Homozygous: Difference between revisions
Jump to navigation
Jump to search
No edit summary |
No edit summary |
||
| Line 1: | Line 1: | ||
Homozygous refers to a situation in which an individual inherits the same [[Alleles|alleles]] of a [[gene|gene]] from both parents. The allele could be [[Dominant allele|dominant]] or [[Recessive|recessive]]. | |||
For example: [[Cystic fibrosis|Cystic Fibrosis]] is a condition which is characterised by thick mucus causing an obstruction in the lungs of the sufferer. Sufferers inherit the recessive allele (a mutation in the CFTR gene) for the disease from both parents. See also [[Albinisim|Albinism]]. | For example: [[Cystic fibrosis|Cystic Fibrosis]] is a condition which is characterised by thick [[mucus|mucus]] causing an obstruction in the [[lungs|lungs]] of the sufferer. Sufferers inherit the [[Recessive_alleles|recessive allele]] (a mutation in the CFTR gene) for the disease from both parents. See also [[Albinisim|Albinism]]. | ||
Revision as of 00:34, 24 October 2014
Homozygous refers to a situation in which an individual inherits the same alleles of a gene from both parents. The allele could be dominant or recessive.
For example: Cystic Fibrosis is a condition which is characterised by thick mucus causing an obstruction in the lungs of the sufferer. Sufferers inherit the recessive allele (a mutation in the CFTR gene) for the disease from both parents. See also Albinism.