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 6376 - 6400 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:3113
  • papillary carcinoma
Mus musculus (house mouse)
DOID:0110467
  • autosomal recessive nonsyndromic deafness 12
  • Aliases:
    • DFNB12
    • autosomal recessive deafness 12
Drosophila melanogaster (fruit fly)
DOID:418
  • systemic scleroderma
  • Aliases:
    • Scleroderma
    • Scleroderma syndrome
    • progressive systemic sclerosis
    • systemic sclerosis
Caenorhabditis elegans
DOID:0112368
  • Coffin-Siris syndrome 5
  • Aliases:
    • CSS5
Homo sapiens (human)
DOID:0080109
  • infantile myofibromatosis
  • Aliases:
    • lipofibromatosis
Caenorhabditis elegans
DOID:0090076
  • hypogonadotropic hypogonadism 18 with or without anosmia
Mus musculus (house mouse)
DOID:3159
  • photosensitivity disease
  • Aliases:
    • Photodermatitis
Homo sapiens (human)
DOID:0050454
  • periventricular nodular heterotopia
  • Aliases:
    • periventricular heterotopia
Drosophila melanogaster (fruit fly)
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:127
  • leiomyoma
  • Aliases:
    • leiomyomatous neoplasm
    • leiomyomatous tumor
Caenorhabditis elegans
DOID:853
  • polymyalgia rheumatica
Mus musculus (house mouse)
DOID:0081317
  • multiple synostoses syndrome 1
Danio rerio (zebrafish)
DOID:1227
  • neutropenia
Rattus norvegicus (Norway rat)
DOID:0050117
  • disease by infectious agent
  • Aliases:
    • infectious disease
Mus musculus (house mouse)
DOID:0070030
  • ITM2B-related cerebral amyloid angiopathy 2
  • Aliases:
    • Cerebellar Ataxia, Cataract, Deafness, and Dementia Or Psychosis
    • FDD
    • Familial Danish Dementia
    • HOOE
    • Heredopathia Ophthalmootoencephalica
Homo sapiens (human)
DOID:0110663
  • congenital myasthenic syndrome 1A
  • Aliases:
    • CMS IIa
    • CMS1A
    • congenital myasthenic syndrome 1A, slow-channel
    • congenital myasthenic syndrome type IIa
Danio rerio (zebrafish)
DOID:0060822
  • syndromic X-linked intellectual disability Cabezas type
  • Aliases:
    • Cabezas syndrome; syndromic X-linked mental retardation 15
    • MRSS
    • MRXS15
    • MRXSC
    • X-linked mental retardation with short stature
    • X-linked mental retardation with short stature, hypogonadism, and abnormal gait
    • mental retardation, X-linked, syndromic 15
    • mental retardation, X-linked, syndromic 15 (Cabezas type)
Mus musculus (house mouse)
DOID:0070139
  • autosomal recessive cutis laxa type IC
  • Aliases:
    • ARCL1C
    • autosomal recessive cutis laxa type 1C
Homo sapiens (human)
DOID:0002116
  • pterygium
  • Aliases:
    • surfer's eye
Rattus norvegicus (Norway rat)
DOID:668
  • myositis ossificans
  • Aliases:
    • Myisitis ossificans
    • Ossification - muscle
Homo sapiens (human)
DOID:1929
  • supravalvular aortic stenosis
  • Aliases:
    • Supra-valvular aortic stenosis
Rattus norvegicus (Norway rat)
DOID:0110859
  • polycystic kidney disease 2
  • Aliases:
    • Apkd2
    • Pkd2
    • Polycystic Kidney Disease, Adult, Type II
Homo sapiens (human)
DOID:963
  • episodic ataxia
  • Aliases:
    • Isaacs syndrome
Mus musculus (house mouse)
DOID:0050564
  • autosomal dominant nonsyndromic deafness
  • Aliases:
    • autosomal dominant deafness
Rattus norvegicus (Norway rat)
DOID:0060901
  • lymphoplasmacytic lymphoma
  • Aliases:
    • Waldenstroem's macroglobulinemia
    • Waldenstrom Macroglobulinemia
    • lymphoplasmacytic lymphoma with IgM gammopathy
Xenopus laevis (African clawed frog)
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