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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 6201 - 6225 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:14735 hereditary angioedema MGI:3580487 Mus musculus (house mouse) 328779 Hs3st6
  • MGI:6194238
DOID:0111156 spermatogenic failure 9 FB:FBgn0030946 Drosophila melanogaster (fruit fly) 32854 CG6659
  • MGI:6194238
DOID:11612 polycystic ovary syndrome HGNC:5218 Homo sapiens (human) 3284 HSD3B2
  • PMID:11739466
DOID:10892 hypospadias HGNC:5218 Homo sapiens (human) 3284 HSD3B2
  • PMID:14764821
DOID:10763 hypertension HGNC:5218 Homo sapiens (human) 3284 HSD3B2
  • MGI:6194238
DOID:12700 hyperprolactinemia HGNC:5218 Homo sapiens (human) 3284 HSD3B2
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:5218 Homo sapiens (human) 3284 HSD3B2
  • PMID:18180323
DOID:1924 hypogonadism HGNC:5217 Homo sapiens (human) 3283 HSD3B1
  • MGI:6194238
DOID:1459 hypothyroidism HGNC:5217 Homo sapiens (human) 3283 HSD3B1
  • MGI:6194238
DOID:10763 hypertension HGNC:5217 Homo sapiens (human) 3283 HSD3B1
  • MGI:6194238
  • PMID:12054649
DOID:12700 hyperprolactinemia HGNC:5217 Homo sapiens (human) 3283 HSD3B1
  • MGI:6194238
DOID:11446 sciatic neuropathy HGNC:5217 Homo sapiens (human) 3283 HSD3B1
  • MGI:6194238
DOID:11612 polycystic ovary syndrome HGNC:5217 Homo sapiens (human) 3283 HSD3B1
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:5217 Homo sapiens (human) 3283 HSD3B1
  • MGI:6194238
DOID:2316 brain ischemia HGNC:587 Homo sapiens (human) 328 APEX1
  • MGI:6194238
DOID:1824 status epilepticus HGNC:587 Homo sapiens (human) 328 APEX1
  • MGI:6194238
DOID:13129 severe pre-eclampsia HGNC:587 Homo sapiens (human) 328 APEX1
  • PMID:24619222
DOID:684 hepatocellular carcinoma HGNC:587 Homo sapiens (human) 328 APEX1
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:587 Homo sapiens (human) 328 APEX1
  • PMID:18712175
DOID:3459 breast carcinoma HGNC:587 Homo sapiens (human) 328 APEX1
  • PMID:11748448
DOID:2394 ovarian cancer HGNC:587 Homo sapiens (human) 328 APEX1
  • PMID:17974506
  • PMID:19787261
DOID:4362 cervical cancer HGNC:587 Homo sapiens (human) 328 APEX1
  • PMID:18503157
  • PMID:19292061
DOID:850 lung disease HGNC:587 Homo sapiens (human) 328 APEX1
  • MGI:6194238

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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