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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 70326 - 70350 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:0110180 Charcot-Marie-Tooth disease axonal type 2CC HGNC:7737 Homo sapiens (human) 4744 NEFH
  • RGD:7240710
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:4886 Homo sapiens (human) 3077 HFE
  • PMID:11473047
  • PMID:9453491
DOID:10652 Alzheimer's disease HGNC:23064 Homo sapiens (human) 119391 GSTO2
  • PMID:14570706
  • PMID:15917099
DOID:2988 antiphospholipid syndrome HGNC:4942 Homo sapiens (human) 3117 HLA-DQA1
  • PMID:11157139
DOID:0060532 latex allergy HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1
  • PMID:15536412
DOID:865 vasculitis HGNC:16 Homo sapiens (human) 12 SERPINA3
  • PMID:12685871
DOID:9970 obesity RGD:71037 Rattus norvegicus (Norway rat) 246075 Prlhr
  • PMID:15854142
DOID:0050741 alcohol dependence HGNC:11042 Homo sapiens (human) 6529 SLC6A1
  • PMID:26727527
DOID:0080294 Charcot-Marie-Tooth disease dominant intermediate G HGNC:7739 Homo sapiens (human) 4747 NEFL
  • RGD:7240710
DOID:0080822 aspirin-induced respiratory disease HGNC:4942 Homo sapiens (human) 3117 HLA-DQA1
  • PMID:25975240
DOID:639 acute disseminated encephalomyelitis HGNC:4953 Homo sapiens (human) 3127 HLA-DRB5
  • PMID:15201511
DOID:10772 thrombotic thrombocytopenic purpura HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1
  • PMID:19922436
DOID:0081366 Paget's disease of bone 3 HGNC:11280 Homo sapiens (human) 8878 SQSTM1
  • RGD:7240710
DOID:1115 sarcoma HGNC:6973 Homo sapiens (human) 4193 MDM2
  • PMID:1614537
DOID:9074 systemic lupus erythematosus HGNC:2505 Homo sapiens (human) 1493 CTLA4
  • PMID:18185908
  • RGD:7240710
DOID:2945 severe acute respiratory syndrome HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1
  • PMID:15243926
  • PMID:19445991
DOID:0050877 pancreatic agenesis HGNC:6107 Homo sapiens (human) 3651 PDX1
  • RGD:7240710
DOID:12930 dilated cardiomyopathy HGNC:6554 Homo sapiens (human) 3953 LEPR
  • PMID:19337797
DOID:0081352 congenital myopathy 20 HGNC:10485 Homo sapiens (human) 6263 RYR3
  • RGD:7240710
DOID:0080538 Sweeney-Cox syndrome HGNC:12428 Homo sapiens (human) 7291 TWIST1
  • RGD:7240710
DOID:13241 Behcet's disease HGNC:5331 Homo sapiens (human) 64127 NOD2
  • PMID:15515785
  • PMID:19748964
DOID:322 myelitis HGNC:4940 Homo sapiens (human) 3115 HLA-DPB1
  • PMID:22884298
DOID:0080600 COVID-19 HGNC:4933 Homo sapiens (human) 3107 HLA-C
  • PMID:32424945
DOID:12858 Huntington's disease HGNC:4585 Homo sapiens (human) 2903 GRIN2A
  • PMID:15742215
  • PMID:17569088
DOID:2986 IgA glomerulonephritis HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:12566518

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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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Last updated: December 9, 2024