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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
GM00981
 
Resource Report
Resource Website
RRID:CVCL_V829 Homo sapiens (Human) Population: African American. PMID:657847
PMID:6617268
PMID:6661932
PMID:23665875
Finite cell line Female GM-981, GM-0981, GM 981 CLO:CLO_0029478,
Coriell:GM00981,
Wikidata:Q54836579
CVCL_V829 2026-08-15 04:28:55 0
GM00956
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00956, RRID:CVCL_X060 Homo sapiens (Human) PMID:6451249 Finite cell line Female GM-956, GM 956 Coriell GM00956 Coriell:GM00956,
Wikidata:Q54836561
CVCL_X060 2026-08-15 04:28:55 0
GM00975
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_JD95 Homo sapiens (Human) Finite cell line Female GM-975 Coriell:GM00975,
Wikidata:Q54836574
CVCL_JD95 2026-08-15 04:28:55 0
GM00946
 
Resource Report
Resource Website
RRID:CVCL_7308 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:14583597
PMID:16260726
PMID:20889555
PMID:29959025
Transformed cell line Female GM-946, GM00946B, GM17210 CLO:CLO_0013891,
CLO:CLO_0029523,
Coriell:GM00946,
Coriell:GM17210,
GEO:GSM569510,
GEO:GSM596274,
GEO:GSM596635,
GEO:GSM924812,
Wikidata:Q54836554
CVCL_7308 2026-08-15 04:28:54 0
GM00958
 
Resource Report
Resource Website
RRID:CVCL_9W79 Homo sapiens (Human) Mucopolysaccharidosis type IVA Population: Caucasian. PMID:8910459 Finite cell line Male GM-958 CLO:CLO_0029522,
Coriell:GM00958,
Wikidata:Q54836563
CVCL_9W79 2026-08-15 04:28:55 0
GM00915
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM00915, RRID:CVCL_CX53 Homo sapiens (Human) Multiple sulfatase deficiency disease Finite cell line Male GM-915 Coriell GM00915 Coriell:GM00915,
Wikidata:Q54836532
CVCL_CX53 2026-08-15 04:28:54 0
GM00947
 
Resource Report
Resource Website
Coriell Cat# GM00947, RRID:CVCL_4W19 Homo sapiens (Human) Isovaleric acidemia Population: Caucasian. Finite cell line Male GM0947, GM-947 Coriell GM00947 CLO:CLO_0029524,
Coriell:GM00947,
Wikidata:Q54836555
CVCL_4W19 2026-08-15 04:28:54 0
GM00959
 
Resource Report
Resource Website
RRID:CVCL_V787 Homo sapiens (Human) Population: Caucasian. PMID:1017324
PMID:6661932
PMID:23665875
Finite cell line Male GM-959, GM-0959, GM 959 CLO:CLO_0029532,
Coriell:GM00959,
Wikidata:Q54836564
CVCL_V787 2026-08-15 04:28:55 0
GM00911
 
Resource Report
Resource Website
RRID:CVCL_4T28 Homo sapiens (Human) Methionine adenosyltransferase deficiency Population: Caucasian. PMID:7560086 Finite cell line Male GM0911, GM-911, GM 00911 CLO:CLO_0029561,
Coriell:GM00911,
Wikidata:Q54836529
CVCL_4T28 2026-08-15 04:28:54 0
GM00959
 
Resource Report
Resource Website
Coriell Cat# GM00959, RRID:CVCL_V787 Homo sapiens (Human) Population: Caucasian. PMID:1017324
PMID:6661932
PMID:23665875
Finite cell line Male GM-959, GM-0959, GM 959 Coriell GM00959 CLO:CLO_0029532,
Coriell:GM00959,
Wikidata:Q54836564
CVCL_V787 2026-08-15 04:28:55 0
GM00978
 
Resource Report
Resource Website
Discontinued
RRID:CVCL_L956 Homo sapiens (Human) Finite cell line Female GM-978, GM00188, GM-188 CLO:CLO_0029500,
Coriell:GM00188,
Coriell:GM00978,
Wikidata:Q54836577
CVCL_L956 2026-08-15 04:28:55 0
GM00915
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_CX53 Homo sapiens (Human) Multiple sulfatase deficiency disease Finite cell line Male GM-915 Coriell:GM00915,
Wikidata:Q54836532
CVCL_CX53 2026-08-15 04:28:54 0
GM00954
 
Resource Report
Resource Website
Coriell Cat# GM00954, RRID:CVCL_V029 Homo sapiens (Human) Argininemia Finite cell line Female GM0954, GM-954 Coriell GM00954 CLO:CLO_0029520,
Coriell:GM00954,
Wikidata:Q54836560
CVCL_V029 2026-08-15 04:28:55 0
GM00969
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_7311 Homo sapiens (Human) Population: Caucasian. PMID:2837086
PMID:3745952
PMID:6458814
PMID:6726265
PMID:7380831
PMID:12665480
PMID:17668376
PMID:19896956
PMID:26831110
PMID:30567591
Finite cell line Female GM0969, GM-969, GM 969, GM00969A, GM 969A, GM0969B, GM00969C, GM00969F, C4 CLO:CLO_0029504,
Coriell:GM00969,
GEO:GSM1316971,
GEO:GSM1317008,
GEO:GSM3124626,
Wikidata:Q54836570
CVCL_7311 2026-08-15 04:28:55 3
GM00919
 
Resource Report
Resource Website
Coriell Cat# GM00919, RRID:CVCL_H176 Homo sapiens (Human) Homocystinuria Finite cell line Female GM-919 Coriell GM00919 CLO:CLO_0029564,
Coriell:GM00919,
Wikidata:Q54836535
CVCL_H176 2026-08-15 04:28:54 0
GM00933
 
Resource Report
Resource Website
RRID:CVCL_4J15 Homo sapiens (Human) Acute intermittent porphyria Donor information: At sampling donor was not affected with acute intermittent porphyria but at significant risk for disease., Characteristics: Has decreased HMBS activity., Population: Caucasian. PMID:1165472 Finite cell line Female GM-933 CLO:CLO_0029570,
Coriell:GM00933,
Wikidata:Q54836542
CVCL_4J15 2026-08-15 04:28:54 0
GM00939
 
Resource Report
Resource Website
RRID:CVCL_W223 Homo sapiens (Human) Acute intermittent porphyria Population: Caucasian. PMID:25326100 Finite cell line Female GM-939 CLO:CLO_0029546,
Coriell:GM00939,
GEO:GSM1266956,
Wikidata:Q54836548
CVCL_W223 2026-08-15 04:28:54 0
GM00958
 
Resource Report
Resource Website
Coriell Cat# GM00958, RRID:CVCL_9W79 Homo sapiens (Human) Mucopolysaccharidosis type IVA Population: Caucasian. PMID:8910459 Finite cell line Male GM-958 Coriell GM00958 CLO:CLO_0029522,
Coriell:GM00958,
Wikidata:Q54836563
CVCL_9W79 2026-08-15 04:28:55 0
GM00917
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_JC77 Homo sapiens (Human) Progeria Finite cell line Female GM-917 Coriell:GM00917,
Wikidata:Q54836533
CVCL_JC77 2026-08-15 04:28:54 0
GM00963
 
Resource Report
Resource Website
Coriell Cat# GM00963, RRID:CVCL_1V22 Homo sapiens (Human) Hurler-Scheie syndrome Population: Caucasian. PMID:30052969 Finite cell line Male GM-963 Coriell GM00963 CLO:CLO_0029506,
Coriell:GM00963,
Wikidata:Q54836567
CVCL_1V22 2026-08-15 04:28:55 0

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