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    SPG27 spastic paraplegia 27 (autosomal recessive) [ Homo sapiens (human) ]

    Gene ID: 414886, updated on 2-Oct-2019

    Summary

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    Gene symbol
    SPG27
    Gene description
    spastic paraplegia 27 (autosomal recessive)
    Primary source
    MIM:609041
    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:
    10q22.1-q24.1

    Bibliography

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    Related articles in PubMed

    1. A new phenotype linked to SPG27 and refinement of the critical region on chromosome. Ribai P, et al. J Neurol, 2006 Jun. PMID 16511635
    2. A novel locus for pure recessive hereditary spastic paraplegia maps to 10q22.1-10q24.1. Meijer IA, et al. Ann Neurol, 2004 Oct. PMID 15455396

    GeneRIFs: Gene References Into Functions

    Phenotypes

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    spastic paraplegia 27 (autosomal recessive)

    General gene information

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    Property

    • phenotype only

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    Molecular Biology Databases