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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 68126 - 68150 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence Code Names References
DOID:11446 sciatic neuropathy HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • MGI:6194238
DOID:9744 type 1 diabetes mellitus MGI:104798 Mus musculus (house mouse) 21926 Tnf
  • MGI:6194238
DOID:10003 sensorineural hearing loss HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1
  • PMID:8712634
DOID:11801 protein-energy malnutrition RGD:68374 Rattus norvegicus (Norway rat) 29445 Cox4i1
  • PMID:18725894
DOID:9352 type 2 diabetes mellitus MGI:1098296 Mus musculus (house mouse) 12894 Cpt1a
  • MGI:6194238
DOID:11198 DiGeorge syndrome MGI:104719 Mus musculus (house mouse) 15531 Ndst1
  • MGI:5284969
DOID:0080750 erythema nodosum MGI:95929 Mus musculus (house mouse) 15007 H2-Q10
  • MGI:6194238
DOID:1826 epilepsy WB:WBGene00012364 Caenorhabditis elegans 179991 zmp-4
  • MGI:6194238
DOID:1875 impotence RGD:3242 Rattus norvegicus (Norway rat) 25265 P2ry1
  • PMID:19303093
DOID:0110170 Charcot-Marie-Tooth disease axonal type 2Q HGNC:23537 Homo sapiens (human) 55526 DHTKD1
  • MGI:6194238
  • RGD:7240710
DOID:591 phobic disorder HGNC:11957 Homo sapiens (human) 9968 MED12
  • PMID:12216017
DOID:0080600 COVID-19 HGNC:9075 Homo sapiens (human) 5345 SERPINF2
  • PMID:32747830
DOID:162 cancer HGNC:29259 Homo sapiens (human) 57551 TAOK1
  • MGI:6194238
DOID:0050545 visceral heterotaxy Xenbase:XB-GENE-5964399 Xenopus tropicalis (tropical clawed frog) 394458 nodal3.1
  • MGI:6194238
DOID:0110798 hereditary spastic paraplegia 46 HGNC:18986 Homo sapiens (human) 57704 GBA2
  • RGD:7240710
DOID:0070249 autosomal dominant Emery-Dreifuss muscular dystrophy 4 FB:FBgn0261836 Drosophila melanogaster (fruit fly) 3771968 Msp300
  • MGI:6194238
DOID:8947 diabetic retinopathy HGNC:3373 Homo sapiens (human) 2033 EP300
  • MGI:6194238
DOID:9256 colorectal cancer HGNC:592 Homo sapiens (human) 331 XIAP
  • PMID:27827395
DOID:10652 Alzheimer's disease HGNC:7230 Homo sapiens (human) 4361 MRE11
  • PMID:15337312
DOID:3770 pulmonary fibrosis FB:FBgn0260004 Drosophila melanogaster (fruit fly) 42514 Snmp1
  • MGI:6194238
DOID:1470 major depressive disorder WB:WBGene00003772 Caenorhabditis elegans 178167 nlr-1
  • MGI:6194238
DOID:3144 cutis laxa HGNC:3219 Homo sapiens (human) 30008 EFEMP2
  • MGI:6194238
DOID:3008 invasive ductal carcinoma MGI:105988 Mus musculus (house mouse) 13522 Adam28
  • MGI:6194238
DOID:1307 dementia RGD:3177 Rattus norvegicus (Norway rat) 24596 Ngfr
  • PMID:8232919
DOID:14330 Parkinson's disease MGI:2444207 Mus musculus (house mouse) 320528 Vps13c
  • 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: December 9, 2024