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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 July 29, 2024
Displaying entries 11176 - 11200 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:0050589 inflammatory bowel disease HGNC:437 Homo sapiens (human) 248 ALPI
  • PMID:29567797
DOID:1024 leprosy HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:20650301
DOID:0111261 fumarase deficiency HGNC:3700 Homo sapiens (human) 2271 FH
  • RGD:7240710
DOID:0080470 developmental and epileptic encephalopathy 36 HGNC:30881 Homo sapiens (human) 79868 ALG13
  • RGD:7240710
DOID:10283 prostate cancer HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:16126332
  • PMID:16492910
  • PMID:17507624
DOID:0110645 long QT syndrome 2 HGNC:31088 Homo sapiens (human) 144245 ALG10B
  • RGD:7240710
DOID:3393 coronary artery disease HGNC:5998 Homo sapiens (human) 9173 IL1RL1
  • PMID:20602249
DOID:9970 obesity HGNC:288 Homo sapiens (human) 155 ADRB3
  • PMID:11882399
  • PMID:9126344
  • PMID:9892244
  • RGD:7240710
DOID:0111460 cardiofaciocutaneous syndrome 1 HGNC:1097 Homo sapiens (human) 673 BRAF
  • RGD:7240710
DOID:0014667 disease of metabolism HGNC:932 Homo sapiens (human) 570 BAAT
  • PMID:12704386
DOID:0080664 diaphyseal medullary stenosis with malignant fibrous histiocytoma HGNC:7413 Homo sapiens (human) 4507 MTAP
  • RGD:7240710
DOID:8619 recurrent hypersomnia HGNC:1938 Homo sapiens (human) 1120 CHKB
  • PMID:19404393
DOID:12732 intermediate uveitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:23378732
DOID:10591 pre-eclampsia HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:20044877
DOID:11832 visual epilepsy HGNC:20499 Homo sapiens (human) 79944 L2HGDH
  • PMID:24894778
DOID:0080379 nephrotic syndrome type 2 HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:9853251
DOID:11650 bronchopulmonary dysplasia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:15286263
DOID:3907 lung squamous cell carcinoma HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:16797832
  • PMID:18298806
DOID:417 autoimmune disease HGNC:270 Homo sapiens (human) 142 PARP1
  • PMID:16026592
DOID:1324 lung cancer HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:20303010
DOID:10763 hypertension HGNC:79 Homo sapiens (human) 28 ABO
  • PMID:32379894
DOID:12129 bulimia nervosa HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:21300128
DOID:4249 Gerstmann-Straussler-Scheinker syndrome HGNC:9449 Homo sapiens (human) 5621 PRNP
  • RGD:7240710
DOID:0111773 46,XY sex reversal 8 HGNC:385 Homo sapiens (human) 1646 AKR1C2
  • RGD:7240710
DOID:9432 renal glycosuria HGNC:11037 Homo sapiens (human) 6524 SLC5A2
  • PMID:12436245
  • PMID:14614622
  • RGD:7240710

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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: August 19, 2024