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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 7051 - 7075 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:14227 azoospermia HGNC:7681 Homo sapiens (human) 8509 NDST2
  • MGI:6194238
DOID:1059 intellectual disability HGNC:7681 Homo sapiens (human) 8509 NDST2
  • MGI:6194238
DOID:1059 intellectual disability HGNC:7680 Homo sapiens (human) 3340 NDST1
  • MGI:6194238
DOID:11198 DiGeorge syndrome HGNC:7680 Homo sapiens (human) 3340 NDST1
  • MGI:6194238
DOID:14227 azoospermia HGNC:7680 Homo sapiens (human) 3340 NDST1
  • MGI:6194238
DOID:0081210 autosomal recessive intellectual developmental disorder 46 HGNC:7680 Homo sapiens (human) 3340 NDST1
  • RGD:7240710
DOID:12716 newborn respiratory distress syndrome HGNC:7680 Homo sapiens (human) 3340 NDST1
  • MGI:6194238
DOID:0060041 autism spectrum disorder HGNC:7680 Homo sapiens (human) 3340 NDST1
  • MGI:6194238
DOID:3827 congenital diaphragmatic hernia HGNC:7680 Homo sapiens (human) 3340 NDST1
  • MGI:6194238
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
DOID:2560 morphine dependence HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • 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: August 19, 2024