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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 66201 - 66225 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:2256 osteochondrodysplasia HGNC:5273 Homo sapiens (human) 3339 HSPG2
  • PMID:11101850
DOID:9744 type 1 diabetes mellitus HGNC:11179 Homo sapiens (human) 6647 SOD1
  • PMID:18423055
DOID:684 hepatocellular carcinoma HGNC:6554 Homo sapiens (human) 3953 LEPR
  • PMID:23090836
DOID:10652 Alzheimer's disease HGNC:6014 Homo sapiens (human) 3565 IL4
  • PMID:20213229
DOID:783 end stage renal disease HGNC:7579 Homo sapiens (human) 4627 MYH9
  • PMID:18794854
  • PMID:19177153
  • PMID:19567477
  • PMID:20144966
  • PMID:21968013
DOID:6846 familial melanoma HGNC:7105 Homo sapiens (human) 4286 MITF
  • RGD:7240710
DOID:1996 rectum adenocarcinoma HGNC:11368 Homo sapiens (human) 6778 STAT6
  • PMID:22121102
DOID:0060278 pontocerebellar hypoplasia type 9 HGNC:469 Homo sapiens (human) 271 AMPD2
  • RGD:7240710
DOID:0112002 immunodeficiency 47 HGNC:868 Homo sapiens (human) 537 ATP6AP1
  • RGD:7240710
DOID:612 primary immunodeficiency disease HGNC:29619 Homo sapiens (human) 219972 MPEG1
  • RGD:7240710
DOID:4644 epidermolysis bullosa simplex HGNC:6442 Homo sapiens (human) 3852 KRT5
  • PMID:1372711
  • RGD:7240710
DOID:0060462 Desbuquois dysplasia HGNC:15516 Homo sapiens (human) 64131 XYLT1
  • RGD:7240710
DOID:783 end stage renal disease HGNC:7155 Homo sapiens (human) 4312 MMP1
  • PMID:19221176
  • PMID:22401717
DOID:399 tuberculosis HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:27393733
DOID:3393 coronary artery disease HGNC:6700 Homo sapiens (human) 7804 LRP8
  • PMID:17847002
  • PMID:18592168
DOID:0050650 familial atrial fibrillation HGNC:6294 Homo sapiens (human) 3784 KCNQ1
  • RGD:7240710
DOID:0090094 hypogonadotropic hypogonadism 1 with or without anosmia HGNC:6211 Homo sapiens (human) 3730 ANOS1
  • RGD:7240710
DOID:13166 allergic bronchopulmonary aspergillosis HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:20646338
DOID:0111133 focal segmental glomerulosclerosis 8 HGNC:14082 Homo sapiens (human) 54443 ANLN
  • RGD:7240710
DOID:0112194 Filippi syndrome HGNC:26877 Homo sapiens (human) 150468 CKAP2L
  • RGD:7240710
DOID:3082 interstitial lung disease HGNC:4893 Homo sapiens (human) 3082 HGF
  • PMID:21520010
DOID:10286 prostate carcinoma HGNC:6065 Homo sapiens (human) 3623 INHA
  • PMID:11818495
DOID:13774 Addison's disease HGNC:7067 Homo sapiens (human) 4261 CIITA
  • PMID:18593762
DOID:0050741 alcohol dependence HGNC:644 Homo sapiens (human) 367 AR
  • PMID:19231085
DOID:0111561 stiff skin syndrome HGNC:3603 Homo sapiens (human) 2200 FBN1
  • 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