Table Filtering
Other Information
Release Statistics Download
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 October 9, 2024
Displaying entries 71076 - 71100 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:0112185 thyroid dyshormonogenesis 1 HGNC:11040 Homo sapiens (human) 6528 SLC5A5
  • RGD:7240710
DOID:0060001 withdrawal disorder HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:11900601
DOID:13810 familial hypercholesterolemia HGNC:9205 Homo sapiens (human) 5445 PON2
  • PMID:16776623
DOID:12365 malaria HGNC:6338 Homo sapiens (human) 3811 KIR3DL1
  • PMID:21889618
DOID:8893 psoriasis HGNC:19100 Homo sapiens (human) 149233 IL23R
  • PMID:17587057
  • PMID:20978829
  • PMID:23093364
DOID:9975 cocaine dependence HGNC:8846 Homo sapiens (human) 8864 PER2
  • PMID:22832851
DOID:2841 asthma HGNC:18274 Homo sapiens (human) 57105 CYSLTR2
  • PMID:15454733
  • PMID:15475736
DOID:14080 glucocorticoid-remediable aldosteronism HGNC:2591 Homo sapiens (human) 1584 CYP11B1
  • RGD:7240710
DOID:0070066 autosomal dominant intellectual developmental disorder 36 HGNC:9302 Homo sapiens (human) 5518 PPP2R1A
  • RGD:7240710
DOID:0050645 arterial tortuosity syndrome HGNC:13444 Homo sapiens (human) 81031 SLC2A10
  • RGD:7240710
DOID:6000 congestive heart failure HGNC:283 Homo sapiens (human) 152 ADRA2C
  • PMID:12374873
DOID:0060307 autosomal dominant intellectual developmental disorder HGNC:29284 Homo sapiens (human) 57609 DIP2B
  • RGD:7240710
DOID:1588 thrombocytopenia HGNC:23657 Homo sapiens (human) 10020 GNE
  • RGD:7240710
DOID:0060639 permanent neonatal diabetes mellitus HGNC:4195 Homo sapiens (human) 2645 GCK
  • RGD:7240710
DOID:0080444 developmental and epileptic encephalopathy 27 HGNC:4586 Homo sapiens (human) 2904 GRIN2B
  • RGD:7240710
DOID:2476 hereditary spastic paraplegia HGNC:20499 Homo sapiens (human) 79944 L2HGDH
  • PMID:24573090
DOID:0050741 alcohol dependence HGNC:4076 Homo sapiens (human) 2555 GABRA2
  • RGD:7240710
DOID:0080459 developmental and epileptic encephalopathy 12 HGNC:15917 Homo sapiens (human) 23236 PLCB1
  • RGD:7240710
DOID:5844 myocardial infarction HGNC:3662 Homo sapiens (human) 2244 FGB
  • PMID:9437197
DOID:0112343 hereditary spastic paraplegia 82 HGNC:8756 Homo sapiens (human) 5833 PCYT2
  • RGD:7240710
DOID:8483 retinal artery occlusion HGNC:6018 Homo sapiens (human) 3569 IL6
  • PMID:15604420
DOID:0070434 hyperphosphatasia with impaired intellectual development syndrome 2 HGNC:23215 Homo sapiens (human) 84720 PIGO
  • RGD:7240710
DOID:13250 diarrhea HGNC:3018 Homo sapiens (human) 1811 SLC26A3
  • PMID:8896562
DOID:14330 Parkinson's disease HGNC:6893 Homo sapiens (human) 4137 MAPT
  • PMID:18162161
  • PMID:18785640
  • PMID:19879020
  • PMID:22221882
DOID:5041 esophageal cancer HGNC:5994 Homo sapiens (human) 7850 IL1R2
  • PMID:31744444

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.1.0

Last updated: December 9, 2024