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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 70651 - 70675 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:9277 primary cerebellar degeneration HGNC:17663 Homo sapiens (human) 10531 PITRM1
  • MGI:6194238
DOID:12930 dilated cardiomyopathy HGNC:16932 Homo sapiens (human) 10529 NEBL
  • PMID:11140941
DOID:0050983 spinocerebellar ataxia type 36 HGNC:15911 Homo sapiens (human) 10528 NOP56
  • RGD:7240710
DOID:0111974 immunodeficiency 59 HGNC:16931 Homo sapiens (human) 10525 HYOU1
  • RGD:7240710
DOID:0070054 Vulto-van Silfout-de Vries syndrome HGNC:14677 Homo sapiens (human) 10522 DEAF1
  • RGD:7240710
DOID:0060611 abdominal obesity-metabolic syndrome HGNC:2740 Homo sapiens (human) 10521 DDX17
  • MGI:6194238
DOID:162 cancer HGNC:2740 Homo sapiens (human) 10521 DDX17
  • MGI:6194238
DOID:1574 alcohol use disorder HGNC:2740 Homo sapiens (human) 10521 DDX17
  • MGI:6194238
DOID:3534 Lafora disease MGI:2145264 Mus musculus (house mouse) 105193 Nhlrc1
  • PMID:20538597
  • PMID:21077101
  • PMID:21882344
  • PMID:22186026
DOID:10871 age related macular degeneration HGNC:3602 Homo sapiens (human) 10516 FBLN5
  • RGD:7240710
DOID:3144 cutis laxa HGNC:3602 Homo sapiens (human) 10516 FBLN5
  • MGI:6194238
  • PMID:12189163
DOID:10595 Charcot-Marie-Tooth disease HGNC:3602 Homo sapiens (human) 10516 FBLN5
  • RGD:7240710
DOID:0070135 autosomal recessive cutis laxa type IA HGNC:3602 Homo sapiens (human) 10516 FBLN5
  • RGD:7240710
DOID:0070136 autosomal dominant cutis laxa 2 HGNC:3602 Homo sapiens (human) 10516 FBLN5
  • RGD:7240710
DOID:7148 rheumatoid arthritis HGNC:10725 Homo sapiens (human) 10512 SEMA3C
  • PMID:15077297
DOID:10652 Alzheimer's disease HGNC:1834 Homo sapiens (human) 1051 CEBPB
  • PMID:12391607
DOID:7148 rheumatoid arthritis HGNC:1834 Homo sapiens (human) 1051 CEBPB
  • PMID:19248099
DOID:2256 osteochondrodysplasia HGNC:1834 Homo sapiens (human) 1051 CEBPB
  • MGI:6194238
DOID:934 viral infectious disease HGNC:1834 Homo sapiens (human) 1051 CEBPB
  • MGI:6194238
DOID:684 hepatocellular carcinoma HGNC:1834 Homo sapiens (human) 1051 CEBPB
  • PMID:30659195
DOID:891 progressive myoclonus epilepsy HGNC:10739 Homo sapiens (human) 10501 SEMA6B
  • RGD:7240710
DOID:3908 lung non-small cell carcinoma HGNC:7669 Homo sapiens (human) 10499 NCOA2
  • PMID:23144319
DOID:10534 stomach cancer HGNC:7669 Homo sapiens (human) 10499 NCOA2
  • PMID:32489143
DOID:7474 malignant pleural mesothelioma HGNC:7669 Homo sapiens (human) 10499 NCOA2
  • PMID:22011668
DOID:0050861 colorectal adenocarcinoma HGNC:7669 Homo sapiens (human) 10499 NCOA2
  • PMID:19198856

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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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