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 6451 - 6475 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▲
DOID:0110741
  • type 1 diabetes mellitus 2
  • Aliases:
    • IDDM2
    • Insulin-Dependent Diabetes Mellitus 2
Homo sapiens (human)
DOID:0110749
  • type 1 diabetes mellitus 10
  • Aliases:
    • IDDM10
    • Insulin-Dependent Diabetes Mellitus 10
Rattus norvegicus (Norway rat)
DOID:0110749
  • type 1 diabetes mellitus 10
  • Aliases:
    • IDDM10
    • Insulin-Dependent Diabetes Mellitus 10
Mus musculus (house mouse)
DOID:0110749
  • type 1 diabetes mellitus 10
  • Aliases:
    • IDDM10
    • Insulin-Dependent Diabetes Mellitus 10
Homo sapiens (human)
DOID:0110751
  • type 1 diabetes mellitus 12
  • Aliases:
    • IDDM12
    • Insulin-Dependent Diabetes Mellitus 12
Homo sapiens (human)
DOID:0110751
  • type 1 diabetes mellitus 12
  • Aliases:
    • IDDM12
    • Insulin-Dependent Diabetes Mellitus 12
Mus musculus (house mouse)
DOID:0110757
  • type 1 diabetes mellitus 20
  • Aliases:
    • IDDM20
    • Insulin-Dependent Diabetes Mellitus 20
Homo sapiens (human)
DOID:0110759
  • type 1 diabetes mellitus 22
  • Aliases:
    • IDDM22
    • Insulin-Dependent Diabetes Mellitus 22
Mus musculus (house mouse)
DOID:0110759
  • type 1 diabetes mellitus 22
  • Aliases:
    • IDDM22
    • Insulin-Dependent Diabetes Mellitus 22
Rattus norvegicus (Norway rat)
DOID:0110759
  • type 1 diabetes mellitus 22
  • Aliases:
    • IDDM22
    • Insulin-Dependent Diabetes Mellitus 22
Homo sapiens (human)
DOID:0110764
  • hereditary spastic paraplegia 11
  • Aliases:
    • HSP-TCC
    • Nakamura-Osame syndrome
    • SPG11
    • autosomal recessive spastic paraplegia 11
    • autosomal recessive spastic paraplegia complicated with thin corpus callosum
    • autosomal recessive spastic paraplegia type 11
    • autosomal recessive spastic paraplegia with mental impairment and thin corpus callosum
    • spastic paraplegia-intellectual disability-thin corpus callosum syndrome
Homo sapiens (human)
DOID:0110765
  • hereditary spastic paraplegia 12
  • Aliases:
    • SPG12
    • autosomal dominant spastic paraplegia 12
    • autosomal dominant spastic paraplegia type 12
Homo sapiens (human)
DOID:0110765
  • hereditary spastic paraplegia 12
  • Aliases:
    • SPG12
    • autosomal dominant spastic paraplegia 12
    • autosomal dominant spastic paraplegia type 12
Mus musculus (house mouse)
DOID:0110766
  • hereditary spastic paraplegia 13
  • Aliases:
    • SPG13
    • autosomal dominant spastic paraplegia 13
Homo sapiens (human)
DOID:0110766
  • hereditary spastic paraplegia 13
  • Aliases:
    • SPG13
    • autosomal dominant spastic paraplegia 13
Mus musculus (house mouse)
DOID:0110766
  • hereditary spastic paraplegia 13
  • Aliases:
    • SPG13
    • autosomal dominant spastic paraplegia 13
Rattus norvegicus (Norway rat)
DOID:0110768
  • hereditary spastic paraplegia 15
  • Aliases:
    • Kjellin syndrome
    • SPG15
    • autosomal recessive spastic paraplegia 15
    • autosomal recessive spastic paraplegia type 15
    • hereditary spastic paraparesis type 15
    • spastic paraplegia and retinal degeneration
    • spastic paraplegia-retinal degeneration syndrome
Homo sapiens (human)
DOID:0110770
  • hereditary spastic paraplegia 17
  • Aliases:
    • SPG17
    • Silver spastic paraplegia syndrome
    • Silver syndrome
    • autosomal dominant spastic paraplegia 17
    • autosomal dominant spastic paraplegia type 17
    • dHMN5B
    • distal hereditary motor neuropathy type 5B
    • spastic paraplegia with amyotrophy of hands and feet
    • spastic paraplegia-amyotrophy of hands and feet
Mus musculus (house mouse)
DOID:0110770
  • hereditary spastic paraplegia 17
  • Aliases:
    • SPG17
    • Silver spastic paraplegia syndrome
    • Silver syndrome
    • autosomal dominant spastic paraplegia 17
    • autosomal dominant spastic paraplegia type 17
    • dHMN5B
    • distal hereditary motor neuropathy type 5B
    • spastic paraplegia with amyotrophy of hands and feet
    • spastic paraplegia-amyotrophy of hands and feet
Homo sapiens (human)
DOID:0110770
  • hereditary spastic paraplegia 17
  • Aliases:
    • SPG17
    • Silver spastic paraplegia syndrome
    • Silver syndrome
    • autosomal dominant spastic paraplegia 17
    • autosomal dominant spastic paraplegia type 17
    • dHMN5B
    • distal hereditary motor neuropathy type 5B
    • spastic paraplegia with amyotrophy of hands and feet
    • spastic paraplegia-amyotrophy of hands and feet
Rattus norvegicus (Norway rat)
DOID:0110771
  • hereditary spastic paraplegia 18
  • Aliases:
    • IDMDC
    • SPG18
    • autosomal recessive spastic paraplegia 18
    • autosomal recessive spastic paraplegia type 18
    • intellectual disability, motor dysfunction and joint contractures
Rattus norvegicus (Norway rat)
DOID:0110771
  • hereditary spastic paraplegia 18
  • Aliases:
    • IDMDC
    • SPG18
    • autosomal recessive spastic paraplegia 18
    • autosomal recessive spastic paraplegia type 18
    • intellectual disability, motor dysfunction and joint contractures
Xenopus laevis (African clawed frog)
DOID:0110771
  • hereditary spastic paraplegia 18
  • Aliases:
    • IDMDC
    • SPG18
    • autosomal recessive spastic paraplegia 18
    • autosomal recessive spastic paraplegia type 18
    • intellectual disability, motor dysfunction and joint contractures
Caenorhabditis elegans
DOID:0110771
  • hereditary spastic paraplegia 18
  • Aliases:
    • IDMDC
    • SPG18
    • autosomal recessive spastic paraplegia 18
    • autosomal recessive spastic paraplegia type 18
    • intellectual disability, motor dysfunction and joint contractures
Mus musculus (house mouse)
DOID:0110771
  • hereditary spastic paraplegia 18
  • Aliases:
    • IDMDC
    • SPG18
    • autosomal recessive spastic paraplegia 18
    • autosomal recessive spastic paraplegia type 18
    • intellectual disability, motor dysfunction and joint contractures
Danio rerio (zebrafish)

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