Table Filtering
Other Information
Release Statistics Download
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 65576 - 65600 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:1380 endometrial cancer HGNC:10839 Homo sapiens (human) 6462 SHBG
  • PMID:17315164
DOID:2367 neuroaxonal dystrophy HGNC:9039 Homo sapiens (human) 8398 PLA2G6
  • PMID:17033970
  • PMID:19138334
DOID:0110917 hereditary spherocytosis type 2 HGNC:11274 Homo sapiens (human) 6710 SPTB
  • RGD:7240710
DOID:14004 thoracic aortic aneurysm HGNC:29673 Homo sapiens (human) 8076 MFAP5
  • RGD:7240710
DOID:2957 pulmonary tuberculosis HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:19199550
DOID:1324 lung cancer HGNC:12828 Homo sapiens (human) 7515 XRCC1
  • PMID:15705867
  • PMID:16652158
  • PMID:17531525
  • PMID:17952468
  • PMID:19061777
  • PMID:24935603
  • PMID:25038912
  • PMID:25584213
  • PMID:27323144
DOID:8544 chronic fatigue syndrome HGNC:4942 Homo sapiens (human) 3117 HLA-DQA1
  • PMID:16049290
DOID:0080925 cytochrome P450 oxidoreductase deficiency HGNC:9208 Homo sapiens (human) 5447 POR
  • RGD:7240710
DOID:5683 hereditary breast ovarian cancer syndrome HGNC:9820 Homo sapiens (human) 5889 RAD51C
  • RGD:7240710
DOID:0081221 autosomal recessive intellectual developmental disorder 59 HGNC:6050 Homo sapiens (human) 3612 IMPA1
  • RGD:7240710
DOID:9538 multiple myeloma HGNC:12680 Homo sapiens (human) 7422 VEGFA
  • PMID:24687381
DOID:0060251 sclerosteosis HGNC:13771 Homo sapiens (human) 50964 SOST
  • PMID:11179006
DOID:0111189 distal myopathy 3 HGNC:5031 Homo sapiens (human) 3178 HNRNPA1
  • RGD:7240710
DOID:4927 Klatskin's tumor HGNC:22950 Homo sapiens (human) 80243 PREX2
  • PMID:33387086
DOID:8549 chronic ulcer of skin HGNC:7176 Homo sapiens (human) 4318 MMP9
  • PMID:21455563
DOID:0070330 multiple mitochondrial dysfunctions syndrome HGNC:4208 Homo sapiens (human) 2653 GCSH
  • RGD:7240710
DOID:10487 Hirschsprung's disease HGNC:12789 Homo sapiens (human) 7479 WNT8B
  • PMID:20972907
DOID:0112205 developmental and epileptic encephalopathy 69 HGNC:1392 Homo sapiens (human) 777 CACNA1E
  • RGD:7240710
DOID:13641 exfoliation syndrome HGNC:7176 Homo sapiens (human) 4318 MMP9
  • PMID:20808730
DOID:8947 diabetic retinopathy HGNC:12711 Homo sapiens (human) 9559 VPS26A
  • PMID:28821857
DOID:1612 breast cancer HGNC:795 Homo sapiens (human) 472 ATM
  • PMID:11200774
  • RGD:7240710
DOID:0111548 ring dermoid of cornea HGNC:9005 Homo sapiens (human) 5308 PITX2
  • RGD:7240710
DOID:8552 chronic myeloid leukemia HGNC:53 Homo sapiens (human) 1244 ABCC2
  • PMID:25060527
DOID:3138 acanthosis nigricans HGNC:3690 Homo sapiens (human) 2261 FGFR3
  • PMID:10377013
  • PMID:18583390
DOID:0112004 immunodeficiency 71 HGNC:704 Homo sapiens (human) 10095 ARPC1B
  • RGD:7240710

About Release Notes Help Feedback

International Collaboration

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.1.0

Last updated: December 9, 2024