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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 11251 - 11275 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▼ References
DOID:0080556 congenital disorder of glycosylation Id HGNC:23056 Homo sapiens (human) 10195 ALG3
  • MGI:6194238
  • RGD:7240710
DOID:5381 bile duct adenoma HGNC:1097 Homo sapiens (human) 673 BRAF
  • MGI:6194238
  • PMID:25704541
DOID:3012 Li-Fraumeni syndrome HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
  • PMID:1631137
DOID:9352 type 2 diabetes mellitus HGNC:4323 Homo sapiens (human) 2739 GLO1
  • MGI:6194238
  • PMID:18413187
DOID:0050884 triosephosphate isomerase deficiency HGNC:12009 Homo sapiens (human) 7167 TPI1
  • MGI:6194238
  • RGD:7240710
DOID:0090031 D-bifunctional protein deficiency HGNC:5213 Homo sapiens (human) 3295 HSD17B4
  • MGI:6194238
  • PMID:16385454
  • PMID:9345094
  • RGD:7240710
DOID:0050657 Bannayan-Riley-Ruvalcaba syndrome HGNC:9588 Homo sapiens (human) 5728 PTEN
  • MGI:6194238
  • RGD:7240710
DOID:0110915 childhood hypophosphatasia HGNC:438 Homo sapiens (human) 249 ALPL
  • MGI:6194238
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:11006 Homo sapiens (human) 6514 SLC2A2
  • MGI:6194238
  • PMID:17636114
  • PMID:8027028
  • RGD:7240710
DOID:0111254 glutaric acidemia I HGNC:4189 Homo sapiens (human) 2639 GCDH
  • MGI:6194238
  • RGD:7240710
DOID:0070216 familial hyperinsulinemic hypoglycemia 3 HGNC:4195 Homo sapiens (human) 2645 GCK
  • MGI:6194238
  • RGD:7240710
DOID:10763 hypertension HGNC:1929 Homo sapiens (human) 1113 CHGA
  • MGI:6194238
  • PMID:20113265
  • PMID:21061160
DOID:0110293 autosomal recessive limb-girdle muscular dystrophy type 2P HGNC:2666 Homo sapiens (human) 1605 DAG1
  • MGI:6194238
  • RGD:7240710
DOID:3413 alpha-mannosidosis HGNC:6826 Homo sapiens (human) 4125 MAN2B1
  • MGI:6194238
  • RGD:7240710
DOID:0080250 erythrokeratodermia variabilis et progressiva 4 HGNC:4021 Homo sapiens (human) 2531 KDSR
  • MGI:6194238
  • RGD:7240710
DOID:0110671 congenital myasthenic syndrome 6 HGNC:1912 Homo sapiens (human) 1103 CHAT
  • MGI:6194238
  • PMID:11172068
  • RGD:7240710
DOID:9743 diabetic neuropathy HGNC:381 Homo sapiens (human) 231 AKR1B1
  • MGI:6194238
  • PMID:9489533
DOID:0081326 oxoglutarate dehydrogenase deficiency HGNC:8124 Homo sapiens (human) 4967 OGDH
  • MGI:6194238
  • RGD:7240710
DOID:12799 mucopolysaccharidosis II HGNC:5389 Homo sapiens (human) 3423 IDS
  • MGI:6194238
  • PMID:1550586
  • PMID:27146977
  • RGD:7240710
DOID:1919 Lesch-Nyhan syndrome HGNC:5157 Homo sapiens (human) 3251 HPRT1
  • MGI:6194238
  • PMID:20638392
  • PMID:24940672
  • RGD:7240710
DOID:0060602 alpha-methylacyl-CoA racemase deficiency HGNC:451 Homo sapiens (human) 23600 AMACR
  • MGI:6194238
  • RGD:7240710
DOID:850 lung disease HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
  • PMID:19897513
DOID:0050773 paraganglioma HGNC:10681 Homo sapiens (human) 6390 SDHB
  • MGI:6194238
  • PMID:11404820
  • RGD:7240710
DOID:12801 mucopolysaccharidosis III HGNC:10818 Homo sapiens (human) 6448 SGSH
  • MGI:6194238
  • PMID:15902564
DOID:12798 mucopolysaccharidosis HGNC:25239 Homo sapiens (human) 153642 ARSK
  • MGI:6194238
  • RGD:7240710

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Last updated: August 19, 2024