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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 5126 - 5150 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:11832 visual epilepsy HGNC:4341 Homo sapiens (human) 2752 GLUL
  • MGI:6194238
DOID:3328 temporal lobe epilepsy HGNC:4341 Homo sapiens (human) 2752 GLUL
  • MGI:6194238
  • PMID:14723991
DOID:114 heart disease HGNC:4341 Homo sapiens (human) 2752 GLUL
  • PMID:26395743
DOID:3525 middle cerebral artery infarction HGNC:4341 Homo sapiens (human) 2752 GLUL
  • MGI:6194238
DOID:5082 liver cirrhosis HGNC:4341 Homo sapiens (human) 2752 GLUL
  • PMID:30950843
DOID:8947 diabetic retinopathy HGNC:4341 Homo sapiens (human) 2752 GLUL
  • MGI:6194238
DOID:12858 Huntington's disease HGNC:4341 Homo sapiens (human) 2752 GLUL
  • PMID:3159462
  • PMID:6237280
DOID:1070 primary open angle glaucoma HGNC:4341 Homo sapiens (human) 2752 GLUL
  • PMID:22974818
DOID:409 liver disease HGNC:4341 Homo sapiens (human) 2752 GLUL
  • PMID:23362937
  • PMID:31335486
DOID:224 transient cerebral ischemia HGNC:4341 Homo sapiens (human) 2752 GLUL
  • MGI:6194238
DOID:3321 GM2 gangliosidosis HGNC:4367 Homo sapiens (human) 2760 GM2A
  • PMID:10364519
DOID:4795 GM2 gangliosidosis, AB variant HGNC:4367 Homo sapiens (human) 2760 GM2A
  • MGI:6194238
  • RGD:7240710
DOID:1067 open-angle glaucoma HGNC:4369 Homo sapiens (human) 2762 GMDS
  • PMID:25173105
DOID:0070255 congenital disorder of glycosylation type IIc HGNC:4369 Homo sapiens (human) 2762 GMDS
  • MGI:6194238
DOID:0111402 mucopolysaccharidosis type IIID HGNC:4422 Homo sapiens (human) 2799 GNS
  • RGD:7240710
DOID:12801 mucopolysaccharidosis III HGNC:4422 Homo sapiens (human) 2799 GNS
  • MGI:6194238
  • PMID:12573255
DOID:0081267 graft-versus-host disease HGNC:79 Homo sapiens (human) 28 ABO
  • PMID:3289150
DOID:9952 acute lymphoblastic leukemia HGNC:79 Homo sapiens (human) 28 ABO
  • PMID:17065136
DOID:4948 gallbladder carcinoma HGNC:79 Homo sapiens (human) 28 ABO
  • PMID:7795450
DOID:1496 echinococcosis HGNC:79 Homo sapiens (human) 28 ABO
  • PMID:2142987
DOID:552 pneumonia HGNC:79 Homo sapiens (human) 28 ABO
  • PMID:4375858
DOID:10763 hypertension HGNC:79 Homo sapiens (human) 28 ABO
  • PMID:32379894
DOID:2237 hepatitis HGNC:79 Homo sapiens (human) 28 ABO
  • PMID:32379894
DOID:1240 leukemia HGNC:79 Homo sapiens (human) 28 ABO
  • PMID:18426641
DOID:583 hemolytic anemia HGNC:79 Homo sapiens (human) 28 ABO
  • PMID:3136561

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

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