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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 66201 - 66225 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▼ Evidence Code Names References
DOID:0080552 congenital disorder of glycosylation Ia WB:WBGene00009925 Caenorhabditis elegans 178364 F52B11.2
  • MGI:6194238
DOID:4001 ovarian carcinoma HGNC:5973 Homo sapiens (human) 3596 IL13
  • PMID:14984938
DOID:0050788 proximal symphalangism Xenbase:XB-GENE-487724 Xenopus tropicalis (tropical clawed frog) 493191 nog
  • MGI:6194238
DOID:9884 muscular dystrophy MGI:101864 Mus musculus (house mouse) 13138 Dag1
  • MGI:6194238
DOID:1936 atherosclerosis HGNC:30620 Homo sapiens (human) 80310 PDGFD
  • PMID:33381146
DOID:446 primary hyperaldosteronism HGNC:2020 Homo sapiens (human) 1181 CLCN2
  • MGI:6194238
  • RGD:7240710
DOID:1024 leprosy MGI:1341295 Mus musculus (house mouse) 21897 Tlr1
  • MGI:6194238
DOID:8991 cervix uteri carcinoma in situ MGI:98790 Mus musculus (house mouse) 21973 Top2a
  • MGI:6194238
DOID:0050558 Ullrich congenital muscular dystrophy HGNC:2211 Homo sapiens (human) 1291 COL6A1
  • MGI:6194238
DOID:4928 intrahepatic cholangiocarcinoma MGI:99255 Mus musculus (house mouse) 14103 Fasl
  • MGI:6194238
DOID:83 cataract RGD:619831 Rattus norvegicus (Norway rat) 246097 Fas
  • MGI:6194238
DOID:1059 intellectual disability MGI:1919834 Mus musculus (house mouse) 72584 Cul4b
  • PMID:22763239
DOID:224 transient cerebral ischemia WB:WBGene00011556 Caenorhabditis elegans 176442 vglu-3
  • MGI:6194238
DOID:3393 coronary artery disease HGNC:7809 Homo sapiens (human) 4804 NGFR
  • PMID:11935372
DOID:4330 non-Langerhans-cell histiocytosis MGI:97551 Mus musculus (house mouse) 18646 Prf1
  • MGI:6194238
DOID:1591 renovascular hypertension HGNC:9445 Homo sapiens (human) 5617 PRL
  • MGI:6194238
DOID:2349 arteriosclerosis MGI:109325 Mus musculus (house mouse) 14068 F7
  • MGI:6194238
DOID:1324 lung cancer HGNC:7107 Homo sapiens (human) 4288 MKI67
  • PMID:29183007
DOID:127 leiomyoma WB:WBGene00000858 Caenorhabditis elegans 177870 cwn-2
  • MGI:6194238
DOID:1574 alcohol use disorder FB:FBgn0000036 Drosophila melanogaster (fruit fly) 42918 nAChRalpha1
  • MGI:6194238
DOID:12365 malaria HGNC:19077 Homo sapiens (human) 259197 NCR3
  • RGD:7240710
DOID:5688 Werner syndrome HGNC:1058 Homo sapiens (human) 641 BLM
  • MGI:6194238
DOID:0060041 autism spectrum disorder HGNC:18748 Homo sapiens (human) 129684 CNTNAP5
  • MGI:6194238
DOID:8466 retinal degeneration HGNC:8807 Homo sapiens (human) 5161 PDHA2
  • MGI:6194238
DOID:0050848 obstructive sleep apnea HGNC:1074 Homo sapiens (human) 655 BMP7
  • 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: December 9, 2024