IFI27L1
Description
The IFI27L1 (interferon alpha inducible protein 27 like 1) is a protein-coding gene located on chromosome 14.
IFI27L1 promotes programmed cell death (apoptosis).
IFI27L1 is also known as FAM14B, ISG12C.
Associated Diseases
- retinitis pigmentosa
- snowflake vitreoretinal degeneration
- Coats disease
- megalocornea
- asthma, nasal polyps, and aspirin intolerance
- birdshot chorioretinopathy
- exudative vitreoretinopathy 2, X-linked
- macular corneal dystrophy
- cataract 50 with or without glaucoma
- Stickler syndrome type 2
- ocular cystinosis
- Wagner disease
- isolated ectopia lentis
- MRCS syndrome
- Norrie disease
- X-linked retinoschisis
