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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 10701 - 10725 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:8577 ulcerative colitis HGNC:10721 Homo sapiens (human) 6403 SELP
  • PMID:21526498
DOID:684 hepatocellular carcinoma HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:21559380
  • PMID:25179842
  • PMID:28578348
DOID:3069 malignant astrocytoma HGNC:1119 Homo sapiens (human) 684 BST2
  • PMID:21565182
DOID:8741 seborrheic dermatitis HGNC:11848 Homo sapiens (human) 7097 TLR2
  • PMID:21566548
DOID:684 hepatocellular carcinoma HGNC:8574 Homo sapiens (human) 5048 PAFAH1B1
  • PMID:21569763
DOID:0080159 Cryptococcal meningitis HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:21592999
DOID:2316 brain ischemia RGD:2081 Rattus norvegicus (Norway rat) 24185 Akt1
  • PMID:21596097
DOID:0050861 colorectal adenocarcinoma HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • PMID:21609933
DOID:1580 diffuse scleroderma HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • PMID:21615510
DOID:0050864 non-arteritic anterior ischemic optic neuropathy HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:21633717
DOID:0081267 graft-versus-host disease HGNC:10720 Homo sapiens (human) 6402 SELL
  • PMID:21635226
DOID:3393 coronary artery disease HGNC:11009 Homo sapiens (human) 6517 SLC2A4
  • PMID:21645024
DOID:9470 bacterial meningitis HGNC:270 Homo sapiens (human) 142 PARP1
  • PMID:21651918
DOID:2377 multiple sclerosis HGNC:29013 Homo sapiens (human) 23274 CLEC16A
  • PMID:21653641
DOID:9884 muscular dystrophy HGNC:1938 Homo sapiens (human) 1120 CHKB
  • PMID:21665002
DOID:1059 intellectual disability HGNC:1938 Homo sapiens (human) 1120 CHKB
  • PMID:21665002
DOID:3393 coronary artery disease HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:21679057
DOID:684 hepatocellular carcinoma RGD:3560 Rattus norvegicus (Norway rat) 25106 Rgn
  • PMID:21683810
DOID:10690 mastitis RGD:3870 Rattus norvegicus (Norway rat) 29260 Tlr4
  • PMID:21691936
DOID:0050848 obstructive sleep apnea HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:21698055
DOID:8778 Crohn's disease HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:21702710
DOID:0060496 respiratory allergy HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:21704886
DOID:0050127 sinusitis HGNC:9053 Homo sapiens (human) 5329 PLAUR
  • PMID:21711960
DOID:9279 hyperhomocysteinemia RGD:2645 Rattus norvegicus (Norway rat) 24377 G6pd
  • PMID:21717134
DOID:10591 pre-eclampsia HGNC:9053 Homo sapiens (human) 5329 PLAUR
  • PMID:21722073

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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