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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 8151 - 8175 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:10652 Alzheimer's disease HGNC:433 Homo sapiens (human) 246 ALOX15
  • PMID:15111312
DOID:8947 diabetic retinopathy HGNC:4323 Homo sapiens (human) 2739 GLO1
  • PMID:21738003
DOID:9352 type 2 diabetes mellitus HGNC:4323 Homo sapiens (human) 2739 GLO1
  • MGI:6194238
  • PMID:18413187
DOID:783 end stage renal disease HGNC:4323 Homo sapiens (human) 2739 GLO1
  • PMID:20185929
DOID:178 vascular disease HGNC:4323 Homo sapiens (human) 2739 GLO1
  • PMID:18079478
DOID:12849 autistic disorder HGNC:4323 Homo sapiens (human) 2739 GLO1
  • PMID:17346350
DOID:9268 glycine encephalopathy HGNC:4313 Homo sapiens (human) 2731 GLDC
  • MGI:6194238
  • PMID:15851735
  • PMID:17361008
  • RGD:7240710
DOID:10534 stomach cancer HGNC:4313 Homo sapiens (human) 2731 GLDC
  • PMID:26722042
DOID:5082 liver cirrhosis HGNC:4311 Homo sapiens (human) 2729 GCLC
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:4311 Homo sapiens (human) 2729 GCLC
  • PMID:12598062
  • RGD:7240710
DOID:1485 cystic fibrosis HGNC:4311 Homo sapiens (human) 2729 GCLC
  • PMID:16690975
DOID:9256 colorectal cancer HGNC:4311 Homo sapiens (human) 2729 GCLC
  • PMID:8705999
DOID:83 cataract HGNC:4311 Homo sapiens (human) 2729 GCLC
  • MGI:6194238
DOID:0111681 glutamate-cysteine ligase deficiency HGNC:4311 Homo sapiens (human) 2729 GCLC
  • RGD:7240710
DOID:9675 pulmonary emphysema HGNC:4311 Homo sapiens (human) 2729 GCLC
  • MGI:6194238
DOID:583 hemolytic anemia HGNC:4311 Homo sapiens (human) 2729 GCLC
  • PMID:10733484
DOID:0060710 autosomal recessive congenital ichthyosis 2 HGNC:430 Homo sapiens (human) 242 ALOX12B
  • RGD:7240710
DOID:12804 mucopolysaccharidosis IV HGNC:4298 Homo sapiens (human) 2720 GLB1
  • PMID:11511921
  • PMID:19091613
DOID:0080502 GM1 gangliosidosis type 1 HGNC:4298 Homo sapiens (human) 2720 GLB1
  • RGD:7240710
DOID:0111392 mucopolysaccharidosis type IVB HGNC:4298 Homo sapiens (human) 2720 GLB1
  • RGD:7240710
DOID:0080501 GM1 gangliosidosis type 2 HGNC:4298 Homo sapiens (human) 2720 GLB1
  • RGD:7240710
DOID:3322 GM1 gangliosidosis HGNC:4298 Homo sapiens (human) 2720 GLB1
  • MGI:6194238
  • PMID:10737981
  • PMID:17309651
DOID:0080489 GM1 gangliosidosis type 3 HGNC:4298 Homo sapiens (human) 2720 GLB1
  • RGD:7240710
DOID:14499 Fabry disease HGNC:4296 Homo sapiens (human) 2717 GLA
  • MGI:6194238
  • PMID:2539398
  • RGD:7240710
DOID:3211 lysosomal storage disease HGNC:4296 Homo sapiens (human) 2717 GLA
  • MGI:6194238

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

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Supported by JST NBDC Grant Number JPMJND2204

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


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