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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 July 29, 2024
Displaying entries 6626 - 6650 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:4195 hyperglycemia HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • MGI:6194238
DOID:224 transient cerebral ischemia HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • MGI:6194238
DOID:2513 basal cell carcinoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:10677095
  • PMID:9539248
  • RGD:7240710
DOID:9452 steatotic liver disease HGNC:84 Homo sapiens (human) 31 ACACA
  • MGI:6194238
DOID:1596 depressive disorder HGNC:2596 Homo sapiens (human) 1544 CYP1A2
  • MGI:6194238
DOID:12930 dilated cardiomyopathy HGNC:2422 Homo sapiens (human) 1431 CS
  • PMID:10354207
  • PMID:8252591
DOID:11832 visual epilepsy HGNC:4341 Homo sapiens (human) 2752 GLUL
  • MGI:6194238
DOID:1936 atherosclerosis HGNC:16049 Homo sapiens (human) 10728 PTGES3
  • PMID:14736553
DOID:0050852 limb ischemia HGNC:2422 Homo sapiens (human) 1431 CS
  • MGI:6194238
DOID:9870 galactosemia HGNC:24063 Homo sapiens (human) 130589 GALM
  • RGD:7240710
DOID:0050158 desquamative interstitial pneumonia HGNC:10802 Homo sapiens (human) 6440 SFTPC
  • MGI:6194238
DOID:9775 diastolic heart failure HGNC:6554 Homo sapiens (human) 3953 LEPR
  • MGI:6194238
DOID:783 end stage renal disease HGNC:9053 Homo sapiens (human) 5329 PLAUR
  • PMID:19926968
DOID:5844 myocardial infarction HGNC:587 Homo sapiens (human) 328 APEX1
  • PMID:18712175
DOID:552 pneumonia HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:17727310
  • PMID:19455553
  • PMID:20051911
DOID:5844 myocardial infarction HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • PMID:15138244
DOID:2978 carbohydrate metabolic disorder HGNC:93 Homo sapiens (human) 38 ACAT1
  • PMID:7617578
DOID:2957 pulmonary tuberculosis HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:18008256
DOID:684 hepatocellular carcinoma HGNC:4250 Homo sapiens (human) 2678 GGT1
  • PMID:10572675
  • PMID:11940314
  • PMID:27793641
DOID:783 end stage renal disease HGNC:8133 Homo sapiens (human) 4973 OLR1
  • MGI:6194238
DOID:10787 premature menopause HGNC:94 Homo sapiens (human) 39 ACAT2
  • MGI:6194238
DOID:9119 acute myeloid leukemia HGNC:4458 Homo sapiens (human) 2821 GPI
  • PMID:6589021
DOID:0112379 muscular dystrophy-dystroglycanopathy type B4 HGNC:3622 Homo sapiens (human) 2218 FKTN
  • RGD:7240710
DOID:10652 Alzheimer's disease HGNC:23064 Homo sapiens (human) 119391 GSTO2
  • PMID:14570706
  • PMID:15917099
DOID:9352 type 2 diabetes mellitus HGNC:18590 Homo sapiens (human) 80339 PNPLA3
  • PMID:31377187

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Supported by JST NBDC Grant Number JPMJND2204

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


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