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, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| OSTM1-20-RE | 20 (40 μL) | 200 μL |  |
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| OSTM1-20-OR | 20 (40 μL) | 200 μL |  |
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| OSTM1-20-GO | 20 (40 μL) | 200 μL |  |
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| OSTM1-20-GR | 20 (40 μL) | 200 μL |  |
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| OSTM1-20-AQ | 20 (40 μL) | 200 μL |  |
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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, Jul 2008]
Gene Symbol : OSTM1
Gene Name : Osteopetrosis associated transmembrane protein 1
Chromosome : CHR 6: 108,074,736-108,041,408
Locus : 6q21
Alt. Genes : RAD50
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