cerebellar ataxia type 43

Summary
Synonym
  • SCA43
Definition
An autosomal dominant cerebellar ataxia characterized by adult-onset, slowly progressive, gait and limb ataxia, often associated with peripheral neuropathy typically affecting the motor system that has_material_basis_in heterozygous mutation in MME on chromosome 3q25.2.
Super Class
autosomal dominant cerebellar ataxia
Disease Ontology
DOID:0111745
Mondo Disease Ontology
ORDO
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
4311 MME membrane metalloendopeptidase
Displaying 1 entry
Gene ID Gene Symbol Description Source
17380 Mme membrane metallo endopeptidase
Displaying 1 entry
Gene ID Gene Symbol Description Source
24590 Mme membrane metallo-endopeptidase
Displaying all 2 entries
Gene ID Gene Symbol Description Source
31547 Nep1 Neprilysin 1
42449 Nep4 Neprilysin 4
Displaying 1 entry
Gene ID Gene Symbol Description Source
188090 nep-2 Neprilysin-2

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.1.0

Last updated: December 9, 2024