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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 3776 - 3800 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:684 hepatocellular carcinoma HGNC:4415 Homo sapiens (human) 27232 GNMT
  • MGI:6194238
DOID:2957 pulmonary tuberculosis HGNC:4180 Homo sapiens (human) 2632 GBE1
  • PMID:28355295
DOID:9744 type 1 diabetes mellitus HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:12743671
DOID:10591 pre-eclampsia HGNC:9053 Homo sapiens (human) 5329 PLAUR
  • PMID:21722073
DOID:2272 vulvovaginal candidiasis HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:17470593
DOID:9352 type 2 diabetes mellitus HGNC:9020 Homo sapiens (human) 5313 PKLR
  • PMID:12196482
  • PMID:19111066
DOID:0070257 congenital disorder of glycosylation type IIe HGNC:18622 Homo sapiens (human) 91949 COG7
  • MGI:6194238
  • RGD:7240710
DOID:0050441 mucosulfatidosis HGNC:20376 Homo sapiens (human) 285362 SUMF1
  • MGI:6194238
  • RGD:7240710
DOID:9409 diabetes insipidus HGNC:4819 Homo sapiens (human) 3037 HAS2
  • MGI:6194238
DOID:0110389 retinitis pigmentosa 73 HGNC:26527 Homo sapiens (human) 138050 HGSNAT
  • RGD:7240710
DOID:0090045 childhood onset GLUT1 deficiency syndrome 2 HGNC:11005 Homo sapiens (human) 6513 SLC2A1
  • RGD:7240710
DOID:0060718 autosomal recessive congenital ichthyosis 9 HGNC:23752 Homo sapiens (human) 204219 CERS3
  • RGD:7240710
DOID:10763 hypertension HGNC:6554 Homo sapiens (human) 3953 LEPR
  • MGI:6194238
  • PMID:10999797
DOID:4448 macular degeneration HGNC:936 Homo sapiens (human) 572 BAD
  • PMID:22773904
DOID:0111257 gamma-glutamyl transpeptidase deficiency HGNC:4250 Homo sapiens (human) 2678 GGT1
  • RGD:7240710
DOID:3429 inclusion body myositis HGNC:2666 Homo sapiens (human) 1605 DAG1
  • PMID:14972325
DOID:11984 hypertrophic cardiomyopathy HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • MGI:6194238
DOID:0060058 lymphoma HGNC:8575 Homo sapiens (human) 5049 PAFAH1B2
  • PMID:11983068
DOID:4195 hyperglycemia HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
DOID:1380 endometrial cancer HGNC:11377 Homo sapiens (human) 6783 SULT1E1
  • PMID:18318428
DOID:0111263 combined malonic and methylmalonic acidemia HGNC:27288 Homo sapiens (human) 197322 ACSF3
  • RGD:7240710
DOID:8549 chronic ulcer of skin HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:8099861
DOID:0050773 paraganglioma HGNC:10981 Homo sapiens (human) 8402 SLC25A11
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • MGI:6194238
  • PMID:12534643
DOID:936 brain disease HGNC:9588 Homo sapiens (human) 5728 PTEN
  • MGI:6194238

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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