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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 2726 - 2750 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:0060639 permanent neonatal diabetes mellitus HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • PMID:15115830
  • PMID:16670688
  • RGD:7240710
DOID:3393 coronary artery disease HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:15115767
  • PMID:17070179
DOID:4481 allergic rhinitis HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:15112973
DOID:10652 Alzheimer's disease HGNC:433 Homo sapiens (human) 246 ALOX15
  • PMID:15111312
DOID:630 genetic disease HGNC:18622 Homo sapiens (human) 91949 COG7
  • PMID:15107842
DOID:1612 breast cancer HGNC:2665 Homo sapiens (human) 1604 CD55
  • PMID:15102687
  • PMID:18676748
DOID:657 adenoma HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • PMID:15100237
DOID:10584 retinitis pigmentosa HGNC:1375 Homo sapiens (human) 762 CA4
  • PMID:15090652
DOID:13241 Behcet's disease HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:15088300
DOID:1612 breast cancer HGNC:545 Homo sapiens (human) 310 ANXA7
  • PMID:15073110
DOID:3393 coronary artery disease HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:15059615
DOID:11983 Prader-Willi syndrome HGNC:18129 Homo sapiens (human) 51738 GHRL
  • PMID:15057669
DOID:12849 autistic disorder HGNC:10982 Homo sapiens (human) 8604 SLC25A12
  • PMID:15056512
DOID:4195 hyperglycemia HGNC:5273 Homo sapiens (human) 3339 HSPG2
  • PMID:15056491
DOID:3312 bipolar disorder HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • PMID:15050861
DOID:13241 Behcet's disease HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:15045629
  • PMID:15961928
DOID:1800 neuroendocrine carcinoma HGNC:3353 Homo sapiens (human) 2026 ENO2
  • PMID:15010880
DOID:0050152 aspiration pneumonia HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:14990394
DOID:12930 dilated cardiomyopathy HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:14984724
DOID:9352 type 2 diabetes mellitus HGNC:10659 Homo sapiens (human) 6383 SDC2
  • PMID:14976204
DOID:3429 inclusion body myositis HGNC:2666 Homo sapiens (human) 1605 DAG1
  • PMID:14972325
DOID:11624 penile benign neoplasm HGNC:9599 Homo sapiens (human) 9536 PTGES
  • PMID:14871981
DOID:61 mitral valve disease HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:14765837
DOID:10892 hypospadias HGNC:5218 Homo sapiens (human) 3284 HSD3B2
  • PMID:14764821
DOID:9352 type 2 diabetes mellitus HGNC:4242 Homo sapiens (human) 9945 GFPT2
  • PMID:14764791

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Supported by JST NBDC Grant Number JPMJND2204

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