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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 71476 - 71500 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:13141 uveitis HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:229083
DOID:14115 toxic shock syndrome HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:28336767
DOID:10534 stomach cancer HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:17035401
DOID:1184 nephrotic syndrome HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:8947 diabetic retinopathy HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:11106834
  • PMID:2157294
  • PMID:23065222
  • PMID:7729604
DOID:12986 leukostasis HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:820 myocarditis HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:3770 pulmonary fibrosis HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:2921 glomerulonephritis HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:790 ocular hypotension HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:3905 lung carcinoma HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:183595
DOID:5844 myocardial infarction HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
  • PMID:7555560
DOID:552 pneumonia HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:17727310
  • PMID:19455553
  • PMID:20051911
DOID:3827 congenital diaphragmatic hernia HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:0110861 autosomal recessive polycystic kidney disease HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:11400 pyelonephritis HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:10504496
DOID:8805 intermediate coronary syndrome HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:11451295
  • PMID:15131005
DOID:418 systemic scleroderma HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:17360781
DOID:0050848 obstructive sleep apnea HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
  • PMID:19482546
  • PMID:20182789
DOID:783 end stage renal disease HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
  • PMID:16385653
  • PMID:20149750
DOID:12236 primary biliary cholangitis HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:4079 heart valve disease HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:12578328
DOID:5419 schizophrenia HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:26296754
DOID:3525 middle cerebral artery infarction HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238

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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