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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 11476 - 11500 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:8778 Crohn's disease Xenbase:XB-GENE-5793241 Xenopus tropicalis (tropical clawed frog) 100135191 ugt1a6
  • MGI:6194238
DOID:11394 adult respiratory distress syndrome RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • MGI:6194238
DOID:0070352 stress-induced childhood-onset neurodegeneration with variable ataxia and seizures WB:WBGene00004051 Caenorhabditis elegans 177683 parg-1
  • MGI:6194238
DOID:12662 paracoccidioidomycosis RGD:2894 Rattus norvegicus (Norway rat) 25556 Il1rl1
  • MGI:6194238
DOID:0080322 polycystic kidney disease Xenbase:XB-GENE-993408 Xenopus tropicalis (tropical clawed frog) 448400 xylt2
  • MGI:6194238
DOID:219 colon cancer RGD:3387 Rattus norvegicus (Norway rat) 65248 Prkaa1
  • MGI:6194238
DOID:11151 cholecystolithiasis WB:WBGene00018206 Caenorhabditis elegans 185500 ugt-61
  • MGI:6194238
DOID:0080570 congenital disorder of glycosylation It FB:FBgn0003076 Drosophila melanogaster (fruit fly) 44010 Pgm1
  • MGI:6194238
DOID:0112374 muscular dystrophy-dystroglycanopathy SGD:S000003431 Saccharomyces cerevisiae S288C 853113 PMT6
  • MGI:6194238
DOID:5154 borna disease HGNC:786 Homo sapiens (human) 468 ATF4
  • MGI:6194238
DOID:9351 diabetes mellitus MGI:96824 Mus musculus (house mouse) 21898 Tlr4
  • MGI:6194238
DOID:2565 macular corneal dystrophy Xenbase:XB-GENE-5812130 Xenopus tropicalis (tropical clawed frog) 496807 chst5
  • MGI:6194238
DOID:28 endocrine system disease FB:FBgn0027538 Drosophila melanogaster (fruit fly) 36585 beta4GalNAcTA CG8536
  • MGI:6194238
DOID:10652 Alzheimer's disease SGD:S000006202 Saccharomyces cerevisiae S288C 855848 ERR2
  • MGI:6194238
DOID:0110870 congenital stationary night blindness 1A HGNC:8082 Homo sapiens (human) 60506 NYX
  • MGI:6194238
  • RGD:7240710
DOID:0050812 spondyloepimetaphyseal dysplasia, Pakistani type HGNC:8604 Homo sapiens (human) 9060 PAPSS2
  • MGI:6194238
  • RGD:7240710
DOID:0080070 mucolipidosis II alpha/beta HGNC:29670 Homo sapiens (human) 79158 GNPTAB
  • MGI:6194238
  • RGD:7240710
DOID:3347 osteosarcoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
  • RGD:7240710
DOID:0110515 autosomal recessive nonsyndromic deafness 63 HGNC:25033 Homo sapiens (human) 220074 LRTOMT
  • MGI:6194238
  • RGD:7240710
DOID:0110544 autosomal dominant nonsyndromic deafness 12 HGNC:11720 Homo sapiens (human) 7007 TECTA
  • MGI:6194238
  • RGD:7240710
DOID:1056 oculocerebrorenal syndrome HGNC:8108 Homo sapiens (human) 4952 OCRL
  • MGI:6194238
  • RGD:7240710
DOID:0111673 Saul-Wilson syndrome HGNC:18620 Homo sapiens (human) 25839 COG4
  • MGI:6194238
  • RGD:7240710
DOID:0111442 optic atrophy 9 HGNC:118 Homo sapiens (human) 50 ACO2
  • MGI:6194238
  • RGD:7240710
DOID:0050775 schneckenbecken dysplasia HGNC:20800 Homo sapiens (human) 23169 SLC35D1
  • MGI:6194238
  • RGD:7240710
DOID:0110728 neuronal ceroid lipofuscinosis 5 HGNC:2076 Homo sapiens (human) 1203 CLN5
  • MGI:6194238
  • RGD:7240710

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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: August 19, 2024