IGFL4 Polyclonal Antibody, 100ul Lentiviral Packaging Mutations in this gene cause

Mutations in this gene cause autosomal recessive nonsyndromic deafness| type 18B

The encoded protein may interact with synaptotagmin to enhance low frequency neurotransmission in quiescent neurons

This gene is highly polymorphic

delta-type and kappa-type

which shows little similarity to any of the other known human DEAD box proteins

IGFL4 Polyclonal Antibody, 100ul Lentiviral Packaging Mutations in this gene causeIGFL4 belongs to the insulin like growth factor (IGF; see MIM 147440) family of signaling molecules that play critical roles in cellular energy metabolism and in growth and development especially prenatal growth (Emtage et al. 2006