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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 3076 - 3100 of 12216 in total
Disease ID Disease Name ▲ Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0050753 cerebellar ataxia HGNC:16268 Homo sapiens (human) 10908 PNPLA6
  • MGI:6194238
DOID:0050753 cerebellar ataxia HGNC:24768 Homo sapiens (human) 375775 PNPLA7
  • MGI:6194238
DOID:0050753 cerebellar ataxia FB:FBgn0032729 Drosophila melanogaster (fruit fly) 35156 L2HGDH
  • MGI:6194238
DOID:0050753 cerebellar ataxia HGNC:20499 Homo sapiens (human) 79944 L2HGDH
  • PMID:24573090
DOID:9246 cerebral amyloid angiopathy HGNC:8133 Homo sapiens (human) 4973 OLR1
  • PMID:16328515
DOID:0060669 cerebral cavernous malformation MGI:1206581 Mus musculus (house mouse) 18706 Pik3ca
  • MGI:6194238
DOID:0060669 cerebral cavernous malformation RGD:620916 Rattus norvegicus (Norway rat) 170911 Pik3ca
  • MGI:6194238
DOID:0060669 cerebral cavernous malformation HGNC:8975 Homo sapiens (human) 5290 PIK3CA
  • RGD:7240710
DOID:0060669 cerebral cavernous malformation HGNC:9588 Homo sapiens (human) 5728 PTEN
  • PMID:19061355
DOID:0080491 cerebral cavernous malformation 1 HGNC:9603 Homo sapiens (human) 5740 PTGIS
  • PMID:26795600
DOID:0050719 cerebral folate receptor alpha deficiency HGNC:3791 Homo sapiens (human) 2348 FOLR1
  • RGD:7240710
DOID:3526 cerebral infarction RGD:3546 Rattus norvegicus (Norway rat) 25703 Rbp4
  • MGI:6194238
DOID:3526 cerebral infarction HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:11596779
DOID:3526 cerebral infarction HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • MGI:6194238
DOID:3526 cerebral infarction HGNC:11609 Homo sapiens (human) 6916 TBXAS1
  • PMID:19403042
DOID:3526 cerebral infarction RGD:2802 Rattus norvegicus (Norway rat) 25459 Hmgb1
  • MGI:6194238
DOID:3526 cerebral infarction HGNC:9603 Homo sapiens (human) 5740 PTGIS
  • MGI:6194238
  • PMID:11130769
  • PMID:28108096
  • PMID:28478978
DOID:3526 cerebral infarction MGI:97879 Mus musculus (house mouse) 19662 Rbp4
  • MGI:6194238
DOID:3526 cerebral infarction RGD:62387 Rattus norvegicus (Norway rat) 29535 Pdx1
  • MGI:6194238
DOID:3526 cerebral infarction HGNC:9922 Homo sapiens (human) 5950 RBP4
  • PMID:19846170
  • PMID:30030781
  • PMID:30038059
DOID:3526 cerebral infarction HGNC:6107 Homo sapiens (human) 3651 PDX1
  • PMID:18506375
DOID:3526 cerebral infarction HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:18201705
DOID:3526 cerebral infarction HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:16173529
DOID:3526 cerebral infarction MGI:102851 Mus musculus (house mouse) 18609 Pdx1
  • MGI:6194238
DOID:3526 cerebral infarction HGNC:3402 Homo sapiens (human) 2053 EPHX2
  • MGI:6194238

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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