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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 5126 - 5150 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:10534 stomach cancer HGNC:7527 Homo sapiens (human) 4595 MUTYH
  • RGD:7240710
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: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
DOID:11206 opioid abuse HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • MGI:6194238
DOID:9744 type 1 diabetes mellitus HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • PMID:15714132
DOID:1596 depressive disorder HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • MGI:6194238
DOID:9974 drug dependence HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • PMID:18828801
DOID:5419 schizophrenia HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • PMID:30664618
DOID:3073 brain glioblastoma multiforme HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • PMID:20219118
DOID:4947 cholangiocarcinoma HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • PMID:12031086
DOID:3312 bipolar disorder HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • PMID:15050861
DOID:0060318 acute promyelocytic leukemia HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • PMID:24296270
DOID:657 adenoma HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • PMID:15100237
DOID:0050700 cardiomyopathy HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • PMID:23462508
DOID:1459 hypothyroidism HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • MGI:6194238
DOID:6000 congestive heart failure HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • MGI:6194238

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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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