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 70701 - 70725 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:2841 asthma HGNC:5998 Homo sapiens (human) 9173 IL1RL1
  • PMID:11463601
  • PMID:19198610
  • PMID:19852851
  • PMID:21150878
  • PMID:21281963
DOID:4483 rhinitis HGNC:5998 Homo sapiens (human) 9173 IL1RL1
  • PMID:19671251
DOID:0081378 amyotrophic lateral sclerosis type 24 HGNC:18591 Homo sapiens (human) 91754 NEK9
  • MGI:6194238
DOID:0060558 lethal congenital contracture syndrome HGNC:18591 Homo sapiens (human) 91754 NEK9
  • RGD:7240710
DOID:1596 depressive disorder HGNC:5298 Homo sapiens (human) 9177 HTR3B
  • PMID:16487942
DOID:1574 alcohol use disorder HGNC:5298 Homo sapiens (human) 9177 HTR3B
  • PMID:20838391
DOID:0080930 primary localized cutaneous amyloidosis 1 HGNC:8507 Homo sapiens (human) 9180 OSMR
  • RGD:7240710
DOID:0080312 neurodevelopmental disorder with midbrain and hindbrain malformations HGNC:682 Homo sapiens (human) 9181 ARHGEF2
  • MGI:6194238
  • RGD:7240710
DOID:162 cancer HGNC:1151 Homo sapiens (human) 9184 BUB3
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I HGNC:30220 Homo sapiens (human) 91869 RFT1
  • MGI:6194238
DOID:0080566 congenital disorder of glycosylation In HGNC:30220 Homo sapiens (human) 91869 RFT1
  • RGD:7240710
DOID:162 cancer HGNC:30220 Homo sapiens (human) 91869 RFT1
  • MGI:6194238
DOID:0110868 congenital stationary night blindness 1D HGNC:10975 Homo sapiens (human) 9187 SLC24A1
  • MGI:6194238
  • RGD:7240710
DOID:9074 systemic lupus erythematosus HGNC:25132 Homo sapiens (human) 91937 TIMD4
  • MGI:6194238
DOID:0112075 nuclear type mitochondrial complex I deficiency 10 HGNC:28086 Homo sapiens (human) 91942 NDUFAF2
  • RGD:7240710
DOID:0070257 congenital disorder of glycosylation type IIe HGNC:18622 Homo sapiens (human) 91949 COG7
  • MGI:6194238
  • RGD:7240710
DOID:630 genetic disease HGNC:18622 Homo sapiens (human) 91949 COG7
  • PMID:15107842
DOID:0110794 hereditary spastic paraplegia 42 HGNC:95 Homo sapiens (human) 9197 SLC33A1
  • RGD:7240710
DOID:1793 pancreatic cancer HGNC:173 Homo sapiens (human) 92 ACVR2A
  • PMID:9714055
DOID:14323 Marfan syndrome HGNC:173 Homo sapiens (human) 92 ACVR2A
  • MGI:6194238
DOID:3883 Lynch syndrome HGNC:173 Homo sapiens (human) 92 ACVR2A
  • PMID:28218421
DOID:4258 Weissenbacher-Zweymuller syndrome HGNC:173 Homo sapiens (human) 92 ACVR2A
  • MGI:6194238
DOID:0050787 juvenile polyposis syndrome HGNC:173 Homo sapiens (human) 92 ACVR2A
  • MGI:6194238
DOID:219 colon cancer HGNC:173 Homo sapiens (human) 92 ACVR2A
  • PMID:14988818
DOID:670 amphetamine abuse HGNC:1678 Homo sapiens (human) 920 CD4
  • MGI:6194238

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