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 7 entries
Gene ID Gene Symbol Description Source
1639 DCTN1 dynactin subunit 1
4744 NEFH neurofilament heavy chain
5630 PRPH peripherin
6623 SNCG synuclein gamma
6647 SOD1 superoxide dismutase 1
6648 SOD2 superoxide dismutase 2
7422 VEGFA vascular endothelial growth factor A
Displaying all 6 entries
Gene ID Gene Symbol Description Source
13191 Dctn1 dynactin 1
20618 Sncg synuclein, gamma
20655 Sod1 superoxide dismutase 1, soluble
20656 Sod2 superoxide dismutase 2, mitochondrial
22339 Vegfa vascular endothelial growth factor A
380684 Nefh neurofilament, heavy polypeptide
Displaying all 4 entries
Gene ID Gene Symbol Description Source
24787 Sod2 superoxide dismutase 2
29167 Dctn1 dynactin subunit 1
64347 Sncg synuclein, gamma
83785 Vegfa vascular endothelial growth factor A
Displaying 1 entry
Gene ID Gene Symbol Description Source
36232 Sod3 Superoxide dismutase 3
Displaying 1 entry
Gene ID Gene Symbol Description Source
30682 vegfaa vascular endothelial growth factor Aa
The Human Phenotype Ontology
Displaying entries 11 - 20 of 36 in total
HPO ID HPO Term
HP:0002145 Frontotemporal dementia
HP:0000716 Depression
HP:0002360 Sleep abnormality
HP:0001257 Spasticity
HP:0000712 Emotional lability
HP:0002017 Nausea and vomiting
HP:0002463 Language impairment
HP:0003487 Babinski sign
HP:0012378 Fatigue
HP:0003324 Generalized muscle weakness
Displaying all 6 entries
Gene ID Gene Symbol Description
5444 PON1 paraoxonase 1
5445 PON2 paraoxonase 2
5446 PON3 paraoxonase 3
55830 GLT8D1 glycosyltransferase 8 domain containing 1
7415 VCP valosin containing protein
9896 FIG4 FIG4 phosphoinositide 5-phosphatase

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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