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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 551 - 575 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:0050861 colorectal adenocarcinoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:8264230
DOID:13189 gout HGNC:9462 Homo sapiens (human) 5631 PRPS1
  • PMID:8253776
DOID:10652 Alzheimer's disease HGNC:11007 Homo sapiens (human) 6515 SLC2A3
  • PMID:8179300
DOID:10652 Alzheimer's disease HGNC:11005 Homo sapiens (human) 6513 SLC2A1
  • PMID:8179300
DOID:0050424 familial adenomatous polyposis HGNC:9065 Homo sapiens (human) 5335 PLCG1
  • PMID:8174133
DOID:10923 sickle cell anemia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:8140855
DOID:2876 laryngeal squamous cell carcinoma HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:8138195
DOID:3008 invasive ductal carcinoma HGNC:8729 Homo sapiens (human) 5111 PCNA
  • PMID:8102204
DOID:8549 chronic ulcer of skin HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:8099861
DOID:1923 disorder of sexual development HGNC:5212 Homo sapiens (human) 3293 HSD17B3
  • PMID:8075637
DOID:479 angiokeratoma HGNC:7631 Homo sapiens (human) 4668 NAGA
  • PMID:8040340
DOID:9268 glycine encephalopathy HGNC:473 Homo sapiens (human) 275 AMT
  • PMID:8005589
  • PMID:9600239
  • PMID:9621520
  • RGD:7240710
DOID:2671 transitional cell carcinoma HGNC:11755 Homo sapiens (human) 7031 TFF1
  • PMID:7965392
DOID:4247 coronary restenosis RGD:3130 Rattus norvegicus (Norway rat) 24577 Myc
  • PMID:7955204
DOID:8472 localized scleroderma HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:7916356
DOID:8505 dermatitis herpetiformis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:7914110
DOID:9970 obesity HGNC:612 Homo sapiens (human) 347 APOD
  • PMID:7913935
DOID:2747 glycogen storage disease SGD:S000004818 Saccharomyces cerevisiae S288C 855245 PFK2
  • PMID:7825568
DOID:2747 glycogen storage disease SGD:S000003472 Saccharomyces cerevisiae S288C 853155 PFK1
  • PMID:7825568
DOID:4948 gallbladder carcinoma HGNC:79 Homo sapiens (human) 28 ABO
  • PMID:7795450
DOID:0050452 mevalonic aciduria HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:7780142
DOID:3454 brain infarction RGD:2870 Rattus norvegicus (Norway rat) 24483 Igf2
  • PMID:7770004
DOID:5204 fructose-1,6-bisphosphatase deficiency HGNC:3606 Homo sapiens (human) 2203 FBP1
  • PMID:7763253
  • RGD:7240710
DOID:11656 cicatricial pemphigoid HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:7750940
DOID:0080162 lupus nephritis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:7750940

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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