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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 9451 - 9475 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:10534 stomach cancer MGI:96560 Mus musculus (house mouse) 16195 Il6st
  • PMID:14699500
DOID:2349 arteriosclerosis HGNC:435 Homo sapiens (human) 240 ALOX5
  • PMID:14702425
DOID:13378 Kawasaki disease HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:14703611
  • PMID:14744383
  • PMID:18710885
  • PMID:8777922
DOID:4450 renal cell carcinoma HGNC:451 Homo sapiens (human) 23600 AMACR
  • PMID:14707866
DOID:0050570 congenital disorder of glycosylation type I SGD:S000000314 Saccharomyces cerevisiae S288C 852407 ALG1
  • PMID:14709599
  • PMID:14973778
  • PMID:22966035
DOID:1214 tympanosclerosis HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:14710000
DOID:3132 porphyria cutanea tarda HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:14714565
DOID:0002116 pterygium HGNC:8125 Homo sapiens (human) 4968 OGG1
  • PMID:14716324
DOID:12783 migraine without aura HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:14718719
DOID:3393 coronary artery disease HGNC:3402 Homo sapiens (human) 2053 EPHX2
  • PMID:14732757
DOID:1936 atherosclerosis HGNC:16049 Homo sapiens (human) 10728 PTGES3
  • PMID:14736553
DOID:4247 coronary restenosis HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:14740296
DOID:0050127 sinusitis HGNC:11848 Homo sapiens (human) 7097 TLR2
  • PMID:14743629
DOID:0050127 sinusitis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:14743629
DOID:1612 breast cancer HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:14744747
DOID:5041 esophageal cancer HGNC:2602 Homo sapiens (human) 1591 CYP24A1
  • PMID:14760115
DOID:9352 type 2 diabetes mellitus HGNC:4242 Homo sapiens (human) 9945 GFPT2
  • PMID:14764791
DOID:10892 hypospadias HGNC:5218 Homo sapiens (human) 3284 HSD3B2
  • PMID:14764821
DOID:61 mitral valve disease HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:14765837
DOID:11624 penile benign neoplasm HGNC:9599 Homo sapiens (human) 9536 PTGES
  • PMID:14871981
DOID:3429 inclusion body myositis HGNC:2666 Homo sapiens (human) 1605 DAG1
  • PMID:14972325
DOID:9352 type 2 diabetes mellitus HGNC:10659 Homo sapiens (human) 6383 SDC2
  • PMID:14976204
DOID:12930 dilated cardiomyopathy HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:14984724
DOID:0050152 aspiration pneumonia HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:14990394
DOID:1800 neuroendocrine carcinoma HGNC:3353 Homo sapiens (human) 2026 ENO2
  • PMID:15010880

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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