autosomal gene

For the vast majority of autosomal genes, expression occurs from both alleles simultaneously.

The actual frequency calculations depend on the ploidy of the species for autosomal genes.

This single autosomal gene has 10 exons.

AGL is an autosomal gene found on chromosome lp21.

All primates share an S opsin encoded by an autosomal gene on chromosome 7.

X-linked genes just like autosomal genes have both dominant and recessive types.

(2006) ran simulations dividing autosomal gene frequencies in selected populations into a given number of clusters.

A recessive autosomal gene for Onion hair which causes roughness and swelling on the hairs.

A recessive autosomal gene spf for sparse fur.

Most of the organic acidemias result from defective autosomal genes for various enzymes important to amino acid metabolism.

Each autosomal gene is therefore represented by two copies, or alleles, with one copy inherited from each parent at fertilisation.

The leucistic colouration is caused by a mutation in an autosomal gene and is recessively inherited.

It is believed most people produce the odorous compounds after eating asparagus, but only about 22% of the population have the autosomal genes required to smell them.

He then conducted further study and found that the dominant autosomal genes, termed the immune response genes, determined the response to certain antigens.

The pseudoautosomal regions get their name because any genes located within them (so far at least 29 have been found) are inherited just like any autosomal genes.

There are some multifactorial autosomal genes which affect only chicks with delayed-feathering and have no effect on fast normal-feathering chicks, neither on adult plumage.

The steps of formation of the testes are dependent on a series of Y-linked, X-linked and autosomal genes actions and interactions.

Kalmus discovered a mutant allele of an autosomal gene that expressed ebony body color and other selective advantages in a pattern that was autosomal dominant.

Comparative transcription profiling of matched pairs of fibroblast clones should eliminate any noise contributed by polymorphisms or mutations of autosomal genes.

However, there have been a few rare cases in which a patient with PDH actually has a mutation in the autosomal gene for the E2 subunit instead.