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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
GM11403
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_5P51 Homo sapiens (Human) PMID:23665875 Finite cell line Male CLO:CLO_0026098,
BioSample:SAMN00800621,
Coriell:GM11403,
Wikidata:Q54845058
CVCL_5P51 2026-08-15 04:31:21 0
GM11380
 
Resource Report
Resource Website
RRID:CVCL_H552 Homo sapiens (Human) Finite cell line Female CLO:CLO_0026081,
Coriell:GM11380,
Wikidata:Q54845041
CVCL_H552 2026-08-15 04:31:20 0
GM11390
 
Resource Report
Resource Website
RRID:CVCL_5P48 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0026082,
Coriell:GM11390,
Wikidata:Q54845050
CVCL_5P48 2026-08-15 04:31:20 0
GM11349
 
Resource Report
Resource Website
Coriell Cat# GM11349, RRID:CVCL_9X19 Homo sapiens (Human) Rhizomelic chondrodysplasia punctata Population: Caucasian. Finite cell line Female Coriell GM11349 CLO:CLO_0026072,
Coriell:GM11349,
Wikidata:Q54845034
CVCL_9X19 2026-08-15 04:31:20 0
GM11386
 
Resource Report
Resource Website
Coriell Cat# GM11386, RRID:CVCL_5P45 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM11386 CLO:CLO_0026085,
Coriell:GM11386,
Wikidata:Q54845046
CVCL_5P45 2026-08-15 04:31:20 0
GM11413
 
Resource Report
Resource Website
RRID:CVCL_DB80 Homo sapiens (Human) Population: Caucasian; Amish. PMID:1680289 Transformed cell line Male GM 11413 CLO:CLO_0020794,
Coriell:GM11413,
Wikidata:Q54845070
CVCL_DB80 2026-08-15 04:31:21 0
GM11338
 
Resource Report
Resource Website
RRID:CVCL_4E06 Homo sapiens (Human) Ring chromosome 21 syndrome Karyotypic information: 46,XX dic,r(21) [36]; 45,XX,-21 [10]; 46,XX,r(21) [4] (Coriell=GM11338)., Population: Caucasian. Finite cell line Female CLO:CLO_0026078,
Coriell:GM11338,
Wikidata:Q54845020
CVCL_4E06 2026-08-15 04:31:20 0
GM11346
 
Resource Report
Resource Website
Coriell Cat# GM11346, RRID:CVCL_2U06 Homo sapiens (Human) Karyotypic information: 45,XY,der(14)(14qter->14p12::18q11->18qter),-18 (Coriell=GM11346)., Population: Caucasian. Finite cell line Male Coriell GM11346 CLO:CLO_0026069,
Coriell:GM11346,
Wikidata:Q54845031
CVCL_2U06 2026-08-15 04:31:19 0
GM11407
 
Resource Report
Resource Website
Coriell Cat# GM11407, RRID:CVCL_9R93 Homo sapiens (Human) Weaver syndrome Transformed cell line Female Coriell GM11407 CLO:CLO_0020790,
Coriell:GM11407,
Wikidata:Q54845063
CVCL_9R93 2026-08-15 04:31:21 0
GM11397
 
Resource Report
Resource Website
Coriell Cat# GM11397, RRID:CVCL_2U07 Homo sapiens (Human) Karyotypic information: 46,XX,t(8;10)(8qter->8p11.2::10q24->10qter;10pter->10q24::8p11.2->8pter) (Coriell=GM11397). Finite cell line Female Coriell GM11397 CLO:CLO_0026095,
Coriell:GM11397,
Wikidata:Q54845055
CVCL_2U07 2026-08-15 04:31:20 0
GM11388
 
Resource Report
Resource Website
Coriell Cat# GM11388, RRID:CVCL_U533 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Male Coriell GM11388 CLO:CLO_0026083,
Coriell:GM11388,
Wikidata:Q54845048
CVCL_U533 2026-08-15 04:31:20 0
GM11349
 
Resource Report
Resource Website
RRID:CVCL_9X19 Homo sapiens (Human) Rhizomelic chondrodysplasia punctata Population: Caucasian. Finite cell line Female CLO:CLO_0026072,
Coriell:GM11349,
Wikidata:Q54845034
CVCL_9X19 2026-08-15 04:31:20 0
GM11402
 
Resource Report
Resource Website
RRID:CVCL_AJ50 Homo sapiens (Human) Hepatocyte nuclear factor 4-alpha associated monogenic diabetes Population: Caucasian., Part of: R-W pedigree MODY cell line collection. PMID:8945471 Transformed cell line Female CLO:CLO_0026097,
Coriell:GM11402,
Wikidata:Q54845057
CVCL_AJ50 2026-08-15 04:31:20 0
GM11401
 
Resource Report
Resource Website
RRID:CVCL_AJ49 Homo sapiens (Human) Hepatocyte nuclear factor 4-alpha associated monogenic diabetes Population: Caucasian., Part of: R-W pedigree MODY cell line collection. PMID:8945471 Transformed cell line Male GM11401A CLO:CLO_0026096,
Coriell:GM11401,
Wikidata:Q54845056
CVCL_AJ49 2026-08-15 04:31:20 0
GM11347
 
Resource Report
Resource Website
Coriell Cat# GM11347, RRID:CVCL_9X17 Homo sapiens (Human) Rhizomelic chondrodysplasia punctata Population: Caucasian. Finite cell line Female Coriell GM11347 CLO:CLO_0026070,
Coriell:GM11347,
Wikidata:Q54845032
CVCL_9X17 2026-08-15 04:31:20 0
GM11408
 
Resource Report
Resource Website
RRID:CVCL_4F64 Homo sapiens (Human) Very long-chain acyl-CoA dehydrogenase deficiency Population: Asian. Finite cell line Male CLO:CLO_0020789,
Coriell:GM11408,
Wikidata:Q54845064
CVCL_4F64 2026-08-15 04:31:21 0
GM11389
 
Resource Report
Resource Website
Coriell Cat# GM11389, RRID:CVCL_5P47 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM11389 CLO:CLO_0026084,
Coriell:GM11389,
Wikidata:Q54845049
CVCL_5P47 2026-08-15 04:31:20 0
GM11419
 
Resource Report
Resource Website
RRID:CVCL_N182 Homo sapiens (Human) Karyotypic information: 49,XYYYY (Coriell=GM11419)., Population: Indian (from Guyana)., Part of: Human variation panel. PMID:23665875 Transformed cell line Male GM17316 CLO:CLO_0013357,
CLO:CLO_0020867,
Coriell:GM11419,
Coriell:GM17316,
Wikidata:Q54845073
CVCL_N182 2026-08-15 04:31:21 0
GM11375
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM11375, RRID:CVCL_UW18 Homo sapiens (Human) Population: Southeast Asian; Khmer Cambodian., Part of: Yale-Stanford Collection from NIGMS Human Genetic Cell Repository., Part of: Human variation panel. Transformed cell line Male 86-174 Coriell GM11375 Coriell:GM11375,
Wikidata:Q93815034
CVCL_UW18 2026-08-15 04:31:20 0
GM11377
 
Resource Report
Resource Website
Coriell Cat# GM11377, RRID:CVCL_N177 Homo sapiens (Human) Population: Southeast Asian; Khmer Cambodian., Part of: Yale-Stanford Collection from NIGMS Human Genetic Cell Repository., Part of: Human variation panel. PMID:14583597 Transformed cell line Male GM17088, 86-194 Coriell GM11377 CLO:CLO_0014488,
CLO:CLO_0026077,
Coriell:GM11377,
Coriell:GM17088,
Wikidata:Q54845040
CVCL_N177 2026-08-15 04:31:20 0

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