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They include: trans-location, deletion, duplication and inversion. A chromosome mutation is an unpredictable change that occurs in a chromosome.

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What are the various kinds of mutations?

Mutations differ and change according to many factors: 1- Site of occurrence: -Genetic mutations -Chromosomal mutations 2- The inheritance: -Somatic mutations -Gamete mutations 3- The origin: -Spontaneous (natural) mutations -Induced mutations 4- The harmful OR useful effects: -Undesirable mutations -Desirable mutations


What are the Different types of Mutations?

a bunch of stuff acxtually 4 major mutations to look at these go to Google and type in your question. if this does not work for you then sucks for you


What are the name of 23 chromosomes in human body?

No, there are 46 chromosomes in one cell. A gamete, or sex cell, has 23 chromosomes because during fertilization, the female and male gametes (egg and sperm, respectively) come together to form a new cell with 46 chromosomes


What causes angleman syndrome?

Angelman syndrome is caused by a deletion or mutation of a gene called UBE3A on chromosome 15. This gene is important for normal brain development and function, and its loss results in the characteristic symptoms of Angelman syndrome, including developmental delays, intellectual disability, and movement problems. About 70% of cases are caused by a deletion on the maternal chromosome 15, while other cases can be caused by mutations in the UBE3A gene.


Did Mendel find all the 7 traits on 7 different chromosome?

Gregor Mendel studied seven different traits in pea plants, but these traits were not necessarily found on seven distinct chromosomes. Instead, each trait is controlled by genes located on different chromosomes, and the principles of Mendelian genetics apply to the inheritance of these traits independently of their chromosomal location.

Related Questions

Is Parkinson disease on chromosome 6?

No, Parkinson's disease is not caused by a mutation on chromosome 6. The exact cause of Parkinson's disease is not fully understood, but it is believed to involve a combination of genetic and environmental factors. Some rare forms of Parkinson's disease are linked to specific gene mutations, but these are not located on chromosome 6.


What causes the MPS I disorders?

Mutations in the alpha-L-iduronidase (IDUA) gene located on chromosome 4 cause the MPS I disorders (Hurler, Hurler-Scheie, and Scheie syndromes


What is the difference between gene and chromosomal mutation?

A gene mutation is a permanent change in the DNA sequence that makes up a gene. Mutations range in size from a single DNA building block (DNA base) to a large segment of a chromosome. A chromosomal mutation is a mutation involving a long segment of DNA, it is a any change in the structure or arrangement of the chromosomes. These mutations can involve deletions, insertions, or inversions of sections of DNA. In some cases, deleted sections may attach to other chromosomes, disrupting both the chromosomes that loses the DNA and the one that gains it.It is also referred to as a chromosomal rearrangement The differences between Gene mutation and Chromosome mutation are ; 1- Chromosome mutations involve changes in the structure of a chromosome OR the loss or gain of a chromosome while Gene mutations involve a change in the nucleotide -base sequence of a gene on a DNA molecule. 2- Chromosomal mutations are changes in the structure or the numbers of chromosomes (a gain or loss). Gene mutations involve changes in the nucleotide sequence of the DNA molecule. 3-A gene mutation is a permanent change in the DNA sequence that makes up a gene. Mutations range in size from a single DNA building block (DNA base) to a large segment of a chromosome while a chromosomal mutation is a mutation involving a long segment of DNA, it is a any change in the structure or arrangement of the chromosomes. These mutations can involve deletions, insertions, or inversions of sections of DNA. In some cases, deleted sections may attach to other chromosomes, disrupting both the chromosomes that loses the DNA and the one that gains it.It is also referred to as a chromosomal rearrangement 4-gene mutation is just a substitute in any old random nucleotide for any old random nucleotide chromosome mutation is missing of chromosome or +1 chromosome (down's syndrome).


What chromosome is Parkinson's disease on?

Chromosome 4


How many chromosomes are in a homologous pair?

in a homologous chromosome there are two chromosomes ( a chromosome and a sister chromosome)


What are the 4 types of DNA?

autosomal dna, X chromosome, Y chromosome,and mitochondrial


What allele and chromosome is huntington's disease found on?

The gene codes for a protein called huntingtin found on the short arm of chromosome 4.


What chromosome is affected by Marfan syndrome?

Since the traits for hemophilia are carried on the X chromosome and not the Y, it is more probable for females to have a chromosome with the mutation. Since the mutation is considered recessive and males only have one X chromosome, they are more likely to portray the phenotype for hemophilia than their female counterparts.


What actors and actresses appeared in Chromosome 4 - 2014?

The cast of Chromosome 4 - 2014 includes: Malachi Brown Thea McCartan as Katharine


What are names of mutations in chromosomes?

1. Duplication - Where a portion of a chromosome is duplicated, resulting in multiple copies of the region. 2. Deletions - When a deletion of a nucleotide (nitrogen bases of a DNA) causes a shift of the mRNA codons. This will cause Alternations of Amino Acids. 3. Insertions - Occurs when an extra nucleotide is added. 4. Inversions - When a portion of a chromosome breaks off and reinserts itself in the same spot but in the reversed position 5. Translocation - When a portion of 2 chromosomes break off and switch locations


There are 4 chromatids in a?

A chromatid is one half of a duplicated chromosome, so typically there are 2 chromatids in a chromosome.


What are the various kinds of mutations?

Mutations differ and change according to many factors: 1- Site of occurrence: -Genetic mutations -Chromosomal mutations 2- The inheritance: -Somatic mutations -Gamete mutations 3- The origin: -Spontaneous (natural) mutations -Induced mutations 4- The harmful OR useful effects: -Undesirable mutations -Desirable mutations