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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 71526 - 71550 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▼ References
DOID:10652 Alzheimer's disease MGI:88059 Mus musculus (house mouse) 11820 App
  • MGI:6194238
  • PMID:10188929
  • PMID:15147316
  • PMID:16279840
  • PMID:24728269
  • PMID:27109181
  • PMID:8798542
DOID:0110864 congenital stationary night blindness 1F MGI:2685267 Mus musculus (house mouse) 242235 Lrit3
  • MGI:6194238
  • PMID:24598786
DOID:2738 pseudoxanthoma elasticum MGI:1351634 Mus musculus (house mouse) 27421 Abcc6
  • MGI:6194238
  • PMID:15888484
  • PMID:16135817
DOID:10587 Krabbe disease MGI:95636 Mus musculus (house mouse) 14420 Galc
  • MGI:6194238
  • PMID:11461188
  • PMID:20441793
  • PMID:21389217
  • PMID:34142127
  • PMID:7417782
  • PMID:7437911
DOID:0111037 glycine N-methyltransferase deficiency MGI:1202304 Mus musculus (house mouse) 14711 Gnmt
  • MGI:6194238
  • PMID:16779654
  • PMID:17937387
DOID:5688 Werner syndrome MGI:109635 Mus musculus (house mouse) 22427 Wrn
  • MGI:6194238
  • PMID:16330174
DOID:2219 Glanzmann's thrombasthenia MGI:96612 Mus musculus (house mouse) 16416 Itgb3
  • MGI:6194238
  • PMID:19933310
DOID:0080053 Albright's hereditary osteodystrophy MGI:95777 Mus musculus (house mouse) 14683 Gnas
  • MGI:6194238
  • PMID:21747923
  • PMID:26671181
DOID:0080124 mitochondrial DNA depletion syndrome 5 MGI:1306775 Mus musculus (house mouse) 20916 Sucla2
  • MGI:6194238
  • PMID:24271779
DOID:0060591 WHIM syndrome MGI:109563 Mus musculus (house mouse) 12767 Cxcr4
  • MGI:6194238
  • PMID:22438253
DOID:0110376 retinitis pigmentosa 41 MGI:1100886 Mus musculus (house mouse) 19126 Prom1
  • MGI:5605698
  • MGI:6194238
  • PMID:19228982
DOID:0110456 dilated cardiomyopathy 1R MGI:87905 Mus musculus (house mouse) 11464 Actc1
  • MGI:6194238
  • PMID:20713897
DOID:8893 psoriasis MGI:103178 Mus musculus (house mouse) 22339 Vegfa
  • MGI:6194238
  • PMID:15100155
DOID:0110500 autosomal recessive nonsyndromic deafness 42 MGI:2146574 Mus musculus (house mouse) 106347 Ildr1
  • MGI:6194238
  • PMID:25217574
  • PMID:25819842
  • PMID:25822906
DOID:0050144 Kartagener syndrome MGI:1100864 Mus musculus (house mouse) 13411 Dnah11
  • MGI:5284969
  • MGI:6194238
DOID:0050946 Charlevoix-Saguenay spastic ataxia MGI:1354724 Mus musculus (house mouse) 50720 Sacs
  • MGI:6194238
  • PMID:22307627
  • PMID:25260547
DOID:0081060 X-linked nephrogenic diabetes insipidus MGI:88123 Mus musculus (house mouse) 12000 Avpr2
  • MGI:6194238
  • PMID:19729836
DOID:1612 breast cancer MGI:1328361 Mus musculus (house mouse) 12021 Bard1
  • MGI:6194238
  • PMID:18443292
DOID:14557 primary pulmonary hypertension MGI:1095407 Mus musculus (house mouse) 12168 Bmpr2
  • MGI:6194238
  • PMID:16027259
  • PMID:18663089
  • PMID:20562228
  • PMID:26076038
DOID:2752 glycogen storage disease II MGI:95609 Mus musculus (house mouse) 14387 Gaa
  • MGI:6194238
  • PMID:10838256
  • PMID:9384603
  • PMID:9668092
DOID:0060041 autism spectrum disorder MGI:1096875 Mus musculus (house mouse) 72145 Wdfy3
  • MGI:6194238
  • PMID:25198012
DOID:9970 obesity MGI:104993 Mus musculus (house mouse) 16847 Lepr
  • MGI:3611487
  • MGI:3778961
  • MGI:3778962
  • MGI:3815208
  • MGI:6194238
  • PMID:12136396
  • PMID:12590922
  • PMID:12594516
  • PMID:12885755
  • PMID:15207242
  • PMID:15389315
  • PMID:15685168
  • PMID:16113078
  • PMID:16443782
  • PMID:19015522
  • PMID:34390703
  • PMID:6991317
  • PMID:6993269
  • PMID:8177042
DOID:0110703 hypotrichosis 6 MGI:2661061 Mus musculus (house mouse) 16769 Dsg4
  • MGI:6194238
  • PMID:10839719
  • PMID:8752833
DOID:0050464 Farber lipogranulomatosis MGI:1277124 Mus musculus (house mouse) 11886 Asah1
  • MGI:6194238
  • PMID:11829492
  • PMID:23681708
  • PMID:29908121
DOID:0110640 congenital muscular dystrophy due to LMNA mutation MGI:96794 Mus musculus (house mouse) 16905 Lmna
  • MGI:6194238
  • PMID:22090424

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: December 9, 2024