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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 7476 - 7500 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:3525 middle cerebral artery infarction HGNC:6783 Homo sapiens (human) 4099 MAG
  • MGI:6194238
DOID:573 nerve compression syndrome HGNC:6783 Homo sapiens (human) 4099 MAG
  • MGI:6194238
DOID:11446 sciatic neuropathy HGNC:6783 Homo sapiens (human) 4099 MAG
  • MGI:6194238
DOID:0110820 hereditary spastic paraplegia 75 HGNC:6783 Homo sapiens (human) 4099 MAG
  • RGD:7240710
DOID:1459 hypothyroidism HGNC:713 Homo sapiens (human) 410 ARSA
  • MGI:6194238
DOID:10581 metachromatic leukodystrophy HGNC:713 Homo sapiens (human) 410 ARSA
  • MGI:6194238
  • PMID:15026521
  • PMID:15375602
  • RGD:7240710
DOID:12800 mucopolysaccharidosis VI HGNC:714 Homo sapiens (human) 411 ARSB
  • MGI:6194238
  • PMID:1550123
  • RGD:7240710
DOID:10763 hypertension FB:FBgn0037671 Drosophila melanogaster (fruit fly) 41104 ATP6AP2
  • MGI:6194238
DOID:0060806 syndromic X-linked intellectual disability Hedera type FB:FBgn0037671 Drosophila melanogaster (fruit fly) 41104 ATP6AP2
  • MGI:6194238
DOID:0112105 X-linked parkinsonism-spasticity syndrome FB:FBgn0037671 Drosophila melanogaster (fruit fly) 41104 ATP6AP2
  • MGI:6194238
DOID:5212 congenital disorder of glycosylation FB:FBgn0037671 Drosophila melanogaster (fruit fly) 41104 ATP6AP2
  • PMID:29127204
DOID:0060309 syndromic X-linked intellectual disability FB:FBgn0037671 Drosophila melanogaster (fruit fly) 41104 ATP6AP2
  • PMID:26376863
DOID:0050571 congenital disorder of glycosylation type II FB:FBgn0037671 Drosophila melanogaster (fruit fly) 41104 ATP6AP2
  • MGI:6194238
DOID:9074 systemic lupus erythematosus FB:FBgn0011740 Drosophila melanogaster (fruit fly) 41126 α-Man-IIa CG18802
  • MGI:6194238
DOID:5419 schizophrenia FB:FBgn0011740 Drosophila melanogaster (fruit fly) 41126 α-Man-IIa CG18802
  • MGI:6194238
DOID:1338 congenital dyserythropoietic anemia FB:FBgn0011740 Drosophila melanogaster (fruit fly) 41126 alpha-Man-IIa CG18802
  • MGI:6194238
DOID:5419 schizophrenia FB:FBgn0011740 Drosophila melanogaster (fruit fly) 41126 alpha-Man-IIa CG18802
  • MGI:6194238
DOID:1338 congenital dyserythropoietic anemia FB:FBgn0011740 Drosophila melanogaster (fruit fly) 41126 α-Man-IIa CG18802
  • MGI:6194238
DOID:9074 systemic lupus erythematosus FB:FBgn0011740 Drosophila melanogaster (fruit fly) 41126 alpha-Man-IIa CG18802
  • MGI:6194238
DOID:2228 thrombocytosis FB:FBgn0005585 Drosophila melanogaster (fruit fly) 41166 Calr CG9429
  • MGI:6194238
DOID:3910 lung adenocarcinoma FB:FBgn0005585 Drosophila melanogaster (fruit fly) 41166 Calr CG9429
  • MGI:6194238
DOID:2224 essential thrombocythemia FB:FBgn0005585 Drosophila melanogaster (fruit fly) 41166 Calr CG9429
  • MGI:6194238
DOID:3748 esophagus squamous cell carcinoma FB:FBgn0005585 Drosophila melanogaster (fruit fly) 41166 Calr CG9429
  • MGI:6194238
DOID:8955 sideroblastic anemia FB:FBgn0005585 Drosophila melanogaster (fruit fly) 41166 Calr CG9429
  • MGI:6194238
DOID:3587 pancreatic ductal carcinoma FB:FBgn0005585 Drosophila melanogaster (fruit fly) 41166 Calr CG9429
  • MGI:6194238

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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


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Last updated: August 19, 2024