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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 67576 - 67600 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:0112297 spondylometaphyseal dysplasia corner fracture type HGNC:3778 Homo sapiens (human) 2335 FN1
  • RGD:7240710
DOID:0050456 Buruli ulcer disease HGNC:10907 Homo sapiens (human) 6556 SLC11A1
  • RGD:7240710
DOID:12365 malaria HGNC:4702 Homo sapiens (human) 2993 GYPA
  • RGD:7240710
DOID:9970 obesity HGNC:2357 Homo sapiens (human) 1394 CRHR1
  • PMID:14724656
DOID:988 mitral valve prolapse HGNC:9052 Homo sapiens (human) 5328 PLAU
  • PMID:15262029
DOID:0050742 nicotine dependence HGNC:281 Homo sapiens (human) 150 ADRA2A
  • PMID:17612790
DOID:234 colon adenocarcinoma HGNC:959 Homo sapiens (human) 581 BAX
  • PMID:9020077
DOID:0110367 retinitis pigmentosa 38 HGNC:7027 Homo sapiens (human) 10461 MERTK
  • RGD:7240710
DOID:2043 hepatitis B HGNC:12530 Homo sapiens (human) 54658 UGT1A1
  • PMID:29239247
DOID:0081442 blepharophimosis-impaired intellectual development syndrome HGNC:11098 Homo sapiens (human) 6595 SMARCA2
  • RGD:7240710
DOID:9277 primary cerebellar degeneration HGNC:24624 Homo sapiens (human) 64374 SIL1
  • RGD:7240710
DOID:0050741 alcohol dependence HGNC:4087 Homo sapiens (human) 2566 GABRG2
  • PMID:15630072
DOID:12449 aplastic anemia HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1
  • PMID:12070003
  • PMID:24979673
  • PMID:7994040
DOID:0112318 Schindler disease type 1 HGNC:7631 Homo sapiens (human) 4668 NAGA
  • RGD:7240710
DOID:0111017 cone-rod dystrophy 10 HGNC:10729 Homo sapiens (human) 64218 SEMA4A
  • RGD:7240710
DOID:3907 lung squamous cell carcinoma HGNC:9177 Homo sapiens (human) 5426 POLE
  • PMID:29650000
DOID:2048 autoimmune hepatitis HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1
  • PMID:10573514
  • PMID:11182227
  • PMID:15763345
  • PMID:17050030
DOID:3908 lung non-small cell carcinoma HGNC:40 Homo sapiens (human) 5243 ABCB1
  • PMID:17534875
DOID:1993 rectum cancer HGNC:12833 Homo sapiens (human) 7520 XRCC5
  • PMID:26735576
DOID:0050647 Arts syndrome HGNC:9462 Homo sapiens (human) 5631 PRPS1
  • RGD:7240710
DOID:0080600 COVID-19 HGNC:1228 Homo sapiens (human) 710 SERPING1
  • PMID:32747830
DOID:2747 glycogen storage disease HGNC:11006 Homo sapiens (human) 6514 SLC2A2
  • PMID:9354798
DOID:3407 carotid artery disease HGNC:6709 Homo sapiens (human) 4049 LTA
  • PMID:17065682
DOID:11383 cryptorchidism HGNC:644 Homo sapiens (human) 367 AR
  • PMID:15472213
  • PMID:15757859
DOID:0080785 Brown-Vialetto-Van Laere syndrome 1 HGNC:16187 Homo sapiens (human) 113278 SLC52A3
  • RGD:7240710

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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