SEL1L3
Description
The SEL1L3 (SEL1L family member 3) is a protein-coding gene located on chromosome 4.
SEL1L3 is also known as Sel-1L3.
Associated Diseases
- ringed hair disease
- Griscelli syndrome type 3
- uncombable hair syndrome
- microcephaly-albinism-digital anomalies syndrome
- pili bifurcati
- oculocutaneous albinism type 3
- alopecia, androgenetic, 1
- wooly hair, autosomal recessive 3
