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genetic code
system of nucleotides triplets in DNA and RNA contain info for synthesizing proteins into 20 amino acids
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gene
fundemental units of heridetery consists of sequence of DNA bases that cary info. for synthesizing protein and ocupies chromosomal locus
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protein
complex molecules formed by chains of amino acids or from polypeptide function as molecules and transprt molecules antibodies enzymes and hormones
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amino acids
molecules formed by proteins
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ribosome
structure composed of RNA found on ER site of protein synthesis
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chromosomes
structurs composed of condensed DNA and supporting proteins
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polypeptide
molecule made of amino acids
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codon
3 nucleotides in mRNA that makes amino acids or the intintion or end of polpypeptide sequence
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mRNA
strand of RNA synthesized in nucleus (transcription)carries info for sequence to amino scids to make specific protein into cytoplasm where ribosome is read and recorded( translation)
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tRNA
RNA molecules that bind to specific amino acids and transprt them to ribosomesto be used in protein synthesis
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nucleus
part f cel where genetic material i8s seperated from everything else by cytoplasm
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genotype
genetic makeup of someone
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transcription
is the process of creating a complementary RNA copy of a sequence of DNA.
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tranlation
messenger RNA (mRNA) produced by transcription is decoded by the ribosome to produce a specific amino acid chain, or polypeptide, that will later fold into an active protein
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polygenic
pheotype traits that result from combined action of more than one gene (complec traits)
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monogenic
diesise from only one gene
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genome
sum total of genes carried by individual
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crossing over
exvhange of gentic material between homologous chromosomes during first prophase of meiosis (gentic recombination)
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mitosis
somatic cell division in which a single cell divides to produce to identical daughtere cells
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phenotype
observable or measurable feature of an organsim. can be anatomical,biochemical or behavioral
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homozogoes
having same allele of gene on both members of homologous chromosomes
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heterozygoes
having two different type of alleles on gene on pair of autosomes
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dominant
the allele expressed when present on only one pair of homologous chromsomes
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recessive
allele not expressed and autosomes
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codominant
only in diploid org. which are two different alleles on autosomes and both are expressed
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DNA
(deoxyribonucleic acid)
double stranded molecule that carries genetic information. Each strand has nucleotides and held together by hydrogen bonds formed by complemanety bases
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meiosis
cell division that occurs in testes or ovaries that leads to gametes
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linkage
genes formed on same chromsomes and are linked. the closer on chromsome the greater linkage and less likely to be seperated during crossing over
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allele
alternative version of a gene. different alleles distinguished by effects on genotype expression on same gene
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trisomy
genetic abnormality in which there are three copies, instead of the normal two, of a particular chromosome
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bases
- variable components of nucleotides that form DNA,RNA.
- DNA=A G T C
- RNA=U replaces thymine
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