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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 69576 - 69600 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0080322 polycystic kidney disease HGNC:6319 Homo sapiens (human) 11127 KIF3A
  • MGI:6194238
DOID:1934 dysostosis HGNC:6319 Homo sapiens (human) 11127 KIF3A
  • MGI:6194238
DOID:10325 silicosis HGNC:6319 Homo sapiens (human) 11127 KIF3A
  • MGI:6194238
  • PMID:32042332
DOID:9256 colorectal cancer HGNC:9682 Homo sapiens (human) 11122 PTPRT
  • PMID:30200630
DOID:3748 esophagus squamous cell carcinoma HGNC:9682 Homo sapiens (human) 11122 PTPRT
  • PMID:25967969
DOID:5419 schizophrenia MGI:2148258 Mus musculus (house mouse) 111174 Taar1
  • PMID:17212650
DOID:0081399 autosomal dominant distal hereditary motor neuronopathy 10 HGNC:19880 Homo sapiens (human) 11117 EMILIN1
  • RGD:7240710
DOID:0081292 traumatic brain injury HGNC:1985 Homo sapiens (human) 11113 CIT
  • MGI:6194238
DOID:0070288 primary autosomal recessive microcephaly 17 HGNC:1985 Homo sapiens (human) 11113 CIT
  • RGD:7240710
DOID:10907 microcephaly HGNC:1985 Homo sapiens (human) 11113 CIT
  • MGI:6194238
DOID:11832 visual epilepsy HGNC:1985 Homo sapiens (human) 11113 CIT
  • MGI:6194238
DOID:0070297 primary microcephaly HGNC:1985 Homo sapiens (human) 11113 CIT
  • PMID:27503289
  • PMID:27519304
DOID:1826 epilepsy HGNC:1985 Homo sapiens (human) 11113 CIT
  • MGI:6194238
DOID:9252 amino acid metabolic disorder HGNC:4907 Homo sapiens (human) 11112 HIBADH
  • MGI:6194238
DOID:1793 pancreatic cancer HGNC:1925 Homo sapiens (human) 1111 CHEK1
  • PMID:18381943
DOID:14330 Parkinson's disease HGNC:236 Homo sapiens (human) 111 ADCY5
  • MGI:6194238
DOID:10763 hypertension HGNC:236 Homo sapiens (human) 111 ADCY5
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:236 Homo sapiens (human) 111 ADCY5
  • MGI:6194238
DOID:0111870 nonphotosensitive trichothiodystrophy 7 MGI:106314 Mus musculus (house mouse) 110960 Tars1
  • MGI:6194238
DOID:9252 amino acid metabolic disorder MGI:106314 Mus musculus (house mouse) 110960 Tars1
  • MGI:6194238
DOID:0111867 nonphotosensitive trichothiodystrophy MGI:106314 Mus musculus (house mouse) 110960 Tars1
  • MGI:6194238
DOID:8398 osteoarthritis HGNC:221 Homo sapiens (human) 11096 ADAMTS5
  • MGI:6194238
  • PMID:11801682
  • PMID:18240210
  • PMID:22961118
DOID:90 degenerative disc disease HGNC:221 Homo sapiens (human) 11096 ADAMTS5
  • MGI:6194238
DOID:12800 mucopolysaccharidosis VI HGNC:221 Homo sapiens (human) 11096 ADAMTS5
  • MGI:6194238
DOID:7148 rheumatoid arthritis HGNC:221 Homo sapiens (human) 11096 ADAMTS5
  • PMID:11801682

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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