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10,882 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
FC3.Tg
 
Resource Report
Resource Website
1+ mentions
Discontinued
IZSLER Cat# BS CL 44, RRID:CVCL_4191 Felis catus (Cat) Virology: Not susceptible to infection by bovine viral diarrhea virus (BVDV) (PubMed=7989438)., Senescence: Can undergo 50 PDL., Part of: Naval Biosciences Laboratory (NBL) collection (transferred to ATCC in 1982). PMID:6160900
PMID:7989438
PMID:15705889
Finite cell line Female Fc3Tg, Fc 3Tg, Fc 3 Tg IZSLER BS CL 44 CLO:CLO_0003015,
CLO:CLO_0003039,
CLDB:cl1215,
CLDB:cl1216,
ATCC:CCL-176,
ATCC:CRL-6570,
ECACC:90073002,
IZSLER:BS CL 44,
Wikidata:Q54833351
CVCL_4191 2026-08-15 04:28:03 1
FC3.Tg
 
Resource Report
Resource Website
1+ mentions
Discontinued
ECACC Cat# 90073002, RRID:CVCL_4191 Felis catus (Cat) Virology: Not susceptible to infection by bovine viral diarrhea virus (BVDV) (PubMed=7989438)., Senescence: Can undergo 50 PDL., Part of: Naval Biosciences Laboratory (NBL) collection (transferred to ATCC in 1982). PMID:6160900
PMID:7989438
PMID:15705889
Finite cell line Female Fc3Tg, Fc 3Tg, Fc 3 Tg ECACC 90073002 CLO:CLO_0003015,
CLO:CLO_0003039,
CLDB:cl1215,
CLDB:cl1216,
ATCC:CCL-176,
ATCC:CRL-6570,
ECACC:90073002,
IZSLER:BS CL 44,
Wikidata:Q54833351
CVCL_4191 2026-08-15 04:28:04 1
FDCP-Mix cl.A4
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_2040 Mus musculus (Mouse) Characteristics: IL3 dependent. PMID:1334022
PMID:3091439
Factor-dependent cell line FDCP-mix, FDCPmix, FDCP MIX A4, FDPC-mix A4, FDCP mix A4, FDCPmixA4 BTO:BTO_0000446,
CLO:CLO_0003074,
DSMZ:ACC-401,
DSMZCellDive:ACC-401,
Lonza:721,
Wikidata:Q54833451
CVCL_2040 2026-08-15 04:28:06 2
GM12593
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_7524 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel. PMID:16260726 Transformed cell line Female GM17238 CLO:CLO_0014332,
CLO:CLO_0018080,
Coriell:GM12593,
Coriell:GM17238,
GEO:GSM569565,
GEO:GSM596302,
GEO:GSM596662,
GEO:GSM924840,
Wikidata:Q54845892
CVCL_7524 2026-08-15 04:31:44 1
GM12593
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM17238, RRID:CVCL_7524 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel. PMID:16260726 Transformed cell line Female GM17238 Coriell GM17238 CLO:CLO_0014332,
CLO:CLO_0018080,
Coriell:GM12593,
Coriell:GM17238,
GEO:GSM569565,
GEO:GSM596302,
GEO:GSM596662,
GEO:GSM924840,
Wikidata:Q54845892
CVCL_7524 2026-08-15 04:31:44 1
GM12891
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_9630 Homo sapiens (Human) Population: Caucasian; Utah residents with ancestry from Northern and Western Europe., Part of: International Genome Sample Resource (1000 genomes project) cell lines., Part of: ENCODE project common cell types; tier 3., Part of: CEPH/Utah pedigree cell line collection. PMID:17122850
PMID:19043577
PMID:19797678
PMID:20398888
PMID:20856902
PMID:21397061
PMID:23325432
PMID:23676674
PMID:27792722
Transformed cell line Male CLO:CLO_0022859,
EFO:EFO_0002785,
BioSample:SAMN00801912,
Coriell:GM12891,
ENCODE:ENCBS041WYJ,
ENCODE:ENCBS270GPL,
ENCODE:ENCBS377ENC,
ENCODE:ENCBS384ENC,
ENCODE:ENCBS388ENC,
ENCODE:ENCBS430ENC,
ENCODE:ENCBS507TOT,
ENCODE:ENCBS606OMD,
ENCODE:ENCBS653UMX,
GEO:GSM112569,
GEO:GSM112872,
GEO:GSM188848,
GEO:GSM273370,
GEO:GSM273371,
GEO:GSM291699,
GEO:GSM315038,
GEO:GSM421104,
GEO:GSM424360,
GEO:GSM486855,
GEO:GSM486856,
GEO:GSM489280,
GEO:GSM489281,
GEO:GSM489293,
GEO:GSM489294,
GEO:GSM649300,
GEO:GSM649855,
GEO:GSM659960,
GEO:GSM660162,
GEO:GSM660369,
GEO:GSM816656,
GEO:GSM905905,
GEO:GSM906000,
GEO:GSM906095,
GEO:GSM957396,
IGSR:NA12891,
Wikidata:Q54846191
CVCL_9630 2026-08-15 04:31:50 1
GM13267
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM13267, RRID:CVCL_4F67 Homo sapiens (Human) Zellweger syndrome Population: Caucasian. Finite cell line Male Coriell GM13267 CLO:CLO_0013123,
BioSample:SAMN00802232,
Coriell:GM13267,
Wikidata:Q54846409
CVCL_4F67 2026-08-15 04:31:54 1
GM13411
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_8A61 Homo sapiens (Human) Leigh disease Population: Chinese. PMID:8042671
PMID:30471880
Finite cell line Male CLO:CLO_0012853,
BioSample:SAMN00802348,
Coriell:GM13411,
Wikidata:Q54846509
CVCL_8A61 2026-08-15 04:31:55 1
GM01202
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_V799 Homo sapiens (Human) Karyotypic information: 49,XXXXY (Coriell=GM01202)., Population: Caucasian. PMID:62390
PMID:6661932
PMID:23665875
Transformed cell line Male GM-1202, GM 1202, GM1202, GM1202A, GM01202C CLO:CLO_0030260,
BioSample:SAMN00803702,
Coriell:GM01202,
Wikidata:Q54836697
CVCL_V799 2026-08-15 04:28:57 1
GM01202
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM01202, RRID:CVCL_V799 Homo sapiens (Human) Karyotypic information: 49,XXXXY (Coriell=GM01202)., Population: Caucasian. PMID:62390
PMID:6661932
PMID:23665875
Transformed cell line Male GM-1202, GM 1202, GM1202, GM1202A, GM01202C Coriell GM01202 CLO:CLO_0030260,
BioSample:SAMN00803702,
Coriell:GM01202,
Wikidata:Q54836697
CVCL_V799 2026-08-15 04:28:57 1
GM01582
 
Resource Report
Resource Website
1+ mentions
Discontinued
Possibly Discontinued
Coriell Cat# GM00240, RRID:CVCL_7323 Homo sapiens (Human) Population: Caucasian. PMID:12665480
PMID:30567591
Finite cell line Female GM1582, GM-1582, GM01582A, GM1582A, GM00240, GM0240, GM-240 Coriell GM00240 CLO:CLO_0031462,
BioSample:SAMN00806939,
Coriell:GM00240,
Coriell:GM01582,
GEO:GSM3124639,
Wikidata:Q54836927
CVCL_7323 2026-08-15 04:29:02 1
GM01582
 
Resource Report
Resource Website
1+ mentions
Possibly Discontinued
Discontinued
Coriell Cat# GM01582, RRID:CVCL_7323 Homo sapiens (Human) Population: Caucasian. PMID:12665480
PMID:30567591
Finite cell line Female GM1582, GM-1582, GM01582A, GM1582A, GM00240, GM0240, GM-240 Coriell GM01582 CLO:CLO_0031462,
BioSample:SAMN00806939,
Coriell:GM00240,
Coriell:GM01582,
GEO:GSM3124639,
Wikidata:Q54836927
CVCL_7323 2026-08-15 04:29:02 1
GM01835
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_D873 Homo sapiens (Human) Schizophrenia Population: Jewish and Caucasian; Scandinavian. PMID:7847674
PMID:21490598
Finite cell line Female GM-1835 CLO:CLO_0031421,
BioSample:SAMN00807213,
Coriell:GM01835,
Wikidata:Q54837112
CVCL_D873 2026-08-15 04:29:07 1
GM01981
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_F589 Homo sapiens (Human) Menkes disease Population: Caucasian. PMID:7438975
PMID:7977350
Finite cell line Male GM-1981, GM1981 CLO:CLO_0032339,
BioSample:SAMN00807346,
Coriell:GM01981,
Wikidata:Q54837212
CVCL_F589 2026-08-15 04:29:09 1
GM02079
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_1H41 Homo sapiens (Human) Huntington's disease Population: Caucasian. PMID:6220707 Finite cell line Female GM-2079, GM 2079, GM02079A CLO:CLO_0032509,
BioSample:SAMN00807468,
Coriell:GM02079,
Wikidata:Q54837291
CVCL_1H41 2026-08-15 04:29:11 1
GM02075
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_CW70 Homo sapiens (Human) Chediak-Higashi syndrome Population: Caucasian. PMID:8896560
PMID:36259166
Finite cell line Female GM-2075, GM02075A CLO:CLO_0032513,
BioSample:SAMN00807462,
Coriell:GM02075,
Wikidata:Q54837288
CVCL_CW70 2026-08-15 04:29:11 1
GM02036
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM02036, RRID:CVCL_7348 Homo sapiens (Human) Population: Caucasian. PMID:17668376
PMID:28284873
PMID:29125828
PMID:32291635
PMID:33038742
PMID:35850241
Finite cell line Female GM2036, GM 02036, GM-02036, GM-2036, GM02036A, GMO2036A, C2036 Coriell GM02036 CLO:CLO_0032573,
BioSample:SAMN00807414,
BioSample:SAMN03253067,
Coriell:GM02036,
GEO:GSM2794402,
Wikidata:Q54837255
CVCL_7348 2026-08-15 04:29:10 4
GM02036
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_7348 Homo sapiens (Human) Population: Caucasian. PMID:17668376
PMID:28284873
PMID:29125828
PMID:32291635
PMID:33038742
PMID:35850241
Finite cell line Female GM2036, GM 02036, GM-02036, GM-2036, GM02036A, GMO2036A, C2036 CLO:CLO_0032573,
BioSample:SAMN00807414,
BioSample:SAMN03253067,
Coriell:GM02036,
GEO:GSM2794402,
Wikidata:Q54837255
CVCL_7348 2026-08-15 04:29:10 4
GM09497
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_AY35 Homo sapiens (Human) Fragile X syndrome Karyotypic information: 46,XY,t(1;3)(3pter->3p22::1p32->1qter;1pter->1p32::3p22->3qter) [3]; 46,XY,t(3;12)(3pter->3q12::12q24.1->12qter;12pter->12q24.1:;3q12->3qter) [3]; 46,XY [13] (Coriell=GM09497)., Population: Caucasian. Finite cell line Male CLO:CLO_0011480,
Coriell:GM09497,
Wikidata:Q54843801
CVCL_AY35 2026-08-15 04:30:47 1
GM09497
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM09497, RRID:CVCL_AY35 Homo sapiens (Human) Fragile X syndrome Karyotypic information: 46,XY,t(1;3)(3pter->3p22::1p32->1qter;1pter->1p32::3p22->3qter) [3]; 46,XY,t(3;12)(3pter->3q12::12q24.1->12qter;12pter->12q24.1:;3q12->3qter) [3]; 46,XY [13] (Coriell=GM09497)., Population: Caucasian. Finite cell line Male Coriell GM09497 CLO:CLO_0011480,
Coriell:GM09497,
Wikidata:Q54843801
CVCL_AY35 2026-08-15 04:30:47 1

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