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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 8276 - 8300 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:0070460 hereditary spastic paraplegia 90B HGNC:20361 Homo sapiens (human) 171546 SPTSSA
  • RGD:7240710
DOID:162 cancer HGNC:11279 Homo sapiens (human) 6713 SQLE
  • MGI:6194238
DOID:9970 obesity HGNC:11284 Homo sapiens (human) 6715 SRD5A1
  • MGI:6194238
DOID:10283 prostate cancer HGNC:11284 Homo sapiens (human) 6715 SRD5A1
  • MGI:6194238
  • PMID:16818707
  • PMID:17720776
DOID:9352 type 2 diabetes mellitus HGNC:11284 Homo sapiens (human) 6715 SRD5A1
  • MGI:6194238
DOID:1459 hypothyroidism HGNC:11284 Homo sapiens (human) 6715 SRD5A1
  • MGI:6194238
DOID:3459 breast carcinoma HGNC:11284 Homo sapiens (human) 6715 SRD5A1
  • PMID:15212687
DOID:11132 prostatic hypertrophy HGNC:11284 Homo sapiens (human) 6715 SRD5A1
  • PMID:15136785
DOID:12700 hyperprolactinemia HGNC:11284 Homo sapiens (human) 6715 SRD5A1
  • MGI:6194238
DOID:12700 hyperprolactinemia HGNC:11285 Homo sapiens (human) 6716 SRD5A2
  • MGI:6194238
DOID:9351 diabetes mellitus HGNC:11285 Homo sapiens (human) 6716 SRD5A2
  • MGI:6194238
DOID:10283 prostate cancer HGNC:11285 Homo sapiens (human) 6716 SRD5A2
  • PMID:10501358
  • PMID:12949937
DOID:10892 hypospadias HGNC:11285 Homo sapiens (human) 6716 SRD5A2
  • PMID:10514539
DOID:3459 breast carcinoma HGNC:11285 Homo sapiens (human) 6716 SRD5A2
  • PMID:15212687
DOID:0080568 congenital disorder of glycosylation Iq HGNC:25812 Homo sapiens (human) 79644 SRD5A3
  • RGD:7240710
DOID:0050570 congenital disorder of glycosylation type I HGNC:25812 Homo sapiens (human) 79644 SRD5A3
  • MGI:6194238
DOID:0050807 Kahrizi syndrome HGNC:25812 Homo sapiens (human) 79644 SRD5A3
  • RGD:7240710
DOID:0081180 autosomal recessive intellectual developmental disorder 12 HGNC:10866 Homo sapiens (human) 6487 ST3GAL3
  • RGD:7240710
DOID:0080414 developmental and epileptic encephalopathy 15 HGNC:10866 Homo sapiens (human) 6487 ST3GAL3
  • RGD:7240710
DOID:0060470 salt and pepper syndrome HGNC:10872 Homo sapiens (human) 8869 ST3GAL5
  • RGD:7240710
DOID:3070 high grade glioma HGNC:10860 Homo sapiens (human) 6480 ST6GAL1
  • MGI:6194238
DOID:1574 alcohol use disorder HGNC:10860 Homo sapiens (human) 6480 ST6GAL1
  • PMID:17697868
DOID:0050589 inflammatory bowel disease HGNC:23614 Homo sapiens (human) 55808 ST6GALNAC1
  • MGI:6194238
DOID:1700 X-linked ichthyosis HGNC:11425 Homo sapiens (human) 412 STS
  • RGD:7240710
DOID:10763 hypertension HGNC:11425 Homo sapiens (human) 412 STS
  • 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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