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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 151 - 175 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:874 bacterial pneumonia HGNC:10803 Homo sapiens (human) 6441 SFTPD
  • MGI:6194238
  • PMID:15271694
DOID:1184 nephrotic syndrome HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • MGI:6194238
  • PMID:15292677
DOID:83 cataract HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
  • PMID:15295623
DOID:2841 asthma HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
  • PMID:15316498
  • PMID:17573729
  • PMID:18489027
  • PMID:19862936
DOID:11721 glycogen storage disease VII HGNC:8877 Homo sapiens (human) 5213 PFKM
  • MGI:6194238
  • PMID:1533013
  • RGD:7240710
DOID:0110728 neuronal ceroid lipofuscinosis 5 MGI:2442253 Mus musculus (house mouse) 211286 Cln5
  • MGI:6194238
  • PMID:15459177
DOID:0110644 long QT syndrome 1 MGI:108083 Mus musculus (house mouse) 16535 Kcnq1
  • MGI:6194238
  • PMID:15498462
DOID:12800 mucopolysaccharidosis VI HGNC:714 Homo sapiens (human) 411 ARSB
  • MGI:6194238
  • PMID:1550123
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:20147 Homo sapiens (human) 51167 CYB5R4
  • MGI:6194238
  • PMID:15504981
DOID:12799 mucopolysaccharidosis II HGNC:5389 Homo sapiens (human) 3423 IDS
  • MGI:6194238
  • PMID:1550586
  • PMID:27146977
  • RGD:7240710
DOID:10652 Alzheimer's disease HGNC:4141 Homo sapiens (human) 2597 GAPDH
  • MGI:6194238
  • PMID:15507493
  • PMID:17387692
  • PMID:18340469
  • PMID:20864222
  • PMID:28087189
DOID:3012 Li-Fraumeni syndrome MGI:98834 Mus musculus (house mouse) 22059 Trp53
  • MGI:6194238
  • PMID:15607980
  • PMID:15607981
  • PMID:7922305
DOID:3322 GM1 gangliosidosis MGI:88151 Mus musculus (house mouse) 12091 Glb1
  • MGI:6194238
  • PMID:15687347
  • PMID:9063740
  • PMID:9071485
  • PMID:9337086
DOID:8584 Burkitt lymphoma MGI:97250 Mus musculus (house mouse) 17869 Myc
  • MGI:6194238
  • PMID:15687498
DOID:9352 type 2 diabetes mellitus HGNC:6081 Homo sapiens (human) 3630 INS
  • MGI:6194238
  • PMID:1569197
  • PMID:3322910
DOID:9352 type 2 diabetes mellitus HGNC:4195 Homo sapiens (human) 2645 GCK
  • MGI:6194238
  • PMID:1570017
  • PMID:8200206
  • PMID:8314445
  • PMID:8325445
  • RGD:7240710
DOID:2741 bilirubin metabolic disorder RGD:3935 Rattus norvegicus (Norway rat) 24861 Ugt1a1
  • MGI:6194238
  • PMID:15753292
DOID:13088 periventricular leukomalacia RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • MGI:6194238
  • PMID:15765524
DOID:9970 obesity HGNC:5209 Homo sapiens (human) 3291 HSD11B2
  • MGI:6194238
  • PMID:15793240
DOID:10588 adrenoleukodystrophy HGNC:29567 Homo sapiens (human) 23205 ACSBG1
  • MGI:6194238
  • PMID:15800013
DOID:684 hepatocellular carcinoma HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
  • PMID:15800977
  • PMID:24720952
  • PMID:24759835
DOID:0060867 macrocephaly-autism syndrome HGNC:9588 Homo sapiens (human) 5728 PTEN
  • MGI:6194238
  • PMID:15805158
  • RGD:7240710
DOID:4450 renal cell carcinoma HGNC:9588 Homo sapiens (human) 5728 PTEN
  • MGI:6194238
  • PMID:15821467
  • PMID:17681738
  • PMID:17886097
DOID:0060887 ossification of the posterior longitudinal ligament of spine HGNC:3356 Homo sapiens (human) 5167 ENPP1
  • MGI:6194238
  • PMID:15834329
DOID:0050559 Fukuyama congenital muscular dystrophy MGI:2179507 Mus musculus (house mouse) 246179 Fktn
  • MGI:6194238
  • PMID:15837576
  • PMID:19017726
  • PMID:22922256

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: August 19, 2024