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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 11951 - 11975 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:2747 glycogen storage disease HGNC:4699 Homo sapiens (human) 2992 GYG1
  • RGD:7240710
DOID:0112223 developmental and epileptic encephalopathy 89 HGNC:4092 Homo sapiens (human) 2571 GAD1
  • RGD:7240710
DOID:0060576 3MC syndrome 2 HGNC:17213 Homo sapiens (human) 78989 COLEC11
  • RGD:7240710
DOID:0050546 congenital adrenal insufficiency HGNC:2590 Homo sapiens (human) 1583 CYP11A1
  • RGD:7240710
DOID:0111411 exudative vitreoretinopathy 4 HGNC:6697 Homo sapiens (human) 4041 LRP5
  • RGD:7240710
DOID:0080721 calvarial doughnut lesions with bone fragility HGNC:28395 Homo sapiens (human) 166929 SGMS2
  • RGD:7240710
DOID:3805 porokeratosis HGNC:3631 Homo sapiens (human) 2224 FDPS
  • RGD:7240710
DOID:0110794 hereditary spastic paraplegia 42 HGNC:95 Homo sapiens (human) 9197 SLC33A1
  • RGD:7240710
DOID:1470 major depressive disorder HGNC:5293 Homo sapiens (human) 3356 HTR2A
  • RGD:7240710
DOID:0111258 pentosuria HGNC:18985 Homo sapiens (human) 51181 DCXR
  • RGD:7240710
DOID:0070403 hypomyelinating leukodystrophy 26 HGNC:16872 Homo sapiens (human) 347734 SLC35B2
  • RGD:7240710
DOID:0112198 spondyloepimetaphyseal dysplasia with joint laxity type 1 HGNC:17978 Homo sapiens (human) 126792 B3GALT6
  • RGD:7240710
DOID:0110267 cataract 44 HGNC:6708 Homo sapiens (human) 4047 LSS
  • RGD:7240710
DOID:0080560 congenital disorder of glycosylation Ih HGNC:23161 Homo sapiens (human) 79053 ALG8
  • RGD:7240710
DOID:2738 pseudoxanthoma elasticum HGNC:15516 Homo sapiens (human) 64131 XYLT1
  • RGD:7240710
DOID:0112160 autosomal dominant nonsyndromic deafness 79 HGNC:21088 Homo sapiens (human) 79966 SCD5
  • RGD:7240710
DOID:0060806 syndromic X-linked intellectual disability Hedera type HGNC:18305 Homo sapiens (human) 10159 ATP6AP2
  • RGD:7240710
DOID:0080554 congenital disorder of glycosylation Ib HGNC:7216 Homo sapiens (human) 4351 MPI
  • RGD:7240710
DOID:612 primary immunodeficiency disease HGNC:8978 Homo sapiens (human) 5294 PIK3CG
  • RGD:7240710
DOID:0080923 bilateral parasagittal parieto-occipital polymicrogyria HGNC:16873 Homo sapiens (human) 9896 FIG4
  • RGD:7240710
DOID:0080288 spinocerebellar ataxia 46 HGNC:17158 Homo sapiens (human) 23646 PLD3
  • RGD:7240710
DOID:0070215 familial hyperinsulinemic hypoglycemia 4 HGNC:4799 Homo sapiens (human) 3033 HADH
  • RGD:7240710
DOID:0080071 mucolipidosis III alpha/beta HGNC:29670 Homo sapiens (human) 79158 GNPTAB
  • RGD:7240710
DOID:0060898 Parkinson's disease 20 HGNC:11503 Homo sapiens (human) 8867 SYNJ1
  • RGD:7240710
DOID:0080738 Ehlers-Danlos syndrome spondylodysplastic type 1 HGNC:930 Homo sapiens (human) 11285 B4GALT7
  • 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