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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
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 Cellosaurus 2026-09-26 06:48:53 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 Cellosaurus 2026-09-26 06:48:55 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 Cellosaurus 2026-09-26 06:48:54 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 Cellosaurus 2026-09-26 06:48:54 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 Cellosaurus 2026-09-26 06:48:54 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 Cellosaurus 2026-09-26 06:48:54 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 Cellosaurus 2026-09-26 06:48:53 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 Cellosaurus 2026-09-26 06:48:55 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 Cellosaurus 2026-09-26 06:48:54 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 Cellosaurus 2026-09-26 06:48:54 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 Cellosaurus 2026-09-26 06:48:54 0
GM02303
 
Resource Report
Resource Website
Coriell Cat# GM02303, RRID:CVCL_BT15 Homo sapiens (Human) Variegate porphyria Transformed cell line Female GM-2303 Coriell GM02303 CLO:CLO_0032208,
BioSample:SAMN00807675,
Coriell:GM02303,
Wikidata:Q54837417
CVCL_BT15 Cellosaurus 2026-09-26 06:48:54 0
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

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