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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 October 9, 2024
Displaying entries 70451 - 70475 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence Code Names References
DOID:2957 pulmonary tuberculosis RGD:2081 Rattus norvegicus (Norway rat) 24185 Akt1
  • MGI:6194238
DOID:1824 status epilepticus HGNC:2159 Homo sapiens (human) 1268 CNR1
  • MGI:6194238
DOID:13359 Ehlers-Danlos syndrome HGNC:11976 Homo sapiens (human) 7148 TNXB
  • PMID:11642233
DOID:0060564 spinal disease HGNC:3755 Homo sapiens (human) 2317 FLNB
  • PMID:14991055
DOID:12177 common variable immunodeficiency HGNC:5351 Homo sapiens (human) 29851 ICOS
  • MGI:6194238
DOID:10325 silicosis HGNC:6319 Homo sapiens (human) 11127 KIF3A
  • MGI:6194238
  • PMID:32042332
DOID:4448 macular degeneration MGI:105384 Mus musculus (house mouse) 15481 Hspa8
  • MGI:6194238
DOID:1289 neurodegenerative disease HGNC:16703 Homo sapiens (human) 57084 SLC17A6
  • MGI:6194238
DOID:11832 visual epilepsy HGNC:13447 Homo sapiens (human) 81539 SLC38A1
  • MGI:6194238
DOID:289 endometriosis MGI:95669 Mus musculus (house mouse) 14473 Gc
  • MGI:6194238
DOID:14766 renal agenesis Xenbase:XB-GENE-1013855 Xenopus tropicalis (tropical clawed frog) 100125202 gfra1
  • MGI:6194238
DOID:1883 hepatitis C RGD:68949 Rattus norvegicus (Norway rat) 116553 Il13
  • MGI:6194238
DOID:127 leiomyoma HGNC:3685 Homo sapiens (human) 2252 FGF7
  • PMID:18566572
DOID:13099 Moyamoya disease MGI:87909 Mus musculus (house mouse) 11475 Acta2
  • MGI:6194238
DOID:14323 Marfan syndrome WB:WBGene00022816 Caenorhabditis elegans 176076 fbn-1
  • MGI:6194238
DOID:1561 cognitive disorder MGI:99841 Mus musculus (house mouse) 15566 Htr7
  • MGI:6194238
DOID:2048 autoimmune hepatitis RGD:620047 Rattus norvegicus (Norway rat) 116562 Il2
  • MGI:6194238
DOID:10652 Alzheimer's disease RGD:619993 Rattus norvegicus (Norway rat) 65262 Atp5f1a
  • PMID:25561935
DOID:0090109 autosomal dominant hypocalcemia HGNC:1514 Homo sapiens (human) 846 CASR
  • PMID:20501971
  • PMID:7874174
  • PMID:8813042
DOID:557 kidney disease MGI:1314884 Mus musculus (house mouse) 21937 Tnfrsf1a
  • MGI:6194238
DOID:0080621 glucocorticoid deficiency 1 HGNC:6930 Homo sapiens (human) 4158 MC2R
  • RGD:7240710
DOID:0050340 opportunistic bacterial infectious disease HGNC:11105 Homo sapiens (human) 6601 SMARCC2
  • MGI:6194238
DOID:0050156 idiopathic pulmonary fibrosis HGNC:14129 Homo sapiens (human) 10919 EHMT2
  • PMID:24652950
DOID:1852 intrahepatic cholestasis WB:WBGene00003995 Caenorhabditis elegans 178215 pgp-1
  • MGI:6194238
DOID:0112010 pituitary adenoma 3 HGNC:4392 Homo sapiens (human) 2778 GNAS
  • RGD:7240710

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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: December 9, 2024