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236,573 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
GM03112
 
Resource Report
Resource Website
RRID:CVCL_L776 Homo sapiens (Human) I-cell disease Population: Caucasian. PMID:16465621 Finite cell line Female GM03112F, GM03112G CLO:CLO_0013554,
BioSample:SAMN00808253,
Coriell:GM03112,
Wikidata:Q54837876
CVCL_L776 2026-09-12 05:32:23 0
GM03056
 
Resource Report
Resource Website
RRID:CVCL_U519 Homo sapiens (Human) Citrullinemia type I Population: Caucasian. PMID:7174798 Finite cell line Male GM3056 CLO:CLO_0013504,
BioSample:SAMN00808231,
Coriell:GM03056,
Wikidata:Q54837844
CVCL_U519 2026-09-12 05:32:22 0
GM03045
 
Resource Report
Resource Website
RRID:CVCL_2Z48 Homo sapiens (Human) Krabbe disease Donor information: Established from monozygotic twin of GM03046 (Cellosaurus=CVCL_2Z49)., Population: Caucasian. PMID:3926002 Finite cell line Female GM 3045, GM3045 CLO:CLO_0013507,
Coriell:GM03045,
Wikidata:Q54837835
CVCL_2Z48 2026-09-12 05:32:22 0
GM03128
 
Resource Report
Resource Website
RRID:CVCL_X061 Homo sapiens (Human) Glycogen storage disease type VII PMID:6451249 Transformed cell line Male GM 3128 CLO:CLO_0013579,
BioSample:SAMN00808261,
Coriell:GM03128,
Wikidata:Q54837890
CVCL_X061 2026-09-12 05:32:23 0
GM03201
 
Resource Report
Resource Website
RRID:CVCL_7378 Homo sapiens (Human) PMID:2112341
PMID:6451249
Transformed cell line Male GM 3201 CLO:CLO_0013392,
BioSample:SAMN00808292,
Coriell:GM03201,
Wikidata:Q54837934
CVCL_7378 2026-09-12 05:32:24 0
GM03217
 
Resource Report
Resource Website
RRID:CVCL_HQ61 Homo sapiens (Human) Idiopathic torsion dystonia Population: Caucasian. Finite cell line Male CLO:CLO_0013381,
BioSample:SAMN00808302,
Coriell:GM03217,
Wikidata:Q54837944
CVCL_HQ61 2026-09-12 05:32:24 0
GM03194
 
Resource Report
Resource Website
RRID:CVCL_AB30 Homo sapiens (Human) Dyskeratosis congenita Transformed cell line Male CLO:CLO_0013395,
BioSample:SAMN00808287,
Coriell:GM03194,
Wikidata:Q54837929
CVCL_AB30 2026-09-12 05:32:24 0
GM03221
 
Resource Report
Resource Website
RRID:CVCL_1U25 Homo sapiens (Human) Autosomal dominant torsion dystonia 1 Population: Caucasian. Finite cell line Female CLO:CLO_0016474,
BioSample:SAMN00808306,
Coriell:GM03221,
Wikidata:Q54837948
CVCL_1U25 2026-09-12 05:32:24 0
GM03240
 
Resource Report
Resource Website
RRID:CVCL_X104 Homo sapiens (Human) PMID:6617268
PMID:6661932
PMID:23665875
Finite cell line Male GM 3240 CLO:CLO_0016736,
BioSample:SAMN00808319,
Coriell:GM03240,
Wikidata:Q54837961
CVCL_X104 2026-09-12 05:32:25 0
GM03240
 
Resource Report
Resource Website
Coriell Cat# GM03240, RRID:CVCL_X104 Homo sapiens (Human) PMID:6617268
PMID:6661932
PMID:23665875
Finite cell line Male GM 3240 Coriell GM03240 CLO:CLO_0016736,
BioSample:SAMN00808319,
Coriell:GM03240,
Wikidata:Q54837961
CVCL_X104 2026-09-12 05:32:25 0
GM03215
 
Resource Report
Resource Website
Coriell Cat# GM03215, RRID:CVCL_HQ59 Homo sapiens (Human) Idiopathic torsion dystonia Population: Caucasian. Finite cell line Female Coriell GM03215 CLO:CLO_0013373,
BioSample:SAMN00808300,
Coriell:GM03215,
Wikidata:Q54837942
CVCL_HQ59 2026-09-12 05:32:24 0
GM03241
 
Resource Report
Resource Website
RRID:CVCL_X281 Homo sapiens (Human) Population: Caucasian. PMID:6661932
PMID:23665875
Finite cell line Female GM 3241, GM03241A CLO:CLO_0016738,
BioSample:SAMN00808320,
Coriell:GM03241,
Wikidata:Q54837962
CVCL_X281 2026-09-12 05:32:25 0
GM03218
 
Resource Report
Resource Website
RRID:CVCL_4N42 Homo sapiens (Human) Autosomal recessive torsion dystonia 2 Population: Caucasian. Finite cell line Male CLO:CLO_0013382,
BioSample:SAMN00808303,
Coriell:GM03218,
Wikidata:Q54837945
CVCL_4N42 2026-09-12 05:32:24 0
GM03137
 
Resource Report
Resource Website
RRID:CVCL_GS61 Homo sapiens (Human) Adenosine deaminase deficiency Karyotypic information: 46,XX,t(1;12)(1qter->1p36::12q15->12qter;12pter->12q15::1p36->1pter) [24]; 46,XX [26] (Coriell=GM03137). PMID:1346349
PMID:1680289
PMID:2567118
Finite cell line Female GM 3137 CLO:CLO_0013521,
Coriell:GM03137,
Wikidata:Q54837897
CVCL_GS61 2026-09-12 05:32:23 0
GM03237
 
Resource Report
Resource Website
RRID:CVCL_F072 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel. PMID:7438795 Transformed cell line Male GM3237, GM18010 CLO:CLO_0016000,
CLO:CLO_0016730,
BioSample:SAMN00808316,
Coriell:GM03237,
Coriell:GM18010,
Wikidata:Q54837958
CVCL_F072 2026-09-12 05:32:24 0
GM03222
 
Resource Report
Resource Website
Coriell Cat# GM03222, RRID:CVCL_HQ64 Homo sapiens (Human) Idiopathic torsion dystonia Population: Jewish; Ashkenazi. Finite cell line Female Coriell GM03222 CLO:CLO_0016473,
BioSample:SAMN00808307,
Coriell:GM03222,
Wikidata:Q54837949
CVCL_HQ64 2026-09-12 05:32:24 0
GM03192
 
Resource Report
Resource Website
Coriell Cat# GM03192, RRID:CVCL_EJ33 Homo sapiens (Human) Population: Caucasian; Irish/Scottish. Finite cell line Female Coriell GM03192 CLO:CLO_0013389,
BioSample:SAMN00808285,
Coriell:GM03192,
Wikidata:Q54837927
CVCL_EJ33 2026-09-12 05:32:24 0
GM03184
 
Resource Report
Resource Website
Coriell Cat# GM03184, RRID:CVCL_X280 Homo sapiens (Human) PMID:6661932
PMID:23665875
Finite cell line Male GM 3184 Coriell GM03184 CLO:CLO_0013415,
Coriell:GM03184,
Wikidata:Q54837912
CVCL_X280 2026-09-12 05:32:23 0
GM03201
 
Resource Report
Resource Website
Coriell Cat# GM03201, RRID:CVCL_7378 Homo sapiens (Human) PMID:2112341
PMID:6451249
Transformed cell line Male GM 3201 Coriell GM03201 CLO:CLO_0013392,
BioSample:SAMN00808292,
Coriell:GM03201,
Wikidata:Q54837934
CVCL_7378 2026-09-12 05:32:24 0
GM03208
 
Resource Report
Resource Website
Coriell Cat# GM03208, RRID:CVCL_4N41 Homo sapiens (Human) Autosomal recessive torsion dystonia 2 Population: Jewish; Ashkenazi. Finite cell line Male Coriell GM03208 CLO:CLO_0013394,
BioSample:SAMN00808294,
Coriell:GM03208,
Wikidata:Q54837936
CVCL_4N41 2026-09-12 05:32:24 0

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