OSTM1 Products

Description

This gene encodes a protein that may be involved in the degradation of G proteins via the ubiquitin-dependent proteasome pathway. The encoded protein binds to members of subfamily A of the regulator of the G-protein signaling (RGS) family through an N-terminal leucine-rich region. This protein also has a central RING finger-like domain and E3 ubiquitin ligase activity. This protein is highly conserved from flies to humans. Defects in this gene may cause the autosomal recessive, infantile malignant form of osteopetrosis. [provided by RefSeq].

Bioinformatics

Product By Gene ID	28962
Alternate Names	GIPN GLGAIP-interacting protein N terminus grey-lethal osteopetrosis HSPC019 OPTB5 osteopetrosis associated transmembrane protein 1 osteopetrosis-associated transmembrane protein 1

Research Areas for OSTM1

Find related products by research area and learn more about each of the different research areas below.

Cancer
Cell Biology
Cell Cycle and Replication
Cytoskeleton Markers
Signal Transduction