SMPX Rabbit Polyclonal Antibody, 20ul Electronic Pipette A genetic variation in IFNGR1

A genetic variation in IFNGR1 is associated with susceptibility to Helicobacter pylori infection

As is typical for genes encoding ribosomal proteins

subcellular location:In the nucleus

This gene encodes a protein containing RNA helicase-DEAD box protein motifs and a caspase recruitment domain (CARD)

This family member is a retinal cone/brain exchanger that can mediate a light-induced decrease in free Ca2+ concentration

SMPX Rabbit Polyclonal Antibody, 20ul Electronic Pipette A genetic variation in IFNGR1This gene encodes a small protein that has no known functional domains. Mutations in this gene are a cause of X linked deafness 4 and the encoded protein may play a role in the maintenance of inner ear cells subjected to mechanical stress. Alternatively spliced transcript variants have been observed for this gene.