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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 70901 - 70925 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:820 myocarditis HGNC:286 Homo sapiens (human) 154 ADRB2
  • MGI:6194238
DOID:1067 open-angle glaucoma HGNC:286 Homo sapiens (human) 154 ADRB2
  • PMID:16785856
DOID:10763 hypertension HGNC:286 Homo sapiens (human) 154 ADRB2
  • MGI:6194238
  • PMID:16041242
  • PMID:16685203
  • PMID:17221209
  • PMID:20484896
  • PMID:20739939
DOID:12361 Graves' disease HGNC:286 Homo sapiens (human) 154 ADRB2
  • PMID:17143563
DOID:1459 hypothyroidism HGNC:286 Homo sapiens (human) 154 ADRB2
  • MGI:6194238
DOID:11612 polycystic ovary syndrome HGNC:286 Homo sapiens (human) 154 ADRB2
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:286 Homo sapiens (human) 154 ADRB2
  • PMID:17221209
DOID:557 kidney disease HGNC:286 Homo sapiens (human) 154 ADRB2
  • MGI:6194238
DOID:9452 steatotic liver disease HGNC:286 Homo sapiens (human) 154 ADRB2
  • PMID:11718682
DOID:8893 psoriasis HGNC:286 Homo sapiens (human) 154 ADRB2
  • PMID:15265530
  • PMID:8763426
DOID:552 pneumonia HGNC:286 Homo sapiens (human) 154 ADRB2
  • MGI:6194238
DOID:4947 cholangiocarcinoma HGNC:286 Homo sapiens (human) 154 ADRB2
  • PMID:16292515
DOID:2942 bronchiolitis HGNC:286 Homo sapiens (human) 154 ADRB2
  • PMID:17687719
DOID:13810 familial hypercholesterolemia HGNC:286 Homo sapiens (human) 154 ADRB2
  • PMID:17020471
DOID:14115 toxic shock syndrome HGNC:286 Homo sapiens (human) 154 ADRB2
  • PMID:16076286
  • PMID:19850944
DOID:0014667 disease of metabolism HGNC:286 Homo sapiens (human) 154 ADRB2
  • PMID:16082424
DOID:5844 myocardial infarction HGNC:286 Homo sapiens (human) 154 ADRB2
  • MGI:6194238
  • PMID:15520258
DOID:1591 renovascular hypertension HGNC:285 Homo sapiens (human) 153 ADRB1
  • MGI:6194238
DOID:0050848 obstructive sleep apnea HGNC:285 Homo sapiens (human) 153 ADRB1
  • PMID:20948559
DOID:9744 type 1 diabetes mellitus HGNC:285 Homo sapiens (human) 153 ADRB1
  • MGI:6194238
DOID:12930 dilated cardiomyopathy HGNC:285 Homo sapiens (human) 153 ADRB1
  • MGI:6194238
DOID:11664 nephrosclerosis HGNC:285 Homo sapiens (human) 153 ADRB1
  • PMID:19745105
DOID:10763 hypertension HGNC:285 Homo sapiens (human) 153 ADRB1
  • MGI:6194238
  • PMID:20398560
DOID:5844 myocardial infarction HGNC:285 Homo sapiens (human) 153 ADRB1
  • MGI:6194238
DOID:13544 low tension glaucoma HGNC:285 Homo sapiens (human) 153 ADRB1
  • PMID:16785856

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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: December 9, 2024