XB-FEAT-6464201
cfap418
nomenclature changes
06.16.2021
Human symbol has changed for genepage ID: 6464201 From C8orf37 to CFAP418 Xenopus symbol has changed for genepage ID: 6464201 From c8orf37 to cfap418
Human name has changed for genepage ID: 6464201 from chromosome 8 open reading frame 37 to cilia and flagella associated protein 418
summary for human CFAP418 from NCBI
This gene encodes a ubiquitously expressed protein of unknown function. It has high levels of mRNA expression in the brain, heart, and retina and the protein co-localizes with polyglutamylated tubulin at the base of the primary cilium in human retinal pigment epithelial cells. Mutations in this gene have been associated with autosomal recessive cone-rod dystrophy (arCRD) and retinitis pigmentosa (arRP). [provided by RefSeq, Mar 2012]