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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 12101 - 12125 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:13628 favism MGI:105979 Mus musculus (house mouse) 14381 G6pdx
  • MGI:6194238
  • PMID:12777375
  • PMID:14751857
  • PMID:3377761
DOID:0111103 maturity-onset diabetes of the young type 4 MGI:102851 Mus musculus (house mouse) 18609 Pdx1
  • MGI:6194238
  • PMID:12697734
DOID:4947 cholangiocarcinoma HGNC:1097 Homo sapiens (human) 673 BRAF
  • MGI:6194238
  • PMID:12692057
DOID:9970 obesity HGNC:392 Homo sapiens (human) 208 AKT2
  • MGI:6194238
  • PMID:12663464
DOID:9352 type 2 diabetes mellitus HGNC:417 Homo sapiens (human) 229 ALDOB
  • MGI:6194238
  • PMID:12646233
DOID:5419 schizophrenia RGD:70982 Rattus norvegicus (Norway rat) 84027 Gsk3b
  • MGI:6194238
  • PMID:12644246
DOID:11476 osteoporosis RGD:3000 Rattus norvegicus (Norway rat) 25608 Lep
  • MGI:6194238
  • PMID:12609558
  • PMID:24250662
DOID:9352 type 2 diabetes mellitus HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
  • PMID:12606537
  • PMID:18162502
  • PMID:18270681
  • PMID:23210442
  • PMID:23251491
DOID:9352 type 2 diabetes mellitus MGI:2153588 Mus musculus (house mouse) 140491 Ppp1r3a
  • MGI:6194238
  • PMID:12606498
DOID:0050852 limb ischemia HGNC:9603 Homo sapiens (human) 5740 PTGIS
  • MGI:6194238
  • PMID:12586736
  • PMID:14568901
DOID:12801 mucopolysaccharidosis III HGNC:4422 Homo sapiens (human) 2799 GNS
  • MGI:6194238
  • PMID:12573255
DOID:7148 rheumatoid arthritis HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
  • PMID:12563673
  • PMID:22660635
  • PMID:25311255
DOID:14504 Niemann-Pick disease HGNC:11120 Homo sapiens (human) 6609 SMPD1
  • MGI:6194238
  • PMID:12556236
DOID:0050589 inflammatory bowel disease HGNC:5466 Homo sapiens (human) 3481 IGF2
  • MGI:6194238
  • PMID:12548059
DOID:9352 type 2 diabetes mellitus HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • MGI:6194238
  • PMID:12534643
DOID:14504 Niemann-Pick disease MGI:1097712 Mus musculus (house mouse) 18145 Npc1
  • MGI:6194238
  • PMID:12528192
  • PMID:15071184
  • PMID:18160655
  • PMID:20007718
  • PMID:21303697
  • PMID:21856732
  • PMID:21896731
  • PMID:22048958
  • PMID:22163015
  • PMID:22869680
  • PMID:23843985
  • PMID:24391715
  • PMID:26019327
  • PMID:6257302
  • PMID:7202025
  • PMID:9950794
DOID:9970 obesity RGD:2796 Rattus norvegicus (Norway rat) 25058 Hk1
  • MGI:6194238
  • PMID:12524468
DOID:206 hereditary multiple exostoses HGNC:3512 Homo sapiens (human) 2131 EXT1
  • MGI:6194238
  • PMID:12490068
  • PMID:17767039
  • PMID:18330718
  • PMID:24297320
  • PMID:25421355
  • PMID:26839764
  • PMID:8981950
DOID:9744 type 1 diabetes mellitus HGNC:1667 Homo sapiens (human) 952 CD38
  • MGI:6194238
  • PMID:12488956
  • PMID:16459468
DOID:0060062 familial juvenile hyperuricemic nephropathy HGNC:12559 Homo sapiens (human) 7369 UMOD
  • MGI:6194238
  • PMID:12471200
  • RGD:7240710
DOID:0060284 paroxysmal nocturnal hemoglobinuria HGNC:8957 Homo sapiens (human) 5277 PIGA
  • MGI:6194238
  • PMID:12424196
  • RGD:7240710
DOID:13359 Ehlers-Danlos syndrome WB:WBGene00005021 Caenorhabditis elegans 176382 sqv-3
  • MGI:6194238
  • PMID:12417421
DOID:10652 Alzheimer's disease HGNC:1912 Homo sapiens (human) 1103 CHAT
  • MGI:6194238
  • PMID:12401548
DOID:0060001 withdrawal disorder RGD:61800 Rattus norvegicus (Norway rat) 29595 Htr2a
  • MGI:6194238
  • PMID:12398913
  • PMID:18801381
  • PMID:26031442
DOID:5844 myocardial infarction HGNC:9053 Homo sapiens (human) 5329 PLAUR
  • MGI:6194238
  • PMID:12393744

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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

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024