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SPG38 spastic paraplegia 38 (autosomal dominant, Silver syndrome) [ Homo sapiens (human) ]

Gene ID: 100049707, updated on 2-Oct-2019

Summary

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Gene symbol
SPG38
Gene description
spastic paraplegia 38 (autosomal dominant, Silver syndrome)
Primary source
MIM:612335
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Genomic context

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Location:
4p16-p15

Bibliography

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Related articles in PubMed

  1. Silver syndrome variant of hereditary spastic paraplegia: A locus to 4p and allelism with SPG4. Orlacchio A, et al. Neurology, 2008 May 20. PMID 18401025

GeneRIFs: Gene References Into Functions

Phenotypes

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spastic paraplegia 38 (autosomal dominant, Silver syndrome)

General gene information

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Property

  • phenotype only

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