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95,747 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
GM13885
 
Resource Report
Resource Website
Coriell Cat# GM13885, RRID:CVCL_HL79 Homo sapiens (Human) Transformed cell line Female Coriell GM13885 BioSample:SAMN00802696,
Coriell:GM13885,
Wikidata:Q54846892
CVCL_HL79 2026-08-15 04:32:03 0
GM13898
 
Resource Report
Resource Website
Coriell Cat# GM13898, RRID:CVCL_1M11 Homo sapiens (Human) Ataxia telangiectasia syndrome Transformed cell line Female Coriell GM13898 CLO:CLO_0033970,
BioSample:SAMN00802712,
Coriell:GM13898,
Wikidata:Q54846902
CVCL_1M11 2026-08-15 04:32:03 0
GM13913
 
Resource Report
Resource Website
RRID:CVCL_N456 Homo sapiens (Human) Population: Caucasian; Russian., Part of: Yale-Stanford Collection from NIGMS Human Genetic Cell Repository. Transformed cell line Female JK3520 CLO:CLO_0033937,
Coriell:GM13913,
Wikidata:Q54846916
CVCL_N456 2026-08-15 04:32:03 0
GM13948
 
Resource Report
Resource Website
RRID:CVCL_5Q22 Homo sapiens (Human) Williams syndrome Transformed cell line Female CLO:CLO_0034001,
BioSample:SAMN00802764,
Coriell:GM13948,
Wikidata:Q54846939
CVCL_5Q22 2026-08-15 04:32:04 0
GM13913
 
Resource Report
Resource Website
Coriell Cat# GM13913, RRID:CVCL_N456 Homo sapiens (Human) Population: Caucasian; Russian., Part of: Yale-Stanford Collection from NIGMS Human Genetic Cell Repository. Transformed cell line Female JK3520 Coriell GM13913 CLO:CLO_0033937,
Coriell:GM13913,
Wikidata:Q54846916
CVCL_N456 2026-08-15 04:32:03 0
GM13951
 
Resource Report
Resource Website
Coriell Cat# GM13951, RRID:CVCL_5Q25 Homo sapiens (Human) Williams syndrome Transformed cell line Female Coriell GM13951 CLO:CLO_0033998,
BioSample:SAMN00802770,
Coriell:GM13951,
Wikidata:Q54846942
CVCL_5Q25 2026-08-15 04:32:10 0
GM13907
 
Resource Report
Resource Website
RRID:CVCL_1M14 Homo sapiens (Human) Ataxia telangiectasia syndrome Transformed cell line Female CLO:CLO_0033974,
BioSample:SAMN00802720,
Coriell:GM13907,
Wikidata:Q54846910
CVCL_1M14 2026-08-15 04:32:10 0
GM13897
 
Resource Report
Resource Website
RRID:CVCL_5Q14 Homo sapiens (Human) Orofacial cleft 1 Transformed cell line Female CLO:CLO_0033967,
BioSample:SAMN00802710,
Coriell:GM13897,
Wikidata:Q54846901
CVCL_5Q14 2026-08-15 04:32:03 0
GM13899
 
Resource Report
Resource Website
Coriell Cat# GM13899, RRID:CVCL_1M12 Homo sapiens (Human) Ataxia telangiectasia syndrome Transformed cell line Female Coriell GM13899 CLO:CLO_0033971,
BioSample:SAMN00802714,
Coriell:GM13899,
Wikidata:Q54846903
CVCL_1M12 2026-08-15 04:32:10 0
GM13897
 
Resource Report
Resource Website
Coriell Cat# GM13897, RRID:CVCL_5Q14 Homo sapiens (Human) Orofacial cleft 1 Transformed cell line Female Coriell GM13897 CLO:CLO_0033967,
BioSample:SAMN00802710,
Coriell:GM13897,
Wikidata:Q54846901
CVCL_5Q14 2026-08-15 04:32:03 0
GM13933
 
Resource Report
Resource Website
RRID:CVCL_FV96 Homo sapiens (Human) Progressive familial intrahepatic cholestasis Transformed cell line Female CLO:CLO_0034023,
BioSample:SAMN00802738,
Coriell:GM13933,
Wikidata:Q54846925
CVCL_FV96 2026-08-15 04:32:03 0
GM13947
 
Resource Report
Resource Website
RRID:CVCL_5Q21 Homo sapiens (Human) Williams syndrome Transformed cell line Female CLO:CLO_0034006,
BioSample:SAMN00802762,
Coriell:GM13947,
Wikidata:Q54846938
CVCL_5Q21 2026-08-15 04:32:10 0
GM13880
 
Resource Report
Resource Website
Coriell Cat# GM13880, RRID:CVCL_5Q11 Homo sapiens (Human) Orofacial cleft 1 Transformed cell line Female Coriell GM13880 CLO:CLO_0033217,
BioSample:SAMN00802690,
Coriell:GM13880,
Wikidata:Q54846889
CVCL_5Q11 2026-08-15 04:32:03 0
GM13909
 
Resource Report
Resource Website
RRID:CVCL_1M15 Homo sapiens (Human) Ataxia telangiectasia syndrome Transformed cell line Female CLO:CLO_0033917,
BioSample:SAMN00802722,
Coriell:GM13909,
Wikidata:Q54846911
CVCL_1M15 2026-08-15 04:32:03 0
GM13915
 
Resource Report
Resource Website
Coriell Cat# GM13915, RRID:CVCL_N458 Homo sapiens (Human) Population: Caucasian; Russian., Part of: Yale-Stanford Collection from NIGMS Human Genetic Cell Repository. Transformed cell line Female JK3536 Coriell GM13915 CLO:CLO_0033932,
Coriell:GM13915,
Wikidata:Q54846918
CVCL_N458 2026-08-15 04:32:10 0
GM13922
 
Resource Report
Resource Website
RRID:CVCL_1M19 Homo sapiens (Human) Ataxia telangiectasia syndrome Transformed cell line Female CLO:CLO_0033940,
BioSample:SAMN00802732,
Coriell:GM13922,
Wikidata:Q54846922
CVCL_1M19 2026-08-15 04:32:03 0
GM13958
 
Resource Report
Resource Website
RRID:CVCL_0R43 Homo sapiens (Human) Hermansky-Pudlak syndrome 1 Transformed cell line Female CLO:CLO_0033844,
Coriell:GM13958,
Wikidata:Q54846949
CVCL_0R43 2026-08-15 04:32:04 0
GM14000
 
Resource Report
Resource Website
Coriell Cat# GM14000, RRID:CVCL_1M36 Homo sapiens (Human) Ataxia telangiectasia syndrome Transformed cell line Female Coriell GM14000 CLO:CLO_0033904,
Coriell:GM14000,
Wikidata:Q54846976
CVCL_1M36 2026-08-15 04:32:10 0
GM14033
 
Resource Report
Resource Website
Coriell Cat# GM14033, RRID:CVCL_5Q31 Homo sapiens (Human) Williams syndrome PMID:23665875 Transformed cell line Female Coriell GM14033 CLO:CLO_0033867,
Coriell:GM14033,
Wikidata:Q54846995
CVCL_5Q31 2026-08-15 04:32:05 0
GM13977
 
Resource Report
Resource Website
RRID:CVCL_L267 Homo sapiens (Human) Cornelia de Lange syndrome Donor information: Established from monozygotic twin of GM13976 (Cellosaurus=CVCL_L266)., Part of: ENCODE project common cell types; tier 3. Transformed cell line Female CLO:CLO_0033829,
EFO:EFO_0005346,
BioSample:SAMN00802797,
Coriell:GM13977,
ENCODE:ENCBS221AAA,
GEO:GSM1008556,
Wikidata:Q54846967
CVCL_L267 2026-08-15 04:32:10 0

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