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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 2801 - 2825 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:4450 renal cell carcinoma HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:17220335
DOID:3659 sialuria HGNC:23657 Homo sapiens (human) 10020 GNE
  • RGD:7240710
DOID:5844 myocardial infarction HGNC:2464 Homo sapiens (human) 1462 VCAN
  • MGI:6194238
DOID:0050742 nicotine dependence HGNC:7956 Homo sapiens (human) 4886 NPY1R
  • PMID:22309839
DOID:3717 gastric adenocarcinoma HGNC:6876 Homo sapiens (human) 1432 MAPK14
  • PMID:32243890
DOID:0111390 mucopolysaccharidosis Ih HGNC:5391 Homo sapiens (human) 3425 IDUA
  • RGD:7240710
DOID:0060248 Simpson-Golabi-Behmel syndrome type 1 HGNC:4451 Homo sapiens (human) 2719 GPC3
  • MGI:6194238
  • RGD:7240710
DOID:3082 interstitial lung disease HGNC:10798 Homo sapiens (human) 653509 SFTPA1
  • PMID:11445799
  • PMID:9216212
  • RGD:7240710
DOID:10763 hypertension HGNC:4555 Homo sapiens (human) 2878 GPX3
  • MGI:6194238
  • PMID:21933611
  • PMID:32034489
DOID:3021 acute kidney failure HGNC:6563 Homo sapiens (human) 3958 LGALS3
  • MGI:6194238
DOID:1074 kidney failure HGNC:30092 Homo sapiens (human) 10135 NAMPT
  • MGI:6194238
DOID:0050855 renal fibrosis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • MGI:6194238
DOID:1459 hypothyroidism HGNC:7962 Homo sapiens (human) 9572 NR1D1
  • MGI:6194238
DOID:1508 candidiasis HGNC:4015 Homo sapiens (human) 2526 FUT4
  • MGI:6194238
DOID:14250 Down syndrome HGNC:11503 Homo sapiens (human) 8867 SYNJ1
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I HGNC:3005 Homo sapiens (human) 8813 DPM1
  • MGI:6194238
DOID:9408 acute myocardial infarction HGNC:10681 Homo sapiens (human) 6390 SDHB
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • MGI:6194238
  • PMID:17259403
  • PMID:19498446
  • PMID:19502414
  • RGD:7240710
DOID:3082 interstitial lung disease HGNC:10803 Homo sapiens (human) 6441 SFTPD
  • PMID:19286849
  • PMID:9216212
DOID:3635 congenital myasthenic syndrome HGNC:10979 Homo sapiens (human) 6576 SLC25A1
  • RGD:7240710
DOID:8577 ulcerative colitis HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • PMID:16432373
DOID:1380 endometrial cancer HGNC:11755 Homo sapiens (human) 7031 TFF1
  • PMID:10835496
DOID:0080552 congenital disorder of glycosylation Ia HGNC:9115 Homo sapiens (human) 5373 PMM2
  • MGI:6194238
  • RGD:7240710
DOID:0080564 congenital disorder of glycosylation Il HGNC:15672 Homo sapiens (human) 79796 ALG9
  • RGD:7240710
DOID:10283 prostate cancer HGNC:11848 Homo sapiens (human) 7097 TLR2
  • PMID:22311043

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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