Mutation Details

DNA changeProtein changeExon/intronTypeReported classificationBatemanSIFTPolyPhenConservedProtein domainRemarksLOVD ID
c.3489_3490delTGp.Glu1164GlyfsX7Exon 26Deletion; frameshiftDisease-causingn.a.n.a.n.a.n.a. Cytopl.  

Patients

Family# Affected relativesClinical featuresRemarksReference
1 6 Adducted thumbs, Aphasia, Mental retardation, Spastic paraplegia Died <1 yr: 0/6 Jouet et al. (1994)

References

YearAuthorTitleJournalVolumePagesWeblink
1994Jouet et al.X-linked spastic paraplegia (SPG1), MASA syndrome and X-linked hydrocephalus result from mutations in the L1 gene Nat. Genet. 7402-407 7920659