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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 5801 - 5825 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:12662 paracoccidioidomycosis HGNC:5998 Homo sapiens (human) 9173 IL1RL1
  • PMID:28992214
DOID:2326 gastroenteritis HGNC:6480 Homo sapiens (human) 3906 LALBA
  • PMID:1327323
DOID:1070 primary open angle glaucoma HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:22831837
DOID:10652 Alzheimer's disease HGNC:404 Homo sapiens (human) 217 ALDH2
  • PMID:15126281
DOID:874 bacterial pneumonia HGNC:5998 Homo sapiens (human) 9173 IL1RL1
  • MGI:6194238
DOID:10763 hypertension HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
DOID:0080899 lung pleomorphic carcinoma HGNC:11026 Homo sapiens (human) 6520 SLC3A2
  • PMID:30300664
DOID:12466 secondary hyperparathyroidism HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
  • PMID:21335517
DOID:0080322 polycystic kidney disease HGNC:4138 Homo sapiens (human) 23193 GANAB
  • PMID:27259053
DOID:9074 systemic lupus erythematosus HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:11607787
  • PMID:15642275
  • PMID:22660635
DOID:6039 uveal melanoma HGNC:6919 Homo sapiens (human) 8930 MBD4
  • RGD:7240710
DOID:4450 renal cell carcinoma HGNC:9588 Homo sapiens (human) 5728 PTEN
  • MGI:6194238
  • PMID:15821467
  • PMID:17681738
  • PMID:17886097
DOID:0111773 46,XY sex reversal 8 HGNC:387 Homo sapiens (human) 1109 AKR1C4
  • RGD:7240710
DOID:1289 neurodegenerative disease HGNC:9387 Homo sapiens (human) 53632 PRKAG3
  • MGI:6194238
DOID:3393 coronary artery disease HGNC:3402 Homo sapiens (human) 2053 EPHX2
  • PMID:14732757
DOID:9952 acute lymphoblastic leukemia HGNC:79 Homo sapiens (human) 28 ABO
  • PMID:17065136
DOID:0070329 mitochondrial DNA depletion syndrome HGNC:10980 Homo sapiens (human) 1468 SLC25A10
  • MGI:6194238
DOID:0014667 disease of metabolism HGNC:8807 Homo sapiens (human) 5161 PDHA2
  • MGI:6194238
DOID:0060537 mitochondrial complex II deficiency HGNC:10680 Homo sapiens (human) 6389 SDHA
  • MGI:6194238
  • RGD:7240710
DOID:4948 gallbladder carcinoma HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:18946757
DOID:5844 myocardial infarction HGNC:9053 Homo sapiens (human) 5329 PLAUR
  • MGI:6194238
  • PMID:12393744
DOID:9269 maple syrup urine disease HGNC:2898 Homo sapiens (human) 1738 DLD
  • RGD:7240710
DOID:684 hepatocellular carcinoma HGNC:418 Homo sapiens (human) 230 ALDOC
  • MGI:6194238
DOID:11394 adult respiratory distress syndrome HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:16135717
  • PMID:21062445
DOID:0111843 Paganini-Miozzo syndrome HGNC:19133 Homo sapiens (human) 90161 HS6ST2
  • RGD:7240710

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

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