QuickView for Wdr62;jsessionid=C6EF2F721E40A501557079DE0CE3D79F;jsessionid=D47F46A5817C11188A9FF4B7F3E1DB19;jsessionid=F9929BDF89258238AAFDC19DBDA21788 (gene)

Summary
General Info

Body Atlas

Most Correlated Tissues

Testis seminiferous tubule
Globus pallidus
Skeletal muscle psoas
Ciliary ganglion
Extraocular muscle

Explore Body Atlas Results

Disease Atlas

Most Correlated Diseases

Multiple organ failure
Placental insufficiency
Ischemia
Microcephalus
Cytomegalovirus infection

Explore Disease Atlas Results

Pharmaco Atlas

Most Correlated Compounds

dyclonine
Tocainide
Ficoll
Nalbuphine
zaprinast

Explore Pharmaco Atlas Results

Knockdown Atlas

Most Correlated Gene Perturbations

MIR508
MLXIP
WRN
HIC1
SPO11

Explore Knockdown Atlas Results

Curated Studies

Most Correlated Studies

Explore Curated Studies Results

Literature

Most Relevant Literature

WDR62-deficiency Causes Autism-like Behaviors Independent of Microcephaly in Mice.
WDR62 variants contribute to congenital heart disease by inhibiting cardiomyocyte proliferation.
WDR62 is required for centriole duplication in spermatogenesis and manchette removal in spermiogenes…
Modeling microcephaly with cerebral organoids reveals a WDR62-CEP170-KIF2A pathway promoting cilium …
Analysis of genome-wide knockout mouse database identifies candidate ciliopathy genes.

Explore Literature Results

Clinical Trials

Most Relevant Clinical Trials

There were no clinical trials for Wdr62;jsessionid=C6EF2F721E40A501557079DE0CE3D79F;jsessionid=D47F46A5817C11188A9FF4B7F3E1DB19;jsessionid=F9929BDF89258238AAFDC19DBDA21788

Explore Clinical Trials Results