Information about Wild Type
A blue lobster (one in two million), an example of a genuine mutant.
A deformed banana, probably a developmental abnormality, not a mutant.
A mutant is an individual, organism, or new genetic character arising or resulting from an instance of mutation, which is a sudden structural change within the DNA of a gene or chromosome of an organism resulting in the creation of a new character or trait not found in the wildtype. In an organism or individual, the new character or trait may or may not be trivial, may occasionally be beneficial, but will usually result in either a genetic disorder or have no phenotypic effect whatsoever. The natural occurrence of genetic mutations is integral to the process of evolution. A more general term for mutant is sport, which includes individuals who vary from type due to mutation, as well as those who vary from type due to other reasons.
Developmental abnormalities not due to genetic change, are frequently referred to as mutants by non-experts. The difference between a developmental abnormality and a mutation is that the former is non-hereditable as the DNA is unchanged. Such abnormalities include extra limbs and occur when a genetically normal embryo develops abnormally.
Occasionally, a body cell in a healthy organism may acquire a mutation caused by a genetic error occurring during routine cell division. This is also known as a "somatic mutation". Such an error may result in cancer.
Creatures with visibly obvious mutations are often regarded as objects of curiosity. Examples include rare blue lobsters,[1] albinos of many species[2][3] and animals with extra digits.[4] A well-known mutation in fruit flies causes the flies to have legs in place of antennas.[5] An American aquarium even displays what it calls a "double mutant" snake that is both albino and has two heads[6], though calling this a double mutation is a misnomer as the two-headed condition is a developmental abnormality and not a genetic mutation.
Similarly striking human mutations also occur occasionally. People who are completely covered in a fur-like coat of hair are one example (see hypertrichosis). There are also cases of newborn babies having an extended tailbone or a sixth finger. Purely internal, less obvious mutations are more common; a small fraction of these cause serious medical conditions or death. (The ratio is probably under 1.5%, as only about 1.5% of the genome encodes protein genes)[7]
Wild type
Wild type (sometimes written wildtype, wild-type or +) is the genetic term used in texts for the typical form of an organism, strain, gene, or characteristic as it was first observed in nature.[8][9] Wild type refers to the most common phenotype in the natural population; however this may, over a period of time, be replaced by a mutant form, which then becomes the new wildtype. The phenotype can be dominant or recessive. Naturally occurring mutant phenotypes play a role in evolution.References
1. ^ WESH NBC affiliate news report
2. ^ Picture of Snowflake, a white ape
3. ^ Pictures of albino (and other) reptiles
4. ^ Polydactyly, pictured in cats
5. ^ Memorial University of Newfoundland page with picture, paragraph about antennapedia mutant flies
6. ^ BBC news report World Aquarium in St. Louis auctioning its albino two-headed rat snake. (The snake did not fetch enough money and was ultimately not sold)].
7. ^ International Human Genome Sequencing Consortium (2001). "Initial sequencing and analysis of the human genome.". Nature 409 (6822): 860-921. PMID 11237011. [1]
8. ^ Robinson Roy (1999), "Genetics for Cat Breeders and Veterinarians", Butterworth Heinemann, ISBN 0-7506-4069-3
9. ^ [2]
2. ^ Picture of Snowflake, a white ape
3. ^ Pictures of albino (and other) reptiles
4. ^ Polydactyly, pictured in cats
5. ^ Memorial University of Newfoundland page with picture, paragraph about antennapedia mutant flies
6. ^ BBC news report World Aquarium in St. Louis auctioning its albino two-headed rat snake. (The snake did not fetch enough money and was ultimately not sold)].
7. ^ International Human Genome Sequencing Consortium (2001). "Initial sequencing and analysis of the human genome.". Nature 409 (6822): 860-921. PMID 11237011. [1]
8. ^ Robinson Roy (1999), "Genetics for Cat Breeders and Veterinarians", Butterworth Heinemann, ISBN 0-7506-4069-3
9. ^ [2]
mutations are changes to the base pair sequence of the genetic material of an organism. Mutations can be caused by copying errors in the genetic material during cell division, by exposure to ultraviolet or ionizing radiation, chemical mutagens, or viruses, or can occur deliberately
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For a non-technical introduction to the topic, see .
A gene is a locatable region of genomic sequence, corresponding to a unit of inheritance, which is associated with regulatory regions, transcribed regions and/or other functional sequence regions...... Click the link for more information.
Figure 1: A representation of a condensed eukaryotic chromosome, as seen during cell division.]] A chromosome is a single large macromolecule of DNA, and constitutes a physically organized form of DNA in a cell.
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character is an attribute of an organism that allows it to be compared with another. In genetics this refers to heritable features which can exist in more than one state.[1] A trait
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A genetic disorder is a condition caused by abnormalities in genes or chromosomes. While some diseases, such as cancer, are due to genetic abnormalities acquired in a few cells during life, the term "genetic disease" most commonly refers to diseases present in all cells of the body
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phenotype describes the total physical appearance of an organism, as opposed to its genotype. This genotype-phenotype distinction was proposed by Wilhelm Johannsen in 1911 to make clear the difference between an organism's heredity and what that heredity produces.
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A somatic cell is generally taken to mean any cell forming the body of an organism: the word "somatic" is derived from the Greek word sōma (σώμα), meaning "body". Somatic cells, by definition, are not germline cells.
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Cell division is a process by which a cell, called the parent cell, divides into two cells, called daughter cells. Cell division is usually a small segment of a larger cell cycle. In meiosis however, a cell is permanently transformed and cannot divide again.
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H. americanus
Binomial name
Homarus americanus
H. Milne-Edwards, 1837
The American lobster, Homarus americanus, is a species of lobster found on the Atlantic coast of North America.
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Binomial name
Homarus americanus
H. Milne-Edwards, 1837
The American lobster, Homarus americanus, is a species of lobster found on the Atlantic coast of North America.
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Albinism
Classification & external resources
Albinistic boy
ICD-10 E 70.3
ICD-9 270.2
OMIM 203100 103470 , 203200 , 203280 ,
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Classification & external resources
Albinistic boy
ICD-10 E 70.3
ICD-9 270.2
OMIM 203100 103470 , 203200 , 203280 ,
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Polydactyly
Classification & external resources
ICD-10 Q 69.
ICD-9 755.0
OMIM 603598
DiseasesDB 24853
eMedicine derm/692
Polydactyly or polydactylism (from the Greek poly = "many" + daktylos
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Classification & external resources
ICD-10 Q 69.
ICD-9 755.0
OMIM 603598
DiseasesDB 24853
eMedicine derm/692
Polydactyly or polydactylism (from the Greek poly = "many" + daktylos
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D. melanogaster
Binomial name
Drosophila melanogaster
Meigen, 1830[1]
Drosophila melanogaster (from the Greek for black-bellied dew-lover
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Binomial name
Drosophila melanogaster
Meigen, 1830[1]
Drosophila melanogaster (from the Greek for black-bellied dew-lover
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Polycephaly is the condition of having more than one head. By far the most common use is in relation to the anatomical head, though the word has also been used for other meanings of "head".
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Hypertrichosis
Classification & external resources
ICD-10 L 68.
ICD-9 704.1
Hypertrichosis or werewolf syndrome is a medical term referring to a condition of excessive body hair.
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Classification & external resources
ICD-10 L 68.
ICD-9 704.1
Hypertrichosis or werewolf syndrome is a medical term referring to a condition of excessive body hair.
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Sexadactyly or hexadactyly is a genetic condition in which a person has six fingers on one or both hands, or six toes on one or both feet. This is a genetically inheritable condition; it is actually autosomal-dominant; and some populations feature a larger proportion of
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Proteins are large organic compounds made of amino acids arranged in a linear chain and joined together by peptide bonds between the carboxyl and amino groups of adjacent amino acid residues.
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The word dominant has several possible meanings:
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- In music theory, the dominant or dominant note (second most important) of a key is that which is a perfect fifth above the tonic; in just intonation the note whose pitch is 1.
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