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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 2251 - 2275 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0080322 polycystic kidney disease HGNC:15517 Homo sapiens (human) 64132 XYLT2
  • MGI:6194238
DOID:2394 ovarian cancer HGNC:8143 Homo sapiens (human) 4978 OPCML
  • RGD:7240710
DOID:0110870 congenital stationary night blindness 1A HGNC:8082 Homo sapiens (human) 60506 NYX
  • MGI:6194238
  • RGD:7240710
DOID:2841 asthma HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:19383228
  • PMID:19484664
DOID:11612 polycystic ovary syndrome HGNC:5215 Homo sapiens (human) 51478 HSD17B7
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:4923 Homo sapiens (human) 3099 HK2
  • PMID:11319725
DOID:2018 hyperinsulinism HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
DOID:12894 Sjogren's syndrome HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
  • PMID:22703762
DOID:3021 acute kidney failure HGNC:11850 Homo sapiens (human) 7099 TLR4
  • MGI:6194238
DOID:0110429 dilated cardiomyopathy 1H HGNC:2592 Homo sapiens (human) 1585 CYP11B2
  • PMID:12031704
DOID:3070 high grade glioma HGNC:5383 Homo sapiens (human) 3418 IDH2
  • MGI:6194238
DOID:14330 Parkinson's disease HGNC:1455 Homo sapiens (human) 811 CALR
  • MGI:6194238
DOID:0080000 muscular disease HGNC:2330 Homo sapiens (human) 1376 CPT2
  • PMID:10873395
DOID:0080844 omodysplasia 1 HGNC:4454 Homo sapiens (human) 10082 GPC6
  • RGD:7240710
DOID:3138 acanthosis nigricans HGNC:11007 Homo sapiens (human) 6515 SLC2A3
  • PMID:11436180
DOID:5453 pulmonary venoocclusive disease HGNC:786 Homo sapiens (human) 468 ATF4
  • MGI:6194238
DOID:1909 melanoma HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:16456816
DOID:684 hepatocellular carcinoma HGNC:5988 Homo sapiens (human) 8809 IL18R1
  • PMID:26893476
DOID:0050812 spondyloepimetaphyseal dysplasia, Pakistani type HGNC:8604 Homo sapiens (human) 9060 PAPSS2
  • MGI:6194238
  • RGD:7240710
DOID:3321 GM2 gangliosidosis HGNC:4367 Homo sapiens (human) 2760 GM2A
  • PMID:10364519
DOID:162 cancer HGNC:10852 Homo sapiens (human) 6472 SHMT2
  • MGI:6194238
DOID:331 central nervous system disease HGNC:118 Homo sapiens (human) 50 ACO2
  • MGI:6194238
DOID:10584 retinitis pigmentosa HGNC:23059 Homo sapiens (human) 63827 BCAN
  • PMID:29150673
DOID:0080630 B-lymphoblastic leukemia/lymphoma HGNC:2638 Homo sapiens (human) 1577 CYP3A5
  • PMID:21225912
DOID:4608 common bile duct neoplasm HGNC:7371 Homo sapiens (human) 10232 MSLN
  • PMID:16416732

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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: August 19, 2024