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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 5151 - 5175 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:2560 morphine dependence HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • MGI:6194238
DOID:1574 alcohol use disorder HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • MGI:6194238
DOID:0050742 nicotine dependence HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • PMID:17085484
DOID:5844 myocardial infarction HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • MGI:6194238
DOID:1793 pancreatic cancer HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • PMID:10374842
  • PMID:11249065
DOID:0050933 ovarian serous carcinoma HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • PMID:25455994
DOID:10652 Alzheimer's disease HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • MGI:6194238
DOID:1059 intellectual disability HGNC:7680 Homo sapiens (human) 3340 NDST1
  • MGI:6194238
DOID:11198 DiGeorge syndrome HGNC:7680 Homo sapiens (human) 3340 NDST1
  • MGI:6194238
DOID:14227 azoospermia HGNC:7680 Homo sapiens (human) 3340 NDST1
  • MGI:6194238
DOID:0081210 autosomal recessive intellectual developmental disorder 46 HGNC:7680 Homo sapiens (human) 3340 NDST1
  • RGD:7240710
DOID:12716 newborn respiratory distress syndrome HGNC:7680 Homo sapiens (human) 3340 NDST1
  • MGI:6194238
DOID:0060041 autism spectrum disorder HGNC:7680 Homo sapiens (human) 3340 NDST1
  • MGI:6194238
DOID:3827 congenital diaphragmatic hernia HGNC:7680 Homo sapiens (human) 3340 NDST1
  • MGI:6194238
DOID:0060041 autism spectrum disorder HGNC:7681 Homo sapiens (human) 8509 NDST2
  • MGI:6194238
DOID:14227 azoospermia HGNC:7681 Homo sapiens (human) 8509 NDST2
  • MGI:6194238
DOID:1059 intellectual disability HGNC:7681 Homo sapiens (human) 8509 NDST2
  • MGI:6194238
DOID:0060041 autism spectrum disorder HGNC:7682 Homo sapiens (human) 9348 NDST3
  • MGI:6194238
DOID:14227 azoospermia HGNC:7682 Homo sapiens (human) 9348 NDST3
  • MGI:6194238
DOID:1059 intellectual disability HGNC:7682 Homo sapiens (human) 9348 NDST3
  • MGI:6194238
DOID:0110734 neurodegeneration with brain iron accumulation HGNC:7694 Homo sapiens (human) 4706 NDUFAB1
  • MGI:6194238
DOID:0080488 mucolipidosis HGNC:7758 Homo sapiens (human) 4758 NEU1
  • RGD:7240710
DOID:3343 glycoproteinosis HGNC:7758 Homo sapiens (human) 4758 NEU1
  • MGI:6194238
DOID:10283 prostate cancer HGNC:785 Homo sapiens (human) 467 ATF3
  • PMID:26522727
  • PMID:26944919
DOID:2957 pulmonary tuberculosis HGNC:785 Homo sapiens (human) 467 ATF3
  • PMID:20856677

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