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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 2626 - 2650 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:5603 T-cell acute lymphoblastic leukemia HGNC:386 Homo sapiens (human) 8644 AKR1C3
  • PMID:26116659
DOID:13406 pulmonary sarcoidosis HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:15763444
DOID:3049 Churg-Strauss syndrome HGNC:4243 Homo sapiens (human) 2674 GFRA1
  • PMID:9853108
DOID:0050775 schneckenbecken dysplasia HGNC:20800 Homo sapiens (human) 23169 SLC35D1
  • MGI:6194238
  • RGD:7240710
DOID:13001 carotid stenosis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • MGI:6194238
DOID:3493 signet ring cell adenocarcinoma HGNC:11755 Homo sapiens (human) 7031 TFF1
  • PMID:18283638
DOID:9744 type 1 diabetes mellitus HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • PMID:19640330
DOID:10595 Charcot-Marie-Tooth disease HGNC:7450 Homo sapiens (human) 8898 MTMR2
  • MGI:6194238
DOID:10763 hypertension HGNC:6080 Homo sapiens (human) 3636 INPPL1
  • PMID:15220217
DOID:0111334 congenital leptin deficiency HGNC:6553 Homo sapiens (human) 3952 LEP
  • RGD:7240710
DOID:3070 high grade glioma HGNC:2172 Homo sapiens (human) 6900 CNTN2
  • PMID:11280781
DOID:12351 alcoholic hepatitis HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:1347281
DOID:9351 diabetes mellitus HGNC:4092 Homo sapiens (human) 2571 GAD1
  • MGI:6194238
DOID:2018 hyperinsulinism HGNC:6619 Homo sapiens (human) 3990 LIPC
  • MGI:6194238
  • PMID:11095452
  • PMID:1592086
DOID:11823 hepatorenal syndrome HGNC:11850 Homo sapiens (human) 7099 TLR4
  • MGI:6194238
DOID:1612 breast cancer HGNC:23531 Homo sapiens (human) 196051 PLPP4
  • PMID:16818692
DOID:684 hepatocellular carcinoma HGNC:4449 Homo sapiens (human) 2817 GPC1
  • PMID:35693827
DOID:1240 leukemia HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:17205986
DOID:0050830 peripheral artery disease HGNC:7956 Homo sapiens (human) 4886 NPY1R
  • PMID:21468772
DOID:224 transient cerebral ischemia HGNC:18451 Homo sapiens (human) 90411 MCFD2
  • MGI:6194238
DOID:3963 thyroid gland carcinoma HGNC:15855 Homo sapiens (human) 22918 CD93
  • PMID:32626543
DOID:0050589 inflammatory bowel disease HGNC:23614 Homo sapiens (human) 55808 ST6GALNAC1
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I HGNC:20266 Homo sapiens (human) 29880 ALG5
  • MGI:6194238
DOID:0070254 congenital disorder of glycosylation type IIb HGNC:24862 Homo sapiens (human) 7841 MOGS
  • RGD:7240710
DOID:824 periodontitis HGNC:3774 Homo sapiens (human) 2331 FMOD
  • PMID:15196146

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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