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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 October 9, 2024
Displaying entries 69451 - 69475 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:9884 muscular dystrophy HGNC:2213 Homo sapiens (human) 1293 COL6A3
  • PMID:9536084
DOID:2747 glycogen storage disease HGNC:9725 Homo sapiens (human) 5836 PYGL
  • PMID:9536091
DOID:3261 hyper IgE recurrent infection syndrome 1 HGNC:6015 Homo sapiens (human) 3566 IL4R
  • PMID:9537881
DOID:332 amyotrophic lateral sclerosis HGNC:10940 Homo sapiens (human) 6506 SLC1A2
  • PMID:9539131
DOID:4362 cervical cancer HGNC:5962 Homo sapiens (human) 3586 IL10
  • PMID:9541628
DOID:4948 gallbladder carcinoma HGNC:11765 Homo sapiens (human) 7039 TGFA
  • PMID:9542514
DOID:11723 Duchenne muscular dystrophy HGNC:7872 Homo sapiens (human) 4842 NOS1
  • PMID:9542584
DOID:11123 Henoch-Schoenlein purpura HGNC:9051 Homo sapiens (human) 5327 PLAT
  • PMID:9543574
DOID:2211 factor XIII deficiency HGNC:6631 Homo sapiens (human) 3998 LMAN1
  • PMID:9546392
DOID:2216 factor V deficiency HGNC:6631 Homo sapiens (human) 3998 LMAN1
  • PMID:9546392
DOID:7148 rheumatoid arthritis HGNC:4187 Homo sapiens (human) 2638 GC
  • PMID:9548303
DOID:10825 essential hypertension MGI:1314883 Mus musculus (house mouse) 21938 Tnfrsf1b
  • PMID:9551933
DOID:13809 familial combined hyperlipidemia MGI:1314883 Mus musculus (house mouse) 21938 Tnfrsf1b
  • PMID:9551933
DOID:2580 rhizomelic chondrodysplasia punctata HGNC:327 Homo sapiens (human) 8540 AGPS
  • PMID:9553082
DOID:820 myocarditis HGNC:6155 Homo sapiens (human) 3689 ITGB2
  • PMID:9556870
DOID:820 myocarditis HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:9556870
DOID:10652 Alzheimer's disease HGNC:2095 Homo sapiens (human) 1191 CLU
  • PMID:9560017
DOID:2377 multiple sclerosis HGNC:4077 Homo sapiens (human) 2556 GABRA3
  • PMID:9561979
DOID:12930 dilated cardiomyopathy HGNC:143 Homo sapiens (human) 70 ACTC1
  • PMID:9563954
DOID:9744 type 1 diabetes mellitus HGNC:9951 Homo sapiens (human) 5967 REG1A
  • PMID:9564847
DOID:12930 dilated cardiomyopathy MGI:107164 Mus musculus (house mouse) 19055 Ppp3ca
  • PMID:9568714
DOID:2349 arteriosclerosis HGNC:3544 Homo sapiens (human) 2155 F7
  • PMID:9569183
DOID:9744 type 1 diabetes mellitus HGNC:601 Homo sapiens (human) 336 APOA2
  • PMID:9578960
DOID:9744 type 1 diabetes mellitus HGNC:600 Homo sapiens (human) 335 APOA1
  • PMID:9578960
DOID:9744 type 1 diabetes mellitus HGNC:6619 Homo sapiens (human) 3990 LIPC
  • PMID:9580247

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: December 9, 2024