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  • Organism:homo sapiens (human) (facet)

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185,176 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
GM50182
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_5T55 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell:GM50182,
Wikidata:Q54854251
CVCL_5T55 2026-07-25 04:38:16 0
GM50194
 
Resource Report
Resource Website
RRID:CVCL_0G72 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Male JL453 CLO:CLO_0014993,
Coriell:GM50194,
Wikidata:Q54854257
CVCL_0G72 2026-07-25 04:38:16 0
GMP-iPSCs-2
 
Resource Report
Resource Website
RRID:CVCL_VD85 Homo sapiens (Human) From: Institute of Zoology, Chinese Academy of Sciences; Beijing; China. PMID:26564165 Induced pluripotent stem cell Male Wikidata:Q54854301 CVCL_VD85 2026-07-25 04:38:17 0
GM5756-T
 
Resource Report
Resource Website
1+ mentions
RRID:CVCL_VQ75 Homo sapiens (Human) Caution: Incorrectly stated in Lonza=1146 to originate from a 18 year old male patient with ataxia telangiectasia., Population: Caucasian. PMID:9922452 Transformed cell line Male GM5756T, 5756T Lonza:1146,
Wikidata:Q93933917
cvcl_7436 CVCL_VQ75 2026-07-25 04:38:16 1
GM50291
 
Resource Report
Resource Website
RRID:CVCL_2U68 Homo sapiens (Human) Transformed cell line Male JL612 CLO:CLO_0014977,
Coriell:GM50291,
Wikidata:Q54854265
CVCL_2U68 2026-07-25 04:38:16 0
GM50346
 
Resource Report
Resource Website
Coriell Cat# GM50346, RRID:CVCL_H994 Homo sapiens (Human) Cerebrooculofacioskeletal syndrome Finite cell line Male Coriell GM50346 CLO:CLO_0012522,
Coriell:GM50346,
Wikidata:Q54854280
CVCL_H994 2026-07-25 04:38:17 0
GM50205
 
Resource Report
Resource Website
RRID:CVCL_5T58 Homo sapiens (Human) Cri du chat syndrome PMID:23665875 Transformed cell line Female BioSample:SAMN00806847,
Coriell:GM50205,
Wikidata:Q54854259
CVCL_5T58 2026-07-25 04:38:16 0
GM50292
 
Resource Report
Resource Website
Coriell Cat# GM50292, RRID:CVCL_5L37 Homo sapiens (Human) Deletion 18p syndrome Transformed cell line Male JL614 Coriell GM50292 CLO:CLO_0014978,
Coriell:GM50292,
Wikidata:Q54854266
CVCL_5L37 2026-07-25 04:38:16 0
GM50292
 
Resource Report
Resource Website
RRID:CVCL_5L37 Homo sapiens (Human) Deletion 18p syndrome Transformed cell line Male JL614 CLO:CLO_0014978,
Coriell:GM50292,
Wikidata:Q54854266
CVCL_5L37 2026-07-25 04:38:16 0
GN00087
 
Resource Report
Resource Website
RRID:CVCL_JC56 Homo sapiens (Human) Part of: International Histocompatibility Workshop cell lines. PMID:9162096 Transformed cell line Sex unspecified GN087 Wikidata:Q54871594 CVCL_JC56 2026-07-25 04:38:17 0
GN00001
 
Resource Report
Resource Website
RRID:CVCL_JC45 Homo sapiens (Human) Part of: International Histocompatibility Workshop cell lines. PMID:9162096 Transformed cell line Sex unspecified GN001 Wikidata:Q54854315 CVCL_JC45 2026-07-25 04:38:17 0
GOL1
 
Resource Report
Resource Website
RRID:CVCL_YE05 Homo sapiens (Human) Infectious mononucleosis PMID:4330463
PMID:4333769
PMID:5287057
Transformed cell line Female Wikidata:Q93934288 CVCL_YE05 2026-07-25 04:38:18 0
GOS-2
 
Resource Report
Resource Website
RRID:CVCL_A3BE Homo sapiens (Human) Glioblastoma PMID:9760066 Cancer cell line Male GOS 2, GOS2 Wikidata:Q105507460 CVCL_A3BE 2026-07-25 04:38:18 0
GN00105
 
Resource Report
Resource Website
RRID:CVCL_JD64 Homo sapiens (Human) Part of: International Histocompatibility Workshop cell lines. Transformed cell line Male IPD-IMGT/HLA:10619,
Wikidata:Q54871597
CVCL_JD64 2026-07-25 04:38:18 0
GN00151
 
Resource Report
Resource Website
RRID:CVCL_JC59 Homo sapiens (Human) Part of: International Histocompatibility Workshop cell lines. PMID:9162096 Transformed cell line Male IPD-IMGT/HLA:10629,
Wikidata:Q54871598
CVCL_JC59 2026-07-25 04:38:18 0
GN00080
 
Resource Report
Resource Website
RRID:CVCL_JC55 Homo sapiens (Human) Part of: International Histocompatibility Workshop cell lines. PMID:9162096 Transformed cell line Sex unspecified GN080 Wikidata:Q54871593 CVCL_JC55 2026-07-25 04:38:17 0
GN00350
 
Resource Report
Resource Website
RRID:CVCL_6G67 Homo sapiens (Human) Part of: International Histocompatibility Workshop cell lines. PMID:11782282 Transformed cell line Male IPD-IMGT/HLA:12148,
Wikidata:Q54871600
CVCL_6G67 2026-07-25 04:38:18 0
Go Je
 
Resource Report
Resource Website
RRID:CVCL_3314 Homo sapiens (Human) Ehlers-Danlos syndrome Finite cell line Female CLO:CLO_0003548,
ATCC:CRL-1381,
BioSample:SAMN03471360,
Wikidata:Q54871610
CVCL_3314 2026-07-25 04:38:18 0
GN00049
 
Resource Report
Resource Website
RRID:CVCL_JC51 Homo sapiens (Human) Part of: International Histocompatibility Workshop cell lines. PMID:9162096 Transformed cell line Sex unspecified GN049 Wikidata:Q54871589 CVCL_JC51 2026-07-25 04:38:17 0
GNM
 
Resource Report
Resource Website
1+ mentions
Contaminated
CCTCC Cat# GDC0185, RRID:CVCL_WL58 Homo sapiens (Human) Human papillomavirus-related endocervical adenocarcinoma Population: African American., Problematic cell line: Contaminated. Shown to be a HeLa derivative (PubMed=26116706). Originally thought to originate from a patient with a gingival carcinoma neck metastasis.. PMID:10779629
PMID:15929393
PMID:26116706
Cancer cell line Female Gingival carcinoma Neck Metastasis CCTCC GDC0185 CCTCC:GDC0185,
Wikidata:Q93934197
cvcl_0030 CVCL_WL58 2026-07-25 04:38:18 2

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