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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 64701 - 64725 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:332 amyotrophic lateral sclerosis HGNC:11741 Homo sapiens (human) 7019 TFAM
  • PMID:22354563
DOID:0080337 mitochondrial DNA depletion syndrome 15 HGNC:11741 Homo sapiens (human) 7019 TFAM
  • RGD:7240710
DOID:12858 Huntington's disease HGNC:11741 Homo sapiens (human) 7019 TFAM
  • PMID:21595933
DOID:1824 status epilepticus HGNC:11741 Homo sapiens (human) 7019 TFAM
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:11741 Homo sapiens (human) 7019 TFAM
  • PMID:17537576
  • PMID:21799244
DOID:9970 obesity HGNC:11741 Homo sapiens (human) 7019 TFAM
  • MGI:6194238
  • PMID:21862610
DOID:14330 Parkinson's disease HGNC:11741 Homo sapiens (human) 7019 TFAM
  • MGI:6194238
  • PMID:17537576
  • PMID:18248889
  • PMID:19925850
DOID:2355 anemia HGNC:11740 Homo sapiens (human) 7018 TF
  • MGI:6194238
  • PMID:23680589
DOID:10976 membranous glomerulonephritis HGNC:11740 Homo sapiens (human) 7018 TF
  • PMID:22328173
DOID:2921 glomerulonephritis HGNC:11740 Homo sapiens (human) 7018 TF
  • PMID:22607047
DOID:4195 hyperglycemia HGNC:11740 Homo sapiens (human) 7018 TF
  • PMID:16936158
DOID:11758 iron deficiency anemia HGNC:11740 Homo sapiens (human) 7018 TF
  • PMID:11703331
DOID:9970 obesity HGNC:11740 Homo sapiens (human) 7018 TF
  • MGI:6194238
DOID:0050649 atransferrinemia HGNC:11740 Homo sapiens (human) 7018 TF
  • MGI:6194238
  • RGD:7240710
DOID:0050425 restless legs syndrome HGNC:11740 Homo sapiens (human) 7018 TF
  • PMID:23369046
DOID:77 gastrointestinal system disease HGNC:11740 Homo sapiens (human) 7018 TF
  • PMID:23055815
DOID:10763 hypertension HGNC:11740 Homo sapiens (human) 7018 TF
  • PMID:14974364
DOID:9744 type 1 diabetes mellitus HGNC:11740 Homo sapiens (human) 7018 TF
  • PMID:22861364
DOID:2237 hepatitis HGNC:11740 Homo sapiens (human) 7018 TF
  • MGI:6194238
DOID:0060419 chromosome 3q29 microdeletion syndrome HGNC:11740 Homo sapiens (human) 7018 TF
  • MGI:6194238
DOID:0050685 small cell carcinoma HGNC:11730 Homo sapiens (human) 7015 TERT
  • PMID:24761905
DOID:9261 nasopharynx carcinoma HGNC:11730 Homo sapiens (human) 7015 TERT
  • PMID:26621837
DOID:3910 lung adenocarcinoma HGNC:11730 Homo sapiens (human) 7015 TERT
  • PMID:19955392
  • PMID:23738012
  • PMID:23908149
  • PMID:24761905
  • PMID:31935503
DOID:8991 cervix uteri carcinoma in situ HGNC:11730 Homo sapiens (human) 7015 TERT
  • PMID:17644806
DOID:11054 urinary bladder cancer HGNC:11730 Homo sapiens (human) 7015 TERT
  • PMID:17644139

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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