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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 70151 - 70175 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:9744 type 1 diabetes mellitus HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:19120272
DOID:4586 familial meningioma HGNC:8800 Homo sapiens (human) 5155 PDGFB
  • RGD:7240710
DOID:0014667 disease of metabolism HGNC:7652 Homo sapiens (human) 4683 NBN
  • PMID:9590180
DOID:0060901 lymphoplasmacytic lymphoma HGNC:6018 Homo sapiens (human) 3569 IL6
  • PMID:19573080
DOID:0111062 familial hypobetalipoproteinemia 1 HGNC:603 Homo sapiens (human) 338 APOB
  • RGD:7240710
DOID:8947 diabetic retinopathy HGNC:1037 Homo sapiens (human) 629 CFB
  • PMID:23864767
DOID:7148 rheumatoid arthritis HGNC:288 Homo sapiens (human) 155 ADRB3
  • PMID:12739037
DOID:10825 essential hypertension HGNC:243 Homo sapiens (human) 118 ADD1
  • RGD:7240710
DOID:0080950 alopecia-mental retardation syndrome 4 HGNC:6708 Homo sapiens (human) 4047 LSS
  • RGD:7240710
DOID:1909 melanoma HGNC:3437 Homo sapiens (human) 2073 ERCC5
  • PMID:21390047
DOID:3907 lung squamous cell carcinoma HGNC:2597 Homo sapiens (human) 1545 CYP1B1
  • PMID:10739169
DOID:0050635 alternating hemiplegia of childhood HGNC:800 Homo sapiens (human) 477 ATP1A2
  • RGD:7240710
DOID:3083 chronic obstructive pulmonary disease HGNC:3327 Homo sapiens (human) 2006 ELN
  • PMID:16081882
DOID:0080030 spondyloepimetaphyseal dysplasia, Missouri type HGNC:7159 Homo sapiens (human) 4322 MMP13
  • RGD:7240710
DOID:0060770 dextro-looped transposition of the great arteries HGNC:10937 Homo sapiens (human) 6573 SLC19A1
  • PMID:22868813
DOID:11372 megacolon RGD:2536 Rattus norvegicus (Norway rat) 50672 Ednrb
  • PMID:8570650
DOID:0110158 Charcot-Marie-Tooth disease type 2I HGNC:7225 Homo sapiens (human) 4359 MPZ
  • RGD:7240710
DOID:2256 osteochondrodysplasia HGNC:2227 Homo sapiens (human) 1311 COMP
  • PMID:7670471
  • PMID:7670472
DOID:0050741 alcohol dependence HGNC:4083 Homo sapiens (human) 2562 GABRB3
  • PMID:14745296
DOID:0110028 age related macular degeneration 5 HGNC:3438 Homo sapiens (human) 2074 ERCC6
  • RGD:7240710
DOID:3526 cerebral infarction HGNC:9403 Homo sapiens (human) 5583 PRKCH
  • RGD:7240710
DOID:9261 nasopharynx carcinoma HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:33616746
DOID:234 colon adenocarcinoma HGNC:11362 Homo sapiens (human) 6772 STAT1
  • PMID:22121102
DOID:1287 cardiovascular system disease HGNC:3662 Homo sapiens (human) 2244 FGB
  • PMID:18278190
DOID:0081122 Catel Manzke syndrome HGNC:20324 Homo sapiens (human) 23483 TGDS
  • RGD:7240710

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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