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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 66501 - 66525 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:14250 Down syndrome HGNC:10786 Homo sapiens (human) 6429 SRSF4
  • PMID:16847874
DOID:2152 ovary epithelial cancer HGNC:10785 Homo sapiens (human) 6428 SRSF3
  • PMID:23748175
DOID:3312 bipolar disorder HGNC:10785 Homo sapiens (human) 6428 SRSF3
  • PMID:18281098
DOID:0050908 myelodysplastic syndrome HGNC:10782 Homo sapiens (human) 9295 SRSF11
  • PMID:24244432
DOID:0060041 autism spectrum disorder HGNC:10782 Homo sapiens (human) 9295 SRSF11
  • PMID:24007566
DOID:4448 macular degeneration HGNC:10781 Homo sapiens (human) 6434 TRA2B
  • PMID:24098751
DOID:14557 primary pulmonary hypertension HGNC:1078 Homo sapiens (human) 659 BMPR2
  • MGI:6194238
  • RGD:7240710
DOID:0081268 pulmonary venoocclusive disease 1 HGNC:1078 Homo sapiens (human) 659 BMPR2
  • RGD:7240710
DOID:2841 asthma HGNC:1078 Homo sapiens (human) 659 BMPR2
  • PMID:18292470
DOID:1681 heart septal defect HGNC:1078 Homo sapiens (human) 659 BMPR2
  • PMID:21070126
DOID:6432 pulmonary hypertension HGNC:1078 Homo sapiens (human) 659 BMPR2
  • MGI:6194238
  • PMID:15775752
  • PMID:19324947
  • PMID:19785764
  • PMID:20002458
  • PMID:20534176
  • PMID:21737550
DOID:0080019 metaphyseal dysplasia HGNC:10778 Homo sapiens (human) 6424 SFRP4
  • RGD:7240710
DOID:8719 in situ carcinoma HGNC:10776 Homo sapiens (human) 6422 SFRP1
  • PMID:15123780
DOID:4450 renal cell carcinoma HGNC:10776 Homo sapiens (human) 6422 SFRP1
  • PMID:20420713
DOID:127 leiomyoma HGNC:10776 Homo sapiens (human) 6422 SFRP1
  • PMID:15972578
DOID:2671 transitional cell carcinoma HGNC:10773 Homo sapiens (human) 2810 SFN
  • PMID:16964403
DOID:8719 in situ carcinoma HGNC:10773 Homo sapiens (human) 2810 SFN
  • PMID:11896620
DOID:2101 vulva squamous cell carcinoma HGNC:10773 Homo sapiens (human) 2810 SFN
  • PMID:11896620
DOID:11054 urinary bladder cancer HGNC:10773 Homo sapiens (human) 2810 SFN
  • PMID:17645415
DOID:1059 intellectual disability HGNC:10773 Homo sapiens (human) 2810 SFN
  • MGI:6194238
DOID:2394 ovarian cancer HGNC:10773 Homo sapiens (human) 2810 SFN
  • PMID:15102672
  • PMID:16773180
DOID:2871 endometrial carcinoma HGNC:10773 Homo sapiens (human) 2810 SFN
  • PMID:16271083
DOID:1793 pancreatic cancer HGNC:10771 Homo sapiens (human) 10262 SF3B4
  • PMID:28351319
DOID:684 hepatocellular carcinoma HGNC:10771 Homo sapiens (human) 10262 SF3B4
  • MGI:6194238
  • PMID:29059470
  • PMID:30391496
DOID:5768 Nager acrofacial dysostosis HGNC:10771 Homo sapiens (human) 10262 SF3B4
  • PMID:22541558
  • PMID:23568615
  • RGD:7240710

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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