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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 10501 - 10525 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:1459 hypothyroidism HGNC:2594 Homo sapiens (human) 1588 CYP19A1
  • MGI:6194238
DOID:14654 prostatitis HGNC:2594 Homo sapiens (human) 1588 CYP19A1
  • PMID:19700748
DOID:1380 endometrial cancer HGNC:2594 Homo sapiens (human) 1588 CYP19A1
  • PMID:18497059
DOID:289 endometriosis HGNC:2594 Homo sapiens (human) 1588 CYP19A1
  • MGI:6194238
  • PMID:8550748
DOID:4914 esophagus adenocarcinoma HGNC:2594 Homo sapiens (human) 1588 CYP19A1
  • PMID:21472143
DOID:8634 prostate carcinoma in situ HGNC:2594 Homo sapiens (human) 1588 CYP19A1
  • PMID:19700748
DOID:13948 bladder neck obstruction HGNC:2594 Homo sapiens (human) 1588 CYP19A1
  • PMID:21356374
DOID:1923 disorder of sexual development HGNC:2594 Homo sapiens (human) 1588 CYP19A1
  • MGI:6194238
DOID:11801 protein-energy malnutrition HGNC:2594 Homo sapiens (human) 1588 CYP19A1
  • MGI:6194238
DOID:10763 hypertension HGNC:2594 Homo sapiens (human) 1588 CYP19A1
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:2594 Homo sapiens (human) 1588 CYP19A1
  • PMID:16882736
  • PMID:18180323
DOID:11612 polycystic ovary syndrome HGNC:2594 Homo sapiens (human) 1588 CYP19A1
  • MGI:6194238
  • PMID:21282199
DOID:12894 Sjogren's syndrome HGNC:2594 Homo sapiens (human) 1588 CYP19A1
  • MGI:6194238
DOID:3891 placental insufficiency HGNC:2594 Homo sapiens (human) 1588 CYP19A1
  • MGI:6194238
DOID:0090122 aromatase excess syndrome HGNC:2594 Homo sapiens (human) 1588 CYP19A1
  • RGD:7240710
DOID:1612 breast cancer HGNC:2594 Homo sapiens (human) 1588 CYP19A1
  • PMID:16875543
  • PMID:23643682
  • PMID:7053713
DOID:2394 ovarian cancer HGNC:2594 Homo sapiens (human) 1588 CYP19A1
  • PMID:18497059
DOID:11476 osteoporosis HGNC:2594 Homo sapiens (human) 1588 CYP19A1
  • PMID:17002564
DOID:0050811 congenital adrenal hyperplasia HGNC:2593 Homo sapiens (human) 1586 CYP17A1
  • PMID:2026124
DOID:1793 pancreatic cancer HGNC:2593 Homo sapiens (human) 1586 CYP17A1
  • PMID:19642097
DOID:10211 cholelithiasis HGNC:2593 Homo sapiens (human) 1586 CYP17A1
  • PMID:16381022
DOID:3121 gallbladder cancer HGNC:2593 Homo sapiens (human) 1586 CYP17A1
  • PMID:16381022
DOID:11446 sciatic neuropathy HGNC:2593 Homo sapiens (human) 1586 CYP17A1
  • MGI:6194238
DOID:1612 breast cancer HGNC:2593 Homo sapiens (human) 1586 CYP17A1
  • PMID:12631398
DOID:10283 prostate cancer HGNC:2593 Homo sapiens (human) 1586 CYP17A1
  • PMID:18645193

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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