Faster access than browser!Similarities between Mutation and Point mutation
Mutation and Point mutation have 41 things in common (in Unionpedia): Adenine, Amino acid, Base pair, Cancer, Cytosine, DNA, DNA replication, Evolution, Frameshift mutation, Gene, Gene product, Genetic code, Genome, Germline mutation, Hemoglobin, Insertion (genetics), Intron, Lysine, Meiosis, Missense mutation, Mutagen, Mutagenesis, Natural selection, Nonsense mutation, Nucleotide, Promoter (genetics), Protein, Purine, Pyrimidine, RNA, ..., Sickle cell disease, Silent mutation, Stop codon, Synonymous substitution, Thymine, Transition (genetics), Transposable element, Transversion, Ultraviolet, Wild type, X-ray. Expand index (11 more) »
Adenine
Adenine (A, Ade) is a nucleobase (a purine derivative).
Adenine and Mutation · Adenine and Point mutation ·
Amino acid
Amino acids are organic compounds containing amine (-NH2) and carboxyl (-COOH) functional groups, along with a side chain (R group) specific to each amino acid.
Amino acid and Mutation · Amino acid and Point mutation ·
Base pair
A base pair (bp) is a unit consisting of two nucleobases bound to each other by hydrogen bonds.
Base pair and Mutation · Base pair and Point mutation ·
Cancer
Cancer is a group of diseases involving abnormal cell growth with the potential to invade or spread to other parts of the body.
Cancer and Mutation · Cancer and Point mutation ·
Cytosine
Cytosine (C) is one of the four main bases found in DNA and RNA, along with adenine, guanine, and thymine (uracil in RNA).
Cytosine and Mutation · Cytosine and Point mutation ·
DNA
Deoxyribonucleic acid (DNA) is a thread-like chain of nucleotides carrying the genetic instructions used in the growth, development, functioning and reproduction of all known living organisms and many viruses.
DNA and Mutation · DNA and Point mutation ·
DNA replication
In molecular biology, DNA replication is the biological process of producing two identical replicas of DNA from one original DNA molecule.
DNA replication and Mutation · DNA replication and Point mutation ·
Evolution
Evolution is change in the heritable characteristics of biological populations over successive generations.
Evolution and Mutation · Evolution and Point mutation ·
Frameshift mutation
A frameshift mutation (also called a framing error or a reading frame shift) is a genetic mutation caused by indels (insertions or deletions) of a number of nucleotides in a DNA sequence that is not divisible by three.
Frameshift mutation and Mutation · Frameshift mutation and Point mutation ·
Gene
In biology, a gene is a sequence of DNA or RNA that codes for a molecule that has a function.
Gene and Mutation · Gene and Point mutation ·
Gene product
A gene product is the biochemical material, either RNA or protein, resulting from expression of a gene.
Gene product and Mutation · Gene product and Point mutation ·
Genetic code
The genetic code is the set of rules used by living cells to translate information encoded within genetic material (DNA or mRNA sequences) into proteins.
Genetic code and Mutation · Genetic code and Point mutation ·
Genome
In the fields of molecular biology and genetics, a genome is the genetic material of an organism.
Genome and Mutation · Genome and Point mutation ·
Germline mutation
A germline mutation, or germinal mutation, is any detectable variation within germ cells (cells that, when fully developed, become sperm and ovum).
Germline mutation and Mutation · Germline mutation and Point mutation ·
Hemoglobin
Hemoglobin (American) or haemoglobin (British); abbreviated Hb or Hgb, is the iron-containing oxygen-transport metalloprotein in the red blood cells of all vertebrates (with the exception of the fish family Channichthyidae) as well as the tissues of some invertebrates.
Hemoglobin and Mutation · Hemoglobin and Point mutation ·
Insertion (genetics)
In genetics, an insertion (also called an insertion mutation) is the addition of one or more nucleotide base pairs into a DNA sequence.
Insertion (genetics) and Mutation · Insertion (genetics) and Point mutation ·
Intron
An intron is any nucleotide sequence within a gene that is removed by RNA splicing during maturation of the final RNA product.
Intron and Mutation · Intron and Point mutation ·
Lysine
Lysine (symbol Lys or K) is an α-amino acid that is used in the biosynthesis of proteins.
Lysine and Mutation · Lysine and Point mutation ·
Meiosis
Meiosis (from Greek μείωσις, meiosis, which means lessening) is a specialized type of cell division that reduces the chromosome number by half, creating four haploid cells, each genetically distinct from the parent cell that gave rise to them.
Meiosis and Mutation · Meiosis and Point mutation ·
Missense mutation
In genetics, a missense mutation is a point mutation in which a single nucleotide change results in a codon that codes for a different amino acid.
Missense mutation and Mutation · Missense mutation and Point mutation ·
Mutagen
In genetics, a mutagen is a physical or chemical agent that changes the genetic material, usually DNA, of an organism and thus increases the frequency of mutations above the natural background level.
Mutagen and Mutation · Mutagen and Point mutation ·
Mutagenesis
Mutagenesis is a process by which the genetic information of an organism is changed, resulting in a mutation.
Mutagenesis and Mutation · Mutagenesis and Point mutation ·
Natural selection
Natural selection is the differential survival and reproduction of individuals due to differences in phenotype.
Mutation and Natural selection · Natural selection and Point mutation ·
Nonsense mutation
In genetics, a point-nonsense mutation is a point mutation in a sequence of DNA that results in a premature stop codon, or a point-nonsense codon in the transcribed mRNA, and in a truncated, incomplete, and usually nonfunctional protein product.
Mutation and Nonsense mutation · Nonsense mutation and Point mutation ·
Nucleotide
Nucleotides are organic molecules that serve as the monomer units for forming the nucleic acid polymers deoxyribonucleic acid (DNA) and ribonucleic acid (RNA), both of which are essential biomolecules within all life-forms on Earth.
Mutation and Nucleotide · Nucleotide and Point mutation ·
Promoter (genetics)
In genetics, a promoter is a region of DNA that initiates transcription of a particular gene.
Mutation and Promoter (genetics) · Point mutation and Promoter (genetics) ·
Protein
Proteins are large biomolecules, or macromolecules, consisting of one or more long chains of amino acid residues.
Mutation and Protein · Point mutation and Protein ·
Purine
A purine is a heterocyclic aromatic organic compound that consists of a pyrimidine ring fused to an imidazole ring.
Mutation and Purine · Point mutation and Purine ·
Pyrimidine
Pyrimidine is an aromatic heterocyclic organic compound similar to pyridine.
Mutation and Pyrimidine · Point mutation and Pyrimidine ·
RNA
Ribonucleic acid (RNA) is a polymeric molecule essential in various biological roles in coding, decoding, regulation, and expression of genes.
Mutation and RNA · Point mutation and RNA ·
Sickle cell disease
Sickle cell disease (SCD) is a group of blood disorders typically inherited from a person's parents.
Mutation and Sickle cell disease · Point mutation and Sickle cell disease ·
Silent mutation
Silent mutations are mutations in DNA that do not have an observable effect on the organism's phenotype.
Mutation and Silent mutation · Point mutation and Silent mutation ·
Stop codon
In the genetic code, a stop codon (or termination codon) is a nucleotide triplet within messenger RNA that signals a termination of translation into proteins.
Mutation and Stop codon · Point mutation and Stop codon ·
Synonymous substitution
A synonymous substitution (often called a silent substitution though they are not always silent) is the evolutionary substitution of one base for another in an exon of a gene coding for a protein, such that the produced amino acid sequence is not modified.
Mutation and Synonymous substitution · Point mutation and Synonymous substitution ·
Thymine
---> Thymine (T, Thy) is one of the four nucleobases in the nucleic acid of DNA that are represented by the letters G–C–A–T.
Mutation and Thymine · Point mutation and Thymine ·
Transition (genetics)
In genetics, a transition is a point mutation that changes a purine nucleotide to another purine (A ↔ G) or a pyrimidine nucleotide to another pyrimidine (C ↔ T).
Mutation and Transition (genetics) · Point mutation and Transition (genetics) ·
Transposable element
A transposable element (TE or transposon) is a DNA sequence that can change its position within a genome, sometimes creating or reversing mutations and altering the cell's genetic identity and genome size.
Mutation and Transposable element · Point mutation and Transposable element ·
Transversion
Transversion, in molecular biology, refers to the substitution of a (two ring) purine for a (one ring) pyrimidine or vice versa, in deoxyribonucleic acid (DNA).
Mutation and Transversion · Point mutation and Transversion ·
Ultraviolet
Ultraviolet (UV) is electromagnetic radiation with a wavelength from 10 nm to 400 nm, shorter than that of visible light but longer than X-rays.
Mutation and Ultraviolet · Point mutation and Ultraviolet ·
Wild type
Wild type (WT) refers to the phenotype of the typical form of a species as it occurs in nature.
Mutation and Wild type · Point mutation and Wild type ·
X-ray
X-rays make up X-radiation, a form of electromagnetic radiation.
The list above answers the following questions
- What Mutation and Point mutation have in common
- What are the similarities between Mutation and Point mutation
Mutation and Point mutation Comparison
Mutation has 296 relations, while Point mutation has 93. As they have in common 41, the Jaccard index is 10.54% = 41 / (296 + 93).
References
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