02207
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM02207, RRID:CVCL_JB90 Homo sapiens (Human) Ehlers-Danlos syndrome, type IV Finite cell line Female GM-2207 Coriell GM02207 Coriell:GM02207,
Wikidata:Q54837372
CVCL_JB90 2026-07-25 04:32:30 0
GM02205
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_L968 Homo sapiens (Human) Population: Caucasian. PMID:6617268
PMID:23665875
PMID:24555846
PMID:25326100
Finite cell line Male GM-2205, GM 2205, GM01515 CLO:CLO_0032263,
BioSample:SAMN00807602,
Coriell:GM01515,
Coriell:GM02205,
GEO:GSM1266975,
GEO:GSM1267054,
GEO:GSM1288438,
Wikidata:Q54837369
CVCL_L968 2026-07-25 04:32:32 0
GM02329
 
Resource Report
Resource Website
RRID:CVCL_X263 Homo sapiens (Human) Trisomy 9 Karyotypic information: 47,XX,+9 [5]; 46,XX [45] (Coriell=GM02329)., Population: Caucasian. PMID:6661932 Finite cell line Female GM-2329, GM 2329 CLO:CLO_0033128,
BioSample:SAMN00807701,
Coriell:GM02329,
Wikidata:Q54837430
CVCL_X263 2026-07-25 04:32:32 0
GM02224
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_CX22 Homo sapiens (Human) Lactic acidosis Finite cell line Female GM-2224 Coriell:GM02224,
Wikidata:Q54837379
CVCL_CX22 2026-07-25 04:32:31 0
GM02291
 
Resource Report
Resource Website
Coriell Cat# GM02291, RRID:CVCL_7357 Homo sapiens (Human) Lesch-Nyhan syndrome Population: Caucasian. PMID:477417 Finite cell line Male GM-2291 Coriell GM02291 CLO:CLO_0003524,
CLO:CLO_0032130,
CLDB:cl1491,
BioSample:SAMN00807656,
Coriell:GM02291,
Wikidata:Q54837407
CVCL_7357 2026-07-25 04:32:33 0
GM02306
 
Resource Report
Resource Website
RRID:CVCL_4N23 Homo sapiens (Human) Autosomal recessive torsion dystonia 2 Population: Caucasian. Finite cell line Male GM-2306 CLO:CLO_0032175,
BioSample:SAMN00807681,
Coriell:GM02306,
Wikidata:Q54837420
CVCL_4N23 2026-07-25 04:32:31 0
GM02305
 
Resource Report
Resource Website
Coriell Cat# GM02305, RRID:CVCL_1U22 Homo sapiens (Human) Autosomal dominant torsion dystonia 1 Population: Caucasian. Transformed cell line Female GM-2305 Coriell GM02305 CLO:CLO_0032207,
BioSample:SAMN00807679,
Coriell:GM02305,
Wikidata:Q54837419
CVCL_1U22 2026-07-25 04:32:31 0
GM02205
 
Resource Report
Resource Website
Discontinued
Coriell Cat# GM01515, RRID:CVCL_L968 Homo sapiens (Human) Population: Caucasian. PMID:6617268
PMID:23665875
PMID:24555846
PMID:25326100
Finite cell line Male GM-2205, GM 2205, GM01515 Coriell GM01515 CLO:CLO_0032263,
BioSample:SAMN00807602,
Coriell:GM01515,
Coriell:GM02205,
GEO:GSM1266975,
GEO:GSM1267054,
GEO:GSM1288438,
Wikidata:Q54837369
CVCL_L968 2026-07-25 04:32:30 0
GM02325
 
Resource Report
Resource Website
Coriell Cat# GM02325, RRID:CVCL_X262 Homo sapiens (Human) Karyotypic information: 47,XX,+der(22)(22pter->22q11.21::16p13.11->16pter)mat (Coriell=GM02325)., Population: Caucasian. PMID:6661932
PMID:23665875
Finite cell line Female GM-2325, GM 2325 Coriell GM02325 CLO:CLO_0032174,
BioSample:SAMN00807695,
Coriell:GM02325,
Wikidata:Q54837427
CVCL_X262 2026-07-25 04:32:32 0
GM02230
 
Resource Report
Resource Website
Coriell Cat# GM02230, RRID:CVCL_4J49 Homo sapiens (Human) Transformed cell line Female GM-2230 Coriell GM02230 CLO:CLO_0032244,
BioSample:SAMN00807618,
Coriell:GM02230,
Wikidata:Q54837384
CVCL_4J49 2026-07-25 04:32:31 0
GM02315
 
Resource Report
Resource Website
RRID:CVCL_8A65 Homo sapiens (Human) Farber lipogranulomatosis PMID:11241842
PMID:21335555
Finite cell line Female GM-2315, FD-1 BTO:BTO_0004460,
CLO:CLO_0032178,
BioSample:SAMN00807687,
Coriell:GM02315,
Wikidata:Q54837423
CVCL_8A65 2026-07-25 04:32:32 0
GM02298
 
Resource Report
Resource Website
RRID:CVCL_5M71 Homo sapiens (Human) Becker's muscular dystrophy Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:6093571
PMID:21354051
PMID:23665875
Finite cell line Male GM-2298, GM2298, GM02298A, HF-B CLO:CLO_0032205,
Coriell:GM02298,
Wikidata:Q54837412
CVCL_5M71 2026-07-25 04:32:31 0

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