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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 11626 - 11650 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:4195 hyperglycemia HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
DOID:114 heart disease HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
  • PMID:23269818
DOID:9970 obesity HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
  • PMID:12606537
  • PMID:18162502
  • PMID:18270681
  • PMID:23210442
  • PMID:23251491
DOID:263 kidney cancer HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • PMID:23150719
DOID:10652 Alzheimer's disease HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
  • PMID:19273754
DOID:11446 sciatic neuropathy HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
DOID:12236 primary biliary cholangitis HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
DOID:0050328 congenital hypothyroidism HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
DOID:0060180 colitis HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
DOID:12930 dilated cardiomyopathy HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
DOID:14330 Parkinson's disease HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
  • PMID:21376232
  • PMID:21595954
DOID:3083 chronic obstructive pulmonary disease HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • PMID:20732852
DOID:3891 placental insufficiency HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
DOID:1074 kidney failure HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
DOID:12858 Huntington's disease HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
  • PMID:17018277
  • PMID:19133136
  • PMID:21211002
  • PMID:21595933
  • PMID:21757867
  • PMID:22589246
  • PMID:24383721
DOID:11716 prediabetes syndrome HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
DOID:1909 melanoma HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • PMID:23416000
DOID:4448 macular degeneration HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • PMID:23335958
DOID:1184 nephrotic syndrome HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
DOID:1907 malignant fibrous histiocytoma HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • PMID:23166610
DOID:7998 hyperthyroidism HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
DOID:10871 age related macular degeneration HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
DOID:8947 diabetic retinopathy HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238

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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