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117,735 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
GM01129
 
Resource Report
Resource Website
RRID:CVCL_2H12 Homo sapiens (Human) Homocystinuria Population: Caucasian. Finite cell line Male GM1129, GM-1129 CLO:CLO_0030168,
BioSample:SAMN00803648,
Coriell:GM01129,
Wikidata:Q54836657
CVCL_2H12 2026-07-25 04:32:13 0
GM01168
 
Resource Report
Resource Website
Coriell Cat# GM01168, RRID:CVCL_1H37 Homo sapiens (Human) Huntington's disease Population: Caucasian. PMID:6458814 Finite cell line Male GM-1168, GM 1168 Coriell GM01168 CLO:CLO_0030210,
BioSample:SAMN00803680,
Coriell:GM01168,
Wikidata:Q54836682
CVCL_1H37 2026-07-25 04:32:13 0
GM01177
 
Resource Report
Resource Website
Possibly Discontinued
Possibly Discontinued
Coriell Cat# AG01177, RRID:CVCL_JB60 Homo sapiens (Human) Progeria From: Montreal Children's Hospital cell repository; Montreal; Canada. PMID:7176709
PMID:7253718
Finite cell line Male GM-1177, GM1177, AG01177, AG-1177, AG 1177, AG1177, WG0360, WG360 Coriell AG01177 Coriell:AG01177,
Coriell:GM01177,
Wikidata:Q54836688
CVCL_JB60 2026-07-25 04:32:13 0
GM01178
 
Resource Report
Resource Website
Coriell Cat# AG01178, RRID:CVCL_CV40 Homo sapiens (Human) Progeria From: Montreal Children's Hospital cell repository; Montreal; Canada. PMID:7253718 Finite cell line Male GM-1178, GM 1178, GM1178, GM01178B, AG01178, AG-1178, AG1178, AG01178B, WG0380, WG380 Coriell AG01178 CLO:CLO_0030204,
CLO:CLO_0036894,
Coriell:AG01178,
Coriell:GM01178,
Wikidata:Q54836689
CVCL_CV40 2026-07-25 04:32:13 0
GM01204
 
Resource Report
Resource Website
RRID:CVCL_U515 Homo sapiens (Human) Citrullinemia type I Population: Caucasian. Transformed cell line Male GM-1204, GM01204A CLO:CLO_0030261,
BioSample:SAMN00803706,
Coriell:GM01204,
Wikidata:Q54836699
CVCL_U515 2026-07-25 04:32:13 0
GM01178
 
Resource Report
Resource Website
Coriell Cat# GM01178, RRID:CVCL_CV40 Homo sapiens (Human) Progeria From: Montreal Children's Hospital cell repository; Montreal; Canada. PMID:7253718 Finite cell line Male GM-1178, GM 1178, GM1178, GM01178B, AG01178, AG-1178, AG1178, AG01178B, WG0380, WG380 Coriell GM01178 CLO:CLO_0030204,
CLO:CLO_0036894,
Coriell:AG01178,
Coriell:GM01178,
Wikidata:Q54836689
CVCL_CV40 2026-07-25 04:32:14 0
GM01183
 
Resource Report
Resource Website
Coriell Cat# GM01183, RRID:CVCL_X242 Homo sapiens (Human) Population: Caucasian. PMID:6661932
PMID:23665875
Finite cell line Male GM-1183, GM 1183 Coriell GM01183 CLO:CLO_0030263,
BioSample:SAMN00803690,
Coriell:GM01183,
Wikidata:Q54836691
CVCL_X242 2026-07-25 04:32:13 0
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 2026-07-25 04:32:13 1
GM01310
 
Resource Report
Resource Website
Coriell Cat# GM01310, RRID:CVCL_7316 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:62390
PMID:16260726
PMID:20889555
PMID:29959025
Transformed cell line Male GM-1310, GM01310B, GM01310C, GM17212 Coriell GM01310 CLO:CLO_0013895,
CLO:CLO_0030914,
BioSample:SAMN00803794,
Coriell:GM01310,
Coriell:GM17212,
GEO:GSM569521,
GEO:GSM596276,
GEO:GSM596637,
GEO:GSM924814,
Wikidata:Q54836762
CVCL_7316 2026-07-25 04:32:15 0
GM01221
 
Resource Report
Resource Website
RRID:CVCL_X244 Homo sapiens (Human) Population: African American. PMID:6293786
PMID:6661932
PMID:23665875
Finite cell line Male GM-1221, GM 1221, GM1221, GM01221A CLO:CLO_0030285,
BioSample:SAMN00803728,
Coriell:GM01221,
Wikidata:Q54836715
CVCL_X244 2026-07-25 04:32:14 0
GM01227
 
Resource Report
Resource Website
Coriell Cat# GM01227, RRID:CVCL_L459 Homo sapiens (Human) Xeroderma pigmentosum Population: Caucasian. PMID:7263770
PMID:7326997
Finite cell line Male GM-1227, GM 1227, GM1227 Coriell GM01227 CLO:CLO_0030281,
BioSample:SAMN00803736,
Coriell:GM01227,
JCRB:KURB1268,
Wikidata:Q54836719
CVCL_L459 2026-07-25 04:32:14 0
GM01253
 
Resource Report
Resource Website
Coriell Cat# GM01253, RRID:CVCL_V803 Homo sapiens (Human) Karyotypic information: 46,XY,rec(3)(qter->p25::q25->qter) (Coriell=GM01253)., Population: African American. PMID:477407
PMID:6661932
Finite cell line Male GM-1253, GM 1253 Coriell GM01253 CLO:CLO_0030936,
BioSample:SAMN00803764,
Coriell:GM01253,
Wikidata:Q54836739
CVCL_V803 2026-07-25 04:32:16 0
GM01250
 
Resource Report
Resource Website
RRID:CVCL_W636 Homo sapiens (Human) 47,XYY syndrome Karyotypic information: 47,XYY (Coriell=GM01250)., Population: African American. PMID:6661932 Finite cell line Male GM-1250, GM 1250 CLO:CLO_0030931,
BioSample:SAMN00803758,
Coriell:GM01250,
Wikidata:Q54836736
CVCL_W636 2026-07-25 04:32:14 0
GM01310
 
Resource Report
Resource Website
RRID:CVCL_7316 Homo sapiens (Human) Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:62390
PMID:16260726
PMID:20889555
PMID:29959025
Transformed cell line Male GM-1310, GM01310B, GM01310C, GM17212 CLO:CLO_0013895,
CLO:CLO_0030914,
BioSample:SAMN00803794,
Coriell:GM01310,
Coriell:GM17212,
GEO:GSM569521,
GEO:GSM596276,
GEO:GSM596637,
GEO:GSM924814,
Wikidata:Q54836762
CVCL_7316 2026-07-25 04:32:16 0
GM01255
 
Resource Report
Resource Website
RRID:CVCL_1V24 Homo sapiens (Human) Hurler-Scheie syndrome Population: Caucasian. PMID:6293786 Finite cell line Male GM-1255, GM1255 CLO:CLO_0030934,
BioSample:SAMN00803768,
Coriell:GM01255,
Wikidata:Q54836741
CVCL_1V24 2026-07-25 04:32:16 0
GM01246
 
Resource Report
Resource Website
RRID:CVCL_H966 Homo sapiens (Human) Hepatocyte nuclear factor 4-alpha associated monogenic diabetes Population: Caucasian., Part of: R-W pedigree MODY cell line collection. PMID:7313555
PMID:8945471
Transformed cell line Male GM-1246, GM 1246, GM01246A CLO:CLO_0030270,
BioSample:SAMN00803754,
Coriell:GM01246,
Wikidata:Q54836734
CVCL_H966 2026-07-25 04:32:14 0
GM01299
 
Resource Report
Resource Website
RRID:CVCL_2N28 Homo sapiens (Human) Propionic acidemia Finite cell line Male GM1299, GM-1299 CLO:CLO_0030927,
Coriell:GM01299,
Wikidata:Q54836753
CVCL_2N28 2026-07-25 04:32:16 0
GM01228
 
Resource Report
Resource Website
Discontinued
Coriell Cat# GM00642, RRID:CVCL_L957 Homo sapiens (Human) Intellectual developmental disorder, X-linked 1 Population: Caucasian. Finite cell line Male GM-1228, GM00642 Coriell GM00642 CLO:CLO_0030282,
BioSample:SAMN00803738,
Coriell:GM00642,
Coriell:GM01228,
Wikidata:Q54836720
CVCL_L957 2026-07-25 04:32:14 0
GM01244
 
Resource Report
Resource Website
RRID:CVCL_AI25 Homo sapiens (Human) Hepatocyte nuclear factor 4-alpha associated monogenic diabetes Population: Caucasian., Part of: R-W pedigree MODY cell line collection. PMID:8945471 Transformed cell line Male GM-1244 CLO:CLO_0030272,
Coriell:GM01244,
Wikidata:Q54836731
CVCL_AI25 2026-07-25 04:32:14 0
GM01323
 
Resource Report
Resource Website
RRID:CVCL_1V18 Homo sapiens (Human) Scheie syndrome Population: Caucasian. Finite cell line Male GM-1323 CLO:CLO_0030899,
BioSample:SAMN00803802,
Coriell:GM01323,
Wikidata:Q54836766
CVCL_1V18 2026-07-25 04:32:15 0

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