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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
GM05854
 
Resource Report
Resource Website
Coriell Cat# GM05854, RRID:CVCL_AX84 Homo sapiens (Human) Transformed cell line Female Coriell GM05854 CLO:CLO_0024700,
Coriell:GM05854,
Wikidata:Q54841962
CVCL_AX84 2026-08-01 05:04:52 0
GM05817
 
Resource Report
Resource Website
RRID:CVCL_N040 Homo sapiens (Human) Population: African American., Part of: Human variation panel. PMID:2567118
PMID:16260726
PMID:20210923
Transformed cell line Female GM 5817, GM17159 CLO:CLO_0013964,
CLO:CLO_0024681,
Coriell:GM05817,
Coriell:GM17159,
GEO:GSM273426,
GEO:GSM569655,
GEO:GSM596224,
GEO:GSM597024,
GEO:GSM924669,
IPD-IMGT/HLA:15817,
Wikidata:Q54841955
CVCL_N040 2026-08-01 05:04:59 0
GM05823+hTERT
 
Resource Report
Resource Website
RRID:CVCL_VL10 Homo sapiens (Human) Ataxia telangiectasia syndrome PMID:11313956
PMID:21149446
Telomerase immortalized cell line Male GM05823-hTert, hTERT+ GM05823 Wikidata:Q93789883 cvcl_7441 CVCL_VL10 2026-08-01 05:04:57 0
GM05854
 
Resource Report
Resource Website
RRID:CVCL_AX84 Homo sapiens (Human) Transformed cell line Female CLO:CLO_0024700,
Coriell:GM05854,
Wikidata:Q54841962
CVCL_AX84 2026-08-01 05:04:57 0
GM05759
 
Resource Report
Resource Website
RRID:CVCL_U944 Homo sapiens (Human) Alagille syndrome Population: Caucasian. PMID:34087995 Finite cell line Female CLO:CLO_0024658,
Coriell:GM05759,
Wikidata:Q54841934
CVCL_U944 2026-08-01 05:04:58 0
GM05794
 
Resource Report
Resource Website
Coriell Cat# GM05794, RRID:CVCL_0Q54 Homo sapiens (Human) Population: Caucasian. Finite cell line Male Coriell GM05794 CLO:CLO_0024687,
Coriell:GM05794,
Wikidata:Q54841942
CVCL_0Q54 2026-08-01 05:04:52 0
GM05880
 
Resource Report
Resource Website
RRID:CVCL_5N36 Homo sapiens (Human) Population: Iraqi. Finite cell line Female CLO:CLO_0024224,
Coriell:GM05880,
Wikidata:Q54841979
CVCL_5N36 2026-08-01 05:04:58 0
GM05796
 
Resource Report
Resource Website
Coriell Cat# GM05796, RRID:CVCL_0Q57 Homo sapiens (Human) Population: Caucasian. Finite cell line Female Coriell GM05796 CLO:CLO_0024685,
Coriell:GM05796,
Wikidata:Q54841944
CVCL_0Q57 2026-08-01 05:04:59 0
GM05798
 
Resource Report
Resource Website
RRID:CVCL_0P68 Homo sapiens (Human) Hepatolenticular degeneration Population: Caucasian. Finite cell line Female CLO:CLO_0024683,
Coriell:GM05798,
Wikidata:Q54841947
CVCL_0P68 2026-08-01 05:04:59 0
GM05855
 
Resource Report
Resource Website
Coriell Cat# GM05855, RRID:CVCL_AX85 Homo sapiens (Human) Transformed cell line Female GM05855B Coriell GM05855 CLO:CLO_0024701,
Coriell:GM05855,
Wikidata:Q54841963
CVCL_AX85 2026-08-01 05:04:57 0
GM05875
 
Resource Report
Resource Website
RRID:CVCL_X328 Homo sapiens (Human) Population: Caucasian. PMID:2095701
PMID:6661932
PMID:23665875
Finite cell line Female GM 5875, GM05875A, GM5875A CLO:CLO_0024237,
Coriell:GM05875,
Wikidata:Q54841971
CVCL_X328 2026-08-01 05:04:59 0
GM05872
 
Resource Report
Resource Website
RRID:CVCL_4F51 Homo sapiens (Human) Medium-chain acyl-CoA dehydrogenase deficiency Population: Caucasian. Finite cell line Female CLO:CLO_0024231,
Coriell:GM05872,
Wikidata:Q54841970
CVCL_4F51 2026-08-01 05:04:52 0
GM05725
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_UR86 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Female GM05725Z Coriell:GM05725,
Wikidata:Q93789618
CVCL_UR86 2026-08-01 05:04:51 0
GM05740
 
Resource Report
Resource Website
RRID:CVCL_Y893 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Male GM05740A CLO:CLO_0024640,
Coriell:GM05740,
Wikidata:Q54841923
CVCL_Y893 2026-08-01 05:04:58 0
GM05724
 
Resource Report
Resource Website
RRID:CVCL_1J26 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Male GM05724A CLO:CLO_0024646,
Coriell:GM05724,
Wikidata:Q54841919
CVCL_1J26 2026-08-01 05:04:58 0
GM05725
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM05725, RRID:CVCL_UR86 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Female GM05725Z Coriell GM05725 Coriell:GM05725,
Wikidata:Q93789618
CVCL_UR86 2026-08-01 05:04:58 0
GM05789
 
Resource Report
Resource Website
RRID:CVCL_7440 Homo sapiens (Human) Smith-Lemli-Opitz syndrome Population: Caucasian. Transformed cell line Female CLO:CLO_0024662,
Coriell:GM05789,
Wikidata:Q54841938
CVCL_7440 2026-08-01 05:04:57 0
GM05726
 
Resource Report
Resource Website
Coriell Cat# GM05726, RRID:CVCL_1J27 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Female GM05726A Coriell GM05726 CLO:CLO_0024647,
Coriell:GM05726,
Wikidata:Q54841920
CVCL_1J27 2026-08-01 05:04:51 0
GM05744
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_US88 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Male GM05744Z Coriell:GM05744,
Wikidata:Q93789658
CVCL_US88 2026-08-01 05:04:51 0
GM05832
 
Resource Report
Resource Website
Coriell Cat# GM05832, RRID:CVCL_X327 Homo sapiens (Human) Population: Caucasian. PMID:6661932
PMID:23665875
Finite cell line Male GM 5832 Coriell GM05832 CLO:CLO_0024707,
Coriell:GM05832,
Wikidata:Q54841956
CVCL_X327 2026-08-01 05:04:59 0

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