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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 8301 - 8325 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:10591 pre-eclampsia HGNC:5208 Homo sapiens (human) 3290 HSD11B1
  • PMID:23659736
DOID:1168 familial hyperlipidemia HGNC:5208 Homo sapiens (human) 3290 HSD11B1
  • MGI:6194238
DOID:0111843 Paganini-Miozzo syndrome HGNC:19133 Homo sapiens (human) 90161 HS6ST2
  • RGD:7240710
DOID:0090075 hypogonadotropic hypogonadism 15 with or without anosmia HGNC:5201 Homo sapiens (human) 9394 HS6ST1
  • RGD:7240710
DOID:14735 hereditary angioedema HGNC:14178 Homo sapiens (human) 64711 HS3ST6
  • RGD:7240710
DOID:3908 lung non-small cell carcinoma HGNC:5195 Homo sapiens (human) 9956 HS3ST2
  • PMID:27777637
DOID:219 colon cancer HGNC:5195 Homo sapiens (human) 9956 HS3ST2
  • PMID:12527896
DOID:1793 pancreatic cancer HGNC:5195 Homo sapiens (human) 9956 HS3ST2
  • PMID:12527896
DOID:1324 lung cancer HGNC:5195 Homo sapiens (human) 9956 HS3ST2
  • PMID:12527896
DOID:0050816 urofacial syndrome HGNC:18374 Homo sapiens (human) 60495 HPSE2
  • MGI:6194238
  • RGD:7240710
DOID:1919 Lesch-Nyhan syndrome HGNC:5157 Homo sapiens (human) 3251 HPRT1
  • MGI:6194238
  • PMID:20638392
  • PMID:24940672
  • RGD:7240710
DOID:0112127 HRPT-related hyperuricemia HGNC:5157 Homo sapiens (human) 3251 HPRT1
  • RGD:7240710
DOID:684 hepatocellular carcinoma HGNC:5157 Homo sapiens (human) 3251 HPRT1
  • MGI:6194238
DOID:2977 primary hyperoxaluria HGNC:25155 Homo sapiens (human) 112817 HOGA1
  • MGI:6194238
DOID:0111672 primary hyperoxaluria type 3 HGNC:25155 Homo sapiens (human) 112817 HOGA1
  • RGD:7240710
DOID:1612 breast cancer HGNC:5012 Homo sapiens (human) 3161 HMMR
  • RGD:7240710
DOID:13619 extrahepatic cholestasis HGNC:5008 Homo sapiens (human) 3158 HMGCS2
  • MGI:6194238
DOID:0081168 HMG-CoA synthase 2 deficiency HGNC:5008 Homo sapiens (human) 3158 HMGCS2
  • MGI:6194238
  • RGD:7240710
DOID:684 hepatocellular carcinoma HGNC:5008 Homo sapiens (human) 3158 HMGCS2
  • PMID:28867541
DOID:9970 obesity HGNC:5007 Homo sapiens (human) 3157 HMGCS1
  • MGI:6194238
DOID:9252 amino acid metabolic disorder HGNC:5005 Homo sapiens (human) 3155 HMGCL
  • PMID:8440722
DOID:4194 glucose metabolism disease HGNC:23302 Homo sapiens (human) 80201 HKDC1
  • MGI:6194238
DOID:4195 hyperglycemia HGNC:23302 Homo sapiens (human) 80201 HKDC1
  • MGI:6194238
DOID:13317 hyperinsulinemic hypoglycemia HGNC:23302 Homo sapiens (human) 80201 HKDC1
  • MGI:6194238
DOID:0050524 maturity-onset diabetes of the young HGNC:23302 Homo sapiens (human) 80201 HKDC1
  • 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: August 19, 2024