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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 July 29, 2024
Displaying entries 11901 - 11925 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0070342 adult-onset type II citrullinemia HGNC:10983 Homo sapiens (human) 10165 SLC25A13
  • PMID:10369257
  • PMID:11153906
  • RGD:7240710
DOID:1852 intrahepatic cholestasis HGNC:10983 Homo sapiens (human) 10165 SLC25A13
  • MGI:6194238
DOID:10763 hypertension HGNC:18305 Homo sapiens (human) 10159 ATP6AP2
  • MGI:6194238
DOID:0112105 X-linked parkinsonism-spasticity syndrome HGNC:18305 Homo sapiens (human) 10159 ATP6AP2
  • RGD:7240710
DOID:0060309 syndromic X-linked intellectual disability HGNC:18305 Homo sapiens (human) 10159 ATP6AP2
  • MGI:6194238
DOID:0060806 syndromic X-linked intellectual disability Hedera type HGNC:18305 Homo sapiens (human) 10159 ATP6AP2
  • RGD:7240710
DOID:0050571 congenital disorder of glycosylation type II HGNC:18305 Homo sapiens (human) 10159 ATP6AP2
  • RGD:7240710
DOID:5212 congenital disorder of glycosylation HGNC:18305 Homo sapiens (human) 10159 ATP6AP2
  • MGI:6194238
DOID:0060227 Adams-Oliver syndrome MGI:2141669 Mus musculus (house mouse) 101351 Eogt
  • MGI:6194238
DOID:8893 psoriasis HGNC:30092 Homo sapiens (human) 10135 NAMPT
  • PMID:22151390
DOID:3407 carotid artery disease HGNC:30092 Homo sapiens (human) 10135 NAMPT
  • PMID:17283255
DOID:3393 coronary artery disease HGNC:30092 Homo sapiens (human) 10135 NAMPT
  • PMID:17283255
DOID:1074 kidney failure HGNC:30092 Homo sapiens (human) 10135 NAMPT
  • MGI:6194238
DOID:3525 middle cerebral artery infarction HGNC:30092 Homo sapiens (human) 10135 NAMPT
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:30092 Homo sapiens (human) 10135 NAMPT
  • MGI:6194238
DOID:6432 pulmonary hypertension HGNC:30092 Homo sapiens (human) 10135 NAMPT
  • MGI:6194238
  • PMID:28202489
DOID:224 transient cerebral ischemia HGNC:30092 Homo sapiens (human) 10135 NAMPT
  • MGI:6194238
  • PMID:25603815
DOID:9970 obesity HGNC:30092 Homo sapiens (human) 10135 NAMPT
  • PMID:17618961
DOID:824 periodontitis HGNC:30092 Homo sapiens (human) 10135 NAMPT
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:30092 Homo sapiens (human) 10135 NAMPT
  • PMID:16234302
  • PMID:18410550
DOID:2871 endometrial carcinoma HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:18519763
DOID:2349 arteriosclerosis HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:11326751
DOID:1612 breast cancer HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:17764565
  • PMID:8673923
DOID:3908 lung non-small cell carcinoma HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:11389090
DOID:3459 breast carcinoma HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:11389090

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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: August 19, 2024