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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
GM08680
 
Resource Report
Resource Website
RRID:CVCL_7489 Homo sapiens (Human) Population: Caucasian. Finite cell line Male GM8680 CLO:CLO_0010615,
Coriell:GM08680,
Wikidata:Q54843244
CVCL_7489 2026-07-25 04:33:56 0
GM08776
 
Resource Report
Resource Website
RRID:CVCL_DF30 Homo sapiens (Human) Retinoblastoma Transformed cell line Female CLO:CLO_0010487,
BioSample:SAMN00798192,
Coriell:GM08776,
Wikidata:Q54843292
CVCL_DF30 2026-07-25 04:33:55 0
GM08779
 
Resource Report
Resource Website
RRID:CVCL_N088 Homo sapiens (Human) Population: African American., Part of: Human variation panel. Transformed cell line Female GM08779A, GM17166 CLO:CLO_0010485,
CLO:CLO_0013990,
BioSample:SAMN00798196,
Coriell:GM08779,
Coriell:GM17166,
GEO:GSM569693,
GEO:GSM596231,
GEO:GSM597065,
GEO:GSM924676,
IPD-IMGT/HLA:20687,
Wikidata:Q54843294
CVCL_N088 2026-07-25 04:33:55 0
GM08768
 
Resource Report
Resource Website
RRID:CVCL_4F60 Homo sapiens (Human) Medium-chain acyl-CoA dehydrogenase deficiency Population: Caucasian. Finite cell line Female CLO:CLO_0010497,
BioSample:SAMN00798176,
Coriell:GM08768,
Wikidata:Q54843283
CVCL_4F60 2026-07-25 04:33:55 0
GM08698
 
Resource Report
Resource Website
Coriell Cat# GM08698, RRID:CVCL_EJ57 Homo sapiens (Human) Transformed cell line Male GM08698A Coriell GM08698 CLO:CLO_0010421,
Coriell:GM08698,
Wikidata:Q54843251
CVCL_EJ57 2026-07-25 04:33:54 0
GM08773
 
Resource Report
Resource Website
Coriell Cat# GM08773, RRID:CVCL_2T58 Homo sapiens (Human) Population: Caucasian. PMID:23665875 Transformed cell line Female Coriell GM08773 CLO:CLO_0010479,
BioSample:SAMN00798186,
Coriell:GM08773,
Wikidata:Q54843289
CVCL_2T58 2026-07-25 04:33:55 0
GM08788
 
Resource Report
Resource Website
RRID:CVCL_EH04 Homo sapiens (Human) Congenital adrenal gland hypoplasia Population: African American. Finite cell line Male CLO:CLO_0010467,
BioSample:SAMN00798206,
Coriell:GM08788,
Wikidata:Q54843299
CVCL_EH04 2026-07-25 04:33:55 0
GM08762
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_5N87 Homo sapiens (Human) Finite cell line Male GM08762A Coriell:GM08762,
Wikidata:Q54843269
CVCL_5N87 2026-07-25 04:33:57 0
GM08739
 
Resource Report
Resource Website
Coriell Cat# GM08739, RRID:CVCL_AW89 Homo sapiens (Human) Autosomal dominant polycystic kidney disease Transformed cell line Female Coriell GM08739 CLO:CLO_0010500,
BioSample:SAMN00798150,
Coriell:GM08739,
Wikidata:Q54843256
CVCL_AW89 2026-07-25 04:33:54 0
GM08794
 
Resource Report
Resource Website
Coriell Cat# GM08794, RRID:CVCL_DA27 Homo sapiens (Human) Neuronal ceroid lipofuscinosis type 3 Transformed cell line Male Coriell GM08794 CLO:CLO_0010469,
BioSample:SAMN00798208,
Coriell:GM08794,
Wikidata:Q54843300
CVCL_DA27 2026-07-25 04:33:55 0
GM08714
 
Resource Report
Resource Website
RRID:CVCL_E128 Homo sapiens (Human) Immunodeficiency-centromeric instability-facial anomalies syndrome 1 Population: Caucasian., Part of: ENCODE project common cell types; tier 3. Transformed cell line Female CLO:CLO_0010422,
EFO:EFO_0005333,
BioSample:SAMN00798144,
Coriell:GM08714,
ENCODE:ENCBS182AAA,
ENCODE:ENCBS477AAA,
ENCODE:ENCBS478AAA,
Wikidata:Q54843253
CVCL_E128 2026-07-25 04:33:54 0
GM08785
 
Resource Report
Resource Website
RRID:CVCL_5N90 Homo sapiens (Human) WAGR syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0010483,
BioSample:SAMN00798200,
Coriell:GM08785,
Wikidata:Q54843296
CVCL_5N90 2026-07-25 04:33:57 0
GM08662
 
Resource Report
Resource Website
RRID:CVCL_2Y91 Homo sapiens (Human) Population: Caucasian; Amish. Transformed cell line Male CLO:CLO_0010604,
BioSample:SAMN00798112,
Coriell:GM08662,
Wikidata:Q54843237
CVCL_2Y91 2026-07-25 04:33:54 0
GM08668
 
Resource Report
Resource Website
RRID:CVCL_F152 Homo sapiens (Human) Porphyria cutanea tarda Transformed cell line Male CLO:CLO_0010614,
BioSample:SAMN00798120,
Coriell:GM08668,
Wikidata:Q54843241
CVCL_F152 2026-07-25 04:33:54 0
GM08799
 
Resource Report
Resource Website
RRID:CVCL_AW92 Homo sapiens (Human) Transformed cell line Male CLO:CLO_0010468,
BioSample:SAMN00798210,
Coriell:GM08799,
Wikidata:Q54843301
CVCL_AW92 2026-07-25 04:33:57 0
GM08729
 
Resource Report
Resource Website
Coriell Cat# GM08729, RRID:CVCL_N086 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:20889555
PMID:29959025
Transformed cell line Male GM17282 Coriell GM08729 CLO:CLO_0010503,
CLO:CLO_0013094,
BioSample:SAMN00798148,
Coriell:GM08729,
Coriell:GM17282,
GEO:GSM569735,
GEO:GSM596346,
GEO:GSM596765,
GEO:GSM924884,
Wikidata:Q54843255
CVCL_N086 2026-07-25 04:33:54 0
GM08801
 
Resource Report
Resource Website
Coriell Cat# GM08801, RRID:CVCL_AW94 Homo sapiens (Human) Autosomal dominant polycystic kidney disease Transformed cell line Female Coriell GM08801 CLO:CLO_0010474,
BioSample:SAMN00798214,
Coriell:GM08801,
Wikidata:Q54843303
CVCL_AW94 2026-07-25 04:33:55 0
GM08813
 
Resource Report
Resource Website
Coriell Cat# GM08813, RRID:CVCL_4H53 Homo sapiens (Human) Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection. Transformed cell line Male Coriell GM08813 CLO:CLO_0010472,
Coriell:GM08813,
Wikidata:Q54843309
CVCL_4H53 2026-07-25 04:33:55 0
GM08869
 
Resource Report
Resource Website
RRID:CVCL_4I99 Homo sapiens (Human) Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection. Transformed cell line Male GM08869A CLO:CLO_0010433,
Coriell:GM08869,
Wikidata:Q54843352
CVCL_4I99 2026-07-25 04:33:59 0
GM08865
 
Resource Report
Resource Website
RRID:CVCL_4H70 Homo sapiens (Human) Depression Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection. Transformed cell line Female CLO:CLO_0010436,
Coriell:GM08865,
Wikidata:Q54843348
CVCL_4H70 2026-07-25 04:33:57 0

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