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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 1676 - 1700 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence Code Names References
DOID:9884 muscular dystrophy MGI:88459 Mus musculus (house mouse) 12833 Col6a1
  • MGI:6194238
DOID:0060759 immunodeficiency with hyper IgM type 5 HGNC:12572 Homo sapiens (human) 7374 UNG
  • RGD:7240710
DOID:9351 diabetes mellitus MGI:95593 Mus musculus (house mouse) 71665 Fuca1
  • MGI:6194238
DOID:178 vascular disease MGI:106675 Mus musculus (house mouse) 11450 Adipoq
  • MGI:6194238
DOID:684 hepatocellular carcinoma HGNC:6554 Homo sapiens (human) 3953 LEPR
  • PMID:23090836
DOID:206 hereditary multiple exostoses Xenbase:XB-GENE-17332106 Xenopus laevis (African clawed frog) 398214 ext1.L
  • MGI:6194238
DOID:674 cleft palate HGNC:10659 Homo sapiens (human) 6383 SDC2
  • PMID:18716610
DOID:3393 coronary artery disease WB:WBGene00000503 Caenorhabditis elegans 180628 cht-1
  • MGI:6194238
DOID:1793 pancreatic cancer MGI:1347050 Mus musculus (house mouse) 26358 Aldh1a7
  • MGI:6194238
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:2394 ovarian cancer RGD:2081 Rattus norvegicus (Norway rat) 24185 Akt1
  • MGI:6194238
DOID:11716 prediabetes syndrome RGD:69247 Rattus norvegicus (Norway rat) 83535 Kcnj11
  • PMID:18001323
DOID:0080556 congenital disorder of glycosylation Id RGD:1306004 Rattus norvegicus (Norway rat) 287983 Alg3
  • MGI:6194238
DOID:8947 diabetic retinopathy MGI:106675 Mus musculus (house mouse) 11450 Adipoq
  • MGI:6194238
DOID:6039 uveal melanoma MGI:1333850 Mus musculus (house mouse) 17193 Mbd4
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I WB:WBGene00022044 Caenorhabditis elegans 176874 dpm-1
  • MGI:6194238
DOID:8778 Crohn's disease FB:FBgn0040256 Drosophila melanogaster (fruit fly) 53507 Ugt35C1
  • MGI:6194238
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:14250 Down syndrome RGD:1307334 Rattus norvegicus (Norway rat) 309686 Pofut2
  • MGI:6194238
DOID:0111458 galactose epimerase deficiency WB:WBGene00008132 Caenorhabditis elegans 173171 gale-1
  • MGI:6194238
DOID:9119 acute myeloid leukemia WB:WBGene00000503 Caenorhabditis elegans 180628 cht-1
  • MGI:6194238

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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