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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 376 - 400 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:0110297 autosomal recessive limb-girdle muscular dystrophy type 2K HGNC:9202 Homo sapiens (human) 10585 POMT1
  • RGD:7240710
DOID:3649 pyruvate decarboxylase deficiency HGNC:21350 Homo sapiens (human) 8050 PDHX
  • RGD:7240710
DOID:6364 migraine HGNC:11892 Homo sapiens (human) 7124 TNF
  • RGD:7240710
DOID:0060448 Fleck corneal dystrophy HGNC:23785 Homo sapiens (human) 200576 PIKFYVE
  • RGD:7240710
DOID:2738 pseudoxanthoma elasticum HGNC:15517 Homo sapiens (human) 64132 XYLT2
  • RGD:7240710
DOID:0111582 hereditary arterial and articular multiple calcification syndrome HGNC:8021 Homo sapiens (human) 4907 NT5E
  • RGD:7240710
DOID:2739 Gilbert syndrome HGNC:12530 Homo sapiens (human) 54658 UGT1A1
  • RGD:7240710
DOID:0112378 muscular dystrophy-dystroglycanopathy type B3 HGNC:19139 Homo sapiens (human) 55624 POMGNT1
  • RGD:7240710
DOID:0111242 congenital muscular dystrophy-dystroglycanopathy type A6 HGNC:6511 Homo sapiens (human) 9215 LARGE1
  • RGD:7240710
DOID:9970 obesity HGNC:10660 Homo sapiens (human) 9672 SDC3
  • RGD:7240710
DOID:0080411 familial adenomatous polyposis 3 HGNC:8028 Homo sapiens (human) 4913 NTHL1
  • RGD:7240710
DOID:0112319 Kanzaki disease HGNC:7631 Homo sapiens (human) 4668 NAGA
  • RGD:7240710
DOID:0060175 succinic semialdehyde dehydrogenase deficiency HGNC:408 Homo sapiens (human) 7915 ALDH5A1
  • RGD:7240710
DOID:0110820 hereditary spastic paraplegia 75 HGNC:6783 Homo sapiens (human) 4099 MAG
  • RGD:7240710
DOID:0070221 progressive familial intrahepatic cholestasis HGNC:10741 Homo sapiens (human) 8482 SEMA7A
  • RGD:7240710
DOID:0070256 congenital disorder of glycosylation type IId HGNC:924 Homo sapiens (human) 2683 B4GALT1
  • RGD:7240710
DOID:0050571 congenital disorder of glycosylation type II HGNC:18619 Homo sapiens (human) 83548 COG3
  • RGD:7240710
DOID:14735 hereditary angioedema HGNC:14178 Homo sapiens (human) 64711 HS3ST6
  • RGD:7240710
DOID:14766 renal agenesis HGNC:4243 Homo sapiens (human) 2674 GFRA1
  • RGD:7240710
DOID:0081337 congenital myopathy HGNC:9639 Homo sapiens (human) 9200 HACD1
  • RGD:7240710
DOID:0111141 delayed sleep phase syndrome HGNC:2384 Homo sapiens (human) 1407 CRY1
  • RGD:7240710
DOID:0050156 idiopathic pulmonary fibrosis HGNC:10799 Homo sapiens (human) 729238 SFTPA2
  • RGD:7240710
DOID:0090075 hypogonadotropic hypogonadism 15 with or without anosmia HGNC:5201 Homo sapiens (human) 9394 HS6ST1
  • RGD:7240710
DOID:0080566 congenital disorder of glycosylation In HGNC:30220 Homo sapiens (human) 91869 RFT1
  • RGD:7240710
DOID:0081381 juvenile amyotrophic lateral sclerosis type 27 HGNC:11277 Homo sapiens (human) 10558 SPTLC1
  • 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: August 19, 2024