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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 Authority Record Last Update Mentions Count
GM04599
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_0L60 Homo sapiens (Human) Population: African American. Finite cell line Male GM04599A Coriell:GM04599,
Wikidata:Q54838586
CVCL_0L60 Cellosaurus 2026-10-31 05:03:20 0
GM04585
 
Resource Report
Resource Website
RRID:CVCL_AA22 Homo sapiens (Human) Population: Caucasian. Transformed cell line Female CLO:CLO_0018901,
Coriell:GM04585,
Wikidata:Q54838574
CVCL_AA22 Cellosaurus 2026-10-31 05:03:20 0
GM04435
 
Resource Report
Resource Website
RRID:CVCL_X307 Homo sapiens (Human) Trisomy 16 PMID:6661932
PMID:11687795
Finite cell line Sex ambiguous GM 4435 CLO:CLO_0019688,
Coriell:GM04435,
GEO:GSM803,
Wikidata:Q54838528
CVCL_X307 Cellosaurus 2026-10-31 05:03:19 0
GM04584
 
Resource Report
Resource Website
RRID:CVCL_1I21 Homo sapiens (Human) Huntington's disease Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease. Transformed cell line Male CLO:CLO_0018900,
Coriell:GM04584,
Wikidata:Q54838573
CVCL_1I21 Cellosaurus 2026-10-31 05:03:20 0
GM04539
 
Resource Report
Resource Website
RRID:CVCL_0M33 Homo sapiens (Human) Cystic fibrosis Population: Caucasian. Finite cell line Female CLO:CLO_0018881,
Coriell:GM04539,
Wikidata:Q54838563
CVCL_0M33 Cellosaurus 2026-10-31 05:03:20 0
GM04478
 
Resource Report
Resource Website
RRID:CVCL_V566 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Female CLO:CLO_0019661,
Coriell:GM04478,
Wikidata:Q54838532
CVCL_V566 Cellosaurus 2026-10-31 05:03:19 0
GM04545
 
Resource Report
Resource Website
RRID:CVCL_0M37 Homo sapiens (Human) Population: Caucasian. Finite cell line Male CLO:CLO_0018874,
Coriell:GM04545,
Wikidata:Q54838567
CVCL_0M37 Cellosaurus 2026-10-31 05:03:20 0
GM04465
 
Resource Report
Resource Website
Coriell Cat# GM04465, RRID:CVCL_CV41 Homo sapiens (Human) Schwartz-Jampel syndrome Population: Caucasian. Finite cell line Female Coriell GM04465 CLO:CLO_0019686,
Coriell:GM04465,
Wikidata:Q54838529
CVCL_CV41 Cellosaurus 2026-10-31 05:03:19 0
GM04502
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM04502, RRID:CVCL_F135 Homo sapiens (Human) Donor information: Established from monozygotic twin of GM04501 (Cellosaurus=CVCL_7409). Finite cell line Male GM04502A, HF21 Coriell GM04502 CLO:CLO_0018818,
Coriell:GM04502,
Wikidata:Q54838542
CVCL_F135 Cellosaurus 2026-10-31 05:03:20 0
GM04496
 
Resource Report
Resource Website
RRID:CVCL_9R20 Homo sapiens (Human) Adrenoleukodystrophy PMID:1634904
PMID:21721033
Finite cell line Male GM 4496 CLO:CLO_0019670,
Coriell:GM04496,
Wikidata:Q54838539
CVCL_9R20 Cellosaurus 2026-10-31 05:03:19 0
GM04616
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM04616, RRID:CVCL_V475 Homo sapiens (Human) Down syndrome Population: Caucasian. PMID:6661932
PMID:17668376
Finite cell line Female GM 4616, GM04616A Coriell GM04616 CLO:CLO_0018955,
Coriell:GM04616,
Wikidata:Q54838601
CVCL_V475 Cellosaurus 2026-10-31 05:03:21 3
GM04628
 
Resource Report
Resource Website
Coriell Cat# GM04628, RRID:CVCL_2T06 Homo sapiens (Human) Karyotypic information: 46,X,t(X;22)(q12;p11) (PubMed=10377420)., Population: Caucasian; Swiss. PMID:10377420 Finite cell line Female GM4628 Coriell GM04628 CLO:CLO_0018936,
Coriell:GM04628,
Wikidata:Q54838610
CVCL_2T06 Cellosaurus 2026-10-31 05:03:21 0
GM04663
 
Resource Report
Resource Website
RRID:CVCL_7415 Homo sapiens (Human) Familial dysautonomia Population: Caucasian. PMID:29762696
PMID:30905397
Finite cell line Female CLO:CLO_0018968,
Coriell:GM04663,
GEO:GSM3592407,
GEO:GSM3592413,
Wikidata:Q54838620
CVCL_7415 Cellosaurus 2026-10-31 05:03:21 0
GM04627
 
Resource Report
Resource Website
RRID:CVCL_X311 Homo sapiens (Human) PMID:6661932 Finite cell line Male GM-4627, GM 4627 CLO:CLO_0018935,
Coriell:GM04627,
Wikidata:Q54838609
CVCL_X311 Cellosaurus 2026-10-31 05:03:21 0
GM04723
 
Resource Report
Resource Website
Coriell Cat# GM04723, RRID:CVCL_Y871 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Female Coriell GM04723 CLO:CLO_0019072,
Coriell:GM04723,
Wikidata:Q54838655
CVCL_Y871 Cellosaurus 2026-10-31 05:03:22 0
GM04734
 
Resource Report
Resource Website
RRID:CVCL_1I28 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Female GM04734A CLO:CLO_0019069,
Coriell:GM04734,
Wikidata:Q54838661
CVCL_1I28 Cellosaurus 2026-10-31 05:03:22 0
GM04610
 
Resource Report
Resource Website
Coriell Cat# GM04610, RRID:CVCL_X309 Homo sapiens (Human) Trisomy 8 Karyotypic information: 47,XX,+8 [75]; 46,XX,+8,dic(14;21)(14qter->14p13::21p13->21qter) [25] (Coriell=GM04610). PMID:6661932 Finite cell line Female GM 4610 Coriell GM04610 CLO:CLO_0018902,
Coriell:GM04610,
Wikidata:Q54838597
CVCL_X309 Cellosaurus 2026-10-31 05:03:21 0
GM04718
 
Resource Report
Resource Website
RRID:CVCL_V569 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Female GM04718A CLO:CLO_0019022,
Coriell:GM04718,
Wikidata:Q54838650
CVCL_V569 Cellosaurus 2026-10-31 05:03:22 0
GM04608
 
Resource Report
Resource Website
Coriell Cat# GM04608, RRID:CVCL_Y797 Homo sapiens (Human) Dystrophia myotonica 1 Population: Caucasian. Finite cell line Female Coriell GM04608 CLO:CLO_0018912,
Coriell:GM04608,
Wikidata:Q54838596
CVCL_Y797 Cellosaurus 2026-10-31 05:03:21 0
GM04708
 
Resource Report
Resource Website
Coriell Cat# GM04708, RRID:CVCL_1I26 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Female GM04708A Coriell GM04708 CLO:CLO_0019025,
Coriell:GM04708,
Wikidata:Q54838642
CVCL_1I26 Cellosaurus 2026-10-31 05:03:22 0

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