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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 7651 - 7675 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
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
DOID:7148 rheumatoid arthritis HGNC:6021 Homo sapiens (human) 3572 IL6ST
  • MGI:6194238
DOID:1459 hypothyroidism WB:WBGene00000833 Caenorhabditis elegans 176437 cts-1
  • MGI:6194238
DOID:10652 Alzheimer's disease WB:WBGene00016204 Caenorhabditis elegans 183000 gsto-1
  • MGI:6194238
DOID:863 nervous system disease MGI:88107 Mus musculus (house mouse) 232975 Atp1a3
  • MGI:6194238
DOID:0050565 autosomal recessive nonsyndromic deafness Xenbase:XB-GENE-6488174 Xenopus laevis (African clawed frog) 108708472 tmtc4.L
  • MGI:6194238
DOID:4988 alcoholic pancreatitis MGI:3576092 Mus musculus (house mouse) 394434 Ugt1a9
  • MGI:6194238
DOID:0050802 Ehlers-Danlos syndrome spondylodysplastic type 2 Xenbase:XB-GENE-6488390 Xenopus laevis (African clawed frog) 108696563 b3galt6.L
  • MGI:6194238
DOID:0111225 centronuclear myopathy X-linked HGNC:7450 Homo sapiens (human) 8898 MTMR2
  • 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