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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 5251 - 5275 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:1793 pancreatic cancer Xenbase:XB-GENE-864803 Xenopus laevis (African clawed frog) 378695 ins.L
  • MGI:6194238
DOID:9744 type 1 diabetes mellitus Xenbase:XB-GENE-864803 Xenopus laevis (African clawed frog) 378695 ins.L
  • MGI:6194238
DOID:0111238 congenital muscular dystrophy-dystroglycanopathy type A13 FB:FBgn0041706 Drosophila melanogaster (fruit fly) 37861 CG3253 CG3253
  • MGI:6194238
DOID:0050560 Walker-Warburg syndrome FB:FBgn0041706 Drosophila melanogaster (fruit fly) 37861 CG3253 CG3253
  • MGI:6194238
DOID:0050588 muscular dystrophy-dystroglycanopathy type B1 FB:FBgn0041706 Drosophila melanogaster (fruit fly) 37861 CG3253 CG3253
  • MGI:6194238
DOID:0111843 Paganini-Miozzo syndrome ZFIN:ZDB-GENE-030909-14 Danio rerio (zebrafish) 378450 hs6st2
  • MGI:6194238
DOID:0060224 atrial fibrillation HGNC:6294 Homo sapiens (human) 3784 KCNQ1
  • PMID:12522251
DOID:2842 Jervell-Lange Nielsen syndrome HGNC:6294 Homo sapiens (human) 3784 KCNQ1
  • MGI:6194238
  • PMID:12051962
  • RGD:7240710
DOID:2843 long QT syndrome HGNC:6294 Homo sapiens (human) 3784 KCNQ1
  • MGI:6194238
  • PMID:15840476
  • PMID:22199116
DOID:9352 type 2 diabetes mellitus HGNC:6294 Homo sapiens (human) 3784 KCNQ1
  • PMID:27281273
DOID:0050793 short QT syndrome HGNC:6294 Homo sapiens (human) 3784 KCNQ1
  • RGD:7240710
DOID:0050650 familial atrial fibrillation HGNC:6294 Homo sapiens (human) 3784 KCNQ1
  • RGD:7240710
DOID:4440 seminoma HGNC:6294 Homo sapiens (human) 3784 KCNQ1
  • PMID:15389592
DOID:10763 hypertension HGNC:6294 Homo sapiens (human) 3784 KCNQ1
  • MGI:6194238
DOID:0110644 long QT syndrome 1 HGNC:6294 Homo sapiens (human) 3784 KCNQ1
  • MGI:6194238
  • RGD:7240710
DOID:2978 carbohydrate metabolic disorder FB:FBgn0023477 Drosophila melanogaster (fruit fly) 37804 Taldo
  • MGI:6194238
DOID:5212 congenital disorder of glycosylation FB:FBgn0011297 Drosophila melanogaster (fruit fly) 37754 Alg3 CG4084
  • MGI:6194238
DOID:0080556 congenital disorder of glycosylation Id FB:FBgn0011297 Drosophila melanogaster (fruit fly) 37754 Alg3 CG4084
  • MGI:6194238
DOID:14500 fucosidosis FB:FBgn0285958 Drosophila melanogaster (fruit fly) 3772574 Fuca
  • MGI:6194238
DOID:9744 type 1 diabetes mellitus FB:FBgn0285958 Drosophila melanogaster (fruit fly) 3772574 Fuca
  • MGI:6194238
DOID:8947 diabetic retinopathy FB:FBgn0285958 Drosophila melanogaster (fruit fly) 3772574 Fuca
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus FB:FBgn0285958 Drosophila melanogaster (fruit fly) 3772574 Fuca
  • MGI:6194238
DOID:9351 diabetes mellitus FB:FBgn0285958 Drosophila melanogaster (fruit fly) 3772574 Fuca
  • MGI:6194238
DOID:206 hereditary multiple exostoses FB:FBgn0029175 Drosophila melanogaster (fruit fly) 3772101 sotv CG8433
  • MGI:6194238
DOID:9351 diabetes mellitus HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • PMID:15292329

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Supported by JST NBDC Grant Number JPMJND2204

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


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