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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 68301 - 68325 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:0111366 familial hepatic adenoma HGNC:11621 Homo sapiens (human) 6927 HNF1A
  • RGD:7240710
DOID:2043 hepatitis B HGNC:15925 Homo sapiens (human) 25939 SAMHD1
  • PMID:24317272
DOID:0111420 familial GPIHBP1 deficiency HGNC:24945 Homo sapiens (human) 338328 GPIHBP1
  • RGD:7240710
DOID:7693 abdominal aortic aneurysm HGNC:613 Homo sapiens (human) 348 APOE
  • PMID:10848855
DOID:0070354 cataract 48 HGNC:30373 Homo sapiens (human) 23268 DNMBP
  • RGD:7240710
DOID:686 liver carcinoma HGNC:5962 Homo sapiens (human) 3586 IL10
  • PMID:28763918
DOID:3907 lung squamous cell carcinoma HGNC:10801 Homo sapiens (human) 6439 SFTPB
  • PMID:12107845
  • PMID:16570259
DOID:9261 nasopharynx carcinoma HGNC:7381 Homo sapiens (human) 4486 MST1R
  • RGD:7240710
DOID:10283 prostate cancer HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:16126332
  • PMID:16492910
  • PMID:17507624
DOID:13166 allergic bronchopulmonary aspergillosis HGNC:15633 Homo sapiens (human) 54106 TLR9
  • PMID:18275280
DOID:865 vasculitis HGNC:7876 Homo sapiens (human) 4846 NOS3
  • PMID:14583572
DOID:10966 lipoid nephrosis HGNC:11368 Homo sapiens (human) 6778 STAT6
  • PMID:12900808
  • PMID:15687724
  • PMID:19011907
DOID:8778 Crohn's disease HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:21702710
DOID:0111153 congenital mirror movement disorder HGNC:2701 Homo sapiens (human) 1630 DCC
  • RGD:7240710
DOID:0110482 autosomal recessive nonsyndromic deafness 24 HGNC:9944 Homo sapiens (human) 5962 RDX
  • RGD:7240710
DOID:612 primary immunodeficiency disease HGNC:11849 Homo sapiens (human) 7098 TLR3
  • RGD:7240710
DOID:2513 basal cell carcinoma HGNC:9871 Homo sapiens (human) 5921 RASA1
  • PMID:8275088
  • RGD:7240710
DOID:5517 stomach carcinoma HGNC:7527 Homo sapiens (human) 4595 MUTYH
  • PMID:15273732
DOID:13241 Behcet's disease HGNC:11365 Homo sapiens (human) 6775 STAT4
  • PMID:20438790
  • PMID:23001997
DOID:0070467 carpal tunnel syndrome 2 HGNC:2227 Homo sapiens (human) 1311 COMP
  • RGD:7240710
DOID:0111212 autosomal dominant distal hereditary motor neuronopathy 9 HGNC:12729 Homo sapiens (human) 7453 WARS1
  • RGD:7240710
DOID:0081182 autosomal recessive intellectual developmental disorder 6 HGNC:4580 Homo sapiens (human) 2898 GRIK2
  • RGD:7240710
DOID:0050211 swine influenza HGNC:8978 Homo sapiens (human) 5294 PIK3CG
  • PMID:29867955
DOID:2256 osteochondrodysplasia HGNC:2187 Homo sapiens (human) 1302 COL11A2
  • PMID:10677296
DOID:332 amyotrophic lateral sclerosis HGNC:613 Homo sapiens (human) 348 APOE
  • PMID:8899655

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International Collaboration

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