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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 8051 - 8075 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:8577 ulcerative colitis HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:20186929
DOID:0060060 non-Hodgkin lymphoma HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:25016003
DOID:3717 gastric adenocarcinoma HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:24228025
  • PMID:27957666
DOID:2527 nephrosis HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:22046528
DOID:9538 multiple myeloma HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:8599825
DOID:2738 pseudoxanthoma elasticum HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:17693525
DOID:8552 chronic myeloid leukemia HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:25436036
DOID:12858 Huntington's disease HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:18588971
DOID:9119 acute myeloid leukemia HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:22930375
  • PMID:26823947
  • PMID:26950655
DOID:11714 gestational diabetes HGNC:4553 Homo sapiens (human) 2876 GPX1
  • MGI:6194238
DOID:0050083 Keshan disease HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:21055077
DOID:0050889 non-syndromic intellectual disability HGNC:4551 Homo sapiens (human) 9524 TECR
  • MGI:6194238
DOID:0081188 autosomal recessive intellectual developmental disorder 14 HGNC:4551 Homo sapiens (human) 9524 TECR
  • RGD:7240710
DOID:11054 urinary bladder cancer HGNC:451 Homo sapiens (human) 23600 AMACR
  • PMID:18648853
DOID:3459 breast carcinoma HGNC:451 Homo sapiens (human) 23600 AMACR
  • PMID:15941950
DOID:0060602 alpha-methylacyl-CoA racemase deficiency HGNC:451 Homo sapiens (human) 23600 AMACR
  • MGI:6194238
  • RGD:7240710
DOID:8634 prostate carcinoma in situ HGNC:451 Homo sapiens (human) 23600 AMACR
  • PMID:18343427
DOID:0111068 congenital bile acid synthesis defect 4 HGNC:451 Homo sapiens (human) 23600 AMACR
  • RGD:7240710
DOID:4450 renal cell carcinoma HGNC:451 Homo sapiens (human) 23600 AMACR
  • PMID:14707866
DOID:0080932 primary localized cutaneous amyloidosis 3 HGNC:4462 Homo sapiens (human) 10457 GPNMB
  • RGD:7240710
DOID:3454 brain infarction HGNC:4462 Homo sapiens (human) 10457 GPNMB
  • MGI:6194238
DOID:0060680 pigment dispersion syndrome HGNC:4462 Homo sapiens (human) 10457 GPNMB
  • MGI:6194238
DOID:2861 congenital nonspherocytic hemolytic anemia HGNC:4458 Homo sapiens (human) 2821 GPI
  • MGI:6194238
  • PMID:17041899
  • PMID:9446754
DOID:14330 Parkinson's disease HGNC:4458 Homo sapiens (human) 2821 GPI
  • MGI:6194238
DOID:9119 acute myeloid leukemia HGNC:4458 Homo sapiens (human) 2821 GPI
  • PMID:6589021

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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