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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 67326 - 67350 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:0080297 Coffin-Siris syndrome 6 HGNC:18037 Homo sapiens (human) 196528 ARID2
  • RGD:7240710
DOID:12704 ataxia telangiectasia HGNC:959 Homo sapiens (human) 581 BAX
  • PMID:19898928
DOID:0060837 isolated microphthalmia 5 HGNC:18121 Homo sapiens (human) 83552 MFRP
  • PMID:19753314
  • RGD:7240710
DOID:1307 dementia HGNC:6701 Homo sapiens (human) 4043 LRPAP1
  • PMID:18721259
DOID:0080447 developmental and epileptic encephalopathy 43 HGNC:4083 Homo sapiens (human) 2562 GABRB3
  • RGD:7240710
DOID:4947 cholangiocarcinoma HGNC:53 Homo sapiens (human) 1244 ABCC2
  • PMID:19451719
DOID:1319 brain cancer HGNC:11730 Homo sapiens (human) 7015 TERT
  • PMID:26014354
DOID:13241 Behcet's disease HGNC:40 Homo sapiens (human) 5243 ABCB1
  • PMID:22705826
DOID:4448 macular degeneration HGNC:34 Homo sapiens (human) 24 ABCA4
  • PMID:9295268
DOID:0112056 X-linked intellectual disability-short stature-overweight syndrome HGNC:19073 Homo sapiens (human) 57187 THOC2
  • RGD:7240710
DOID:0070114 Niemann-Pick disease type C2 HGNC:14537 Homo sapiens (human) 10577 NPC2
  • RGD:7240710
DOID:1883 hepatitis C HGNC:1606 Homo sapiens (human) 1234 CCR5
  • PMID:14673528
  • PMID:27304910
  • RGD:7240710
DOID:0111640 autosomal recessive nonsyndromic deafness 111 HGNC:3496 Homo sapiens (human) 10205 MPZL2
  • RGD:7240710
DOID:12361 Graves' disease HGNC:19100 Homo sapiens (human) 149233 IL23R
  • PMID:18073300
  • PMID:19021011
DOID:10923 sickle cell anemia HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:20831548
DOID:0060669 cerebral cavernous malformation HGNC:9204 Homo sapiens (human) 5444 PON1
  • PMID:26122242
DOID:0110652 long QT syndrome 11 HGNC:379 Homo sapiens (human) 10142 AKAP9
  • RGD:7240710
DOID:0050773 paraganglioma HGNC:10682 Homo sapiens (human) 6391 SDHC
  • PMID:11062460
  • RGD:7240710
DOID:11984 hypertrophic cardiomyopathy HGNC:11947 Homo sapiens (human) 7137 TNNI3
  • PMID:15698845
DOID:0060610 megacystis-microcolon-intestinal hypoperistalsis syndrome HGNC:6647 Homo sapiens (human) 25802 LMOD1
  • RGD:7240710
DOID:1793 pancreatic cancer HGNC:1100 Homo sapiens (human) 672 BRCA1
  • RGD:7240710
DOID:1307 dementia HGNC:5465 Homo sapiens (human) 3480 IGF1R
  • PMID:16983186
DOID:0111076 progressive familial heart block type IB HGNC:17993 Homo sapiens (human) 54795 TRPM4
  • RGD:7240710
DOID:417 autoimmune disease HGNC:18187 Homo sapiens (human) 54414 SIAE
  • RGD:7240710
DOID:6432 pulmonary hypertension HGNC:9611 Homo sapiens (human) 5747 PTK2
  • PMID:16244766

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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