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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 4401 - 4425 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:11446 sciatic neuropathy HGNC:5217 Homo sapiens (human) 3283 HSD3B1
  • MGI:6194238
DOID:11612 polycystic ovary syndrome HGNC:5217 Homo sapiens (human) 3283 HSD3B1
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:5217 Homo sapiens (human) 3283 HSD3B1
  • MGI:6194238
DOID:11612 polycystic ovary syndrome HGNC:5218 Homo sapiens (human) 3284 HSD3B2
  • PMID:11739466
DOID:10892 hypospadias HGNC:5218 Homo sapiens (human) 3284 HSD3B2
  • PMID:14764821
DOID:10763 hypertension HGNC:5218 Homo sapiens (human) 3284 HSD3B2
  • MGI:6194238
DOID:12700 hyperprolactinemia HGNC:5218 Homo sapiens (human) 3284 HSD3B2
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:5218 Homo sapiens (human) 3284 HSD3B2
  • PMID:18180323
DOID:10763 hypertension HGNC:5273 Homo sapiens (human) 3339 HSPG2
  • MGI:6194238
DOID:2256 osteochondrodysplasia HGNC:5273 Homo sapiens (human) 3339 HSPG2
  • PMID:11101850
DOID:0090032 Silverman-Handmaker type dyssegmental dysplasia HGNC:5273 Homo sapiens (human) 3339 HSPG2
  • MGI:6194238
  • RGD:7240710
DOID:0060770 dextro-looped transposition of the great arteries HGNC:5273 Homo sapiens (human) 3339 HSPG2
  • MGI:6194238
DOID:3407 carotid artery disease HGNC:5273 Homo sapiens (human) 3339 HSPG2
  • PMID:16620836
DOID:4195 hyperglycemia HGNC:5273 Homo sapiens (human) 3339 HSPG2
  • PMID:15056491
DOID:13481 thanatophoric dysplasia HGNC:5273 Homo sapiens (human) 3339 HSPG2
  • MGI:6194238
DOID:0090005 Schwartz-Jampel syndrome 1 HGNC:5273 Homo sapiens (human) 3339 HSPG2
  • MGI:6194238
  • RGD:7240710
DOID:4989 pancreatitis HGNC:5293 Homo sapiens (human) 3356 HTR2A
  • MGI:6194238
DOID:9975 cocaine dependence HGNC:5293 Homo sapiens (human) 3356 HTR2A
  • MGI:6194238
  • PMID:23241418
DOID:0060041 autism spectrum disorder HGNC:5293 Homo sapiens (human) 3356 HTR2A
  • MGI:6194238
DOID:1574 alcohol use disorder HGNC:5293 Homo sapiens (human) 3356 HTR2A
  • MGI:6194238
DOID:1596 depressive disorder HGNC:5293 Homo sapiens (human) 3356 HTR2A
  • MGI:6194238
DOID:9452 steatotic liver disease HGNC:5293 Homo sapiens (human) 3356 HTR2A
  • PMID:33081272
DOID:0050742 nicotine dependence HGNC:5293 Homo sapiens (human) 3356 HTR2A
  • MGI:6194238
  • PMID:25366721
  • PMID:28900078
DOID:2537 inflammatory and toxic neuropathy HGNC:5293 Homo sapiens (human) 3356 HTR2A
  • MGI:6194238
DOID:0080546 non-alcoholic fatty liver HGNC:5293 Homo sapiens (human) 3356 HTR2A
  • PMID:33081272

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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