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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 4601 - 4625 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:9427 hypertensive encephalopathy HGNC:1033 Homo sapiens (human) 627 BDNF
  • MGI:6194238
DOID:1459 hypothyroidism HGNC:1033 Homo sapiens (human) 627 BDNF
  • MGI:6194238
DOID:1824 status epilepticus HGNC:1033 Homo sapiens (human) 627 BDNF
  • MGI:6194238
  • PMID:19686240
DOID:2559 opiate dependence HGNC:1033 Homo sapiens (human) 627 BDNF
  • PMID:21890593
DOID:13406 pulmonary sarcoidosis HGNC:1033 Homo sapiens (human) 627 BDNF
  • PMID:16315781
DOID:3525 middle cerebral artery infarction HGNC:1033 Homo sapiens (human) 627 BDNF
  • MGI:6194238
DOID:8805 intermediate coronary syndrome HGNC:1033 Homo sapiens (human) 627 BDNF
  • PMID:16186425
DOID:10126 keratoconus HGNC:1033 Homo sapiens (human) 627 BDNF
  • PMID:23489213
DOID:0050741 alcohol dependence HGNC:1033 Homo sapiens (human) 627 BDNF
  • MGI:6194238
DOID:1561 cognitive disorder HGNC:1033 Homo sapiens (human) 627 BDNF
  • PMID:23517654
DOID:1555 urticaria HGNC:1033 Homo sapiens (human) 627 BDNF
  • PMID:21676041
DOID:8725 vascular dementia HGNC:1033 Homo sapiens (human) 627 BDNF
  • MGI:6194238
DOID:9719 neovascular inflammatory vitreoretinopathy HGNC:1033 Homo sapiens (human) 627 BDNF
  • PMID:18405896
DOID:2377 multiple sclerosis HGNC:1033 Homo sapiens (human) 627 BDNF
  • PMID:20656764
DOID:12689 acoustic neuroma HGNC:1033 Homo sapiens (human) 627 BDNF
  • PMID:19937367
DOID:9470 bacterial meningitis HGNC:1033 Homo sapiens (human) 627 BDNF
  • MGI:6194238
DOID:1679 cystitis HGNC:1033 Homo sapiens (human) 627 BDNF
  • MGI:6194238
DOID:1094 attention deficit hyperactivity disorder HGNC:1033 Homo sapiens (human) 627 BDNF
  • MGI:6194238
DOID:12858 Huntington's disease HGNC:1033 Homo sapiens (human) 627 BDNF
  • PMID:17885687
  • PMID:18093249
DOID:2055 post-traumatic stress disorder HGNC:1033 Homo sapiens (human) 627 BDNF
  • MGI:6194238
  • PMID:23319005
DOID:1686 glaucoma HGNC:1033 Homo sapiens (human) 627 BDNF
  • MGI:6194238
  • PMID:19422885
DOID:1470 major depressive disorder HGNC:1033 Homo sapiens (human) 627 BDNF
  • PMID:21803060
DOID:0060041 autism spectrum disorder HGNC:1033 Homo sapiens (human) 627 BDNF
  • PMID:21984201
DOID:0060731 congenital central hypoventilation syndrome HGNC:1033 Homo sapiens (human) 627 BDNF
  • PMID:11840487
DOID:14330 Parkinson's disease HGNC:1033 Homo sapiens (human) 627 BDNF
  • PMID:10208589
  • PMID:16565926

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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