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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 5176 - 5200 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:12783 migraine without aura RGD:2554 Rattus norvegicus (Norway rat) 24334 Eno2
  • MGI:6194238
DOID:0090001 Fraser syndrome HGNC:23399 Homo sapiens (human) 158326 FREM1
  • MGI:6194238
DOID:3328 temporal lobe epilepsy RGD:619850 Rattus norvegicus (Norway rat) 94203 Pgf
  • MGI:6194238
DOID:1289 neurodegenerative disease ZFIN:ZDB-GENE-020416-4 Danio rerio (zebrafish) 560753 tpi1b
  • MGI:6194238
DOID:11121 pulpitis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • MGI:6194238
DOID:1574 alcohol use disorder HGNC:4092 Homo sapiens (human) 2571 GAD1
  • MGI:6194238
DOID:0050912 colon adenoma FB:FBgn0026597 Drosophila melanogaster (fruit fly) 43565 Axn
  • MGI:6194238
DOID:0081292 traumatic brain injury MGI:98834 Mus musculus (house mouse) 22059 Trp53
  • MGI:6194238
DOID:0080108 myoglobinuria HGNC:13345 Homo sapiens (human) 23175 LPIN1
  • MGI:6194238
DOID:0070253 congenital disorder of glycosylation type IIa FB:FBgn0039738 Drosophila melanogaster (fruit fly) 43563 Mgat2 CG7921
  • MGI:6194238
DOID:9146 visceral leishmaniasis RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • MGI:6194238
DOID:13544 low tension glaucoma MGI:98834 Mus musculus (house mouse) 22059 Trp53
  • MGI:6194238
DOID:2355 anemia MGI:104798 Mus musculus (house mouse) 21926 Tnf
  • MGI:6194238
DOID:0050908 myelodysplastic syndrome RGD:3889 Rattus norvegicus (Norway rat) 24842 Tp53
  • MGI:6194238
DOID:0050559 Fukuyama congenital muscular dystrophy ZFIN:ZDB-GENE-070410-96 Danio rerio (zebrafish) 100006345 fktn
  • MGI:6194238
DOID:3635 congenital myasthenic syndrome HGNC:1912 Homo sapiens (human) 1103 CHAT
  • MGI:6194238
DOID:2739 Gilbert syndrome RGD:3935 Rattus norvegicus (Norway rat) 24861 Ugt1a1
  • MGI:6194238
DOID:3454 brain infarction MGI:96434 Mus musculus (house mouse) 16002 Igf2
  • MGI:6194238
DOID:0050560 Walker-Warburg syndrome MGI:2179507 Mus musculus (house mouse) 246179 Fktn
  • MGI:6194238
DOID:9261 nasopharynx carcinoma MGI:98834 Mus musculus (house mouse) 22059 Trp53
  • MGI:6194238
DOID:0080552 congenital disorder of glycosylation Ia RGD:2870 Rattus norvegicus (Norway rat) 24483 Igf2
  • MGI:6194238
DOID:10591 pre-eclampsia HGNC:6554 Homo sapiens (human) 3953 LEPR
  • MGI:6194238
DOID:10952 nephritis RGD:2053 Rattus norvegicus (Norway rat) 25591 Parp1
  • MGI:6194238
DOID:0110958 Gaucher's disease type II WB:WBGene00021160 Caenorhabditis elegans 177314 gba-4
  • MGI:6194238
DOID:854 collagen disease MGI:1341296 Mus musculus (house mouse) 21899 Tlr6
  • 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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