Table Filtering
Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
Resources Genes Glycoproteins Lectins Glycolipids Glycans Pathways Diseases Organisms
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Other Information
Release Statistics Download
Tools
SugarDrawer GlycanBuilder Glycan Converters GlycoMaple GlycomeAtlas LM-GlycomeAtlas GALAXY MCAW GlycoSim GRable
Search Tools
Cross Search Glycan Search Publication Search Programmatic Access
Standards Ontologies Notations
Guidelines
MIRAGE
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 January 28, 2025
Displaying entries 5876 - 5900 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence References
DOID:1909 melanoma HGNC:21686 Homo sapiens (human) 8635 RNASET2 mutant phenotype evidence used in manual assertion
  • PMID:27014725
DOID:0112182 mismatch repair cancer syndrome HGNC:21686 Homo sapiens (human) 8635 RNASET2 inference by association of genotype from phenotype used in manual assertion
  • PMID:28218421
DOID:3883 Lynch syndrome HGNC:21686 Homo sapiens (human) 8635 RNASET2 inference by association of genotype from phenotype used in manual assertion
  • PMID:28218421
DOID:0050861 colorectal adenocarcinoma HGNC:21686 Homo sapiens (human) 8635 RNASET2 mutant phenotype evidence used in manual assertion
  • PMID:27014725
DOID:0081007 RNASET2-deficient cystic leukoencephalopathy HGNC:21686 Homo sapiens (human) 8635 RNASET2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1324 lung cancer HGNC:21686 Homo sapiens (human) 8635 RNASET2 inference by association of genotype from phenotype used in manual assertion
  • PMID:29193083
DOID:234 colon adenocarcinoma HGNC:21686 Homo sapiens (human) 8635 RNASET2 mutant phenotype evidence used in manual assertion
  • PMID:30842415
DOID:0111926 spermatogenic failure 39 HGNC:2946 Homo sapiens (human) 8632 DNAH17 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1059 intellectual disability HGNC:1733 Homo sapiens (human) 8621 CDK13 inference by association of genotype from phenotype used in manual assertion
  • PMID:29021403
  • PMID:29222009
DOID:0112247 congenital heart defects, dysmorphic facial features, and intellectual developmental disorder HGNC:1733 Homo sapiens (human) 8621 CDK13 inference by association of genotype from phenotype used in manual assertion
  • PMID:27479907
  • PMID:28807008
  • PMID:29021403
  • PMID:29393965
  • RGD:7240710
DOID:684 hepatocellular carcinoma HGNC:1733 Homo sapiens (human) 8621 CDK13 inference by association of genotype from phenotype used in manual assertion
  • PMID:22912832
DOID:10286 prostate carcinoma HGNC:1733 Homo sapiens (human) 8621 CDK13 mutant phenotype evidence used in manual assertion
  • PMID:33390186
DOID:12849 autistic disorder HGNC:10982 Homo sapiens (human) 8604 SLC25A12 inference by association of genotype from phenotype used in manual assertion
  • PMID:15056512
DOID:0080349 developmental and epileptic encephalopathy 39 HGNC:10982 Homo sapiens (human) 8604 SLC25A12 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050432 Asperger syndrome HGNC:10982 Homo sapiens (human) 8604 SLC25A12 inference by association of genotype from phenotype used in manual assertion
  • PMID:24679184
DOID:11476 osteoporosis HGNC:11926 Homo sapiens (human) 8600 TNFSF11 inference by association of genotype from phenotype used in manual assertion
  • PMID:17002564
DOID:0110943 autosomal recessive osteopetrosis 2 HGNC:11926 Homo sapiens (human) 8600 TNFSF11 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0090048 dystonia 16 HGNC:9438 Homo sapiens (human) 8575 PRKRA inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060807 syndromic X-linked intellectual disability Najm type HGNC:1497 Homo sapiens (human) 8573 CASK inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:14711 FG syndrome HGNC:1497 Homo sapiens (human) 8573 CASK inference by association of genotype from phenotype used in manual assertion
  • PMID:19200522
DOID:0110199 Charcot-Marie-Tooth disease dominant intermediate C HGNC:12840 Homo sapiens (human) 8565 YARS1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3459 breast carcinoma HGNC:19074 Homo sapiens (human) 8563 THOC5 inference by association of genotype from phenotype used in manual assertion
  • PMID:16959974
DOID:0070399 hypomyelinating leukodystrophy 18 HGNC:13709 Homo sapiens (human) 8560 DEGS1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3082 interstitial lung disease HGNC:566 Homo sapiens (human) 8546 AP3B1 inference by association of genotype from phenotype used in manual assertion
  • PMID:22009278
DOID:3770 pulmonary fibrosis HGNC:566 Homo sapiens (human) 8546 AP3B1 inference by association of genotype from phenotype used in manual assertion
  • PMID:12125811
Download data in CSV format Download data in TSV format Download data in JSON format
About Release Notes Help Feedback
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 v4.2.1

Last updated: April 7, 2025