amyotrophic lateral sclerosis type 10

Summary
Synonym
  • ALS10
  • TARDBP-related frontotemporal lobar degeneration with TDP43 inclusions
  • amyotrophic lateral sclerosis 10
  • amyotrophic lateral sclerosis 10, with or without frontotemporal dementia
Definition
An amyotrophic lateral sclerosis that has_material_basis_in mutation in the TARDBP gene on chromosome 1.
Super Class
amyotrophic lateral sclerosis
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
23435 TARDBP TAR DNA binding protein
The Human Phenotype Ontology
Displaying entries 21 - 30 of 63 in total
HPO ID HPO Term
HP:0007373 Motor neuron atrophy
HP:0002878 Respiratory failure
HP:0009027 Foot dorsiflexor weakness
HP:0003470 Paralysis
HP:0012531 Pain
HP:0007340 Lower limb muscle weakness
HP:0002795 Abnormal respiratory system physiology
HP:0008955 Progressive distal muscular atrophy
HP:0003394 Muscle spasm
HP:0012473 Tongue atrophy
Displaying all 6 entries
Gene ID Gene Symbol Description
7415 VCP valosin containing protein
5444 PON1 paraoxonase 1
5445 PON2 paraoxonase 2
5446 PON3 paraoxonase 3
55830 GLT8D1 glycosyltransferase 8 domain containing 1
9896 FIG4 FIG4 phosphoinositide 5-phosphatase

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