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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 68876 - 68900 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:2747 glycogen storage disease SGD:S000003472 Saccharomyces cerevisiae S288C 853155 PFK1
  • PMID:7825568
DOID:2747 glycogen storage disease SGD:S000004818 Saccharomyces cerevisiae S288C 855245 PFK2
  • PMID:7825568
DOID:0111054 von Willebrand's disease 3 HGNC:12726 Homo sapiens (human) 7450 VWF
  • PMID:7831648
  • RGD:7240710
DOID:3393 coronary artery disease HGNC:8941 Homo sapiens (human) 5265 SERPINA1
  • PMID:7832094
DOID:14757 Ehlers-Danlos syndrome hypermobility type HGNC:2201 Homo sapiens (human) 1281 COL3A1
  • PMID:7833919
DOID:409 liver disease HGNC:2321 Homo sapiens (human) 1371 CPOX
  • PMID:7849704
DOID:13252 mesenteric vascular occlusion RGD:2857 Rattus norvegicus (Norway rat) 25464 Icam1
  • PMID:7858885
DOID:0080046 Stickler syndrome MGI:88446 Mus musculus (house mouse) 12814 Col11a1
  • PMID:7859283
DOID:0080677 otospondylomegaepiphyseal dysplasia, autosomal dominant HGNC:2187 Homo sapiens (human) 1302 COL11A2
  • PMID:7859284
  • RGD:7240710
DOID:874 bacterial pneumonia RGD:61819 Rattus norvegicus (Norway rat) 54320 Pdpn
  • PMID:7864138
DOID:1123 spondyloarthropathy HGNC:2200 Homo sapiens (human) 1280 COL2A1
  • PMID:7866404
DOID:3587 pancreatic ductal carcinoma HGNC:7029 Homo sapiens (human) 4233 MET
  • PMID:7866999
DOID:0111337 Jackson-Weiss syndrome HGNC:3689 Homo sapiens (human) 2263 FGFR2
  • PMID:7874170
  • RGD:7240710
DOID:3042 allergic contact dermatitis HGNC:3763 Homo sapiens (human) 2321 FLT1
  • PMID:7876550
DOID:3042 allergic contact dermatitis HGNC:6307 Homo sapiens (human) 3791 KDR
  • PMID:7876550
DOID:4258 Weissenbacher-Zweymuller syndrome MGI:102806 Mus musculus (house mouse) 11480 Acvr2a
  • PMID:7885474
DOID:0060762 restrictive dermopathy MGI:95586 Mus musculus (house mouse) 14313 Fst
  • PMID:7885475
DOID:11726 Emery-Dreifuss muscular dystrophy HGNC:3331 Homo sapiens (human) 2010 EMD
  • PMID:7894480
DOID:1826 epilepsy RGD:68946 Rattus norvegicus (Norway rat) 29237 Penk
  • PMID:7898641
DOID:11832 visual epilepsy RGD:3810 Rattus norvegicus (Norway rat) 24808 Tacr3
  • PMID:7898759
DOID:0111676 high molecular weight kininogen deficiency HGNC:6383 Homo sapiens (human) 3827 KNG1
  • PMID:7901207
  • RGD:7240710
DOID:3459 breast carcinoma HGNC:12780 Homo sapiens (human) 7472 WNT2
  • PMID:7903963
DOID:4001 ovarian carcinoma HGNC:7850 Homo sapiens (human) 4831 NME2
  • PMID:7907945
DOID:4450 renal cell carcinoma HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:7912320
DOID:9970 obesity HGNC:612 Homo sapiens (human) 347 APOD
  • PMID:7913935

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: December 9, 2024