amyotrophic lateral sclerosis type 1

Summary
Synonym
  • ALS1
  • amyotrophic lateral sclerosis 1
Definition
An amyotrophic lateral sclerosis that has_material_basis_in mutation in the SOD1 gene on chromosome 21. The most common type of familial ALS.
Super Class
amyotrophic lateral sclerosis autosomal dominant disease autosomal recessive disease
Related Genes
Displaying all 4 entries
Gene ID Gene Symbol Description Source
1639 DCTN1 dynactin subunit 1
4744 NEFH neurofilament heavy chain
5630 PRPH peripherin
6647 SOD1 superoxide dismutase 1
Displaying all 4 entries
Gene ID Gene Symbol Description Source
20618 Sncg synuclein, gamma
20655 Sod1 superoxide dismutase 1, soluble
20656 Sod2 superoxide dismutase 2, mitochondrial
22339 Vegfa vascular endothelial growth factor A
The Human Phenotype Ontology
Displaying entries 1 - 10 of 36 in total
HPO ID HPO Term
HP:0000708 Atypical behavior
HP:0000217 Xerostomia
HP:0000712 Emotional lability
HP:0002878 Respiratory failure
HP:0012531 Pain
HP:0002017 Nausea and vomiting
HP:0007340 Lower limb muscle weakness
HP:0001257 Spasticity
HP:0003470 Paralysis
HP:0009027 Foot dorsiflexor weakness
Displaying all 6 entries
Gene ID Gene Symbol Description
5445 PON2 paraoxonase 2
5444 PON1 paraoxonase 1
5446 PON3 paraoxonase 3
55830 GLT8D1 glycosyltransferase 8 domain containing 1
7415 VCP valosin containing protein
9896 FIG4 FIG4 phosphoinositide 5-phosphatase

About Release Notes Help Feedback

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 v4.4.0

Last updated: December 8, 2025