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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 68401 - 68425 of 71927 in total
Disease ID Disease Name ▼ Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:12842 Guillain-Barre syndrome RGD:2432 Rattus norvegicus (Norway rat) 25307 Cst3
  • MGI:6194238
DOID:0060672 Grn-related frontotemporal lobar degeneration with Tdp43 inclusions RGD:61983 Rattus norvegicus (Norway rat) 29143 Grn
  • MGI:6194238
DOID:0060672 Grn-related frontotemporal lobar degeneration with Tdp43 inclusions MGI:95832 Mus musculus (house mouse) 14824 Grn
  • MGI:6194238
  • PMID:25155018
  • PMID:29382817
  • PMID:29511098
DOID:0060672 Grn-related frontotemporal lobar degeneration with Tdp43 inclusions HGNC:4601 Homo sapiens (human) 2896 GRN
  • MGI:6194238
  • PMID:19649643
  • RGD:7240710
DOID:0060672 Grn-related frontotemporal lobar degeneration with Tdp43 inclusions HGNC:11571 Homo sapiens (human) 23435 TARDBP
  • MGI:6194238
DOID:0060832 Griscelli syndrome type 1 HGNC:7602 Homo sapiens (human) 4644 MYO5A
  • MGI:6194238
  • RGD:7240710
DOID:0060832 Griscelli syndrome type 1 RGD:3143 Rattus norvegicus (Norway rat) 25017 Myo5a
  • MGI:6194238
DOID:0060832 Griscelli syndrome type 1 MGI:105976 Mus musculus (house mouse) 17918 Myo5a
  • MGI:5607575
  • MGI:6194238
  • PMID:21508232
DOID:14761 Greig cephalopolysyndactyly syndrome MGI:95729 Mus musculus (house mouse) 14634 Gli3
  • MGI:6194238
  • PMID:8387379
DOID:14761 Greig cephalopolysyndactyly syndrome HGNC:4319 Homo sapiens (human) 2737 GLI3
  • MGI:6194238
  • PMID:10441342
  • PMID:15739154
  • PMID:22903559
  • PMID:24736735
  • RGD:7240710
DOID:0111588 Greenberg dysplasia HGNC:6518 Homo sapiens (human) 3930 LBR
  • PMID:21327084
  • RGD:7240710
DOID:0111588 Greenberg dysplasia MGI:2138281 Mus musculus (house mouse) 98386 Lbr
  • MGI:6194238
DOID:12361 Graves' disease HGNC:1324 Homo sapiens (human) 721 C4B
  • PMID:21943165
DOID:12361 Graves' disease HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • PMID:18997483
  • PMID:20583542
DOID:12361 Graves' disease MGI:105304 Mus musculus (house mouse) 16194 Il6ra
  • MGI:6194238
DOID:12361 Graves' disease MGI:96548 Mus musculus (house mouse) 16183 Il2
  • MGI:6194238
DOID:12361 Graves' disease ZFIN:ZDB-GENE-990415-273 Danio rerio (zebrafish) 30682 vegfaa
  • MGI:6194238
DOID:12361 Graves' disease MGI:103178 Mus musculus (house mouse) 22339 Vegfa
  • MGI:6194238
DOID:12361 Graves' disease HGNC:2505 Homo sapiens (human) 1493 CTLA4
  • PMID:10369864
  • PMID:10404810
  • PMID:12780750
  • PMID:14986169
  • PMID:15785242
  • PMID:20352109
  • PMID:9672157
  • PMID:9861324
DOID:12361 Graves' disease SGD:S000004525 Saccharomyces cerevisiae S288C 854942 OGG1
  • MGI:6194238
DOID:12361 Graves' disease RGD:620005 Rattus norvegicus (Norway rat) 24233 C4a
  • MGI:6194238
DOID:12361 Graves' disease RGD:619831 Rattus norvegicus (Norway rat) 246097 Fas
  • MGI:6194238
DOID:12361 Graves' disease HGNC:6156 Homo sapiens (human) 3690 ITGB3
  • PMID:23109646
DOID:12361 Graves' disease MGI:88336 Mus musculus (house mouse) 21939 Cd40
  • MGI:6194238
DOID:12361 Graves' disease MGI:95931 Mus musculus (house mouse) 15013 H2-Q2
  • MGI:6194238

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International Collaboration

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