ଯୋଡିରେ ଶରୀର କୋଷ କିନ୍ତୁ ଶୁକ୍ରାଣୁ ଏକ କ୍ରୋମୋଜୋମ ପରି ଦେଖାଯାଏ |, ଏକ କ୍ରୋମୋଜୋମ୍ ଏକ ଯ sex ନ କ୍ରୋମୋଜୋମ୍ ନୁହେଁ |,

autosome తెలుగు అర్థానికి ఉదాహరణ:

ଏହା ଏକ ଅଟୋସୋମାଲ ରିସିସିଭ ଭାବରେ ଉତ୍ତରାଧିକାରୀ ସୂତ୍ରରେ ମିଳିଥାଏ | ଜୋବର୍ଟ ବା ବାର୍ଡେଟ-ବିଏଡ୍ଲ ସିଣ୍ଡ୍ରୋମମାନଙ୍କର ଏକ ଅଂଶ ଭାବରେ ମଧ୍ୟ ଏହା ଥାଏ ।

ଜଣେ ବ୍ୟକ୍ତିର ଯେ କୌଣସି ଦୁଇ କପି ଜିନର ଅଟୋସୋମାଲ ଡୋମିନାଣ୍ଟ ମ୍ୟୁଟେସନ‌କୁ ହଣ୍ଟିଙ୍ଗଟିନ କୁହାଯାଏ ।

ସାଧାରଣତଃ ଏହା ଅଟୋସୋମାଲ ରିସିସିଭ (autosomal recessive) ପାଟର୍ଣ୍ଣରେ ଇନହେରିଟ ହୁଏ, କିନ୍ତୁ ମ୍ୟୁଟେସନ ଅନୁଯାୟୀ ବେଳେବେଳେ ଅଟୋସୋମାଲ ଡୋମିନାଣ୍ଟ (autosomal dominant) ହୋଇଯାଏ ।

|ସି.ଏଫ୍. ଏକ ଅଟୋସୋମାଲ ରିସିସିଭ୍ ବିକାର ।

ଉତ୍ତରାଧିକାର (inherited from a person's parents) ସୁତ୍ରରେ ଅଟୋସୋମାଲ ରିସିସିଭ (autosomal recessive) ଭାବରେ ଏହି ଅନୁବଂଶିକ ରୋଗ ମିଳେ ।

ଏହା ଏକ୍ସ-ଲିଙ୍କଡ ରିସିସିଭ (X-linked recessive), ଅଟୋସୋମାଲ (autosomal recessive), ବା ଅଟୋସୋମାଲ ଡୋମିନାଣ୍ଟ autosomal dominant ଯୋଗୁ ହୋଇପାରେ ।

ଏମାନଙ୍କ ମଧରୁ କେତେକ ଅଟୋସୋମାଲ ଡୋମିନାଣ୍ଟ (autosomal dominant) ହୋଇଥିବା ବେଳେ କେତେକ ଅଟୋସୋମାଲ ରିସିସିଭ (autosomal recessive) ହୋଇଥାଏ ।

ଅଳ୍ପ ସଂଖ୍ୟକ କେତେକ କେଶ୍‌ରେ ପିଆରକେଏଜି୨ (PRKAG2) ଜିନର ମ୍ୟୁଟେସନ (mutation) ହୋଇ ଉତ୍ତରାଧିକାର ସୂତ୍ରରେ ପିତାମାତାଙ୍କଠାରୁ ଅଟୋସୋମାଲ ଡୋମିନାଣ୍ଟ (autosomal dominant) ଫେସନରେ ଇନହେରିଟ (inherited) ହୋଇଥାଏ ।

|ଟିସିଏସ ଏକ ଅଟୋସୋମାଲ ଡୋମିନାଣ୍ଟ (autosomal dominant) ରୋଗ ।

autosome's Usage Examples:

contains 44 autosomes and two sex chromosomes.

PAR1 region boundary ZBED1 in mice, some PAR1 genes have transferred to autosomes.

the ratio between the number of X chromosomes and the number of sets of autosomes in an organism.

Humans have two copies of chromosome 1, as they do with all of the autosomes, which are the non-sex chromosomes.

For the human species, whose genome includes 22 pairs of autosomes and 2 sex chromosomes, a complete genome sequence will involve 46 separate.

recessive are used to describe gene variants on non-sex chromosomes (autosomes) and their associated traits, while those on sex chromosomes (allosomes).

of X chromosomes to sets of autosomes (A) exceeds 1.

the defective (mutated) gene that causes the disorder is located on an autosome, and the disorder occurs when two copies of this defective gene are inherited.

Though a 48-chromosome complement involving the autosomes would be unsurvivable, 48,XYYY and other high-level sex chromosome aneuploidies such as XXXY.

An autosome is chromosome that is not a sex chromosome (an allosome).

chromosome can also contain satellites, although these are thought to be translocations from autosomes.

In an X0 sex-determination system, males and females receive an equal number of autosomes, but when it comes to sex.

defective gene responsible for the disorder is located on an autosome (chromosome 6 is an autosome), and two copies of the defective gene (one inherited from.