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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 71401 - 71425 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:2152 ovary epithelial cancer HGNC:9599 Homo sapiens (human) 9536 PTGES
  • PMID:17107625
DOID:289 endometriosis HGNC:9599 Homo sapiens (human) 9536 PTGES
  • PMID:17295901
DOID:9206 Barrett's esophagus HGNC:9599 Homo sapiens (human) 9536 PTGES
  • MGI:6194238
DOID:8719 in situ carcinoma HGNC:9599 Homo sapiens (human) 9536 PTGES
  • PMID:14499677
  • PMID:14871981
DOID:2671 transitional cell carcinoma HGNC:9599 Homo sapiens (human) 9536 PTGES
  • MGI:6194238
  • PMID:14499677
DOID:13976 peptic esophagitis HGNC:9599 Homo sapiens (human) 9536 PTGES
  • MGI:6194238
DOID:2870 endometrial adenocarcinoma HGNC:9599 Homo sapiens (human) 9536 PTGES
  • PMID:11592775
DOID:2615 papilloma HGNC:9599 Homo sapiens (human) 9536 PTGES
  • MGI:6194238
DOID:11624 penile benign neoplasm HGNC:9599 Homo sapiens (human) 9536 PTGES
  • PMID:14871981
DOID:326 ischemia HGNC:9599 Homo sapiens (human) 9536 PTGES
  • MGI:6194238
DOID:0060074 ductal carcinoma in situ HGNC:9599 Homo sapiens (human) 9536 PTGES
  • PMID:16353170
DOID:5082 liver cirrhosis HGNC:3364 Homo sapiens (human) 954 ENTPD2
  • PMID:15651265
DOID:10763 hypertension HGNC:3364 Homo sapiens (human) 954 ENTPD2
  • MGI:6194238
DOID:12236 primary biliary cholangitis HGNC:3364 Homo sapiens (human) 954 ENTPD2
  • PMID:15651265
DOID:3070 high grade glioma HGNC:3364 Homo sapiens (human) 954 ENTPD2
  • PMID:19558578
DOID:14330 Parkinson's disease HGNC:10700 Homo sapiens (human) 9554 SEC22B
  • MGI:6194238
DOID:0050908 myelodysplastic syndrome HGNC:4740 Homo sapiens (human) 9555 MACROH2A1
  • MGI:6194238
DOID:1319 brain cancer HGNC:12711 Homo sapiens (human) 9559 VPS26A
  • MGI:6194238
DOID:8947 diabetic retinopathy HGNC:12711 Homo sapiens (human) 9559 VPS26A
  • PMID:28821857
DOID:9352 type 2 diabetes mellitus HGNC:12711 Homo sapiens (human) 9559 VPS26A
  • PMID:27281273
DOID:0112333 pontocerebellar hypoplasia type 16 HGNC:7102 Homo sapiens (human) 9562 MINPP1
  • RGD:7240710
DOID:3969 thyroid gland papillary carcinoma HGNC:7102 Homo sapiens (human) 9562 MINPP1
  • RGD:7240710
DOID:2377 multiple sclerosis HGNC:4795 Homo sapiens (human) 9563 H6PD
  • PMID:19935835
DOID:0090139 cortisone reductase deficiency HGNC:4795 Homo sapiens (human) 9563 H6PD
  • PMID:12858176
DOID:0090141 cortisone reductase deficiency 1 HGNC:4795 Homo sapiens (human) 9563 H6PD
  • RGD:7240710

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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