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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 65601 - 65625 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:1790 malignant mesothelioma HGNC:18420 Homo sapiens (human) 29072 SETD2
  • PMID:27834213
DOID:1324 lung cancer HGNC:3430 Homo sapiens (human) 2064 ERBB2
  • RGD:7240710
DOID:3908 lung non-small cell carcinoma HGNC:18170 Homo sapiens (human) 51727 CMPK1
  • PMID:21642870
DOID:0070296 primary autosomal recessive microcephaly HGNC:28952 Homo sapiens (human) 23310 NCAPD3
  • RGD:7240710
DOID:0111672 primary hyperoxaluria type 3 HGNC:25155 Homo sapiens (human) 112817 HOGA1
  • RGD:7240710
DOID:0110317 hypertrophic cardiomyopathy 11 HGNC:143 Homo sapiens (human) 70 ACTC1
  • RGD:7240710
DOID:1924 hypogonadism HGNC:4510 Homo sapiens (human) 84634 KISS1R
  • PMID:12944565
DOID:10534 stomach cancer HGNC:7527 Homo sapiens (human) 4595 MUTYH
  • RGD:7240710
DOID:12361 Graves' disease HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1
  • PMID:10468909
  • PMID:11272094
DOID:9352 type 2 diabetes mellitus HGNC:11005 Homo sapiens (human) 6513 SLC2A1
  • PMID:18613291
  • PMID:7516306
  • PMID:9789717
DOID:5844 myocardial infarction HGNC:6692 Homo sapiens (human) 4035 LRP1
  • PMID:12402342
DOID:3883 Lynch syndrome HGNC:11773 Homo sapiens (human) 7048 TGFBR2
  • PMID:28218421
DOID:9352 type 2 diabetes mellitus HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:24452036
DOID:0081101 nonautoimmune hyperthyroidism HGNC:12373 Homo sapiens (human) 7253 TSHR
  • PMID:18306976
  • RGD:7240710
DOID:10825 essential hypertension HGNC:2638 Homo sapiens (human) 1577 CYP3A5
  • RGD:7240710
DOID:0110272 cataract 40 HGNC:7820 Homo sapiens (human) 4810 NHS
  • RGD:7240710
DOID:3907 lung squamous cell carcinoma HGNC:11730 Homo sapiens (human) 7015 TERT
  • PMID:23908149
  • PMID:31935503
DOID:0081102 familial gestational hyperthyroidism HGNC:12373 Homo sapiens (human) 7253 TSHR
  • RGD:7240710
DOID:6846 familial melanoma HGNC:11730 Homo sapiens (human) 7015 TERT
  • RGD:7240710
DOID:0060639 permanent neonatal diabetes mellitus HGNC:59 Homo sapiens (human) 6833 ABCC8
  • RGD:7240710
DOID:0111732 Eiken syndrome HGNC:9608 Homo sapiens (human) 5745 PTH1R
  • PMID:15525660
  • RGD:7240710
DOID:0050475 Weill-Marchesani syndrome HGNC:6715 Homo sapiens (human) 4053 LTBP2
  • PMID:22539340
  • RGD:7240710
DOID:848 arthritis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:19395541
DOID:769 neuroblastoma HGNC:14234 Homo sapiens (human) 64324 NSD1
  • PMID:20018718
DOID:2560 morphine dependence HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:30211780

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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: December 9, 2024