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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 126 - 150 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:4481 allergic rhinitis HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:15112973
DOID:3827 congenital diaphragmatic hernia HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:0111128 focal segmental glomerulosclerosis 1 HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:11123 Henoch-Schoenlein purpura HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:15315169
DOID:0050848 obstructive sleep apnea HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
  • PMID:19482546
  • PMID:20182789
DOID:11476 osteoporosis HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:2987 familial mediterranean fever HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:24680475
DOID:783 end stage renal disease HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
  • PMID:16385653
  • PMID:20149750
DOID:5844 myocardial infarction HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
  • PMID:7555560
DOID:1612 breast cancer HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:23828384
DOID:10763 hypertension HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
  • PMID:17283861
DOID:3083 chronic obstructive pulmonary disease HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:19493329
  • PMID:20096799
  • PMID:20156752
DOID:2355 anemia HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:18156303
  • PMID:23141116
DOID:0050855 renal fibrosis HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
  • PMID:10504496
DOID:0110861 autosomal recessive polycystic kidney disease HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:3587 pancreatic ductal carcinoma HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:17481528
DOID:12930 dilated cardiomyopathy HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:9270088
DOID:8432 polycythemia HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:18339134
DOID:418 systemic scleroderma HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:17360781
DOID:3770 pulmonary fibrosis HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:12236 primary biliary cholangitis HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:3905 lung carcinoma HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:183595
DOID:0060071 pre-malignant neoplasm HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:684 hepatocellular carcinoma HGNC:16066 Homo sapiens (human) 55331 ACER3
  • PMID:30097213
DOID:0080547 metabolic dysfunction-associated steatohepatitis HGNC:16066 Homo sapiens (human) 55331 ACER3
  • PMID:31949129

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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