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117,735 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
GM03857
 
Resource Report
Resource Website
RRID:CVCL_DD75 Homo sapiens (Human) Hereditary optic atrophy Population: Jewish. Transformed cell line Male GM3857, GM03857A CLO:CLO_0015618,
BioSample:SAMN00808569,
Coriell:GM03857,
Wikidata:Q54838273
CVCL_DD75 Cellosaurus 2026-09-26 06:49:11 0
GM04081
 
Resource Report
Resource Website
RRID:CVCL_0R01 Homo sapiens (Human) Primary carnitine deficiency Population: Caucasian. Finite cell line Male CLO:CLO_0016224,
Coriell:GM04081,
Wikidata:Q54838384
CVCL_0R01 Cellosaurus 2026-09-26 06:49:13 0
GM04126
 
Resource Report
Resource Website
RRID:CVCL_V820 Homo sapiens (Human) Wolf-Hirschhorn syndrome Population: Caucasian. PMID:6617268
PMID:6661932
PMID:23665875
Finite cell line Male GM 4126 CLO:CLO_0016204,
Coriell:GM04126,
Wikidata:Q54838392
CVCL_V820 Cellosaurus 2026-09-26 06:49:13 0
GM04079
 
Resource Report
Resource Website
RRID:CVCL_T821 Homo sapiens (Human) Friedreich ataxia Caution: Indicated by Coriell to have 420 and 541 GAA repeats., Population: Caucasian. Transformed cell line Male CLO:CLO_0016225,
Coriell:GM04079,
Wikidata:Q54838383
CVCL_T821 Cellosaurus 2026-09-26 06:49:13 0
GM03998
 
Resource Report
Resource Website
RRID:CVCL_IZ39 Homo sapiens (Human) Hyperlipoproteinemia, type I Population: Caucasian. Finite cell line Male CLO:CLO_0016074,
Coriell:GM03998,
Wikidata:Q54838364
CVCL_IZ39 Cellosaurus 2026-09-26 06:49:13 0
GM03940
 
Resource Report
Resource Website
RRID:CVCL_CY31 Homo sapiens (Human) Familial adenomatous polyposis Donor information: At sampling donor was not affected with familial adenomatous polyposis but at risk for disease., Population: Caucasian. Finite cell line Male CLO:CLO_0016105,
Coriell:GM03940,
Wikidata:Q54838334
CVCL_CY31 Cellosaurus 2026-09-26 06:49:12 0
GM04025
 
Resource Report
Resource Website
RRID:CVCL_1N28 Homo sapiens (Human) Fragile X syndrome Population: African American. PMID:1672039
PMID:25776194
PMID:33426406
Transformed cell line Male GM4025B, GM04025C, GM04025E CLO:CLO_0016229,
Coriell:GM04025,
Wikidata:Q54838374
CVCL_1N28 Cellosaurus 2026-09-26 06:49:13 0
GM03941
 
Resource Report
Resource Website
Coriell Cat# GM03941, RRID:CVCL_CY32 Homo sapiens (Human) Familial adenomatous polyposis Donor information: At sampling donor was not affected with familial adenomatous polyposis but at risk for disease., Population: Caucasian. Transformed cell line Male GM03941B Coriell GM03941 CLO:CLO_0016108,
Coriell:GM03941,
Wikidata:Q54838336
CVCL_CY32 Cellosaurus 2026-09-26 06:49:12 0
GM03929
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_5M87 Homo sapiens (Human) Duchenne muscular dystrophy Population: Caucasian., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:6726265
PMID:7253718
PMID:21354051
PMID:23665875
Transformed cell line Male GM03929A, AG03929, AG 3929, AG3929 CLO:CLO_0016136,
Coriell:AG03929,
Coriell:GM03929,
Wikidata:Q54838329
CVCL_5M87 Cellosaurus 2026-09-26 06:49:12 0
GM03932
 
Resource Report
Resource Website
Coriell Cat# GM03932, RRID:CVCL_9S53 Homo sapiens (Human) Limb-girdle muscular dystrophy type 2A Population: Caucasian. Finite cell line Male Coriell GM03932 CLO:CLO_0016132,
Coriell:GM03932,
Wikidata:Q54838331
CVCL_9S53 Cellosaurus 2026-09-26 06:49:12 0
GM04034
 
Resource Report
Resource Website
RRID:CVCL_F112 Homo sapiens (Human) Dystrophia myotonica 1 Population: Caucasian. PMID:23680132 Transformed cell line Male CLO:CLO_0016232,
Coriell:GM04034,
Wikidata:Q54838377
CVCL_F112 Cellosaurus 2026-09-26 06:49:13 0
GM03941
 
Resource Report
Resource Website
RRID:CVCL_CY32 Homo sapiens (Human) Familial adenomatous polyposis Donor information: At sampling donor was not affected with familial adenomatous polyposis but at risk for disease., Population: Caucasian. Transformed cell line Male GM03941B CLO:CLO_0016108,
Coriell:GM03941,
Wikidata:Q54838336
CVCL_CY32 Cellosaurus 2026-09-26 06:49:12 0
GM04107
 
Resource Report
Resource Website
Coriell Cat# GM04107, RRID:CVCL_9Q95 Homo sapiens (Human) LEOPARD syndrome Population: Caucasian. Finite cell line Male Coriell GM04107 CLO:CLO_0016210,
Coriell:GM04107,
Wikidata:Q54838389
CVCL_9Q95 Cellosaurus 2026-09-26 06:49:13 0
GM03955
 
Resource Report
Resource Website
RRID:CVCL_CY44 Homo sapiens (Human) Familial adenomatous polyposis Population: Caucasian. Transformed cell line Male CLO:CLO_0016093,
Coriell:GM03955,
Wikidata:Q54838350
CVCL_CY44 Cellosaurus 2026-09-26 06:49:13 0
GM03986
 
Resource Report
Resource Website
RRID:CVCL_F111 Homo sapiens (Human) Dystrophia myotonica 1 Population: Caucasian. PMID:23680132 Transformed cell line Male GM03986A CLO:CLO_0016057,
Coriell:GM03986,
Wikidata:Q54838355
CVCL_F111 Cellosaurus 2026-09-26 06:49:13 0
GM04126
 
Resource Report
Resource Website
Coriell Cat# GM04126, RRID:CVCL_V820 Homo sapiens (Human) Wolf-Hirschhorn syndrome Population: Caucasian. PMID:6617268
PMID:6661932
PMID:23665875
Finite cell line Male GM 4126 Coriell GM04126 CLO:CLO_0016204,
Coriell:GM04126,
Wikidata:Q54838392
CVCL_V820 Cellosaurus 2026-09-26 06:49:13 0
GM04106
 
Resource Report
Resource Website
Coriell Cat# GM04106, RRID:CVCL_9Q94 Homo sapiens (Human) LEOPARD syndrome Population: Caucasian. Transformed cell line Male Coriell GM04106 CLO:CLO_0016209,
Coriell:GM04106,
Wikidata:Q54838388
CVCL_9Q94 Cellosaurus 2026-09-26 06:49:13 0
GM04078
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_T820 Homo sapiens (Human) Friedreich ataxia Caution: Indicated by Coriell to have 420 and 541 GAA repeats., Population: Caucasian. PMID:27002638
PMID:28444186
PMID:29125828
Finite cell line Male GM-4078, F4078, 4078 CLO:CLO_0016228,
ChEMBL-Cells:CHEMBL4802059,
Coriell:GM04078,
GEO:GSM2794424,
PubChem_Cell_line:CVCL_T820,
Wikidata:Q54838382
CVCL_T820 Cellosaurus 2026-09-26 06:49:13 1
GM04106
 
Resource Report
Resource Website
RRID:CVCL_9Q94 Homo sapiens (Human) LEOPARD syndrome Population: Caucasian. Transformed cell line Male CLO:CLO_0016209,
Coriell:GM04106,
Wikidata:Q54838388
CVCL_9Q94 Cellosaurus 2026-09-26 06:49:13 0
GM04125
 
Resource Report
Resource Website
RRID:CVCL_1Q58 Homo sapiens (Human) Karyotypic information: 46,XY,t(15;18)(15pter->15q15::18p11.3->18pter;18qter->18p11.3::15q15->15qter) (Coriell=GM04125)., Population: Caucasian. Finite cell line Male CLO:CLO_0016208,
Coriell:GM04125,
Wikidata:Q54838391
CVCL_1Q58 Cellosaurus 2026-09-26 06:49:13 0

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