Rho guanine nucleotide exchange factor (GEF) 3, also known as ARHGEF3, is a human gene. [5]
In biology, a gene is a sequence of nucleotides in DNA or RNA that codes for a molecule that has a function. During gene expression, the DNA is first copied into RNA. The RNA can be directly functional or be the intermediate template for a protein that performs a function. The transmission of genes to an organism's offspring is the basis of the inheritance of phenotypic trait. These genes make up different DNA sequences called genotypes. Genotypes along with environmental and developmental factors determine what the phenotypes will be. Most biological traits are under the influence of polygenes as well as gene–environment interactions. Some genetic traits are instantly visible, such as eye color or number of limbs, and some are not, such as blood type, risk for specific diseases, or the thousands of basic biochemical processes that constitute life.
Rho GTPases play a fundamental role in numerous cellular processes that are initiated by extracellular stimuli that work through G protein-coupled receptors. The encoded protein may form complex with G proteins and stimulate Rho-dependent signals. This protein is similar to the NET1A protein. [5]
ARHGEF3 has been shown to interact with RHOA [6] and RHOB. [6]
Ras homolog gene family, member A (RhoA) is a small GTPase protein in the Rho family. While the effects of RhoA activity are not all well known, it is primarily associated with cytoskeleton regulation, mostly actin stress fibers formation and actomyosin contractility. In humans, it is encoded by the gene RHOA. It acts upon several effectors. Among them, ROCK1 and DIAPH1 are the best described. RhoA, and the other Rho GTPases, are part of a larger family of related proteins known as the Ras superfamily, a family of proteins involved in the regulation and timing of cell division. RhoA is one of the oldest Rho GTPases, with homologues present in the genomes since 1.5 billions years. As a consequence, RhoA is somehow involved in many cellular processes which emerged throughout evolution. RhoA specifically is regarded as a prominent regulatory factor in other functions such as the regulation of cytoskeletal dynamics, transcription, cell cycle progression and cell transformation.
Ras homolog gene family, member B, also known as RHOB, is a protein which in humans is encoded by the RHOB gene.
Rho guanine nucleotide exchange factor 2 is a protein that in humans is encoded by the ARHGEF2 gene.
Rho guanine nucleotide exchange factor 12 is a protein that in humans is encoded by the ARHGEF12 gene.
Ras-related protein Rab-5B is a protein that in humans is encoded by the RAB5B gene.
Synaptotagmin-3 is a protein that in humans is encoded by the SYT3 gene.
Beta-taxilin is a protein that in humans is encoded by the TXLNB gene.
Uncharacterized protein KIAA1267 is a protein that in humans is encoded by the KIAA1267 gene.
Protein YIPF3 is a protein that in humans is encoded by the YIPF3 gene. Along with YIPF4, it is concentrated in the cis-Golgi region. There the two form a complex and may be involved in the maintenance of the Golgi structure.
LisH domain-containing protein ARMC9 is a protein that in humans is encoded by the ARMC9 gene.
Transmembrane protein 47 is a protein that in humans is encoded by the TMEM47 gene.
High-mobility group protein B3 is a protein that in humans is encoded by the HMGB3 gene.
Hippocalcin like 4, also known as HPCAL4, is a human gene.
Synaptotagmin-13 is a protein that in humans is encoded by the SYT13 gene.
FERM, RhoGEF and pleckstrin domain-containing protein 1 is a protein that in humans is encoded by the FARP1 gene.
Metalloreductase STEAP3 is an enzyme that in humans is encoded by the STEAP3 gene.
Zinc finger protein 34 is a protein that in humans is encoded by the ZNF34 gene.
Rho guanine nucleotide exchange factor 9 is a protein that in humans is encoded by the ARHGEF9 gene.
IQ domain-containing protein E is a protein that in humans is encoded by the IQCE gene.
Leiomodin-3 is a protein that in humans is encoded by the LMOD3 gene.
Uncharacterized protein KIAA1539 is a protein that in humans is encoded by the KIAA1539 gene.
The human ARHGEF10 gene encodes the protein Rho guanine nucleotide exchange factor 10.
The UCSC Genome Browser is an on-line, and downloadable, genome browser hosted by the University of California, Santa Cruz (UCSC). It is an interactive website offering access to genome sequence data from a variety of vertebrate and invertebrate species and major model organisms, integrated with a large collection of aligned annotations. The Browser is a graphical viewer optimized to support fast interactive performance and is an open-source, web-based tool suite built on top of a MySQL database for rapid visualization, examination, and querying of the data at many levels. The Genome Browser Database, browsing tools, downloadable data files, and documentation can all be found on the UCSC Genome Bioinformatics website.
In computing, a Digital Object Identifier or DOI is a persistent identifier or handle used to uniquely identify objects, standardized by the International Organization for Standardization (ISO). An implementation of the Handle System, DOIs are in wide use mainly to identify academic, professional, and government information, such as journal articles, research reports and data sets, and official publications though they also have been used to identify other types of information resources, such as commercial videos.
PubMed Central (PMC) is a free digital repository that archives publicly accessible full-text scholarly articles that have been published within the biomedical and life sciences journal literature. As one of the major research databases within the suite of resources that have been developed by the National Center for Biotechnology Information (NCBI), PubMed Central is much more than just a document repository. Submissions into PMC undergo an indexing and formatting procedure which results in enhanced metadata, medical ontology, and unique identifiers which all enrich the XML structured data for each article on deposit. Content within PMC can easily be interlinked to many other NCBI databases and accessed via Entrez search and retrieval systems, further enhancing the public's ability to freely discover, read and build upon this portfolio of biomedical knowledge.
This article on a gene on human chromosome 3 is a stub. You can help Wikipedia by expanding it. |