Gene table: search width pubmed_id = 23176824


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

protein
All allelic disease phenotypes - locus/disease symbols
Neuropathy, hereditary sensory and autonomic, type IX, with developmental delay - (AR)
14.114
23176824
TECPR2 (14q32)
Tectonin beta-propeller repeat containing 2
* Spastic paraplegia 49, autosomal recessive - SPG49
* Neuropathy, hereditary sensory and autonomic, type IX, with developmental delay - HSAN9