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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 11301 - 11325 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▼ References
DOID:0060001 withdrawal disorder HGNC:5293 Homo sapiens (human) 3356 HTR2A
  • MGI:6194238
  • PMID:19060480
DOID:0080563 congenital disorder of glycosylation Ik HGNC:18294 Homo sapiens (human) 56052 ALG1
  • MGI:6194238
  • RGD:7240710
DOID:0050558 Ullrich congenital muscular dystrophy HGNC:2211 Homo sapiens (human) 1291 COL6A1
  • MGI:6194238
  • RGD:7240710
DOID:3659 sialuria HGNC:10933 Homo sapiens (human) 26503 SLC17A5
  • MGI:6194238
  • PMID:10581036
  • RGD:7240710
DOID:0111103 maturity-onset diabetes of the young type 4 HGNC:6107 Homo sapiens (human) 3651 PDX1
  • MGI:6194238
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:6126 Homo sapiens (human) 8660 IRS2
  • MGI:6194238
  • PMID:11030756
  • RGD:7240710
DOID:10609 rickets HGNC:2606 Homo sapiens (human) 1594 CYP27B1
  • MGI:6194238
  • PMID:9486994
DOID:0060246 MASA syndrome HGNC:6470 Homo sapiens (human) 3897 L1CAM
  • MGI:6194238
  • PMID:7920660
  • PMID:8786080
  • PMID:9643285
  • RGD:7240710
DOID:0080887 vitamin D-dependent rickets type 1B HGNC:20580 Homo sapiens (human) 120227 CYP2R1
  • MGI:6194238
  • RGD:7240710
DOID:10763 hypertension HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
  • PMID:16202847
DOID:409 liver disease HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • MGI:6194238
  • PMID:17950035
  • PMID:20392357
DOID:0110660 congenital myasthenic syndrome 12 HGNC:4241 Homo sapiens (human) 2673 GFPT1
  • MGI:6194238
  • RGD:7240710
DOID:0050809 mucopolysaccharidosis IX HGNC:5320 Homo sapiens (human) 3373 HYAL1
  • MGI:6194238
  • RGD:7240710
DOID:1561 cognitive disorder HGNC:2228 Homo sapiens (human) 1312 COMT
  • MGI:6194238
  • PMID:16542182
  • PMID:31301644
DOID:0050663 Bethlem myopathy HGNC:2211 Homo sapiens (human) 1291 COL6A1
  • MGI:6194238
  • PMID:8782832
  • RGD:7240710
DOID:0050797 peroxisomal acyl-CoA oxidase deficiency HGNC:119 Homo sapiens (human) 51 ACOX1
  • MGI:6194238
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
  • PMID:18564365
DOID:0110859 polycystic kidney disease 2 HGNC:9009 Homo sapiens (human) 5311 PKD2
  • MGI:6194238
  • RGD:7240710
DOID:3633 beta-mannosidosis HGNC:6831 Homo sapiens (human) 4126 MANBA
  • MGI:6194238
  • RGD:7240710
DOID:14692 Smith-Lemli-Opitz syndrome HGNC:2860 Homo sapiens (human) 1717 DHCR7
  • MGI:6194238
  • PMID:9683613
  • RGD:7240710
DOID:12800 mucopolysaccharidosis VI HGNC:714 Homo sapiens (human) 411 ARSB
  • MGI:6194238
  • PMID:1550123
  • RGD:7240710
DOID:3652 Leigh disease HGNC:10680 Homo sapiens (human) 6389 SDHA
  • MGI:6194238
  • PMID:7550341
DOID:10763 hypertension HGNC:5217 Homo sapiens (human) 3283 HSD3B1
  • MGI:6194238
  • PMID:12054649
DOID:13359 Ehlers-Danlos syndrome HGNC:930 Homo sapiens (human) 11285 B4GALT7
  • MGI:6194238
  • PMID:10473568
DOID:0110474 autosomal recessive nonsyndromic deafness 18B HGNC:8516 Homo sapiens (human) 340990 OTOG
  • MGI:6194238
  • RGD:7240710

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Last updated: August 19, 2024