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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 64801 - 64825 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:11555 Fuchs' endothelial dystrophy HGNC:11634 Homo sapiens (human) 6925 TCF4
  • RGD:7240710
DOID:5419 schizophrenia HGNC:11634 Homo sapiens (human) 6925 TCF4
  • MGI:6194238
DOID:3883 Lynch syndrome HGNC:11634 Homo sapiens (human) 6925 TCF4
  • PMID:28218421
DOID:0060488 Pitt-Hopkins syndrome HGNC:11634 Homo sapiens (human) 6925 TCF4
  • MGI:6194238
  • RGD:7240710
DOID:0060037 developmental disorder of mental health HGNC:11634 Homo sapiens (human) 6925 TCF4
  • MGI:6194238
DOID:9970 obesity HGNC:11634 Homo sapiens (human) 6925 TCF4
  • MGI:6194238
DOID:0081140 agammaglobulinemia 8A HGNC:11633 Homo sapiens (human) 6929 TCF3
  • RGD:7240710
DOID:10283 prostate cancer HGNC:11633 Homo sapiens (human) 6929 TCF3
  • PMID:22564737
DOID:0081143 agammaglobulinemia 8B HGNC:11633 Homo sapiens (human) 6929 TCF3
  • RGD:7240710
DOID:9256 colorectal cancer HGNC:11633 Homo sapiens (human) 6929 TCF3
  • PMID:19828471
  • PMID:23940558
  • PMID:24454819
  • PMID:25375219
DOID:9970 obesity HGNC:11633 Homo sapiens (human) 6929 TCF3
  • MGI:6194238
DOID:0060037 developmental disorder of mental health HGNC:11633 Homo sapiens (human) 6929 TCF3
  • MGI:6194238
DOID:0060488 Pitt-Hopkins syndrome HGNC:11633 Homo sapiens (human) 6929 TCF3
  • MGI:6194238
DOID:0060041 autism spectrum disorder HGNC:11631 Homo sapiens (human) 6942 TCF20
  • MGI:6194238
DOID:0080354 Phelan-McDermid syndrome HGNC:11631 Homo sapiens (human) 6942 TCF20
  • MGI:6194238
DOID:2340 craniosynostosis HGNC:11623 Homo sapiens (human) 6938 TCF12
  • RGD:7240710
DOID:0060037 developmental disorder of mental health HGNC:11623 Homo sapiens (human) 6938 TCF12
  • MGI:6194238
DOID:9970 obesity HGNC:11623 Homo sapiens (human) 6938 TCF12
  • MGI:6194238
DOID:0060488 Pitt-Hopkins syndrome HGNC:11623 Homo sapiens (human) 6938 TCF12
  • MGI:6194238
DOID:0090070 hypogonadotropic hypogonadism HGNC:11623 Homo sapiens (human) 6938 TCF12
  • RGD:7240710
DOID:9744 type 1 diabetes mellitus HGNC:11621 Homo sapiens (human) 6927 HNF1A
  • RGD:7240710
DOID:10591 pre-eclampsia HGNC:11621 Homo sapiens (human) 6927 HNF1A
  • PMID:31825269
DOID:4450 renal cell carcinoma HGNC:11621 Homo sapiens (human) 6927 HNF1A
  • RGD:7240710
DOID:9281 phenylketonuria HGNC:11621 Homo sapiens (human) 6927 HNF1A
  • MGI:6194238
DOID:11714 gestational diabetes HGNC:11621 Homo sapiens (human) 6927 HNF1A
  • PMID:16752173

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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