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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 October 9, 2024
Displaying entries 61626 - 61650 of 71927 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:14929 Homo sapiens (human) 23411 SIRT1
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:14929 Homo sapiens (human) 23411 SIRT1
  • MGI:6194238
DOID:11476 osteoporosis HGNC:14929 Homo sapiens (human) 23411 SIRT1
  • MGI:6194238
DOID:1936 atherosclerosis HGNC:14929 Homo sapiens (human) 23411 SIRT1
  • MGI:6194238
DOID:14330 Parkinson's disease HGNC:14929 Homo sapiens (human) 23411 SIRT1
  • MGI:6194238
DOID:1826 epilepsy HGNC:14929 Homo sapiens (human) 23411 SIRT1
  • MGI:6194238
  • PMID:23644113
DOID:9970 obesity HGNC:14929 Homo sapiens (human) 23411 SIRT1
  • MGI:6194238
DOID:9669 senile cataract HGNC:14929 Homo sapiens (human) 23411 SIRT1
  • PMID:21501079
DOID:1574 alcohol use disorder HGNC:14929 Homo sapiens (human) 23411 SIRT1
  • MGI:6194238
DOID:9452 steatotic liver disease HGNC:14929 Homo sapiens (human) 23411 SIRT1
  • MGI:6194238
DOID:4448 macular degeneration HGNC:14929 Homo sapiens (human) 23411 SIRT1
  • PMID:21890195
DOID:1875 impotence HGNC:14929 Homo sapiens (human) 23411 SIRT1
  • MGI:6194238
DOID:9975 cocaine dependence HGNC:14929 Homo sapiens (human) 23411 SIRT1
  • MGI:6194238
DOID:10283 prostate cancer HGNC:14929 Homo sapiens (human) 23411 SIRT1
  • MGI:6194238
  • PMID:23038275
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:14929 Homo sapiens (human) 23411 SIRT1
  • MGI:6194238
  • PMID:20033348
  • PMID:22902550
DOID:10652 Alzheimer's disease HGNC:14929 Homo sapiens (human) 23411 SIRT1
  • MGI:6194238
DOID:12387 nephrogenic diabetes insipidus HGNC:14929 Homo sapiens (human) 23411 SIRT1
  • MGI:6194238
DOID:12858 Huntington's disease HGNC:14929 Homo sapiens (human) 23411 SIRT1
  • PMID:18538940
  • PMID:9949199
DOID:0050741 alcohol dependence HGNC:14921 Homo sapiens (human) 50833 TAS2R16
  • RGD:7240710
DOID:674 cleft palate HGNC:1491 Homo sapiens (human) 832 CAPZB
  • MGI:6194238
DOID:1307 dementia HGNC:1491 Homo sapiens (human) 832 CAPZB
  • MGI:6194238
DOID:0070011 Seckel syndrome 7 HGNC:14906 Homo sapiens (human) 51199 NIN
  • RGD:7240710
DOID:4483 rhinitis HGNC:14900 Homo sapiens (human) 50616 IL22
  • PMID:21535180
DOID:3382 liposarcoma HGNC:14900 Homo sapiens (human) 50616 IL22
  • MGI:6194238
DOID:2841 asthma HGNC:14900 Homo sapiens (human) 50616 IL22
  • MGI:6194238
  • PMID:21297073
  • PMID:21535180

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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: December 9, 2024