KCTD5
Description
The KCTD5 (potassium channel tetramerization domain containing 5) is a protein-coding gene located on chromosome 16.
KCTD5 interacts with CUL3, suggesting a role as a substrate adapter in an E3 ligase complex. It does not affect the function of Kv channels Kv2.1/KCNB1, Kv1.2/KCNA2, Kv4.2/KCND2, and Kv3.4/KCNC4.
KCTD5 is also known as -.
Associated Diseases
- cancer
- hypoparathyroidism, familial isolated, 2
- pseudohypoparathyroidism type 2
- 22q11.2 deletion syndrome
- familial isolated hyperparathyroidism
- adamantinoma
- blue diaper syndrome
- ulna metaphyseal dysplasia syndrome
- familial isolated hypoparathyroidism due to agenesis of parathyroid gland
