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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 3726 - 3750 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:2394 ovarian cancer HGNC:11755 Homo sapiens (human) 7031 TFF1
  • PMID:17624412
DOID:3702 cervical adenocarcinoma HGNC:11755 Homo sapiens (human) 7031 TFF1
  • PMID:10727981
DOID:0060180 colitis HGNC:11755 Homo sapiens (human) 7031 TFF1
  • MGI:6194238
DOID:10283 prostate cancer HGNC:11755 Homo sapiens (human) 7031 TFF1
  • PMID:10458410
  • PMID:16467092
DOID:11054 urinary bladder cancer HGNC:11755 Homo sapiens (human) 7031 TFF1
  • PMID:18283638
DOID:10534 stomach cancer HGNC:11755 Homo sapiens (human) 7031 TFF1
  • MGI:6194238
DOID:0080365 endometrial hyperplasia HGNC:11755 Homo sapiens (human) 7031 TFF1
  • PMID:9221798
DOID:13550 angle-closure glaucoma HGNC:11743 Homo sapiens (human) 7021 TFAP2B
  • MGI:6194238
DOID:535 sleep disorder HGNC:11743 Homo sapiens (human) 7021 TFAP2B
  • MGI:6194238
DOID:13832 patent ductus arteriosus HGNC:11743 Homo sapiens (human) 7021 TFAP2B
  • MGI:6194238
  • PMID:10802654
  • RGD:7240710
DOID:0060563 Char syndrome HGNC:11743 Homo sapiens (human) 7021 TFAP2B
  • MGI:6194238
  • RGD:7240710
DOID:0110544 autosomal dominant nonsyndromic deafness 12 HGNC:11720 Homo sapiens (human) 7007 TECTA
  • MGI:6194238
  • RGD:7240710
DOID:10003 sensorineural hearing loss HGNC:11720 Homo sapiens (human) 7007 TECTA
  • PMID:9590290
  • PMID:9949200
DOID:0110479 autosomal recessive nonsyndromic deafness 21 HGNC:11720 Homo sapiens (human) 7007 TECTA
  • RGD:7240710
DOID:0050889 non-syndromic intellectual disability HGNC:4551 Homo sapiens (human) 9524 TECR
  • MGI:6194238
DOID:0081188 autosomal recessive intellectual developmental disorder 14 HGNC:4551 Homo sapiens (human) 9524 TECR
  • RGD:7240710
DOID:9970 obesity SGD:S000003424 Saccharomyces cerevisiae S288C 853106 TDH3
  • MGI:6194238
DOID:0050827 rheumatic heart disease SGD:S000003424 Saccharomyces cerevisiae S288C 853106 TDH3
  • MGI:6194238
DOID:10652 Alzheimer's disease SGD:S000003424 Saccharomyces cerevisiae S288C 853106 TDH3
  • MGI:6194238
DOID:8947 diabetic retinopathy SGD:S000003424 Saccharomyces cerevisiae S288C 853106 TDH3
  • MGI:6194238
DOID:1826 epilepsy SGD:S000003424 Saccharomyces cerevisiae S288C 853106 TDH3
  • MGI:6194238
DOID:0060108 brain glioma SGD:S000003424 Saccharomyces cerevisiae S288C 853106 TDH3
  • MGI:6194238
DOID:3525 middle cerebral artery infarction SGD:S000003424 Saccharomyces cerevisiae S288C 853106 TDH3
  • MGI:6194238
DOID:3319 lymphangioleiomyomatosis SGD:S000003424 Saccharomyces cerevisiae S288C 853106 TDH3
  • MGI:6194238
DOID:0050866 oral squamous cell carcinoma SGD:S000003424 Saccharomyces cerevisiae S288C 853106 TDH3
  • MGI:6194238

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International Collaboration

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