Question: Genes are associated with?
Answer: Genotype
55 orthologous genes are associated with human height
There are three different genes that have been associated with CMT4 as of early 2001. They are called MTMR2, EGR2, and NDRG1. More research is required to understand how mutations in these genes cause CMT.
Stability genes are one of the three main genes, that when mutated are associated with cell progression towards tumorigenicity. It's normal function is to control the rate of mutation, but if mutated it off-balances, effecting oncogene and tumor suppressor function. In other words, accelerating the mutation process.
Regions of the chromosome with few functional genes are called gene deserts or gene-poor regions. These regions typically have a lower density of genes compared to other parts of the chromosome, and are often associated with non-coding DNA or regulatory elements.
No - the father's genes are not always the dominant genes.
55 orthologous genes are associated with human height
Some associated genes of human mitochondrial genome are the Eukaryotic cells and the cell nucleus. Mitochondrial DNA is inherited only from the mother's ovum.
There are three different genes that have been associated with CMT4 as of early 2001. They are called MTMR2, EGR2, and NDRG1. More research is required to understand how mutations in these genes cause CMT.
The reason is that most of the genetic conditions are related to changes in particular genes on chromosome 11.
mutation
Sequencing of the entire genetic make-up of the zebrafish has revealed that 70 per cent of protein-coding human genes are related to genes found in the zebrafish and that 84 per cent of genes known to be associated with human disease have a zebrafish counterpart.
Stability genes are one of the three main genes, that when mutated are associated with cell progression towards tumorigenicity. It's normal function is to control the rate of mutation, but if mutated it off-balances, effecting oncogene and tumor suppressor function. In other words, accelerating the mutation process.
Regions of the chromosome with few functional genes are called gene deserts or gene-poor regions. These regions typically have a lower density of genes compared to other parts of the chromosome, and are often associated with non-coding DNA or regulatory elements.
Activation of meiosis-specific genes is associated with depolyploidization of human tumor cells following radiation-induced mitotic catastrophe.
Not in the scientific sence as the genes are not located on the sex chromosomes. It can rarley be caused by genes from the father mutating as the equivolent genes from the mother are almost silent due to gene imprinting. So in a more general sence it may be associated with the gender of the parent from whom deleted gene copys were recieved.
Chromosome is A thread like linear strand of DNA and associated proteins in the nucleus!!!!!!
Polygenic genes are usually dominant genes.