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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 70201 - 70225 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:321 tropical spastic paraparesis HGNC:11914 Homo sapiens (human) 8784 TNFRSF18
  • PMID:20945034
  • PMID:28101786
DOID:13608 biliary atresia HGNC:2907 Homo sapiens (human) 8788 DLK1
  • PMID:14743499
DOID:3070 high grade glioma HGNC:2907 Homo sapiens (human) 8788 DLK1
  • PMID:16288219
DOID:0080006 bone development disease HGNC:11908 Homo sapiens (human) 8792 TNFRSF11A
  • PMID:10615125
DOID:0081365 Paget's disease of bone 2 HGNC:11908 Homo sapiens (human) 8792 TNFRSF11A
  • RGD:7240710
DOID:0111542 familial expansile osteolysis HGNC:11908 Homo sapiens (human) 8792 TNFRSF11A
  • RGD:7240710
DOID:820 myocarditis HGNC:11908 Homo sapiens (human) 8792 TNFRSF11A
  • MGI:6194238
DOID:11476 osteoporosis HGNC:11908 Homo sapiens (human) 8792 TNFRSF11A
  • PMID:17002564
DOID:10534 stomach cancer HGNC:11908 Homo sapiens (human) 8792 TNFRSF11A
  • PMID:28035468
DOID:0110946 autosomal recessive osteopetrosis 7 HGNC:11908 Homo sapiens (human) 8792 TNFRSF11A
  • RGD:7240710
DOID:5408 Paget's disease of bone HGNC:11908 Homo sapiens (human) 8792 TNFRSF11A
  • MGI:6194238
  • PMID:10615125
DOID:219 colon cancer HGNC:11907 Homo sapiens (human) 8793 TNFRSF10D
  • MGI:6194238
DOID:8398 osteoarthritis HGNC:11907 Homo sapiens (human) 8793 TNFRSF10D
  • MGI:6194238
DOID:219 colon cancer HGNC:11906 Homo sapiens (human) 8794 TNFRSF10C
  • MGI:6194238
DOID:8398 osteoarthritis HGNC:11906 Homo sapiens (human) 8794 TNFRSF10C
  • MGI:6194238
DOID:219 colon cancer HGNC:11905 Homo sapiens (human) 8795 TNFRSF10B
  • MGI:6194238
DOID:5520 head and neck squamous cell carcinoma HGNC:11905 Homo sapiens (human) 8795 TNFRSF10B
  • RGD:7240710
DOID:8398 osteoarthritis HGNC:11905 Homo sapiens (human) 8795 TNFRSF10B
  • MGI:6194238
DOID:3007 breast ductal carcinoma HGNC:11904 Homo sapiens (human) 8797 TNFRSF10A
  • PMID:17011986
DOID:219 colon cancer HGNC:11904 Homo sapiens (human) 8797 TNFRSF10A
  • MGI:6194238
DOID:4450 renal cell carcinoma HGNC:11904 Homo sapiens (human) 8797 TNFRSF10A
  • PMID:16865223
  • PMID:17184908
DOID:4362 cervical cancer HGNC:11904 Homo sapiens (human) 8797 TNFRSF10A
  • PMID:16271751
DOID:5520 head and neck squamous cell carcinoma HGNC:11904 Homo sapiens (human) 8797 TNFRSF10A
  • PMID:16217763
DOID:11054 urinary bladder cancer HGNC:11904 Homo sapiens (human) 8797 TNFRSF10A
  • PMID:16217763
DOID:8398 osteoarthritis HGNC:11904 Homo sapiens (human) 8797 TNFRSF10A
  • MGI:6194238

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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: December 9, 2024