Table Filtering
Other Information
Release Statistics Download
Guidelines
MIRAGE
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 October 9, 2024
Displaying entries 61701 - 61725 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:1911 endodermal sinus tumor HGNC:12781 Homo sapiens (human) 7482 WNT2B
  • PMID:16822086
DOID:3307 teratoma HGNC:12781 Homo sapiens (human) 7482 WNT2B
  • PMID:16822086
DOID:0060774 congenital diarrhea HGNC:12781 Homo sapiens (human) 7482 WNT2B
  • RGD:7240710
DOID:0112192 tetraamelia syndrome 1 HGNC:12782 Homo sapiens (human) 7473 WNT3
  • RGD:7240710
DOID:1459 hypothyroidism HGNC:15983 Homo sapiens (human) 89780 WNT3A
  • MGI:6194238
DOID:0111526 Mullerian aplasia and hyperandrogenism HGNC:12783 Homo sapiens (human) 54361 WNT4
  • RGD:7240710
DOID:3021 acute kidney failure HGNC:12783 Homo sapiens (human) 54361 WNT4
  • MGI:6194238
DOID:2871 endometrial carcinoma HGNC:12783 Homo sapiens (human) 54361 WNT4
  • PMID:9099960
DOID:2871 endometrial carcinoma HGNC:12784 Homo sapiens (human) 7474 WNT5A
  • PMID:9099960
DOID:0060254 Robinow syndrome HGNC:12784 Homo sapiens (human) 7474 WNT5A
  • MGI:6194238
DOID:219 colon cancer HGNC:12784 Homo sapiens (human) 7474 WNT5A
  • MGI:6194238
DOID:0060766 autosomal dominant Robinow syndrome 1 HGNC:12784 Homo sapiens (human) 7474 WNT5A
  • RGD:7240710
DOID:127 leiomyoma HGNC:16265 Homo sapiens (human) 81029 WNT5B
  • PMID:15972578
DOID:0112181 Schinzel type phocomelia HGNC:12786 Homo sapiens (human) 7476 WNT7A
  • RGD:7240710
DOID:127 leiomyoma HGNC:12786 Homo sapiens (human) 7476 WNT7A
  • PMID:11232041
DOID:0090067 Fuhrmann syndrome HGNC:12786 Homo sapiens (human) 7476 WNT7A
  • MGI:6194238
  • RGD:7240710
DOID:1618 breast fibroadenoma HGNC:12787 Homo sapiens (human) 7477 WNT7B
  • PMID:8168088
DOID:11054 urinary bladder cancer HGNC:12787 Homo sapiens (human) 7477 WNT7B
  • PMID:9461004
DOID:1612 breast cancer HGNC:12787 Homo sapiens (human) 7477 WNT7B
  • PMID:15492823
DOID:10487 Hirschsprung's disease HGNC:12789 Homo sapiens (human) 7479 WNT8B
  • PMID:20972907
DOID:4947 cholangiocarcinoma HGNC:12778 Homo sapiens (human) 7483 WNT9A
  • PMID:31687280
DOID:1793 pancreatic cancer HGNC:12778 Homo sapiens (human) 7483 WNT9A
  • PMID:18772397
DOID:1612 breast cancer HGNC:12778 Homo sapiens (human) 7483 WNT9A
  • PMID:11713592
DOID:0050477 Liddle syndrome HGNC:16804 Homo sapiens (human) 11060 WWP2
  • MGI:6194238
DOID:0081126 DeSanto-Shinawi syndrome MGI:2387357 Mus musculus (house mouse) 225131 Wac
  • MGI:6194238

About Release Notes Help Feedback

International Collaboration

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.1.0

Last updated: December 9, 2024