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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
GM02292
 
Resource Report
Resource Website
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 CLO:CLO_0032131,
BioSample:SAMN00807658,
Coriell:GM02292,
Wikidata:Q54837408
CVCL_D868 Cellosaurus 2026-09-26 06:48:54 0
GM02304
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_1U21 Homo sapiens (Human) Autosomal dominant torsion dystonia 1 Population: Caucasian. Finite cell line Female GM-2304 CLO:CLO_0032209,
BioSample:SAMN00807677,
Coriell:GM02304,
Wikidata:Q54837418
CVCL_1U21 Cellosaurus 2026-09-26 06:48:54 1
GM02232
 
Resource Report
Resource Website
Coriell Cat# GM02232, RRID:CVCL_BT12 Homo sapiens (Human) Beta thalassemia Population: Caucasian; Greek. Transformed cell line Female GM-2232, GM02232A Coriell GM02232 CLO:CLO_0032243,
BioSample:SAMN00807620,
Coriell:GM02232,
Wikidata:Q54837385
CVCL_BT12 Cellosaurus 2026-09-26 06:48:54 0
GM02270
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM02270, RRID:CVCL_UR70 Homo sapiens (Human) Population: Caucasian. Finite cell line Male GM2270, GM02270A, GM2270A Coriell GM02270 Coriell:GM02270,
Wikidata:Q93576868
CVCL_UR70 Cellosaurus 2026-09-26 06:48:54 0
GM02255
 
Resource Report
Resource Website
Coriell Cat# GM02255, RRID:CVCL_4N21 Homo sapiens (Human) Autosomal recessive torsion dystonia 2 Finite cell line Female GM-2255 Coriell GM02255 CLO:CLO_0032157,
Coriell:GM02255,
Wikidata:Q54837395
CVCL_4N21 Cellosaurus 2026-09-26 06:48:54 0
GM02293
 
Resource Report
Resource Website
Coriell Cat# GM02293, RRID:CVCL_M995 Homo sapiens (Human) Ehlers-Danlos syndrome Population: Cuban., Part of: Human variation panel. Finite cell line Female GM-2293, GM17353 Coriell GM02293 CLO:CLO_0013723,
CLO:CLO_0032132,
BioSample:SAMN00807660,
Coriell:GM02293,
Coriell:GM17353,
Wikidata:Q54837409
CVCL_M995 Cellosaurus 2026-09-26 06:48:54 0
GM02325
 
Resource Report
Resource Website
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 CLO:CLO_0032174,
BioSample:SAMN00807695,
Coriell:GM02325,
Wikidata:Q54837427
CVCL_X262 Cellosaurus 2026-09-26 06:48:54 0
GM02307
 
Resource Report
Resource Website
RRID:CVCL_4N24 Homo sapiens (Human) Autosomal recessive torsion dystonia 2 Population: Caucasian. Transformed cell line Male GM-2307 CLO:CLO_0032176,
BioSample:SAMN00807683,
Coriell:GM02307,
Wikidata:Q54837421
CVCL_4N24 Cellosaurus 2026-09-26 06:48:54 0
GM02254
 
Resource Report
Resource Website
Coriell Cat# GM17221, RRID:CVCL_7355 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:16260726
PMID:20889555
PMID:29959025
Transformed cell line Female GM-2254, GM17221 Coriell GM17221 CLO:CLO_0014377,
CLO:CLO_0032160,
BioSample:SAMN00807638,
Coriell:GM02254,
Coriell:GM17221,
GEO:GSM569550,
GEO:GSM596285,
GEO:GSM596645,
GEO:GSM924823,
Wikidata:Q54837394
CVCL_7355 Cellosaurus 2026-09-26 06:48:54 0
GM02229
 
Resource Report
Resource Website
RRID:CVCL_4J48 Homo sapiens (Human) Transformed cell line Female GM-2229, GM02229A CLO:CLO_0032241,
BioSample:SAMN00807616,
Coriell:GM02229,
Wikidata:Q54837383
CVCL_4J48 Cellosaurus 2026-09-26 06:48:54 0
GM02314
 
Resource Report
Resource Website
RRID:CVCL_8A64 Homo sapiens (Human) Farber lipogranulomatosis Population: Caucasian; Irish. PMID:21418647
PMID:25326100
Finite cell line Female GM-2314 CLO:CLO_0032177,
BioSample:SAMN00807685,
Coriell:GM02314,
GEO:GSM651168,
GEO:GSM651169,
GEO:GSM1266974,
GEO:GSM1267053,
Wikidata:Q54837422
CVCL_8A64 Cellosaurus 2026-09-26 06:48:54 0
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 Cellosaurus 2026-09-26 06:48:54 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 Cellosaurus 2026-09-26 06:48:54 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 Cellosaurus 2026-09-26 06:48:54 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 Cellosaurus 2026-09-26 06:48:54 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 Cellosaurus 2026-09-26 06:48:55 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 Cellosaurus 2026-09-26 06:48:54 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 Cellosaurus 2026-09-26 06:48:54 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 Cellosaurus 2026-09-26 06:48:54 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 Cellosaurus 2026-09-26 06:48:54 0

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