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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 6926 - 6950 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0050753 cerebellar ataxia HGNC:24768 Homo sapiens (human) 375775 PNPLA7
  • MGI:6194238
DOID:1432 blindness HGNC:24768 Homo sapiens (human) 375775 PNPLA7
  • MGI:6194238
DOID:1289 neurodegenerative disease HGNC:24768 Homo sapiens (human) 375775 PNPLA7
  • MGI:6194238
DOID:2476 hereditary spastic paraplegia HGNC:24768 Homo sapiens (human) 375775 PNPLA7
  • MGI:6194238
DOID:0110657 congenital myasthenic syndrome 8 HGNC:329 Homo sapiens (human) 375790 AGRN
  • MGI:6194238
  • RGD:7240710
DOID:9351 diabetes mellitus HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • PMID:15292329
DOID:0070218 familial hyperinsulinemic hypoglycemia 2 HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • MGI:6194238
  • PMID:17259403
  • PMID:19498446
  • PMID:19502414
  • RGD:7240710
DOID:10763 hypertension HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • MGI:6194238
DOID:0060639 permanent neonatal diabetes mellitus HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • PMID:15115830
  • PMID:16670688
  • RGD:7240710
DOID:11716 prediabetes syndrome HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • MGI:6194238
DOID:11446 sciatic neuropathy HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • MGI:6194238
DOID:11832 visual epilepsy HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • MGI:6194238
DOID:2018 hyperinsulinism HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • PMID:15998776
DOID:1824 status epilepticus HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • MGI:6194238
DOID:0080855 Parkinsonism HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • MGI:6194238
DOID:0111110 maturity-onset diabetes of the young type 13 HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • RGD:7240710
DOID:206 hereditary multiple exostoses FB:FBgn0029175 Drosophila melanogaster (fruit fly) 3772101 sotv CG8433
  • MGI:6194238
DOID:14500 fucosidosis FB:FBgn0285958 Drosophila melanogaster (fruit fly) 3772574 Fuca
  • MGI:6194238
DOID:9744 type 1 diabetes mellitus FB:FBgn0285958 Drosophila melanogaster (fruit fly) 3772574 Fuca
  • MGI:6194238
DOID:8947 diabetic retinopathy FB:FBgn0285958 Drosophila melanogaster (fruit fly) 3772574 Fuca
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus FB:FBgn0285958 Drosophila melanogaster (fruit fly) 3772574 Fuca
  • MGI:6194238
DOID:9351 diabetes mellitus FB:FBgn0285958 Drosophila melanogaster (fruit fly) 3772574 Fuca
  • MGI:6194238
DOID:5212 congenital disorder of glycosylation FB:FBgn0011297 Drosophila melanogaster (fruit fly) 37754 Alg3 CG4084
  • MGI:6194238
DOID:0080556 congenital disorder of glycosylation Id FB:FBgn0011297 Drosophila melanogaster (fruit fly) 37754 Alg3 CG4084
  • 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