Gene table: search width pubmed_id = 16399879


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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, with spastic paraplegia, autosomal recessive - (AR)
14.136
16333315
16399879
CCT5 (5p15.2)
Chaperonin containing TCP1 subunit 5
* Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive