Basic information
- Full name
- RNA binding motif protein 10
- Ensembl
- ENSG00000182872.16
- Summary
- 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.[provided by RefSeq, Mar 2011]
- Annotation
- Cancer driver (TSG)
Protein product
- ENST00000377604.8 Primary ENSP00000366829.3 (35 phosphosites)
- ENST00000329236.8
- ENST00000345781.10
- ENST00000628161.2
Phosphosites on the primary protein product
Tumor and normal comparison
| Signed p-values | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| Data type | Meta P | BRCA | CCRCC | COAD | GBM | HNSCC | LSCC | LUAD | OV | PDAC | UCEC |
mRNA expression at gene level
Protein expression
Phenotype and mutation association
Manhattan plot summarizing associations of phenotypes and mutations across all cohorts and omics data types
Associations of the protein abundance of RBM10 with phenotypes and mutations
| Signed p-values | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| Phenotype | Meta P | BRCA | CCRCC | COAD | GBM | HNSCC | LSCC | LUAD | OV | PDAC | UCEC |
Cis-association
Associations between omics data of RBM10
Trans-association
Associations of the protein abundance of RBM10 and the protein abundance of other genes
| Signed p-values | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| Gene | Meta P | BRCA | CCRCC | COAD | GBM | HNSCC | LSCC | LUAD | OV | PDAC | UCEC |
Gene set enrichment analysis
Submit genes and the common logarithm of the p-values of their association with to WebGestalt.