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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 70226 - 70250 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:10652 Alzheimer's disease HGNC:8023 Homo sapiens (human) 4908 NTF3
  • PMID:9502217
DOID:9976 heroin dependence HGNC:4087 Homo sapiens (human) 2566 GABRG2
  • PMID:17440936
DOID:0080136 multiple mitochondrial dysfunctions syndrome 4 HGNC:19857 Homo sapiens (human) 122961 ISCA2
  • RGD:7240710
DOID:1580 diffuse scleroderma HGNC:5973 Homo sapiens (human) 3596 IL13
  • PMID:16832637
DOID:2394 ovarian cancer HGNC:8975 Homo sapiens (human) 5290 PIK3CA
  • RGD:7240710
DOID:3908 lung non-small cell carcinoma HGNC:10680 Homo sapiens (human) 6389 SDHA
  • PMID:25576295
DOID:10534 stomach cancer HGNC:12637 Homo sapiens (human) 7403 KDM6A
  • PMID:32867456
DOID:6498 seborrheic keratosis HGNC:8975 Homo sapiens (human) 5290 PIK3CA
  • RGD:7240710
DOID:341 peripheral vascular disease HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:15295097
DOID:9269 maple syrup urine disease HGNC:2898 Homo sapiens (human) 1738 DLD
  • RGD:7240710
DOID:9743 diabetic neuropathy HGNC:12519 Homo sapiens (human) 7352 UCP3
  • PMID:16373902
DOID:0111872 nonphotosensitive trichothiodystrophy 6 HGNC:4651 Homo sapiens (human) 2961 GTF2E2
  • RGD:7240710
DOID:0080736 Ehlers-Danlos syndrome musculocontractural type 1 HGNC:24464 Homo sapiens (human) 113189 CHST14
  • PMID:20004762
  • PMID:26373698
  • RGD:7240710
DOID:4780 anti-basement membrane glomerulonephritis HGNC:3619 Homo sapiens (human) 2214 FCGR3A
  • PMID:19640933
  • PMID:19946017
DOID:12849 autistic disorder HGNC:10761 Homo sapiens (human) 9869 SETDB1
  • PMID:23055267
DOID:0050908 myelodysplastic syndrome HGNC:1785 Homo sapiens (human) 1027 CDKN1B
  • PMID:9171997
DOID:1682 congenital heart disease HGNC:7577 Homo sapiens (human) 4625 MYH7
  • PMID:18159245
DOID:0050908 myelodysplastic syndrome HGNC:6973 Homo sapiens (human) 4193 MDM2
  • PMID:22668018
DOID:0060307 autosomal dominant intellectual developmental disorder HGNC:25777 Homo sapiens (human) 64864 RFX7
  • RGD:7240710
DOID:0060704 lymphoproliferative syndrome HGNC:11364 Homo sapiens (human) 6774 STAT3
  • PMID:22859607
DOID:3070 high grade glioma HGNC:5962 Homo sapiens (human) 3586 IL10
  • PMID:20406895
DOID:0050646 distal arthrogryposis HGNC:16305 Homo sapiens (human) 170689 ADAMTS15
  • RGD:7240710
DOID:0080199 colorectal carcinoma HGNC:8975 Homo sapiens (human) 5290 PIK3CA
  • PMID:17546593
DOID:0060468 Holt-Oram syndrome HGNC:15924 Homo sapiens (human) 57167 SALL4
  • PMID:12843316
DOID:10003 sensorineural hearing loss HGNC:4172 Homo sapiens (human) 2625 GATA3
  • PMID:10935639

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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