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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
GM04374
 
Resource Report
Resource Website
Coriell Cat# GM04374, RRID:CVCL_GS63 Homo sapiens (Human) Tyrosinemia type II Population: Native North American. Finite cell line Female Coriell GM04374 CLO:CLO_0019341,
Coriell:GM04374,
Wikidata:Q54838504
CVCL_GS63 2026-08-08 05:00:14 0
GM04376
 
Resource Report
Resource Website
Coriell Cat# GM04376, RRID:CVCL_AB34 Homo sapiens (Human) Triploidy syndrome Karyotypic information: 69,XXX (Coriell=GM04376)., Population: Caucasian. Finite cell line Female GM04376A Coriell GM04376 CLO:CLO_0019336,
Coriell:GM04376,
Wikidata:Q54838508
CVCL_AB34 2026-08-08 05:00:15 0
GM04297
 
Resource Report
Resource Website
RRID:CVCL_5M91 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0019633,
Coriell:GM04297,
Wikidata:Q54838472
CVCL_5M91 2026-08-08 05:00:13 0
GM04290
 
Resource Report
Resource Website
Coriell Cat# GM04290, RRID:CVCL_1I18 Homo sapiens (Human) Huntington's disease Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease., Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Female Coriell GM04290 CLO:CLO_0019631,
Coriell:GM04290,
Wikidata:Q54838471
CVCL_1I18 2026-08-08 05:00:14 0
GM04289
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM04289, RRID:CVCL_US61 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Female GM04289C Coriell GM04289 Coriell:GM04289,
Wikidata:Q93587500
CVCL_US61 2026-08-08 05:00:13 0
GM04305
 
Resource Report
Resource Website
RRID:CVCL_IJ33 Homo sapiens (Human) Galactosialidosis Transformed cell line Female CLO:CLO_0019629,
Coriell:GM04305,
Wikidata:Q54838474
CVCL_IJ33 2026-08-08 05:00:14 0
GM04329
 
Resource Report
Resource Website
RRID:CVCL_2Z44 Homo sapiens (Human) Campomelic dysplasia Population: Caucasian. Finite cell line Female CLO:CLO_0019571,
Coriell:GM04329,
Wikidata:Q54838486
CVCL_2Z44 2026-08-08 05:00:13 0
GM04315
 
Resource Report
Resource Website
RRID:CVCL_5M92 Homo sapiens (Human) Population: African American., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:21354051
PMID:23665875
Finite cell line Female CLO:CLO_0019552,
Coriell:GM04315,
Wikidata:Q54838479
CVCL_5M92 2026-08-08 05:00:13 0
GM04347
 
Resource Report
Resource Website
Coriell Cat# GM04347, RRID:CVCL_4D84 Homo sapiens (Human) Transformed cell line Female Coriell GM04347 CLO:CLO_0019567,
Coriell:GM04347,
Wikidata:Q54838497
CVCL_4D84 2026-08-08 05:00:14 0
GM04326
 
Resource Report
Resource Website
RRID:CVCL_0Q83 Homo sapiens (Human) Citrullinemia type I Population: Caucasian. Finite cell line Female GM4326 CLO:CLO_0019535,
Coriell:GM04326,
Wikidata:Q54838484
CVCL_0Q83 2026-08-08 05:00:13 0
GM04504
 
Resource Report
Resource Website
RRID:CVCL_7411 Homo sapiens (Human) Donor information: Established from monozygotic twin of GM04503 (Cellosaurus=CVCL_7410)., Part of: ENCODE project common cell types; tier 3. PMID:30567591 Finite cell line Female GM04504A, HF23 CLO:CLO_0018812,
Coriell:GM04504,
ENCODE:ENCBS016ENC,
ENCODE:ENCBS388KHM,
GEO:GSM3124652,
Wikidata:Q54838544
CVCL_7411 2026-08-08 05:00:15 0
GM04516
 
Resource Report
Resource Website
Coriell Cat# GM04516, RRID:CVCL_AW70 Homo sapiens (Human) Sideroblastic anemia Population: Caucasian. Finite cell line Female Coriell GM04516 CLO:CLO_0018850,
Coriell:GM04516,
Wikidata:Q54838554
CVCL_AW70 2026-08-08 05:00:16 0
GM04514
 
Resource Report
Resource Website
RRID:CVCL_X308 Homo sapiens (Human) Population: Caucasian. PMID:6661932 Finite cell line Female GM 4514 CLO:CLO_0018832,
Coriell:GM04514,
Wikidata:Q54838552
CVCL_X308 2026-08-08 05:00:15 0
GM04601
 
Resource Report
Resource Website
RRID:CVCL_Y793 Homo sapiens (Human) Dystrophia myotonica 1 Population: Caucasian. Finite cell line Female CLO:CLO_0018919,
Coriell:GM04601,
Wikidata:Q54838587
CVCL_Y793 2026-08-08 05:00:16 0
GM04516
 
Resource Report
Resource Website
RRID:CVCL_AW70 Homo sapiens (Human) Sideroblastic anemia Population: Caucasian. Finite cell line Female CLO:CLO_0018850,
Coriell:GM04516,
Wikidata:Q54838554
CVCL_AW70 2026-08-08 05:00:15 0
GM04505
 
Resource Report
Resource Website
Coriell Cat# GM04505, RRID:CVCL_7412 Homo sapiens (Human) Donor information: Established from monozygotic twin of GM04506 (Cellosaurus=CVCL_7413)., Population: Caucasian. PMID:30567591 Finite cell line Female GM04505A, HF24 Coriell GM04505 CLO:CLO_0018816,
Coriell:GM04505,
GEO:GSM3124650,
Wikidata:Q54838545
CVCL_7412 2026-08-08 05:00:15 0
GM04592
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_V473 Homo sapiens (Human) Down syndrome Population: Caucasian. PMID:6661932
PMID:23665875
Finite cell line Female GM 4592, GM04592A CLO:CLO_0018882,
Coriell:GM04592,
Wikidata:Q54838578
CVCL_V473 2026-08-08 05:00:15 1
GM04595
 
Resource Report
Resource Website
RRID:CVCL_GY22 Homo sapiens (Human) Charcot-Marie-Tooth neuropathy X type 1 Population: Caucasian. Finite cell line Female CLO:CLO_0018887,
Coriell:GM04595,
Wikidata:Q54838581
CVCL_GY22 2026-08-08 05:00:15 0
GM04513
 
Resource Report
Resource Website
Coriell Cat# GM04513, RRID:CVCL_X119 Homo sapiens (Human) Karyotypic information: 47,XX,+del(2)(qter->p23) [38]; 47,XX,+2 [12] (Coriell=GM04513)., Population: Caucasian. PMID:6617268
PMID:6661932
Finite cell line Female GM 4513 Coriell GM04513 CLO:CLO_0018827,
Coriell:GM04513,
Wikidata:Q54838551
CVCL_X119 2026-08-08 05:00:16 0
GM04506
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_7413 Homo sapiens (Human) Donor information: Established from monozygotic twin of GM04505 (Cellosaurus=CVCL_7412)., Population: Caucasian. PMID:21490598 Finite cell line Female GM04506A, HF25 CLO:CLO_0018815,
Coriell:GM04506,
Wikidata:Q54838546
CVCL_7413 2026-08-08 05:00:15 3

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