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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 51 - 75 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:0111773 46,XY sex reversal 8 HGNC:387 Homo sapiens (human) 1109 AKR1C4
  • RGD:7240710
DOID:9269 maple syrup urine disease HGNC:2898 Homo sapiens (human) 1738 DLD
  • RGD:7240710
DOID:0111843 Paganini-Miozzo syndrome HGNC:19133 Homo sapiens (human) 90161 HS6ST2
  • RGD:7240710
DOID:0110736 neurodegeneration with brain iron accumulation 2b HGNC:9039 Homo sapiens (human) 8398 PLA2G6
  • RGD:7240710
DOID:1700 X-linked ichthyosis HGNC:11425 Homo sapiens (human) 412 STS
  • RGD:7240710
DOID:0110409 retinitis pigmentosa 46 HGNC:5385 Homo sapiens (human) 3420 IDH3B
  • RGD:7240710
DOID:0111070 congenital bile acid synthesis defect 3 HGNC:2652 Homo sapiens (human) 9420 CYP7B1
  • RGD:7240710
DOID:0112218 developmental and epileptic encephalopathy 83 HGNC:12527 Homo sapiens (human) 7360 UGP2
  • RGD:7240710
DOID:0111451 progressive myoclonus epilepsy 8 HGNC:14253 Homo sapiens (human) 10715 CERS1
  • RGD:7240710
DOID:3659 sialuria HGNC:23657 Homo sapiens (human) 10020 GNE
  • RGD:7240710
DOID:0111390 mucopolysaccharidosis Ih HGNC:5391 Homo sapiens (human) 3425 IDUA
  • RGD:7240710
DOID:3635 congenital myasthenic syndrome HGNC:10979 Homo sapiens (human) 6576 SLC25A1
  • RGD:7240710
DOID:0080564 congenital disorder of glycosylation Il HGNC:15672 Homo sapiens (human) 79796 ALG9
  • RGD:7240710
DOID:0070434 hyperphosphatasia with impaired intellectual development syndrome 2 HGNC:23215 Homo sapiens (human) 84720 PIGO
  • RGD:7240710
DOID:0111236 congenital muscular dystrophy-dystroglycanopathy type A3 HGNC:19139 Homo sapiens (human) 55624 POMGNT1
  • RGD:7240710
DOID:0110676 congenital myasthenic syndrome 13 HGNC:2995 Homo sapiens (human) 1798 DPAGT1
  • RGD:7240710
DOID:0080140 multiple congenital anomalies-hypotonia-seizures syndrome 3 HGNC:14938 Homo sapiens (human) 51604 PIGT
  • RGD:7240710
DOID:0112105 X-linked parkinsonism-spasticity syndrome HGNC:18305 Homo sapiens (human) 10159 ATP6AP2
  • RGD:7240710
DOID:0111231 congenital muscular dystrophy-dystroglycanopathy type A8 HGNC:25902 Homo sapiens (human) 84892 POMGNT2
  • RGD:7240710
DOID:5723 optic atrophy HGNC:29622 Homo sapiens (human) 27349 MCAT
  • RGD:7240710
DOID:0111527 spinal muscular atrophy with progressive myoclonic epilepsy HGNC:735 Homo sapiens (human) 427 ASAH1
  • RGD:7240710
DOID:0080576 spondyloepimetaphyseal dysplasia, Genevieve-type HGNC:19237 Homo sapiens (human) 54187 NANS
  • RGD:7240710
DOID:0080575 Larsen-like syndrome B3GAT3 type HGNC:923 Homo sapiens (human) 26229 B3GAT3
  • RGD:7240710
DOID:0050636 familial visceral amyloidosis HGNC:6740 Homo sapiens (human) 4069 LYZ
  • RGD:7240710
DOID:10825 essential hypertension HGNC:2638 Homo sapiens (human) 1577 CYP3A5
  • RGD:7240710

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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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