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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 63401 - 63425 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:2218 blood platelet disease HGNC:12013 Homo sapiens (human) 7171 TPM4
  • RGD:7240710
DOID:1289 neurodegenerative disease HGNC:12009 Homo sapiens (human) 7167 TPI1
  • MGI:6194238
DOID:2978 carbohydrate metabolic disorder HGNC:12009 Homo sapiens (human) 7167 TPI1
  • PMID:9338582
DOID:162 cancer HGNC:12009 Homo sapiens (human) 7167 TPI1
  • MGI:6194238
DOID:0050884 triosephosphate isomerase deficiency HGNC:12009 Homo sapiens (human) 7167 TPI1
  • MGI:6194238
  • RGD:7240710
DOID:9282 ocular hypertension HGNC:12009 Homo sapiens (human) 7167 TPI1
  • MGI:6194238
DOID:1596 depressive disorder HGNC:12008 Homo sapiens (human) 7166 TPH1
  • MGI:6194238
  • PMID:16165107
  • PMID:17134762
DOID:10930 borderline personality disorder HGNC:12008 Homo sapiens (human) 7166 TPH1
  • PMID:16495936
DOID:1574 alcohol use disorder HGNC:12008 Homo sapiens (human) 7166 TPH1
  • PMID:15654285
DOID:9478 postpartum depression HGNC:12008 Homo sapiens (human) 7166 TPH1
  • PMID:15544576
DOID:1094 attention deficit hyperactivity disorder HGNC:12008 Homo sapiens (human) 7166 TPH1
  • PMID:16389593
  • PMID:20921119
DOID:10652 Alzheimer's disease HGNC:12008 Homo sapiens (human) 7166 TPH1
  • PMID:15182943
DOID:0060041 autism spectrum disorder HGNC:12008 Homo sapiens (human) 7166 TPH1
  • MGI:6194238
DOID:5419 schizophrenia HGNC:12008 Homo sapiens (human) 7166 TPH1
  • PMID:15211625
DOID:0060249 scoliosis HGNC:12008 Homo sapiens (human) 7166 TPH1
  • PMID:18794762
  • PMID:21192222
  • PMID:21308753
DOID:0060412 chromosome 1q41-q42 deletion syndrome HGNC:12000 Homo sapiens (human) 7159 TP53BP2
  • MGI:6194238
DOID:0111067 congenital bile acid synthesis defect 6 HGNC:120 Homo sapiens (human) 8309 ACOX2
  • RGD:7240710
DOID:6432 pulmonary hypertension HGNC:11999 Homo sapiens (human) 7158 TP53BP1
  • PMID:24270264
DOID:0080630 B-lymphoblastic leukemia/lymphoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:22699455
DOID:3702 cervical adenocarcinoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:17354237
DOID:0050834 CHARGE syndrome HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
DOID:7575 pancreatic intraductal papillary-mucinous neoplasm HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:28930868
DOID:3012 Li-Fraumeni syndrome HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
  • PMID:1631137
DOID:0050866 oral squamous cell carcinoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:27283772
DOID:0112182 mismatch repair cancer syndrome HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:28218421

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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