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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 9126 - 9150 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence Code Names References
DOID:150 disease of mental health HGNC:4416 Homo sapiens (human) 8443 GNPAT
  • MGI:6194238
DOID:0111391 mucopolysaccharidosis IVA HGNC:4122 Homo sapiens (human) 2588 GALNS
  • RGD:7240710
DOID:1920 hyperuricemia ZFIN:ZDB-GENE-980526-110 Danio rerio (zebrafish) 30262 ins
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus FB:FBgn0027074 Drosophila melanogaster (fruit fly) 35137 Ugt36F1
  • MGI:6194238
DOID:0060710 autosomal recessive congenital ichthyosis 2 HGNC:430 Homo sapiens (human) 242 ALOX12B
  • RGD:7240710
DOID:0080718 GNE myopathy RGD:69239 Rattus norvegicus (Norway rat) 114711 Gne
  • MGI:6194238
DOID:3178 skin papilloma MGI:1346060 Mus musculus (house mouse) 24088 Tlr2
  • MGI:6194238
DOID:0014667 disease of metabolism Xenbase:XB-GENE-864803 Xenopus laevis (African clawed frog) 378695 ins.L
  • MGI:6194238
DOID:0111069 congenital bile acid synthesis defect 2 HGNC:388 Homo sapiens (human) 6718 AKR1D1
  • RGD:7240710
DOID:3908 lung non-small cell carcinoma FB:FBgn0040261 Drosophila melanogaster (fruit fly) 53512 Ugt37E1
  • MGI:6194238
DOID:0111680 essential fructosuria HGNC:6315 Homo sapiens (human) 3795 KHK
  • RGD:7240710
DOID:0050328 congenital hypothyroidism MGI:1342774 Mus musculus (house mouse) 19017 Ppargc1a
  • MGI:6194238
DOID:0080537 hypermanganesemia with dystonia 2 HGNC:20858 Homo sapiens (human) 23516 SLC39A14
  • RGD:7240710
DOID:526 human immunodeficiency virus infectious disease MGI:104993 Mus musculus (house mouse) 16847 Lepr
  • MGI:6194238
DOID:8552 chronic myeloid leukemia RGD:2081 Rattus norvegicus (Norway rat) 24185 Akt1
  • MGI:6194238
DOID:9970 obesity HGNC:119 Homo sapiens (human) 51 ACOX1
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:2641 Homo sapiens (human) 10858 CYP46A1
  • PMID:12232784
DOID:4852 pleomorphic xanthoastrocytoma MGI:88190 Mus musculus (house mouse) 109880 Braf
  • MGI:6194238
DOID:13564 aspergillosis HGNC:1641 Homo sapiens (human) 30835 CD209
  • PMID:21381282
DOID:0070162 hereditary sensory and autonomic neuropathy type 1 HGNC:16253 Homo sapiens (human) 55304 SPTLC3
  • MGI:6194238
DOID:13452 scleritis MGI:104798 Mus musculus (house mouse) 21926 Tnf
  • MGI:6194238
DOID:3669 intermittent claudication HGNC:10886 Homo sapiens (human) 22933 SIRT2
  • MGI:6194238
DOID:0111681 glutamate-cysteine ligase deficiency HGNC:4311 Homo sapiens (human) 2729 GCLC
  • RGD:7240710
DOID:417 autoimmune disease MGI:96413 Mus musculus (house mouse) 15926 Idh1
  • MGI:6194238
DOID:0050571 congenital disorder of glycosylation type II SGD:S000000959 Saccharomyces cerevisiae S288C 856901 COG3
  • MGI:6194238

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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