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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 3926 - 3950 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:10763 hypertension HGNC:5209 Homo sapiens (human) 3291 HSD11B2
  • MGI:6194238
  • PMID:9683587
DOID:9970 obesity HGNC:5209 Homo sapiens (human) 3291 HSD11B2
  • MGI:6194238
  • PMID:15793240
DOID:5844 myocardial infarction HGNC:5209 Homo sapiens (human) 3291 HSD11B2
  • MGI:6194238
DOID:655 inherited metabolic disorder HGNC:5209 Homo sapiens (human) 3291 HSD11B2
  • PMID:9683587
DOID:9744 type 1 diabetes mellitus HGNC:5209 Homo sapiens (human) 3291 HSD11B2
  • PMID:11916625
  • PMID:16616286
DOID:9352 type 2 diabetes mellitus HGNC:5209 Homo sapiens (human) 3291 HSD11B2
  • PMID:17519316
DOID:5199 ureteral obstruction HGNC:5209 Homo sapiens (human) 3291 HSD11B2
  • MGI:6194238
DOID:0050696 fetal alcohol spectrum disorder HGNC:5209 Homo sapiens (human) 3291 HSD11B2
  • MGI:6194238
DOID:3008 invasive ductal carcinoma HGNC:5210 Homo sapiens (human) 3292 HSD17B1
  • PMID:10682658
DOID:9970 obesity HGNC:18646 Homo sapiens (human) 51144 HSD17B12
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:5212 Homo sapiens (human) 3293 HSD17B3
  • PMID:18180323
DOID:9970 obesity HGNC:5212 Homo sapiens (human) 3293 HSD17B3
  • MGI:6194238
DOID:1923 disorder of sexual development HGNC:5212 Homo sapiens (human) 3293 HSD17B3
  • PMID:8075637
DOID:0112248 17-beta hydroxysteroid dehydrogenase 3 deficiency HGNC:5212 Homo sapiens (human) 3293 HSD17B3
  • MGI:6194238
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:5212 Homo sapiens (human) 3293 HSD17B3
  • MGI:6194238
DOID:3146 lipid metabolism disorder HGNC:5213 Homo sapiens (human) 3295 HSD17B4
  • MGI:6194238
DOID:0050857 Perrault syndrome HGNC:5213 Homo sapiens (human) 3295 HSD17B4
  • RGD:7240710
DOID:10763 hypertension HGNC:5213 Homo sapiens (human) 3295 HSD17B4
  • MGI:6194238
DOID:13366 Stiff-Person syndrome HGNC:5213 Homo sapiens (human) 3295 HSD17B4
  • PMID:12225901
DOID:0090031 D-bifunctional protein deficiency HGNC:5213 Homo sapiens (human) 3295 HSD17B4
  • MGI:6194238
  • PMID:16385454
  • PMID:9345094
  • RGD:7240710
DOID:9970 obesity HGNC:5213 Homo sapiens (human) 3295 HSD17B4
  • MGI:6194238
DOID:11612 polycystic ovary syndrome HGNC:5215 Homo sapiens (human) 51478 HSD17B7
  • MGI:6194238
DOID:1701 steroid inherited metabolic disorder HGNC:5215 Homo sapiens (human) 51478 HSD17B7
  • MGI:6194238
DOID:1924 hypogonadism HGNC:5217 Homo sapiens (human) 3283 HSD3B1
  • MGI:6194238
DOID:1459 hypothyroidism HGNC:5217 Homo sapiens (human) 3283 HSD3B1
  • MGI:6194238

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

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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