TM138 Rabbit Polyclonal Antibody, 50ul Microplate Mixer A pseudogene of this gene

A pseudogene of this gene is located on chromosome 13

conotruncal heart defects and facial dysmorphology

is a nuclear protein belonging to the nuclear hormone receptor family and NR2 subfamily with a nuclear receptor DNA-binding domain

Lid lock prevents accidental opening of cap and evaporation of samples during long-term storage

a microsomal enzyme complex responsible for the interconversion of cortisol and cortisone

TM138 Rabbit Polyclonal Antibody, 50ul Microplate Mixer A pseudogene of this geneThis gene encodes a multi pass transmembrane protein. Reduced expression of this gene in mouse fibroblasts causes short cilia and failure of ciliogenesis. Expression of this gene is tightly coordinated with expression of the neighboring gene TMEM216. Mutations in this gene are associated with the autosomal recessive neurodevelopmental disorder Joubert Syndrome. Alternative splicing results in multiple transcript variants.