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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 4501 - 4525 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:3908 lung non-small cell carcinoma RGD:3935 Rattus norvegicus (Norway rat) 24861 Ugt1a1
  • MGI:6194238
DOID:2043 hepatitis B RGD:3935 Rattus norvegicus (Norway rat) 24861 Ugt1a1
  • MGI:6194238
DOID:2394 ovarian cancer RGD:3935 Rattus norvegicus (Norway rat) 24861 Ugt1a1
  • MGI:6194238
DOID:9744 type 1 diabetes mellitus RGD:3935 Rattus norvegicus (Norway rat) 24861 Ugt1a1
  • PMID:9841869
DOID:10211 cholelithiasis RGD:3935 Rattus norvegicus (Norway rat) 24861 Ugt1a1
  • MGI:6194238
DOID:11151 cholecystolithiasis RGD:3935 Rattus norvegicus (Norway rat) 24861 Ugt1a1
  • MGI:6194238
DOID:3803 Crigler-Najjar syndrome RGD:3935 Rattus norvegicus (Norway rat) 24861 Ugt1a1
  • MGI:6194238
  • PMID:22765254
DOID:2739 Gilbert syndrome RGD:3935 Rattus norvegicus (Norway rat) 24861 Ugt1a1
  • MGI:6194238
DOID:2741 bilirubin metabolic disorder RGD:3935 Rattus norvegicus (Norway rat) 24861 Ugt1a1
  • MGI:6194238
  • PMID:15753292
DOID:9352 type 2 diabetes mellitus RGD:3935 Rattus norvegicus (Norway rat) 24861 Ugt1a1
  • PMID:23545594
DOID:0110914 infantile hypophosphatasia HGNC:438 Homo sapiens (human) 249 ALPL
  • MGI:6194238
  • RGD:7240710
DOID:4676 uremia HGNC:438 Homo sapiens (human) 249 ALPL
  • MGI:6194238
DOID:8719 in situ carcinoma HGNC:438 Homo sapiens (human) 249 ALPL
  • PMID:10547581
DOID:0110915 childhood hypophosphatasia HGNC:438 Homo sapiens (human) 249 ALPL
  • MGI:6194238
  • RGD:7240710
DOID:13809 familial combined hyperlipidemia HGNC:438 Homo sapiens (human) 249 ALPL
  • PMID:16336518
DOID:2349 arteriosclerosis HGNC:438 Homo sapiens (human) 249 ALPL
  • PMID:17010978
DOID:0110913 adult hypophosphatasia HGNC:438 Homo sapiens (human) 249 ALPL
  • MGI:6194238
  • RGD:7240710
DOID:9452 steatotic liver disease HGNC:438 Homo sapiens (human) 249 ALPL
  • PMID:16197789
DOID:14213 hypophosphatasia HGNC:438 Homo sapiens (human) 249 ALPL
  • PMID:8406453
DOID:1591 renovascular hypertension RGD:2059 Rattus norvegicus (Norway rat) 24925 Adrb1
  • PMID:15592645
  • PMID:17278011
DOID:5844 myocardial infarction RGD:2059 Rattus norvegicus (Norway rat) 24925 Adrb1
  • PMID:17143192
DOID:4195 hyperglycemia RGD:2059 Rattus norvegicus (Norway rat) 24925 Adrb1
  • PMID:21831645
DOID:12930 dilated cardiomyopathy RGD:2059 Rattus norvegicus (Norway rat) 24925 Adrb1
  • PMID:18287209
DOID:13544 low tension glaucoma RGD:2059 Rattus norvegicus (Norway rat) 24925 Adrb1
  • MGI:6194238
DOID:0050848 obstructive sleep apnea RGD:2059 Rattus norvegicus (Norway rat) 24925 Adrb1
  • MGI:6194238

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

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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