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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 67926 - 67950 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:12306 vitiligo HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:19439879
  • PMID:20613769
  • PMID:23868633
DOID:1909 melanoma HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:9758419
DOID:3770 pulmonary fibrosis HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:21190578
DOID:0080592 Klippel-Feil syndrome 4 HGNC:18150 Homo sapiens (human) 84700 MYO18B
  • RGD:7240710
DOID:3762 cytochrome-c oxidase deficiency disease HGNC:16232 Homo sapiens (human) 84701 COX4I2
  • MGI:6194238
DOID:9256 colorectal cancer HGNC:6128 Homo sapiens (human) 8471 IRS4
  • PMID:29185229
  • PMID:29353348
  • PMID:30410539
DOID:1324 lung cancer HGNC:6128 Homo sapiens (human) 8471 IRS4
  • PMID:33894221
DOID:10914 amnestic disorder HGNC:6128 Homo sapiens (human) 8471 IRS4
  • MGI:6194238
DOID:1059 intellectual disability HGNC:6128 Homo sapiens (human) 8471 IRS4
  • MGI:6194238
DOID:4194 glucose metabolism disease HGNC:6128 Homo sapiens (human) 8471 IRS4
  • MGI:6194238
DOID:3908 lung non-small cell carcinoma HGNC:6128 Homo sapiens (human) 8471 IRS4
  • PMID:33894221
DOID:9352 type 2 diabetes mellitus HGNC:6128 Homo sapiens (human) 8471 IRS4
  • MGI:6194238
DOID:0111835 congenital nongoitrous hypothyroidism 9 HGNC:6128 Homo sapiens (human) 8471 IRS4
  • RGD:7240710
DOID:0070434 hyperphosphatasia with impaired intellectual development syndrome 2 HGNC:23215 Homo sapiens (human) 84720 PIGO
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:8127 Homo sapiens (human) 8473 OGT
  • MGI:6194238
DOID:1712 aortic valve stenosis HGNC:8127 Homo sapiens (human) 8473 OGT
  • PMID:22128088
DOID:0080240 non-syndromic X-linked intellectual disability 106 HGNC:8127 Homo sapiens (human) 8473 OGT
  • MGI:6194238
  • RGD:7240710
DOID:6000 congestive heart failure HGNC:8127 Homo sapiens (human) 8473 OGT
  • MGI:6194238
DOID:9351 diabetes mellitus HGNC:8127 Homo sapiens (human) 8473 OGT
  • MGI:6194238
DOID:684 hepatocellular carcinoma HGNC:1552 Homo sapiens (human) 84733 CBX2
  • PMID:35693827
DOID:0050866 oral squamous cell carcinoma HGNC:1552 Homo sapiens (human) 84733 CBX2
  • PMID:24885002
DOID:162 cancer HGNC:1552 Homo sapiens (human) 84733 CBX2
  • MGI:6194238
DOID:14447 gonadal dysgenesis HGNC:1552 Homo sapiens (human) 84733 CBX2
  • PMID:23219007
DOID:0111776 46,XY sex reversal 5 HGNC:1552 Homo sapiens (human) 84733 CBX2
  • RGD:7240710
DOID:2921 glomerulonephritis HGNC:20675 Homo sapiens (human) 84735 CNDP1
  • PMID:20851293

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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