THIK-2 Polyclonal Antibody, 50ul Oligo Pool Mutations in this gene cause

Mutations in this gene cause mitochondrial complex I deficiency

Mutations in this gene are associated with glutamate formiminotransferase deficiency

KPNA2 (karyopherin subunit alpha 2) protein interacts with the NLSs of DNA helicase Q1 and SV40 T antigen and may be involved in the nuclear transport of proteins

and has a broad array of biological activities

Also localized to the nucleolus

THIK-2 Polyclonal Antibody, 50ul Oligo Pool Mutations in this gene causeKCNK12 (potassium two pore domain channel subfamily K member 12) encodes one of the members of the superfamily of potassium channel proteins containing two pore forming P domains. The product of KCNK12 has not been shown to be a functional channel, however, it may require other non pore forming proteins for activity.