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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 70301 - 70325 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:3717 gastric adenocarcinoma HGNC:450 Homo sapiens (human) 60529 ALX4
  • PMID:27895854
DOID:1324 lung cancer HGNC:450 Homo sapiens (human) 60529 ALX4
  • PMID:24037716
DOID:2340 craniosynostosis HGNC:450 Homo sapiens (human) 60529 ALX4
  • RGD:7240710
DOID:4926 bronchiolo-alveolar adenocarcinoma HGNC:450 Homo sapiens (human) 60529 ALX4
  • PMID:24037716
DOID:0112038 non-syndromic X-linked intellectual disability 1 HGNC:450 Homo sapiens (human) 60529 ALX4
  • MGI:6194238
DOID:0060285 parietal foramina HGNC:450 Homo sapiens (human) 60529 ALX4
  • MGI:6194238
  • RGD:7240710
DOID:0081046 frontonasal dysplasia 2 HGNC:450 Homo sapiens (human) 60529 ALX4
  • RGD:7240710
DOID:9256 colorectal cancer HGNC:450 Homo sapiens (human) 60529 ALX4
  • PMID:17101318
  • PMID:26918234
DOID:684 hepatocellular carcinoma HGNC:450 Homo sapiens (human) 60529 ALX4
  • MGI:6194238
  • PMID:28081728
  • PMID:31132711
DOID:14213 hypophosphatasia HGNC:438 Homo sapiens (human) 249 ALPL
  • PMID:8406453
DOID:4676 uremia HGNC:438 Homo sapiens (human) 249 ALPL
  • MGI:6194238
DOID:9452 steatotic liver disease HGNC:438 Homo sapiens (human) 249 ALPL
  • PMID:16197789
DOID:0110914 infantile hypophosphatasia HGNC:438 Homo sapiens (human) 249 ALPL
  • MGI:6194238
  • RGD:7240710
DOID:2349 arteriosclerosis HGNC:438 Homo sapiens (human) 249 ALPL
  • PMID:17010978
DOID:13809 familial combined hyperlipidemia HGNC:438 Homo sapiens (human) 249 ALPL
  • PMID:16336518
DOID:0110913 adult hypophosphatasia HGNC:438 Homo sapiens (human) 249 ALPL
  • MGI:6194238
  • RGD:7240710
DOID:8719 in situ carcinoma HGNC:438 Homo sapiens (human) 249 ALPL
  • PMID:10547581
DOID:0110915 childhood hypophosphatasia HGNC:438 Homo sapiens (human) 249 ALPL
  • MGI:6194238
  • RGD:7240710
DOID:0080326 familial hypertrophic cardiomyopathy HGNC:17574 Homo sapiens (human) 57538 ALPK3
  • RGD:7240710
DOID:0050589 inflammatory bowel disease HGNC:437 Homo sapiens (human) 248 ALPI
  • PMID:29567797
DOID:8778 Crohn's disease HGNC:437 Homo sapiens (human) 248 ALPI
  • PMID:22783049
DOID:8577 ulcerative colitis HGNC:437 Homo sapiens (human) 248 ALPI
  • PMID:22783049
DOID:3770 pulmonary fibrosis HGNC:435 Homo sapiens (human) 240 ALOX5
  • PMID:8621765
DOID:2316 brain ischemia HGNC:435 Homo sapiens (human) 240 ALOX5
  • MGI:6194238
DOID:4947 cholangiocarcinoma HGNC:435 Homo sapiens (human) 240 ALOX5
  • PMID:18507031

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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