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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 7776 - 7800 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▼
DOID:0112000
  • immunodeficiency 34
  • Aliases:
    • AMCBX2
    • IMD34
    • X-linked MSMD due to CYBB deficiency
    • X-linked mendelian susceptibility to mycobacterial diseases due to CYBB deficiency
    • familial atypical mycobacteriosis X-linked 2
    • immunodeficiency 34, mycobacteriosis, X-linked
Homo sapiens (human)
DOID:0111999
  • immunodeficiency 61
  • Aliases:
    • IMD61
Homo sapiens (human)
DOID:0111998
  • immunodeficiency 66
  • Aliases:
    • IMD66
Mus musculus (house mouse)
DOID:0111998
  • immunodeficiency 66
  • Aliases:
    • IMD66
Homo sapiens (human)
DOID:0111997
  • immunodeficiency 63
  • Aliases:
    • IL2RB deficiency
    • IMD63
    • immunodeficiency 63 with lymphoproliferation and autoimmunity
Homo sapiens (human)
DOID:0111997
  • immunodeficiency 63
  • Aliases:
    • IL2RB deficiency
    • IMD63
    • immunodeficiency 63 with lymphoproliferation and autoimmunity
Rattus norvegicus (Norway rat)
DOID:0111997
  • immunodeficiency 63
  • Aliases:
    • IL2RB deficiency
    • IMD63
    • immunodeficiency 63 with lymphoproliferation and autoimmunity
Mus musculus (house mouse)
DOID:0111996
  • immunodeficiency 51
  • Aliases:
    • CANDF5
    • IMD51
    • familial candidiasis 5
Homo sapiens (human)
DOID:0111996
  • immunodeficiency 51
  • Aliases:
    • CANDF5
    • IMD51
    • familial candidiasis 5
Mus musculus (house mouse)
DOID:0111996
  • immunodeficiency 51
  • Aliases:
    • CANDF5
    • IMD51
    • familial candidiasis 5
Caenorhabditis elegans
DOID:0111995
  • immunodeficiency 28
  • Aliases:
    • IFNGR2 deficiency
    • IMD28
    • MSMD due to complete IFNgammaR2 deficiency
    • MSMD due to complete interferon gamma receptor 2 deficiency
    • Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency
    • Mendelian susceptibility to mycobacterial diseases due to complete interferon gamma receptor 2 deficiency
    • immunodeficiency 28, mycobacteriosis
Homo sapiens (human)
DOID:0111995
  • immunodeficiency 28
  • Aliases:
    • IFNGR2 deficiency
    • IMD28
    • MSMD due to complete IFNgammaR2 deficiency
    • MSMD due to complete interferon gamma receptor 2 deficiency
    • Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency
    • Mendelian susceptibility to mycobacterial diseases due to complete interferon gamma receptor 2 deficiency
    • immunodeficiency 28, mycobacteriosis
Mus musculus (house mouse)
DOID:0111994
  • immunodeficiency 45
  • Aliases:
    • IMD45
Homo sapiens (human)
DOID:0111994
  • immunodeficiency 45
  • Aliases:
    • IMD45
Mus musculus (house mouse)
DOID:0111992
  • immunodeficiency 53
  • Aliases:
    • IMD53
Homo sapiens (human)
DOID:0111991
  • immunodeficiency 62
  • Aliases:
    • IMD62
Mus musculus (house mouse)
DOID:0111990
  • immunodeficiency 30
  • Aliases:
    • IMD30
    • MSMD due to complete IL12RB1 deficiency
    • MSMD due to complete interleukin 12 receptor beta 1 deficiency
    • Mendelian susceptibility to interleukin 12 receptor beta 1 deficiency
    • Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency
Mus musculus (house mouse)
DOID:0111990
  • immunodeficiency 30
  • Aliases:
    • IMD30
    • MSMD due to complete IL12RB1 deficiency
    • MSMD due to complete interleukin 12 receptor beta 1 deficiency
    • Mendelian susceptibility to interleukin 12 receptor beta 1 deficiency
    • Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency
Homo sapiens (human)
DOID:0111989
  • immunodeficiency 35
  • Aliases:
    • IMD35
    • TYK2 deficiency
    • autosomal recessiv HIES with atypical mycobacteriosis
    • autosomal recessive hyper-IgE syndrome with atypical mycobacteriosis
    • susceptibility to infection due to TYK2 deficiency
    • tyrosine kinase 2 deficiency
Homo sapiens (human)
DOID:0111988
  • immunodeficiency 12
  • Aliases:
    • IMD12
    • combined immunodeficiency due to MALT1 deficiency
Homo sapiens (human)
DOID:0111984
  • immunodeficiency 58
  • Aliases:
    • IMD58
    • severe combined immunodeficiency due to CARMIL2 deficiency
Homo sapiens (human)
DOID:0111983
  • immunodeficiency 52
  • Aliases:
    • IMD52
    • severe combined immunodeficiency due to LAT deficiency
Homo sapiens (human)
DOID:0111982
  • immunodeficiency 56
  • Aliases:
    • IL21R immunodeficiency
    • IMD56
    • combined immunodeficiency due to IL21R deficiency
Mus musculus (house mouse)
DOID:0111982
  • immunodeficiency 56
  • Aliases:
    • IL21R immunodeficiency
    • IMD56
    • combined immunodeficiency due to IL21R deficiency
Homo sapiens (human)
DOID:0111981
  • immunodeficiency 43
  • Aliases:
    • B2M deficiency
    • IMD43
    • beta-2-microglobulin deficiency
    • hypercatabolic hypoproteinemia
Homo sapiens (human)
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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: August 19, 2024