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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 8351 - 8375 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:2352 hemochromatosis HGNC:4887 Homo sapiens (human) 148738 HJV
  • PMID:14647275
DOID:12801 mucopolysaccharidosis III HGNC:26527 Homo sapiens (human) 138050 HGSNAT
  • MGI:6194238
DOID:0110389 retinitis pigmentosa 73 HGNC:26527 Homo sapiens (human) 138050 HGSNAT
  • RGD:7240710
DOID:0111393 mucopolysaccharidosis type IIIC HGNC:26527 Homo sapiens (human) 138050 HGSNAT
  • RGD:7240710
DOID:3323 Sandhoff disease HGNC:4879 Homo sapiens (human) 3074 HEXB
  • MGI:6194238
  • PMID:2147027
  • RGD:7240710
DOID:12377 spinal muscular atrophy HGNC:4879 Homo sapiens (human) 3074 HEXB
  • PMID:1720305
DOID:3211 lysosomal storage disease HGNC:4879 Homo sapiens (human) 3074 HEXB
  • MGI:6194238
DOID:3320 Tay-Sachs disease HGNC:4878 Homo sapiens (human) 3073 HEXA
  • MGI:6194238
  • RGD:7240710
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: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: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

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: August 19, 2024