PLXNA1 (Plexin A1) is a Protein Coding gene. Diseases associated with PLXNA1 include Hereditary Congenital Facial Paresis. Among its related pathways are Developmental Biology and Neuroscience. GO annotations related to this gene include receptor activity and semaphorin receptor activity. An important paralog of this gene is PLXNA3.
Aliases： NOV; NOVP; PLXN1; PLEXIN-A1
Entrez GeneID： 5361
Swissprot ： Q9UIW2
WB Predicted band size： 211kDa
Host/Isotype： Mouse IgG2b
Species Reactivity： Human
Immunogen ： Purified recombinant fragment of human PLXNA1 (AA: 1100-1200) expressed in E. Coli.
