U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

SPG41 spastic paraplegia 41 (autosomal dominant) [ Homo sapiens (human) ]

Gene ID: 100359402, updated on 2-Oct-2019

Summary

Go to the top of the page Help
Gene symbol
SPG41
Gene description
spastic paraplegia 41 (autosomal dominant)
Primary source
MIM:613364
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Summary
This locus was defined in a Chinese family. Nineteen individuals were genotyped and the interval was defined between D11S1324 and D11S1933. [provided by RefSeq, Feb 2010]

Genomic context

Go to the top of the page Help
Location:
11p14.1-p11.2

Bibliography

Go to the top of the pageHelp

Related articles in PubMed

  1. A novel candidate locus on chromosome 11p14.1-p11.2 for autosomal dominant hereditary spastic paraplegia. Zhao GH, et al. Chin Med J (Engl), 2008 Mar 5. PMID 18364116
  2. Mutational spectrum of the SPG4 (SPAST) and SPG3A (ATL1) genes in Spanish patients with hereditary spastic paraplegia. Alvarez V, et al. BMC Neurol, 2010 Oct 8. PMID 20932283, Free PMC Article

GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. Observational study of gene-disease association. (HuGE Navigator)
    Title: Mutational spectrum of the SPG4 (SPAST) and SPG3A (ATL1) genes in Spanish patients with hereditary spastic paraplegia.
Submit: New GeneRIF Correction

Phenotypes

Go to the top of the page Help
spastic paraplegia 41 (autosomal dominant)

General gene information

Go to the top of the page Help

Property

  • phenotype only

Gene LinkOut

The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

Molecular Biology Databases