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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
GM03125
 
Resource Report
Resource Website
RRID:CVCL_5R36 Homo sapiens (Human) Karyotypic information: 46,XY,del(2)(pter->q23::q32.2->qter) (Coriell=GM03125)., Population: Caucasian. Finite cell line Male CLO:CLO_0013586,
BioSample:SAMN00808259,
Coriell:GM03125,
Wikidata:Q54837887
CVCL_5R36 Cellosaurus 2026-09-26 06:49:03 0
GM03125
 
Resource Report
Resource Website
Coriell Cat# GM03125, RRID:CVCL_5R36 Homo sapiens (Human) Karyotypic information: 46,XY,del(2)(pter->q23::q32.2->qter) (Coriell=GM03125)., Population: Caucasian. Finite cell line Male Coriell GM03125 CLO:CLO_0013586,
BioSample:SAMN00808259,
Coriell:GM03125,
Wikidata:Q54837887
CVCL_5R36 Cellosaurus 2026-09-26 06:49:03 0
GM03066
 
Resource Report
Resource Website
RRID:CVCL_9Q93 Homo sapiens (Human) I-cell disease Population: Caucasian. PMID:16465621 Finite cell line Female GM03066C CLO:CLO_0013477,
BioSample:SAMN00808234,
Coriell:GM03066,
Wikidata:Q54837848
CVCL_9Q93 Cellosaurus 2026-09-26 06:49:02 0
GM03033
 
Resource Report
Resource Website
Coriell Cat# GM03033, RRID:CVCL_4Z83 Homo sapiens (Human) Population: Caucasian; Sardinian. Finite cell line Female Coriell GM03033 CLO:CLO_0012619,
BioSample:SAMN00808216,
Coriell:GM03033,
Wikidata:Q54837825
CVCL_4Z83 Cellosaurus 2026-09-26 06:49:02 0
GM03093
 
Resource Report
Resource Website
RRID:CVCL_UH44 Homo sapiens (Human) Donor information: Established from a patient suffering from an unknown defect in the pyruvate dehydrogenase complex., Population: Caucasian. PMID:5032527
PMID:7299037
Finite cell line Female GM 3093, GM3093 CLO:CLO_0013486,
BioSample:SAMN00808248,
Coriell:GM03093,
Wikidata:Q93582268
CVCL_UH44 Cellosaurus 2026-09-26 06:49:02 0
GM03075
 
Resource Report
Resource Website
Coriell Cat# GM03075, RRID:CVCL_CW74 Homo sapiens (Human) Population: Caucasian. PMID:24555846
PMID:25326100
Finite cell line Male Coriell GM03075 CLO:CLO_0013461,
BioSample:SAMN00808240,
Coriell:GM03075,
GEO:GSM1257702,
GEO:GSM1266987,
GEO:GSM1267064,
GEO:GSM1288448,
Wikidata:Q54837856
CVCL_CW74 Cellosaurus 2026-09-26 06:49:02 0
GM03038
 
Resource Report
Resource Website
RRID:CVCL_M935 Homo sapiens (Human) Alpha thalassemia Population: Southeast Asian; Vietnamese. Finite cell line Male CLO:CLO_0012628,
BioSample:SAMN00808220,
Coriell:GM03038,
Wikidata:Q54837830
CVCL_M935 Cellosaurus 2026-09-26 06:49:02 0
GM03044
 
Resource Report
Resource Website
RRID:CVCL_7371 Homo sapiens (Human) Smith-Lemli-Opitz syndrome Karyotypic information: 45,XY,der(13;14)(13qter->13q10::14q10->14qter) (Coriell=GM03044)., Population: Caucasian. Finite cell line Male CLO:CLO_0012622,
BioSample:SAMN00808224,
Coriell:GM03044,
Wikidata:Q54837834
CVCL_7371 Cellosaurus 2026-09-26 06:49:02 0
GM03124
 
Resource Report
Resource Website
RRID:CVCL_7375 Homo sapiens (Human) Niemann-Pick disease, type C1 Population: Caucasian. Transformed cell line Female CLO:CLO_0013587,
BioSample:SAMN00808258,
Coriell:GM03124,
Wikidata:Q54837886
CVCL_7375 Cellosaurus 2026-09-26 06:49:03 0
GM03051
 
Resource Report
Resource Website
RRID:CVCL_4N36 Homo sapiens (Human) Population: Jewish; Ashkenazi. PMID:3375249 Finite cell line Male GM3051 CLO:CLO_0013501,
BioSample:SAMN00808226,
Coriell:GM03051,
Wikidata:Q54837838
CVCL_4N36 Cellosaurus 2026-09-26 06:49:02 0
GM03085
 
Resource Report
Resource Website
Coriell Cat# GM03085, RRID:CVCL_X278 Homo sapiens (Human) Karyotypic information: 46,XY,rec(3)(qter->p25::q21->qter)pat (Coriell=GM03085)., Population: Caucasian; French Canadian. PMID:6661932 Finite cell line Male GM 3085 Coriell GM03085 CLO:CLO_0013498,
BioSample:SAMN00808244,
Coriell:GM03085,
Wikidata:Q54837862
CVCL_X278 Cellosaurus 2026-09-26 06:49:02 0
GM03070
 
Resource Report
Resource Website
Coriell Cat# GM03070, RRID:CVCL_EF92 Homo sapiens (Human) Congenital sucrase-isomaltase deficiency Transformed cell line Male Coriell GM03070 CLO:CLO_0013478,
BioSample:SAMN00808235,
Coriell:GM03070,
Wikidata:Q54837849
CVCL_EF92 Cellosaurus 2026-09-26 06:49:02 0
GM03081
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM03081, RRID:CVCL_UR78 Homo sapiens (Human) Finite cell line Female GM03081A Coriell GM03081 Coriell:GM03081,
Wikidata:Q93582195
CVCL_UR78 Cellosaurus 2026-09-26 06:49:02 0
GM03070
 
Resource Report
Resource Website
RRID:CVCL_EF92 Homo sapiens (Human) Congenital sucrase-isomaltase deficiency Transformed cell line Male CLO:CLO_0013478,
BioSample:SAMN00808235,
Coriell:GM03070,
Wikidata:Q54837849
CVCL_EF92 Cellosaurus 2026-09-26 06:49:02 0
GM03128
 
Resource Report
Resource Website
Coriell Cat# GM03128, RRID:CVCL_X061 Homo sapiens (Human) Glycogen storage disease type VII PMID:6451249 Transformed cell line Male GM 3128 Coriell GM03128 CLO:CLO_0013579,
BioSample:SAMN00808261,
Coriell:GM03128,
Wikidata:Q54837890
CVCL_X061 Cellosaurus 2026-09-26 06:49:03 0
GM03126
 
Resource Report
Resource Website
Coriell Cat# GM03126, RRID:CVCL_X102 Homo sapiens (Human) Tetralogy of Fallot Karyotypic information: 46,XX,der(1)(pter->p13.1::q21.1->p13.1::q21.1->q42.3) (Coriell=GM03126)., Population: African American. PMID:6617268
PMID:6661932
Finite cell line Female GM 3126 Coriell GM03126 CLO:CLO_0013585,
BioSample:SAMN00808260,
Coriell:GM03126,
Wikidata:Q54837888
CVCL_X102 Cellosaurus 2026-09-26 06:49:03 0
GM03031
 
Resource Report
Resource Website
Coriell Cat# GM03031, RRID:CVCL_4Z82 Homo sapiens (Human) Population: Caucasian; Sardinian. Finite cell line Female Coriell GM03031 CLO:CLO_0012620,
BioSample:SAMN00808215,
Coriell:GM03031,
Wikidata:Q54837824
CVCL_4Z82 Cellosaurus 2026-09-26 06:49:02 0
GM03120
 
Resource Report
Resource Website
RRID:CVCL_X054 Homo sapiens (Human) Karyotypic information: 45,X,-Y,inv(9)(p11;q13) [13]; 46,XY,inv(9)(p11;q13) [7] (Coriell=GM03120). PMID:6617268 Finite cell line Female GM 3120 CLO:CLO_0013583,
Coriell:GM03120,
Wikidata:Q54837882
CVCL_X054 Cellosaurus 2026-09-26 06:49:03 0
GM03037
 
Resource Report
Resource Website
Coriell Cat# GM03037, RRID:CVCL_M934 Homo sapiens (Human) Alpha thalassemia Population: Southeast Asian; Vietnamese., Part of: Human variation panel. Finite cell line Male GM17082 Coriell GM03037 CLO:CLO_0012630,
CLO:CLO_0014481,
BioSample:SAMN00808219,
Coriell:GM03037,
Coriell:GM17082,
Wikidata:Q54837829
CVCL_M934 Cellosaurus 2026-09-26 06:49:02 0
GM03071
 
Resource Report
Resource Website
RRID:CVCL_M936 Homo sapiens (Human) Myopathy due to myoadenylate deaminase deficiency Population: Caucasian. PMID:25326100 Finite cell line Male CLO:CLO_0013465,
BioSample:SAMN00808236,
Coriell:GM03071,
GEO:GSM1266989,
Wikidata:Q54837850
CVCL_M936 Cellosaurus 2026-09-26 06:49:02 0

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