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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 69801 - 69825 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:3393 coronary artery disease HGNC:13916 Homo sapiens (human) 55937 APOM
  • PMID:17674965
DOID:9744 type 1 diabetes mellitus HGNC:13916 Homo sapiens (human) 55937 APOM
  • PMID:19007767
DOID:557 kidney disease HGNC:14868 Homo sapiens (human) 80833 APOL3
  • MGI:6194238
DOID:557 kidney disease HGNC:618 Homo sapiens (human) 8542 APOL1
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:616 Homo sapiens (human) 350 APOH
  • MGI:6194238
  • PMID:15322656
DOID:0060903 thrombosis HGNC:616 Homo sapiens (human) 350 APOH
  • MGI:6194238
DOID:4449 macular retinal edema HGNC:616 Homo sapiens (human) 350 APOH
  • PMID:16080911
DOID:8947 diabetic retinopathy HGNC:616 Homo sapiens (human) 350 APOH
  • PMID:18695102
DOID:2349 arteriosclerosis HGNC:616 Homo sapiens (human) 350 APOH
  • PMID:6613192
DOID:341 peripheral vascular disease HGNC:616 Homo sapiens (human) 350 APOH
  • PMID:17626983
DOID:9352 type 2 diabetes mellitus HGNC:616 Homo sapiens (human) 350 APOH
  • PMID:16126948
DOID:9351 diabetes mellitus HGNC:616 Homo sapiens (human) 350 APOH
  • PMID:18695102
  • PMID:9377806
DOID:2988 antiphospholipid syndrome HGNC:616 Homo sapiens (human) 350 APOH
  • PMID:24642748
DOID:12365 malaria HGNC:613 Homo sapiens (human) 348 APOE
  • PMID:24116184
DOID:3525 middle cerebral artery infarction HGNC:613 Homo sapiens (human) 348 APOE
  • MGI:6194238
DOID:0050639 primary cutaneous amyloidosis HGNC:613 Homo sapiens (human) 348 APOE
  • PMID:9740234
DOID:4606 bile duct cancer HGNC:613 Homo sapiens (human) 348 APOE
  • PMID:18296645
DOID:1168 familial hyperlipidemia HGNC:613 Homo sapiens (human) 348 APOE
  • MGI:6194238
DOID:1070 primary open angle glaucoma HGNC:613 Homo sapiens (human) 348 APOE
  • PMID:15525904
  • PMID:17706090
DOID:3310 atopic dermatitis HGNC:613 Homo sapiens (human) 348 APOE
  • PMID:19116453
DOID:13580 cholestasis HGNC:613 Homo sapiens (human) 348 APOE
  • PMID:19055369
DOID:0050851 glomerulosclerosis HGNC:613 Homo sapiens (human) 348 APOE
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:613 Homo sapiens (human) 348 APOE
  • PMID:18950899
DOID:3526 cerebral infarction HGNC:613 Homo sapiens (human) 348 APOE
  • PMID:17016617
DOID:12930 dilated cardiomyopathy HGNC:613 Homo sapiens (human) 348 APOE
  • PMID:16714771

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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: December 9, 2024