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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 70251 - 70275 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:14735 hereditary angioedema HGNC:484 Homo sapiens (human) 284 ANGPT1
  • RGD:7240710
DOID:6432 pulmonary hypertension HGNC:484 Homo sapiens (human) 284 ANGPT1
  • MGI:6194238
DOID:8719 in situ carcinoma HGNC:484 Homo sapiens (human) 284 ANGPT1
  • MGI:6194238
DOID:10808 gastric ulcer HGNC:484 Homo sapiens (human) 284 ANGPT1
  • MGI:6194238
DOID:1574 alcohol use disorder HGNC:484 Homo sapiens (human) 284 ANGPT1
  • MGI:6194238
DOID:2870 endometrial adenocarcinoma HGNC:484 Homo sapiens (human) 284 ANGPT1
  • PMID:17295646
DOID:5844 myocardial infarction HGNC:484 Homo sapiens (human) 284 ANGPT1
  • MGI:6194238
DOID:2732 Rothmund-Thomson syndrome HGNC:19988 Homo sapiens (human) 64682 ANAPC1
  • RGD:7240710
DOID:9268 glycine encephalopathy HGNC:473 Homo sapiens (human) 275 AMT
  • PMID:8005589
  • PMID:9600239
  • PMID:9621520
  • RGD:7240710
DOID:0110814 hereditary spastic paraplegia 63 HGNC:469 Homo sapiens (human) 271 AMPD2
  • RGD:7240710
DOID:0060278 pontocerebellar hypoplasia type 9 HGNC:469 Homo sapiens (human) 271 AMPD2
  • RGD:7240710
DOID:0060264 pontocerebellar hypoplasia HGNC:469 Homo sapiens (human) 271 AMPD2
  • MGI:6194238
DOID:13382 megaloblastic anemia HGNC:14604 Homo sapiens (human) 81693 AMN
  • PMID:12590260
DOID:557 kidney disease HGNC:14604 Homo sapiens (human) 81693 AMN
  • MGI:6194238
DOID:0050700 cardiomyopathy HGNC:14604 Homo sapiens (human) 81693 AMN
  • MGI:6194238
DOID:11446 sciatic neuropathy HGNC:24075 Homo sapiens (human) 386724 AMIGO3
  • MGI:6194238
DOID:3717 gastric adenocarcinoma HGNC:24073 Homo sapiens (human) 347902 AMIGO2
  • PMID:15107827
DOID:1967 leiomyosarcoma HGNC:465 Homo sapiens (human) 269 AMHR2
  • PMID:17988723
DOID:0050791 persistent Mullerian duct syndrome HGNC:465 Homo sapiens (human) 269 AMHR2
  • MGI:6194238
  • RGD:7240710
DOID:4441 dysgerminoma HGNC:465 Homo sapiens (human) 269 AMHR2
  • PMID:17988723
DOID:2999 granulosa cell tumor HGNC:464 Homo sapiens (human) 268 AMH
  • PMID:19359032
DOID:9970 obesity HGNC:464 Homo sapiens (human) 268 AMH
  • PMID:17109858
DOID:4001 ovarian carcinoma HGNC:464 Homo sapiens (human) 268 AMH
  • PMID:16533786
DOID:11612 polycystic ovary syndrome HGNC:464 Homo sapiens (human) 268 AMH
  • PMID:17224152
DOID:0050791 persistent Mullerian duct syndrome HGNC:464 Homo sapiens (human) 268 AMH
  • RGD:7240710

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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: December 9, 2024