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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 2576 - 2600 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:2738 pseudoxanthoma elasticum HGNC:15517 Homo sapiens (human) 64132 XYLT2
  • RGD:7240710
DOID:2738 pseudoxanthoma elasticum HGNC:15516 Homo sapiens (human) 64131 XYLT1
  • RGD:7240710
DOID:557 kidney disease HGNC:15516 Homo sapiens (human) 64131 XYLT1
  • MGI:6194238
DOID:0060462 Desbuquois dysplasia HGNC:15516 Homo sapiens (human) 64131 XYLT1
  • RGD:7240710
DOID:9744 type 1 diabetes mellitus HGNC:15516 Homo sapiens (human) 64131 XYLT1
  • PMID:16759312
DOID:0060480 left ventricular noncompaction HGNC:20862 Homo sapiens (human) 64116 SLC39A8
  • MGI:6194238
DOID:0070266 congenital disorder of glycosylation type IIn HGNC:20862 Homo sapiens (human) 64116 SLC39A8
  • RGD:7240710
DOID:0060250 idiopathic scoliosis HGNC:20862 Homo sapiens (human) 64116 SLC39A8
  • MGI:6194238
DOID:2754 glycogen storage disease VI RGD:620687 Rattus norvegicus (Norway rat) 64035 Pygl
  • MGI:6194238
  • PMID:17705025
  • PMID:21646031
DOID:2747 glycogen storage disease RGD:620687 Rattus norvegicus (Norway rat) 64035 Pygl
  • MGI:6194238
DOID:3650 lactic acidosis RGD:620687 Rattus norvegicus (Norway rat) 64035 Pygl
  • MGI:6194238
  • PMID:17705025
DOID:10652 Alzheimer's disease HGNC:10721 Homo sapiens (human) 6403 SELP
  • PMID:21484243
DOID:3310 atopic dermatitis HGNC:10721 Homo sapiens (human) 6403 SELP
  • PMID:12929084
DOID:1936 atherosclerosis HGNC:10721 Homo sapiens (human) 6403 SELP
  • MGI:6194238
DOID:0080998 acute necrotizing pancreatitis HGNC:10721 Homo sapiens (human) 6403 SELP
  • MGI:6194238
DOID:8577 ulcerative colitis HGNC:10721 Homo sapiens (human) 6403 SELP
  • PMID:21526498
DOID:13378 Kawasaki disease HGNC:10721 Homo sapiens (human) 6403 SELP
  • PMID:20079717
DOID:9352 type 2 diabetes mellitus HGNC:10721 Homo sapiens (human) 6403 SELP
  • PMID:17598012
DOID:676 juvenile rheumatoid arthritis HGNC:10721 Homo sapiens (human) 6403 SELP
  • PMID:21124648
DOID:8805 intermediate coronary syndrome HGNC:10721 Homo sapiens (human) 6403 SELP
  • PMID:21162967
DOID:3083 chronic obstructive pulmonary disease HGNC:10721 Homo sapiens (human) 6403 SELP
  • PMID:20646456
DOID:0060180 colitis HGNC:10721 Homo sapiens (human) 6403 SELP
  • MGI:6194238
DOID:12894 Sjogren's syndrome HGNC:10721 Homo sapiens (human) 6403 SELP
  • PMID:19832990
DOID:4780 anti-basement membrane glomerulonephritis HGNC:10721 Homo sapiens (human) 6403 SELP
  • MGI:6194238
DOID:0112313 brain small vessel disease HGNC:10721 Homo sapiens (human) 6403 SELP
  • PMID:20885295

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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