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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 6601 - 6625 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:9744 type 1 diabetes mellitus HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • PMID:15714132
DOID:3526 cerebral infarction HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:18201705
DOID:0050475 Weill-Marchesani syndrome HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:15223607
DOID:0111420 familial GPIHBP1 deficiency HGNC:24945 Homo sapiens (human) 338328 GPIHBP1
  • RGD:7240710
DOID:900 hepatopulmonary syndrome HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:1312 focal segmental glomerulosclerosis HGNC:6619 Homo sapiens (human) 3990 LIPC
  • MGI:6194238
DOID:10316 pneumoconiosis HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:19273541
DOID:8577 ulcerative colitis HGNC:10721 Homo sapiens (human) 6403 SELP
  • PMID:21526498
DOID:2526 prostate adenocarcinoma HGNC:8976 Homo sapiens (human) 5291 PIK3CB
  • PMID:18755892
DOID:0070266 congenital disorder of glycosylation type IIn HGNC:20862 Homo sapiens (human) 64116 SLC39A8
  • RGD:7240710
DOID:3910 lung adenocarcinoma HGNC:380 Homo sapiens (human) 10327 AKR1A1
  • PMID:30727821
DOID:8398 osteoarthritis HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:22527881
DOID:3649 pyruvate decarboxylase deficiency HGNC:8806 Homo sapiens (human) 5160 PDHA1
  • MGI:6194238
  • PMID:10679936
  • PMID:20002461
  • RGD:7240710
DOID:2349 arteriosclerosis HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:11326751
DOID:1596 depressive disorder HGNC:9031 Homo sapiens (human) 5320 PLA2G2A
  • PMID:22331023
DOID:0112248 17-beta hydroxysteroid dehydrogenase 3 deficiency HGNC:5212 Homo sapiens (human) 3293 HSD17B3
  • MGI:6194238
  • RGD:7240710
DOID:11054 urinary bladder cancer HGNC:3353 Homo sapiens (human) 2026 ENO2
  • PMID:17951193
DOID:0110429 dilated cardiomyopathy 1H HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:14676433
DOID:0050464 Farber lipogranulomatosis HGNC:735 Homo sapiens (human) 427 ASAH1
  • MGI:6194238
  • RGD:7240710
DOID:13241 Behcet's disease HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:15045629
  • PMID:15961928
DOID:2957 pulmonary tuberculosis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:18212516
  • PMID:20650298
DOID:5082 liver cirrhosis HGNC:6563 Homo sapiens (human) 3958 LGALS3
  • PMID:16549783
DOID:10763 hypertension HGNC:2642 Homo sapiens (human) 1579 CYP4A11
  • MGI:6194238
  • PMID:16144986
DOID:9352 type 2 diabetes mellitus HGNC:6344 Homo sapiens (human) 9365 KL
  • MGI:6194238
DOID:1612 breast cancer HGNC:380 Homo sapiens (human) 10327 AKR1A1
  • PMID:25526449

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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