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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 65226 - 65250 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:870 neuropathy Xenbase:XB-GENE-876969 Xenopus tropicalis (tropical clawed frog) 780198 mpz
  • MGI:6194238
DOID:0050540 Charcot-Marie-Tooth disease type 3 Xenbase:XB-GENE-876969 Xenopus tropicalis (tropical clawed frog) 780198 mpz
  • MGI:6194238
DOID:0110157 Charcot-Marie-Tooth disease type 2J Xenbase:XB-GENE-876969 Xenopus tropicalis (tropical clawed frog) 780198 mpz
  • MGI:6194238
DOID:9743 diabetic neuropathy Xenbase:XB-GENE-876969 Xenopus tropicalis (tropical clawed frog) 780198 mpz
  • MGI:6194238
DOID:0110200 Charcot-Marie-Tooth disease dominant intermediate D Xenbase:XB-GENE-876969 Xenopus tropicalis (tropical clawed frog) 780198 mpz
  • MGI:6194238
DOID:10595 Charcot-Marie-Tooth disease Xenbase:XB-GENE-876969 Xenopus tropicalis (tropical clawed frog) 780198 mpz
  • MGI:6194238
DOID:0090111 PCWH syndrome Xenbase:XB-GENE-876969 Xenopus tropicalis (tropical clawed frog) 780198 mpz
  • MGI:6194238
DOID:0050645 arterial tortuosity syndrome Xenbase:XB-GENE-950490 Xenopus tropicalis (tropical clawed frog) 780388 slc2a10
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:6700 Homo sapiens (human) 7804 LRP8
  • PMID:12399018
  • PMID:20208369
DOID:3393 coronary artery disease HGNC:6700 Homo sapiens (human) 7804 LRP8
  • PMID:17847002
  • PMID:18592168
DOID:5419 schizophrenia HGNC:6700 Homo sapiens (human) 7804 LRP8
  • PMID:22419519
DOID:5844 myocardial infarction HGNC:6700 Homo sapiens (human) 7804 LRP8
  • PMID:17847002
  • PMID:18592168
  • RGD:7240710
DOID:1307 dementia HGNC:6700 Homo sapiens (human) 7804 LRP8
  • PMID:17614163
DOID:0110818 hereditary spastic paraplegia 73 MGI:2446526 Mus musculus (house mouse) 78070 Cpt1c
  • MGI:6194238
DOID:0070395 developmental and epileptic encephalopathy 110 HGNC:1399 Homo sapiens (human) 781 CACNA2D1
  • RGD:7240710
DOID:3454 brain infarction HGNC:1399 Homo sapiens (human) 781 CACNA2D1
  • MGI:6194238
DOID:0060041 autism spectrum disorder HGNC:29905 Homo sapiens (human) 7812 CSDE1
  • MGI:6194238
DOID:0080379 nephrotic syndrome type 2 HGNC:13394 Homo sapiens (human) 7827 NPHS2
  • RGD:7240710
DOID:10976 membranous glomerulonephritis HGNC:13394 Homo sapiens (human) 7827 NPHS2
  • MGI:6194238
DOID:1184 nephrotic syndrome HGNC:13394 Homo sapiens (human) 7827 NPHS2
  • MGI:6194238
DOID:576 proteinuria HGNC:13394 Homo sapiens (human) 7827 NPHS2
  • MGI:6194238
DOID:8634 prostate carcinoma in situ MGI:1916603 Mus musculus (house mouse) 78284 Creb3l4
  • MGI:6194238
DOID:2526 prostate adenocarcinoma MGI:1916603 Mus musculus (house mouse) 78284 Creb3l4
  • MGI:6194238
DOID:0110221 Brugada syndrome 4 HGNC:1402 Homo sapiens (human) 783 CACNB2
  • RGD:7240710
DOID:10763 hypertension HGNC:1402 Homo sapiens (human) 783 CACNB2
  • PMID:24338417

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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