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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 3326 - 3350 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:1612 breast cancer HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
  • PMID:26666818
  • RGD:7240710
DOID:1070 primary open angle glaucoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:23049825
DOID:0112182 mismatch repair cancer syndrome HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:28218421
DOID:2531 hematologic cancer HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:28387921
DOID:2671 transitional cell carcinoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:18270948
DOID:8725 vascular dementia HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
DOID:2998 testicular cancer HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
DOID:0081267 graft-versus-host disease HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:16393253
DOID:1350 paranasal sinus benign neoplasm HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:22575263
  • PMID:23369851
DOID:3717 gastric adenocarcinoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:30554333
DOID:0060074 ductal carcinoma in situ HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:17119686
DOID:2729 dyskeratosis congenita 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:9538 multiple myeloma HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:12745272
  • PMID:22261445
  • PMID:24611901
DOID:0081292 traumatic brain injury HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
DOID:0002116 pterygium HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:19065760
DOID:3969 thyroid gland papillary carcinoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:19286843
DOID:705 Leber hereditary optic neuropathy HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:15838728
DOID:4971 myelofibrosis HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:26123119
DOID:684 hepatocellular carcinoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
  • PMID:29749584
  • RGD:7240710
DOID:5940 malignant peripheral nerve sheath tumor HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
DOID:11650 bronchopulmonary dysplasia HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
DOID:9261 nasopharynx carcinoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:9929165
  • RGD:7240710
DOID:9256 colorectal cancer HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
  • PMID:28910954
  • PMID:29286614
  • RGD:7240710
DOID:3393 coronary artery disease HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:29482350

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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