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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 67551 - 67575 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:8947 diabetic retinopathy HGNC:1511 Homo sapiens (human) 842 CASP9
  • PMID:18369072
DOID:332 amyotrophic lateral sclerosis HGNC:1511 Homo sapiens (human) 842 CASP9
  • MGI:6194238
DOID:2945 severe acute respiratory syndrome HGNC:1511 Homo sapiens (human) 842 CASP9
  • PMID:19635508
DOID:2055 post-traumatic stress disorder HGNC:1511 Homo sapiens (human) 842 CASP9
  • MGI:6194238
DOID:12930 dilated cardiomyopathy HGNC:1511 Homo sapiens (human) 842 CASP9
  • MGI:6194238
DOID:3908 lung non-small cell carcinoma HGNC:1511 Homo sapiens (human) 842 CASP9
  • PMID:16231180
  • PMID:17285546
  • PMID:20661084
  • PMID:20972334
DOID:10763 hypertension HGNC:1511 Homo sapiens (human) 842 CASP9
  • MGI:6194238
DOID:1793 pancreatic cancer HGNC:1511 Homo sapiens (human) 842 CASP9
  • PMID:19209030
  • PMID:20357690
DOID:224 transient cerebral ischemia HGNC:1511 Homo sapiens (human) 842 CASP9
  • MGI:6194238
DOID:11650 bronchopulmonary dysplasia HGNC:1511 Homo sapiens (human) 842 CASP9
  • MGI:6194238
DOID:9256 colorectal cancer HGNC:1511 Homo sapiens (human) 842 CASP9
  • PMID:21538054
  • PMID:23303631
DOID:746 adenomatoid tumor HGNC:20456 Homo sapiens (human) 84231 TRAF7
  • PMID:29148537
DOID:684 hepatocellular carcinoma HGNC:20456 Homo sapiens (human) 84231 TRAF7
  • PMID:31730901
DOID:1788 peritoneal mesothelioma HGNC:20456 Homo sapiens (human) 84231 TRAF7
  • PMID:30171198
DOID:0111437 optic atrophy 7 HGNC:25382 Homo sapiens (human) 84233 TMEM126A
  • RGD:7240710
DOID:0070139 autosomal recessive cutis laxa type IC HGNC:6717 Homo sapiens (human) 8425 LTBP4
  • RGD:7240710
DOID:3144 cutis laxa HGNC:6717 Homo sapiens (human) 8425 LTBP4
  • MGI:6194238
DOID:0081328 familial hyperinsulinemic hypoglycemia 8 HGNC:29681 Homo sapiens (human) 84275 SLC25A33
  • MGI:6194238
DOID:0060669 cerebral cavernous malformation HGNC:11403 Homo sapiens (human) 8428 STK24
  • MGI:6194238
DOID:6000 congestive heart failure HGNC:18145 Homo sapiens (human) 84295 PHF6
  • PMID:33779075
DOID:0080199 colorectal carcinoma HGNC:18145 Homo sapiens (human) 84295 PHF6
  • PMID:28675510
DOID:684 hepatocellular carcinoma HGNC:18145 Homo sapiens (human) 84295 PHF6
  • PMID:30888215
  • PMID:31329335
DOID:9119 acute myeloid leukemia HGNC:18145 Homo sapiens (human) 84295 PHF6
  • PMID:31186809
DOID:0050681 Borjeson-Forssman-Lehmann syndrome HGNC:18145 Homo sapiens (human) 84295 PHF6
  • MGI:6194238
  • RGD:7240710
DOID:9955 hypoplastic left heart syndrome HGNC:28184 Homo sapiens (human) 84303 CHCHD6
  • 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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Last updated: December 9, 2024