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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 7176 - 7200 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:783 end stage renal disease HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:16801331
DOID:2272 vulvovaginal candidiasis HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:17470593
DOID:1070 primary open angle glaucoma HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:22335808
DOID:0080159 Cryptococcal meningitis HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:21592999
DOID:2957 pulmonary tuberculosis HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:19199550
DOID:13241 Behcet's disease HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:15693089
  • PMID:15730518
DOID:2043 hepatitis B HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:16231358
DOID:8778 Crohn's disease HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:21702710
DOID:4247 coronary restenosis HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:15790942
DOID:12375 bronchopneumonia HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:19804807
DOID:594 panic disorder HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:24856568
DOID:874 bacterial pneumonia HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:18641104
DOID:3312 bipolar disorder HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:24856568
DOID:11162 respiratory failure HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:18582923
DOID:0080162 lupus nephritis HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:24850777
DOID:0050697 chorioamnionitis HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:15723707
DOID:12306 vitiligo HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:17337399
  • PMID:19416237
DOID:10457 Legionnaires' disease HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:19073229
DOID:14067 Plasmodium falciparum malaria HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:18396436
DOID:3385 bacterial vaginosis HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:17470593
DOID:12177 common variable immunodeficiency HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:10652157
DOID:57 aortic valve insufficiency HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:18400978
DOID:13166 allergic bronchopulmonary aspergillosis HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:11474427
  • PMID:16487239
DOID:0060496 respiratory allergy HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:16487239
DOID:9744 type 1 diabetes mellitus HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:18361935

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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