Gene table: search width pubmed_id = 16826527


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Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Spastic paraplegia 31, autosomal dominant - (AD)
15.14
16565863
16826527
REEP1 (2p11.2)
Receptor accessory protein 1(M)
* Neuropathy, distal hereditary motor, autosomal recessive 6 - HMNR6
* Distal spinal muscular atrophy, type VB - DSMAVB
* Spastic paraplegia 31 - SPG31
* Neuronopathy, distal hereditary motor, autosomal dominant 12 - HMND12