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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 January 28, 2025
Displaying entries 76 - 100 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence References ▲
DOID:0060041 autism spectrum disorder MGI:1930016 Mus musculus (house mouse) 58234 Shank3 author statement supported by traceable reference
  • MGI:5499103
  • PMID:21167025
  • PMID:21423165
  • PMID:21558424
  • PMID:26134648
  • PMID:26559786
  • PMID:26687841
  • PMID:26886798
  • PMID:27189882
  • PMID:27492494
  • PMID:30610205
DOID:0110965 brachydactyly type A2 MGI:95688 Mus musculus (house mouse) 14563 Gdf5 author statement supported by traceable reference
  • MGI:5509308
DOID:0110977 brachydactyly type A1C MGI:95688 Mus musculus (house mouse) 14563 Gdf5 author statement supported by traceable reference
  • MGI:5509308
DOID:0080052 acromesomelic dysplasia, Grebe type MGI:95688 Mus musculus (house mouse) 14563 Gdf5 author statement supported by traceable reference
  • MGI:5509308
DOID:0110970 brachydactyly type C MGI:95688 Mus musculus (house mouse) 14563 Gdf5 author statement supported by traceable reference
  • MGI:5509308
DOID:0050794 multiple synostoses syndrome MGI:95688 Mus musculus (house mouse) 14563 Gdf5 author statement supported by traceable reference
  • MGI:5509308
DOID:0080051 acromesomelic dysplasia, Hunter-Thompson type MGI:95688 Mus musculus (house mouse) 14563 Gdf5 author statement supported by traceable reference
  • MGI:5509308
DOID:0050790 fibular hypoplasia and complex brachydactyly MGI:95688 Mus musculus (house mouse) 14563 Gdf5 author statement supported by traceable reference
  • MGI:5509308
DOID:0110726 neuronal ceroid lipofuscinosis 2 MGI:1336194 Mus musculus (house mouse) 12751 Tpp1 author statement supported by traceable reference
  • MGI:5511005
  • PMID:15483130
  • PMID:18343701
DOID:0110148 Charcot-Marie-Tooth disease type 1A MGI:97631 Mus musculus (house mouse) 18858 Pmp22 author statement supported by traceable reference
  • MGI:5515889
  • PMID:11331611
  • PMID:12090404
  • PMID:1303281
  • PMID:15363066
  • PMID:15703401
  • PMID:15755691
DOID:0060843 hereditary neuropathy with liability to pressure palsies MGI:97631 Mus musculus (house mouse) 18858 Pmp22 author statement supported by traceable reference
  • MGI:5515889
  • PMID:16436605
  • PMID:7581450
DOID:0050540 Charcot-Marie-Tooth disease type 3 MGI:97631 Mus musculus (house mouse) 18858 Pmp22 author statement supported by traceable reference
  • MGI:5515889
DOID:0110153 Charcot-Marie-Tooth disease type 1E MGI:97631 Mus musculus (house mouse) 18858 Pmp22 author statement supported by traceable reference
  • MGI:5515889
DOID:0050328 congenital hypothyroidism MGI:98849 Mus musculus (house mouse) 22095 Tshr author statement supported by traceable reference
  • MGI:5571363
  • PMID:10575115
  • PMID:12432094
  • PMID:17932107
DOID:0110376 retinitis pigmentosa 41 MGI:1100886 Mus musculus (house mouse) 19126 Prom1 author statement supported by traceable reference
  • MGI:5605698
  • PMID:19228982
DOID:0050632 oculocutaneous albinism MGI:97454 Mus musculus (house mouse) 18431 Oca2 author statement supported by traceable reference
  • MGI:5607140
DOID:0060832 Griscelli syndrome type 1 MGI:105976 Mus musculus (house mouse) 17918 Myo5a author statement supported by traceable reference
  • MGI:5607575
  • PMID:21508232
DOID:0060757 sclerosteosis 2 MGI:2442252 Mus musculus (house mouse) 228357 Lrp4 author statement supported by traceable reference
  • MGI:5688518
  • PMID:28477420
DOID:0110725 neuronal ceroid lipofuscinosis 10 MGI:88562 Mus musculus (house mouse) 13033 Ctsd author statement supported by traceable reference
  • MGI:5751705
  • PMID:18498441
  • PMID:26232697
DOID:0060696 hyperekplexia 1 MGI:95747 Mus musculus (house mouse) 14654 Glra1 author statement supported by traceable reference
  • MGI:5790609
  • PMID:12954867
  • PMID:17114051
  • PMID:8733750
DOID:1838 Menkes disease MGI:99400 Mus musculus (house mouse) 11977 Atp7a author statement supported by traceable reference
  • MGI:60964
  • PMID:10098864
  • PMID:13103353
  • PMID:16338116
  • PMID:1819648
  • PMID:20831904
  • PMID:25456742
  • PMID:4858102
  • PMID:6685755
DOID:11836 clubfoot MGI:1921303 Mus musculus (house mouse) 74053 Grip1 author statement supported by traceable reference
  • MGI:61605
DOID:9970 obesity MGI:101932 Mus musculus (house mouse) 12876 Cpe author statement supported by traceable reference
  • MGI:61833
  • PMID:2250094
DOID:0110011 advanced sleep phase syndrome 1 MGI:1195265 Mus musculus (house mouse) 18627 Per2 author statement supported by traceable reference
  • MGI:6197761
DOID:0050473 Alstrom syndrome MGI:1934606 Mus musculus (house mouse) 236266 Alms1 author statement supported by traceable reference
  • MGI:6197902
  • MGI:6197907
  • PMID:16000322
  • PMID:16516152
  • PMID:17206865
  • PMID:28859131

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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 8, 2025