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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 3626 - 3650 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:916 liver benign neoplasm HGNC:417 Homo sapiens (human) 229 ALDOB
  • MGI:6194238
DOID:8283 peritonitis HGNC:417 Homo sapiens (human) 229 ALDOB
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:417 Homo sapiens (human) 229 ALDOB
  • MGI:6194238
  • PMID:12646233
DOID:0050439 Usher syndrome HGNC:24102 Homo sapiens (human) 22901 ARSG
  • RGD:7240710
DOID:12798 mucopolysaccharidosis HGNC:24102 Homo sapiens (human) 22901 ARSG
  • MGI:6194238
DOID:1883 hepatitis C HGNC:18788 Homo sapiens (human) 22914 KLRK1
  • PMID:26518141
  • PMID:27091211
DOID:4231 histiocytoma HGNC:18788 Homo sapiens (human) 22914 KLRK1
  • MGI:6194238
DOID:11168 anogenital venereal wart HGNC:18788 Homo sapiens (human) 22914 KLRK1
  • PMID:23754510
DOID:0060704 lymphoproliferative syndrome HGNC:18788 Homo sapiens (human) 22914 KLRK1
  • PMID:22105417
DOID:399 tuberculosis HGNC:18788 Homo sapiens (human) 22914 KLRK1
  • PMID:23922903
DOID:321 tropical spastic paraparesis HGNC:18788 Homo sapiens (human) 22914 KLRK1
  • PMID:22170554
DOID:3963 thyroid gland carcinoma HGNC:15855 Homo sapiens (human) 22918 CD93
  • PMID:32626543
DOID:9975 cocaine dependence HGNC:10886 Homo sapiens (human) 22933 SIRT2
  • MGI:6194238
DOID:3669 intermittent claudication HGNC:10886 Homo sapiens (human) 22933 SIRT2
  • MGI:6194238
DOID:3070 high grade glioma HGNC:10886 Homo sapiens (human) 22933 SIRT2
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:10886 Homo sapiens (human) 22933 SIRT2
  • MGI:6194238
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
DOID:4621 holoprosencephaly HGNC:29185 Homo sapiens (human) 23007 PLCH1
  • RGD:7240710
DOID:0110798 hereditary spastic paraplegia 46 MGI:2654325 Mus musculus (house mouse) 230101 Gba2
  • MGI:6194238
DOID:9256 colorectal cancer MGI:2444664 Mus musculus (house mouse) 230145 Galnt12
  • 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

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Supported by JST NBDC Grant Number JPMJND2204

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


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