| Gene Symbol | RBM10 |
| Entrez Gene ID | 8241 |
| Full Name | RNA binding motif protein 10 |
| Synonyms | DXS8237E,GPATC9,GPATCH9,S1-1,TARPS,ZRANB5 |
| General protein information |
|
| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| 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]. |
| Disorder MIM: | |
| Disorder Html: | TARP syndrome, 311900 (3) |








































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