Table Filtering
Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
Resources Genes Glycoproteins Lectins Glycolipids Glycans Pathways Diseases Organisms
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Other Information
Release Statistics Download
Tools
SugarDrawer GlycanBuilder Glycan Converters GlycoMaple GlycomeAtlas LM-GlycomeAtlas GALAXY MCAW GlycoSim GRable
Search Tools
Cross Search Glycan Search Publication Search Programmatic Access
Standards Ontologies Notations
GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources October 9, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 1951 - 1975 of 4649 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▼
DOID:0111918
  • spermatogenic failure 40
  • Aliases:
    • SPGF40
Homo sapiens (human)
DOID:0111917
  • spermatogenic failure 43
  • Aliases:
    • SPGF43
Homo sapiens (human)
DOID:0111916
  • spermatogenic failure 28
  • Aliases:
    • SPGF28
Homo sapiens (human)
DOID:0111913
  • spermatogenic failure 30
  • Aliases:
    • SPGF30
Homo sapiens (human)
DOID:0111911
  • spermatogenic failure 34
  • Aliases:
    • SPGF34
Homo sapiens (human)
DOID:0111910
  • spermatogenic failure
  • Aliases:
    • SPGF
Homo sapiens (human)
DOID:0111909
  • autosomal dominant thrombophilia due to protein C deficiency
  • Aliases:
    • THPH3
    • autosomal dominant PROC deficiency
    • autosomal dominant protein C deficiency
Homo sapiens (human)
DOID:0111908
  • thrombophilia due to thrombomodulin defect
  • Aliases:
    • THBD-related bleeding disorder
    • THBD-related coagulopathy
    • THPH12
    • thrombomodulin-related bleeding disorder
    • thrombomodulin-related coagulopathy
Homo sapiens (human)
DOID:0111907
  • thrombophilia due to thrombin defect
  • Aliases:
    • THPH1
    • prothrombin-related thrombophilia
    • thrombophilia due to factor 2 defect
Homo sapiens (human)
DOID:0111905
  • autosomal recessive thrombophilia due to protein S deficiency
  • Aliases:
    • THPH6
    • autosomal recessive thrombophilia due to congenital protein S deficiency
    • severe hereditary thrombophilia due to congenital protein S deficiency
Homo sapiens (human)
DOID:0111904
  • autosomal recessive thrombophilia due to protein C deficiency
  • Aliases:
    • THPH4
    • autosomal recessive PROC deficiency
    • autosomal recessive protein C deficiency
Homo sapiens (human)
DOID:0111903
  • thrombophilia due to HRG deficiency
  • Aliases:
    • THPH11
    • hereditary thrombophilia due to congenital HRG deficiency
    • hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
Homo sapiens (human)
DOID:0111902
  • thrombophilia due to activated protein C resistance
  • Aliases:
    • APC resistance
    • PCCF deficiency
    • PROC cofactor deficiency
    • THPH2
    • activated protein C resistance
    • thrombophilia V
    • thrombophilia due to deficiency of activated protein C cofactor
Homo sapiens (human)
DOID:0111901
  • heparin cofactor II deficiency
  • Aliases:
    • HCF 2 deficiency
    • HCF II deficiency
    • THPH10
    • thrombophilia due to heparin cofactor II deficiency
Homo sapiens (human)
DOID:0111900
  • autosomal dominant thrombophilia due to protein S deficiency
  • Aliases:
    • THPH5
Homo sapiens (human)
DOID:0111899
  • X-linked thrombophilia due to factor IX defect
  • Aliases:
    • THPH8
Homo sapiens (human)
DOID:0111898
  • CK syndrome
  • Aliases:
    • X-linked intellectual disability-microcephaly-cortical malformation-thin habitus syndrome
Homo sapiens (human)
DOID:0111896
  • Diamond-Blackfan anemia 18
  • Aliases:
    • DBA18
    • RPL18-related Diamond-Blackfan anemia
Homo sapiens (human)
DOID:0111892
  • Diamond-Blackfan anemia 11
  • Aliases:
    • DBA11
    • RPL26-related Diamond-Blackfan anemia
Homo sapiens (human)
DOID:0111887
  • Diamond-blackfan anemia 3
  • Aliases:
    • DBA3
    • RPS24-related Diamond-Blackfan anemia
Homo sapiens (human)
DOID:0111883
  • Diamond-Blackfan anemia 5
  • Aliases:
    • DBA5
    • RPL35A-related Diamond-Blackfan anemia
Homo sapiens (human)
DOID:0111876
  • linear skin defects with multiple congenital anomalies 3
  • Aliases:
    • LSDMCA3
    • linear skin defects with cardiomyopathy and other congenital anomalies
Homo sapiens (human)
DOID:0111872
  • nonphotosensitive trichothiodystrophy 6
  • Aliases:
    • TTD6
Homo sapiens (human)
DOID:0111870
  • nonphotosensitive trichothiodystrophy 7
  • Aliases:
    • TTD7
Homo sapiens (human)
DOID:0111867
  • nonphotosensitive trichothiodystrophy
Homo sapiens (human)
Download data in CSV format Download data in TSV format Download data in JSON format
About Release Notes Help Feedback

Click here to visit the beta site.

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