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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 62176 - 62200 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:2018 hyperinsulinism HGNC:59 Homo sapiens (human) 6833 ABCC8
  • PMID:12199344
DOID:11446 sciatic neuropathy HGNC:59 Homo sapiens (human) 6833 ABCC8
  • MGI:6194238
DOID:1824 status epilepticus HGNC:59 Homo sapiens (human) 6833 ABCC8
  • MGI:6194238
DOID:0080855 Parkinsonism HGNC:59 Homo sapiens (human) 6833 ABCC8
  • MGI:6194238
DOID:0070219 familial hyperinsulinemic hypoglycemia 1 HGNC:59 Homo sapiens (human) 6833 ABCC8
  • RGD:7240710
DOID:11832 visual epilepsy HGNC:59 Homo sapiens (human) 6833 ABCC8
  • MGI:6194238
DOID:0110187 Charcot-Marie-Tooth disease type 4K HGNC:11474 Homo sapiens (human) 6834 SURF1
  • RGD:7240710
DOID:0070491 mitochondrial complex IV deficiency nuclear type 1 HGNC:11474 Homo sapiens (human) 6834 SURF1
  • MGI:6194238
  • RGD:7240710
DOID:3652 Leigh disease HGNC:11474 Homo sapiens (human) 6834 SURF1
  • MGI:6194238
  • PMID:9843204
DOID:0112139 nuclear type mitochondrial complex I deficiency 35 MGI:1915592 Mus musculus (house mouse) 68342 Ndufb10
  • MGI:6194238
DOID:0081267 graft-versus-host disease MGI:95937 Mus musculus (house mouse) 68395 H2-Q8
  • MGI:6194238
DOID:3069 malignant astrocytoma HGNC:1119 Homo sapiens (human) 684 BST2
  • PMID:21565182
DOID:10534 stomach cancer HGNC:1119 Homo sapiens (human) 684 BST2
  • PMID:26832883
DOID:12894 Sjogren's syndrome HGNC:1119 Homo sapiens (human) 684 BST2
  • PMID:30249485
DOID:0050866 oral squamous cell carcinoma HGNC:1119 Homo sapiens (human) 684 BST2
  • PMID:24706327
DOID:635 acquired immunodeficiency syndrome HGNC:1119 Homo sapiens (human) 684 BST2
  • PMID:26885809
DOID:3748 esophagus squamous cell carcinoma HGNC:1119 Homo sapiens (human) 684 BST2
  • PMID:26832883
DOID:1380 endometrial cancer HGNC:1119 Homo sapiens (human) 684 BST2
  • PMID:22729361
  • PMID:26498112
DOID:0112108 myofibrillar myopathy 10 HGNC:11480 Homo sapiens (human) 6840 SVIL
  • RGD:7240710
DOID:0112136 severe congenital neutropenia 4 MGI:1915651 Mus musculus (house mouse) 68401 G6pc3
  • MGI:6194238
DOID:0050717 methylmalonic aciduria and homocystinuria type cblF MGI:1915671 Mus musculus (house mouse) 68421 Lmbrd1
  • MGI:6194238
DOID:0111626 D-glyceric aciduria RGD:1591498 Rattus norvegicus (Norway rat) 684314 Glyctk
  • MGI:6194238
DOID:11446 sciatic neuropathy RGD:1589169 Rattus norvegicus (Norway rat) 684516 Kcnc4
  • PMID:17855600
DOID:10652 Alzheimer's disease RGD:1589169 Rattus norvegicus (Norway rat) 684516 Kcnc4
  • MGI:6194238
DOID:1824 status epilepticus RGD:1589169 Rattus norvegicus (Norway rat) 684516 Kcnc4
  • PMID:17942314
  • PMID:20971086

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

Acknowledgements

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