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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 126 - 150 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:8947 diabetic retinopathy WB:WBGene00001683 Caenorhabditis elegans 174603 gpd-1
  • MGI:6194238
DOID:0110296 autosomal recessive limb-girdle muscular dystrophy type 2M WB:WBGene00020307 Caenorhabditis elegans 173469 T07D3.4
  • MGI:6194238
DOID:2861 congenital nonspherocytic hemolytic anemia WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238
DOID:9884 muscular dystrophy WB:WBGene00020307 Caenorhabditis elegans 173469 T07D3.4
  • MGI:6194238
DOID:3211 lysosomal storage disease WB:WBGene00020509 Caenorhabditis elegans 180533 hex-1
  • MGI:6194238
DOID:0080855 Parkinsonism WB:WBGene00008706 Caenorhabditis elegans 178535 gba-3
  • MGI:6194238
DOID:9279 hyperhomocysteinemia WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238
DOID:13276 Mycoplasma pneumoniae pneumonia WB:WBGene00016207 Caenorhabditis elegans 183002 C29E4.10
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I WB:WBGene00007464 Caenorhabditis elegans 174542 algn-8
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus WB:WBGene00000503 Caenorhabditis elegans 180628 cht-1
  • MGI:6194238
DOID:3525 middle cerebral artery infarction WB:WBGene00001685 Caenorhabditis elegans 180601 gpd-3
  • MGI:6194238
DOID:0080411 familial adenomatous polyposis 3 WB:WBGene00011201 Caenorhabditis elegans 187770 nth-1
  • MGI:6194238
DOID:0060713 autosomal recessive congenital ichthyosis 4B WB:WBGene00008431 Caenorhabditis elegans 174386 piga-1
  • MGI:6194238
DOID:1793 pancreatic cancer WB:WBGene00044303 Caenorhabditis elegans 3564879 hst-3.2
  • MGI:6194238
DOID:2741 bilirubin metabolic disorder WB:WBGene00010904 Caenorhabditis elegans 175591 ugt-62
  • MGI:6194238
DOID:0110444 dilated cardiomyopathy 1X WB:WBGene00020924 Caenorhabditis elegans 189104 W02B3.4
  • MGI:6194238
DOID:0110284 autosomal recessive limb-girdle muscular dystrophy type 2L WB:WBGene00020307 Caenorhabditis elegans 173469 T07D3.4
  • MGI:6194238
DOID:6000 congestive heart failure WB:WBGene00000503 Caenorhabditis elegans 180628 cht-1
  • MGI:6194238
DOID:0112250 Gaucher's disease type IIIC WB:WBGene00008706 Caenorhabditis elegans 178535 gba-3
  • MGI:6194238
DOID:0110957 Gaucher's disease type I WB:WBGene00008706 Caenorhabditis elegans 178535 gba-3
  • MGI:6194238
DOID:7998 hyperthyroidism WB:WBGene00010904 Caenorhabditis elegans 175591 ugt-62
  • MGI:6194238
DOID:206 hereditary multiple exostoses WB:WBGene00004361 Caenorhabditis elegans 176502 rib-2
  • PMID:17237233
DOID:12217 Lewy body dementia WB:WBGene00016340 Caenorhabditis elegans 183155 gba-2
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I WB:WBGene00007435 Caenorhabditis elegans 182392 algn-6
  • MGI:6194238
DOID:12783 migraine without aura WB:WBGene00011884 Caenorhabditis elegans 174423 enol-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