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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 10951 - 10975 of 12216 in total
Disease ID ▼ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0060900 Parkinson's disease 14 HGNC:9039 Homo sapiens (human) 8398 PLA2G6
  • MGI:6194238
  • RGD:7240710
DOID:0060898 Parkinson's disease 20 HGNC:11503 Homo sapiens (human) 8867 SYNJ1
  • RGD:7240710
DOID:0060894 early-onset Parkinson's disease HGNC:11504 Homo sapiens (human) 8871 SYNJ2
  • MGI:6194238
DOID:0060894 early-onset Parkinson's disease HGNC:11503 Homo sapiens (human) 8867 SYNJ1
  • MGI:6194238
DOID:0060892 late onset Parkinson's disease WB:WBGene00008706 Caenorhabditis elegans 178535 gba-3
  • MGI:6194238
DOID:0060892 late onset Parkinson's disease HGNC:251 Homo sapiens (human) 126 ADH1C
  • RGD:7240710
DOID:0060892 late onset Parkinson's disease MGI:95665 Mus musculus (house mouse) 14466 Gba1
  • MGI:6194238
DOID:0060892 late onset Parkinson's disease HGNC:4177 Homo sapiens (human) 2629 GBA1
  • RGD:7240710
DOID:0060892 late onset Parkinson's disease WB:WBGene00021160 Caenorhabditis elegans 177314 gba-4
  • MGI:6194238
DOID:0060892 late onset Parkinson's disease HGNC:9498 Homo sapiens (human) 5660 PSAP
  • RGD:7240710
DOID:0060887 ossification of the posterior longitudinal ligament of spine RGD:628825 Rattus norvegicus (Norway rat) 85496 Enpp1
  • MGI:6194238
DOID:0060887 ossification of the posterior longitudinal ligament of spine MGI:97370 Mus musculus (house mouse) 18605 Enpp1
  • MGI:6194238
  • PMID:24770645
  • PMID:9359030
  • PMID:9662402
DOID:0060887 ossification of the posterior longitudinal ligament of spine HGNC:3356 Homo sapiens (human) 5167 ENPP1
  • MGI:6194238
  • PMID:15834329
DOID:0060867 macrocephaly-autism syndrome HGNC:9588 Homo sapiens (human) 5728 PTEN
  • MGI:6194238
  • PMID:15805158
  • RGD:7240710
DOID:0060856 right atrial isomerism HGNC:18292 Homo sapiens (human) 55997 CFC1
  • MGI:6194238
DOID:0060849 osteoporosis-pseudoglioma syndrome MGI:1278315 Mus musculus (house mouse) 16973 Lrp5
  • MGI:6194238
  • PMID:11956231
  • PMID:24225945
DOID:0060849 osteoporosis-pseudoglioma syndrome HGNC:6697 Homo sapiens (human) 4041 LRP5
  • MGI:6194238
  • PMID:11719191
  • PMID:16679074
  • RGD:7240710
DOID:0060841 isolated microphthalmia 8 HGNC:409 Homo sapiens (human) 220 ALDH1A3
  • RGD:7240710
DOID:0060806 syndromic X-linked intellectual disability Hedera type FB:FBgn0037671 Drosophila melanogaster (fruit fly) 41104 ATP6AP2
  • MGI:6194238
DOID:0060806 syndromic X-linked intellectual disability Hedera type HGNC:18305 Homo sapiens (human) 10159 ATP6AP2
  • RGD:7240710
DOID:0060786 hypomyelinating leukodystrophy HGNC:13709 Homo sapiens (human) 8560 DEGS1
  • MGI:6194238
DOID:0060778 congenital diarrhea 7 with exudative enteropathy HGNC:2843 Homo sapiens (human) 8694 DGAT1
  • RGD:7240710
DOID:0060774 congenital diarrhea HGNC:16526 Homo sapiens (human) 51703 ACSL5
  • RGD:7240710
DOID:0060770 dextro-looped transposition of the great arteries HGNC:5273 Homo sapiens (human) 3339 HSPG2
  • MGI:6194238
DOID:0060770 dextro-looped transposition of the great arteries HGNC:18292 Homo sapiens (human) 55997 CFC1
  • MGI:6194238

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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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