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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 Authority Record Last Update Mentions Count
GM02303
 
Resource Report
Resource Website
RRID:CVCL_BT15 Homo sapiens (Human) Variegate porphyria Transformed cell line Female GM-2303 CLO:CLO_0032208,
BioSample:SAMN00807675,
Coriell:GM02303,
Wikidata:Q54837417
CVCL_BT15 Cellosaurus 2026-10-31 05:02:52 0
GM02214
 
Resource Report
Resource Website
Coriell Cat# GM02214, RRID:CVCL_H179 Homo sapiens (Human) Metachromatic leukodystrophy Donor information: At sampling donor was not affected with metachromatic leukodystrophy but at risk for disease., Population: Caucasian. Finite cell line Male GM-2214 Coriell GM02214 CLO:CLO_0032259,
BioSample:SAMN00807610,
Coriell:GM02214,
Wikidata:Q54837376
CVCL_H179 Cellosaurus 2026-10-31 05:02:51 0
GM02228
 
Resource Report
Resource Website
RRID:CVCL_U949 Homo sapiens (Human) Alkaptonuria Population: Caucasian. Finite cell line Male GM2228, GM-2228 CLO:CLO_0032242,
BioSample:SAMN00807614,
Coriell:GM02228,
Wikidata:Q54837382
CVCL_U949 Cellosaurus 2026-10-31 05:02:52 0
GM02316
 
Resource Report
Resource Website
Coriell Cat# GM02316, RRID:CVCL_8A66 Homo sapiens (Human) Population: Caucasian; Irish. PMID:21418647
PMID:24555846
PMID:25326100
Finite cell line Male GM-2316 Coriell GM02316 CLO:CLO_0032169,
BioSample:SAMN00807689,
Coriell:GM02316,
GEO:GSM651150,
GEO:GSM651151,
GEO:GSM1257697,
GEO:GSM1266972,
GEO:GSM1267051,
GEO:GSM1288439,
GEO:GSM1314047,
Wikidata:Q54837424
CVCL_8A66 Cellosaurus 2026-10-31 05:02:53 0
GM02269
 
Resource Report
Resource Website
Coriell Cat# GM02269, RRID:CVCL_H180 Homo sapiens (Human) Finite cell line Male GM-2269 Coriell GM02269 CLO:CLO_0032123,
BioSample:SAMN00807648,
Coriell:GM02269,
Wikidata:Q54837401
CVCL_H180 Cellosaurus 2026-10-31 05:02:52 0
GM02206
 
Resource Report
Resource Website
Discontinued
Coriell Cat# GM01514, RRID:CVCL_L969 Homo sapiens (Human) Ehlers-Danlos syndrome Population: Caucasian. PMID:6617268
PMID:23665875
PMID:25326100
Finite cell line Female GM-2206 GM 2206, GM01514 Coriell GM01514 CLO:CLO_0032262,
BioSample:SAMN00807604,
Coriell:GM01514,
Coriell:GM02206,
GEO:GSM1266977,
Wikidata:Q54837370
CVCL_L969 Cellosaurus 2026-10-31 05:02:51 0
GM02206
 
Resource Report
Resource Website
Discontinued
Coriell Cat# GM02206, RRID:CVCL_L969 Homo sapiens (Human) Ehlers-Danlos syndrome Population: Caucasian. PMID:6617268
PMID:23665875
PMID:25326100
Finite cell line Female GM-2206 GM 2206, GM01514 Coriell GM02206 CLO:CLO_0032262,
BioSample:SAMN00807604,
Coriell:GM01514,
Coriell:GM02206,
GEO:GSM1266977,
Wikidata:Q54837370
CVCL_L969 Cellosaurus 2026-10-31 05:02:51 0
GM02209
 
Resource Report
Resource Website
Coriell Cat# GM02209, RRID:CVCL_CZ04 Homo sapiens (Human) Population: Caucasian. PMID:7438795 Finite cell line Female GM2209 Coriell GM02209 CLO:CLO_0032261,
BioSample:SAMN00807606,
Coriell:GM02209,
Wikidata:Q54837373
CVCL_CZ04 Cellosaurus 2026-10-31 05:02:51 0
GM02215
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_JB88 Homo sapiens (Human) Autosomal dominant torsion dystonia 1 Finite cell line Male GM-2215 Coriell:GM02215,
Wikidata:Q54837377
CVCL_JB88 Cellosaurus 2026-10-31 05:02:51 0
GM02328
 
Resource Report
Resource Website
Coriell Cat# GM02328, RRID:CVCL_DD69 Homo sapiens (Human) Osteogenesis imperfecta Population: Caucasian. PMID:6689020 Finite cell line Male GM-2328, IMR-2328 Coriell GM02328 CLO:CLO_0032180,
BioSample:SAMN00807699,
Coriell:GM02328,
Wikidata:Q54837429
CVCL_DD69 Cellosaurus 2026-10-31 05:02:53 0
GM02307
 
Resource Report
Resource Website
Coriell Cat# GM02307, RRID:CVCL_4N24 Homo sapiens (Human) Autosomal recessive torsion dystonia 2 Population: Caucasian. Transformed cell line Male GM-2307 Coriell GM02307 CLO:CLO_0032176,
BioSample:SAMN00807683,
Coriell:GM02307,
Wikidata:Q54837421
CVCL_4N24 Cellosaurus 2026-10-31 05:02:53 0
GM02301
 
Resource Report
Resource Website
Coriell Cat# GM02301, RRID:CVCL_IL10 Homo sapiens (Human) Androgen insensitivity syndrome Population: African American. Finite cell line Sex ambiguous GM-2301 Coriell GM02301 CLO:CLO_0032199,
BioSample:SAMN00807671,
Coriell:GM02301,
Wikidata:Q54837415
CVCL_IL10 Cellosaurus 2026-10-31 05:02:52 0
GM02299
 
Resource Report
Resource Website
RRID:CVCL_IL08 Homo sapiens (Human) Androgen insensitivity syndrome Population: African American. Finite cell line Sex ambiguous GM-2299 CLO:CLO_0032202,
BioSample:SAMN00807667,
Coriell:GM02299,
Wikidata:Q54837413
CVCL_IL08 Cellosaurus 2026-10-31 05:02:52 0
GM02305
 
Resource Report
Resource Website
RRID:CVCL_1U22 Homo sapiens (Human) Autosomal dominant torsion dystonia 1 Population: Caucasian. Transformed cell line Female GM-2305 CLO:CLO_0032207,
BioSample:SAMN00807679,
Coriell:GM02305,
Wikidata:Q54837419
CVCL_1U22 Cellosaurus 2026-10-31 05:02:53 0
GM02229
 
Resource Report
Resource Website
Coriell Cat# GM02229, RRID:CVCL_4J48 Homo sapiens (Human) Transformed cell line Female GM-2229, GM02229A Coriell GM02229 CLO:CLO_0032241,
BioSample:SAMN00807616,
Coriell:GM02229,
Wikidata:Q54837383
CVCL_4J48 Cellosaurus 2026-10-31 05:02:52 0
GM02230
 
Resource Report
Resource Website
RRID:CVCL_4J49 Homo sapiens (Human) Transformed cell line Female GM-2230 CLO:CLO_0032244,
BioSample:SAMN00807618,
Coriell:GM02230,
Wikidata:Q54837384
CVCL_4J49 Cellosaurus 2026-10-31 05:02:52 0
GM02205
 
Resource Report
Resource Website
Discontinued
Coriell Cat# GM02205, RRID:CVCL_L968 Homo sapiens (Human) Population: Caucasian. PMID:6617268
PMID:23665875
PMID:24555846
PMID:25326100
Finite cell line Male GM-2205, GM 2205, GM01515 Coriell GM02205 CLO:CLO_0032263,
BioSample:SAMN00807602,
Coriell:GM01515,
Coriell:GM02205,
GEO:GSM1266975,
GEO:GSM1267054,
GEO:GSM1288438,
Wikidata:Q54837369
CVCL_L968 Cellosaurus 2026-10-31 05:02:51 0
GM02293
 
Resource Report
Resource Website
RRID:CVCL_M995 Homo sapiens (Human) Ehlers-Danlos syndrome Population: Cuban., Part of: Human variation panel. Finite cell line Female GM-2293, GM17353 CLO:CLO_0013723,
CLO:CLO_0032132,
BioSample:SAMN00807660,
Coriell:GM02293,
Coriell:GM17353,
Wikidata:Q54837409
CVCL_M995 Cellosaurus 2026-10-31 05:02:52 0
GM02304
 
Resource Report
Resource Website
1+ mentions
Coriell Cat# GM02304, RRID:CVCL_1U21 Homo sapiens (Human) Autosomal dominant torsion dystonia 1 Population: Caucasian. Finite cell line Female GM-2304 Coriell GM02304 CLO:CLO_0032209,
BioSample:SAMN00807677,
Coriell:GM02304,
Wikidata:Q54837418
CVCL_1U21 Cellosaurus 2026-10-31 05:02:53 1
GM02300
 
Resource Report
Resource Website
RRID:CVCL_IL09 Homo sapiens (Human) Androgen insensitivity syndrome Population: African American. Finite cell line Sex ambiguous GM-2300, GM02300A CLO:CLO_0032203,
BioSample:SAMN00807669,
Coriell:GM02300,
Wikidata:Q54837414
CVCL_IL09 Cellosaurus 2026-10-31 05:02:52 0

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