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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
GM11982
 
Resource Report
Resource Website
RRID:CVCL_5C44 Homo sapiens (Human) Part of: International Histocompatibility Workshop cell lines., Part of: CEPH/Utah pedigree cell line collection. PMID:15514893
PMID:20856902
Transformed cell line Female CEPH-1362-NA11982, 1362-8568 CLO:CLO_0020526,
Coriell:GM11982,
dbMHC:48655,
GEO:GSM25516,
GEO:GSM30077,
GEO:GSM316216,
GEO:GSM316217,
GEO:GSM316218,
GEO:GSM420715,
GEO:GSM957419,
IHW:IHW01129,
IPD-IMGT/HLA:25926,
Wikidata:Q54845416
CVCL_5C44 2026-08-01 05:06:33 0
GM11972
 
Resource Report
Resource Website
RRID:CVCL_F156 Homo sapiens (Human) Transformed cell line Female CLO:CLO_0020547,
Coriell:GM11972,
Wikidata:Q54845405
CVCL_F156 2026-08-01 05:06:33 0
GM11926
 
Resource Report
Resource Website
RRID:CVCL_5C40 Homo sapiens (Human) Part of: CEPH/Utah pedigree cell line collection. PMID:14583597
PMID:15514893
PMID:20856902
Transformed cell line Female CLO:CLO_0020249,
Coriell:GM11926,
GEO:GSM25504,
GEO:GSM30210,
GEO:GSM316318,
GEO:GSM316319,
GEO:GSM316320,
GEO:GSM420703,
Wikidata:Q54845359
CVCL_5C40 2026-08-01 05:06:32 0
GM11932
 
Resource Report
Resource Website
Coriell Cat# GM11932, RRID:CVCL_0V40 Homo sapiens (Human) Population: Caucasian; Utah residents with ancestry from Northern and Western Europe., Part of: International Genome Sample Resource (1000 genomes project) cell lines., Part of: CEPH/Utah pedigree cell line collection. PMID:14583597
PMID:15514893
PMID:19797678
PMID:20856902
PMID:29116076
Transformed cell line Male Coriell GM11932 CLO:CLO_0020239,
ArrayExpress:E-MTAB-5835,
Coriell:GM11932,
GEO:GSM25512,
GEO:GSM25513,
GEO:GSM30216,
GEO:GSM314886,
GEO:GSM314887,
GEO:GSM420711,
GEO:GSM420712,
GEO:GSM906141,
GEO:GSM906142,
GEO:GSM1719768,
IGSR:NA11932,
Wikidata:Q54845371
CVCL_0V40 2026-08-01 05:06:32 0
GM11958
 
Resource Report
Resource Website
RRID:CVCL_5L14 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male CLO:CLO_0020108,
Coriell:GM11958,
Wikidata:Q54845390
CVCL_5L14 2026-08-01 05:06:33 0
GM12000
 
Resource Report
Resource Website
RRID:CVCL_5C58 Homo sapiens (Human) Part of: CEPH/Utah pedigree cell line collection. PMID:20856902
PMID:21418647
Transformed cell line Female CLO:CLO_0020486,
Coriell:GM12000,
GEO:GSM316276,
GEO:GSM316277,
GEO:GSM316278,
GEO:GSM420734,
GEO:GSM651087,
GEO:GSM651088,
GEO:GSM957439,
Wikidata:Q54845435
CVCL_5C58 2026-08-01 05:06:34 0
GM12035
 
Resource Report
Resource Website
Coriell Cat# GM12035, RRID:CVCL_5C62 Homo sapiens (Human) Part of: International Histocompatibility Workshop cell lines., Part of: CEPH/Utah pedigree cell line collection. PMID:20856902 Transformed cell line Male CEPH-1346-NA12035, 1346-8362 Coriell GM12035 CLO:CLO_0020442,
Coriell:GM12035,
dbMHC:48612,
GEO:GSM25532,
GEO:GSM316501,
GEO:GSM316502,
GEO:GSM316503,
GEO:GSM420742,
IHW:IHW01085,
IPD-IMGT/HLA:25883,
Wikidata:Q54845468
CVCL_5C62 2026-08-01 05:06:40 0
GM11996
 
Resource Report
Resource Website
RRID:CVCL_5C54 Homo sapiens (Human) Part of: International Histocompatibility Workshop cell lines., Part of: CEPH/Utah pedigree cell line collection. PMID:15514893 Transformed cell line Male CEPH-1362-NA11996, 1362-8929 CLO:CLO_0020507,
Coriell:GM11996,
dbMHC:48669,
GEO:GSM30095,
GEO:GSM316525,
GEO:GSM316526,
GEO:GSM316527,
GEO:GSM957433,
IHW:IHW01139,
IPD-IMGT/HLA:25936,
Wikidata:Q54845431
CVCL_5C54 2026-08-01 05:06:34 0
GM11988
 
Resource Report
Resource Website
RRID:CVCL_5C50 Homo sapiens (Human) Part of: International Histocompatibility Workshop cell lines., Part of: CEPH/Utah pedigree cell line collection. PMID:15514893
PMID:20856902
PMID:24924344
Transformed cell line Female CEPH-1362-NA11988, 1362-8567 CLO:CLO_0020525,
Coriell:GM11988,
dbMHC:48661,
GEO:GSM25522,
GEO:GSM30087,
GEO:GSM316228,
GEO:GSM316229,
GEO:GSM316230,
GEO:GSM420721,
GEO:GSM957425,
IHW:IHW01128,
IPD-IMGT/HLA:25925,
Wikidata:Q54845423
CVCL_5C50 2026-08-01 05:06:33 0
GM12050
 
Resource Report
Resource Website
RRID:CVCL_5C73 Homo sapiens (Human) Part of: International Histocompatibility Workshop cell lines., Part of: CEPH/Utah pedigree cell line collection. PMID:20856902 Transformed cell line Male CEPH-1344-NA12050, 1344-8349 CLO:CLO_0020419,
Coriell:GM12050,
dbMHC:48601,
GEO:GSM420761,
GEO:GSM659918,
GEO:GSM660129,
GEO:GSM660335,
IHW:IHW01070,
IPD-IMGT/HLA:25868,
PRIDE:PXD025499,
Wikidata:Q54845485
CVCL_5C73 2026-08-01 05:06:36 0
GM11993
 
Resource Report
Resource Website
Coriell Cat# GM11993, RRID:CVCL_7516 Homo sapiens (Human) Population: Caucasian; Utah residents with ancestry from Northern and Western Europe., Part of: International Histocompatibility Workshop cell lines., Part of: International Genome Sample Resource (1000 genomes project) cell lines., Part of: CEPH/Utah pedigree cell line collection. PMID:15514893
PMID:17122850
PMID:19797678
PMID:20398888
PMID:20856902
PMID:21397061
PMID:23676674
PMID:24037378
PMID:26621101
PMID:27617755
PMID:31048460
Transformed cell line Female CEPH-1362-NA11993, 1362-8572 Coriell GM11993 CLO:CLO_0020508,
EFO:EFO_0001125,
ArrayExpress:E-GEUV-1,
ArrayExpress:E-GEUV-2,
ArrayExpress:E-GEUV-3,
ArrayExpress:E-MTAB-3656,
ArrayExpress:E-MTAB-3657,
Coriell:GM11993,
dbMHC:48666,
GEO:GSM25526,
GEO:GSM25527,
GEO:GSM30092,
GEO:GSM112519,
GEO:GSM112824,
GEO:GSM188798,
GEO:GSM207783,
GEO:GSM273303,
GEO:GSM273304,
GEO:GSM314892,
GEO:GSM314893,
GEO:GSM420725,
GEO:GSM420726,
GEO:GSM424337,
GEO:GSM486773,
GEO:GSM486774,
GEO:GSM648866,
GEO:GSM659995,
GEO:GSM660201,
GEO:GSM660406,
GEO:GSM905857,
GEO:GSM905952,
GEO:GSM906047,
GEO:GSM957347,
GEO:GSM957373,
GEO:GSM957430,
IGSR:NA11993,
IHW:IHW01133,
IPD-IMGT/HLA:25930,
Wikidata:Q54845428
CVCL_7516 2026-08-01 05:06:34 0
GM12014
 
Resource Report
Resource Website
RRID:CVCL_X346 Homo sapiens (Human) Mevalonate kinase deficiency Population: Caucasian. Finite cell line Male CLO:CLO_0020467,
Coriell:GM12014,
Wikidata:Q54845449
CVCL_X346 2026-08-01 05:06:40 0
GM12016
 
Resource Report
Resource Website
Coriell Cat# GM12016, RRID:CVCL_5J55 Homo sapiens (Human) Alagille syndrome Transformed cell line Female Coriell GM12016 CLO:CLO_0020465,
BioSample:SAMN00801071,
Coriell:GM12016,
Wikidata:Q54845452
CVCL_5J55 2026-08-01 05:06:34 0
GM12004
 
Resource Report
Resource Website
RRID:CVCL_9602 Homo sapiens (Human) Population: Caucasian; Utah residents with ancestry from Northern and Western Europe., Part of: International Genome Sample Resource (1000 genomes project) cell lines., Part of: CEPH/Utah pedigree cell line collection. PMID:14583597
PMID:17122850
PMID:19043577
PMID:19797678
PMID:20398888
PMID:20856902
PMID:21397061
PMID:21418647
PMID:24037378
PMID:27617755
Transformed cell line Female CLO:CLO_0020480,
EFO:EFO_0001129,
ArrayExpress:E-GEUV-1,
ArrayExpress:E-GEUV-2,
ArrayExpress:E-GEUV-3,
BioSample:SAMN00801051,
Coriell:GM12004,
GEO:GSM112523,
GEO:GSM112828,
GEO:GSM188802,
GEO:GSM273310,
GEO:GSM291637,
GEO:GSM314899,
GEO:GSM420738,
GEO:GSM424340,
GEO:GSM486781,
GEO:GSM486782,
GEO:GSM649295,
GEO:GSM651099,
GEO:GSM651100,
GEO:GSM659948,
GEO:GSM660168,
GEO:GSM660376,
GEO:GSM905861,
GEO:GSM905956,
GEO:GSM906051,
GEO:GSM957342,
GEO:GSM957350,
GEO:GSM957376,
GEO:GSM957443,
GEO:GSM980644,
GEO:GSM980646,
GEO:GSM1261036,
GEO:GSM1719774,
IGSR:NA12004,
Wikidata:Q54845439
CVCL_9602 2026-08-01 05:06:40 0
GM12000
 
Resource Report
Resource Website
Coriell Cat# GM12000, RRID:CVCL_5C58 Homo sapiens (Human) Part of: CEPH/Utah pedigree cell line collection. PMID:20856902
PMID:21418647
Transformed cell line Female Coriell GM12000 CLO:CLO_0020486,
Coriell:GM12000,
GEO:GSM316276,
GEO:GSM316277,
GEO:GSM316278,
GEO:GSM420734,
GEO:GSM651087,
GEO:GSM651088,
GEO:GSM957439,
Wikidata:Q54845435
CVCL_5C58 2026-08-01 05:06:34 0
GM12047
 
Resource Report
Resource Website
Coriell Cat# GM12047, RRID:CVCL_5C70 Homo sapiens (Human) Part of: International Histocompatibility Workshop cell lines., Part of: CEPH/Utah pedigree cell line collection. PMID:20856902 Transformed cell line Female CEPH-1344-NA12047, 1344-8348 Coriell GM12047 CLO:CLO_0020422,
Coriell:GM12047,
dbMHC:48598,
GEO:GSM420758,
GEO:GSM659921,
GEO:GSM660132,
GEO:GSM660338,
IHW:IHW01069,
IPD-IMGT/HLA:25867,
Wikidata:Q54845482
CVCL_5C70 2026-08-01 05:06:35 0
GM12014
 
Resource Report
Resource Website
Coriell Cat# GM12014, RRID:CVCL_X346 Homo sapiens (Human) Mevalonate kinase deficiency Population: Caucasian. Finite cell line Male Coriell GM12014 CLO:CLO_0020467,
Coriell:GM12014,
Wikidata:Q54845449
CVCL_X346 2026-08-01 05:06:35 0
GM12044
 
Resource Report
Resource Website
Coriell Cat# GM12044, RRID:CVCL_9605 Homo sapiens (Human) Population: Caucasian; Utah residents with ancestry from Northern and Western Europe., Part of: International Histocompatibility Workshop cell lines., Part of: International Genome Sample Resource (1000 genomes project) cell lines., Part of: CEPH/Utah pedigree cell line collection. PMID:15514893
PMID:17122850
PMID:19043577
PMID:19797678
PMID:20398888
PMID:20856902
PMID:21397061
PMID:23676674
PMID:24037378
PMID:27617755
PMID:29116076
PMID:35931342
Transformed cell line Female CEPH-1346-NA12044, 1346-8363 Coriell GM12044 CLO:CLO_0020425,
EFO:EFO_0001133,
ArrayExpress:E-GEUV-1,
ArrayExpress:E-GEUV-2,
ArrayExpress:E-GEUV-3,
ArrayExpress:E-MTAB-5835,
BioSample:SAMN00801101,
Coriell:GM12044,
dbMHC:48621,
GEO:GSM25542,
GEO:GSM25543,
GEO:GSM30040,
GEO:GSM112527,
GEO:GSM112832,
GEO:GSM188806,
GEO:GSM273315,
GEO:GSM273316,
GEO:GSM291642,
GEO:GSM314904,
GEO:GSM314905,
GEO:GSM420752,
GEO:GSM420753,
GEO:GSM424344,
GEO:GSM486789,
GEO:GSM486790,
GEO:GSM648941,
GEO:GSM957380,
GEO:GSM1719778,
IGSR:NA12044,
IHW:IHW01086,
IPD-IMGT/HLA:25884,
Wikidata:Q54845477
CVCL_9605 2026-08-01 05:06:35 0
GM11992
 
Resource Report
Resource Website
Coriell Cat# GM11992, RRID:CVCL_7515 Homo sapiens (Human) Population: Caucasian; Utah residents with ancestry from Northern and Western Europe., Part of: International Histocompatibility Workshop cell lines., Part of: International Genome Sample Resource (1000 genomes project) cell lines., Part of: CEPH/Utah pedigree cell line collection. PMID:15514893
PMID:17122850
PMID:19043577
PMID:19797678
PMID:20398888
PMID:20856902
PMID:21397061
PMID:23676674
PMID:24037378
PMID:27617755
PMID:29116076
PMID:31048460
Transformed cell line Male CEPH-1362-NA11992, 1362-8573 Coriell GM11992 CLO:CLO_0020500,
EFO:EFO_0001124,
ArrayExpress:E-GEUV-1,
ArrayExpress:E-GEUV-2,
ArrayExpress:E-GEUV-3,
ArrayExpress:E-MTAB-3656,
ArrayExpress:E-MTAB-3657,
ArrayExpress:E-MTAB-5835,
Coriell:GM11992,
dbMHC:48665,
GEO:GSM25524,
GEO:GSM25525,
GEO:GSM30091,
GEO:GSM112518,
GEO:GSM112823,
GEO:GSM188796,
GEO:GSM273301,
GEO:GSM273302,
GEO:GSM291631,
GEO:GSM314890,
GEO:GSM314891,
GEO:GSM420723,
GEO:GSM420724,
GEO:GSM424336,
GEO:GSM486771,
GEO:GSM486772,
GEO:GSM648942,
GEO:GSM659997,
GEO:GSM660204,
GEO:GSM660408,
GEO:GSM905856,
GEO:GSM905951,
GEO:GSM906046,
GEO:GSM957346,
GEO:GSM957372,
GEO:GSM957429,
GEO:GSM1719770,
IGSR:NA11992,
IHW:IHW01134,
IPD-IMGT/HLA:25931,
Wikidata:Q54845427
CVCL_7515 2026-08-01 05:06:33 0
GM11987
 
Resource Report
Resource Website
Coriell Cat# GM11987, RRID:CVCL_5C49 Homo sapiens (Human) Part of: International Histocompatibility Workshop cell lines., Part of: CEPH/Utah pedigree cell line collection. PMID:15514893
PMID:20856902
Transformed cell line Male CEPH-1362-NA11987, 1362-8565 Coriell GM11987 CLO:CLO_0020524,
Coriell:GM11987,
dbMHC:48660,
GEO:GSM25521,
GEO:GSM30086,
GEO:GSM316519,
GEO:GSM316520,
GEO:GSM316521,
GEO:GSM420720,
GEO:GSM957424,
IHW:IHW01126,
IPD-IMGT/HLA:25923,
Wikidata:Q54845422
CVCL_5C49 2026-08-01 05:06:34 0

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