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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 68876 - 68900 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:10652 Alzheimer's disease HGNC:29 Homo sapiens (human) 19 ABCA1
  • PMID:15024730
DOID:10652 Alzheimer's disease HGNC:12680 Homo sapiens (human) 7422 VEGFA
  • PMID:15732116
DOID:0110167 Charcot-Marie-Tooth disease axonal type 2K HGNC:14201 Homo sapiens (human) 56704 JPH1
  • RGD:7240710
DOID:3393 coronary artery disease HGNC:9232 Homo sapiens (human) 5465 PPARA
  • PMID:16043164
DOID:12859 choreatic disease HGNC:4942 Homo sapiens (human) 3117 HLA-DQA1
  • PMID:17559688
DOID:0111801 syndromic microphthalmia 3 HGNC:11195 Homo sapiens (human) 6657 SOX2
  • RGD:7240710
DOID:0050567 orofacial cleft HGNC:15814 Homo sapiens (human) 55902 ACSS2
  • PMID:27229527
  • PMID:28543373
DOID:8986 narcolepsy HGNC:7197 Homo sapiens (human) 4340 MOG
  • RGD:7240710
DOID:10003 sensorineural hearing loss HGNC:3522 Homo sapiens (human) 2070 EYA4
  • PMID:15735644
DOID:0070286 primary autosomal recessive microcephaly 3 HGNC:18672 Homo sapiens (human) 55755 CDK5RAP2
  • PMID:17764569
  • PMID:23587236
  • RGD:7240710
DOID:0050753 cerebellar ataxia HGNC:29168 Homo sapiens (human) 23322 RPGRIP1L
  • PMID:17558409
DOID:674 cleft palate HGNC:7432 Homo sapiens (human) 4522 MTHFD1
  • PMID:18661527
DOID:9452 steatotic liver disease HGNC:286 Homo sapiens (human) 154 ADRB2
  • PMID:11718682
DOID:5408 Paget's disease of bone HGNC:17142 Homo sapiens (human) 10133 OPTN
  • PMID:20436471
DOID:4752 multiple system atrophy HGNC:6367 Homo sapiens (human) 5653 KLK6
  • PMID:12928483
DOID:2154 nephroblastoma HGNC:1101 Homo sapiens (human) 675 BRCA2
  • PMID:15689453
  • RGD:7240710
DOID:1727 retinal vein occlusion HGNC:3542 Homo sapiens (human) 2153 F5
  • PMID:10511031
  • PMID:10634550
  • PMID:16113792
DOID:630 genetic disease HGNC:18622 Homo sapiens (human) 91949 COG7
  • PMID:15107842
DOID:0112180 urocanase deficiency HGNC:26444 Homo sapiens (human) 131669 UROC1
  • RGD:7240710
DOID:0050791 persistent Mullerian duct syndrome HGNC:464 Homo sapiens (human) 268 AMH
  • RGD:7240710
DOID:14735 hereditary angioedema HGNC:6383 Homo sapiens (human) 3827 KNG1
  • RGD:7240710
DOID:0111210 autosomal dominant distal hereditary motor neuronopathy 6 HGNC:28844 Homo sapiens (human) 81545 FBXO38
  • RGD:7240710
DOID:0111715 Schaaf-Yang syndrome HGNC:6814 Homo sapiens (human) 54551 MAGEL2
  • RGD:7240710
DOID:0081223 glycosylphosphatidylinositol biosynthesis defect 16 HGNC:8960 Homo sapiens (human) 5279 PIGC
  • RGD:7240710
DOID:7147 ankylosing spondylitis HGNC:14872 Homo sapiens (human) 54829 ASPN
  • PMID:20144272

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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