ST7-OT3
Description
The ST7-OT3 (ST7 overlapping transcript 3) is a ncRNA gene located on chromosome 7.
ST7 overlapping transcript 3 (non-protein coding), also known as ST7-OT3, is a long non-coding RNA. In humans, it is found on chromosome 7 in a locus spanning a translocation breakpoint associated with autism. It overlaps the ST7 gene, spanning intron 10 to exon 14 of ST7. Some isoforms of ST7 may use exons from ST7-OT3.
May act as a tumor suppressor.
ST7-OT3 is also known as NCRNA00026, ST7, ST7OT3.
Associated Diseases
- uncombable hair syndrome
- Griscelli syndrome type 3
- hypotrichosis simplex
- Clouston syndrome
- Waardenburg syndrome, IIa 2F
