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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:3493 signet ring cell adenocarcinoma HGNC:11755 Homo sapiens (human) 7031 TFF1
  • PMID:18283638
DOID:1380 endometrial cancer HGNC:11755 Homo sapiens (human) 7031 TFF1
  • PMID:10835496
DOID:2671 transitional cell carcinoma HGNC:11755 Homo sapiens (human) 7031 TFF1
  • PMID:7965392
DOID:10808 gastric ulcer HGNC:11755 Homo sapiens (human) 7031 TFF1
  • MGI:6194238
DOID:0060074 ductal carcinoma in situ HGNC:11755 Homo sapiens (human) 7031 TFF1
  • PMID:15375487
DOID:2394 ovarian cancer HGNC:11755 Homo sapiens (human) 7031 TFF1
  • PMID:17624412
DOID:3702 cervical adenocarcinoma HGNC:11755 Homo sapiens (human) 7031 TFF1
  • PMID:10727981
DOID:0060180 colitis HGNC:11755 Homo sapiens (human) 7031 TFF1
  • MGI:6194238
DOID:10283 prostate cancer HGNC:11755 Homo sapiens (human) 7031 TFF1
  • PMID:10458410
  • PMID:16467092
DOID:11054 urinary bladder cancer HGNC:11755 Homo sapiens (human) 7031 TFF1
  • PMID:18283638
DOID:10534 stomach cancer HGNC:11755 Homo sapiens (human) 7031 TFF1
  • MGI:6194238
DOID:0080365 endometrial hyperplasia HGNC:11755 Homo sapiens (human) 7031 TFF1
  • PMID:9221798
DOID:13550 angle-closure glaucoma HGNC:11743 Homo sapiens (human) 7021 TFAP2B
  • MGI:6194238
DOID:535 sleep disorder HGNC:11743 Homo sapiens (human) 7021 TFAP2B
  • MGI:6194238
DOID:13832 patent ductus arteriosus HGNC:11743 Homo sapiens (human) 7021 TFAP2B
  • MGI:6194238
  • PMID:10802654
  • RGD:7240710
DOID:0060563 Char syndrome HGNC:11743 Homo sapiens (human) 7021 TFAP2B
  • MGI:6194238
  • RGD:7240710
DOID:0110544 autosomal dominant nonsyndromic deafness 12 HGNC:11720 Homo sapiens (human) 7007 TECTA
  • MGI:6194238
  • RGD:7240710
DOID:10003 sensorineural hearing loss HGNC:11720 Homo sapiens (human) 7007 TECTA
  • PMID:9590290
  • PMID:9949200
DOID:0110479 autosomal recessive nonsyndromic deafness 21 HGNC:11720 Homo sapiens (human) 7007 TECTA
  • RGD:7240710
DOID:13268 porphyria HGNC:117 Homo sapiens (human) 48 ACO1
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:117 Homo sapiens (human) 48 ACO1
  • MGI:6194238
DOID:1724 duodenal ulcer HGNC:117 Homo sapiens (human) 48 ACO1
  • MGI:6194238
DOID:10763 hypertension HGNC:11609 Homo sapiens (human) 6916 TBXAS1
  • MGI:6194238
DOID:3526 cerebral infarction HGNC:11609 Homo sapiens (human) 6916 TBXAS1
  • PMID:19403042
DOID:0060903 thrombosis HGNC:11609 Homo sapiens (human) 6916 TBXAS1
  • 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