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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 15626 - 15650 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▼
DOID:0050559
  • Fukuyama congenital muscular dystrophy
Mus musculus (house mouse)
DOID:0050559
  • Fukuyama congenital muscular dystrophy
Rattus norvegicus (Norway rat)
DOID:0050559
  • Fukuyama congenital muscular dystrophy
Drosophila melanogaster (fruit fly)
DOID:0050559
  • Fukuyama congenital muscular dystrophy
Caenorhabditis elegans
DOID:0050558
  • Ullrich congenital muscular dystrophy
  • Aliases:
    • ULLRICH DISEASE
    • Ullrich scleroatonic muscular dystrophy
Homo sapiens (human)
DOID:0050558
  • Ullrich congenital muscular dystrophy
  • Aliases:
    • ULLRICH DISEASE
    • Ullrich scleroatonic muscular dystrophy
Mus musculus (house mouse)
DOID:0050558
  • Ullrich congenital muscular dystrophy
  • Aliases:
    • ULLRICH DISEASE
    • Ullrich scleroatonic muscular dystrophy
Caenorhabditis elegans
DOID:0050557
  • congenital muscular dystrophy
Rattus norvegicus (Norway rat)
DOID:0050557
  • congenital muscular dystrophy
Homo sapiens (human)
DOID:0050557
  • congenital muscular dystrophy
Caenorhabditis elegans
DOID:0050557
  • congenital muscular dystrophy
Mus musculus (house mouse)
DOID:0050554
  • X-linked sideroblastic anemia with ataxia
  • Aliases:
    • Anemia sideroblastic and spinocerebellar ataxia
    • Anemia, sideroblastic, spinocerebellar ataxia
    • X-linked sideroblastic anaemia and ataxia
    • X-linked sideroblastic anaemia with ataxia
    • X-linked sideroblastic anemia and ataxia
Homo sapiens (human)
DOID:0050548
  • hereditary sensory neuropathy
  • Aliases:
    • familial dysautonomia, type II
    • hereditary sensory and autonomic neuropathy
Drosophila melanogaster (fruit fly)
DOID:0050548
  • hereditary sensory neuropathy
  • Aliases:
    • familial dysautonomia, type II
    • hereditary sensory and autonomic neuropathy
Homo sapiens (human)
DOID:0050548
  • hereditary sensory neuropathy
  • Aliases:
    • familial dysautonomia, type II
    • hereditary sensory and autonomic neuropathy
Saccharomyces cerevisiae S288C
DOID:0050548
  • hereditary sensory neuropathy
  • Aliases:
    • familial dysautonomia, type II
    • hereditary sensory and autonomic neuropathy
Rattus norvegicus (Norway rat)
DOID:0050548
  • hereditary sensory neuropathy
  • Aliases:
    • familial dysautonomia, type II
    • hereditary sensory and autonomic neuropathy
Mus musculus (house mouse)
DOID:0050547
  • familial medullary thyroid carcinoma
  • Aliases:
    • THYROID CARCINOMA, FAMILIAL MEDULLARY
Homo sapiens (human)
DOID:0050547
  • familial medullary thyroid carcinoma
  • Aliases:
    • THYROID CARCINOMA, FAMILIAL MEDULLARY
Danio rerio (zebrafish)
DOID:0050547
  • familial medullary thyroid carcinoma
  • Aliases:
    • THYROID CARCINOMA, FAMILIAL MEDULLARY
Rattus norvegicus (Norway rat)
DOID:0050547
  • familial medullary thyroid carcinoma
  • Aliases:
    • THYROID CARCINOMA, FAMILIAL MEDULLARY
Mus musculus (house mouse)
DOID:0050547
  • familial medullary thyroid carcinoma
  • Aliases:
    • THYROID CARCINOMA, FAMILIAL MEDULLARY
Xenopus laevis (African clawed frog)
DOID:0050546
  • congenital adrenal insufficiency
  • Aliases:
    • ADRENAL INSUFFICIENCY, CONGENITAL, WITH 46,XY SEX REVERSAL, PARTIAL OR COMPLETE
    • Adrenal insufficiency, congenital, with 46,XY sex reversal
    • P450scc DEFICIENCY
Homo sapiens (human)
DOID:0050545
  • visceral heterotaxy
  • Aliases:
    • heterotaxia
    • situs ambiguus
Xenopus laevis (African clawed frog)
DOID:0050545
  • visceral heterotaxy
  • Aliases:
    • heterotaxia
    • situs ambiguus
Saccharomyces cerevisiae S288C
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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