RPGR1 Rabbit Polyclonal Antibody, 20ul General Lab Use Mutations in CYP7B1 have been

Mutations in CYP7B1 have been associated with hereditary spastic paraplegia (SPG5 or HSP)

and other cytokines by acting as a molecular adaptor between diverse receptor tyrosine kinases and downstream effectors

and thus play a role in cell migration

which is required for transcriptional activation of genes normally repressed by chromatin

This gene encodes a nuclear protein with three C2H2-type zinc fingers| and functions as a transcriptional repressor

RPGR1 Rabbit Polyclonal Antibody, 20ul General Lab Use Mutations in CYP7B1 have beenThis gene encodes a photoreceptor protein that interacts with retinitis pigmentosa GTPase regulator protein and is a key component of cone and rod photoreceptor cells. Mutations in this gene lead to autosomal recessive congenital blindness.