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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 69701 - 69725 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:0080226 autosomal dominant intellectual developmental disorder 56 HGNC:2092 Homo sapiens (human) 1213 CLTC
  • RGD:7240710
DOID:2526 prostate adenocarcinoma HGNC:1709 Homo sapiens (human) 928 CD9
  • PMID:17406028
DOID:0112219 developmental and epileptic encephalopathy 84 HGNC:12525 Homo sapiens (human) 7358 UGDH
  • RGD:7240710
DOID:10584 retinitis pigmentosa HGNC:6055 Homo sapiens (human) 3617 IMPG1
  • RGD:7240710
DOID:0080734 Ehlers-Danlos syndrome kyphoscoliotic type 1 HGNC:9081 Homo sapiens (human) 5351 PLOD1
  • RGD:7240710
DOID:2671 transitional cell carcinoma HGNC:5173 Homo sapiens (human) 3265 HRAS
  • PMID:19303097
DOID:9849 Meniere's disease HGNC:4932 Homo sapiens (human) 3106 HLA-B
  • PMID:12542204
DOID:8577 ulcerative colitis HGNC:2602 Homo sapiens (human) 1591 CYP24A1
  • PMID:28811712
DOID:3138 acanthosis nigricans HGNC:19165 Homo sapiens (human) 9882 TBC1D4
  • PMID:19470471
DOID:4971 myelofibrosis HGNC:1455 Homo sapiens (human) 811 CALR
  • PMID:24997152
  • PMID:25860380
  • RGD:7240710
DOID:0060903 thrombosis HGNC:3662 Homo sapiens (human) 2244 FGB
  • PMID:17469143
DOID:2058 chronic mucocutaneous candidiasis HGNC:1343 Homo sapiens (human) 10758 TRAF3IP2
  • RGD:7240710
DOID:0080612 anterior segment dysgenesis 7 HGNC:14966 Homo sapiens (human) 7837 PXDN
  • RGD:7240710
DOID:114 heart disease HGNC:11050 Homo sapiens (human) 6532 SLC6A4
  • PMID:10381332
DOID:9253 gastrointestinal stromal tumor HGNC:11730 Homo sapiens (human) 7015 TERT
  • PMID:26372813
DOID:12894 Sjogren's syndrome HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1
  • PMID:11555411
DOID:1470 major depressive disorder HGNC:11957 Homo sapiens (human) 9968 MED12
  • PMID:12216017
DOID:0060558 lethal congenital contracture syndrome HGNC:13841 Homo sapiens (human) 57211 ADGRG6
  • RGD:7240710
DOID:2559 opiate dependence HGNC:1358 Homo sapiens (human) 735 C9
  • PMID:18438686
DOID:0060892 late onset Parkinson's disease HGNC:4947 Homo sapiens (human) 3122 HLA-DRA
  • PMID:21791235
DOID:0060765 autosomal dominant Robinow syndrome 2 HGNC:3084 Homo sapiens (human) 1855 DVL1
  • RGD:7240710
DOID:783 end stage renal disease RGD:2238 Rattus norvegicus (Norway rat) 24237 C6
  • PMID:11912252
DOID:0080575 Larsen-like syndrome B3GAT3 type HGNC:923 Homo sapiens (human) 26229 B3GAT3
  • RGD:7240710
DOID:1574 alcohol use disorder HGNC:90 Homo sapiens (human) 35 ACADS
  • PMID:20554694
DOID:3070 high grade glioma HGNC:886 Homo sapiens (human) 546 ATRX
  • PMID:23104868

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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