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 1876 - 1900 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism Source
DOID:0110782
  • hereditary spastic paraplegia 31
  • Aliases:
    • SPG31
    • autosomal dominant spastic paraplegia 31
    • autosomal dominant spastic paraplegia type 31
Mus musculus (house mouse)
DOID:0080350
  • retinitis pigmentosa 77
Mus musculus (house mouse)
DOID:0070432
  • hyperphosphatasia with impaired intellectual development syndrome 5
  • Aliases:
    • GPIBD11
    • HPMRS5
    • glycosylphosphatidylinositol biosynthesis defect 11
    • hyperphosphatasia with mental retardation syndrome 5
Mus musculus (house mouse)
DOID:3493
  • signet ring cell adenocarcinoma
  • Aliases:
    • Signet ring carcinoma
    • Signet ring cell carcinoma
Homo sapiens (human)
DOID:3702
  • cervical adenocarcinoma
  • Aliases:
    • adenocarcinoma cervix uteri
    • adenocarcinoma of cervix
    • adenocarcinoma of the uterine Cervix
Homo sapiens (human)
DOID:0080943
  • 46,XX sex reversal 5
Homo sapiens (human)
DOID:0060563
  • Char syndrome
Homo sapiens (human)
DOID:0080337
  • mitochondrial DNA depletion syndrome 15
Homo sapiens (human)
DOID:12934
  • Kearns-Sayre syndrome
Homo sapiens (human)
DOID:0050649
  • atransferrinemia
  • Aliases:
    • familial hypotransferrinemia
Homo sapiens (human)
DOID:0060717
  • autosomal recessive congenital ichthyosis 8
  • Aliases:
    • ARCI8
    • lamellar ichthyosis 4
    • late-onset lamellar ichthyosis
Mus musculus (house mouse)
DOID:0070016
  • autosomal dominant dyskeratosis congenita 2
  • Aliases:
    • DKCA2
Homo sapiens (human)
DOID:9513
  • plasma cell leukemia
  • Aliases:
    • plasma cell leukaemia
    • plasmacytic leukaemia
    • plasmacytic leukemia
Homo sapiens (human)
DOID:0080268
  • autosomal dominant nonsyndromic deafness 72
Mus musculus (house mouse)
DOID:0050792
  • multiple cutaneous and mucosal venous malformations
  • Aliases:
    • VMCM
    • cutaneomucosal venous malformation
    • mucocutaneous venous malformations
Homo sapiens (human)
DOID:12176
  • goiter
  • Aliases:
    • goitre
Homo sapiens (human)
DOID:0080141
  • mosaic variegated aneuploidy syndrome 1
Homo sapiens (human)
DOID:0080641
  • tongue carcinoma
Homo sapiens (human)
DOID:0060304
  • dyschromatosis universalis hereditaria
Mus musculus (house mouse)
DOID:0110479
  • autosomal recessive nonsyndromic deafness 21
  • Aliases:
    • DFNB21
    • autosomal recessive deafness 21
Homo sapiens (human)
DOID:0110544
  • autosomal dominant nonsyndromic deafness 12
  • Aliases:
    • DFNA12
    • DFNA8
    • autosomal dominant deafness 12
    • autosomal dominant deafness 8
Homo sapiens (human)
DOID:0111228
  • Sveinsson chorioretinal atrophy
  • Aliases:
    • HPCD
    • SCRA
    • atrophia areata
    • helicoid peripapillary chorioretinal degeneration
    • peripapillary chorioretinal degeneration, Icelandic type
Homo sapiens (human)
DOID:14069
  • cerebral malaria
  • Aliases:
    • Malarial encephalitis
Mus musculus (house mouse)
DOID:0110456
  • dilated cardiomyopathy 1R
  • Aliases:
    • CMD1R
Homo sapiens (human)
DOID:0110110
  • atrial heart septal defect 5
  • Aliases:
    • ASD5
    • atrial septal defect 5
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