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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 70901 - 70925 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:0110770 hereditary spastic paraplegia 17 HGNC:15832 Homo sapiens (human) 26580 BSCL2
  • RGD:7240710
DOID:0080420 developmental and epileptic encephalopathy 62 HGNC:10590 Homo sapiens (human) 6328 SCN3A
  • RGD:7240710
DOID:0112353 spermatogenic failure 64 HGNC:28521 Homo sapiens (human) 286151 FBXO43
  • RGD:7240710
DOID:0112145 retinitis pigmentosa 88 HGNC:15946 Homo sapiens (human) 94137 RP1L1
  • RGD:7240710
DOID:0060387 chondrodysplasia Blomstrand type HGNC:9608 Homo sapiens (human) 5745 PTH1R
  • RGD:7240710
DOID:0060386 Chilblain lupus HGNC:15925 Homo sapiens (human) 25939 SAMHD1
  • RGD:7240710
DOID:0060767 autosomal dominant Robinow syndrome 3 HGNC:3087 Homo sapiens (human) 1857 DVL3
  • RGD:7240710
DOID:0080460 developmental and epileptic encephalopathy 34 HGNC:13818 Homo sapiens (human) 57468 SLC12A5
  • RGD:7240710
DOID:0081378 amyotrophic lateral sclerosis type 24 HGNC:7744 Homo sapiens (human) 4750 NEK1
  • RGD:7240710
DOID:612 primary immunodeficiency disease HGNC:23357 Homo sapiens (human) 28985 MCTS1
  • RGD:7240710
DOID:2218 blood platelet disease HGNC:3749 Homo sapiens (human) 2313 FLI1
  • RGD:7240710
DOID:1172 hyperlipoproteinemia type IV HGNC:17288 Homo sapiens (human) 116519 APOA5
  • RGD:7240710
DOID:13777 epidermodysplasia verruciformis HGNC:18021 Homo sapiens (human) 11322 TMC6
  • RGD:7240710
DOID:0111969 immunodeficiency 39 HGNC:6122 Homo sapiens (human) 3665 IRF7
  • RGD:7240710
DOID:0110292 autosomal recessive limb-girdle muscular dystrophy type 2O HGNC:19139 Homo sapiens (human) 55624 POMGNT1
  • RGD:7240710
DOID:11555 Fuchs' endothelial dystrophy HGNC:26504 Homo sapiens (human) 123624 AGBL1
  • RGD:7240710
DOID:0110857 posterior polymorphous corneal dystrophy 3 HGNC:11642 Homo sapiens (human) 6935 ZEB1
  • RGD:7240710
DOID:0080046 Stickler syndrome HGNC:2217 Homo sapiens (human) 1297 COL9A1
  • RGD:7240710
DOID:0070252 autosomal dominant Emery-Dreifuss muscular dystrophy 7 HGNC:28472 Homo sapiens (human) 79188 TMEM43
  • RGD:7240710
DOID:0111141 delayed sleep phase syndrome HGNC:2384 Homo sapiens (human) 1407 CRY1
  • RGD:7240710
DOID:0110592 autosomal dominant nonsyndromic deafness 70 HGNC:6944 Homo sapiens (human) 4171 MCM2
  • RGD:7240710
DOID:0111019 cone-rod dystrophy 12 HGNC:9454 Homo sapiens (human) 8842 PROM1
  • RGD:7240710
DOID:0081274 peroxisome biogenesis disorder 14B HGNC:8853 Homo sapiens (human) 8799 PEX11B
  • RGD:7240710
DOID:0110589 autosomal dominant nonsyndromic deafness 68 HGNC:17513 Homo sapiens (human) 9455 HOMER2
  • RGD:7240710
DOID:0080285 developmental and epileptic encephalopathy 58 HGNC:8032 Homo sapiens (human) 4915 NTRK2
  • RGD:7240710

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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