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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 69801 - 69825 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:684 hepatocellular carcinoma HGNC:6091 Homo sapiens (human) 3643 INSR
  • MGI:6194238
  • PMID:23633480
DOID:13269 hereditary coproporphyria MGI:104841 Mus musculus (house mouse) 12892 Cpox
  • MGI:6194238
  • PMID:23631845
  • PMID:28600349
DOID:783 end stage renal disease HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • MGI:6194238
  • PMID:23619522
DOID:10763 hypertension RGD:2582 Rattus norvegicus (Norway rat) 25149 Esr2
  • MGI:6194238
  • PMID:23608653
DOID:9351 diabetes mellitus HGNC:12762 Homo sapiens (human) 7466 WFS1
  • MGI:6194238
  • PMID:23595122
DOID:0110726 neuronal ceroid lipofuscinosis 2 ZFIN:ZDB-GENE-030131-6654 Danio rerio (zebrafish) 798347 tpp1
  • MGI:6194238
  • PMID:23587805
DOID:0111030 hemochromatosis type 3 RGD:1310152 Rattus norvegicus (Norway rat) 288562 Tfr2
  • MGI:6194238
  • PMID:23582421
DOID:1596 depressive disorder HGNC:6018 Homo sapiens (human) 3569 IL6
  • MGI:6194238
  • PMID:23571152
  • PMID:28083615
  • PMID:31396300
DOID:13580 cholestasis MGI:97569 Mus musculus (house mouse) 18670 Abcb4
  • MGI:6194238
  • PMID:23545228
DOID:0110612 primary ciliary dyskinesia 10 MGI:1923566 Mus musculus (house mouse) 109065 Dnaaf2
  • MGI:6194238
  • PMID:23525783
  • PMID:31107948
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:9868 Homo sapiens (human) 5919 RARRES2
  • MGI:6194238
  • PMID:23507574
DOID:684 hepatocellular carcinoma HGNC:40 Homo sapiens (human) 5243 ABCB1
  • MGI:6194238
  • PMID:23488625
  • PMID:24175826
DOID:3347 osteosarcoma MGI:98834 Mus musculus (house mouse) 22059 Trp53
  • MGI:6194238
  • PMID:23486187
DOID:0110766 hereditary spastic paraplegia 13 MGI:96242 Mus musculus (house mouse) 15510 Hspd1
  • MGI:6194238
  • PMID:23466696
DOID:289 endometriosis HGNC:8824 Homo sapiens (human) 5176 SERPINF1
  • MGI:6194238
  • PMID:23466670
DOID:10591 pre-eclampsia HGNC:3349 Homo sapiens (human) 2022 ENG
  • MGI:6194238
  • PMID:23460287
DOID:90 degenerative disc disease HGNC:16953 Homo sapiens (human) 10631 POSTN
  • MGI:6194238
  • PMID:23453657
DOID:332 amyotrophic lateral sclerosis HGNC:6169 Homo sapiens (human) 3700 ITIH4
  • MGI:6194238
  • PMID:23436019
DOID:0060741 methylmalonic acidemia due to transcobalamin receptor defect MGI:1860083 Mus musculus (house mouse) 54219 Cd320
  • MGI:6194238
  • PMID:23430977
DOID:8947 diabetic retinopathy HGNC:29079 Homo sapiens (human) 23028 KDM1A
  • MGI:6194238
  • PMID:23423566
DOID:784 chronic kidney disease HGNC:910 Homo sapiens (human) 563 AZGP1
  • MGI:6194238
  • PMID:23423258
DOID:0110350 osteogenesis imperfecta type 6 MGI:108080 Mus musculus (house mouse) 20317 Serpinf1
  • MGI:6194238
  • PMID:23413146
DOID:10763 hypertension RGD:2825 Rattus norvegicus (Norway rat) 24464 Hp
  • MGI:6194238
  • PMID:23401751
DOID:0050777 Joubert syndrome HGNC:21474 Homo sapiens (human) 56623 INPP5E
  • MGI:6194238
  • PMID:23386033
DOID:0050742 nicotine dependence WB:WBGene00001053 Caenorhabditis elegans 179347 dop-2
  • MGI:6194238
  • PMID:23351035

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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