C1orf127
Description
The C1ORF127 (chromosome 1 open reading frame 127) is a protein-coding gene located on chromosome 1.
C1ORF127 is a human gene located on chromosome 1. Its function is currently unknown, but it has been associated with certain diseases and cellular processes. Further research is needed to understand its precise role.
The functional description of C1ORF127 is not well-understood. It is a protein-coding gene that has been associated with certain diseases and cellular processes, but its precise role remains unclear. Further research is needed to fully elucidate its function.
C1ORF127 is also known as -.
Associated Diseases
- alopecia
- glaucoma
- heterotaxy, visceral, 9, autosomal, with male infertility
- visceral heterotaxy
- right atrial isomerism
- primary ciliary dyskinesia
- ciliary dyskinesia, primary, 40
- ciliary dyskinesia, primary, 39
- renal-hepatic-pancreatic dysplasia
- congenital heart defects, multiple types, 6
- heterotaxy, visceral, 5, autosomal
- ciliary dyskinesia, primary, 49, without situs inversus
- primary ciliary dyskinesia 5
