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 6326 - 6350 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:9775
  • diastolic heart failure
Caenorhabditis elegans
DOID:678
  • progressive supranuclear palsy
  • Aliases:
    • Steele-Richardson-Olszewski syndrome
    • progressive supranuclear ophthalmoplegia
Saccharomyces cerevisiae S288C
DOID:0111189
  • distal myopathy 3
  • Aliases:
    • MPD3
    • distal muscular dystrophy 3
    • distal myopathy type 3
Homo sapiens (human)
DOID:0081110
  • keratosis palmoplantaris striata 3
Homo sapiens (human)
DOID:0110883
  • inflammatory bowel disease 17
  • Aliases:
    • IBD17
Mus musculus (house mouse)
DOID:0111238
  • congenital muscular dystrophy-dystroglycanopathy type A13
  • Aliases:
    • MDDGA13
    • Walker-Warburg syndrome or muscle-eye-brain disease, B3GNT1-related
    • Walker-Warburg syndrome or muscle-eye-brain disease, B4GNT1-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A13
Mus musculus (house mouse)
DOID:0081097
  • Rafiq syndrome
  • Aliases:
    • MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15
Homo sapiens (human)
DOID:3500
  • gallbladder adenocarcinoma
  • Aliases:
    • adenocarcinoma of the gallbladder
Xenopus tropicalis (tropical clawed frog)
DOID:3908
  • lung non-small cell carcinoma
  • Aliases:
    • NSCLC
    • Non-small cell lung cancer
    • non-small cell lung carcinoma
Drosophila melanogaster (fruit fly)
DOID:0110427
  • dilated cardiomyopathy 1V
  • Aliases:
    • CMD1V
Xenopus laevis (African clawed frog)
DOID:0110865
  • congenital stationary night blindness 1B
  • Aliases:
    • CSNB1B
    • autosomal recessive complete congenital stationary night blindness
    • congenital stationary night blindness 1B autosomal recessive
Mus musculus (house mouse)
DOID:0110377
  • retinitis pigmentosa 49
  • Aliases:
    • RP49
Mus musculus (house mouse)
DOID:0050814
  • temtamy preaxial brachydactyly syndrome
  • Aliases:
    • PREAXIAL BRACHYDACTYLY SYNDROME, TEMTAMY TYPE
Drosophila melanogaster (fruit fly)
DOID:0060612
  • abdominal obesity-metabolic syndrome 3
Mus musculus (house mouse)
DOID:668
  • myositis ossificans
  • Aliases:
    • Myisitis ossificans
    • Ossification - muscle
Drosophila melanogaster (fruit fly)
DOID:9074
  • systemic lupus erythematosus
  • Aliases:
    • Lupus Erythematosus, systemic
    • SLE - Lupus Erythematosus, systemic
    • disseminated lupus erythematosus
Drosophila melanogaster (fruit fly)
DOID:0110013
  • advanced sleep phase syndrome 3
  • Aliases:
    • FASPS3
    • familial advanced sleep phase syndrome 3
Drosophila melanogaster (fruit fly)
DOID:10907
  • microcephaly
  • Aliases:
    • Microcephalus
    • microencephaly
Danio rerio (zebrafish)
DOID:0070248
  • autosomal recessive Emery-Dreifuss muscular dystrophy 3
  • Aliases:
    • EDMD3
    • Emery-Dreifuss muscular dystrophy 3, autosomal recessive
Rattus norvegicus (Norway rat)
DOID:0070297
  • primary microcephaly
  • Aliases:
    • true microcephaly
Homo sapiens (human)
DOID:10787
  • premature menopause
  • Aliases:
    • Menopause - premature
    • Menopause praecox
Drosophila melanogaster (fruit fly)
DOID:1387
  • hypolipoproteinemia
  • Aliases:
    • Hypolipoproteinaemia
Homo sapiens (human)
DOID:14213
  • hypophosphatasia
  • Aliases:
    • deficiency of alkaline phosphatase
Rattus norvegicus (Norway rat)
DOID:62
  • aortic valve disease
Caenorhabditis elegans
DOID:0080957
  • primary hypoalphalipoproteinemia 1
  • Aliases:
    • familial HDL deficiency
    • familial hypoalphalipoproteinemia
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