regulatory mutation

См. также в других словарях:

• mutation — mutational, adj. mutationally, adv. /myooh tay sheuhn/, n. 1. Biol. a. a sudden departure from the parent type in one or more heritable characteristics, caused by a change in a gene or a chromosome. b. an individual, species, or the like,… …   Universalium

• Gene regulatory network — A gene regulatory network (also called a GRN or genetic regulatory network ) is a collection of DNA segments in a cell which interact with each other (indirectly through their RNA and protein expression products) and with other substances in the… …   Wikipedia

• Neutral mutation — In genetics, a neutral mutation is a mutation that has no effect on fitness. In other words, it is neutral with respect to natural selection. For example, some mutations in a DNA triplet or codon do not change which amino acid is introduced: this …   Wikipedia

• Steroidogenic acute regulatory protein — protein Name=steroidogenic acute regulatory proteinth caption= width= HGNCid=11359 Symbol=StAR AltSymbols= EntrezGene=6770 OMIM=600617 RefSeq=NM 000349 UniProt=P49675 PDB= ECnumber= Chromosome=8 Arm=p Band=11.2 LocusSupplementaryData=The… …   Wikipedia

• Glucokinase regulatory protein — protein Name = caption = width = HGNCid = 4196 Symbol = GCKR AltSymbols = EntrezGene = 2646 OMIM = 600842 RefSeq = NM 001486 UniProt = Q14397 PDB = ECnumber = Chromosome = 2 Arm = p Band = 23 LocusSupplementaryData = The glucokinase regulatory… …   Wikipedia

• gain of function mutation — Gene mutation that results in higher than normal levels of activity of the gene product, for example by deletion of a regulatory phosphorylation site on the protein. Examples are oncogenic mutations in genes involved in growth control …   Dictionary of molecular biology

• constitutive mutation — a mutation that causes a gene usually under regulatory control to be expressed constantly, independent of regulation …   Medical dictionary

• Androgen insensitivity syndrome — Classification and external resources AIS results when the function of the androgen receptor (AR) is impaired. The AR protein (pictured) mediates the effects of androgens in the human body. ICD 10 E …   Wikipedia

• Gray (horse) — Nearly all Lipizzaner horses have gray coats. They are typically born bay or black, and their hair coat will be pure white before they are 10 years old …   Wikipedia

• Dominant white — This dominant white Thoroughbred stallion (W2/+) has one form of dominant white. His skin, hooves, and coat lack pigment cells, giving him a pink skinned white coat. Dominant white is a group of genetically related coat color conditions in the… …   Wikipedia

• BCKDHA — Branched chain keto acid dehydrogenase E1, alpha polypeptide, also known as BCKDHA, is a human gene.cite web | title = Entrez Gene: BCKDHA branched chain keto acid dehydrogenase E1, alpha polypeptide| url =… …   Wikipedia