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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 64401 - 64425 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0070354 cataract 48 HGNC:11805 Homo sapiens (human) 7074 TIAM1
  • MGI:6194238
DOID:224 transient cerebral ischemia HGNC:11804 Homo sapiens (human) 7073 TIAL1
  • MGI:6194238
DOID:12510 retinal ischemia HGNC:11801 Homo sapiens (human) 7070 THY1
  • MGI:6194238
DOID:5679 retinal disease HGNC:11801 Homo sapiens (human) 7070 THY1
  • MGI:6194238
DOID:1891 optic nerve disease HGNC:118 Homo sapiens (human) 50 ACO2
  • MGI:6194238
DOID:331 central nervous system disease HGNC:118 Homo sapiens (human) 50 ACO2
  • MGI:6194238
DOID:0111442 optic atrophy 9 HGNC:118 Homo sapiens (human) 50 ACO2
  • MGI:6194238
  • RGD:7240710
DOID:14330 Parkinson's disease HGNC:118 Homo sapiens (human) 50 ACO2
  • MGI:6194238
DOID:1289 neurodegenerative disease HGNC:118 Homo sapiens (human) 50 ACO2
  • MGI:6194238
DOID:0050883 infantile cerebellar-retinal degeneration HGNC:118 Homo sapiens (human) 50 ACO2
  • MGI:6194238
  • RGD:7240710
DOID:4450 renal cell carcinoma HGNC:11796 Homo sapiens (human) 7067 THRA
  • PMID:11756220
DOID:1612 breast cancer HGNC:11796 Homo sapiens (human) 7067 THRA
  • PMID:12082618
DOID:0070128 congenital nongoitrous hypothyroidism 6 HGNC:11796 Homo sapiens (human) 7067 THRA
  • RGD:7240710
DOID:1459 hypothyroidism HGNC:11796 Homo sapiens (human) 7067 THRA
  • MGI:6194238
DOID:11633 thyroid hormone resistance syndrome HGNC:11796 Homo sapiens (human) 7067 THRA
  • MGI:6194238
DOID:5160 arteriosclerosis obliterans HGNC:11795 Homo sapiens (human) 7066 THPO
  • PMID:10822072
DOID:6432 pulmonary hypertension HGNC:11795 Homo sapiens (human) 7066 THPO
  • PMID:12487786
DOID:14115 toxic shock syndrome HGNC:11795 Homo sapiens (human) 7066 THPO
  • PMID:20467749
DOID:5082 liver cirrhosis HGNC:11795 Homo sapiens (human) 7066 THPO
  • PMID:9794189
DOID:1588 thrombocytopenia HGNC:11795 Homo sapiens (human) 7066 THPO
  • MGI:6194238
  • RGD:7240710
DOID:12449 aplastic anemia HGNC:11795 Homo sapiens (human) 7066 THPO
  • PMID:22686250
  • PMID:24085763
DOID:2224 essential thrombocythemia HGNC:11795 Homo sapiens (human) 7066 THPO
  • PMID:9425899
  • RGD:7240710
DOID:2228 thrombocytosis HGNC:11795 Homo sapiens (human) 7066 THPO
  • PMID:9694695
DOID:0080600 COVID-19 HGNC:11785 Homo sapiens (human) 7057 THBS1
  • PMID:32696007
DOID:4947 cholangiocarcinoma HGNC:11785 Homo sapiens (human) 7057 THBS1
  • PMID:11927969
  • PMID:12213730
  • PMID:16465407

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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