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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 10226 - 10250 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:11716 prediabetes syndrome MGI:107501 Mus musculus (house mouse) 16514 Kcnj11
  • MGI:6194238
DOID:1824 status epilepticus MGI:107501 Mus musculus (house mouse) 16514 Kcnj11
  • MGI:6194238
DOID:0080569 congenital disorder of glycosylation Ir HGNC:2728 Homo sapiens (human) 1650 DDOST
  • RGD:7240710
DOID:0111773 46,XY sex reversal 8 HGNC:385 Homo sapiens (human) 1646 AKR1C2
  • RGD:7240710
DOID:9970 obesity HGNC:385 Homo sapiens (human) 1646 AKR1C2
  • PMID:15494612
DOID:9970 obesity HGNC:384 Homo sapiens (human) 1645 AKR1C1
  • PMID:15494612
DOID:0080572 congenital disorder of glycosylation Iw MGI:105124 Mus musculus (house mouse) 16430 Stt3a
  • MGI:6194238
DOID:2841 asthma HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:19383228
  • PMID:19484664
DOID:3526 cerebral infarction HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:11596779
DOID:576 proteinuria HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
  • PMID:10193250
DOID:3393 coronary artery disease HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:12975417
DOID:12932 endomyocardial fibrosis HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:9970 obesity HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
  • PMID:17164796
DOID:10534 stomach cancer HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:17035401
DOID:0050864 non-arteritic anterior ischemic optic neuropathy HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:21633717
DOID:9538 multiple myeloma HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:22345095
DOID:1205 allergic disease HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:10200023
DOID:0080600 COVID-19 HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:32286246
  • PMID:32386188
DOID:3500 gallbladder adenocarcinoma HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:20438364
DOID:0080599 Coronavirus infectious disease HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:17108019
DOID:11400 pyelonephritis HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:10504496
DOID:1591 renovascular hypertension HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:13580 cholestasis HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:9744 type 1 diabetes mellitus HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:1336356
  • PMID:9025006
DOID:5419 schizophrenia HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:26296754

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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: August 19, 2024