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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 9601 - 9625 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0060222 Scheie syndrome HGNC:5391 Homo sapiens (human) 3425 IDUA
  • RGD:7240710
DOID:4195 hyperglycemia HGNC:2623 Homo sapiens (human) 1559 CYP2C9
  • PMID:17597710
DOID:10223 dermatomyositis HGNC:11848 Homo sapiens (human) 7097 TLR2
  • PMID:19953283
DOID:14330 Parkinson's disease HGNC:8999 Homo sapiens (human) 23761 PISD
  • MGI:6194238
DOID:11446 sciatic neuropathy HGNC:11850 Homo sapiens (human) 7099 TLR4
  • MGI:6194238
DOID:2300 spondylolysis HGNC:10994 Homo sapiens (human) 1836 SLC26A2
  • PMID:26077908
DOID:3908 lung non-small cell carcinoma HGNC:10682 Homo sapiens (human) 6391 SDHC
  • PMID:25576295
DOID:418 systemic scleroderma HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:17360781
DOID:4914 esophagus adenocarcinoma HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:22715394
DOID:255 hemangioma HGNC:11005 Homo sapiens (human) 6513 SLC2A1
  • PMID:10665907
DOID:3393 coronary artery disease HGNC:9232 Homo sapiens (human) 5465 PPARA
  • PMID:16043164
DOID:11981 morbid obesity HGNC:15814 Homo sapiens (human) 55902 ACSS2
  • PMID:22384010
DOID:2224 essential thrombocythemia HGNC:1455 Homo sapiens (human) 811 CALR
  • PMID:24496303
  • PMID:25860380
  • RGD:7240710
DOID:5844 myocardial infarction HGNC:6971 Homo sapiens (human) 4191 MDH2
  • MGI:6194238
DOID:4195 hyperglycemia HGNC:4925 Homo sapiens (human) 3101 HK3
  • MGI:6194238
DOID:0060894 early-onset Parkinson's disease HGNC:11503 Homo sapiens (human) 8867 SYNJ1
  • MGI:6194238
DOID:3748 esophagus squamous cell carcinoma HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:11860825
DOID:783 end stage renal disease HGNC:6677 Homo sapiens (human) 4023 LPL
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:5218 Homo sapiens (human) 3284 HSD3B2
  • PMID:18180323
DOID:3525 middle cerebral artery infarction HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:10721 Homo sapiens (human) 6403 SELP
  • MGI:6194238
  • PMID:12165563
  • PMID:17391113
  • PMID:21162967
DOID:1793 pancreatic cancer HGNC:6081 Homo sapiens (human) 3630 INS
  • PMID:19152242
  • PMID:19375425
  • PMID:19572116
DOID:10690 mastitis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • MGI:6194238
DOID:0080507 Cornelia de Lange syndrome 3 HGNC:2468 Homo sapiens (human) 9126 SMC3
  • MGI:6194238
  • RGD:7240710
DOID:2799 bronchiolitis obliterans HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:19104434

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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