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SPG16 spastic paraplegia 16 (complicated, X-linked recessive) [ Homo sapiens (human) ]

Gene ID: 57760, updated on 31-Aug-2024

Summary

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Official Symbol
SPG16provided by HGNC
Official Full Name
spastic paraplegia 16 (complicated, X-linked recessive)provided by HGNC
Primary source
MIM:300266
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
SPG

Genomic context

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Location:
Xq11.2

Bibliography

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Related articles in PubMed

  1. Segregation of a pure form of spastic paraplegia and NOR insertion into Xq11.2. Tamagaki A, et al. Am J Med Genet, 2000 Sep 4. PMID 10982474
  2. Novel syndromic form of X-linked complicated spastic paraplegia. Claes S, et al. Am J Med Genet, 2000 Sep 4. PMID 10982473
  3. Evidence of a third locus in X-linked recessive spastic paraplegia. Steinmüller R, et al. Hum Genet, 1997 Aug. PMID 9254866

GeneRIFs: Gene References Into Functions

Phenotypes

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Associated conditions

Description Tests
spastic paraplegia 16 (complicated, X-linked recessive)
OMIM: 300266GeneReviews: Not available

General gene information

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Markers

Property

  • phenotype only

Gene LinkOut

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