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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 65751 - 65775 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:1612 breast cancer HGNC:11100 Homo sapiens (human) 6597 SMARCA4
  • MGI:6194238
DOID:3672 rhabdoid cancer HGNC:11100 Homo sapiens (human) 6597 SMARCA4
  • RGD:7240710
DOID:1574 alcohol use disorder HGNC:11100 Homo sapiens (human) 6597 SMARCA4
  • MGI:6194238
DOID:684 hepatocellular carcinoma HGNC:11100 Homo sapiens (human) 6597 SMARCA4
  • PMID:24556940
DOID:10283 prostate cancer HGNC:11098 Homo sapiens (human) 6595 SMARCA2
  • PMID:17075831
DOID:162 cancer HGNC:11098 Homo sapiens (human) 6595 SMARCA2
  • MGI:6194238
DOID:0081442 blepharophimosis-impaired intellectual development syndrome HGNC:11098 Homo sapiens (human) 6595 SMARCA2
  • RGD:7240710
DOID:0050340 opportunistic bacterial infectious disease HGNC:11098 Homo sapiens (human) 6595 SMARCA2
  • MGI:6194238
DOID:1574 alcohol use disorder HGNC:11098 Homo sapiens (human) 6595 SMARCA2
  • MGI:6194238
DOID:0081441 Nicolaides-Baraitser syndrome HGNC:11098 Homo sapiens (human) 6595 SMARCA2
  • MGI:6194238
  • RGD:7240710
DOID:331 central nervous system disease HGNC:11097 Homo sapiens (human) 6594 SMARCA1
  • MGI:6194238
DOID:3827 congenital diaphragmatic hernia HGNC:11087 Homo sapiens (human) 6586 SLIT3
  • MGI:6194238
DOID:9562 primary ciliary dyskinesia HGNC:11086 Homo sapiens (human) 9353 SLIT2
  • MGI:6194238
DOID:0050144 Kartagener syndrome HGNC:11086 Homo sapiens (human) 9353 SLIT2
  • MGI:6194238
DOID:0050545 visceral heterotaxy HGNC:11086 Homo sapiens (human) 9353 SLIT2
  • MGI:6194238
DOID:4780 anti-basement membrane glomerulonephritis HGNC:11086 Homo sapiens (human) 9353 SLIT2
  • MGI:6194238
DOID:3827 congenital diaphragmatic hernia HGNC:11086 Homo sapiens (human) 9353 SLIT2
  • MGI:6194238
DOID:0060224 atrial fibrillation HGNC:11086 Homo sapiens (human) 9353 SLIT2
  • PMID:33236535
DOID:2975 cystic kidney disease HGNC:11086 Homo sapiens (human) 9353 SLIT2
  • MGI:6194238
DOID:13207 proliferative diabetic retinopathy HGNC:11086 Homo sapiens (human) 9353 SLIT2
  • PMID:28973045
DOID:8947 diabetic retinopathy HGNC:11086 Homo sapiens (human) 9353 SLIT2
  • MGI:6194238
DOID:224 transient cerebral ischemia HGNC:11086 Homo sapiens (human) 9353 SLIT2
  • MGI:6194238
DOID:0080745 polymyositis HGNC:11086 Homo sapiens (human) 9353 SLIT2
  • PMID:32213157
DOID:10223 dermatomyositis HGNC:11086 Homo sapiens (human) 9353 SLIT2
  • PMID:32213157
DOID:0060825 Christianson syndrome HGNC:11079 Homo sapiens (human) 10479 SLC9A6
  • MGI:6194238
  • RGD:7240710

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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