TMEM38B Back

transmembrane protein 38B

External References:      Wikipedia GeneCards HUGO COSMIC Google Scholar

NCBI Description of TMEM38B
This gene encodes an intracellular monovalent cation channel that functions in maintenance of intracellular calcium release. Mutations in this gene may be associated with autosomal recessive osteogenesis. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments.

Community Annotation of TMEM38B Add / Edit TMEM38B: Annotations

No community annotations yet for TMEM38B.
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

TMEM38B is highly significantly mutated in
(none)
TMEM38B is significantly mutated in
(none)
TMEM38B is near significance in
(none)

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

Data details


• Mutation list for TMEM38B