RESP18
Description
The RESP18 (regulated endocrine specific protein 18) is a protein-coding gene located on chromosome 2.
RESP18 is thought to have a crucial regulatory function within corticotrophs.
RESP18 is also known as -.
Associated Diseases
- X-linked retinal dysplasia
- retinitis pigmentosa
- severe early-childhood-onset retinal dystrophy
- reticular dystrophy of the retinal pigment epithelium
- hypertriglyceridemia 2
- cholesterol-ester transfer protein deficiency
- X-linked retinoschisis
- age related macular degeneration 4
- age related macular degeneration 7
- age related macular degeneration 11
- late-onset retinal degeneration
- birdshot chorioretinopathy
- coloboma of optic nerve
- homozygous familial hypercholesterolemia
