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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 4576 - 4600 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:438 autoimmune disease of the nervous system HGNC:543 Homo sapiens (human) 308 ANXA5
  • PMID:15486486
DOID:418 systemic scleroderma HGNC:543 Homo sapiens (human) 308 ANXA5
  • PMID:21124692
DOID:7998 hyperthyroidism HGNC:543 Homo sapiens (human) 308 ANXA5
  • MGI:6194238
DOID:0080379 nephrotic syndrome type 2 HGNC:543 Homo sapiens (human) 308 ANXA5
  • PMID:17999093
DOID:5844 myocardial infarction HGNC:543 Homo sapiens (human) 308 ANXA5
  • MGI:6194238
  • PMID:12200370
  • PMID:16025836
  • PMID:8814351
DOID:12217 Lewy body dementia HGNC:543 Homo sapiens (human) 308 ANXA5
  • PMID:23576984
DOID:3587 pancreatic ductal carcinoma HGNC:543 Homo sapiens (human) 308 ANXA5
  • PMID:19488907
DOID:234 colon adenocarcinoma HGNC:545 Homo sapiens (human) 310 ANXA7
  • PMID:17708571
DOID:10283 prostate cancer HGNC:545 Homo sapiens (human) 310 ANXA7
  • PMID:17708571
DOID:4159 skin cancer HGNC:545 Homo sapiens (human) 310 ANXA7
  • PMID:17708571
DOID:0060060 non-Hodgkin lymphoma HGNC:545 Homo sapiens (human) 310 ANXA7
  • PMID:17708571
DOID:2394 ovarian cancer HGNC:545 Homo sapiens (human) 310 ANXA7
  • PMID:17708571
DOID:1612 breast cancer HGNC:545 Homo sapiens (human) 310 ANXA7
  • PMID:15073110
DOID:7148 rheumatoid arthritis HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:11247331
  • PMID:19556211
DOID:2377 multiple sclerosis HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:10417663
DOID:1657 ventricular septal defect HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:21238444
DOID:5082 liver cirrhosis HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:28650518
DOID:8398 osteoarthritis HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:22527881
DOID:1612 breast cancer HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:18719053
DOID:1574 alcohol use disorder HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:30277635
DOID:0080552 congenital disorder of glycosylation Ia HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:19207313
DOID:12217 Lewy body dementia HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:19276553
DOID:3594 choriocarcinoma HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:17556377
DOID:635 acquired immunodeficiency syndrome HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:11232005
DOID:11476 osteoporosis HGNC:5466 Homo sapiens (human) 3481 IGF2
  • MGI:6194238

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Last updated: August 19, 2024