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One of the non-X or non-Y chromosomes

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14y ago

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Is angelman syndrome autosomal?

"Autosomal" means the syndrome or disorder of interest is pertaining to a chromosome that is not a sex chromosome, either X or Y. Angelman and Prader-Willi Syndrome are both caused by a deletion (or disruption of a gene) on chromosome 15, which is an autosomal chromosome and not a sex chromosome. Therefore, yes, Angelman syndrome is considered an autosomal syndrome.


Is chromosome 19 autosomal or sex chromosome?

Chromosome#19 is autosomal cell when refering to the human system. The #23 chromsomes is the sex cell in the human body system.


What are the 4 types of DNA?

autosomal dna, X chromosome, Y chromosome,and mitochondrial


What are the specific names of autosomal chromosomes like sex chromosomes?

Y chromosome is autosomal dominant chromosome. When it is present, the sex of the child is male. When both the chromosomes are X, then the sex of the child is female. X chomosome is called as autosomal recessive chromosome.


What is the difference between sex chromosome an autosomal chromosome?

the autosome do not control the sex organs . but the sex chromosome control the sex organs


What are autosomal characteristics?

An Autosomal Characteristic... Examples would be your eye color. An autosome is a chromosome that is not a sex chromosome. So and autosomal characteristic is what you think of when you think about the genes that you inherit from your parents.


What are chromosome pair 1 through 22 called?

autosomal chromosomes ;)


Is progeria autosomal or sex-linked?

Progeria is neither autosomal nor sex-linked. It is caused by a spontaneous mutation in the LMNA gene, which is located on chromosome 1.


What chromosome is affected by meckel syndrome?

Meckel Syndrome (type 1)is an autosomal recessive trait carried on chromosome 17.


In humans what chromosome pairs 1 through 22 called?

autosomal chromosomes


What are the three types of nondisjunction?

The three types of nondisjunction are autosomal nondisjunction, sex chromosome nondisjunction, and structural chromosome nondisjunction. Autosomal nondisjunction involves the failure of homologous chromosomes to separate during cell division. Sex chromosome nondisjunction involves the failure of sex chromosomes to separate. Structural chromosome nondisjunction involves the incorrect separation of chromosome parts during cell division.


Autosomal abnormality resulting in three copies of chromosome 21 is known as?

Trisomey-21