NIFK
Description
The NIFK (nucleolar protein interacting with the FHA domain of MKI67) is a protein-coding gene located on chromosome 2.
NIFK is also known as MKI67IP, Nopp34.
Associated Diseases
- cancer
- retinitis pigmentosa
- X-linked retinal dysplasia
- severe early-childhood-onset retinal dystrophy
- congenital primary aphakia
- microphthalmia, isolated, with coloboma 10
- Coats disease
- snowflake vitreoretinal degeneration
- exudative vitreoretinopathy 2, X-linked
- uveal coloboma-cleft lip and palate-intellectual disability
- isolated aniridia
