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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 12051 - 12075 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
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:9352 type 2 diabetes mellitus HGNC:6081 Homo sapiens (human) 3630 INS
  • MGI:6194238
  • PMID:1569197
  • PMID:3322910
DOID:8584 Burkitt lymphoma MGI:97250 Mus musculus (house mouse) 17869 Myc
  • MGI:6194238
  • PMID:15687498
DOID:3322 GM1 gangliosidosis MGI:88151 Mus musculus (house mouse) 12091 Glb1
  • MGI:6194238
  • PMID:15687347
  • PMID:9063740
  • PMID:9071485
  • PMID:9337086
DOID:3012 Li-Fraumeni syndrome MGI:98834 Mus musculus (house mouse) 22059 Trp53
  • MGI:6194238
  • PMID:15607980
  • PMID:15607981
  • PMID:7922305
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:12799 mucopolysaccharidosis II HGNC:5389 Homo sapiens (human) 3423 IDS
  • MGI:6194238
  • PMID:1550586
  • PMID:27146977
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:20147 Homo sapiens (human) 51167 CYB5R4
  • MGI:6194238
  • PMID:15504981
DOID:12800 mucopolysaccharidosis VI HGNC:714 Homo sapiens (human) 411 ARSB
  • MGI:6194238
  • PMID:1550123
  • RGD:7240710
DOID:0110644 long QT syndrome 1 MGI:108083 Mus musculus (house mouse) 16535 Kcnq1
  • MGI:6194238
  • PMID:15498462
DOID:0110728 neuronal ceroid lipofuscinosis 5 MGI:2442253 Mus musculus (house mouse) 211286 Cln5
  • MGI:6194238
  • PMID:15459177
DOID:11721 glycogen storage disease VII HGNC:8877 Homo sapiens (human) 5213 PFKM
  • MGI:6194238
  • PMID:1533013
  • RGD:7240710
DOID:2841 asthma HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
  • PMID:15316498
  • PMID:17573729
  • PMID:18489027
  • PMID:19862936
DOID:83 cataract HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
  • PMID:15295623
DOID:1184 nephrotic syndrome HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • MGI:6194238
  • PMID:15292677
DOID:874 bacterial pneumonia HGNC:10803 Homo sapiens (human) 6441 SFTPD
  • MGI:6194238
  • PMID:15271694
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • MGI:6194238
  • PMID:15239085
  • PMID:18713296
  • PMID:22269154
  • PMID:26042596
  • PMID:27860427
DOID:9352 type 2 diabetes mellitus HGNC:392 Homo sapiens (human) 208 AKT2
  • MGI:6194238
  • PMID:15166380
  • PMID:18204829
  • PMID:18972094
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus RGD:2670 Rattus norvegicus (Norway rat) 24385 Gck
  • MGI:6194238
  • PMID:15138155
  • PMID:22234649
DOID:4483 rhinitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
  • PMID:15120189
DOID:10763 hypertension HGNC:12518 Homo sapiens (human) 7351 UCP2
  • MGI:6194238
  • PMID:15106800
DOID:0111100 maturity-onset diabetes of the young type 2 MGI:1270854 Mus musculus (house mouse) 103988 Gck
  • MGI:6194238
  • PMID:15102714
  • PMID:15161764
  • PMID:15569412
  • PMID:17353190
  • PMID:19952346
  • PMID:24447392
  • PMID:7553875
  • PMID:7665557
  • PMID:8530440
  • PMID:9867845
DOID:0050741 alcohol dependence RGD:61800 Rattus norvegicus (Norway rat) 29595 Htr2a
  • MGI:6194238
  • PMID:15080502
  • PMID:8822536
DOID:0050770 polycystic liver disease HGNC:9411 Homo sapiens (human) 5589 PRKCSH
  • MGI:6194238
  • PMID:15057895
  • RGD:7240710
DOID:10581 metachromatic leukodystrophy HGNC:713 Homo sapiens (human) 410 ARSA
  • MGI:6194238
  • PMID:15026521
  • PMID:15375602
  • RGD:7240710

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: August 19, 2024