SP5
Description
The SP5 (Sp5 transcription factor) is a protein-coding gene located on chromosome 2.
SP5 refers to the human gene SP5.
SP5 binds to GC boxes in promoter regions, acting as a potential transcriptional activator. It plays a crucial role in regulating the changes in gene expression required for establishing patterns during embryonic development.
SP5 is also known as -.
Associated Diseases
- schizophrenia 15
- Phelan-McDermid syndrome
- hemoglobin D disease
- primary familial polycythemia due to EPO receptor mutation