ADNP

activity dependent neuroprotector homeobox

Ensembl:
ENSG00000101126
UniProt:
Q9H2P0
OMIM:
611386
Synonyms:
ADNP1, KIAA0784

Cilia effects upon perturbation of ADNP

Ciliogenesis screen results (4 screens)

  • Kim2016: Not Reported
  • Wheway et al. 2015 (siRNA) [siRNA]: Ciliogenesis Defect (z=-8.89) PMID:26167766
  • Breslow et al. 2018 (CRISPR) [CRISPR]: No Significant Effect PMID:29459680
  • Roosing et al. 2015 (siRNA) [siRNA]: No effect PMID:26595381

Phenotypes

Human ciliopathy phenotype:
ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder; ADNP-related multiple congenital anomalies-intellectual disability-autism spectrum disorder; Intellectual disability

Subcellular localization

basal body, cilia, nucleus

Functional category

  • Ciliary assembly/disassembly
  • Neurogenesis & migration

Function

ADNP has localized in basal body, cilia.