ATP9B
Description
The ATP9B (ATPase phospholipid transporting 9B (putative)) is a protein-coding gene located on chromosome 18.
ATP9B is also known as ATPASEP, ATPIIB, HUSSY-20, NEO1L, hMMR1.
Associated Diseases
- osteoarthritis
- Griscelli syndrome type 3
- uncombable hair syndrome
- oculocutaneous albinism type 3
- microcephaly-albinism-digital anomalies syndrome
- Tietz syndrome
- ermine phenotype
- hypotrichosis simplex
- Waardenburg syndrome, IIa 2F
- Clouston syndrome
- Waardenburg syndrome type 2A
