KANSL1L
Description
The KANSL1L (KAT8 regulatory NSL complex subunit 1 like) is a protein-coding gene located on chromosome 2.
KANSL1L is also known as C2orf67, MSL1v2.
Associated Diseases
- retinitis pigmentosa
- birdshot chorioretinopathy
- colobomatous microphthalmia - obesity - hypogenitalism - intellectual disability syndrome
- exudative vitreoretinopathy 2, X-linked
- snowflake vitreoretinal degeneration
- Coats disease
- X-linked retinoschisis
- megalocornea
