FoxR1 Polyclonal Antibody, 50ul Vector Construction Defects in PEX19 are a

Defects in PEX19 are a cause of Zellweger syndrome (ZWS)

Rudhira/BCAS3 (Breast Cancer Amplified Sequence 3) is a conserved protein expressed in the embryonic vasculature and malignant tumors

This gene encodes a large multidomain protein of the phosphoinositide 3-kinase-related kinases (PIKK) family

and mitochondrial neurogastrointestinal encephalopathy

This record represents the most centromeric copy which is in intron 22 of the F8 gene

FoxR1 Polyclonal Antibody, 50ul Vector Construction Defects in PEX19 are aFOXR1 encodes a member of the forkhead box (FOX) family of transcription factors. FOX family members are monomeric, helix turn helix proteins with a core DNA binding domain of approximately 110 aa. Many FOX transcription factors play roles in determining cell fates during early development. Forkhead box protein R1 lacks the C terminal basic region found in many other FOX family members. It is located within the 11q23. 3 region which is commonly