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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 6826 - 6850 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:13608 biliary atresia HGNC:4250 Homo sapiens (human) 2678 GGT1
  • PMID:29056230
DOID:2913 acute pancreatitis HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
DOID:1062 Fanconi syndrome HGNC:11006 Homo sapiens (human) 6514 SLC2A2
  • RGD:7240710
DOID:6000 congestive heart failure HGNC:11009 Homo sapiens (human) 6517 SLC2A4
  • PMID:18778861
DOID:11446 sciatic neuropathy HGNC:14076 Homo sapiens (human) 29956 CERS2
  • MGI:6194238
DOID:10825 essential hypertension HGNC:9603 Homo sapiens (human) 5740 PTGIS
  • RGD:7240710
DOID:1287 cardiovascular system disease HGNC:3356 Homo sapiens (human) 5167 ENPP1
  • PMID:21282363
DOID:9744 type 1 diabetes mellitus HGNC:3575 Homo sapiens (human) 9415 FADS2
  • MGI:6194238
DOID:104 bacterial infectious disease HGNC:11022 Homo sapiens (human) 7355 SLC35A2
  • MGI:6194238
DOID:0112315 brain small vessel disease 3 HGNC:26182 Homo sapiens (human) 79709 COLGALT1
  • RGD:7240710
DOID:14227 azoospermia HGNC:7682 Homo sapiens (human) 9348 NDST3
  • MGI:6194238
DOID:1596 depressive disorder HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • MGI:6194238
DOID:3146 lipid metabolism disorder HGNC:4803 Homo sapiens (human) 3032 HADHB
  • MGI:6194238
DOID:13359 Ehlers-Danlos syndrome HGNC:2705 Homo sapiens (human) 1634 DCN
  • MGI:6194238
DOID:0110657 congenital myasthenic syndrome 8 HGNC:329 Homo sapiens (human) 375790 AGRN
  • MGI:6194238
  • RGD:7240710
DOID:10763 hypertension HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • MGI:6194238
DOID:0050833 orotic aciduria HGNC:12563 Homo sapiens (human) 7372 UMPS
  • MGI:6194238
  • RGD:7240710
DOID:12930 dilated cardiomyopathy HGNC:17997 Homo sapiens (human) 79147 FKRP
  • PMID:15833432
DOID:9408 acute myocardial infarction HGNC:5998 Homo sapiens (human) 9173 IL1RL1
  • MGI:6194238
DOID:2747 glycogen storage disease HGNC:8931 Homo sapiens (human) 5261 PHKG2
  • MGI:6194238
  • PMID:8896567
DOID:10534 stomach cancer HGNC:1119 Homo sapiens (human) 684 BST2
  • PMID:26832883
DOID:0050648 atelosteogenesis HGNC:10994 Homo sapiens (human) 1836 SLC26A2
  • RGD:7240710
DOID:5419 schizophrenia HGNC:9232 Homo sapiens (human) 5465 PPARA
  • MGI:6194238
DOID:11650 bronchopulmonary dysplasia HGNC:2666 Homo sapiens (human) 1605 DAG1
  • PMID:17196572
DOID:3121 gallbladder cancer HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:18287863
  • PMID:18990008

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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