PDZK1
Encyclopedia
Na/H(+) exchange regulatory cofactor NHE-RF3 is a protein
that in humans is encoded by the PDZK1 gene
.
with AKAP10
, FARP2
, Sodium-hydrogen antiporter 3 regulator 1
, SLC22A12
, SLK
, SLC22A4
, CLCN3
, PDZK1IP1
, Cystic fibrosis transmembrane conductance regulator
and SLC34A3
.
Protein
Proteins are biochemical compounds consisting of one or more polypeptides typically folded into a globular or fibrous form, facilitating a biological function. A polypeptide is a single linear polymer chain of amino acids bonded together by peptide bonds between the carboxyl and amino groups of...
that in humans is encoded by the PDZK1 gene
Gene
A gene is a molecular unit of heredity of a living organism. It is a name given to some stretches of DNA and RNA that code for a type of protein or for an RNA chain that has a function in the organism. Living beings depend on genes, as they specify all proteins and functional RNA chains...
.
Interactions
PDZK1 has been shown to interactProtein-protein interaction
Protein–protein interactions occur when two or more proteins bind together, often to carry out their biological function. Many of the most important molecular processes in the cell such as DNA replication are carried out by large molecular machines that are built from a large number of protein...
with AKAP10
AKAP10
A kinase anchor protein 10, mitochondrial is an enzyme that in humans is encoded by the AKAP10 gene.-Interactions:AKAP10 has been shown to interact with PDZK1 and PRKAR1A.-Further reading:...
, FARP2
FARP2
FERM, RhoGEF and pleckstrin domain-containing protein 2 is a protein that in humans is encoded by the FARP2 gene.-Further reading:...
, Sodium-hydrogen antiporter 3 regulator 1
Sodium-hydrogen antiporter 3 regulator 1
Sodium-hydrogen antiporter 3 regulator 1 is a regulator of Sodium-hydrogen antiporter 3. It is encoded by the gene SLC9A3R1. It is also known as ERM Binding Protein 50 or Na+/H+ Exchanger Regulatory Factor...
, SLC22A12
SLC22A12
Solute carrier family 22 , member 12, also known as SLC22A12 and URAT1, is a protein which in humans is encoded by the SLC22A12 gene.-Function:...
, SLK
SLK (gene)
STE20-like serine/threonine-protein kinase is an enzyme that in humans is encoded by the SLK gene.-Interactions:SLK has been shown to interact with PDZK1.-Further reading:...
, SLC22A4
SLC22A4
Solute carrier family 22, member 4, also known as SLC22A4, is a human gene; the encoded protein is an ergothioneine transporter.- Function :The encoded protein is an integral protein of the plasma membrane containing 12 transmembrane segments...
, CLCN3
CLCN3
H/Cl exchange transporter 3 is a protein that in humans is encoded by the CLCN3 gene....
, PDZK1IP1
PDZK1IP1
PDZK1-interacting protein 1 is a protein that in humans is encoded by the PDZK1IP1 gene.-Further reading:...
, Cystic fibrosis transmembrane conductance regulator
Cystic fibrosis transmembrane conductance regulator
Cystic fibrosis transmembrane conductance regulator is a protein that in humans is encoded by the CFTR gene.CFTR is a ABC transporter-class ion channel that transports chloride and thiocyanate ions across epithelial cell membranes...
and SLC34A3
SLC34A3
Sodium-dependent phosphate transport protein 2C is a protein that in humans is encoded by the SLC34A3 gene.- Function :SLC34A3 contributes to the maintenance of inorganic phosphate concentration at the kidney.-Clinical Correlation:...
.
Related gene problems
- TAR syndromeTAR syndromeTAR Syndrome is a rare genetic disorder that is characterized by the absence of the radius bone in the forearm, and a dramatically reduced platelet count...
- 1q21.1 deletion syndrome1q21.1 deletion syndrome1q21.1 deletion syndrome or 1q21.1 microdeletion is a rare aberration of chromosome 1. , the international rare chromosome disorder group, has 48 genetically confirmed registered cases of this deletion worldwide ....
- 1q21.1 duplication syndrome1q21.1 duplication syndrome1q21.1 duplication syndrome or 1q21.1 microduplication is a rare aberration of chromosome 1. , the international rare chromosome disorder group, has 38 genetically confirmed registered cases of this duplication worldwide ....