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SPG29 spastic paraplegia 29 (autosomal dominant) [ Homo sapiens (human) ]

Gene ID: 619379, updated on 31-Aug-2024

Summary

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Official Symbol
SPG29provided by HGNC
Official Full Name
spastic paraplegia 29 (autosomal dominant)provided by HGNC
Primary source
MIM:609727
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:
1p31.1-p21.1

Bibliography

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Related articles in PubMed

  1. New locus for hereditary spastic paraplegia maps to chromosome 1p31.1-1p21.1. Orlacchio A, et al. Ann Neurol, 2005 Sep. PMID 16130112

GeneRIFs: Gene References Into Functions

Phenotypes

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Associated conditions

Description Tests
spastic paraplegia 29 (autosomal dominant)
OMIM: 609727GeneReviews: Not available

General gene information

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Property

  • phenotype only

Gene LinkOut

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