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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 69201 - 69225 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:4971 myelofibrosis HGNC:7132 Homo sapiens (human) 4297 KMT2A
  • PMID:35731275
DOID:10283 prostate cancer HGNC:9884 Homo sapiens (human) 5925 RB1
  • PMID:18383208
DOID:2671 transitional cell carcinoma HGNC:7325 Homo sapiens (human) 4436 MSH2
  • PMID:22883484
DOID:2352 hemochromatosis HGNC:11762 Homo sapiens (human) 7036 TFR2
  • PMID:10802645
DOID:2043 hepatitis B HGNC:6014 Homo sapiens (human) 3565 IL4
  • PMID:28051794
DOID:0050431 arrhythmogenic right ventricular cardiomyopathy HGNC:11769 Homo sapiens (human) 7043 TGFB3
  • PMID:7951245
DOID:7188 autoimmune thyroiditis HGNC:11764 Homo sapiens (human) 7038 TG
  • PMID:14657345
  • RGD:7240710
DOID:9261 nasopharynx carcinoma HGNC:2336 Homo sapiens (human) 1380 CR2
  • PMID:23612877
DOID:1793 pancreatic cancer HGNC:6844 Homo sapiens (human) 6416 MAP2K4
  • PMID:18772397
DOID:684 hepatocellular carcinoma HGNC:5423 Homo sapiens (human) 3440 IFNA2
  • PMID:29080269
DOID:0080379 nephrotic syndrome type 2 HGNC:12338 Homo sapiens (human) 7225 TRPC6
  • PMID:21511817
DOID:9974 drug dependence HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • PMID:18828801
DOID:6543 acne HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:18615253
DOID:5844 myocardial infarction HGNC:8133 Homo sapiens (human) 4973 OLR1
  • PMID:12646194
  • RGD:7240710
DOID:12894 Sjogren's syndrome HGNC:1606 Homo sapiens (human) 1234 CCR5
  • PMID:12412204
  • PMID:23773920
DOID:0080254 orofaciodigital syndrome XVI HGNC:28128 Homo sapiens (human) 84314 TMEM107
  • RGD:7240710
DOID:2843 long QT syndrome HGNC:493 Homo sapiens (human) 287 ANK2
  • PMID:12571597
DOID:0080315 megalencephalic leukoencephalopathy with subcortical cysts HGNC:637 Homo sapiens (human) 361 AQP4
  • RGD:7240710
DOID:1574 alcohol use disorder HGNC:4586 Homo sapiens (human) 2904 GRIN2B
  • PMID:14573320
  • PMID:16911840
DOID:10983 Alport syndrome HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1
  • PMID:15182324
DOID:9743 diabetic neuropathy HGNC:404 Homo sapiens (human) 217 ALDH2
  • PMID:15318096
DOID:0070168 spermatogenic failure 3 HGNC:10788 Homo sapiens (human) 6431 SRSF6
  • PMID:24661730
DOID:987 alopecia RGD:735015 Rattus norvegicus (Norway rat) 291754 Dsg4
  • PMID:15617564
DOID:0081023 retinal cone dystrophy 4 HGNC:20202 Homo sapiens (human) 93589 CACNA2D4
  • RGD:7240710
DOID:0080669 posterior polymorphous corneal dystrophy 4 HGNC:2799 Homo sapiens (human) 79977 GRHL2
  • RGD:7240710

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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