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Alliance of Genome Resources

Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.

Source Last Updated
Alliance of Genome Resources October 9, 2024
Displaying entries 69001 - 69025 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▼ References
DOID:11476 osteoporosis HGNC:5465 Homo sapiens (human) 3480 IGF1R
  • PMID:18079194
DOID:4029 gastritis RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • PMID:25335260
DOID:1520 colon carcinoma HGNC:12680 Homo sapiens (human) 7422 VEGFA
  • PMID:18657413
DOID:8283 peritonitis RGD:2582 Rattus norvegicus (Norway rat) 25149 Esr2
  • PMID:23063870
DOID:1107 esophageal carcinoma HGNC:11364 Homo sapiens (human) 6774 STAT3
  • PMID:25724470
DOID:2394 ovarian cancer HGNC:7652 Homo sapiens (human) 4683 NBN
  • PMID:16424057
DOID:12236 primary biliary cholangitis HGNC:8066 Homo sapiens (human) 23636 NUP62
  • PMID:12753810
DOID:684 hepatocellular carcinoma HGNC:14524 Homo sapiens (human) 9043 SPAG9
  • PMID:29344208
DOID:3328 temporal lobe epilepsy HGNC:6893 Homo sapiens (human) 4137 MAPT
  • PMID:28595035
DOID:0060224 atrial fibrillation HGNC:6266 Homo sapiens (human) 3762 KCNJ5
  • PMID:11693772
DOID:5082 liver cirrhosis HGNC:5423 Homo sapiens (human) 3440 IFNA2
  • PMID:7646558
DOID:9953 acute biphenotypic leukemia HGNC:24948 Homo sapiens (human) 84444 DOT1L
  • PMID:23801631
DOID:783 end stage renal disease RGD:2993 Rattus norvegicus (Norway rat) 24530 Lcat
  • PMID:15280162
DOID:14115 toxic shock syndrome RGD:2004 Rattus norvegicus (Norway rat) 24153 A2m
  • PMID:2424486
DOID:0081267 graft-versus-host disease HGNC:6000 Homo sapiens (human) 3557 IL1RN
  • PMID:8049450
DOID:1612 breast cancer HGNC:4566 Homo sapiens (human) 2885 GRB2
  • PMID:17372910
DOID:12704 ataxia telangiectasia HGNC:5438 Homo sapiens (human) 3458 IFNG
  • PMID:6432389
DOID:2377 multiple sclerosis HGNC:5434 Homo sapiens (human) 3456 IFNB1
  • PMID:15389896
DOID:12858 Huntington's disease HGNC:9437 Homo sapiens (human) 5610 EIF2AK2
  • PMID:11468270
  • PMID:15567511
DOID:0060284 paroxysmal nocturnal hemoglobinuria HGNC:1318 Homo sapiens (human) 718 C3
  • PMID:6915939
DOID:4074 pancreatic adenocarcinoma HGNC:3113 Homo sapiens (human) 1869 E2F1
  • PMID:28797284
DOID:1825 childhood absence epilepsy RGD:3199 Rattus norvegicus (Norway rat) 25340 Npy5r
  • PMID:17331209
DOID:9970 obesity RGD:620630 Rattus norvegicus (Norway rat) 85268 Hrh3
  • PMID:17189541
DOID:10283 prostate cancer HGNC:3430 Homo sapiens (human) 2064 ERBB2
  • PMID:16771730
DOID:9352 type 2 diabetes mellitus HGNC:4923 Homo sapiens (human) 3099 HK2
  • PMID:11319725

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024