NFXL1
Description
The NFXL1 (nuclear transcription factor, X-box binding like 1) is a protein-coding gene located on chromosome 4.
NFXL1 is also known as CDZFP, HOZFP, OZFP, URCC5.
Associated Diseases
- Gollop-Wolfgang complex
- tibia, hypoplasia or aplasia of, with polydactyly
- Blount disease
- acheiropody
- syndactyly type 4
- acromesomelic dysplasia 2C, Hunter-Thompson type
- laurin-Sandrow syndrome
- spondyloepimetaphyseal dysplasia, Missouri type
- fibular aplasia-ectrodactyly syndrome
- acromesomelic dysplasia 2A
- tibial hemimelia
- acromesomelic dysplasia 2B
- mesomelic dysplasia, Savarirayan type
- Osebold-Remondini syndrome
- chromosome 17P13.3, telomeric, duplication syndrome
- Fuhrmann syndrome
- Langer mesomelic dysplasia
- tibial aplasia-ectrodactyly syndrome
