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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 10051 - 10075 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0050770 polycystic liver disease HGNC:12518 Homo sapiens (human) 7351 UCP2
  • MGI:6194238
DOID:9970 obesity HGNC:12518 Homo sapiens (human) 7351 UCP2
  • PMID:11381268
  • PMID:17870627
DOID:783 end stage renal disease HGNC:12518 Homo sapiens (human) 7351 UCP2
  • PMID:18242170
  • PMID:19406964
DOID:9452 steatotic liver disease HGNC:12518 Homo sapiens (human) 7351 UCP2
  • MGI:6194238
DOID:12858 Huntington's disease HGNC:12518 Homo sapiens (human) 7351 UCP2
  • PMID:23029535
DOID:3407 carotid artery disease HGNC:12518 Homo sapiens (human) 7351 UCP2
  • PMID:15604415
DOID:6000 congestive heart failure HGNC:12518 Homo sapiens (human) 7351 UCP2
  • MGI:6194238
DOID:224 transient cerebral ischemia HGNC:12518 Homo sapiens (human) 7351 UCP2
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:12518 Homo sapiens (human) 7351 UCP2
  • MGI:6194238
  • PMID:10382588
DOID:13603 obstructive jaundice HGNC:12518 Homo sapiens (human) 7351 UCP2
  • MGI:6194238
DOID:9743 diabetic neuropathy HGNC:12518 Homo sapiens (human) 7351 UCP2
  • PMID:16373902
DOID:10763 hypertension HGNC:12518 Homo sapiens (human) 7351 UCP2
  • MGI:6194238
  • PMID:15106800
DOID:1459 hypothyroidism HGNC:12518 Homo sapiens (human) 7351 UCP2
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:12518 Homo sapiens (human) 7351 UCP2
  • MGI:6194238
  • PMID:18308829
DOID:0050861 colorectal adenocarcinoma HGNC:12020 Homo sapiens (human) 8460 TPST1
  • PMID:27354594
DOID:162 cancer HGNC:12009 Homo sapiens (human) 7167 TPI1
  • MGI:6194238
DOID:0050884 triosephosphate isomerase deficiency HGNC:12009 Homo sapiens (human) 7167 TPI1
  • MGI:6194238
  • RGD:7240710
DOID:2978 carbohydrate metabolic disorder HGNC:12009 Homo sapiens (human) 7167 TPI1
  • PMID:9338582
DOID:9282 ocular hypertension HGNC:12009 Homo sapiens (human) 7167 TPI1
  • MGI:6194238
DOID:1289 neurodegenerative disease HGNC:12009 Homo sapiens (human) 7167 TPI1
  • MGI:6194238
DOID:0111067 congenital bile acid synthesis defect 6 HGNC:120 Homo sapiens (human) 8309 ACOX2
  • RGD:7240710
DOID:0080202 adenoid cystic carcinoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:16249115
DOID:3347 osteosarcoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
  • RGD:7240710
DOID:12361 Graves' disease HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:17980001
DOID:3070 high grade glioma HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:17599090
  • 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