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 63201 - 63225 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:10487 Hirschsprung's disease HGNC:1628 Homo sapiens (human) 929 CD14
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:10195920
  • PMID:14587643
  • PMID:17436151
DOID:3407 carotid artery disease HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:15640605
  • PMID:16873708
DOID:824 periodontitis HGNC:1628 Homo sapiens (human) 929 CD14
  • MGI:6194238
DOID:10763 hypertension HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:22072187
DOID:0060036 intrinsic cardiomyopathy HGNC:1620 Homo sapiens (human) 908 CCT6A
  • MGI:6194238
DOID:0050548 hereditary sensory neuropathy SGD:S000002302 Saccharomyces cerevisiae S288C 851412 CCT4
  • MGI:6194238
DOID:0060036 intrinsic cardiomyopathy SGD:S000002302 Saccharomyces cerevisiae S288C 851412 CCT4
  • MGI:6194238
DOID:0060036 intrinsic cardiomyopathy HGNC:1617 Homo sapiens (human) 10575 CCT4
  • MGI:6194238
DOID:0050548 hereditary sensory neuropathy HGNC:1617 Homo sapiens (human) 10575 CCT4
  • MGI:6194238
DOID:0060036 intrinsic cardiomyopathy HGNC:1616 Homo sapiens (human) 7203 CCT3
  • MGI:6194238
DOID:1508 candidiasis HGNC:1615 Homo sapiens (human) 10576 CCT2
  • MGI:6194238
DOID:14791 Leber congenital amaurosis HGNC:1615 Homo sapiens (human) 10576 CCT2
  • MGI:6194238
DOID:9975 cocaine dependence HGNC:29349 Homo sapiens (human) 401145 CCSER1
  • PMID:18438686
DOID:2841 asthma HGNC:1610 Homo sapiens (human) 10803 CCR9
  • PMID:16210593
DOID:552 pneumonia HGNC:1608 Homo sapiens (human) 1236 CCR7
  • PMID:16394278
DOID:13406 pulmonary sarcoidosis HGNC:1608 Homo sapiens (human) 1236 CCR7
  • PMID:12626344
DOID:12894 Sjogren's syndrome HGNC:1608 Homo sapiens (human) 1236 CCR7
  • MGI:6194238
DOID:418 systemic scleroderma HGNC:1607 Homo sapiens (human) 1235 CCR6
  • PMID:21742595
DOID:2986 IgA glomerulonephritis HGNC:1607 Homo sapiens (human) 1235 CCR6
  • PMID:23192593
DOID:8893 psoriasis HGNC:1607 Homo sapiens (human) 1235 CCR6
  • PMID:10843722
DOID:1564 fungal infectious disease HGNC:1607 Homo sapiens (human) 1235 CCR6
  • PMID:22287435
DOID:0060061 primary cutaneous T-cell non-Hodgkin lymphoma HGNC:1607 Homo sapiens (human) 1235 CCR6
  • PMID:22048239
DOID:224 transient cerebral ischemia HGNC:1607 Homo sapiens (human) 1235 CCR6
  • MGI:6194238
DOID:2920 membranoproliferative glomerulonephritis HGNC:1607 Homo sapiens (human) 1235 CCR6
  • MGI:6194238

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