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30 Cards in this Set

  • Front
  • Back

Homozygous?

Homo - two of the same


Zygous - parents 2 of the same genes from parents

Heterozygous

Two different genes heteron- 2 different

Genotype

In dna

Phenotype

The physical things the dna codes for

What is genetics

Study of genes, heredity and the variation of inherited characteristics and it’s properties

DNA

Deoxyribonucleic Acid is the hereditary material in humans and almost all other organisms. Nearly every cell in a persons body has the same DNA. Stored as a code : guanine, cytosine, thymine, adenine

RNA

Ribonucleic acid, essential in various biological roles: coding decoding and expression of genes.

MRNA

It’s function is to act as an intermediary between genetic information in DNA and amino acid.

Central dogma of molecular

Two step process describing process transcription and translation by which information in genes flows into proteins DNA, RNA, protein

What is transcription

Synthesis of an rna copy of a segment of dna RNA is synthesised by the enzyme of RNA polymerase

Mendelian inheritance

The way certain characteristics are transmitted from one generation to another in an organism eg. Alleles sepereate during gamete formation and randomly unite at fertilisation


And law of independent assortment states alleles get sorted into gametes independently eg the allele a gamete receives for one gene eg hitchhikers thumb and attached earlobes are not traits that would influence each other where as being ginger and having freckles are on the same allele so would inherent them both

Chromosome

Dna molecule with part or all of genetic material of an organism. We have 23 pairs of chromosomes. 23rd chromosome determines sex. On chromosomes are alleles which determine phenotypes and genotypes

Gene

Found in almost every cells nucleus and are made of dna segments of dna called genes are the ingredients each gene adds a specific protein to the recipe. Proteins build regulate and maintain your body

Dominant and recessive genes

Individuals receive 2 versions of a gene known as alleles if the alleles of a gene are different one allele will be expressed it is the dominant gene recessive genes are the ones that are masked and will sometimes make up a persons genotype but not be present in their phenotype

Autosomes

All chromosomes apart from sex chromosomes there are 22 autosome pairs in humans they are highly similar in shape and length

Trisomy 21

Downsyndrome, caused by additional copy of 21st chromosome caused by non disjunction of gametogenisis - when a pair of chromosomes did not seperate

Transcription

Process of transcribing or making a copy of genetic information stored in dna strand into rna

Translation

Process of translating sequence of mRNA molecule to a sequence of amino acids during protein synthesis

Translocation

Results in unusual rearrangement of chromosomes including balanced and unbalanced translocation two fragments of chromosomes are switched

Mitosis

Essential process involving equal division of genetic material from parent cell into two identical daughter cells from sperm and egg

Meiosis

Type of cell division resulting in 4 daughter cells each with half the number of chromosomes of the parent cell

Miosis

Excessive construction of the pupil of the eye

Punnet square

Square diagram used to predict genotypes of a particular cross or breeding experiment

Cri du chat

Known as 5pminus syndrome genetic condition where deletion of genetic material occurs

Apoptosis

A form of cell death in Which a programmes sequence of events leads to elimination of cells without releasing harmful substances into surrounding area - helps maintain healthy old and unnecessary cells

Haploid

Term used when a cell has half the number of chromosomes after meiosis

Diploid

Cell or organism with paired chromosomes eg human sex cells

Karyotype

Picture of a persons chromosomes

Mutation

Alteration in the nucleotide sequence of the genome of an organism

Telomere

Region of repetitive nucleotide sequences at abc end of a chromosome which protects the end of the chromosome from deterioration or from fusion with neighbouring chromosomes