TPRN Back

taperin

External References:      Wikipedia GeneCards HUGO COSMIC Google Scholar

NCBI Description of TPRN
This locus encodes a sensory epithelial protein. It was defined by linkage analysis in three Pakistani families to lie between D9S1818 (centromeric) and D9SH6 (telomeric). Mutations at this locus have been associated with autosomal recessive deafness. Sequence Note: This RefSeq record was created from transcript and genomic sequence data because no single transcript was available for the full length of the gene. The extent of this transcript is supported by mouse NM_175286.4 and supporting mouse transcripts.

Community Annotation of TPRN Add / Edit TPRN: Annotations

No community annotations yet for TPRN.
Sort mutations by: Tumor type  Mutation type  Position  
Straightedge cursor Expand

Figure notes


• "Mouse over" a mutation to see details.
• Missense green saturation indicates evolutionary conservation of the mutated positions.
• Red hashes in protein strip are splice sites.
• Blue-white-red bars are log2 copy ratio distributions (–1 to +1) from Zack et al. (2013).


Legend

TPRN is highly significantly mutated in
(none)
TPRN is significantly mutated in
(none)
TPRN is near significance in
(none)

Click on a tumor type to see its full list of significant genes.

Data details


• Mutation list for TPRN