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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 65626 - 65650 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:14330 Parkinson's disease HGNC:24113 Homo sapiens (human) 79572 ATP13A3
  • MGI:6194238
DOID:0060893 juvenile-onset Parkinson's disease HGNC:24113 Homo sapiens (human) 79572 ATP13A3
  • MGI:6194238
DOID:2476 hereditary spastic paraplegia HGNC:24113 Homo sapiens (human) 79572 ATP13A3
  • MGI:6194238
DOID:0060556 Kufor-Rakeb syndrome HGNC:24113 Homo sapiens (human) 79572 ATP13A3
  • MGI:6194238
DOID:332 amyotrophic lateral sclerosis HGNC:24113 Homo sapiens (human) 79572 ATP13A3
  • MGI:6194238
DOID:14503 neuronal ceroid lipofuscinosis HGNC:24113 Homo sapiens (human) 79572 ATP13A3
  • MGI:6194238
DOID:14557 primary pulmonary hypertension HGNC:24113 Homo sapiens (human) 79572 ATP13A3
  • RGD:7240710
DOID:0060309 syndromic X-linked intellectual disability HGNC:29873 Homo sapiens (human) 79576 NKAP
  • RGD:7240710
DOID:5520 head and neck squamous cell carcinoma HGNC:16783 Homo sapiens (human) 79577 CDC73
  • PMID:26124004
DOID:13543 hyperparathyroidism HGNC:16783 Homo sapiens (human) 79577 CDC73
  • MGI:6194238
  • RGD:7240710
DOID:3910 lung adenocarcinoma HGNC:16783 Homo sapiens (human) 79577 CDC73
  • PMID:21692036
DOID:1540 parathyroid carcinoma HGNC:16783 Homo sapiens (human) 79577 CDC73
  • PMID:27490759
  • RGD:7240710
DOID:9256 colorectal cancer HGNC:16783 Homo sapiens (human) 79577 CDC73
  • PMID:21315421
DOID:0050866 oral squamous cell carcinoma HGNC:16783 Homo sapiens (human) 79577 CDC73
  • PMID:24257751
DOID:2876 laryngeal squamous cell carcinoma HGNC:16783 Homo sapiens (human) 79577 CDC73
  • PMID:27334641
DOID:0050694 Brown-Vialetto-Van Laere syndrome HGNC:30224 Homo sapiens (human) 79581 SLC52A2
  • MGI:6194238
DOID:0080786 Brown-Vialetto-Van Laere syndrome 2 HGNC:30224 Homo sapiens (human) 79581 SLC52A2
  • RGD:7240710
DOID:0110989 Joubert syndrome 20 HGNC:37234 Homo sapiens (human) 79583 TMEM231
  • RGD:7240710
DOID:0050778 Meckel syndrome HGNC:37234 Homo sapiens (human) 79583 TMEM231
  • MGI:6194238
  • RGD:7240710
DOID:4501 orofaciodigital syndrome HGNC:37234 Homo sapiens (human) 79583 TMEM231
  • MGI:6194238
DOID:9970 obesity HGNC:26161 Homo sapiens (human) 79585 CORO7
  • MGI:6194238
DOID:1682 congenital heart disease HGNC:29813 Homo sapiens (human) 79595 SAP130
  • MGI:6194238
DOID:9955 hypoplastic left heart syndrome HGNC:29813 Homo sapiens (human) 79595 SAP130
  • MGI:6194238
DOID:326 ischemia HGNC:1437 Homo sapiens (human) 796 CALCA
  • MGI:6194238
DOID:11400 pyelonephritis HGNC:1437 Homo sapiens (human) 796 CALCA
  • PMID:15286264

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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