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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 5551 - 5575 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:4079 heart valve disease MGI:1278315 Mus musculus (house mouse) 16973 Lrp5
  • MGI:6194238
DOID:10629 microphthalmia MGI:1278315 Mus musculus (house mouse) 16973 Lrp5
  • MGI:6194238
DOID:0110937 autosomal dominant osteopetrosis 1 MGI:1278315 Mus musculus (house mouse) 16973 Lrp5
  • MGI:6194238
DOID:898 autosomal dominant polycystic kidney disease MGI:1278315 Mus musculus (house mouse) 16973 Lrp5
  • MGI:6194238
DOID:0050636 familial visceral amyloidosis FB:FBgn0004425 Drosophila melanogaster (fruit fly) 38125 LysB CG1179
  • MGI:6194238
DOID:0050636 familial visceral amyloidosis FB:FBgn0004427 Drosophila melanogaster (fruit fly) 38127 LysD CG9118
  • MGI:6194238
DOID:0050636 familial visceral amyloidosis FB:FBgn0004428 Drosophila melanogaster (fruit fly) 38128 LysE CG1180
  • MGI:6194238
DOID:0050636 familial visceral amyloidosis FB:FBgn0004429 Drosophila melanogaster (fruit fly) 38129 LysP CG9116
  • MGI:6194238
DOID:0050636 familial visceral amyloidosis FB:FBgn0004430 Drosophila melanogaster (fruit fly) 38130 LysS CG1165
  • MGI:6194238
DOID:0050636 familial visceral amyloidosis FB:FBgn0004431 Drosophila melanogaster (fruit fly) 38122 LysX CG9120
  • MGI:6194238
DOID:0050636 familial visceral amyloidosis MGI:96902 Mus musculus (house mouse) 17110 Lyz1
  • MGI:6194238
DOID:0050636 familial visceral amyloidosis MGI:96897 Mus musculus (house mouse) 17105 Lyz2
  • MGI:6194238
DOID:2377 multiple sclerosis HGNC:6783 Homo sapiens (human) 4099 MAG
  • PMID:2419505
DOID:3525 middle cerebral artery infarction HGNC:6783 Homo sapiens (human) 4099 MAG
  • MGI:6194238
DOID:573 nerve compression syndrome HGNC:6783 Homo sapiens (human) 4099 MAG
  • MGI:6194238
DOID:11446 sciatic neuropathy HGNC:6783 Homo sapiens (human) 4099 MAG
  • MGI:6194238
DOID:0110820 hereditary spastic paraplegia 75 HGNC:6783 Homo sapiens (human) 4099 MAG
  • RGD:7240710
DOID:9266 cystinuria SGD:S000003524 Saccharomyces cerevisiae S288C 853209 MAL12
  • MGI:6194238
DOID:9266 cystinuria SGD:S000000503 Saccharomyces cerevisiae S288C 852602 MAL32
  • MGI:6194238
DOID:0081097 Rafiq syndrome HGNC:6823 Homo sapiens (human) 11253 MAN1B1
  • RGD:7240710
DOID:1338 congenital dyserythropoietic anemia HGNC:6824 Homo sapiens (human) 4124 MAN2A1
  • MGI:6194238
DOID:9074 systemic lupus erythematosus HGNC:6824 Homo sapiens (human) 4124 MAN2A1
  • MGI:6194238
DOID:5419 schizophrenia HGNC:6825 Homo sapiens (human) 4122 MAN2A2
  • MGI:6194238
DOID:3413 alpha-mannosidosis HGNC:6826 Homo sapiens (human) 4125 MAN2B1
  • MGI:6194238
  • RGD:7240710
DOID:3633 beta-mannosidosis HGNC:6831 Homo sapiens (human) 4126 MANBA
  • MGI:6194238
  • RGD:7240710

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Supported by JST NBDC Grant Number JPMJND2204

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


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