ZNF878
Description
The ZNF878 (zinc finger protein 878) is a protein-coding gene located on chromosome 19.
Potentially involved in the regulation of gene expression.
ZNF878 is also known as -.
Associated Diseases
- X-linked retinal dysplasia
- choroidal dystrophy, central areolar, 1
- severe early-childhood-onset retinal dystrophy
- age related macular degeneration 4
- age related macular degeneration 7
- age related macular degeneration 11
- X-linked retinoschisis
- retinitis pigmentosa
- erythroleukemia, familial, susceptibility to
- exudative vitreoretinopathy 2, X-linked
- coloboma of optic nerve
- hereditary neutrophilia
- snowflake vitreoretinal degeneration
