IFT172
Description
The IFT172 (intraflagellar transport 172) is a protein-coding gene located on chromosome 2.
IFT172 is also known as BBS20, NPHP17, RP71, SLB, SRTD10, osm-1, wim.
Associated Diseases
- Retinitis pigmentosa
- Short-Rib thoracic dysplasia 10 with or without polydactyly
- Retinitis pigmentosa 71
- Bardet-Biedl syndrome
- Jeune syndrome
- Bardet-Biedl syndrome 20
