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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 5401 - 5425 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:1564 fungal infectious disease HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:24886325
DOID:3526 cerebral infarction HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:11596779
DOID:3908 lung non-small cell carcinoma HGNC:1455 Homo sapiens (human) 811 CALR
  • PMID:26842877
  • PMID:29228584
DOID:11054 urinary bladder cancer HGNC:4922 Homo sapiens (human) 3098 HK1
  • MGI:6194238
DOID:12361 Graves' disease HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:17980001
DOID:9352 type 2 diabetes mellitus HGNC:11240 Homo sapiens (human) 8877 SPHK1
  • PMID:17265031
DOID:9719 neovascular inflammatory vitreoretinopathy HGNC:6697 Homo sapiens (human) 4041 LRP5
  • PMID:15346351
DOID:4947 cholangiocarcinoma HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • PMID:19621664
DOID:0050866 oral squamous cell carcinoma HGNC:1455 Homo sapiens (human) 811 CALR
  • PMID:28599487
DOID:576 proteinuria HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
  • PMID:10193250
DOID:0050741 alcohol dependence HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
  • PMID:29912265
DOID:3071 gliosarcoma HGNC:9604 Homo sapiens (human) 5742 PTGS1
  • MGI:6194238
DOID:0050524 maturity-onset diabetes of the young HGNC:4923 Homo sapiens (human) 3099 HK2
  • MGI:6194238
DOID:3526 cerebral infarction HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • MGI:6194238
DOID:9970 obesity HGNC:4141 Homo sapiens (human) 2597 GAPDH
  • MGI:6194238
DOID:684 hepatocellular carcinoma HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
  • PMID:15800977
  • PMID:24720952
  • PMID:24759835
DOID:9452 steatotic liver disease HGNC:4803 Homo sapiens (human) 3032 HADHB
  • MGI:6194238
DOID:10591 pre-eclampsia HGNC:386 Homo sapiens (human) 8644 AKR1C3
  • MGI:6194238
  • PMID:19681734
DOID:0080855 Parkinsonism HGNC:4243 Homo sapiens (human) 2674 GFRA1
  • MGI:6194238
DOID:2349 arteriosclerosis HGNC:381 Homo sapiens (human) 231 AKR1B1
  • PMID:16127462
DOID:0050570 congenital disorder of glycosylation type I HGNC:19358 Homo sapiens (human) 79087 ALG12
  • MGI:6194238
DOID:0111240 congenital muscular dystrophy-dystroglycanopathy type A2 HGNC:19743 Homo sapiens (human) 29954 POMT2
  • RGD:7240710
DOID:3146 lipid metabolism disorder HGNC:2859 Homo sapiens (human) 1718 DHCR24
  • PMID:11519011
DOID:0112147 retinitis pigmentosa 90 HGNC:5384 Homo sapiens (human) 3419 IDH3A
  • RGD:7240710
DOID:4194 glucose metabolism disease HGNC:8976 Homo sapiens (human) 5291 PIK3CB
  • MGI:6194238

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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