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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 10601 - 10625 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:0050700 cardiomyopathy RGD:2721 Rattus norvegicus (Norway rat) 24401 Got1
  • PMID:20733562
DOID:0070433 hyperphosphatasia with impaired intellectual development syndrome 1 HGNC:26031 Homo sapiens (human) 55650 PIGV
  • PMID:20802478
  • RGD:7240710
DOID:11963 esophagitis HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • PMID:20811626
DOID:11963 esophagitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:20811626
DOID:13406 pulmonary sarcoidosis HGNC:11848 Homo sapiens (human) 7097 TLR2
  • PMID:20813038
DOID:4483 rhinitis HGNC:16711 Homo sapiens (human) 10333 TLR6
  • PMID:20815312
DOID:10923 sickle cell anemia HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:20831548
DOID:0080855 Parkinsonism HGNC:4177 Homo sapiens (human) 2629 GBA1
  • PMID:20838799
DOID:1612 breast cancer HGNC:16049 Homo sapiens (human) 10728 PTGES3
  • PMID:20847343
DOID:936 brain disease HGNC:3353 Homo sapiens (human) 2026 ENO2
  • PMID:20847541
DOID:2957 pulmonary tuberculosis HGNC:785 Homo sapiens (human) 467 ATF3
  • PMID:20856677
DOID:0080599 Coronavirus infectious disease HGNC:1641 Homo sapiens (human) 30835 CD209
  • PMID:20864747
DOID:3596 placental site trophoblastic tumor HGNC:4451 Homo sapiens (human) 2719 GPC3
  • PMID:20868507
DOID:3498 pancreatic ductal adenocarcinoma HGNC:8978 Homo sapiens (human) 5294 PIK3CG
  • PMID:20876794
DOID:0112313 brain small vessel disease HGNC:10721 Homo sapiens (human) 6403 SELP
  • PMID:20885295
DOID:3770 pulmonary fibrosis HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:20888745
DOID:10754 otitis media HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:20926702
DOID:1287 cardiovascular system disease HGNC:18129 Homo sapiens (human) 51738 GHRL
  • PMID:20930430
DOID:0050771 pheochromocytoma HGNC:6470 Homo sapiens (human) 3897 L1CAM
  • PMID:20937862
DOID:14330 Parkinson's disease HGNC:9039 Homo sapiens (human) 8398 PLA2G6
  • PMID:20938027
  • PMID:21368765
DOID:14499 Fabry disease HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:20941593
DOID:3572 intracranial sinus thrombosis HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:20946167
DOID:5419 schizophrenia HGNC:922 Homo sapiens (human) 135152 B3GAT2
  • PMID:20950796
DOID:7147 ankylosing spondylitis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:20952467
DOID:3132 porphyria cutanea tarda HGNC:2596 Homo sapiens (human) 1544 CYP1A2
  • PMID:20957336

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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