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Gene entry

CCT5

chaperonin containing TCP1 subunit 5

Chromosome
5
Cytoband
5p15.2
Variants (rsID)
9

CCT5 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 5 (region 5p15.2). Its official name is “chaperonin containing TCP1 subunit 5”. The reference table lists 9 variants (rsID) for this gene.

Clinically classified variants

3 reference-table entries with clinical significance.

  • rs11557652Benignsingle nucleotide variantHereditary sensory and autonomic neuropathy with spastic paraplegia
  • rs118203986Conflicting interpretationssingle nucleotide variantHereditary sensory and autonomic neuropathy with spastic paraplegia
  • rs141675330Conflicting interpretationssingle nucleotide variantHereditary sensory and autonomic neuropathy with spastic paraplegia

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.