EMR4 Polyclonal Antibody, 50ul Cell Culture Flasks Mutations in this gene have

Mutations in this gene have been associated with infantile epileptic encephalopathy-4

The protein is localized to the nucleus

Caffey Disease and idiopathic osteoporosis

Several alternatively spliced transcript variants of SCN2A have been described

and Aland Island eye disease

EMR4 Polyclonal Antibody, 50ul Cell Culture Flasks Mutations in this gene haveEMR4P is a member of the EGF TM7 receptor gene family which is thought to play a role in leukocyte adhesion and migration. In other vertebrates, including nonhuman primates, EMR4P encodes a protein containing N terminal EGF domains and a C terminal transmembrane domain. Sequence evidence for the human gene, however, indicates nucleotide deletion in the genomic sequence would result in frameshift and early termination of translation. A protein