RBM8A
Encyclopedia
RNA-binding protein 8A is a protein
that in humans is encoded by the RBM8A gene
.
with IPO13
, MAGOH
and UPF3A
.
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 RBM8A 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
RBM8A 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 IPO13
IPO13
Importin-13 is a protein that in humans is encoded by the IPO13 gene.-Interactions:IPO13 has been shown to interact with RBM8A, PAX6, ALX1, EIF1AX and UBE2I.-Further reading:...
, MAGOH
MAGOH
Protein mago nashi homolog is a protein that in humans is encoded by the MAGOH gene.-Interactions:MAGOH has been shown to interact with RBM8A and NXF1.-Further reading:...
and UPF3A
UPF3A
Regulator of nonsense transcripts 3A is a protein that in humans is encoded by the UPF3A gene.-Interactions:UPF3A has been shown to interact with RBM8A, UPF2 and UPF1.-Further reading:...
.
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 ....