A given gene is present on exactly two chromosomes in a somatic cell.
In a homologous pair, there are two chromosomes, one inherited from each parent, and they are similar in size, shape, and gene location. However, they can differ in the specific alleles present for each gene; for example, one chromosome may carry a gene for brown eyes while the other carries a gene for blue eyes. This genetic variation contributes to the diversity of traits in offspring.
my Doctor told me that there is DNA with one strand and there is with three and if i prove that he will award me so please help me
At the end of telophase, there are two sets of replicated chromosomes present in each cell. This is because during telophase, the duplicated chromosomes have separated and two identical sets of chromosomes are formed in preparation for cytokinesis.
One of the different alleles would be at the same gene locus on each of the paired chromosomes.
Humans typically have about 23,000 genes, organized into 23 pairs of chromosomes. Each pair consists of one chromosome inherited from each parent, resulting in a total of 46 chromosomes. Thus, in terms of gene pairs, humans have approximately 23,000 pairs of genes, with each gene generally existing in two copies (one from each parent).
Typically, there are two alleles present in a gene, one inherited from each parent.
The kind of alleles for a gene that are carried on homologous chromosomes are many. These are for similar genes which may be slightly different like the eyes, hairline, dentures and so much more.
my Doctor told me that there is DNA with one strand and there is with three and if i prove that he will award me so please help me
It depends on which chromosomes were present as to what the abnormality would be, if any. If they were missing one or had one extra there would be developmental abnormalities.
At the end of telophase, there are two sets of replicated chromosomes present in each cell. This is because during telophase, the duplicated chromosomes have separated and two identical sets of chromosomes are formed in preparation for cytokinesis.
A somatic cell typically contains 46 individual chromosomes. These chromosomes exist in pairs, with one set inherited from each parent.
There is no one gene for schizophrenia. However, there are many different genes that may contribute to schizophrenia. A gene on chromosome 1 in the 22 family is implicated in schizophrenia, as well as genes on chromosomes 11 and 6.
Homologous chromosomes are present in diploid cells, which contain two sets of chromosomes (one inherited from each parent). In contrast, haploid cells contain only one set of chromosomes.
Chromosomes. Strictly speaking they are not halves but just grouped into pairs. A pair represents a gene.
One of the different alleles would be at the same gene locus on each of the paired chromosomes.
Humans typically have about 23,000 genes, organized into 23 pairs of chromosomes. Each pair consists of one chromosome inherited from each parent, resulting in a total of 46 chromosomes. Thus, in terms of gene pairs, humans have approximately 23,000 pairs of genes, with each gene generally existing in two copies (one from each parent).
A sex linked trait.