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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 11326 - 11350 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:0090056 dystonia 12 HGNC:9039 Homo sapiens (human) 8398 PLA2G6
  • PMID:19087156
DOID:9296 cleft lip HGNC:9202 Homo sapiens (human) 10585 POMT1
  • PMID:18640039
DOID:83 cataract HGNC:8125 Homo sapiens (human) 4968 OGG1
  • PMID:22306120
DOID:12849 autistic disorder HGNC:10982 Homo sapiens (human) 8604 SLC25A12
  • PMID:15056512
DOID:446 primary hyperaldosteronism HGNC:2592 Homo sapiens (human) 1585 CYP11B2
  • PMID:1731223
DOID:0080784 urinary tract infection HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:19543401
DOID:4448 macular degeneration HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:15829498
  • PMID:18172114
  • PMID:19628747
DOID:0080738 Ehlers-Danlos syndrome spondylodysplastic type 1 HGNC:930 Homo sapiens (human) 11285 B4GALT7
  • RGD:7240710
DOID:9993 hypoglycemia HGNC:392 Homo sapiens (human) 208 AKT2
  • PMID:21979934
DOID:4511 breast angiosarcoma HGNC:8975 Homo sapiens (human) 5290 PIK3CA
  • PMID:32123305
DOID:684 hepatocellular carcinoma HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:26890368
DOID:182 calcinosis HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:17825092
DOID:0070262 congenital disorder of glycosylation type IIj HGNC:18620 Homo sapiens (human) 25839 COG4
  • RGD:7240710
DOID:2596 larynx cancer HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:23516596
DOID:2747 glycogen storage disease HGNC:9386 Homo sapiens (human) 51422 PRKAG2
  • PMID:15877279
DOID:10825 essential hypertension HGNC:5208 Homo sapiens (human) 3290 HSD11B1
  • PMID:26671915
DOID:2986 IgA glomerulonephritis HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:12566518
DOID:5419 schizophrenia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:15927374
DOID:4362 cervical cancer HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:19823053
DOID:0111234 congenital muscular dystrophy-dystroglycanopathy A7 HGNC:37276 Homo sapiens (human) 729920 CRPPA
  • RGD:7240710
DOID:3526 cerebral infarction HGNC:6623 Homo sapiens (human) 9388 LIPG
  • PMID:17016617
DOID:12205 dengue disease HGNC:1641 Homo sapiens (human) 30835 CD209
  • PMID:16274635
  • RGD:7240710
DOID:9261 nasopharynx carcinoma HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:26582733
DOID:684 hepatocellular carcinoma HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:21907168
DOID:8986 narcolepsy HGNC:1938 Homo sapiens (human) 1120 CHKB
  • PMID:18820697

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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