LONRF3
Description
The LONRF3 (LON peptidase N-terminal domain and ring finger 3) is a protein-coding gene located on chromosome X.
LONRF3 is also known as RNF127.
Associated Diseases
- hypoparathyroidism, familial isolated, 2
- familial isolated hyperparathyroidism
- blue diaper syndrome
- pseudohypoparathyroidism type 2
- cholesterol-ester transfer protein deficiency
- adamantinoma
- 22q11.2 deletion syndrome
- familial isolated hypoparathyroidism due to agenesis of parathyroid gland
- ulna metaphyseal dysplasia syndrome
- tuberculosis
