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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 6601 - 6625 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:6432 pulmonary hypertension HGNC:4820 Homo sapiens (human) 3038 HAS3
  • MGI:6194238
DOID:3525 middle cerebral artery infarction HGNC:4819 Homo sapiens (human) 3037 HAS2
  • MGI:6194238
DOID:9409 diabetes insipidus HGNC:4819 Homo sapiens (human) 3037 HAS2
  • MGI:6194238
DOID:6432 pulmonary hypertension HGNC:4819 Homo sapiens (human) 3037 HAS2
  • MGI:6194238
DOID:6432 pulmonary hypertension HGNC:4818 Homo sapiens (human) 3036 HAS1
  • MGI:6194238
DOID:0112136 severe congenital neutropenia 4 RGD:727875 Rattus norvegicus (Norway rat) 303565 G6pc3
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:4799 Homo sapiens (human) 3033 HADH
  • MGI:6194238
DOID:0070215 familial hyperinsulinemic hypoglycemia 4 HGNC:4799 Homo sapiens (human) 3033 HADH
  • RGD:7240710
DOID:9970 obesity HGNC:4799 Homo sapiens (human) 3033 HADH
  • MGI:6194238
DOID:0080558 congenital disorder of glycosylation If RGD:1307699 Rattus norvegicus (Norway rat) 303244 Mpdu1
  • MGI:6194238
DOID:9452 steatotic liver disease HGNC:4803 Homo sapiens (human) 3032 HADHB
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:4803 Homo sapiens (human) 3032 HADHB
  • PMID:11430884
DOID:3146 lipid metabolism disorder HGNC:4803 Homo sapiens (human) 3032 HADHB
  • MGI:6194238
DOID:0111277 mitochondrial trifunctional protein deficiency HGNC:4803 Homo sapiens (human) 3032 HADHB
  • MGI:6194238
  • RGD:7240710
DOID:700 mitochondrial metabolism disease HGNC:4803 Homo sapiens (human) 3032 HADHB
  • PMID:8651282
DOID:9452 steatotic liver disease HGNC:4801 Homo sapiens (human) 3030 HADHA
  • MGI:6194238
  • PMID:7846063
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:4801 Homo sapiens (human) 3030 HADHA
  • MGI:6194238
DOID:0111277 mitochondrial trifunctional protein deficiency HGNC:4801 Homo sapiens (human) 3030 HADHA
  • RGD:7240710
DOID:3146 lipid metabolism disorder HGNC:4801 Homo sapiens (human) 3030 HADHA
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:4801 Homo sapiens (human) 3030 HADHA
  • PMID:25260493
DOID:10763 hypertension ZFIN:ZDB-GENE-980526-110 Danio rerio (zebrafish) 30262 ins
  • MGI:6194238
DOID:8398 osteoarthritis ZFIN:ZDB-GENE-980526-110 Danio rerio (zebrafish) 30262 ins
  • MGI:6194238
DOID:3587 pancreatic ductal carcinoma ZFIN:ZDB-GENE-980526-110 Danio rerio (zebrafish) 30262 ins
  • MGI:6194238
DOID:9351 diabetes mellitus ZFIN:ZDB-GENE-980526-110 Danio rerio (zebrafish) 30262 ins
  • MGI:6194238
DOID:8947 diabetic retinopathy ZFIN:ZDB-GENE-980526-110 Danio rerio (zebrafish) 30262 ins
  • 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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