Phenotype Image Detail

Image

Caption

Mutant (E14.5) has severe craniofacial defects consistent with otocephaly which include microcephaly with cyclopia, proboscis, and agnathia

Copyright

This image is from the Laboratory of Dr. Cecilia Lo, a member of the Cardiovascular Development Consortium (CvDC), Bench to Bassinet (B2B) program of the National Heart Lung and Blood Institute (NHLBI), and is displayed with the permission of the authors. J:175213

Associated Alleles

Symbol	Name
Pcsk6^b2b2830Clo	proprotein convertase subtilisin/kexin type 6; Bench to Bassinet Program (B2B/CVDC), mutation 2830 Cecilia Lo