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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 11951 - 11975 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:3650 lactic acidosis RGD:620687 Rattus norvegicus (Norway rat) 64035 Pygl
  • MGI:6194238
  • PMID:17705025
DOID:2754 glycogen storage disease VI RGD:620687 Rattus norvegicus (Norway rat) 64035 Pygl
  • MGI:6194238
  • PMID:17705025
  • PMID:21646031
DOID:2754 glycogen storage disease VI HGNC:9725 Homo sapiens (human) 5836 PYGL
  • MGI:6194238
  • PMID:17705025
  • PMID:21646031
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:11006 Homo sapiens (human) 6514 SLC2A2
  • MGI:6194238
  • PMID:17636114
  • PMID:8027028
  • RGD:7240710
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:16940 Homo sapiens (human) 84649 DGAT2
  • MGI:6194238
  • PMID:17618857
DOID:0110184 Charcot-Marie-Tooth disease type 4J SGD:S000005269 Saccharomyces cerevisiae S288C 855392 FIG4
  • MGI:6194238
  • PMID:17572665
DOID:684 hepatocellular carcinoma RGD:2870 Rattus norvegicus (Norway rat) 24483 Igf2
  • MGI:6194238
  • PMID:17554210
DOID:12716 newborn respiratory distress syndrome HGNC:10803 Homo sapiens (human) 6441 SFTPD
  • MGI:6194238
  • PMID:17524024
DOID:83 cataract RGD:2092 Rattus norvegicus (Norway rat) 24192 Akr1b1
  • MGI:6194238
  • PMID:17444799
  • PMID:18452283
DOID:13317 hyperinsulinemic hypoglycemia MGI:1270854 Mus musculus (house mouse) 103988 Gck
  • MGI:6194238
  • PMID:17353190
DOID:10652 Alzheimer's disease RGD:2661 Rattus norvegicus (Norway rat) 24383 Gapdh
  • MGI:6194238
  • PMID:17324518
DOID:9970 obesity HGNC:9922 Homo sapiens (human) 5950 RBP4
  • MGI:6194238
  • PMID:17292720
DOID:10763 hypertension HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
  • PMID:17283861
DOID:9352 type 2 diabetes mellitus HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • MGI:6194238
  • PMID:17259403
  • PMID:19498446
  • PMID:19502414
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus RGD:3267 Rattus norvegicus (Norway rat) 362282 Pck1
  • MGI:6194238
  • PMID:17242918
DOID:206 hereditary multiple exostoses WB:WBGene00004360 Caenorhabditis elegans 178080 rib-1
  • MGI:6194238
  • PMID:17237233
DOID:10763 hypertension HGNC:4553 Homo sapiens (human) 2876 GPX1
  • MGI:6194238
  • PMID:17198913
DOID:9352 type 2 diabetes mellitus HGNC:9922 Homo sapiens (human) 5950 RBP4
  • MGI:6194238
  • PMID:17174134
  • PMID:17875187
  • PMID:18496666
  • PMID:18973209
  • PMID:19506831
  • PMID:20058618
  • PMID:20436266
  • PMID:21645024
  • PMID:24647386
DOID:9970 obesity HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
  • PMID:17164796
DOID:9352 type 2 diabetes mellitus RGD:620925 Rattus norvegicus (Norway rat) 83516 Ppargc1a
  • MGI:6194238
  • PMID:17158179
  • PMID:22824914
DOID:10763 hypertension HGNC:2228 Homo sapiens (human) 1312 COMT
  • MGI:6194238
  • PMID:17143180
DOID:4195 hyperglycemia HGNC:6107 Homo sapiens (human) 3651 PDX1
  • MGI:6194238
  • PMID:17131142
DOID:9352 type 2 diabetes mellitus HGNC:6554 Homo sapiens (human) 3953 LEPR
  • MGI:6194238
  • PMID:17065694
  • PMID:18439701
  • PMID:22215535
DOID:1926 Gaucher's disease HGNC:4177 Homo sapiens (human) 2629 GBA1
  • MGI:6194238
  • PMID:17059888
  • PMID:18586596
  • PMID:21112800
DOID:2861 congenital nonspherocytic hemolytic anemia HGNC:4458 Homo sapiens (human) 2821 GPI
  • MGI:6194238
  • PMID:17041899
  • PMID:9446754

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