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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 8551 - 8575 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:4500 hypokalemia HGNC:381 Homo sapiens (human) 231 AKR1B1
  • MGI:6194238
DOID:1205 allergic disease HGNC:381 Homo sapiens (human) 231 AKR1B1
  • MGI:6194238
DOID:10534 stomach cancer HGNC:381 Homo sapiens (human) 231 AKR1B1
  • PMID:23808167
DOID:9743 diabetic neuropathy HGNC:381 Homo sapiens (human) 231 AKR1B1
  • MGI:6194238
  • PMID:9489533
DOID:9870 galactosemia HGNC:381 Homo sapiens (human) 231 AKR1B1
  • MGI:6194238
DOID:4195 hyperglycemia HGNC:381 Homo sapiens (human) 231 AKR1B1
  • MGI:6194238
DOID:83 cataract HGNC:381 Homo sapiens (human) 231 AKR1B1
  • MGI:6194238
  • PMID:21329682
  • PMID:24360973
DOID:8947 diabetic retinopathy HGNC:381 Homo sapiens (human) 231 AKR1B1
  • MGI:6194238
  • PMID:16701918
  • PMID:19587357
  • PMID:21067572
DOID:9352 type 2 diabetes mellitus HGNC:381 Homo sapiens (human) 231 AKR1B1
  • PMID:15569136
DOID:684 hepatocellular carcinoma HGNC:381 Homo sapiens (human) 231 AKR1B1
  • MGI:6194238
  • PMID:19422879
DOID:332 amyotrophic lateral sclerosis HGNC:17074 Homo sapiens (human) 23098 SARM1
  • MGI:6194238
DOID:1289 neurodegenerative disease HGNC:17074 Homo sapiens (human) 23098 SARM1
  • MGI:6194238
DOID:0070433 hyperphosphatasia with impaired intellectual development syndrome 1 MGI:2442480 Mus musculus (house mouse) 230801 Pigv
  • MGI:6194238
DOID:9970 obesity MGI:2685541 Mus musculus (house mouse) 230796 Wdtc1
  • MGI:6194238
DOID:9970 obesity HGNC:29175 Homo sapiens (human) 23038 WDTC1
  • MGI:6194238
DOID:916 liver benign neoplasm MGI:87995 Mus musculus (house mouse) 230163 Aldob
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus MGI:87995 Mus musculus (house mouse) 230163 Aldob
  • MGI:6194238
DOID:9869 hereditary fructose intolerance syndrome MGI:87995 Mus musculus (house mouse) 230163 Aldob
  • MGI:6194238
DOID:8283 peritonitis MGI:87995 Mus musculus (house mouse) 230163 Aldob
  • MGI:6194238
DOID:9256 colorectal cancer MGI:2444664 Mus musculus (house mouse) 230145 Galnt12
  • MGI:6194238
DOID:0110798 hereditary spastic paraplegia 46 MGI:2654325 Mus musculus (house mouse) 230101 Gba2
  • MGI:6194238
DOID:4621 holoprosencephaly HGNC:29185 Homo sapiens (human) 23007 PLCH1
  • RGD:7240710
DOID:684 hepatocellular carcinoma HGNC:418 Homo sapiens (human) 230 ALDOC
  • MGI:6194238
DOID:5154 borna disease HGNC:418 Homo sapiens (human) 230 ALDOC
  • MGI:6194238
DOID:438 autoimmune disease of the nervous system HGNC:418 Homo sapiens (human) 230 ALDOC
  • PMID:16356555

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Supported by JST NBDC Grant Number JPMJND2204

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


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