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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 66526 - 66550 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:8553 pyoderma gangrenosum RGD:621320 Rattus norvegicus (Norway rat) 81687 Mmp9
  • MGI:6194238
DOID:2841 asthma RGD:621320 Rattus norvegicus (Norway rat) 81687 Mmp9
  • MGI:6194238
  • PMID:16191269
DOID:11476 osteoporosis RGD:621320 Rattus norvegicus (Norway rat) 81687 Mmp9
  • MGI:6194238
DOID:1686 glaucoma RGD:621320 Rattus norvegicus (Norway rat) 81687 Mmp9
  • MGI:6194238
DOID:6432 pulmonary hypertension RGD:621320 Rattus norvegicus (Norway rat) 81687 Mmp9
  • MGI:6194238
  • PMID:17133179
  • PMID:23087098
DOID:13382 megaloblastic anemia HGNC:14604 Homo sapiens (human) 81693 AMN
  • PMID:12590260
DOID:557 kidney disease HGNC:14604 Homo sapiens (human) 81693 AMN
  • MGI:6194238
DOID:0050700 cardiomyopathy HGNC:14604 Homo sapiens (human) 81693 AMN
  • MGI:6194238
DOID:10273 heart conduction disease HGNC:1462 Homo sapiens (human) 817 CAMK2D
  • MGI:6194238
DOID:1826 epilepsy HGNC:1462 Homo sapiens (human) 817 CAMK2D
  • MGI:6194238
DOID:1591 renovascular hypertension HGNC:1462 Homo sapiens (human) 817 CAMK2D
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:1462 Homo sapiens (human) 817 CAMK2D
  • MGI:6194238
DOID:104 bacterial infectious disease HGNC:19191 Homo sapiens (human) 81704 DOCK8
  • PMID:25724123
DOID:2043 hepatitis B HGNC:19191 Homo sapiens (human) 81704 DOCK8
  • PMID:32297155
DOID:0080594 hyper IgE recurrent infection syndrome 2 HGNC:19191 Homo sapiens (human) 81704 DOCK8
  • PMID:21763205
  • RGD:7240710
DOID:9744 type 1 diabetes mellitus HGNC:19191 Homo sapiens (human) 81704 DOCK8
  • MGI:6194238
DOID:934 viral infectious disease HGNC:19191 Homo sapiens (human) 81704 DOCK8
  • PMID:25724123
DOID:3310 atopic dermatitis HGNC:19191 Homo sapiens (human) 81704 DOCK8
  • PMID:22476911
DOID:0090110 immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome HGNC:19191 Homo sapiens (human) 81704 DOCK8
  • PMID:29058101
DOID:809 cocaine abuse RGD:69281 Rattus norvegicus (Norway rat) 81721 Chrna6
  • MGI:6194238
DOID:1574 alcohol use disorder RGD:69281 Rattus norvegicus (Norway rat) 81721 Chrna6
  • MGI:6194238
DOID:3635 congenital myasthenic syndrome RGD:69281 Rattus norvegicus (Norway rat) 81721 Chrna6
  • MGI:6194238
DOID:0050742 nicotine dependence RGD:69281 Rattus norvegicus (Norway rat) 81721 Chrna6
  • MGI:6194238
DOID:0110670 congenital myasthenic syndrome 9 RGD:3211 Rattus norvegicus (Norway rat) 81725 Musk
  • MGI:6194238
DOID:0111377 fetal akinesia deformation sequence syndrome 1 RGD:3211 Rattus norvegicus (Norway rat) 81725 Musk
  • MGI:6194238

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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: December 9, 2024