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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 751 - 775 of 71927 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:399 Homo sapiens (human) 213 ALB
  • PMID:11849406
DOID:14525 Reye syndrome HGNC:399 Homo sapiens (human) 213 ALB
  • MGI:6194238
DOID:4947 cholangiocarcinoma HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:10776430
  • PMID:17545000
  • PMID:20431764
DOID:0050625 biliary tract benign neoplasm HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:20358256
DOID:112 esophageal varix HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:8664482
DOID:3525 middle cerebral artery infarction HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:22227456
DOID:11266 Hantavirus hemorrhagic fever with renal syndrome HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:14555823
DOID:3587 pancreatic ductal carcinoma HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:19011933
DOID:13603 obstructive jaundice HGNC:399 Homo sapiens (human) 213 ALB
  • MGI:6194238
DOID:0080600 COVID-19 HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:32198776
  • PMID:32427582
DOID:8893 psoriasis HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:22607558
DOID:1793 pancreatic cancer HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:18154768
  • PMID:20508721
DOID:13580 cholestasis HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:6431134
DOID:620 blood protein disease HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:20603593
DOID:14089 root caries HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:17959907
DOID:5082 liver cirrhosis HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:23285146
DOID:6000 congestive heart failure HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:22158777
DOID:9675 pulmonary emphysema HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:24365562
DOID:8924 autoimmune thrombocytopenic purpura HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:6683982
DOID:0050782 Zollinger-Ellison syndrome HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:908508
DOID:1168 familial hyperlipidemia HGNC:399 Homo sapiens (human) 213 ALB
  • MGI:6194238
DOID:3908 lung non-small cell carcinoma HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:23778417
DOID:1184 nephrotic syndrome HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:22203175
DOID:13576 twin-to-twin transfusion syndrome HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:23208016
DOID:684 hepatocellular carcinoma HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:22392353
  • PMID:23892757
  • PMID:29040987

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