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MIRAGE
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 326 - 350 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:0090132 complex cortical dysplasia with other brain malformations 7 MGI:1920960 Mus musculus (house mouse) 73710 Tubb2b
  • MGI:6194238
  • PMID:23727838
DOID:0110194 Charcot-Marie-Tooth disease type 4B3 MGI:1925230 Mus musculus (house mouse) 77980 Sbf1
  • MGI:6194238
  • PMID:34718573
DOID:0050144 Kartagener syndrome MGI:1100864 Mus musculus (house mouse) 13411 Dnah11
  • MGI:5284969
  • MGI:6194238
DOID:0110957 Gaucher's disease type I MGI:95665 Mus musculus (house mouse) 14466 Gba1
  • MGI:6194238
  • PMID:16954197
  • PMID:17079175
  • PMID:20962279
  • PMID:35711931
DOID:0111020 cone-rod dystrophy 9 MGI:105376 Mus musculus (house mouse) 11502 Adam9
  • MGI:6194238
  • PMID:19409519
DOID:12134 factor VIII deficiency MGI:88383 Mus musculus (house mouse) 14069 F8
  • MGI:6194238
  • PMID:7647782
DOID:10588 adrenoleukodystrophy MGI:1349215 Mus musculus (house mouse) 11666 Abcd1
  • MGI:6194238
  • PMID:11875044
  • PMID:15489218
  • PMID:9126326
  • PMID:9256488
  • PMID:9418970
DOID:0060684 autosomal dominant nocturnal frontal lobe epilepsy 3 MGI:87891 Mus musculus (house mouse) 11444 Chrnb2
  • MGI:6194238
  • PMID:19153075
  • PMID:20603624
DOID:0080119 mitochondrial DNA depletion syndrome 1 MGI:1920212 Mus musculus (house mouse) 72962 Tymp
  • MGI:6194238
  • PMID:12077348
DOID:0090071 hypogonadotropic hypogonadism 11 with or without anosmia MGI:892968 Mus musculus (house mouse) 21338 Tacr3
  • MGI:6194238
  • PMID:22253416
DOID:0110266 cataract 9 multiple types MGI:88515 Mus musculus (house mouse) 12954 Cryaa
  • MGI:6194238
  • PMID:11687536
  • PMID:18056999
  • PMID:19619312
  • PMID:8812430
  • PMID:9023351
DOID:0110555 autosomal dominant nonsyndromic deafness 25 MGI:3039629 Mus musculus (house mouse) 216227 Slc17a8
  • MGI:6194238
  • PMID:18674745
DOID:0090118 congenital amegakaryocytic thrombocytopenia MGI:97076 Mus musculus (house mouse) 17480 Mpl
  • MGI:6194238
  • PMID:10611229
DOID:12259 hemophilia B MGI:88384 Mus musculus (house mouse) 14071 F9
  • MGI:6194238
  • PMID:26964564
  • PMID:9326649
  • PMID:9354664
  • PMID:9639513
DOID:1270 hereditary hemorrhagic telangiectasia MGI:1338946 Mus musculus (house mouse) 11482 Acvrl1
  • MGI:6194238
  • PMID:12588795
  • PMID:17911384
  • PMID:19805914
  • PMID:25082229
DOID:3209 junctional epidermolysis bullosa MGI:88450 Mus musculus (house mouse) 12821 Col17a1
  • MGI:6194238
  • PMID:37796769
DOID:0050535 exudative vitreoretinopathy MGI:108520 Mus musculus (house mouse) 14366 Fzd4
  • MGI:6194238
  • PMID:20159112
  • PMID:33497368
DOID:1928 Williams-Beuren syndrome MGI:104572 Mus musculus (house mouse) 16885 Limk1
  • MGI:6194238
  • PMID:12123613
DOID:0110033 autosomal recessive Alport syndrome MGI:104688 Mus musculus (house mouse) 12828 Col4a3
  • MGI:6194238
  • PMID:20197625
  • PMID:24262794
  • PMID:8947561
  • PMID:8956999
  • PMID:9682811
DOID:2752 glycogen storage disease II MGI:95609 Mus musculus (house mouse) 14387 Gaa
  • MGI:6194238
  • PMID:10838256
  • PMID:9384603
  • PMID:9668092
DOID:0110867 congenital stationary night blindness 1C MGI:1330305 Mus musculus (house mouse) 17364 Trpm1
  • MGI:6194238
  • MGI:7619842
  • MGI:7620509
DOID:0050800 cerebral creatine deficiency syndrome 1 MGI:2147834 Mus musculus (house mouse) 102857 Slc6a8
  • MGI:6194238
  • PMID:21249153
  • PMID:22751104
  • PMID:25485098
  • PMID:27466184
  • PMID:30013483
DOID:0110678 congenital myasthenic syndrome 4A MGI:87894 Mus musculus (house mouse) 11448 Chrne
  • MGI:6194238
  • PMID:9151734
DOID:9884 muscular dystrophy MGI:2447586 Mus musculus (house mouse) 243853 Fkrp
  • MGI:6194238
  • PMID:28859131
DOID:9352 type 2 diabetes mellitus MGI:2153588 Mus musculus (house mouse) 140491 Ppp1r3a
  • MGI:6194238
  • PMID:12606498

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