IFI27L2
Description
The IFI27L2 (interferon alpha inducible protein 27 like 2) is a protein-coding gene located on chromosome 14.
IFI27L2 is involved in the apoptotic process, promoting cell death.
IFI27L2 is also known as FAM14A, ISG12B, TLH29.
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
