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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 3926 - 3950 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
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: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: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:162 cancer HGNC:11279 Homo sapiens (human) 6713 SQLE
  • MGI:6194238
DOID:0070459 hereditary spastic paraplegia 90A HGNC:20361 Homo sapiens (human) 171546 SPTSSA
  • RGD:7240710
DOID:0070460 hereditary spastic paraplegia 90B HGNC:20361 Homo sapiens (human) 171546 SPTSSA
  • RGD:7240710
DOID:0070162 hereditary sensory and autonomic neuropathy type 1 HGNC:16253 Homo sapiens (human) 55304 SPTLC3
  • MGI:6194238
DOID:0070157 hereditary sensory and autonomic neuropathy type 1C HGNC:11278 Homo sapiens (human) 9517 SPTLC2
  • RGD:7240710
DOID:8893 psoriasis HGNC:11278 Homo sapiens (human) 9517 SPTLC2
  • MGI:6194238
DOID:0070162 hereditary sensory and autonomic neuropathy type 1 HGNC:11278 Homo sapiens (human) 9517 SPTLC2
  • MGI:6194238
DOID:0070152 hereditary sensory and autonomic neuropathy type 1A HGNC:11277 Homo sapiens (human) 10558 SPTLC1
  • MGI:6194238
  • RGD:7240710
DOID:0070162 hereditary sensory and autonomic neuropathy type 1 HGNC:11277 Homo sapiens (human) 10558 SPTLC1
  • MGI:6194238
DOID:0050548 hereditary sensory neuropathy HGNC:11277 Homo sapiens (human) 10558 SPTLC1
  • MGI:6194238
DOID:0081381 juvenile amyotrophic lateral sclerosis type 27 HGNC:11277 Homo sapiens (human) 10558 SPTLC1
  • RGD:7240710

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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