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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 65401 - 65425 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:0081268 pulmonary venoocclusive disease 1 HGNC:1078 Homo sapiens (human) 659 BMPR2
  • RGD:7240710
DOID:2841 asthma HGNC:1078 Homo sapiens (human) 659 BMPR2
  • PMID:18292470
DOID:1681 heart septal defect HGNC:1078 Homo sapiens (human) 659 BMPR2
  • PMID:21070126
DOID:6432 pulmonary hypertension HGNC:1078 Homo sapiens (human) 659 BMPR2
  • MGI:6194238
  • PMID:15775752
  • PMID:19324947
  • PMID:19785764
  • PMID:20002458
  • PMID:20534176
  • PMID:21737550
DOID:0110965 brachydactyly type A2 HGNC:1077 Homo sapiens (human) 658 BMPR1B
  • RGD:7240710
DOID:0081237 acromesomelic dysplasia-3 HGNC:1077 Homo sapiens (human) 658 BMPR1B
  • RGD:7240710
DOID:0050787 juvenile polyposis syndrome HGNC:1077 Homo sapiens (human) 658 BMPR1B
  • MGI:6194238
DOID:6432 pulmonary hypertension HGNC:1077 Homo sapiens (human) 658 BMPR1B
  • PMID:19324947
DOID:2256 osteochondrodysplasia HGNC:1077 Homo sapiens (human) 658 BMPR1B
  • PMID:15805157
DOID:2841 asthma HGNC:1077 Homo sapiens (human) 658 BMPR1B
  • PMID:18292470
DOID:0110978 brachydactyly type A1D HGNC:1077 Homo sapiens (human) 658 BMPR1B
  • RGD:7240710
DOID:384 Wolff-Parkinson-White syndrome HGNC:1076 Homo sapiens (human) 657 BMPR1A
  • MGI:6194238
DOID:0111686 hereditary mixed polyposis syndrome 2 HGNC:1076 Homo sapiens (human) 657 BMPR1A
  • RGD:7240710
DOID:5295 intestinal disease HGNC:1076 Homo sapiens (human) 657 BMPR1A
  • PMID:11381269
  • PMID:16525031
  • PMID:16685657
DOID:14289 Ebstein anomaly HGNC:1076 Homo sapiens (human) 657 BMPR1A
  • MGI:6194238
DOID:6432 pulmonary hypertension HGNC:1076 Homo sapiens (human) 657 BMPR1A
  • PMID:19324947
DOID:0060389 chromosome 10q23 deletion syndrome HGNC:1076 Homo sapiens (human) 657 BMPR1A
  • MGI:6194238
DOID:0050787 juvenile polyposis syndrome HGNC:1076 Homo sapiens (human) 657 BMPR1A
  • MGI:6194238
  • PMID:11536076
  • RGD:7240710
DOID:8398 osteoarthritis HGNC:1076 Homo sapiens (human) 657 BMPR1A
  • MGI:6194238
DOID:2559 opiate dependence HGNC:24154 Homo sapiens (human) 168667 BMPER
  • PMID:18438686
DOID:9970 obesity HGNC:1075 Homo sapiens (human) 656 BMP8B
  • MGI:6194238
DOID:9351 diabetes mellitus HGNC:1075 Homo sapiens (human) 656 BMP8B
  • MGI:6194238
DOID:9970 obesity HGNC:21650 Homo sapiens (human) 353500 BMP8A
  • MGI:6194238
DOID:9351 diabetes mellitus HGNC:21650 Homo sapiens (human) 353500 BMP8A
  • MGI:6194238
DOID:9351 diabetes mellitus HGNC:1074 Homo sapiens (human) 655 BMP7
  • 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