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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 October 9, 2024
Displaying entries 11976 - 12000 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:10825 essential hypertension HGNC:17866 Homo sapiens (human) 26762 HAVCR1
  • PMID:22923545
DOID:4450 renal cell carcinoma HGNC:17866 Homo sapiens (human) 26762 HAVCR1
  • PMID:23352434
DOID:557 kidney disease HGNC:17866 Homo sapiens (human) 26762 HAVCR1
  • PMID:23547217
DOID:2378 relapsing-remitting multiple sclerosis HGNC:17866 Homo sapiens (human) 26762 HAVCR1
  • PMID:15153541
DOID:0060180 colitis HGNC:17866 Homo sapiens (human) 26762 HAVCR1
  • MGI:6194238
DOID:2527 nephrosis HGNC:17866 Homo sapiens (human) 26762 HAVCR1
  • MGI:6194238
DOID:3021 acute kidney failure HGNC:17866 Homo sapiens (human) 26762 HAVCR1
  • MGI:6194238
  • PMID:23319831
DOID:2986 IgA glomerulonephritis HGNC:17866 Homo sapiens (human) 26762 HAVCR1
  • PMID:21467131
  • PMID:23135864
DOID:1591 renovascular hypertension HGNC:17866 Homo sapiens (human) 26762 HAVCR1
  • PMID:22923545
DOID:3310 atopic dermatitis HGNC:17866 Homo sapiens (human) 26762 HAVCR1
  • PMID:16159638
DOID:684 hepatocellular carcinoma HGNC:17866 Homo sapiens (human) 26762 HAVCR1
  • PMID:35693827
DOID:9352 type 2 diabetes mellitus HGNC:17869 Homo sapiens (human) 27125 AFF4
  • MGI:6194238
DOID:8923 skin melanoma HGNC:17869 Homo sapiens (human) 27125 AFF4
  • PMID:33417923
DOID:9256 colorectal cancer HGNC:17869 Homo sapiens (human) 27125 AFF4
  • PMID:35223479
DOID:0111113 nephronophthisis 2 HGNC:17870 Homo sapiens (human) 27130 INVS
  • MGI:6194238
  • PMID:12872123
  • RGD:7240710
DOID:0060340 ciliopathy HGNC:17870 Homo sapiens (human) 27130 INVS
  • MGI:6194238
DOID:10763 hypertension HGNC:17870 Homo sapiens (human) 27130 INVS
  • PMID:19177160
DOID:6419 tetralogy of Fallot HGNC:17870 Homo sapiens (human) 27130 INVS
  • MGI:6194238
DOID:0070435 hyperphosphatasia with impaired intellectual development syndrome 3 HGNC:17893 Homo sapiens (human) 27315 PGAP2
  • RGD:7240710
DOID:0050888 syndromic intellectual disability HGNC:17896 Homo sapiens (human) 27339 PRPF19
  • MGI:6194238
DOID:224 transient cerebral ischemia HGNC:17909 Homo sapiens (human) 80824 DUSP16
  • MGI:6194238
DOID:9744 type 1 diabetes mellitus HGNC:17927 Homo sapiens (human) 29843 SENP1
  • MGI:6194238
DOID:1612 breast cancer HGNC:17933 Homo sapiens (human) 84148 KAT8
  • PMID:22199269
DOID:4467 clear cell renal cell carcinoma HGNC:17933 Homo sapiens (human) 84148 KAT8
  • PMID:23394073
DOID:1094 attention deficit hyperactivity disorder HGNC:17938 Homo sapiens (human) 50632 CALY
  • MGI:6194238
  • PMID:16172615

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