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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 8676 - 8700 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:552 pneumonia HGNC:29595 Homo sapiens (human) 130120 REG3G
  • MGI:6194238
DOID:2913 acute pancreatitis HGNC:29595 Homo sapiens (human) 130120 REG3G
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:29595 Homo sapiens (human) 130120 REG3G
  • MGI:6194238
DOID:10588 adrenoleukodystrophy HGNC:29567 Homo sapiens (human) 23205 ACSBG1
  • MGI:6194238
  • PMID:15800013
DOID:0112349 hereditary spastic paraplegia 81 HGNC:29361 Homo sapiens (human) 85465 SELENOI
  • RGD:7240710
DOID:4621 holoprosencephaly HGNC:29185 Homo sapiens (human) 23007 PLCH1
  • RGD:7240710
DOID:9970 obesity HGNC:29175 Homo sapiens (human) 23038 WDTC1
  • MGI:6194238
DOID:0050773 paraganglioma HGNC:2911 Homo sapiens (human) 1743 DLST
  • RGD:7240710
DOID:10652 Alzheimer's disease HGNC:2911 Homo sapiens (human) 1743 DLST
  • PMID:10227647
DOID:2377 multiple sclerosis HGNC:29013 Homo sapiens (human) 23274 CLEC16A
  • PMID:21653641
DOID:9744 type 1 diabetes mellitus HGNC:29013 Homo sapiens (human) 23274 CLEC16A
  • PMID:18946483
  • PMID:19221398
DOID:13774 Addison's disease HGNC:29013 Homo sapiens (human) 23274 CLEC16A
  • PMID:18593762
DOID:7148 rheumatoid arthritis HGNC:29013 Homo sapiens (human) 23274 CLEC16A
  • PMID:19221398
DOID:1289 neurodegenerative disease HGNC:29013 Homo sapiens (human) 23274 CLEC16A
  • MGI:6194238
DOID:9269 maple syrup urine disease HGNC:2898 Homo sapiens (human) 1738 DLD
  • RGD:7240710
DOID:0014667 disease of metabolism HGNC:2898 Homo sapiens (human) 1738 DLD
  • MGI:6194238
DOID:3650 lactic acidosis HGNC:2896 Homo sapiens (human) 1737 DLAT
  • MGI:6194238
DOID:3649 pyruvate decarboxylase deficiency HGNC:2896 Homo sapiens (human) 1737 DLAT
  • MGI:6194238
  • RGD:7240710
DOID:0110219 Brugada syndrome 2 HGNC:28956 Homo sapiens (human) 23171 GPD1L
  • RGD:7240710
DOID:13189 gout HGNC:288 Homo sapiens (human) 155 ADRB3
  • PMID:21285172
DOID:0110429 dilated cardiomyopathy 1H HGNC:288 Homo sapiens (human) 155 ADRB3
  • PMID:20123316
DOID:8947 diabetic retinopathy HGNC:288 Homo sapiens (human) 155 ADRB3
  • PMID:9313761
DOID:7148 rheumatoid arthritis HGNC:288 Homo sapiens (human) 155 ADRB3
  • PMID:12739037
DOID:9970 obesity HGNC:288 Homo sapiens (human) 155 ADRB3
  • PMID:11882399
  • PMID:9126344
  • PMID:9892244
  • RGD:7240710
DOID:10652 Alzheimer's disease HGNC:288 Homo sapiens (human) 155 ADRB3
  • PMID:17440948

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Supported by JST NBDC Grant Number JPMJND2204

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


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