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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 71051 - 71075 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:3083 chronic obstructive pulmonary disease HGNC:12680 Homo sapiens (human) 7422 VEGFA
  • MGI:6194238
  • PMID:15681497
DOID:14499 Fabry disease WB:WBGene00011095 Caenorhabditis elegans 179660 gana-1
  • MGI:6194238
  • PMID:15676072
DOID:11984 hypertrophic cardiomyopathy HGNC:6501 Homo sapiens (human) 3920 LAMP2
  • MGI:6194238
  • PMID:15673802
  • PMID:16144992
DOID:14503 neuronal ceroid lipofuscinosis WB:WBGene00004092 Caenorhabditis elegans 191744 ppt-1
  • MGI:6194238
  • PMID:15672447
DOID:5844 myocardial infarction RGD:2493 Rattus norvegicus (Norway rat) 24310 Ace
  • MGI:6194238
  • PMID:15671045
  • PMID:21975128
  • PMID:23959549
DOID:0110030 alpha thalassemia-X-linked intellectual disability syndrome MGI:103067 Mus musculus (house mouse) 22589 Atrx
  • MGI:6194238
  • PMID:15668733
  • PMID:19088125
DOID:2349 arteriosclerosis RGD:2965 Rattus norvegicus (Norway rat) 25589 Kdr
  • MGI:6194238
  • PMID:15665766
DOID:0050741 alcohol dependence RGD:2677 Rattus norvegicus (Norway rat) 25453 Gdnf
  • MGI:6194238
  • PMID:15659598
  • PMID:19232578
  • PMID:24801661
DOID:12894 Sjogren's syndrome MGI:95484 Mus musculus (house mouse) 14102 Fas
  • MGI:6194238
  • PMID:1565490
  • PMID:17208228
  • PMID:7957574
  • PMID:8163351
DOID:0110052 amelogenesis imperfecta type 1B MGI:1333772 Mus musculus (house mouse) 13801 Enam
  • MGI:6194238
  • PMID:15649948
  • PMID:24603688
DOID:0110721 neuronal ceroid lipofuscinosis 1 MGI:1298204 Mus musculus (house mouse) 19063 Ppt1
  • MGI:6194238
  • PMID:15649713
  • PMID:22031903
  • PMID:25205113
DOID:0111035 CADASIL 1 MGI:99460 Mus musculus (house mouse) 18131 Notch3
  • MGI:6194238
  • PMID:15645445
  • PMID:21940951
  • PMID:25917818
  • PMID:26563570
DOID:10763 hypertension HGNC:1029 Homo sapiens (human) 623 BDKRB1
  • MGI:6194238
  • PMID:15643125
DOID:0090078 hypogonadotropic hypogonadism 7 with or without anosmia MGI:95790 Mus musculus (house mouse) 14715 Gnrhr
  • MGI:6194238
  • PMID:15625238
DOID:3012 Li-Fraumeni syndrome MGI:98834 Mus musculus (house mouse) 22059 Trp53
  • MGI:6194238
  • PMID:15607980
  • PMID:15607981
  • PMID:7922305
DOID:0090004 progressive pseudorheumatoid arthropathy of childhood MGI:2685581 Mus musculus (house mouse) 327743 Ccn6
  • MGI:6194238
  • PMID:15601861
  • PMID:24040393
DOID:8893 psoriasis MGI:103038 Mus musculus (house mouse) 20848 Stat3
  • MGI:6194238
  • PMID:15592573
DOID:0110826 Usher syndrome type 1 HGNC:7606 Homo sapiens (human) 4647 MYO7A
  • MGI:6194238
  • PMID:15592175
DOID:3883 Lynch syndrome HGNC:7329 Homo sapiens (human) 2956 MSH6
  • MGI:6194238
  • PMID:15571801
  • PMID:28218421
  • PMID:7604266
DOID:0050700 cardiomyopathy HGNC:7577 Homo sapiens (human) 4625 MYH7
  • MGI:6194238
  • PMID:15556047
DOID:850 lung disease HGNC:6018 Homo sapiens (human) 3569 IL6
  • MGI:6194238
  • PMID:15547537
DOID:9352 type 2 diabetes mellitus HGNC:11283 Homo sapiens (human) 6714 SRC
  • MGI:6194238
  • PMID:15542065
DOID:0080652 calcium oxalate nephrolithiasis RGD:2102 Rattus norvegicus (Norway rat) 25377 Ambp
  • MGI:6194238
  • PMID:15533056
DOID:0060062 familial juvenile hyperuricemic nephropathy MGI:102674 Mus musculus (house mouse) 22242 Umod
  • MGI:6194238
  • PMID:15522986
  • PMID:20472742
DOID:5844 myocardial infarction HGNC:286 Homo sapiens (human) 154 ADRB2
  • MGI:6194238
  • PMID:15520258

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Last updated: December 9, 2024