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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 1576 - 1600 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:9352 type 2 diabetes mellitus HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:21143859
DOID:0060326 myelomeningocele HGNC:11005 Homo sapiens (human) 6513 SLC2A1
  • PMID:21135204
  • PMID:23427181
DOID:10763 hypertension HGNC:3353 Homo sapiens (human) 2026 ENO2
  • PMID:21130083
DOID:9352 type 2 diabetes mellitus HGNC:8971 Homo sapiens (human) 5286 PIK3C2A
  • PMID:21127054
DOID:418 systemic scleroderma HGNC:543 Homo sapiens (human) 308 ANXA5
  • PMID:21124692
DOID:676 juvenile rheumatoid arthritis HGNC:10721 Homo sapiens (human) 6403 SELP
  • PMID:21124648
DOID:7147 ankylosing spondylitis HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • PMID:21122270
DOID:0080322 polycystic kidney disease RGD:3130 Rattus norvegicus (Norway rat) 24577 Myc
  • PMID:21119215
DOID:8778 Crohn's disease HGNC:9053 Homo sapiens (human) 5329 PLAUR
  • PMID:21114432
DOID:9452 steatotic liver disease RGD:3932 Rattus norvegicus (Norway rat) 54315 Ucp2
  • PMID:21114362
DOID:2986 IgA glomerulonephritis HGNC:11847 Homo sapiens (human) 7096 TLR1
  • PMID:21108742
DOID:0080178 mucositis RGD:3269 Rattus norvegicus (Norway rat) 25737 Pcna
  • PMID:21080177
DOID:0050083 Keshan disease HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:21055077
DOID:13241 Behcet's disease HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • PMID:21044750
DOID:11204 allergic conjunctivitis HGNC:9031 Homo sapiens (human) 5320 PLA2G2A
  • PMID:21042565
DOID:6432 pulmonary hypertension HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:21034646
DOID:3132 porphyria cutanea tarda HGNC:2596 Homo sapiens (human) 1544 CYP1A2
  • PMID:20957336
DOID:7147 ankylosing spondylitis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:20952467
DOID:5419 schizophrenia HGNC:922 Homo sapiens (human) 135152 B3GAT2
  • PMID:20950796
DOID:3572 intracranial sinus thrombosis HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:20946167
DOID:14499 Fabry disease HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:20941593
DOID:14330 Parkinson's disease HGNC:9039 Homo sapiens (human) 8398 PLA2G6
  • PMID:20938027
  • PMID:21368765
DOID:0050771 pheochromocytoma HGNC:6470 Homo sapiens (human) 3897 L1CAM
  • PMID:20937862
DOID:1287 cardiovascular system disease HGNC:18129 Homo sapiens (human) 51738 GHRL
  • PMID:20930430
DOID:10754 otitis media HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:20926702

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Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: August 19, 2024