SWS Rabbit Polyclonal Antibody, 20ul Glassware Allelic variants of this gene

Allelic variants of this gene are associated with the autosomal-recessive disorder Joubert syndrome

sgRNA (single-guide RNA) is a key component in the CRISPR-Cas9 gene-editing system

Diseases associated with SEPT2 include gastrointestinal anthrax and acute orbital inflammation

supports the notion that it is a candidate gene for neuroblastoma

SWS Rabbit Polyclonal Antibody, 20ul Glassware Allelic variants of this geneThis gene belongs to the G protein coupled receptor 1 family opsin subfamily. It encodes the blue cone pigment gene which is one of three types of cone photoreceptors responsible for normal color vision. Defects in this gene are the cause of tritan color blindness (tritanopia). Affected individuals lack blue and yellow sensory mechanisms while retaining those for red and green. Defective blue vision is characteristic.