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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 5776 - 5800 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0111671 primary hyperoxaluria type 2 HGNC:4570 Homo sapiens (human) 9380 GRHPR
  • MGI:6194238
  • RGD:7240710
DOID:341 peripheral vascular disease HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:15295097
DOID:13550 angle-closure glaucoma HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:23961996
DOID:0080855 Parkinsonism HGNC:4177 Homo sapiens (human) 2629 GBA1
  • PMID:20838799
DOID:10652 Alzheimer's disease HGNC:24864 Homo sapiens (human) 26330 GAPDHS
  • PMID:15507493
DOID:7998 hyperthyroidism HGNC:4553 Homo sapiens (human) 2876 GPX1
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:15917 Homo sapiens (human) 23236 PLCB1
  • MGI:6194238
DOID:824 periodontitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:5041 esophageal cancer HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:11833070
  • PMID:26782562
DOID:4367 apparent mineralocorticoid excess syndrome HGNC:5209 Homo sapiens (human) 3291 HSD11B2
  • RGD:7240710
DOID:8805 intermediate coronary syndrome HGNC:9588 Homo sapiens (human) 5728 PTEN
  • PMID:32595526
DOID:653 purine-pyrimidine metabolic disorder HGNC:12563 Homo sapiens (human) 7372 UMPS
  • PMID:9042911
DOID:0112216 developmental and epileptic encephalopathy 80 HGNC:8959 Homo sapiens (human) 9488 PIGB
  • RGD:7240710
DOID:1205 allergic disease HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:10200023
DOID:0110210 Charcot-Marie-Tooth disease X-linked recessive 5 HGNC:9462 Homo sapiens (human) 5631 PRPS1
  • MGI:6194238
  • RGD:7240710
DOID:3650 lactic acidosis HGNC:9725 Homo sapiens (human) 5836 PYGL
  • MGI:6194238
  • PMID:17705025
DOID:0050811 congenital adrenal hyperplasia HGNC:2593 Homo sapiens (human) 1586 CYP17A1
  • PMID:2026124
DOID:326 ischemia HGNC:392 Homo sapiens (human) 208 AKT2
  • MGI:6194238
DOID:0080388 nephrotic syndrome type 7 HGNC:2852 Homo sapiens (human) 8526 DGKE
  • RGD:7240710
DOID:0060041 autism spectrum disorder HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:25325218
DOID:8947 diabetic retinopathy HGNC:4323 Homo sapiens (human) 2739 GLO1
  • PMID:21738003
DOID:1485 cystic fibrosis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:20717938
DOID:4440 seminoma HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:10886088
DOID:1927 sphingolipidosis HGNC:735 Homo sapiens (human) 427 ASAH1
  • PMID:11241842
DOID:1485 cystic fibrosis HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:19466271
  • PMID:20302606

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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