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The function of the encoded protein is not known. Additionally we are shipping C16orf35 Antibodies (23) and many more products for this protein.
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This study demonstrated that mutation of NPRL3 in familial focal epilepsies and focal cortical dysplasia.
NPRL3 mutations are significant cause of focal epilepsy.
Mutations in NPRL3 are a novel cause of familial cortical dysplasia.
NPRL3 is a candidate gene for harbouring mutations in individuals with developmental abnormalities of the cardiovascular system.
NPRL3 is a target gene of the BACH1 (show BACH1 Proteins) transcription factor according to ChIP-seq analysis in HEK (show EPHA3 Proteins) 293 cells.
C16orf35 can modulate differentially the specific activities of selected p73 (show TP73 Proteins) isoforms.
The function of the encoded protein is not known.
, alpha globin regulatory element containing
, alpha-globin regulatory element-containing gene protein
, nitrogen permease regulator 3-like protein
, proximal locus to the hemoglobin alpha chain complex
, -14 gene protein
, conserved gene telomeric to alpha globin cluster