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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 6626 - 6650 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:9970 obesity HGNC:9155 Homo sapiens (human) 5406 PNLIP
  • MGI:6194238
DOID:0080552 congenital disorder of glycosylation Ia HGNC:9115 Homo sapiens (human) 5373 PMM2
  • MGI:6194238
  • RGD:7240710
DOID:0050570 congenital disorder of glycosylation type I HGNC:9115 Homo sapiens (human) 5373 PMM2
  • MGI:6194238
DOID:5212 congenital disorder of glycosylation HGNC:9115 Homo sapiens (human) 5373 PMM2
  • PMID:10066032
  • PMID:11058896
DOID:0050570 congenital disorder of glycosylation type I HGNC:9114 Homo sapiens (human) 5372 PMM1
  • MGI:6194238
DOID:0080552 congenital disorder of glycosylation Ia HGNC:9114 Homo sapiens (human) 5372 PMM1
  • MGI:6194238
DOID:684 hepatocellular carcinoma HGNC:9083 Homo sapiens (human) 8985 PLOD3
  • PMID:29059470
DOID:1459 hypothyroidism HGNC:9083 Homo sapiens (human) 8985 PLOD3
  • MGI:6194238
DOID:6000 congestive heart failure HGNC:9068 Homo sapiens (human) 5338 PLD2
  • MGI:6194238
DOID:11832 visual epilepsy HGNC:9068 Homo sapiens (human) 5338 PLD2
  • MGI:6194238
DOID:4450 renal cell carcinoma HGNC:9068 Homo sapiens (human) 5338 PLD2
  • PMID:11185526
DOID:0080633 developmental cardiac valvular defect HGNC:9068 Homo sapiens (human) 5338 PLD2
  • MGI:6194238
DOID:11832 visual epilepsy HGNC:9067 Homo sapiens (human) 5337 PLD1
  • MGI:6194238
DOID:3498 pancreatic ductal adenocarcinoma HGNC:9067 Homo sapiens (human) 5337 PLD1
  • PMID:27713167
DOID:0080633 developmental cardiac valvular defect HGNC:9067 Homo sapiens (human) 5337 PLD1
  • MGI:6194238
  • RGD:7240710
DOID:0090064 familial cold autoinflammatory syndrome 3 HGNC:9066 Homo sapiens (human) 5336 PLCG2
  • RGD:7240710
DOID:10652 Alzheimer's disease HGNC:9065 Homo sapiens (human) 5335 PLCG1
  • PMID:8534418
DOID:3459 breast carcinoma HGNC:9065 Homo sapiens (human) 5335 PLCG1
  • PMID:1683701
DOID:684 hepatocellular carcinoma HGNC:9065 Homo sapiens (human) 5335 PLCG1
  • PMID:30623526
DOID:3908 lung non-small cell carcinoma HGNC:9065 Homo sapiens (human) 5335 PLCG1
  • PMID:33928024
DOID:3910 lung adenocarcinoma HGNC:9065 Homo sapiens (human) 5335 PLCG1
  • PMID:33077911
DOID:9408 acute myocardial infarction HGNC:9065 Homo sapiens (human) 5335 PLCG1
  • MGI:6194238
DOID:0050866 oral squamous cell carcinoma HGNC:9065 Homo sapiens (human) 5335 PLCG1
  • PMID:25085076
  • PMID:26464646
DOID:219 colon cancer HGNC:9065 Homo sapiens (human) 5335 PLCG1
  • MGI:6194238
DOID:2876 laryngeal squamous cell carcinoma HGNC:9065 Homo sapiens (human) 5335 PLCG1
  • PMID:33466212

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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