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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 4001 - 4025 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:684 hepatocellular carcinoma HGNC:2468 Homo sapiens (human) 9126 SMC3
  • PMID:29996118
DOID:1059 intellectual disability HGNC:2468 Homo sapiens (human) 9126 SMC3
  • PMID:25655089
DOID:0080507 Cornelia de Lange syndrome 3 HGNC:2468 Homo sapiens (human) 9126 SMC3
  • MGI:6194238
  • RGD:7240710
DOID:684 hepatocellular carcinoma FB:FBgn0015615 Drosophila melanogaster (fruit fly) 32627 SMC3
  • MGI:6194238
DOID:9432 renal glycosuria HGNC:11037 Homo sapiens (human) 6524 SLC5A2
  • PMID:12436245
  • PMID:14614622
  • RGD:7240710
DOID:10763 hypertension HGNC:11037 Homo sapiens (human) 6524 SLC5A2
  • MGI:6194238
DOID:0080899 lung pleomorphic carcinoma HGNC:11026 Homo sapiens (human) 6520 SLC3A2
  • PMID:30300664
DOID:2671 transitional cell carcinoma HGNC:11026 Homo sapiens (human) 6520 SLC3A2
  • MGI:6194238
DOID:0050865 tongue squamous cell carcinoma HGNC:11026 Homo sapiens (human) 6520 SLC3A2
  • PMID:24762957
DOID:0080202 adenoid cystic carcinoma HGNC:11026 Homo sapiens (human) 6520 SLC3A2
  • PMID:23516127
DOID:3908 lung non-small cell carcinoma HGNC:11026 Homo sapiens (human) 6520 SLC3A2
  • PMID:22110199
  • PMID:24782339
  • PMID:25084765
DOID:5517 stomach carcinoma HGNC:11026 Homo sapiens (human) 6520 SLC3A2
  • PMID:29179459
DOID:3910 lung adenocarcinoma HGNC:11026 Homo sapiens (human) 6520 SLC3A2
  • PMID:19171406
DOID:9266 cystinuria HGNC:11025 Homo sapiens (human) 6519 SLC3A1
  • MGI:6194238
  • PMID:8054986
  • RGD:7240710
DOID:0060480 left ventricular noncompaction HGNC:20862 Homo sapiens (human) 64116 SLC39A8
  • MGI:6194238
DOID:0070266 congenital disorder of glycosylation type IIn HGNC:20862 Homo sapiens (human) 64116 SLC39A8
  • RGD:7240710
DOID:0060250 idiopathic scoliosis HGNC:20862 Homo sapiens (human) 64116 SLC39A8
  • MGI:6194238
DOID:0080537 hypermanganesemia with dystonia 2 HGNC:20858 Homo sapiens (human) 23516 SLC39A14
  • RGD:7240710
DOID:2749 glycogen storage disease Ia HGNC:4061 Homo sapiens (human) 2542 SLC37A4
  • MGI:6194238
DOID:0081330 glycogen storage disease Ib HGNC:4061 Homo sapiens (human) 2542 SLC37A4
  • PMID:9428641
  • RGD:7240710
DOID:0081331 glycogen storage disease Ic HGNC:4061 Homo sapiens (human) 2542 SLC37A4
  • RGD:7240710
DOID:0050571 congenital disorder of glycosylation type II HGNC:4061 Homo sapiens (human) 2542 SLC37A4
  • RGD:7240710
DOID:0050775 schneckenbecken dysplasia HGNC:20800 Homo sapiens (human) 23169 SLC35D1
  • MGI:6194238
  • RGD:7240710
DOID:0050571 congenital disorder of glycosylation type II HGNC:20197 Homo sapiens (human) 55343 SLC35C1
  • MGI:6194238
DOID:0070255 congenital disorder of glycosylation type IIc HGNC:20197 Homo sapiens (human) 55343 SLC35C1
  • MGI:6194238
  • PMID:11326280
  • RGD:7240710

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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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