XB-FEAT-6464201: Difference between revisions
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imported>Xenbase (Created page with " = ''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: 6464...") |
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Revision as of 15:00, 8 July 2021
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]