VRTN
Description
The VRTN (vertebrae development associated) is a protein-coding gene located on chromosome 14.
VRTN is a human gene. Its protein product acts as a transcription factor that regulates the development of thoracic vertebrae.
VRTN is also known as C14orf115, vertnin.
Associated Diseases
- lysosomal storage disease
- autosomal recessive spondylocostal dysostosis
- autosomal dominant brachyolmia
- autosomal dominant spondylocostal dysostosis
- Scheuermann disease
- Becker nevus syndrome
- thoracomelic dysplasia
- osteomesopyknosis
- spondyloepiphyseal dysplasia tarda, autosomal dominant
- thoracolaryngopelvic dysplasia
- ichthyosis-cheek-eyebrow syndrome
- brachyolmia type 1, toledo type
- hydrocephaly-tall stature-joint laxity syndrome
