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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 11876 - 11900 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▼ Evidence Code Names References
DOID:5212 congenital disorder of glycosylation ZFIN:ZDB-GENE-030131-6093 Danio rerio (zebrafish) 334161 alg1
  • MGI:6194238
DOID:9952 acute lymphoblastic leukemia HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:16676594
  • PMID:22964275
  • PMID:23725389
DOID:0060611 abdominal obesity-metabolic syndrome HGNC:18448 Homo sapiens (human) 79661 NEIL1
  • MGI:6194238
DOID:2394 ovarian cancer Xenbase:XB-GENE-5793241 Xenopus tropicalis (tropical clawed frog) 100135191 ugt1a6
  • MGI:6194238
DOID:0060250 idiopathic scoliosis HGNC:20862 Homo sapiens (human) 64116 SLC39A8
  • MGI:6194238
DOID:11054 urinary bladder cancer SGD:S000001949 Saccharomyces cerevisiae S288C 850614 HXK1
  • MGI:6194238
DOID:10223 dermatomyositis MGI:96824 Mus musculus (house mouse) 21898 Tlr4
  • MGI:6194238
DOID:1793 pancreatic cancer HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • PMID:10374842
  • PMID:11249065
DOID:8719 in situ carcinoma HGNC:9599 Homo sapiens (human) 9536 PTGES
  • PMID:14499677
  • PMID:14871981
DOID:1380 endometrial cancer HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:17023034
DOID:0090145 dopamine beta-hydroxylase deficiency SGD:S000003571 Saccharomyces cerevisiae S288C 853418 KAR2
  • MGI:6194238
DOID:0080600 COVID-19 RGD:628609 Rattus norvegicus (Norway rat) 65270 Abo3
  • MGI:6194238
DOID:0111040 glycogen storage disease IXd MGI:97576 Mus musculus (house mouse) 18679 Phka1
  • MGI:6194238
  • PMID:7874115
DOID:0080132 Sengers syndrome HGNC:21869 Homo sapiens (human) 55750 AGK
  • RGD:7240710
DOID:1440 Machado-Joseph disease HGNC:4242 Homo sapiens (human) 9945 GFPT2
  • MGI:6194238
DOID:28 endocrine system disease HGNC:924 Homo sapiens (human) 2683 B4GALT1
  • MGI:6194238
DOID:83 cataract SGD:S000004060 Saccharomyces cerevisiae S288C 850759 XYL2
  • MGI:6194238
DOID:0060224 atrial fibrillation HGNC:11848 Homo sapiens (human) 7097 TLR2
  • PMID:19167648
DOID:438 autoimmune disease of the nervous system WB:WBGene00017166 Caenorhabditis elegans 175827 aldo-2
  • MGI:6194238
DOID:9970 obesity WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238
DOID:4194 glucose metabolism disease MGI:1270854 Mus musculus (house mouse) 103988 Gck
  • MGI:6194238
DOID:3525 middle cerebral artery infarction WB:WBGene00001686 Caenorhabditis elegans 174578 gpd-4
  • MGI:6194238
DOID:2048 autoimmune hepatitis MGI:106675 Mus musculus (house mouse) 11450 Adipoq
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease RGD:3932 Rattus norvegicus (Norway rat) 54315 Ucp2
  • MGI:6194238
  • PMID:18543254
  • PMID:21359922
DOID:4928 intrahepatic cholangiocarcinoma HGNC:5383 Homo sapiens (human) 3418 IDH2
  • PMID:22824796

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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