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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 1201 - 1225 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:10652 Alzheimer's disease HGNC:936 Homo sapiens (human) 572 BAD
  • PMID:9507158
DOID:9352 type 2 diabetes mellitus HGNC:936 Homo sapiens (human) 572 BAD
  • MGI:6194238
DOID:1875 impotence HGNC:936 Homo sapiens (human) 572 BAD
  • MGI:6194238
DOID:0080855 Parkinsonism HGNC:936 Homo sapiens (human) 572 BAD
  • MGI:6194238
DOID:10286 prostate carcinoma HGNC:936 Homo sapiens (human) 572 BAD
  • PMID:11781193
DOID:3070 high grade glioma HGNC:936 Homo sapiens (human) 572 BAD
  • MGI:6194238
DOID:219 colon cancer HGNC:936 Homo sapiens (human) 572 BAD
  • MGI:6194238
DOID:2316 brain ischemia HGNC:936 Homo sapiens (human) 572 BAD
  • MGI:6194238
DOID:8398 osteoarthritis HGNC:936 Homo sapiens (human) 572 BAD
  • PMID:19217321
DOID:9743 diabetic neuropathy HGNC:936 Homo sapiens (human) 572 BAD
  • MGI:6194238
DOID:3770 pulmonary fibrosis HGNC:936 Homo sapiens (human) 572 BAD
  • MGI:6194238
DOID:1459 hypothyroidism HGNC:936 Homo sapiens (human) 572 BAD
  • MGI:6194238
DOID:1612 breast cancer HGNC:936 Homo sapiens (human) 572 BAD
  • PMID:17004114
DOID:10808 gastric ulcer HGNC:936 Homo sapiens (human) 572 BAD
  • MGI:6194238
DOID:10584 retinitis pigmentosa HGNC:23059 Homo sapiens (human) 63827 BCAN
  • PMID:29150673
DOID:3525 middle cerebral artery infarction HGNC:23059 Homo sapiens (human) 63827 BCAN
  • MGI:6194238
DOID:3070 high grade glioma HGNC:23059 Homo sapiens (human) 63827 BCAN
  • MGI:6194238
  • PMID:16061654
  • PMID:23253190
DOID:9269 maple syrup urine disease HGNC:986 Homo sapiens (human) 593 BCKDHA
  • PMID:1943689
  • PMID:8037208
  • RGD:7240710
DOID:9269 maple syrup urine disease HGNC:987 Homo sapiens (human) 594 BCKDHB
  • MGI:6194238
  • PMID:2022752
DOID:7998 hyperthyroidism HGNC:1027 Homo sapiens (human) 622 BDH1
  • MGI:6194238
DOID:0080600 COVID-19 HGNC:1027 Homo sapiens (human) 622 BDH1
  • PMID:32456948
DOID:12858 Huntington's disease SGD:S000001943 Saccharomyces cerevisiae S288C 850608 BNA6
  • MGI:6194238
DOID:0111630 familial erythrocytosis 8 HGNC:1093 Homo sapiens (human) 669 BPGM
  • PMID:1421379
  • RGD:7240710
DOID:0070352 stress-induced childhood-onset neurodegeneration with variable ataxia and seizures HGNC:1094 Homo sapiens (human) 670 BPHL
  • MGI:6194238
DOID:5742 pancreatic acinar cell adenocarcinoma HGNC:1097 Homo sapiens (human) 673 BRAF
  • PMID:25266736

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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