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) |