You should search up the info on these chromosomes:
chromosome 1
chromosome 14
chromosome 21
there is also other genes:
presenilin 1 (PS1 or PSEN1)
presenilin 2 (PS2 or PSEN2)
amyloid precursor protein (APP)
Mutation is caused when chunks of chromosomes cut taken or fall off. So the chromosome with the DNA causes a mutation which sometimes is helpful but mosty hard to live with.
The specific location of the mutation that causes X-ALD is on the ABCD1 gene on the X-chromosome. Please note that there isn't a specific mutation in the ABCD1 gene that causes X-ALD or can be related in any way to the different clinical presentations of the disease.
mutations
Trisomy 13, also known as Patau syndrome, is a chromosomal mutation where there is an extra copy of chromosome 13 in each cell. This condition can lead to various physical and intellectual disabilities.
Aneuploidy mutation causes a change in the number of chromosomes. Aneuploidy occurs during cell division when the chromosomes do not separate properly resulting in a change in the number of chromosomes.
An Inversion mutation is a mutation that causes a reversal in the order of a segment of a chromosome within the chromosome, or a gene.
mutation
Mutation is caused when chunks of chromosomes cut taken or fall off. So the chromosome with the DNA causes a mutation which sometimes is helpful but mosty hard to live with.
An extra copy of Chromosome 18
non-disjunction
The specific location of the mutation that causes X-ALD is on the ABCD1 gene on the X-chromosome. Please note that there isn't a specific mutation in the ABCD1 gene that causes X-ALD or can be related in any way to the different clinical presentations of the disease.
mutations
Four types of chromosomal mutations are Down syndrome (which is a mutation in which there are three copies of chromosome 21), Kinefelter Syndrome (which is a mutation in which a male has an extra X-chromosome), Turner Syndrome (which is a mutation in which a female is missing an X-chromosome), and Patau Syndrome (which is a mutation in which there are three copies of chromosome 13).
caused by a mutation in a gene called myelin protein zero (MPZ) located on chromosome 1.
Trisomy 13, also known as Patau syndrome, is a chromosomal mutation where there is an extra copy of chromosome 13 in each cell. This condition can lead to various physical and intellectual disabilities.
A mutation is the term for any permanent change in a gene or chromosome. Mutations can be caused by various factors, such as errors during DNA replication or exposure to certain environmental factors like radiation or chemicals.
Mutation