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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
GM2
 
Resource Report
Resource Website
RRID:CVCL_Z795 Drosophila melanogaster (Fruit fly) Part of: modENCODE project cell lines., Group: Insect cell line. PMID:811480
PMID:4626439
PMID:21177962
PMID:24434506
PMID:24985917
PMID:26772746
Spontaneously immortalized cell line Male CLO:CLO_0003535,
EFO:EFO_0005747,
CLDB:cl1502,
DGRC:39,
ENCODE:ENCBS405IST,
FlyBase_Cell_line:FBtc0000039,
Wikidata:Q54850771
CVCL_Z795 2026-09-05 10:58:46 0
GM20089 iPSC
 
Resource Report
Resource Website
RRID:CVCL_UD93 Homo sapiens (Human) Glycogen storage disease type II PMID:25488666 Induced pluripotent stem cell Female Pompe 1 Wikidata:Q93864397 cvcl_1l16 CVCL_UD93 2026-09-05 10:58:46 0
GM20182
 
Resource Report
Resource Website
RRID:CVCL_GS90 Homo sapiens (Human) Deafness, autosomal recessive 28 Transformed cell line Male CLO:CLO_0027945,
Coriell:GM20182,
Wikidata:Q54850827
CVCL_GS90 2026-09-05 10:58:47 0
GM20073
 
Resource Report
Resource Website
RRID:CVCL_1M98 Homo sapiens (Human) Leukoencephalopathy with vanishing white matter Transformed cell line Female CLO:CLO_0028360,
Coriell:GM20073,
Wikidata:Q54850792
CVCL_1M98 2026-09-05 10:58:46 0
GM20033
 
Resource Report
Resource Website
RRID:CVCL_9Y51 Homo sapiens (Human) Donohue syndrome Population: Turkish. Finite cell line Male CLO:CLO_0028356,
Coriell:GM20033,
Wikidata:Q54850788
CVCL_9Y51 2026-09-05 10:58:46 0
GM20192
 
Resource Report
Resource Website
RRID:CVCL_DB97 Homo sapiens (Human) Population: Pakistani. PMID:17186462 Transformed cell line Male CLO:CLO_0027944,
Coriell:GM20192,
Wikidata:Q54850834
CVCL_DB97 2026-09-05 10:58:47 0
GM20122
 
Resource Report
Resource Website
RRID:CVCL_1L20 Homo sapiens (Human) Glycogen storage disease type II Population: African American. PMID:33375166 Finite cell line Male CLO:CLO_0027717,
Coriell:GM20122,
Wikidata:Q54850805
CVCL_1L20 2026-09-05 10:58:47 0
GM20218
 
Resource Report
Resource Website
RRID:CVCL_DA88 Homo sapiens (Human) Langer mesomelic dysplasia Population: Caucasian. Transformed cell line Female CLO:CLO_0027965,
Coriell:GM20218,
Wikidata:Q54850850
CVCL_DA88 2026-09-05 10:58:47 0
GM20214
 
Resource Report
Resource Website
RRID:CVCL_DA84 Homo sapiens (Human) Langer mesomelic dysplasia Population: Caucasian. Transformed cell line Female CLO:CLO_0028000,
Coriell:GM20214,
Wikidata:Q54850846
CVCL_DA84 2026-09-05 10:58:47 0
GM19983
 
Resource Report
Resource Website
RRID:CVCL_1A89 Homo sapiens (Human) Population: African ancestry in Southwest USA (ASW)., Part of: International Genome Sample Resource (1000 genomes project) cell lines. PMID:21397061 Transformed cell line Female CLO:CLO_0028361,
Coriell:GM19983,
GEO:GSM650214,
IGSR:NA19983,
Wikidata:Q54850765
CVCL_1A89 2026-09-05 10:58:46 0
GM20213
 
Resource Report
Resource Website
RRID:CVCL_DA83 Homo sapiens (Human) Langer mesomelic dysplasia Population: Caucasian. Transformed cell line Male CLO:CLO_0027999,
Coriell:GM20213,
Wikidata:Q54850845
CVCL_DA83 2026-09-05 10:58:47 0
GM20127
 
Resource Report
Resource Website
Coriell Cat# GM20127, RRID:CVCL_N883 Homo sapiens (Human) Population: African ancestry in Southwest USA (ASW)., Part of: International Genome Sample Resource (1000 genomes project) cell lines. PMID:21397061 Transformed cell line Female Coriell GM20127 CLO:CLO_0027706,
Coriell:GM20127,
GEO:GSM650218,
GEO:GSM1720352,
IGSR:NA20127,
Wikidata:Q54850810
CVCL_N883 2026-09-05 10:58:47 0
GM20175
 
Resource Report
Resource Website
RRID:CVCL_HQ12 Homo sapiens (Human) Deafness, autosomal recessive 39 Transformed cell line Male Coriell:GM20175,
Wikidata:Q54850826
CVCL_HQ12 2026-09-05 10:58:47 0
GM20074
 
Resource Report
Resource Website
RRID:CVCL_1M99 Homo sapiens (Human) Leukoencephalopathy with vanishing white matter Transformed cell line Male CLO:CLO_0028311,
Coriell:GM20074,
Wikidata:Q54850793
CVCL_1M99 2026-09-05 10:58:46 0
GM20197
 
Resource Report
Resource Website
RRID:CVCL_GS95 Homo sapiens (Human) Deafness, autosomal recessive 49 Population: Pakistani. PMID:17186462 Transformed cell line Female CLO:CLO_0027985,
Coriell:GM20197,
Wikidata:Q54850837
CVCL_GS95 2026-09-05 10:58:47 0
GM20295
 
Resource Report
Resource Website
RRID:CVCL_1B00 Homo sapiens (Human) Population: African ancestry in Southwest USA (ASW)., Part of: International Genome Sample Resource (1000 genomes project) cell lines. PMID:21397061 Transformed cell line Male CLO:CLO_0027857,
Coriell:GM20295,
GEO:GSM650235,
IGSR:NA20295,
Wikidata:Q54850901
CVCL_1B00 2026-09-05 10:58:48 0
GM20302
 
Resource Report
Resource Website
RRID:CVCL_1B04 Homo sapiens (Human) Population: African ancestry in Southwest USA (ASW)., Part of: International Genome Sample Resource (1000 genomes project) cell lines. PMID:21397061 Transformed cell line Male CLO:CLO_0027884,
Coriell:GM20302,
GEO:GSM650242,
IGSR:NA20302,
Wikidata:Q54850908
CVCL_1B04 2026-09-05 10:58:48 0
GM20294
 
Resource Report
Resource Website
RRID:CVCL_N891 Homo sapiens (Human) Population: African ancestry in Southwest USA (ASW)., Part of: International Genome Sample Resource (1000 genomes project) cell lines. PMID:21397061 Transformed cell line Female CLO:CLO_0027858,
BioSample:SAMN00007843,
Coriell:GM20294,
GEO:GSM650234,
GEO:GSM1720361,
IGSR:NA20294,
Wikidata:Q54850900
CVCL_N891 2026-09-05 10:58:48 0
GM20316
 
Resource Report
Resource Website
Coriell Cat# GM20316, RRID:CVCL_1B07 Homo sapiens (Human) Population: African ancestry in Southwest USA (ASW)., Part of: International Genome Sample Resource (1000 genomes project) cell lines. PMID:21397061 Transformed cell line Male Coriell GM20316 CLO:CLO_0027882,
Coriell:GM20316,
GEO:GSM650244,
IGSR:NA20316,
Wikidata:Q54850929
CVCL_1B07 2026-09-05 10:58:49 0
GM20273
 
Resource Report
Resource Website
RRID:CVCL_0R35 Homo sapiens (Human) Gaucher disease Population: Lebanese. Finite cell line Male CLO:CLO_0027829,
Coriell:GM20273,
Wikidata:Q54850881
CVCL_0R35 2026-09-05 10:58:48 0

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