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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 9201 - 9225 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0081427 autosomal recessive distal hereditary motor neuronopathy 8 MGI:98266 Mus musculus (house mouse) 20322 Sord
  • MGI:6194238
DOID:83 cataract MGI:98266 Mus musculus (house mouse) 20322 Sord
  • PMID:18760274
DOID:9743 diabetic neuropathy MGI:98266 Mus musculus (house mouse) 20322 Sord
  • MGI:6194238
DOID:1712 aortic valve stenosis HGNC:3354 Homo sapiens (human) 2027 ENO3
  • MGI:6194238
DOID:0080855 Parkinsonism HGNC:3353 Homo sapiens (human) 2026 ENO2
  • MGI:6194238
DOID:14115 toxic shock syndrome HGNC:3353 Homo sapiens (human) 2026 ENO2
  • MGI:6194238
DOID:11054 urinary bladder cancer HGNC:3353 Homo sapiens (human) 2026 ENO2
  • PMID:17951193
DOID:10763 hypertension HGNC:3353 Homo sapiens (human) 2026 ENO2
  • PMID:21130083
DOID:3459 breast carcinoma HGNC:3353 Homo sapiens (human) 2026 ENO2
  • PMID:16608642
DOID:1800 neuroendocrine carcinoma HGNC:3353 Homo sapiens (human) 2026 ENO2
  • PMID:15010880
DOID:11832 visual epilepsy HGNC:3353 Homo sapiens (human) 2026 ENO2
  • MGI:6194238
DOID:936 brain disease HGNC:3353 Homo sapiens (human) 2026 ENO2
  • PMID:20847541
DOID:12783 migraine without aura HGNC:3353 Homo sapiens (human) 2026 ENO2
  • PMID:21293918
DOID:10283 prostate cancer HGNC:3353 Homo sapiens (human) 2026 ENO2
  • PMID:15239127
DOID:10652 Alzheimer's disease HGNC:3350 Homo sapiens (human) 2023 ENO1
  • PMID:17387692
DOID:10763 hypertension HGNC:3350 Homo sapiens (human) 2023 ENO1
  • MGI:6194238
DOID:0080573 congenital disorder of glycosylation Ix HGNC:30611 Homo sapiens (human) 201595 STT3B
  • RGD:7240710
DOID:0080572 congenital disorder of glycosylation Iw HGNC:30611 Homo sapiens (human) 201595 STT3B
  • MGI:6194238
DOID:162 cancer HGNC:9640 Homo sapiens (human) 201562 HACD2
  • MGI:6194238
DOID:8778 Crohn's disease HGNC:23785 Homo sapiens (human) 200576 PIKFYVE
  • MGI:6194238
DOID:0060448 Fleck corneal dystrophy HGNC:23785 Homo sapiens (human) 200576 PIKFYVE
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:27301 Homo sapiens (human) 200186 CRTC2
  • MGI:6194238
DOID:0110658 congenital myasthenic syndrome 15 HGNC:28287 Homo sapiens (human) 199857 ALG14
  • RGD:7240710
DOID:162 cancer FB:FBgn0266438 Drosophila melanogaster (fruit fly) 19835548 PIG-Z
  • MGI:6194238
DOID:0070433 hyperphosphatasia with impaired intellectual development syndrome 1 FB:FBgn0265174 Drosophila melanogaster (fruit fly) 19835383 PIG-V
  • MGI:6194238

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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