CUTC
Description
The CUTC (cutC copper transporter) is a protein-coding gene located on chromosome 10.
CUTC refers to the human gene encoding the copper homeostasis protein cutC homolog.
CUTC may play a role in copper homeostasis. It can bind one Cu(1+) per subunit. This function is supported by evidence from PubMed IDs 16182249 and 19878721.
CUTC is also known as CGI-32.
Associated Diseases
- Leigh syndrome
- cytochrome-c oxidase deficiency disease
- fatal infantile encephalocardiomyopathy
- diverticulitis
- colorectal cancer
- common variable immunodeficiency
- microphthalmia with limb anomalies
