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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 1 - 25 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:5419 schizophrenia MGI:1858224 Mus musculus (house mouse) 53374 Chst3
  • MGI:3604450
DOID:9970 obesity MGI:104993 Mus musculus (house mouse) 16847 Lepr
  • MGI:3611487
  • MGI:3778961
  • MGI:3778962
  • MGI:3815208
  • MGI:6194238
  • PMID:12136396
  • PMID:12590922
  • PMID:12594516
  • PMID:12885755
  • PMID:15207242
  • PMID:15389315
  • PMID:15685168
  • PMID:16113078
  • PMID:16443782
  • PMID:19015522
  • PMID:34390703
  • PMID:6991317
  • PMID:6993269
  • PMID:8177042
DOID:9352 type 2 diabetes mellitus MGI:104993 Mus musculus (house mouse) 16847 Lepr
  • MGI:3611487
  • MGI:6194238
  • PMID:16113078
  • PMID:22609345
  • PMID:25157166
DOID:12803 Sly syndrome MGI:95872 Mus musculus (house mouse) 110006 Gusb
  • MGI:3801433
  • MGI:6194238
  • PMID:11228259
  • PMID:12403825
  • PMID:12700165
  • PMID:2111021
  • PMID:2495302
  • PMID:9774663
DOID:0110637 muscular dystrophy-dystroglycanopathy type B6 MGI:1342270 Mus musculus (house mouse) 16795 Large1
  • MGI:4454310
  • MGI:6194238
DOID:11198 DiGeorge syndrome MGI:104719 Mus musculus (house mouse) 15531 Ndst1
  • MGI:5284969
DOID:9970 obesity MGI:104663 Mus musculus (house mouse) 16846 Lep
  • MGI:5447547
  • MGI:6194238
  • PMID:12136396
  • PMID:12885755
  • PMID:16394172
DOID:0110011 advanced sleep phase syndrome 1 MGI:1195265 Mus musculus (house mouse) 18627 Per2
  • MGI:6194238
  • MGI:6197761
DOID:10763 hypertension HGNC:2592 Homo sapiens (human) 1585 CYP11B2
  • MGI:6194238
  • PMID:10024332
DOID:1064 cystinosis HGNC:2518 Homo sapiens (human) 1497 CTNS
  • MGI:6194238
  • PMID:10068513
  • PMID:11565547
  • PMID:18578013
  • PMID:9537412
  • PMID:9792862
  • RGD:7240710
DOID:2741 bilirubin metabolic disorder HGNC:12530 Homo sapiens (human) 54658 UGT1A1
  • MGI:6194238
  • PMID:10091405
  • PMID:15753292
  • PMID:16609363
  • PMID:21993917
  • RGD:7240710
DOID:576 proteinuria HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
  • PMID:10193250
DOID:7148 rheumatoid arthritis MGI:104798 Mus musculus (house mouse) 21926 Tnf
  • MGI:6194238
  • PMID:10204494
  • PMID:26195802
  • PMID:29618659
DOID:11211 buphthalmos HGNC:2597 Homo sapiens (human) 1545 CYP1B1
  • MGI:6194238
  • PMID:10227395
  • PMID:12567107
  • PMID:16490498
  • PMID:19247456
  • PMID:19593207
  • PMID:19597567
  • PMID:20664688
  • PMID:23922489
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:12518 Homo sapiens (human) 7351 UCP2
  • MGI:6194238
  • PMID:10382588
DOID:9352 type 2 diabetes mellitus HGNC:9291 Homo sapiens (human) 5506 PPP1R3A
  • MGI:6194238
  • PMID:10389856
  • PMID:10868947
  • PMID:11793847
  • PMID:12831406
  • PMID:19553562
  • PMID:9653600
  • PMID:9726244
  • RGD:7240710
DOID:3413 alpha-mannosidosis MGI:107286 Mus musculus (house mouse) 17159 Man2b1
  • MGI:6194238
  • PMID:10400983
  • PMID:16014715
DOID:850 lung disease RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • MGI:6194238
  • PMID:10455887
  • PMID:11126266
  • PMID:15461830
DOID:13359 Ehlers-Danlos syndrome HGNC:930 Homo sapiens (human) 11285 B4GALT7
  • MGI:6194238
  • PMID:10473568
DOID:14687 diastrophic dysplasia HGNC:10994 Homo sapiens (human) 1836 SLC26A2
  • MGI:6194238
  • PMID:10482955
  • RGD:7240710
DOID:0050855 renal fibrosis HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
  • PMID:10504496
DOID:0110276 autosomal recessive limb-girdle muscular dystrophy type 2B MGI:1349385 Mus musculus (house mouse) 26903 Dysf
  • MGI:6194238
  • PMID:10508505
  • PMID:12736685
  • PMID:15254015
  • PMID:30292141
DOID:4195 hyperglycemia RGD:62387 Rattus norvegicus (Norway rat) 29535 Pdx1
  • MGI:6194238
  • PMID:10512364
  • PMID:12438314
DOID:9352 type 2 diabetes mellitus HGNC:6107 Homo sapiens (human) 3651 PDX1
  • MGI:6194238
  • PMID:10545531
  • PMID:15170499
  • PMID:15734849
  • RGD:7240710
DOID:10652 Alzheimer's disease HGNC:9604 Homo sapiens (human) 5742 PTGS1
  • MGI:6194238
  • PMID:10560656

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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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