I learned this last year I should know this
The gene that determines male biological traits is called the SRY gene, which is located on the Y chromosome. This gene plays a crucial role in the development of male sex characteristics during embryonic development.
It is called gene replication or gene duplication.
The defective gene in Hurler syndrome is located on chromosome 4. This gene carries instructions for making an enzyme called alpha-L-iduronidase, which is essential for breaking down certain complex molecules in the body. When this gene is mutated, the enzyme is deficient, leading to the accumulation of harmful substances in the cells.
A promoter <--- Gradpoint/NovaNet A promoter is located at the beginning of a gene. A promoter functions by facilitating transcription of that gene
The DNA sequence that signals a gene's start is called a promoter region. This region is crucial for the initiation of transcription, where an enzyme called RNA polymerase binds to the promoter and begins the process of copying the gene into messenger RNA. Promoter regions are typically located near the gene's transcription start site.
A gene pair is called an allele. An allele is an alternative form of a gene that is located on a specific chromosome at a specific place.
The gene associated with Marfan syndrome is located on chromosome 15. It is called the FBN1 gene, which provides instructions for making a protein called fibrillin-1. Mutations in this gene can lead to the characteristic features of Marfan syndrome.
The answer to your question is Hybrid.
The gene located on the X chromosome that codes for a protein involved in producing eye pigment is called the OPN1LW gene. Mutations in this gene can lead to color vision deficiencies, such as red-green color blindness.
The gene that determines male biological traits is called the SRY gene, which is located on the Y chromosome. This gene plays a crucial role in the development of male sex characteristics during embryonic development.
Allele
alleles are located in the chromosomes.
It is a mutated gene called PKD1 located on chromosome 16.
Gene contain hereditary information that is transferred from parents to offspring. They are located in the nucleus of a cell.
Dystrophin gene / Xp21 gene / DMD gene: Found at locus Xp21 of the X chromosome, this is why it's called the (Xp21 gene) It's the gene responsible for Duchenne muscular dystrophy(DMD) when mutated, this is why it's called (DMD gene)
The expression of a gene is called the phenotype.
It is called gene replication or gene duplication.