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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 63676 - 63700 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0050834 CHARGE syndrome HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
DOID:7575 pancreatic intraductal papillary-mucinous neoplasm HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:28930868
DOID:3012 Li-Fraumeni syndrome HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
  • PMID:1631137
DOID:0050866 oral squamous cell carcinoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:27283772
DOID:0112182 mismatch repair cancer syndrome HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:28218421
DOID:5773 oral submucous fibrosis HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:23776093
DOID:2870 endometrial adenocarcinoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:1540970
DOID:2998 testicular cancer HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
DOID:0050745 diffuse large B-cell lymphoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
DOID:1909 melanoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:16094622
  • PMID:23568549
DOID:1035 aggressive NK-cell leukemia HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
DOID:0080199 colorectal carcinoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:29560751
DOID:0111503 Li-Fraumeni syndrome 1 HGNC:11998 Homo sapiens (human) 7157 TP53
  • RGD:7240710
DOID:705 Leber hereditary optic neuropathy HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:15838728
DOID:5940 malignant peripheral nerve sheath tumor HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
DOID:1350 paranasal sinus benign neoplasm HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:22575263
  • PMID:23369851
DOID:0001816 angiosarcoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
DOID:0050865 tongue squamous cell carcinoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
DOID:11650 bronchopulmonary dysplasia HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
DOID:7614 meninges sarcoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
DOID:13544 low tension glaucoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:20357201
DOID:1115 sarcoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
  • PMID:31089155
DOID:3748 esophagus squamous cell carcinoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:28789369
DOID:326 ischemia HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
DOID:0002116 pterygium HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:19065760

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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: December 9, 2024