FEZF1

FEZ family zinc finger 1

Ensembl:
ENSG00000128610
UniProt:
A0PJY2
OMIM:
613301
Synonyms:
ZNF312B

Cilia effects upon perturbation of FEZF1

Ciliogenesis screen results (1 screen)

  • Breslow et al. 2018 (CRISPR) [CRISPR]: No Significant Effect PMID:29459680

Phenotypes

Human ciliopathy phenotype:
hypogonadotropic hypogonadism

Ciliopathy associations

  • Kallmann Syndrome

Subcellular localization

cytosol, nucleoplasm

Functional category

  • Motile cilium & axoneme

Function

Mutations in FEZF1 cause Kallmann Syndrome (PMID: 25192046).