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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 5926 - 5950 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:4556 lung large cell carcinoma FB:FBgn0004647 Drosophila melanogaster (fruit fly) 31293 N CG3936
  • MGI:6194238
DOID:479 angiokeratoma HGNC:7631 Homo sapiens (human) 4668 NAGA
  • PMID:8040340
DOID:0112318 Schindler disease type 1 HGNC:7631 Homo sapiens (human) 4668 NAGA
  • RGD:7240710
DOID:0112319 Kanzaki disease HGNC:7631 Homo sapiens (human) 4668 NAGA
  • RGD:7240710
DOID:2367 neuroaxonal dystrophy HGNC:7631 Homo sapiens (human) 4668 NAGA
  • PMID:2243144
DOID:14499 Fabry disease HGNC:7631 Homo sapiens (human) 4668 NAGA
  • MGI:6194238
DOID:10754 otitis media HGNC:7632 Homo sapiens (human) 4669 NAGLU
  • MGI:6194238
DOID:0110178 Charcot-Marie-Tooth disease axonal type 2V HGNC:7632 Homo sapiens (human) 4669 NAGLU
  • RGD:7240710
DOID:0111394 mucopolysaccharidosis type IIIB HGNC:7632 Homo sapiens (human) 4669 NAGLU
  • RGD:7240710
DOID:12801 mucopolysaccharidosis III HGNC:7632 Homo sapiens (human) 4669 NAGLU
  • MGI:6194238
  • PMID:11136549
  • PMID:11668611
  • PMID:4261742
DOID:8893 psoriasis HGNC:30092 Homo sapiens (human) 10135 NAMPT
  • PMID:22151390
DOID:3407 carotid artery disease HGNC:30092 Homo sapiens (human) 10135 NAMPT
  • PMID:17283255
DOID:3393 coronary artery disease HGNC:30092 Homo sapiens (human) 10135 NAMPT
  • PMID:17283255
DOID:1074 kidney failure HGNC:30092 Homo sapiens (human) 10135 NAMPT
  • MGI:6194238
DOID:3525 middle cerebral artery infarction HGNC:30092 Homo sapiens (human) 10135 NAMPT
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:30092 Homo sapiens (human) 10135 NAMPT
  • MGI:6194238
DOID:6432 pulmonary hypertension HGNC:30092 Homo sapiens (human) 10135 NAMPT
  • MGI:6194238
  • PMID:28202489
DOID:224 transient cerebral ischemia HGNC:30092 Homo sapiens (human) 10135 NAMPT
  • MGI:6194238
  • PMID:25603815
DOID:9970 obesity HGNC:30092 Homo sapiens (human) 10135 NAMPT
  • PMID:17618961
DOID:824 periodontitis HGNC:30092 Homo sapiens (human) 10135 NAMPT
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:30092 Homo sapiens (human) 10135 NAMPT
  • PMID:16234302
  • PMID:18410550
DOID:0080576 spondyloepimetaphyseal dysplasia, Genevieve-type FB:FBgn0038045 Drosophila melanogaster (fruit fly) 41528 NANS
  • MGI:6194238
DOID:0080576 spondyloepimetaphyseal dysplasia, Genevieve-type HGNC:19237 Homo sapiens (human) 54187 NANS
  • RGD:7240710
DOID:3525 middle cerebral artery infarction HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • MGI:6194238
  • PMID:32962079
DOID:3892 insulinoma HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • PMID:8972754

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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: August 19, 2024