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 9726 - 9750 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:2476 hereditary spastic paraplegia HGNC:16268 Homo sapiens (human) 10908 PNPLA6
  • MGI:6194238
DOID:0110790 hereditary spastic paraplegia 39 HGNC:16268 Homo sapiens (human) 10908 PNPLA6
  • RGD:7240710
DOID:1432 blindness HGNC:16268 Homo sapiens (human) 10908 PNPLA6
  • MGI:6194238
DOID:0111271 Oliver-McFarlane syndrome HGNC:16268 Homo sapiens (human) 10908 PNPLA6
  • RGD:7240710
DOID:0111265 Boucher-Neuhauser syndrome HGNC:16268 Homo sapiens (human) 10908 PNPLA6
  • RGD:7240710
DOID:1289 neurodegenerative disease HGNC:16268 Homo sapiens (human) 10908 PNPLA6
  • MGI:6194238
DOID:1930 Laurence-Moon syndrome HGNC:16268 Homo sapiens (human) 10908 PNPLA6
  • RGD:7240710
DOID:0070162 hereditary sensory and autonomic neuropathy type 1 HGNC:16253 Homo sapiens (human) 55304 SPTLC3
  • MGI:6194238
DOID:0070430 combined oxidative phosphorylation deficiency 57 HGNC:16148 Homo sapiens (human) 54675 CRLS1
  • RGD:7240710
DOID:684 hepatocellular carcinoma HGNC:16066 Homo sapiens (human) 55331 ACER3
  • PMID:30097213
DOID:0080547 metabolic dysfunction-associated steatohepatitis HGNC:16066 Homo sapiens (human) 55331 ACER3
  • PMID:31949129
DOID:10579 leukodystrophy HGNC:16066 Homo sapiens (human) 55331 ACER3
  • MGI:6194238
DOID:1936 atherosclerosis HGNC:16049 Homo sapiens (human) 10728 PTGES3
  • PMID:14736553
DOID:3181 oligodendroglioma HGNC:16049 Homo sapiens (human) 10728 PTGES3
  • PMID:19347995
DOID:1612 breast cancer HGNC:16049 Homo sapiens (human) 10728 PTGES3
  • PMID:20847343
DOID:2841 asthma HGNC:16037 Homo sapiens (human) 29095 ORMDL2
  • MGI:6194238
DOID:2841 asthma HGNC:16036 Homo sapiens (human) 94101 ORMDL1
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:15917 Homo sapiens (human) 23236 PLCB1
  • MGI:6194238
  • PMID:8534418
DOID:5844 myocardial infarction HGNC:15917 Homo sapiens (human) 23236 PLCB1
  • MGI:6194238
DOID:0050908 myelodysplastic syndrome HGNC:15917 Homo sapiens (human) 23236 PLCB1
  • PMID:16820933
  • PMID:21109771
DOID:0080459 developmental and epileptic encephalopathy 12 HGNC:15917 Homo sapiens (human) 23236 PLCB1
  • RGD:7240710
DOID:5419 schizophrenia HGNC:15917 Homo sapiens (human) 23236 PLCB1
  • MGI:6194238
DOID:9970 obesity HGNC:15917 Homo sapiens (human) 23236 PLCB1
  • MGI:6194238
DOID:9119 acute myeloid leukemia HGNC:15917 Homo sapiens (human) 23236 PLCB1
  • PMID:20516454
DOID:3963 thyroid gland carcinoma HGNC:15855 Homo sapiens (human) 22918 CD93
  • PMID:32626543

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