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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 65351 - 65375 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0050741 alcohol dependence RGD:620735 Rattus norvegicus (Norway rat) 78980 Tas2r118
  • MGI:6194238
DOID:0050651 atrioventricular septal defect HGNC:14630 Homo sapiens (human) 78987 CRELD1
  • RGD:7240710
DOID:1681 heart septal defect HGNC:14630 Homo sapiens (human) 78987 CRELD1
  • PMID:12632326
DOID:674 cleft palate HGNC:17213 Homo sapiens (human) 78989 COLEC11
  • MGI:6194238
DOID:0060576 3MC syndrome 2 HGNC:17213 Homo sapiens (human) 78989 COLEC11
  • RGD:7240710
DOID:9280 carbamoyl phosphate synthetase I deficiency disease HGNC:1424 Homo sapiens (human) 790 CAD
  • MGI:6194238
DOID:3247 rhabdomyosarcoma HGNC:1424 Homo sapiens (human) 790 CAD
  • MGI:6194238
DOID:0050833 orotic aciduria HGNC:1424 Homo sapiens (human) 790 CAD
  • MGI:6194238
DOID:0080419 developmental and epileptic encephalopathy 50 HGNC:1424 Homo sapiens (human) 790 CAD
  • RGD:7240710
DOID:4450 renal cell carcinoma HGNC:1424 Homo sapiens (human) 790 CAD
  • MGI:6194238
DOID:684 hepatocellular carcinoma HGNC:1424 Homo sapiens (human) 790 CAD
  • MGI:6194238
DOID:417 autoimmune disease HGNC:347 Homo sapiens (human) 79026 AHNAK
  • MGI:6194238
DOID:50 thyroid gland disease HGNC:30972 Homo sapiens (human) 79048 SECISBP2
  • RGD:7240710
DOID:0080560 congenital disorder of glycosylation Ih HGNC:23161 Homo sapiens (human) 79053 ALG8
  • RGD:7240710
DOID:0050570 congenital disorder of glycosylation type I HGNC:23161 Homo sapiens (human) 79053 ALG8
  • MGI:6194238
DOID:4239 alveolar soft part sarcoma HGNC:13825 Homo sapiens (human) 79058 ASPSCR1
  • RGD:7240710
DOID:14330 Parkinson's disease HGNC:22408 Homo sapiens (human) 79065 ATG9A
  • MGI:6194238
DOID:4450 renal cell carcinoma HGNC:24678 Homo sapiens (human) 79068 FTO
  • PMID:30648791
DOID:1287 cardiovascular system disease HGNC:24678 Homo sapiens (human) 79068 FTO
  • PMID:20400278
DOID:0080334 aortic valve disease 2 HGNC:24678 Homo sapiens (human) 79068 FTO
  • PMID:26431034
DOID:4467 clear cell renal cell carcinoma HGNC:24678 Homo sapiens (human) 79068 FTO
  • PMID:30648791
  • PMID:32817424
DOID:11446 sciatic neuropathy HGNC:24678 Homo sapiens (human) 79068 FTO
  • MGI:6194238
DOID:0081292 traumatic brain injury HGNC:24678 Homo sapiens (human) 79068 FTO
  • MGI:6194238
DOID:3393 coronary artery disease HGNC:24678 Homo sapiens (human) 79068 FTO
  • PMID:24622111
  • PMID:28167353
DOID:10763 hypertension HGNC:24678 Homo sapiens (human) 79068 FTO
  • PMID:20031594

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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