SRRM3
Description
The SRRM3 (serine/arginine repetitive matrix 3) is a protein-coding gene located on chromosome 7.
The SRRM3 gene is a human gene that encodes a protein involved in regulating gene expression. It is a member of the SR protein family, which are known to play a role in RNA splicing. The SRRM3 gene is located on chromosome 19 and is made up of 16 exons. The protein encoded by this gene is thought to be involved in the regulation of alternative splicing, a process that allows for the production of multiple protein isoforms from a single gene.
This gene may be involved in regulating the invasiveness of breast cancer cells. It may also play a role in breast cancer progression through its interaction with RYBP.
SRRM3 is also known as -.
Associated Diseases
- spinocerebellar ataxia type 15/16
- spinocerebellar ataxia type 35
- infantile-onset autosomal recessive nonprogressive cerebellar ataxia
- spinocerebellar ataxia type 12
- spinocerebellar ataxia type 37
- spinocerebellar ataxia type 31
- spinocerebellar ataxia type 23
- spinocerebellar ataxia type 20
- spinocerebellar ataxia type 17
- spastic ataxia 2
- spinocerebellar ataxia type 29
- autosomal recessive spinocerebellar ataxia 17
