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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 65201 - 65225 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:8634 prostate carcinoma in situ HGNC:1131 Homo sapiens (human) 7832 BTG2
  • PMID:11470758
DOID:0080998 acute necrotizing pancreatitis HGNC:1131 Homo sapiens (human) 7832 BTG2
  • MGI:6194238
DOID:4450 renal cell carcinoma HGNC:1131 Homo sapiens (human) 7832 BTG2
  • PMID:14996721
DOID:1227 neutropenia HGNC:11301 Homo sapiens (human) 6729 SRP54
  • MGI:6194238
DOID:0112135 severe congenital neutropenia 8 HGNC:11301 Homo sapiens (human) 6729 SRP54
  • MGI:6194238
  • RGD:7240710
DOID:0060479 Shwachman-Diamond syndrome HGNC:11301 Homo sapiens (human) 6729 SRP54
  • MGI:6194238
DOID:6000 congestive heart failure HGNC:11291 Homo sapiens (human) 6722 SRF
  • PMID:11893590
DOID:3319 lymphangioleiomyomatosis HGNC:11291 Homo sapiens (human) 6722 SRF
  • PMID:12654640
DOID:10763 hypertension HGNC:11291 Homo sapiens (human) 6722 SRF
  • MGI:6194238
DOID:0050700 cardiomyopathy HGNC:11291 Homo sapiens (human) 6722 SRF
  • PMID:12874181
DOID:12930 dilated cardiomyopathy HGNC:11291 Homo sapiens (human) 6722 SRF
  • MGI:6194238
DOID:684 hepatocellular carcinoma HGNC:11291 Homo sapiens (human) 6722 SRF
  • MGI:6194238
DOID:2527 nephrosis HGNC:11290 Homo sapiens (human) 6721 SREBF2
  • MGI:6194238
DOID:8725 vascular dementia HGNC:11290 Homo sapiens (human) 6721 SREBF2
  • PMID:16082694
DOID:9352 type 2 diabetes mellitus HGNC:11290 Homo sapiens (human) 6721 SREBF2
  • PMID:15644403
DOID:3407 carotid artery disease HGNC:11290 Homo sapiens (human) 6721 SREBF2
  • PMID:12801623
DOID:3393 coronary artery disease HGNC:11290 Homo sapiens (human) 6721 SREBF2
  • PMID:28367087
DOID:11832 visual epilepsy HGNC:11290 Homo sapiens (human) 6721 SREBF2
  • MGI:6194238
DOID:1115 sarcoma HGNC:11290 Homo sapiens (human) 6721 SREBF2
  • PMID:31089155
DOID:9744 type 1 diabetes mellitus HGNC:11290 Homo sapiens (human) 6721 SREBF2
  • PMID:18682608
DOID:9455 lipid storage disease HGNC:11290 Homo sapiens (human) 6721 SREBF2
  • MGI:6194238
DOID:557 kidney disease HGNC:11290 Homo sapiens (human) 6721 SREBF2
  • MGI:6194238
DOID:9970 obesity HGNC:11290 Homo sapiens (human) 6721 SREBF2
  • MGI:6194238
DOID:783 end stage renal disease HGNC:11290 Homo sapiens (human) 6721 SREBF2
  • MGI:6194238
DOID:10283 prostate cancer HGNC:11290 Homo sapiens (human) 6721 SREBF2
  • PMID:15026365

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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