Table Filtering
Other Information
Release Statistics Download
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 66601 - 66625 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▼ References
DOID:4928 intrahepatic cholangiocarcinoma HGNC:6407 Homo sapiens (human) 3845 KRAS
  • MGI:6194238
  • PMID:24139215
DOID:0110124 Bardet-Biedl syndrome 2 HGNC:967 Homo sapiens (human) 583 BBS2
  • MGI:6194238
  • RGD:7240710
DOID:0070113 Niemann-Pick disease type C1 HGNC:7897 Homo sapiens (human) 4864 NPC1
  • MGI:6194238
  • RGD:7240710
DOID:0110827 Usher syndrome type 2 HGNC:12601 Homo sapiens (human) 7399 USH2A
  • MGI:6194238
  • PMID:12112664
  • PMID:15025721
  • PMID:17405132
  • PMID:18665195
  • PMID:22009552
DOID:0050994 episodic ataxia type 6 HGNC:10941 Homo sapiens (human) 6507 SLC1A3
  • MGI:6194238
  • RGD:7240710
DOID:10763 hypertension HGNC:286 Homo sapiens (human) 154 ADRB2
  • MGI:6194238
  • PMID:16041242
  • PMID:16685203
  • PMID:17221209
  • PMID:20484896
  • PMID:20739939
DOID:10587 Krabbe disease HGNC:4115 Homo sapiens (human) 2581 GALC
  • MGI:6194238
  • RGD:7240710
DOID:0060903 thrombosis HGNC:3535 Homo sapiens (human) 2147 F2
  • MGI:6194238
  • PMID:12632020
  • PMID:21070754
DOID:3633 beta-mannosidosis HGNC:6831 Homo sapiens (human) 4126 MANBA
  • MGI:6194238
  • RGD:7240710
DOID:0060933 developmental delay, dysmorphic facies, and brain anomalies HGNC:23156 Homo sapiens (human) 11338 U2AF2
  • MGI:6194238
  • RGD:7240710
DOID:9279 hyperhomocysteinemia HGNC:1550 Homo sapiens (human) 875 CBS
  • MGI:6194238
  • PMID:10704624
DOID:0111078 tibial muscular dystrophy HGNC:12403 Homo sapiens (human) 7273 TTN
  • MGI:6194238
  • RGD:7240710
DOID:0050660 Beare-Stevenson cutis gyrata syndrome HGNC:3689 Homo sapiens (human) 2263 FGFR2
  • MGI:6194238
  • RGD:7240710
DOID:0111277 mitochondrial trifunctional protein deficiency HGNC:4803 Homo sapiens (human) 3032 HADHB
  • MGI:6194238
  • RGD:7240710
DOID:409 liver disease HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • MGI:6194238
  • PMID:17950035
  • PMID:20392357
DOID:2736 Hajdu-Cheney syndrome HGNC:7882 Homo sapiens (human) 4853 NOTCH2
  • MGI:6194238
  • RGD:7240710
DOID:0110454 dilated cardiomyopathy 1S HGNC:7577 Homo sapiens (human) 4625 MYH7
  • MGI:6194238
  • RGD:7240710
DOID:0060556 Kufor-Rakeb syndrome HGNC:30213 Homo sapiens (human) 23400 ATP13A2
  • MGI:6194238
  • RGD:7240710
DOID:0050887 Townes-Brocks syndrome HGNC:10524 Homo sapiens (human) 6299 SALL1
  • MGI:6194238
  • RGD:7240710
DOID:0110869 congenital stationary night blindness 1E HGNC:31371 Homo sapiens (human) 440435 GPR179
  • MGI:6194238
  • RGD:7240710
DOID:10763 hypertension HGNC:3146 Homo sapiens (human) 1889 ECE1
  • MGI:6194238
  • PMID:15126915
DOID:0111385 inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 HGNC:12666 Homo sapiens (human) 7415 VCP
  • MGI:6194238
  • RGD:7240710
DOID:0060878 hypoparathyroidism-deafness-renal disease syndrome HGNC:4172 Homo sapiens (human) 2625 GATA3
  • MGI:6194238
  • RGD:7240710
DOID:0080887 vitamin D-dependent rickets type 1B HGNC:20580 Homo sapiens (human) 120227 CYP2R1
  • MGI:6194238
  • RGD:7240710
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
  • PMID:23269818

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