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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 7876 - 7900 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:13317 hyperinsulinemic hypoglycemia HGNC:4923 Homo sapiens (human) 3099 HK2
  • MGI:6194238
DOID:4195 hyperglycemia HGNC:4923 Homo sapiens (human) 3099 HK2
  • MGI:6194238
DOID:4194 glucose metabolism disease HGNC:4923 Homo sapiens (human) 3099 HK2
  • MGI:6194238
DOID:11054 urinary bladder cancer HGNC:4922 Homo sapiens (human) 3098 HK1
  • MGI:6194238
DOID:9970 obesity HGNC:4922 Homo sapiens (human) 3098 HK1
  • MGI:6194238
  • PMID:131232
DOID:2355 anemia HGNC:4922 Homo sapiens (human) 3098 HK1
  • PMID:19651813
DOID:9538 multiple myeloma HGNC:4922 Homo sapiens (human) 3098 HK1
  • PMID:19996089
DOID:2861 congenital nonspherocytic hemolytic anemia HGNC:4922 Homo sapiens (human) 3098 HK1
  • PMID:7655856
DOID:0110196 Charcot-Marie-Tooth disease type 4G HGNC:4922 Homo sapiens (human) 3098 HK1
  • RGD:7240710
DOID:4194 glucose metabolism disease HGNC:4922 Homo sapiens (human) 3098 HK1
  • MGI:6194238
DOID:10584 retinitis pigmentosa HGNC:4922 Homo sapiens (human) 3098 HK1
  • PMID:25190649
  • RGD:7240710
DOID:9952 acute lymphoblastic leukemia HGNC:4922 Homo sapiens (human) 3098 HK1
  • PMID:21921332
DOID:6432 pulmonary hypertension HGNC:4922 Homo sapiens (human) 3098 HK1
  • MGI:6194238
DOID:10923 sickle cell anemia HGNC:4922 Homo sapiens (human) 3098 HK1
  • PMID:5686464
DOID:9256 colorectal cancer HGNC:4922 Homo sapiens (human) 3098 HK1
  • MGI:6194238
DOID:1574 alcohol use disorder HGNC:491 Homo sapiens (human) 27329 ANGPTL3
  • MGI:6194238
DOID:0111061 familial hypobetalipoproteinemia 2 HGNC:491 Homo sapiens (human) 27329 ANGPTL3
  • RGD:7240710
DOID:0111027 hemochromatosis type 2A HGNC:4887 Homo sapiens (human) 148738 HJV
  • MGI:6194238
  • RGD:7240710
DOID:2352 hemochromatosis HGNC:4887 Homo sapiens (human) 148738 HJV
  • PMID:14647275
DOID:3323 Sandhoff disease HGNC:4879 Homo sapiens (human) 3074 HEXB
  • MGI:6194238
  • PMID:2147027
  • RGD:7240710
DOID:12377 spinal muscular atrophy HGNC:4879 Homo sapiens (human) 3074 HEXB
  • PMID:1720305
DOID:3211 lysosomal storage disease HGNC:4879 Homo sapiens (human) 3074 HEXB
  • MGI:6194238
DOID:3320 Tay-Sachs disease HGNC:4878 Homo sapiens (human) 3073 HEXA
  • MGI:6194238
  • RGD:7240710
DOID:6432 pulmonary hypertension HGNC:4820 Homo sapiens (human) 3038 HAS3
  • MGI:6194238
DOID:3525 middle cerebral artery infarction HGNC:4819 Homo sapiens (human) 3037 HAS2
  • MGI:6194238

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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