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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 65376 - 65400 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:7693 abdominal aortic aneurysm HGNC:24678 Homo sapiens (human) 79068 FTO
  • PMID:32042813
DOID:5844 myocardial infarction HGNC:24678 Homo sapiens (human) 79068 FTO
  • PMID:20031593
  • PMID:26772723
DOID:9970 obesity HGNC:24678 Homo sapiens (human) 79068 FTO
  • MGI:6194238
  • PMID:21919686
  • PMID:23111453
  • PMID:23134754
  • PMID:29540276
  • PMID:31801409
DOID:9538 multiple myeloma HGNC:24678 Homo sapiens (human) 79068 FTO
  • PMID:34274946
DOID:10825 essential hypertension HGNC:24678 Homo sapiens (human) 79068 FTO
  • PMID:23691120
DOID:13963 nuclear senile cataract HGNC:24678 Homo sapiens (human) 79068 FTO
  • PMID:19329528
DOID:224 transient cerebral ischemia HGNC:24678 Homo sapiens (human) 79068 FTO
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:24678 Homo sapiens (human) 79068 FTO
  • MGI:6194238
  • PMID:21294771
  • PMID:25303482
  • PMID:28890888
  • PMID:29154870
  • PMID:29410390
  • PMID:32061761
DOID:9743 diabetic neuropathy HGNC:24678 Homo sapiens (human) 79068 FTO
  • PMID:29154870
DOID:6000 congestive heart failure HGNC:24678 Homo sapiens (human) 79068 FTO
  • PMID:29997116
  • PMID:33748197
DOID:9477 pulmonary embolism HGNC:24678 Homo sapiens (human) 79068 FTO
  • PMID:25161014
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:24678 Homo sapiens (human) 79068 FTO
  • MGI:6194238
DOID:0080559 congenital disorder of glycosylation Ig HGNC:19358 Homo sapiens (human) 79087 ALG12
  • RGD:7240710
DOID:0050570 congenital disorder of glycosylation type I HGNC:19358 Homo sapiens (human) 79087 ALG12
  • MGI:6194238
DOID:0112136 severe congenital neutropenia 4 ZFIN:ZDB-GENE-061215-19 Danio rerio (zebrafish) 790919 g6pc3
  • MGI:6194238
DOID:9212 pityriasis rubra pilaris HGNC:16446 Homo sapiens (human) 79092 CARD14
  • RGD:7240710
DOID:0080475 psoriasis 2 HGNC:16446 Homo sapiens (human) 79092 CARD14
  • MGI:6194238
  • RGD:7240710
DOID:0080118 mitochondrial complex III deficiency nuclear type 9 HGNC:34399 Homo sapiens (human) 790955 UQCC3
  • RGD:7240710
DOID:1459 hypothyroidism RGD:628761 Rattus norvegicus (Norway rat) 79107 Duox2
  • MGI:6194238
DOID:0050328 congenital hypothyroidism RGD:628761 Rattus norvegicus (Norway rat) 79107 Duox2
  • MGI:6194238
DOID:1498 cholera RGD:628761 Rattus norvegicus (Norway rat) 79107 Duox2
  • MGI:6194238
DOID:0050338 primary bacterial infectious disease RGD:628761 Rattus norvegicus (Norway rat) 79107 Duox2
  • MGI:6194238
DOID:0112189 thyroid dyshormonogenesis 6 RGD:628761 Rattus norvegicus (Norway rat) 79107 Duox2
  • MGI:6194238
DOID:8778 Crohn's disease RGD:628761 Rattus norvegicus (Norway rat) 79107 Duox2
  • MGI:6194238
DOID:8577 ulcerative colitis RGD:628761 Rattus norvegicus (Norway rat) 79107 Duox2
  • 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