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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 July 29, 2024
Displaying entries 6476 - 6500 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:4362 cervical cancer HGNC:8907 Homo sapiens (human) 5238 PGM3
  • PMID:508567
DOID:3307 teratoma HGNC:8907 Homo sapiens (human) 5238 PGM3
  • PMID:5259759
DOID:0111953 immunodeficiency 23 HGNC:8907 Homo sapiens (human) 5238 PGM3
  • RGD:7240710
DOID:162 cancer HGNC:8907 Homo sapiens (human) 5238 PGM3
  • MGI:6194238
DOID:0050161 lower respiratory tract disease FB:FBgn0035976 Drosophila melanogaster (fruit fly) 39063 PGRP-LC CG4432
  • PMID:33826881
DOID:0050161 lower respiratory tract disease FB:FBgn0030695 Drosophila melanogaster (fruit fly) 32534 PGRP-LE CG8995
  • PMID:33826881
DOID:2747 glycogen storage disease HGNC:8925 Homo sapiens (human) 5255 PHKA1
  • PMID:12825073
DOID:1459 hypothyroidism HGNC:8925 Homo sapiens (human) 5255 PHKA1
  • MGI:6194238
DOID:0111040 glycogen storage disease IXd HGNC:8925 Homo sapiens (human) 5255 PHKA1
  • MGI:6194238
  • RGD:7240710
DOID:0050545 visceral heterotaxy HGNC:8926 Homo sapiens (human) 5256 PHKA2
  • MGI:6194238
DOID:0111042 glycogen storage disease IXa HGNC:8926 Homo sapiens (human) 5256 PHKA2
  • MGI:6194238
  • PMID:28283841
  • PMID:28627441
  • PMID:8733134
  • RGD:7240710
DOID:2747 glycogen storage disease HGNC:8926 Homo sapiens (human) 5256 PHKA2
  • PMID:7711737
DOID:0111041 glycogen storage disease IXb HGNC:8927 Homo sapiens (human) 5257 PHKB
  • MGI:6194238
  • RGD:7240710
DOID:5082 liver cirrhosis HGNC:8931 Homo sapiens (human) 5261 PHKG2
  • PMID:9384616
DOID:2747 glycogen storage disease HGNC:8931 Homo sapiens (human) 5261 PHKG2
  • MGI:6194238
  • PMID:8896567
DOID:0111043 glycogen storage disease IXc HGNC:8931 Homo sapiens (human) 5261 PHKG2
  • RGD:7240710
DOID:0112347 hereditary spastic paraplegia 84 HGNC:8983 Homo sapiens (human) 5297 PI4KA
  • RGD:7240710
DOID:0060413 chromosome 22q11.2 deletion syndrome, distal HGNC:8983 Homo sapiens (human) 5297 PI4KA
  • MGI:6194238
DOID:0050564 autosomal dominant nonsyndromic deafness HGNC:8984 Homo sapiens (human) 5298 PI4KB
  • RGD:7240710
DOID:0080139 multiple congenital anomalies-hypotonia-seizures syndrome 2 FB:FBgn0034270 Drosophila melanogaster (fruit fly) 37020 PIG-A
  • MGI:6194238
DOID:0060284 paroxysmal nocturnal hemoglobinuria FB:FBgn0034270 Drosophila melanogaster (fruit fly) 37020 PIG-A
  • MGI:6194238
DOID:0060713 autosomal recessive congenital ichthyosis 4B FB:FBgn0034270 Drosophila melanogaster (fruit fly) 37020 PIG-A
  • MGI:6194238
DOID:0112216 developmental and epileptic encephalopathy 80 FB:FBgn0035464 Drosophila melanogaster (fruit fly) 38446 PIG-B
  • MGI:6194238
DOID:10112 sleeping sickness FB:FBgn0035464 Drosophila melanogaster (fruit fly) 38446 PIG-B
  • MGI:6194238
DOID:0070433 hyperphosphatasia with impaired intellectual development syndrome 1 FB:FBgn0265174 Drosophila melanogaster (fruit fly) 19835383 PIG-V
  • 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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