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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 9601 - 9625 of 15957 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism Source
DOID:0080240
  • non-syndromic X-linked intellectual disability 106
  • Aliases:
    • MRX106
    • X-linked mental retardation 106
Rattus norvegicus (Norway rat)
DOID:13910
  • red color blindness
  • Aliases:
    • Protan defect
    • Protanopia
Mus musculus (house mouse)
DOID:13909
  • red-green color blindness
  • Aliases:
    • Deutan defect
    • Deuteranopia
    • Reduced red-green discrimination
Mus musculus (house mouse)
DOID:0050679
  • blue cone monochromacy
Mus musculus (house mouse)
DOID:13909
  • red-green color blindness
  • Aliases:
    • Deutan defect
    • Deuteranopia
    • Reduced red-green discrimination
Rattus norvegicus (Norway rat)
DOID:0050679
  • blue cone monochromacy
Rattus norvegicus (Norway rat)
DOID:13910
  • red color blindness
  • Aliases:
    • Protan defect
    • Protanopia
Rattus norvegicus (Norway rat)
DOID:11661
  • blue color blindness
  • Aliases:
    • Tritan defect
    • Tritanopia
Mus musculus (house mouse)
DOID:11661
  • blue color blindness
  • Aliases:
    • Tritan defect
    • Tritanopia
Rattus norvegicus (Norway rat)
DOID:0110372
  • retinitis pigmentosa 4
  • Aliases:
    • RP4
Rattus norvegicus (Norway rat)
DOID:0110372
  • retinitis pigmentosa 4
  • Aliases:
    • RP4
Mus musculus (house mouse)
DOID:0080686
  • tubular aggregate myopathy 2
Mus musculus (house mouse)
DOID:0111976
  • immunodeficiency 9
  • Aliases:
    • CID due to ORAI1 deficiency
    • IMD9
    • combined immunodeficiency due to ORAI1 deficiency
    • immune dysfunction with T-cell inactivation due to calcium entry defect 1
Mus musculus (house mouse)
DOID:0080686
  • tubular aggregate myopathy 2
Rattus norvegicus (Norway rat)
DOID:0111976
  • immunodeficiency 9
  • Aliases:
    • CID due to ORAI1 deficiency
    • IMD9
    • combined immunodeficiency due to ORAI1 deficiency
    • immune dysfunction with T-cell inactivation due to calcium entry defect 1
Rattus norvegicus (Norway rat)
DOID:14365
  • systemic primary carnitine deficiency disease
  • Aliases:
    • carnitine transporter deficiency
    • carnitine uptake defect
    • deficiency of plasma-membrane carnitine transporter
    • primary carnitine deficiency
    • renal carnitine transport defect
Drosophila melanogaster (fruit fly)
DOID:0080930
  • primary localized cutaneous amyloidosis 1
  • Aliases:
    • familial primary localized cutaneous amyloidosis-1
Mus musculus (house mouse)
DOID:0080930
  • primary localized cutaneous amyloidosis 1
  • Aliases:
    • familial primary localized cutaneous amyloidosis-1
Rattus norvegicus (Norway rat)
DOID:0080569
  • congenital disorder of glycosylation Ir
  • Aliases:
    • congenital disorder of glycosylation 1r
Drosophila melanogaster (fruit fly)
DOID:612
  • primary immunodeficiency disease
  • Aliases:
    • hypoimmunity
    • immune deficiency disorder
    • immunodeficiency syndrome
Drosophila melanogaster (fruit fly)
DOID:104
  • bacterial infectious disease
Drosophila melanogaster (fruit fly)
DOID:0081183
  • autosomal recessive intellectual developmental disorder 7
Drosophila melanogaster (fruit fly)
DOID:0111839
  • congenital disorder of glycosylation Icc
  • Aliases:
    • congenital disorder of glycosylation type Icc
Drosophila melanogaster (fruit fly)
DOID:0080319
  • X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia
  • Aliases:
    • XMEN
Drosophila melanogaster (fruit fly)
DOID:0110939
  • autosomal recessive osteopetrosis 5
  • Aliases:
    • OPTB5
    • infantile malignant osteopetrosis 3
Mus musculus (house mouse)
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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

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Last updated: December 9, 2024