| Gene Symbol | RCBTB1 |
| Entrez Gene ID | 55213 |
| Full Name | RCC1 and BTB domain containing protein 1 |
| Synonyms | CLLD7,CLLL7,GLP,RDEOA |
| General protein information |
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| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| Summary | This gene encodes a protein with an N-terminal RCC1 domain and a C-terminal BTB (broad complex, tramtrack and bric-a-brac) domain. In rat, over-expression of this gene in vascular smooth muscle cells induced cellular hypertrophy. In rat, the C-terminus of RCBTB1 interacts with the angiotensin II receptor-1A. In humans, this gene maps to a region of chromosome 13q that is frequently deleted in B-cell chronic lymphocytic leukemia and other lymphoid malignancies. [provided by RefSeq, Jul 2008]. |
| Disorder MIM: | |
| Disorder Html: | Retinal dystrophy with or without extraocular anomalies, 617175 (3) |








































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