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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 8276 - 8300 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0050866 oral squamous cell carcinoma HGNC:4141 Homo sapiens (human) 2597 GAPDH
  • MGI:6194238
DOID:1826 epilepsy HGNC:4141 Homo sapiens (human) 2597 GAPDH
  • MGI:6194238
DOID:0080322 polycystic kidney disease HGNC:4138 Homo sapiens (human) 23193 GANAB
  • PMID:27259053
DOID:0050770 polycystic liver disease HGNC:4138 Homo sapiens (human) 23193 GANAB
  • PMID:27259053
  • PMID:31462075
DOID:0110860 polycystic kidney disease 3 HGNC:4138 Homo sapiens (human) 23193 GANAB
  • RGD:7240710
DOID:9870 galactosemia HGNC:4135 Homo sapiens (human) 2592 GALT
  • MGI:6194238
DOID:0111459 classic galactosemia HGNC:4135 Homo sapiens (human) 2592 GALT
  • MGI:6194238
  • RGD:7240710
DOID:0111063 hyperphosphatemic familial tumoral calcinosis HGNC:4125 Homo sapiens (human) 2591 GALNT3
  • MGI:6194238
DOID:0050571 congenital disorder of glycosylation type II HGNC:4124 Homo sapiens (human) 2590 GALNT2
  • RGD:7240710
DOID:4079 heart valve disease HGNC:4123 Homo sapiens (human) 2589 GALNT1
  • MGI:6194238
DOID:12804 mucopolysaccharidosis IV HGNC:4122 Homo sapiens (human) 2588 GALNS
  • MGI:6194238
DOID:0111391 mucopolysaccharidosis IVA HGNC:4122 Homo sapiens (human) 2588 GALNS
  • RGD:7240710
DOID:83 cataract HGNC:4118 Homo sapiens (human) 2584 GALK1
  • PMID:7670469
DOID:14695 galactokinase deficiency HGNC:4118 Homo sapiens (human) 2584 GALK1
  • RGD:7240710
DOID:0110777 hereditary spastic paraplegia 26 HGNC:4117 Homo sapiens (human) 2583 B4GALNT1
  • RGD:7240710
DOID:1588 thrombocytopenia HGNC:4116 Homo sapiens (human) 2582 GALE
  • MGI:6194238
DOID:9870 galactosemia HGNC:4116 Homo sapiens (human) 2582 GALE
  • MGI:6194238
DOID:0111458 galactose epimerase deficiency HGNC:4116 Homo sapiens (human) 2582 GALE
  • RGD:7240710
DOID:13276 Mycoplasma pneumoniae pneumonia HGNC:4115 Homo sapiens (human) 2581 GALC
  • PMID:12225900
  • PMID:27490360
  • PMID:29301655
  • PMID:30396892
DOID:10587 Krabbe disease HGNC:4115 Homo sapiens (human) 2581 GALC
  • MGI:6194238
  • RGD:7240710
DOID:1909 melanoma HGNC:4115 Homo sapiens (human) 2581 GALC
  • MGI:6194238
DOID:11949 Creutzfeldt-Jakob disease HGNC:4115 Homo sapiens (human) 2581 GALC
  • PMID:30009661
DOID:14501 Sjogren-Larsson syndrome HGNC:411 Homo sapiens (human) 222 ALDH3B2
  • MGI:6194238
DOID:14501 Sjogren-Larsson syndrome HGNC:410 Homo sapiens (human) 221 ALDH3B1
  • MGI:6194238
DOID:1574 alcohol use disorder HGNC:4093 Homo sapiens (human) 2572 GAD2
  • MGI:6194238

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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: August 19, 2024