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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 October 9, 2024
Displaying entries 69476 - 69500 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:1574 alcohol use disorder RGD:69426 Rattus norvegicus (Norway rat) 29335 Oprk1
  • MGI:6194238
  • PMID:28511993
DOID:1574 alcohol use disorder RGD:3233 Rattus norvegicus (Norway rat) 24613 Oprd1
  • MGI:6194238
  • PMID:28511993
  • PMID:7501658
DOID:13133 HELLP syndrome RGD:619831 Rattus norvegicus (Norway rat) 246097 Fas
  • MGI:6194238
  • PMID:28501275
DOID:13133 HELLP syndrome RGD:3880 Rattus norvegicus (Norway rat) 25385 Faslg
  • MGI:6194238
  • PMID:28501275
DOID:10652 Alzheimer's disease FB:FBgn0039234 Drosophila melanogaster (fruit fly) 42964 Nct
  • MGI:6194238
  • PMID:28495961
DOID:11252 microcytic anemia MGI:109547 Mus musculus (house mouse) 13430 Dnm2
  • MGI:6194238
  • PMID:28466468
DOID:0080312 neurodevelopmental disorder with midbrain and hindbrain malformations MGI:103264 Mus musculus (house mouse) 16800 Arhgef2
  • MGI:6194238
  • PMID:28453519
DOID:1596 depressive disorder HGNC:1963 Homo sapiens (human) 1142 CHRNB3
  • MGI:6194238
  • PMID:28420875
DOID:1596 depressive disorder RGD:621544 Rattus norvegicus (Norway rat) 171131 Chrnb3
  • MGI:6194238
  • PMID:28420875
DOID:0110673 congenital myasthenic syndrome 19 MGI:1277201 Mus musculus (house mouse) 12817 Col13a1
  • MGI:6194238
  • PMID:28369367
DOID:0080092 myofibrillar myopathy 1 HGNC:2770 Homo sapiens (human) 1674 DES
  • MGI:6194238
  • PMID:28341603
  • RGD:7240710
DOID:12801 mucopolysaccharidosis III MGI:1922862 Mus musculus (house mouse) 75612 Gns
  • MGI:6194238
  • PMID:28334745
DOID:10652 Alzheimer's disease HGNC:8824 Homo sapiens (human) 5176 SERPINF1
  • MGI:6194238
  • PMID:28320113
DOID:0110279 autosomal recessive limb-girdle muscular dystrophy type 2E HGNC:10806 Homo sapiens (human) 6443 SGCB
  • MGI:6194238
  • PMID:28284983
  • RGD:7240710
DOID:0111042 glycogen storage disease IXa HGNC:8926 Homo sapiens (human) 5256 PHKA2
  • MGI:6194238
  • PMID:28283841
  • PMID:28627441
  • PMID:8733134
  • RGD:7240710
DOID:9452 steatotic liver disease RGD:3000 Rattus norvegicus (Norway rat) 25608 Lep
  • MGI:6194238
  • PMID:28281237
DOID:9452 steatotic liver disease HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
  • PMID:28281237
DOID:10652 Alzheimer's disease RGD:70514 Rattus norvegicus (Norway rat) 140908 Cdk5
  • MGI:6194238
  • PMID:28269780
DOID:0080195 Marinesco-Sjogren syndrome SGD:S000005391 Saccharomyces cerevisiae S288C 854126 SIL1
  • MGI:6194238
  • PMID:28257000
DOID:898 autosomal dominant polycystic kidney disease MGI:1099818 Mus musculus (house mouse) 18764 Pkd2
  • MGI:6194238
  • PMID:28244683
DOID:3883 Lynch syndrome HGNC:7127 Homo sapiens (human) 4292 MLH1
  • MGI:6194238
  • PMID:28218421
DOID:684 hepatocellular carcinoma HGNC:583 Homo sapiens (human) 324 APC
  • MGI:6194238
  • PMID:28203651
  • RGD:7240710
DOID:6432 pulmonary hypertension RGD:631365 Rattus norvegicus (Norway rat) 297508 Nampt
  • MGI:6194238
  • PMID:28202489
DOID:6432 pulmonary hypertension HGNC:30092 Homo sapiens (human) 10135 NAMPT
  • MGI:6194238
  • PMID:28202489
DOID:0070113 Niemann-Pick disease type C1 MGI:1097712 Mus musculus (house mouse) 18145 Npc1
  • MGI:6194238
  • PMID:28167839

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Last updated: December 9, 2024