myelin protein zero

Summary
Gene Symbol
  • MPZ
Organism
Homo sapiens (human)
NCBI Gene
4359
PubChem
4359
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Alternative splicing
  • Cell membrane
  • Charcot-Marie-Tooth disease
  • Deafness
  • Dejerine-Sottas syndrome
  • Direct protein sequencing
  • Disease variant
  • Disulfide bond
  • Glycoprotein
  • Immunoglobulin domain
  • Neurodegeneration
  • Phosphoprotein
  • Proteomics identification
  • Reference proteome
  • Signal
  • Transmembrane helix
Proteins
Displaying all 2 entries
UniProt Protein Name
P25189
  • Myelin peripheral protein
  • Myelin protein zero
A0A5F9ZI26
  • Myelin peripheral protein
  • Myelin protein zero
Gene Ontology (GO)
OrthoDB (Group)
Group level
Eukaryota
Group Name
myelin protein P0
Functional Category
  • M: Cell wall/membrane/envelope biogenesis
  • O: Posttranslational modification, protein turnover, chaperones
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying all 10 entries
DO ID Disease Name Source
DOID:0050540 Charcot-Marie-Tooth disease type 3
DOID:0090111 PCWH syndrome
DOID:0110152 Charcot-Marie-Tooth disease type 1B
DOID:0110157 Charcot-Marie-Tooth disease type 2J
DOID:0110158 Charcot-Marie-Tooth disease type 2I
DOID:0110200 Charcot-Marie-Tooth disease dominant intermediate D
DOID:10595 Charcot-Marie-Tooth disease
DOID:11446 sciatic neuropathy
DOID:870 neuropathy
DOID:9743 diabetic neuropathy

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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