RBM10 Back

RNA binding motif protein 10

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NCBI Description of RBM10

This gene encodes a nuclear protein that belongs to a family proteins that contain an RNA-binding motif. The encoded protein associates with hnRNP proteins and may be involved in regulating alternative splicing. Defects in this gene are the cause of the X-linked recessive disorder, TARP syndrome. Alternate splicing results in multiple transcript variants.

Community Annotation of RBM10 Add / Edit RBM10: Annotations

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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).


RBM10 is highly significantly mutated in
Lung adenocarcinoma
19 patients (4%)
RBM10 is significantly mutated in
combined cohort
53 patients (1%)
RBM10 is near significance in
8 patients (3%)

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

Data details

Mutation list for RBM10