TIMM23B
Description
The TIMM23B (translocase of inner mitochondrial membrane 23 homolog B) is a protein-coding gene located on chromosome 10.
This protein might play a role in moving proteins with transit peptides across the mitochondrial inner membrane. It may be part of the PAM complex.
TIMM23B is also known as -.
Associated Diseases
- hypotrichosis simplex
- trichodysplasia-xeroderma syndrome
- alopecia universalis congenita
- hypotrichosis 4
- uncombable hair syndrome
- hypotrichosis 5
- Clouston syndrome
- pure hair and nail ectodermal dysplasia
- Alzheimer disease
- progressive supranuclear palsy
