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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 71476 - 71500 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:8398 osteoarthritis HGNC:221 Homo sapiens (human) 11096 ADAMTS5
  • MGI:6194238
  • PMID:11801682
  • PMID:18240210
  • PMID:22961118
DOID:0110156 Charcot-Marie-Tooth disease type 2B1 MGI:96794 Mus musculus (house mouse) 16905 Lmna
  • MGI:6194238
  • PMID:11799477
  • PMID:22331516
DOID:0060490 Schimke immuno-osseous dysplasia HGNC:11102 Homo sapiens (human) 50485 SMARCAL1
  • MGI:6194238
  • PMID:11799392
  • RGD:7240710
DOID:0060162 dentatorubral-pallidoluysian atrophy FB:FBgn0010825 Drosophila melanogaster (fruit fly) 46156 Gug
  • MGI:6194238
  • PMID:11792320
  • PMID:20339376
DOID:0050144 Kartagener syndrome HGNC:2950 Homo sapiens (human) 1767 DNAH5
  • MGI:6194238
  • PMID:11788826
DOID:10487 Hirschsprung's disease MGI:107430 Mus musculus (house mouse) 14573 Gdnf
  • MGI:6194238
  • PMID:11774071
  • PMID:12668632
  • PMID:8657307
DOID:0110953 Waardenburg syndrome type 4A MGI:102720 Mus musculus (house mouse) 13618 Ednrb
  • MGI:6194238
  • PMID:11773966
  • PMID:15294878
DOID:10952 nephritis HGNC:11158 Homo sapiens (human) 6632 SNRPD1
  • MGI:6194238
  • PMID:11771960
DOID:14789 spondyloepiphyseal dysplasia congenita MGI:88452 Mus musculus (house mouse) 12824 Col2a1
  • MGI:6194238
  • PMID:11771668
  • PMID:12968670
  • PMID:22028304
  • PMID:25917818
  • PMID:7590256
DOID:10763 hypertension RGD:2168 Rattus norvegicus (Norway rat) 24212 Atp1a2
  • MGI:6194238
  • PMID:11768735
DOID:9256 colorectal cancer RGD:2082 Rattus norvegicus (Norway rat) 25233 Akt2
  • MGI:6194238
  • PMID:11756242
DOID:9256 colorectal cancer HGNC:392 Homo sapiens (human) 208 AKT2
  • MGI:6194238
  • PMID:11756242
DOID:0060651 MYH-9 related disease HGNC:7579 Homo sapiens (human) 4627 MYH9
  • MGI:6194238
  • PMID:11752022
  • PMID:11935325
  • PMID:16806139
  • RGD:7240710
DOID:9074 systemic lupus erythematosus MGI:88337 Mus musculus (house mouse) 21947 Cd40lg
  • MGI:6194238
  • PMID:11751940
DOID:384 Wolff-Parkinson-White syndrome HGNC:9386 Homo sapiens (human) 51422 PRKAG2
  • MGI:6194238
  • PMID:11748095
  • PMID:15611370
  • RGD:7240710
DOID:0050427 xeroderma pigmentosum SGD:S000002827 Saccharomyces cerevisiae S288C 852028 RAD30
  • MGI:6194238
  • PMID:11743006
DOID:0110299 autosomal recessive limb-girdle muscular dystrophy type 2I HGNC:17997 Homo sapiens (human) 79147 FKRP
  • MGI:6194238
  • PMID:11741828
  • PMID:15580560
  • PMID:16634037
  • PMID:17113772
  • PMID:17994539
  • PMID:18671187
  • PMID:21296577
  • PMID:25048216
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:11784 Homo sapiens (human) 7056 THBD
  • MGI:6194238
  • PMID:11738074
  • PMID:17195062
DOID:1485 cystic fibrosis HGNC:1884 Homo sapiens (human) 1080 CFTR
  • MGI:6194238
  • PMID:11732487
  • PMID:1283149
  • PMID:1284535
  • PMID:1370365
  • PMID:1379413
  • PMID:1380943
  • PMID:17099022
  • PMID:17902144
  • PMID:19202204
  • PMID:19620404
  • PMID:19880712
  • PMID:2344617
  • PMID:9254853
  • PMID:9429141
  • PMID:9439669
  • RGD:7240710
DOID:0060849 osteoporosis-pseudoglioma syndrome HGNC:6697 Homo sapiens (human) 4041 LRP5
  • MGI:6194238
  • PMID:11719191
  • PMID:16679074
  • RGD:7240710
DOID:9744 type 1 diabetes mellitus MGI:107656 Mus musculus (house mouse) 15978 Ifng
  • MGI:6194238
  • PMID:11714835
DOID:0060730 torsion dystonia 1 WB:WBGene00003870 Caenorhabditis elegans 174433 ooc-5
  • MGI:6194238
  • PMID:11714689
DOID:0050560 Walker-Warburg syndrome HGNC:19139 Homo sapiens (human) 55624 POMGNT1
  • MGI:6194238
  • PMID:11709191
  • PMID:15236414
  • PMID:22554691
  • PMID:23689641
DOID:10763 hypertension HGNC:7873 Homo sapiens (human) 4843 NOS2
  • MGI:6194238
  • PMID:11702222
DOID:9352 type 2 diabetes mellitus HGNC:6656 Homo sapiens (human) 4012 LNPEP
  • MGI:6194238
  • PMID:11701721

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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 9, 2024