IL17RD

interleukin 17 receptor D

Ensembl:
ENSG00000144730
UniProt:
Q8NFM7
OMIM:
606807
Synonyms:
FLJ35755, IL-17RD, IL17RLM, SEF

Cilia effects upon perturbation of IL17RD

Ciliogenesis screen results (3 screens)

  • Wheway et al. 2015 (siRNA) [siRNA]: No effect PMID:26167766
  • Breslow et al. 2018 (CRISPR) [CRISPR]: No Significant Effect PMID:29459680
  • Roosing et al. 2015 (siRNA) [siRNA]: No effect PMID:26595381

Phenotypes

Mouse phenotype:
abnormal heart left ventricle morphology

Ciliopathy associations

  • Kallmann Syndrome

Subcellular localization

golgi apparatus, nucleoplasm

Functional category

  • Motile cilium & axoneme

Function

Mutations in IL17RD cause Kallmann Syndrome (PMID: 36138264; 38628584).