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 July 29, 2024
Displaying entries 9851 - 9875 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:9952 acute lymphoblastic leukemia HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:16676594
  • PMID:22964275
  • PMID:23725389
DOID:0060611 abdominal obesity-metabolic syndrome HGNC:18448 Homo sapiens (human) 79661 NEIL1
  • MGI:6194238
DOID:0060250 idiopathic scoliosis HGNC:20862 Homo sapiens (human) 64116 SLC39A8
  • MGI:6194238
DOID:1793 pancreatic cancer HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • PMID:10374842
  • PMID:11249065
DOID:8719 in situ carcinoma HGNC:9599 Homo sapiens (human) 9536 PTGES
  • PMID:14499677
  • PMID:14871981
DOID:1380 endometrial cancer HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:17023034
DOID:0080132 Sengers syndrome HGNC:21869 Homo sapiens (human) 55750 AGK
  • RGD:7240710
DOID:1440 Machado-Joseph disease HGNC:4242 Homo sapiens (human) 9945 GFPT2
  • MGI:6194238
DOID:28 endocrine system disease HGNC:924 Homo sapiens (human) 2683 B4GALT1
  • MGI:6194238
DOID:0060224 atrial fibrillation HGNC:11848 Homo sapiens (human) 7097 TLR2
  • PMID:19167648
DOID:4928 intrahepatic cholangiocarcinoma HGNC:5383 Homo sapiens (human) 3418 IDH2
  • PMID:22824796
DOID:2921 glomerulonephritis HGNC:11609 Homo sapiens (human) 6916 TBXAS1
  • MGI:6194238
DOID:10591 pre-eclampsia HGNC:5208 Homo sapiens (human) 3290 HSD11B1
  • PMID:23659736
DOID:3310 atopic dermatitis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:19764566
  • PMID:23821954
DOID:1123 spondyloarthropathy HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:11211 buphthalmos HGNC:2597 Homo sapiens (human) 1545 CYP1B1
  • MGI:6194238
  • PMID:10227395
  • PMID:12567107
  • PMID:16490498
  • PMID:19247456
  • PMID:19593207
  • PMID:19597567
  • PMID:20664688
  • PMID:23922489
  • RGD:7240710
DOID:767 muscular atrophy HGNC:7452 Homo sapiens (human) 9110 MTMR4
  • MGI:6194238
DOID:1168 familial hyperlipidemia HGNC:5208 Homo sapiens (human) 3290 HSD11B1
  • MGI:6194238
DOID:0090005 Schwartz-Jampel syndrome 1 HGNC:5273 Homo sapiens (human) 3339 HSPG2
  • MGI:6194238
  • RGD:7240710
DOID:1289 neurodegenerative disease HGNC:29013 Homo sapiens (human) 23274 CLEC16A
  • MGI:6194238
DOID:0050628 advanced sleep phase syndrome HGNC:8846 Homo sapiens (human) 8864 PER2
  • PMID:11232563
DOID:9744 type 1 diabetes mellitus HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:19120272
DOID:526 human immunodeficiency virus infectious disease HGNC:2615 Homo sapiens (human) 1555 CYP2B6
  • PMID:18281305
  • PMID:21862974
DOID:11714 gestational diabetes HGNC:4553 Homo sapiens (human) 2876 GPX1
  • MGI:6194238
DOID:5212 congenital disorder of glycosylation HGNC:18305 Homo sapiens (human) 10159 ATP6AP2
  • 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 v4.0.0

Last updated: August 19, 2024