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95,747 Results - per page

Show More Columns | Download Top 1000 Results

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
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 2026-07-25 04:32:10 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 2026-07-25 04:32:11 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 2026-07-25 04:32:09 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 2026-07-25 04:32:09 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 2026-07-25 04:32:09 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 2026-07-25 04:32:09 0
GM00922
 
Resource Report
Resource Website
Coriell Cat# GM17209, RRID:CVCL_7307 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:7313555
PMID:16260726
PMID:20889555
PMID:29959025
Transformed cell line Female GM-922, GM 0922, GM00922A, GM17209 Coriell GM17209 CLO:CLO_0013875,
CLO:CLO_0029565,
Coriell:GM00922,
Coriell:GM17209,
GEO:GSM569629,
GEO:GSM596273,
GEO:GSM596634,
GEO:GSM924811,
Wikidata:Q54836536
CVCL_7307 2026-07-25 04:32:09 0
GM00954
 
Resource Report
Resource Website
RRID:CVCL_V029 Homo sapiens (Human) Argininemia Finite cell line Female GM0954, GM-954 CLO:CLO_0029520,
Coriell:GM00954,
Wikidata:Q54836560
CVCL_V029 2026-07-25 04:32:10 0
GM00935
 
Resource Report
Resource Website
Coriell Cat# GM00935, RRID:CVCL_V785 Homo sapiens (Human) Population: Caucasian. PMID:826372
PMID:21418647
PMID:24555846
PMID:25326100
Finite cell line Female GM-935 Coriell GM00935 CLO:CLO_0029539,
Coriell:GM00935,
GEO:GSM651164,
GEO:GSM651165,
GEO:GSM1257720,
GEO:GSM1266910,
GEO:GSM1267004,
GEO:GSM1288422,
Wikidata:Q54836544
CVCL_V785 2026-07-25 04:32:10 0
GM00962
 
Resource Report
Resource Website
Coriell Cat# GM00962, RRID:CVCL_W225 Homo sapiens (Human) Hereditary coproporphyria Population: Caucasian. Finite cell line Female GM-962 Coriell GM00962 CLO:CLO_0029499,
Coriell:GM00962,
Wikidata:Q54836566
CVCL_W225 2026-07-25 04:32:10 0
GM00935
 
Resource Report
Resource Website
RRID:CVCL_V785 Homo sapiens (Human) Population: Caucasian. PMID:826372
PMID:21418647
PMID:24555846
PMID:25326100
Finite cell line Female GM-935 CLO:CLO_0029539,
Coriell:GM00935,
GEO:GSM651164,
GEO:GSM651165,
GEO:GSM1257720,
GEO:GSM1266910,
GEO:GSM1267004,
GEO:GSM1288422,
Wikidata:Q54836544
CVCL_V785 2026-07-25 04:32:09 0
GM01108
 
Resource Report
Resource Website
RRID:CVCL_1V04 Homo sapiens (Human) Population: Caucasian. Finite cell line Female GM-1108, GM01108A CLO:CLO_0030189,
BioSample:SAMN00803632,
Coriell:GM01108,
Wikidata:Q54836647
CVCL_1V04 2026-07-25 04:32:13 0
GM01095
 
Resource Report
Resource Website
Coriell Cat# GM01095, RRID:CVCL_0L99 Homo sapiens (Human) Population: Caucasian. PMID:24555846
PMID:25326100
Finite cell line Female GM-1095 Coriell GM01095 CLO:CLO_0030181,
BioSample:SAMN00803622,
Coriell:GM01095,
GEO:GSM1257681,
GEO:GSM1266958,
GEO:GSM1267041,
GEO:GSM1288425,
Wikidata:Q54836642
CVCL_0L99 2026-07-25 04:32:13 0
GM01029
 
Resource Report
Resource Website
RRID:CVCL_V795 Homo sapiens (Human) Population: Caucasian. Transformed cell line Female GM-1029, GM01029A CLO:CLO_0030377,
BioSample:SAMN00803579,
Coriell:GM01029,
Wikidata:Q54836613
CVCL_V795 2026-07-25 04:32:11 0
GM01000
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM01000, RRID:CVCL_CX07 Homo sapiens (Human) Maple syrup urine disease Finite cell line Female GM-1000 Coriell GM01000 Coriell:GM01000,
Wikidata:Q54836595
CVCL_CX07 2026-07-25 04:32:11 0
GM01007
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_JB65 Homo sapiens (Human) Refsum disease Finite cell line Female GM-1007 Coriell:GM01007,
Wikidata:Q54836596
CVCL_JB65 2026-07-25 04:32:11 0
GM01017
 
Resource Report
Resource Website
Coriell Cat# GM01017, RRID:CVCL_6B41 Homo sapiens (Human) Metachromatic leukodystrophy Transformed cell line Female GM-1017 Coriell GM01017 CLO:CLO_0029493,
BioSample:SAMN00803561,
Coriell:GM01017,
Wikidata:Q54836603
CVCL_6B41 2026-07-25 04:32:11 0
GM01022
 
Resource Report
Resource Website
Coriell Cat# GM01022, RRID:CVCL_V790 Homo sapiens (Human) Maroteaux-Lamy syndrome Population: Caucasian. PMID:806052
PMID:826372
Transformed cell line Female GM-1022, GM01022A Coriell GM01022 CLO:CLO_0029494,
BioSample:SAMN00803567,
Coriell:GM01022,
Wikidata:Q54836607
CVCL_V790 2026-07-25 04:32:11 0
GM01070
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM01070, RRID:CVCL_CX38 Homo sapiens (Human) Finite cell line Female GM-1070 Coriell GM01070 Coriell:GM01070,
Wikidata:Q54836631
CVCL_CX38 2026-07-25 04:32:12 0
GM01007
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM01007, RRID:CVCL_JB65 Homo sapiens (Human) Refsum disease Finite cell line Female GM-1007 Coriell GM01007 Coriell:GM01007,
Wikidata:Q54836596
CVCL_JB65 2026-07-25 04:32:11 0

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