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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 1851 - 1875 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:0080199 colorectal carcinoma SGD:S000002779 Saccharomyces cerevisiae S288C 851977 CTS2
  • MGI:6194238
DOID:2841 asthma SGD:S000002779 Saccharomyces cerevisiae S288C 851977 CTS2
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus SGD:S000002779 Saccharomyces cerevisiae S288C 851977 CTS2
  • MGI:6194238
DOID:3770 pulmonary fibrosis SGD:S000002779 Saccharomyces cerevisiae S288C 851977 CTS2
  • MGI:6194238
DOID:1909 melanoma SGD:S000002779 Saccharomyces cerevisiae S288C 851977 CTS2
  • MGI:6194238
DOID:0080540 galactosialidosis HGNC:9251 Homo sapiens (human) 5476 CTSA
  • RGD:7240710
DOID:3211 lysosomal storage disease HGNC:9251 Homo sapiens (human) 5476 CTSA
  • PMID:8514852
DOID:0070254 congenital disorder of glycosylation type IIb SGD:S000002995 Saccharomyces cerevisiae S288C 852857 CWH41
  • MGI:6194238
DOID:10783 methemoglobinemia HGNC:2873 Homo sapiens (human) 1727 CYB5R3
  • PMID:11295830
DOID:1612 breast cancer HGNC:2873 Homo sapiens (human) 1727 CYB5R3
  • PMID:25225034
DOID:0060076 estrogen-receptor negative breast cancer HGNC:2873 Homo sapiens (human) 1727 CYB5R3
  • PMID:26351264
DOID:9352 type 2 diabetes mellitus HGNC:20147 Homo sapiens (human) 51167 CYB5R4
  • MGI:6194238
  • PMID:15504981
DOID:1824 status epilepticus HGNC:2590 Homo sapiens (human) 1583 CYP11A1
  • MGI:6194238
DOID:1924 hypogonadism HGNC:2590 Homo sapiens (human) 1583 CYP11A1
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:2590 Homo sapiens (human) 1583 CYP11A1
  • MGI:6194238
DOID:10763 hypertension HGNC:2590 Homo sapiens (human) 1583 CYP11A1
  • MGI:6194238
DOID:0050546 congenital adrenal insufficiency HGNC:2590 Homo sapiens (human) 1583 CYP11A1
  • RGD:7240710
DOID:4195 hyperglycemia HGNC:2590 Homo sapiens (human) 1583 CYP11A1
  • MGI:6194238
DOID:2527 nephrosis HGNC:2590 Homo sapiens (human) 1583 CYP11A1
  • MGI:6194238
DOID:11446 sciatic neuropathy HGNC:2590 Homo sapiens (human) 1583 CYP11A1
  • MGI:6194238
DOID:0050811 congenital adrenal hyperplasia HGNC:2590 Homo sapiens (human) 1583 CYP11A1
  • PMID:12161514
DOID:3454 brain infarction HGNC:2591 Homo sapiens (human) 1584 CYP11B1
  • MGI:6194238
DOID:10763 hypertension HGNC:2591 Homo sapiens (human) 1584 CYP11B1
  • MGI:6194238
DOID:446 primary hyperaldosteronism HGNC:2591 Homo sapiens (human) 1584 CYP11B1
  • PMID:1731223
DOID:0050891 adrenal cortical adenoma HGNC:2591 Homo sapiens (human) 1584 CYP11B1
  • PMID:12457455

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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