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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
GM01742
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_CX27 Homo sapiens (Human) I-cell disease Finite cell line Female GM-1742 Coriell:GM01742,
Wikidata:Q54837054
CVCL_CX27 2026-07-25 04:32:25 0
GM01667
 
Resource Report
Resource Website
Coriell Cat# GM01667, RRID:CVCL_X082 Homo sapiens (Human) Karyotypic information: 46,XX,del(9)(qter>p22) (Coriell=GM01667)., Population: Caucasian. PMID:6617268
PMID:6661932
Finite cell line Female GM-1667, GM 1667 Coriell GM01667 CLO:CLO_0030954,
BioSample:SAMN00807055,
Coriell:GM01667,
Wikidata:Q54836999
CVCL_X082 2026-07-25 04:32:21 0
GM01658
 
Resource Report
Resource Website
RRID:CVCL_2Z69 Homo sapiens (Human) Nevoid basal cell carcinoma syndrome Population: Caucasian. Finite cell line Male GM-1658 CLO:CLO_0030940,
BioSample:SAMN00807039,
Coriell:GM01658,
Wikidata:Q54836990
CVCL_2Z69 2026-07-25 04:32:21 0
GM01673
 
Resource Report
Resource Website
RRID:CVCL_0D84 Homo sapiens (Human) Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency Population: Caucasian. PMID:7909321 Finite cell line Male GM1673, GM-1673 CLO:CLO_0030951,
BioSample:SAMN00807059,
Coriell:GM01673,
Wikidata:Q54837006
CVCL_0D84 2026-07-25 04:32:21 0
GM01667
 
Resource Report
Resource Website
RRID:CVCL_X082 Homo sapiens (Human) Karyotypic information: 46,XX,del(9)(qter>p22) (Coriell=GM01667)., Population: Caucasian. PMID:6617268
PMID:6661932
Finite cell line Female GM-1667, GM 1667 CLO:CLO_0030954,
BioSample:SAMN00807055,
Coriell:GM01667,
Wikidata:Q54836999
CVCL_X082 2026-07-25 04:32:23 0
GM01739
 
Resource Report
Resource Website
RRID:CVCL_0M02 Homo sapiens (Human) Mucopolysaccharidosis type IIIA Population: Caucasian. Finite cell line Female GM-1739 CLO:CLO_0030992,
BioSample:SAMN00807127,
Coriell:GM01739,
Wikidata:Q54837050
CVCL_0M02 2026-07-25 04:32:22 0
GM01706
 
Resource Report
Resource Website
Discontinued
Coriell Cat# GM00237, RRID:CVCL_7334 Homo sapiens (Human) Population: Caucasian. PMID:30567591 Finite cell line Female GM1706, GM-1706, GM 1706, GM01706A, GM1706A, GM00237, GM0237 Coriell GM00237 CLO:CLO_0030976,
BioSample:SAMN00807091,
Coriell:GM00237,
Coriell:GM01706,
GEO:GSM3124688,
Wikidata:Q54837025
CVCL_7334 2026-07-25 04:32:22 0
GM01663
 
Resource Report
Resource Website
RRID:CVCL_V810 Homo sapiens (Human) Karyotypic information: 46,XY,der(17)(17qter->17p13::13q14->13qter)mat (Coriell=GM01663)., Population: Caucasian. PMID:761481
PMID:6661932
PMID:7329430
PMID:7471105
Finite cell line Male GM-1663, GM 1663, GM1663 CLO:CLO_0030957,
BioSample:SAMN00807049,
Coriell:GM01663,
Wikidata:Q54836995
CVCL_V810 2026-07-25 04:32:23 0
GM01685
 
Resource Report
Resource Website
RRID:CVCL_U518 Homo sapiens (Human) Citrullinemia type I Population: Caucasian. Transformed cell line Male GM-1685 CLO:CLO_0030967,
BioSample:SAMN00807077,
Coriell:GM01685,
Wikidata:Q54837016
CVCL_U518 2026-07-25 04:32:21 0
GM01740
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_JC92 Homo sapiens (Human) Ataxia telangiectasia syndrome Finite cell line Male GM-1740, GM01740A BioSample:SAMN00807129,
Coriell:GM01740,
Wikidata:Q54837051
CVCL_JC92 2026-07-25 04:32:25 0
GM01724
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM01724, RRID:CVCL_X254 Homo sapiens (Human) Population: Caucasian. Finite cell line Female GM-1724 Coriell GM01724 Coriell:GM01724,
Wikidata:Q54837038
CVCL_X254 2026-07-25 04:32:22 0
GM01726
 
Resource Report
Resource Website
Coriell Cat# GM01726, RRID:CVCL_2Z71 Homo sapiens (Human) Nevoid basal cell carcinoma syndrome Population: Caucasian. Transformed cell line Female GM-1726, GM01726A Coriell GM01726 CLO:CLO_0030982,
BioSample:SAMN00807117,
Coriell:GM01726,
Wikidata:Q54837040
CVCL_2Z71 2026-07-25 04:32:24 0
GM01730
 
Resource Report
Resource Website
Coriell Cat# GM01730, RRID:CVCL_1R61 Homo sapiens (Human) Karyotypic information: 46,XX,der(21)(21qter->21p11::Xq11->Xqter)mat (Coriell=GM01730)., Population: African American. Finite cell line Female GM-1730, GM01730C Coriell GM01730 CLO:CLO_0030997,
BioSample:SAMN00807121,
Coriell:GM01730,
Wikidata:Q54837042
CVCL_1R61 2026-07-25 04:32:22 0
GM01736
 
Resource Report
Resource Website
RRID:CVCL_1F09 Homo sapiens (Human) Xeroderma pigmentosum, complementation group C Population: Caucasian. Finite cell line Female GM-1736, GM1736 CLO:CLO_0030994,
BioSample:SAMN00807123,
Coriell:GM01736,
Wikidata:Q54837044
CVCL_1F09 2026-07-25 04:32:22 0
GM01727
 
Resource Report
Resource Website
RRID:CVCL_X083 Homo sapiens (Human) Karyotypic information: 46,XY,del(18)(qter>p11) (Coriell=GM01727)., Population: Caucasian. PMID:6617268
PMID:6661932
Finite cell line Male GM-1727, GM 1727 CLO:CLO_0030998,
BioSample:SAMN00807119,
Coriell:GM01727,
Wikidata:Q54837041
CVCL_X083 2026-07-25 04:32:22 0
GM01691
 
Resource Report
Resource Website
Coriell Cat# GM01691, RRID:CVCL_AM86 Homo sapiens (Human) Ehlers-Danlos syndrome, type II Population: Caucasian. Finite cell line Male GM-1691 Coriell GM01691 CLO:CLO_0030960,
BioSample:SAMN00807079,
Coriell:GM01691,
Wikidata:Q54837017
CVCL_AM86 2026-07-25 04:32:21 0
GM01721
 
Resource Report
Resource Website
Coriell Cat# GM01721, RRID:CVCL_JC91 Homo sapiens (Human) Androgen insensitivity syndrome Population: Caucasian. Finite cell line Sex ambiguous GM-1721 Coriell GM01721 CLO:CLO_0030979,
BioSample:SAMN00807111,
Coriell:GM01721,
Wikidata:Q54837035
CVCL_JC91 2026-07-25 04:32:22 0
GM01744
 
Resource Report
Resource Website
RRID:CVCL_AD63 Homo sapiens (Human) Maple syrup urine disease Population: Caucasian. Finite cell line Female GM1744, GM-1744 CLO:CLO_0030991,
BioSample:SAMN00807135,
Coriell:GM01744,
Wikidata:Q54837057
CVCL_AD63 2026-07-25 04:32:25 0
GM01662
 
Resource Report
Resource Website
RRID:CVCL_F602 Homo sapiens (Human) Lesch-Nyhan syndrome Population: Caucasian. PMID:3021482
PMID:3296189
PMID:6087154
PMID:14555701
Finite cell line Male GM-1662, GM 1662, GM1662, GM01662A CLO:CLO_0030958,
BioSample:SAMN00807047,
Coriell:GM01662,
Wikidata:Q54836994
CVCL_F602 2026-07-25 04:32:21 0
GM01685
 
Resource Report
Resource Website
Coriell Cat# GM01685, RRID:CVCL_U518 Homo sapiens (Human) Citrullinemia type I Population: Caucasian. Transformed cell line Male GM-1685 Coriell GM01685 CLO:CLO_0030967,
BioSample:SAMN00807077,
Coriell:GM01685,
Wikidata:Q54837016
CVCL_U518 2026-07-25 04:32:23 0

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