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 4551 - 4575 of 15957 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism Source
DOID:13533
  • osteopetrosis
  • Aliases:
    • Albers-Schonberg disease
    • marble bone
Rattus norvegicus (Norway rat)
DOID:0110731
  • neuronal ceroid lipofuscinosis 3
  • Aliases:
    • Batten disease
    • CLN3
    • juvenile neuronal ceroid lipofuscinosis
Rattus norvegicus (Norway rat)
DOID:0111815
  • low molecular weight proteinuria with hypercalciuric nephrocalcinosis
Rattus norvegicus (Norway rat)
DOID:0050699
  • Dent disease
  • Aliases:
    • Dent disease 1
    • Dent disease 2
    • Dent's disease
Rattus norvegicus (Norway rat)
DOID:0111798
  • X-linked nephrolithiasis type I
  • Aliases:
    • NPHL1
    • X-linked nephrolithiasis with renal failure
    • X-linked recessive urolithiasis type 1
    • XRN
    • nephrolithiasis 1
    • nephrolithiasis X-linked recessive type 1
Mus musculus (house mouse)
DOID:447
  • renal tubular transport disease
  • Aliases:
    • inborn renal tubular transport disorder
Mus musculus (house mouse)
DOID:0080353
  • X-linked recessive hypophosphatemic rickets
Mus musculus (house mouse)
DOID:0050450
  • Gitelman syndrome
  • Aliases:
    • HYPOMAGNESEMIA-HYPOKALEMIA, PRIMARY RENOTUBULAR, WITH HYPOCALCIURIA
Mus musculus (house mouse)
DOID:0110146
  • Bartter disease type 4b
  • Aliases:
    • BARTS4B
    • Bartter syndrome, type 4b, digenic
    • neonatal Bartter syndrome type 4B with sensorineural deafness
Mus musculus (house mouse)
DOID:0110144
  • Bartter disease type 3
  • Aliases:
    • BARTS3
    • Bartter syndrome type 3
    • classic Bartter syndrome
Mus musculus (house mouse)
DOID:445
  • Bartter disease
  • Aliases:
    • Aldosteronism with hyperplasia of the adrenal cortex
    • Bartter's syndrome
Mus musculus (house mouse)
DOID:0050450
  • Gitelman syndrome
  • Aliases:
    • HYPOMAGNESEMIA-HYPOKALEMIA, PRIMARY RENOTUBULAR, WITH HYPOCALCIURIA
Rattus norvegicus (Norway rat)
DOID:0110146
  • Bartter disease type 4b
  • Aliases:
    • BARTS4B
    • Bartter syndrome, type 4b, digenic
    • neonatal Bartter syndrome type 4B with sensorineural deafness
Rattus norvegicus (Norway rat)
DOID:0110144
  • Bartter disease type 3
  • Aliases:
    • BARTS3
    • Bartter syndrome type 3
    • classic Bartter syndrome
Rattus norvegicus (Norway rat)
DOID:445
  • Bartter disease
  • Aliases:
    • Aldosteronism with hyperplasia of the adrenal cortex
    • Bartter's syndrome
Rattus norvegicus (Norway rat)
DOID:1928
  • Williams-Beuren syndrome
  • Aliases:
    • Fanconi Schlesinger syndrome
    • WBS
Mus musculus (house mouse)
DOID:10605
  • short bowel syndrome
  • Aliases:
    • acquired short bowel syndrome
    • short gut syndrome
Rattus norvegicus (Norway rat)
DOID:10605
  • short bowel syndrome
  • Aliases:
    • acquired short bowel syndrome
    • short gut syndrome
Mus musculus (house mouse)
DOID:0110721
  • neuronal ceroid lipofuscinosis 1
  • Aliases:
    • CLN1
    • neuronal ceroid lipofuscinosis 1 variable age of onset
Mus musculus (house mouse)
DOID:0110728
  • neuronal ceroid lipofuscinosis 5
  • Aliases:
    • CLN5
    • neuronal ceroid lipofuscinosis 5 variable age of onset
Mus musculus (house mouse)
DOID:535
  • sleep disorder
  • Aliases:
    • Non-organic sleep disorder
Mus musculus (house mouse)
DOID:0050921
  • pharynx squamous cell carcinoma
Mus musculus (house mouse)
DOID:9261
  • nasopharynx carcinoma
  • Aliases:
    • Nasopharyngeal carcinoma
    • malignant Nasopharyngeal tumor
    • malignant neoplasm of nasopharynx
    • nasopharynx cancer
Rattus norvegicus (Norway rat)
DOID:0050921
  • pharynx squamous cell carcinoma
Rattus norvegicus (Norway rat)
DOID:0110828
  • Usher syndrome type 3
  • Aliases:
    • USH3
Mus musculus (house mouse)
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