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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 13376 - 13400 of 15957 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism Source
DOID:0070113
  • Niemann-Pick disease type C1
  • Aliases:
    • NPC1
Caenorhabditis elegans
DOID:0070112
  • Niemann-Pick disease type B
Saccharomyces cerevisiae S288C
DOID:0070112
  • Niemann-Pick disease type B
Homo sapiens (human)
DOID:0070112
  • Niemann-Pick disease type B
Mus musculus (house mouse)
DOID:0070112
  • Niemann-Pick disease type B
Caenorhabditis elegans
DOID:0070111
  • Niemann-Pick disease type A
Caenorhabditis elegans
DOID:0070111
  • Niemann-Pick disease type A
Homo sapiens (human)
DOID:0070111
  • Niemann-Pick disease type A
Saccharomyces cerevisiae S288C
DOID:0070111
  • Niemann-Pick disease type A
Mus musculus (house mouse)
DOID:0070098
  • oculocutaneous albinism type IV
  • Aliases:
    • OCA4
Homo sapiens (human)
DOID:0070098
  • oculocutaneous albinism type IV
  • Aliases:
    • OCA4
Mus musculus (house mouse)
DOID:0070097
  • oculocutaneous albinism type III
  • Aliases:
    • OCA3
    • Rufous Oculocutaneous Albinism
Mus musculus (house mouse)
DOID:0070097
  • oculocutaneous albinism type III
  • Aliases:
    • OCA3
    • Rufous Oculocutaneous Albinism
Homo sapiens (human)
DOID:0070097
  • oculocutaneous albinism type III
  • Aliases:
    • OCA3
    • Rufous Oculocutaneous Albinism
Caenorhabditis elegans
DOID:0070096
  • oculocutaneous albinism type II
  • Aliases:
    • OCA2
    • Oculocutaneous Albinism, Tyrosinase-Positive
Homo sapiens (human)
DOID:0070096
  • oculocutaneous albinism type II
  • Aliases:
    • OCA2
    • Oculocutaneous Albinism, Tyrosinase-Positive
Mus musculus (house mouse)
DOID:0070095
  • oculocutaneous albinism type IB
  • Aliases:
    • Albinism, Yellow Mutant Type
    • OCA1B
Mus musculus (house mouse)
DOID:0070095
  • oculocutaneous albinism type IB
  • Aliases:
    • Albinism, Yellow Mutant Type
    • OCA1B
Caenorhabditis elegans
DOID:0070095
  • oculocutaneous albinism type IB
  • Aliases:
    • Albinism, Yellow Mutant Type
    • OCA1B
Homo sapiens (human)
DOID:0070094
  • oculocutaneous albinism type IA
  • Aliases:
    • OCA1A
    • Oculocutaneous Albinism, Tyrosinase-Negative
Caenorhabditis elegans
DOID:0070094
  • oculocutaneous albinism type IA
  • Aliases:
    • OCA1A
    • Oculocutaneous Albinism, Tyrosinase-Negative
Mus musculus (house mouse)
DOID:0070094
  • oculocutaneous albinism type IA
  • Aliases:
    • OCA1A
    • Oculocutaneous Albinism, Tyrosinase-Negative
Homo sapiens (human)
DOID:0070093
  • schizophrenia 18
  • Aliases:
    • Chromosome 7q36.3 Duplication Syndrome, 362-Kb
    • SCZD18
Mus musculus (house mouse)
DOID:0070093
  • schizophrenia 18
  • Aliases:
    • Chromosome 7q36.3 Duplication Syndrome, 362-Kb
    • SCZD18
Homo sapiens (human)
DOID:0070093
  • schizophrenia 18
  • Aliases:
    • Chromosome 7q36.3 Duplication Syndrome, 362-Kb
    • SCZD18
Rattus norvegicus (Norway rat)
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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