NBPF1/9/10/12/14/15/16/20 Polyclonal Antibody, 100ul ROS/Nitric Oxide Detection This gene contains a variable

This gene contains a variable number of tandem repeat (VNTR) polymorphism in the coding region that may influence the function of the encoded protein

and it is required for the association of centromere-associated protein E with the kinetochore

These proteins are putative RNA helicases

Mutations in this gene cause lissencephaly type 3 (LIS3) - a neurological condition characterized by microcephaly

The C-terminus of the protein encoded by this gene binds topoisomerase I

NBPF1/9/10/12/14/15/16/20 Polyclonal Antibody, 100ul ROS/Nitric Oxide Detection This gene contains a variableNBPF1 is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1. This gene family has experienced its greatest expansion within the human lineage and has expanded, to a lesser extent, among primates in general. Members of this gene family are characterized by tandemly repeated copies of DUF1220 protein domains. Gene copy number