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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 1601 - 1625 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:3770 pulmonary fibrosis HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:20888745
DOID:0112313 brain small vessel disease HGNC:10721 Homo sapiens (human) 6403 SELP
  • PMID:20885295
DOID:3498 pancreatic ductal adenocarcinoma HGNC:8978 Homo sapiens (human) 5294 PIK3CG
  • PMID:20876794
DOID:3596 placental site trophoblastic tumor HGNC:4451 Homo sapiens (human) 2719 GPC3
  • PMID:20868507
DOID:0080599 Coronavirus infectious disease HGNC:1641 Homo sapiens (human) 30835 CD209
  • PMID:20864747
DOID:2957 pulmonary tuberculosis HGNC:785 Homo sapiens (human) 467 ATF3
  • PMID:20856677
DOID:936 brain disease HGNC:3353 Homo sapiens (human) 2026 ENO2
  • PMID:20847541
DOID:1612 breast cancer HGNC:16049 Homo sapiens (human) 10728 PTGES3
  • PMID:20847343
DOID:0080855 Parkinsonism HGNC:4177 Homo sapiens (human) 2629 GBA1
  • PMID:20838799
DOID:10923 sickle cell anemia HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:20831548
DOID:4483 rhinitis HGNC:16711 Homo sapiens (human) 10333 TLR6
  • PMID:20815312
DOID:13406 pulmonary sarcoidosis HGNC:11848 Homo sapiens (human) 7097 TLR2
  • PMID:20813038
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:0070433 hyperphosphatasia with impaired intellectual development syndrome 1 HGNC:26031 Homo sapiens (human) 55650 PIGV
  • PMID:20802478
  • RGD:7240710
DOID:0050700 cardiomyopathy RGD:2721 Rattus norvegicus (Norway rat) 24401 Got1
  • PMID:20733562
DOID:3083 chronic obstructive pulmonary disease HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • PMID:20732852
DOID:783 end stage renal disease HGNC:11848 Homo sapiens (human) 7097 TLR2
  • PMID:20729266
DOID:783 end stage renal disease HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:20729266
DOID:10652 Alzheimer's disease HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • PMID:20727007
  • PMID:22213409
DOID:5016 hepatocellular clear cell carcinoma HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:20723213
DOID:5016 hepatocellular clear cell carcinoma HGNC:6554 Homo sapiens (human) 3953 LEPR
  • PMID:20723213
DOID:1485 cystic fibrosis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:20717938
DOID:2377 multiple sclerosis HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • PMID:20714168
DOID:3042 allergic contact dermatitis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:20711192

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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