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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 64476 - 64500 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:767 muscular atrophy HGNC:11776 Homo sapiens (human) 7050 TGIF1
  • MGI:6194238
DOID:10754 otitis media HGNC:11776 Homo sapiens (human) 7050 TGIF1
  • MGI:6194238
DOID:2870 endometrial adenocarcinoma HGNC:11774 Homo sapiens (human) 7049 TGFBR3
  • PMID:15745937
DOID:9352 type 2 diabetes mellitus HGNC:11773 Homo sapiens (human) 7048 TGFBR2
  • MGI:6194238
DOID:4947 cholangiocarcinoma HGNC:11773 Homo sapiens (human) 7048 TGFBR2
  • MGI:6194238
DOID:219 colon cancer HGNC:11773 Homo sapiens (human) 7048 TGFBR2
  • PMID:14988818
DOID:3587 pancreatic ductal carcinoma HGNC:11773 Homo sapiens (human) 7048 TGFBR2
  • PMID:10547197
DOID:3883 Lynch syndrome HGNC:11773 Homo sapiens (human) 7048 TGFBR2
  • PMID:28218421
DOID:3748 esophagus squamous cell carcinoma HGNC:11773 Homo sapiens (human) 7048 TGFBR2
  • RGD:7240710
DOID:557 kidney disease HGNC:11773 Homo sapiens (human) 7048 TGFBR2
  • MGI:6194238
DOID:1793 pancreatic cancer HGNC:11773 Homo sapiens (human) 7048 TGFBR2
  • PMID:11866987
  • PMID:18772397
  • PMID:9365135
  • PMID:9850059
DOID:0070273 hereditary nonpolyposis colorectal cancer type 6 HGNC:11773 Homo sapiens (human) 7048 TGFBR2
  • RGD:7240710
DOID:4762 vasculogenic impotence HGNC:11773 Homo sapiens (human) 7048 TGFBR2
  • PMID:14718046
DOID:2920 membranoproliferative glomerulonephritis HGNC:11773 Homo sapiens (human) 7048 TGFBR2
  • MGI:6194238
DOID:0112182 mismatch repair cancer syndrome HGNC:11773 Homo sapiens (human) 7048 TGFBR2
  • PMID:28218421
DOID:10283 prostate cancer HGNC:11773 Homo sapiens (human) 7048 TGFBR2
  • MGI:6194238
DOID:0110214 cleft soft palate HGNC:11773 Homo sapiens (human) 7048 TGFBR2
  • MGI:6194238
DOID:0070234 Loeys-Dietz syndrome 2 HGNC:11773 Homo sapiens (human) 7048 TGFBR2
  • RGD:7240710
DOID:0050466 Loeys-Dietz syndrome HGNC:11773 Homo sapiens (human) 7048 TGFBR2
  • MGI:6194238
DOID:3770 pulmonary fibrosis HGNC:11773 Homo sapiens (human) 7048 TGFBR2
  • MGI:6194238
DOID:14323 Marfan syndrome HGNC:11773 Homo sapiens (human) 7048 TGFBR2
  • MGI:6194238
  • PMID:15235604
DOID:11198 DiGeorge syndrome HGNC:11773 Homo sapiens (human) 7048 TGFBR2
  • MGI:6194238
DOID:6432 pulmonary hypertension HGNC:11773 Homo sapiens (human) 7048 TGFBR2
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:11773 Homo sapiens (human) 7048 TGFBR2
  • MGI:6194238
DOID:684 hepatocellular carcinoma HGNC:11773 Homo sapiens (human) 7048 TGFBR2
  • MGI:6194238

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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