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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 62926 - 62950 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0111130 focal segmental glomerulosclerosis 5 MGI:1917685 Mus musculus (house mouse) 70435 Inf2
  • MGI:6194238
DOID:1682 congenital heart disease HGNC:3122 Homo sapiens (human) 7044 LEFTY2
  • PMID:25111179
DOID:0060455 Thiel-Behnke corneal dystrophy HGNC:11771 Homo sapiens (human) 7045 TGFBI
  • RGD:7240710
DOID:0080530 granular corneal dystrophy 1 HGNC:11771 Homo sapiens (human) 7045 TGFBI
  • RGD:7240710
DOID:0060453 Reis-Bucklers corneal dystrophy HGNC:11771 Homo sapiens (human) 7045 TGFBI
  • RGD:7240710
DOID:2566 corneal dystrophy HGNC:11771 Homo sapiens (human) 7045 TGFBI
  • MGI:6194238
  • PMID:9054935
DOID:557 kidney disease HGNC:11771 Homo sapiens (human) 7045 TGFBI
  • MGI:6194238
DOID:0060447 epithelial basement membrane dystrophy HGNC:11771 Homo sapiens (human) 7045 TGFBI
  • RGD:7240710
DOID:0060444 granular corneal dystrophy 2 HGNC:11771 Homo sapiens (human) 7045 TGFBI
  • RGD:7240710
DOID:10155 intestinal cancer MGI:1917706 Mus musculus (house mouse) 70456 Mpc2
  • MGI:6194238
DOID:0050466 Loeys-Dietz syndrome HGNC:11772 Homo sapiens (human) 7046 TGFBR1
  • MGI:6194238
DOID:11054 urinary bladder cancer HGNC:11772 Homo sapiens (human) 7046 TGFBR1
  • PMID:9363992
DOID:0070235 Loeys-Dietz syndrome 1 HGNC:11772 Homo sapiens (human) 7046 TGFBR1
  • RGD:7240710
DOID:3498 pancreatic ductal adenocarcinoma HGNC:11772 Homo sapiens (human) 7046 TGFBR1
  • PMID:17297450
DOID:5585 Ferguson-Smith tumor HGNC:11772 Homo sapiens (human) 7046 TGFBR1
  • RGD:7240710
DOID:2256 osteochondrodysplasia HGNC:11772 Homo sapiens (human) 7046 TGFBR1
  • MGI:6194238
DOID:418 systemic scleroderma HGNC:11772 Homo sapiens (human) 7046 TGFBR1
  • MGI:6194238
DOID:557 kidney disease HGNC:11772 Homo sapiens (human) 7046 TGFBR1
  • MGI:6194238
DOID:9256 colorectal cancer HGNC:11772 Homo sapiens (human) 7046 TGFBR1
  • PMID:24880985
DOID:5844 myocardial infarction HGNC:11772 Homo sapiens (human) 7046 TGFBR1
  • MGI:6194238
DOID:127 leiomyoma HGNC:11772 Homo sapiens (human) 7046 TGFBR1
  • MGI:6194238
DOID:8398 osteoarthritis HGNC:11772 Homo sapiens (human) 7046 TGFBR1
  • MGI:6194238
DOID:3883 Lynch syndrome HGNC:11772 Homo sapiens (human) 7046 TGFBR1
  • PMID:17613544
DOID:6432 pulmonary hypertension HGNC:11772 Homo sapiens (human) 7046 TGFBR1
  • MGI:6194238
DOID:0112194 Filippi syndrome MGI:1917716 Mus musculus (house mouse) 70466 Ckap2l
  • 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