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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 1851 - 1875 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:10964 cholesteatoma of middle ear HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:9455944
DOID:10811 nasal cavity cancer HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:19950227
DOID:10534 stomach cancer HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:27323394
  • PMID:28387921
DOID:4926 bronchiolo-alveolar adenocarcinoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
DOID:1380 endometrial cancer HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
DOID:0050834 CHARGE syndrome HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
DOID:12894 Sjogren's syndrome HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
  • PMID:22703762
DOID:8725 vascular dementia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:11273064
DOID:10241 thalassemia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:11732868
DOID:9408 acute myocardial infarction HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:0080750 erythema nodosum HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:12198697
DOID:9588 encephalitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:8283 peritonitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
  • PMID:26601826
DOID:9008 psoriatic arthritis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:9326391
DOID:0081120 Graves ophthalmopathy HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:15219383
  • PMID:16191343
  • PMID:8444271
DOID:1407 anterior uveitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:15851552
DOID:1227 neutropenia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:15986200
DOID:0050589 inflammatory bowel disease HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:12306 vitiligo HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:16911396
DOID:8505 dermatitis herpetiformis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:7914110
DOID:12930 dilated cardiomyopathy HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:14984724
DOID:0050697 chorioamnionitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:15128916
DOID:12849 autistic disorder HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:26418275
DOID:874 bacterial pneumonia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:10650487
  • PMID:7546648
DOID:10923 sickle cell anemia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:8140855

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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: August 19, 2024