Copy of `Superglossary - Genetics`
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Superglossary - Genetics
Category: Sciences > Genetics
Date & country: 11/12/2013, USA Words: 460
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AchondroplasiaThe most common and well known form of short limbed dwarfism characterized by a normal trunk size wi
Additive Genetic EffectsWhen the combined effects of alleles at different loci are equal to the sum of their individual effe
Adenine (A)A nitrogenous base, one member of the base pair a- t (adenine- thymine).
Advanced Maternal AgeWomen over age 34 (age 35 at delivery) at increased risk for nondisjunction trisomy in fetus.
Affected Relative PairIndividuals related by blood, each of whom is affected with the same trait. Examples are affected si
Aggregation TechniqueA technique used in model organism studies in which embryos at the 8-cell stage of development are p
AlcoholismA chronic and progressive condition characterized by the inability to control the consumption of alc
AlleleAlternative form of a genetic locus
AllogeneicVariation in alleles among members of the same species.
Alpha-Fetoprotein (AFP)A protein excreted by the fetus into the amniotic fluid and from there into the mother's bloodstream
Alternative SplicingDifferent ways of combining a gene's exons to make variants of the complete protein
Alu Repetitive SequenceThe most common dispersed repeated dna sequence in the human genome accounting for 5% of human dna.
Amino AcidAny of a class of 20 molecules that are combined to form proteins in living things. The sequence of
Amino Acid SequenceThe linear order of the amino acids in a protein or peptide.
AmniocentesisPrenatal diagnosis method using cells in the amniotic fluid to determine the number and kind of chro
AmniocyteCells obtained by amniocentesis.
AmplificationAn increase in the number of copies of a specific dna fragment
AmplificationAny process by which specific dna sequences are replicated disproportionately greater than their rep
AneuploidyState of having variant chromosome number (too many or too few). (i.e. Down syndrome, turner syndrom
Angelman SyndromeA condition characterized by severe mental deficiency, developmental delay and growth deficiency, pu
AnticipationEach generation of offspring has increased severity of a genetic disorder
AntisenseNucleic acid that has a sequence exactly opposite to an mrna molecule made by the body
Apert SyndromeA condition caused by the premature closure of the sutures of the skull bones, resulting in an alter
ApoptosisProgrammed cell death, the body's normal method of disposing of damaged, unwanted, or unneeded cells
Arrayed LibraryIndividual primary recombinant clones (hosted in phage, cosmid, yac, or other vector) that are place
Artificial InseminationThe placement of sperm into a female reproductive tract or the mixing of male and female gametes by
AssemblyPutting sequenced fragments of dna into their correct chromosomal positions.
AutoradiographyA technique that uses x-ray film to visualize radioactively labeled molecules or fragments of molecu
Autosomal DominantA gene on one of the non-sex chromosomes that is always expressed, even if only one copy is present.
AutosomeA chromosome not involved in sex determination. The diploid human genome consists of 46 chromosomes,
Avuncular RelationshipThe genetic relationship between nieces and nephews and their aunts and uncles.
BackcrossA cross between an animal that is heterozygous for alleles obtained from two parental strains and a
BacteriophageA virus whose host is a bacterium
Barr BodyThe condensed single x-chromosome seen in the nuclei of somatic cells of female mammals. Base pair a
BaseOne of the molecules that form dna and rna molecules.
Base Pair (BP)Two nitrogenous bases (adenine and thymine or guanine and cytosine) held together by weak bonds. Two
Base SequenceA partnership of organic bases found in dna and rna
Base Sequence AnalysisA method, sometimes automated, for determining the base sequence.
Baysian AnalysisA mathematical method to further refine recurrence risk taking into account other known factors.
Becker Muscular DystrophyX-linked condition characterized by progressive muscle weakness and wasting
Behavioral GeneticsThe study of genes that may influence behavior.
BioinformaticsThe science of managing and analyzing biological data using advanced computing techniques. Especiall
BioremediationThe use of biological organisms such as plants or microbes to aid in removing hazardous substances f
BiotechnologyA set of biological techniques developed through basic research and now applied to research and prod
Birth DefectAny harmful trait, physical or biochemical, present at birth, whether a result of a genetic mutation
BlastA computer program that identifies homologous (similar) genes in different organisms, such as human,
CancerDiseases in which abnormal cells divide and grow unchecked. Cancer can spread from its original site
Capillary ArrayGel-filled silica capillaries used to separate fragments for dna sequencing. The small diameter of t
CarcinogenSomething which causes cancer to occur by causing changes in a cell's dna.
CarrierAn individual who possesses an unexpressed, recessive trait.
CdnaComplementary dna produced from a rna template by the action of rna- dependent dna polymerase.
Cdna LibraryA collection of dna sequences that code for genes. The sequences are generated in the laboratory fro
CellThe basic unit of any living organism that carries on the biochemical processes of life.
Centimorgan (CM)A unit of measure of recombination frequency. One centimorgan is equal to a 1% chance that a marker
CentromereA region of a chromosome to which spindle traction fibers attach during mitosis and meiosis
Charcot-Marie Tooth DiseaseA condition characterized by degeneration of the motor and sensory nerves that control movement and
Chimera (Pl Chimaera)An organism that contains cells or tissues with a different genotype. These can be mutated cells of
ChimeraplastyAn experimental targeted repair process in which a desirable sequence of dna is combined with rna to
Chloroplast ChromosomeCircular dna found in the photosynthesizing organelle (chloroplast) of plants instead of the cell nu
Chorionic Villus SamplingAn invasive prenatal diagnostic procedure involving removal of villi from the human chorion to obtai
ChromomereOne of the serially aligned beads or granules of a eukaryotic chromosome, resulting from local coili
Chromosomal DeletionThe loss of part of a chromosome's dna.
Chromosomal InversionChromosome segments that have been turned 180 degrees. The gene sequence for the segment is reversed
ChromosomeThe self-replicating genetic structure of cells containing the cellular dna that bears in its nucleo
Chromosome BandingA technique for staining chromosomes so that bands appear in a unique pattern particular to the chro
Chromosome PaintingAttachment of certain fluorescent dyes to targeted parts of the chromosome. Used as a diagnositic fo
Chromosome Region PA designation for the short arm of a chromosome.
Chromosome Region QA designation for the long arm of a chromosome.
ChromosomesThe self- replicating genetic structures of cells containing the cellular dna that bears in its nucl
Cleft PalateCongenital condition with cleft lip alone, or with cleft palate
CloneAn exact copy made of biological material such as a dna segment (e.g., a gene or other region), a wh
Cloned DNAAny dna fragment that passively replicates in the host organism after it has been joined to a clonin
ClonesA group of cells derived from a single ancestor.
CloningUsing specialized DNA technology to produce multiple, exact copies of a single gene or other segment
Cloning VectorDna molecule originating from a virus, a plasmid, or the cell of a higher organism into which anothe
CodominanceSituation in which two different alleles for a genetic trait are both expressed.
CodonA sequence of three nucleotides in mrna that specifies an amino acid.
Coisogenic Or CongenicNearly identical strains of an organism
Comparative GenomicsThe study of human genetics by comparisons with model organisms such as mice, the fruit fly, and the
Complementary DNA (CDNA)Dna that is synthesized from a messenger rna template
Complementary SequenceNucleic acid base sequence that can form a double-stranded structure with another dna fragment by fo
Complex TraitTrait that has a genetic component that does not follow strict mendelian inheritance. May involve th
ConfidentialityIn genetics, the expectation that genetic material and the information gained from testing that mate
CongenitalAny trait present at birth, whether the result of a genetic or nongenetic factor.
ConsanguinityGenetic relationship. Consanguineous individuals have at least one common ancestor in the preceding
Conservative ChangeAn amino acid change that does not affect significantly the function of the protein.
Conserved SequenceA base sequence in a dna molecule (or an amino acid sequence in a protein) that has remained essenti
Constitutive AblationGene expression that results in cell death.
ContigGroup of cloned (copied) pieces of dna representing overlapping regions of a particular chromosome.
Contig MapA map depicting the relative order of a linked library of overlapping clones representing a complete
ContigsGroups of clones representing overlapping regions of a genome.
Contiguous GenesGenes physically close on a chromosome that when acting together express a phenotype.
Cornelia De Lange SyndromeCondition involving growth deficiency, significant developmental delay, anomalies of the extremities
CosmidArtificially constructed cloning vector containing the cos gene of phage lambda. Cosmids can be pack
Cpg IslandsAreas of multiple cg repeats in dna.
Cri-Du-Chat SyndromeA chromosomal condition (monosomy 5p). Name comes from the distinctive mewing cry of affected infant
Crossing OverThe breaking during meiosis of one maternal and one paternal chromosome, the exchange of correspondi
CrossoversThe exchange of genetic material between two paired chromosome during meiosis.
Cystic FibrosisAn autosomal recessive genetic condition of the exocrine glands, which causes the body to produce ex
CytogeneticsThe study of the physical appearance of chromosomes.