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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 65526 - 65550 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:3459 breast carcinoma HGNC:1052 Homo sapiens (human) 274 BIN1
  • PMID:10652430
DOID:2526 prostate adenocarcinoma HGNC:1052 Homo sapiens (human) 274 BIN1
  • PMID:12532338
DOID:0111220 centronuclear myopathy 2 HGNC:1052 Homo sapiens (human) 274 BIN1
  • MGI:6194238
  • RGD:7240710
DOID:1925 Coffin-Siris syndrome HGNC:21111 Homo sapiens (human) 23506 BICRAL
  • MGI:6194238
DOID:0112370 Coffin-Siris syndrome 12 HGNC:4332 Homo sapiens (human) 29998 BICRA
  • RGD:7240710
DOID:0050545 visceral heterotaxy HGNC:19351 Homo sapiens (human) 80114 BICC1
  • MGI:6194238
DOID:2975 cystic kidney disease HGNC:19351 Homo sapiens (human) 80114 BICC1
  • MGI:6194238
DOID:0110861 autosomal recessive polycystic kidney disease HGNC:19351 Homo sapiens (human) 80114 BICC1
  • MGI:6194238
DOID:898 autosomal dominant polycystic kidney disease HGNC:19351 Homo sapiens (human) 80114 BICC1
  • MGI:6194238
DOID:0111682 diffuse cystic renal dysplasia HGNC:19351 Homo sapiens (human) 80114 BICC1
  • RGD:7240710
DOID:10534 stomach cancer HGNC:1044 Homo sapiens (human) 633 BGN
  • PMID:33470887
DOID:0112150 X-linked spondyloepimetaphyseal dysplasia HGNC:1044 Homo sapiens (human) 633 BGN
  • RGD:7240710
DOID:0111861 Meester-Loeys syndrome HGNC:1044 Homo sapiens (human) 633 BGN
  • RGD:7240710
DOID:0110264 cataract 33 HGNC:1040 Homo sapiens (human) 631 BFSP1
  • RGD:7240710
DOID:0111637 autosomal recessive nonsyndromic deafness 112 HGNC:13652 Homo sapiens (human) 55814 BDP1
  • RGD:7240710
DOID:1679 cystitis HGNC:1033 Homo sapiens (human) 627 BDNF
  • MGI:6194238
DOID:9470 bacterial meningitis HGNC:1033 Homo sapiens (human) 627 BDNF
  • MGI:6194238
DOID:2559 opiate dependence HGNC:1033 Homo sapiens (human) 627 BDNF
  • PMID:21890593
DOID:4483 rhinitis HGNC:1033 Homo sapiens (human) 627 BDNF
  • MGI:6194238
  • PMID:21723144
DOID:14330 Parkinson's disease HGNC:1033 Homo sapiens (human) 627 BDNF
  • PMID:10208589
  • PMID:16565926
DOID:0050741 alcohol dependence HGNC:1033 Homo sapiens (human) 627 BDNF
  • MGI:6194238
DOID:12894 Sjogren's syndrome HGNC:1033 Homo sapiens (human) 627 BDNF
  • PMID:18830907
DOID:418 systemic scleroderma HGNC:1033 Homo sapiens (human) 627 BDNF
  • PMID:21085492
DOID:12689 acoustic neuroma HGNC:1033 Homo sapiens (human) 627 BDNF
  • PMID:19937367
DOID:13544 low tension glaucoma HGNC:1033 Homo sapiens (human) 627 BDNF
  • PMID:19861219

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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