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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
GM16866
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM16866, RRID:CVCL_4F75 Homo sapiens (Human) Peroxisome biogenesis disorder 7A Population: Caucasian. PMID:12851857
PMID:16257970
Finite cell line Female Coriell GM16866 CLO:CLO_0018133,
Coriell:GM16866,
Wikidata:Q54848793
CVCL_4F75 2026-09-05 10:58:05 1
GM16769
 
Resource Report
Resource Website
RRID:CVCL_AB19 Homo sapiens (Human) Population: Jewish; Ashkenazi. Transformed cell line Male CLO:CLO_0018434,
Coriell:GM16769,
Wikidata:Q54848729
CVCL_AB19 2026-09-05 10:58:04 0
GM16965
 
Resource Report
Resource Website
Coriell Cat# GM16965, RRID:CVCL_4D31 Homo sapiens (Human) Population: Caucasian; Amish. Transformed cell line Female Coriell GM16965 CLO:CLO_0018083,
Coriell:GM16965,
Wikidata:Q54848820
CVCL_4D31 2026-09-05 10:58:06 0
GM16786
 
Resource Report
Resource Website
RRID:CVCL_CZ70 Homo sapiens (Human) Population: Caucasian; Sardinian. Transformed cell line Male CLO:CLO_0018385,
Coriell:GM16786,
Wikidata:Q54848739
CVCL_CZ70 2026-09-05 10:58:05 0
GM16968
 
Resource Report
Resource Website
Coriell Cat# GM16968, RRID:CVCL_4D34 Homo sapiens (Human) Population: Caucasian; Amish. Finite cell line Female Coriell GM16968 CLO:CLO_0018085,
Coriell:GM16968,
Wikidata:Q54848823
CVCL_4D34 2026-09-05 10:58:06 0
GM16866
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_4F75 Homo sapiens (Human) Peroxisome biogenesis disorder 7A Population: Caucasian. PMID:12851857
PMID:16257970
Finite cell line Female CLO:CLO_0018133,
Coriell:GM16866,
Wikidata:Q54848793
CVCL_4F75 2026-09-05 10:58:05 1
GM16772
 
Resource Report
Resource Website
RRID:CVCL_AB22 Homo sapiens (Human) Familial dysautonomia Donor information: Established from monozygotic twin of GM16771 (Cellosaurus=CVCL_AB21)., Population: Jewish; Ashkenazi. Transformed cell line Female CLO:CLO_0018441,
Coriell:GM16772,
Wikidata:Q54848732
CVCL_AB22 2026-09-05 10:58:04 0
GM16879
 
Resource Report
Resource Website
RRID:CVCL_4D25 Homo sapiens (Human) Population: Caucasian; Amish. Finite cell line Male CLO:CLO_0018135,
Coriell:GM16879,
Wikidata:Q54848797
CVCL_4D25 2026-09-05 10:58:05 0
GM16824
 
Resource Report
Resource Website
RRID:CVCL_U889 Homo sapiens (Human) Alexander disease Population: Caucasian. Transformed cell line Male ALX-1 CLO:CLO_0018420,
Coriell:GM16824,
Wikidata:Q54848759
CVCL_U889 2026-09-05 10:58:05 0
GM16966
 
Resource Report
Resource Website
RRID:CVCL_4D32 Homo sapiens (Human) Population: Caucasian; Amish. Finite cell line Female CLO:CLO_0018082,
Coriell:GM16966,
Wikidata:Q54848821
CVCL_4D32 2026-09-05 10:58:06 0
GM16799
 
Resource Report
Resource Website
RRID:CVCL_1F67 Homo sapiens (Human) Population: Caucasian. Transformed cell line Female CLO:CLO_0018398,
Coriell:GM16799,
Wikidata:Q54848749
CVCL_1F67 2026-09-05 10:58:05 0
GM16807
 
Resource Report
Resource Website
Coriell Cat# GM16807, RRID:CVCL_N270 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel. Transformed cell line Male GM18100 Coriell GM16807 CLO:CLO_0018419,
Coriell:GM16807,
Coriell:GM18100,
Wikidata:Q54848754
CVCL_N270 2026-09-05 10:58:05 0
GM16864
 
Resource Report
Resource Website
RRID:CVCL_6B22 Homo sapiens (Human) Emery-Dreifuss muscular dystrophy 1, X-linked Transformed cell line Male CLO:CLO_0018131,
Coriell:GM16864,
Wikidata:Q54848791
CVCL_6B22 2026-09-05 10:58:05 0
GM16809
 
Resource Report
Resource Website
Coriell Cat# GM16809, RRID:CVCL_5Q80 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM16809 Coriell:GM16809,
Wikidata:Q54848756
CVCL_5Q80 2026-09-05 10:58:05 0
GM16809
 
Resource Report
Resource Website
RRID:CVCL_5Q80 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM16809,
Wikidata:Q54848756
CVCL_5Q80 2026-09-05 10:58:05 0
GM16784
 
Resource Report
Resource Website
Coriell Cat# GM16784, RRID:CVCL_DS92 Homo sapiens (Human) Ichthyosis Population: Caucasian; Sardinian. Transformed cell line Male Coriell GM16784 CLO:CLO_0018437,
BioSample:SAMN00804679,
Coriell:GM16784,
Wikidata:Q54848736
CVCL_DS92 2026-09-05 10:58:05 0
GM16785
 
Resource Report
Resource Website
RRID:CVCL_DS93 Homo sapiens (Human) Ichthyosis Population: Caucasian; Sardinian. Transformed cell line Male CLO:CLO_0018438,
Coriell:GM16785,
Wikidata:Q54848738
CVCL_DS93 2026-09-05 10:58:05 0
GM16925
 
Resource Report
Resource Website
RRID:CVCL_4D28 Homo sapiens (Human) Osteogenesis imperfecta type IV Population: Caucasian; Amish. Finite cell line Male CLO:CLO_0018113,
Coriell:GM16925,
Wikidata:Q54848807
CVCL_4D28 2026-09-05 10:58:05 0
GM16878
 
Resource Report
Resource Website
RRID:CVCL_4D24 Homo sapiens (Human) Population: Caucasian; Amish. Transformed cell line Male CLO:CLO_0018132,
BioSample:SAMN00804737,
Coriell:GM16878,
Wikidata:Q54848795
CVCL_4D24 2026-09-05 10:58:05 0
GM16787
 
Resource Report
Resource Website
Coriell Cat# GM16787, RRID:CVCL_CZ71 Homo sapiens (Human) Population: Caucasian; Sardinian. Transformed cell line Female Coriell GM16787 CLO:CLO_0018383,
Coriell:GM16787,
Wikidata:Q54848740
CVCL_CZ71 2026-09-05 10:58:05 0

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