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SCNN1G

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Anti-SCNN1G Recombinant Antibody Products

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For Research Use Only. Not For Clinical Use.


Nonvoltage-gated, amiloride-sensitive, sodium channels control fluid and electrolyte transport across epithelia in many organs. These channels are heteromeric complexes consisting of 3 subunits: alpha, beta, and gamma. This gene encodes the gamma subunit, and mutations in this gene have been associated with Liddle syndrome. [provided by RefSeq, Apr 2009]
Protein class

Disease related genes, FDA approved drug targets, Human disease related genes, Transporters

Predicted location

Membrane

Single cell type specificity

Cell type enriched (Collecting duct cells)

Immune cell specificity

Not detected in immune cells

Cell line specificity

Group enriched (hTCEpi, RT4)

Interaction

Heterotrimer containing an alpha/SCNN1A, a beta/SCNN1B and a gamma/SCNN1G subunit. An additional delta/SCNN1D subunit exists only in some organisms and can replace the alpha/SCNN1A subunit to form an alternative channel with specific properties (PubMed:7762608). Interacts with NEDD4; via the WW domains (PubMed:11244092, PubMed:12167593). Interacts with NEDD4L; via the WW domains (PubMed:11244092). Interacts with WWP1; via the WW domains (PubMed:9169421). Interacts with WWP2; via the WW domains (PubMed:9169421, PubMed:12167593). Interacts with the full-length immature form of PCSK9 (pro-PCSK9) (PubMed:22493497).

Molecular function

Ion channel, Sodium channel

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