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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 October 9, 2024
Displaying entries 62701 - 62725 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:3717 gastric adenocarcinoma HGNC:12825 Homo sapiens (human) 7514 XPO1
  • PMID:28373767
  • PMID:30115935
DOID:3748 esophagus squamous cell carcinoma HGNC:12825 Homo sapiens (human) 7514 XPO1
  • PMID:24898882
  • PMID:25148895
DOID:0080941 acquired angioedema HGNC:12823 Homo sapiens (human) 7512 XPNPEP2
  • RGD:7240710
DOID:0050427 xeroderma pigmentosum HGNC:12816 Homo sapiens (human) 7508 XPC
  • MGI:6194238
  • PMID:8298653
DOID:3114 serous cystadenocarcinoma HGNC:12816 Homo sapiens (human) 7508 XPC
  • PMID:21751198
DOID:1324 lung cancer HGNC:12816 Homo sapiens (human) 7508 XPC
  • MGI:6194238
DOID:1793 pancreatic cancer HGNC:12816 Homo sapiens (human) 7508 XPC
  • PMID:18559563
DOID:0110844 xeroderma pigmentosum group C HGNC:12816 Homo sapiens (human) 7508 XPC
  • MGI:6194238
  • RGD:7240710
DOID:10487 Hirschsprung's disease HGNC:12789 Homo sapiens (human) 7479 WNT8B
  • PMID:20972907
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: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: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: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:0112192 tetraamelia syndrome 1 HGNC:12782 Homo sapiens (human) 7473 WNT3
  • RGD:7240710
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

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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: December 9, 2024