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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 7351 - 7375 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence Code Names References
DOID:0110859 polycystic kidney disease 2 HGNC:9009 Homo sapiens (human) 5311 PKD2
  • MGI:6194238
  • RGD:7240710
DOID:557 kidney disease RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • MGI:6194238
DOID:0050565 autosomal recessive nonsyndromic deafness FB:FBgn0038324 Drosophila melanogaster (fruit fly) 41867 Tmtc4
  • MGI:6194238
DOID:417 autoimmune disease HGNC:18187 Homo sapiens (human) 54414 SIAE
  • RGD:7240710
DOID:2957 pulmonary tuberculosis MGI:87986 Mus musculus (house mouse) 11651 Akt1
  • MGI:6194238
DOID:11446 sciatic neuropathy HGNC:2593 Homo sapiens (human) 1586 CYP17A1
  • MGI:6194238
DOID:3827 congenital diaphragmatic hernia MGI:104798 Mus musculus (house mouse) 21926 Tnf
  • MGI:6194238
DOID:12716 newborn respiratory distress syndrome HGNC:10802 Homo sapiens (human) 6440 SFTPC
  • MGI:6194238
  • PMID:7537464
DOID:9206 Barrett's esophagus HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
  • PMID:12105834
  • PMID:23011828
DOID:0050811 congenital adrenal hyperplasia HGNC:2600 Homo sapiens (human) 1589 CYP21A2
  • PMID:12930931
DOID:3633 beta-mannosidosis HGNC:6831 Homo sapiens (human) 4126 MANBA
  • MGI:6194238
  • RGD:7240710
DOID:0050570 congenital disorder of glycosylation type I ZFIN:ZDB-GENE-040426-1270 Danio rerio (zebrafish) 393598 alg9
  • MGI:6194238
DOID:4948 gallbladder carcinoma Xenbase:XB-GENE-6488967 Xenopus laevis (African clawed frog) 108698211 abo.2.L
  • MGI:6194238
DOID:9970 obesity SGD:S000005185 Saccharomyces cerevisiae S288C 855480 ZWF1
  • MGI:6194238
DOID:2986 IgA glomerulonephritis MGI:104798 Mus musculus (house mouse) 21926 Tnf
  • MGI:6194238
DOID:3534 Lafora disease SGD:S000004248 Saccharomyces cerevisiae S288C 850962 GSY2
  • MGI:6194238
DOID:2394 ovarian cancer HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:10493953
DOID:14067 Plasmodium falciparum malaria HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:18396436
DOID:0080600 COVID-19 MGI:104798 Mus musculus (house mouse) 21926 Tnf
  • MGI:6194238
DOID:3371 chondrosarcoma ZFIN:ZDB-GENE-050211-4 Danio rerio (zebrafish) 497280 ext1b
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I MGI:97075 Mus musculus (house mouse) 110119 Mpi
  • MGI:6194238
  • PMID:16339137
DOID:10211 cholelithiasis FB:FBgn0040261 Drosophila melanogaster (fruit fly) 53512 Ugt37E1
  • MGI:6194238
DOID:2977 primary hyperoxaluria HGNC:25155 Homo sapiens (human) 112817 HOGA1
  • MGI:6194238
DOID:169 neuroendocrine tumor HGNC:1455 Homo sapiens (human) 811 CALR
  • PMID:16293970
DOID:3393 coronary artery disease HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:12655278
  • PMID:16338763

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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