| 영문 | recessive | 한글 | 열성 |
|---|---|---|---|
| 설명 | 대립형질 중 잡종 제1대에서 숨어서 나타나지 않는 형질. 우성에 대응되는 말이다. 나타나는 쪽에 대해 열성이라 하고, 그 형질을 열성형질이라고 한다. 제2대(F2)에서는 열성형질은 분리되어 1/3의 비율로 나타난다. 유전적 대립형질에는 우성과 열성이 있고, 이것들은 우성유전자와 열성유전자에 의해 지배된다. 예를 들면, 어떤 우성형질을 지배하는 유전자를 A라 하고, 그것에 대응하는 열성유전자를 a라고 하면, 우성유전자를 가진 어버이(AA)와 열성유전자를 가진 어버이(aa)의 교배에 의하여 생긴 잡종 제1대(F1)는 Aa가 되어 우성형질을 나타낸다. Aa 유전자를 가진 F1끼리를 교배하면 잡종 제2대(F2)에서는 AA:Aa:aa가 1:2:1의 비율로 분리되어 열성형질은 F2대에 1/3의 비율로 생긴다. 우성-열성이란 형질의 가치 우열을 말하는 것이 아니다. 열성이 뒤떨어졌다는 인상을 준다고 하여 열성을 잠성으로, 우성을 현성으로 하자고 주장하는 학자도 있다. |
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| MEN | Multiple Endocrine Neoplasia ; AD Trait 1. MEN Type I(= Wermer Syndro... |
|---|---|
| PBT | Paul-Bunnell test; phenacetin breath test; piebald trait; profile-based therapy |
| PTD | percutaneous transluminal dilatation; permanent total disability; personality trait disorder; preter... |
| SCT | secretin; sex chromatin test; sexual compatibility test; sickle-cell trait; sperm cytotoxicity; spin... |
| STAI | State Trait Anxiety Inventory |
| QTL | Aquantitative trait locus |
|---|---|
| AR | Autosomal Recessive |
| AR-JP | Autosomal recessive juvenile parkinsonism |
| ARPKD | Autosomal recessive polycystic kidney disease |
| ARRP | Autosomal recessive retinitis pigmentosa |
| recessive trait | See: dominance of traits. (05 Mar 2000) |
|---|
| autosomal recessive | <genetics> Mutation carried on an autosome that is deleterious only in homozygotes. (02 Jan 1998) |
|---|---|
| genes, recessive | Genes that are reflected in the phenotype only in the homozygous state. (12 Dec 1998) |
| recessive | <genetics> An allele or mutation that is only expressed phenotypically when it is present in the homozygous form. In the heterozygote it is obscured by dominant alleles. (18 Nov 1997) |
| recessive, autosomal | A gene on a nonsex chromosome (an autosome) that expresses itself only when there is no different gene present at that locus (spot on the chromosome). For example, cystic fibrosis (cf) is an autosomal recessive disorder. A cf child has the cf gene on both chromosome 7's (and so is said to be homozygous for cf). (12 Dec 1998) |
| recessive character | An inherited character determined by an allele in homozygous state only. See: dominance of traits. (05 Mar 2000) |
| recessive gene | A gene that is expressed onlywhen it is present in two copies or if theother copy is missing. (09 Oct 1997) |
| recessive inheritance | dominance of traits |
| recessive oncogene | <molecular biology> A single copy of this gene issufficient to suppress cell proliferation, the loss of both copies of the gene contributes to cancer formation. (09 Oct 1997) |
| recessive, x-linked | A gene on the X chromosome that expresses itself only when there is no different gene present at that locus (spot on the chromosome). For example, duchenne muscular dystrophy (dmd) is an x-linked recessive disorder. A dmd boy has the dmd gene on his sole x chromosome (and so is said to be hemizgous for dmd). Although it is much rarer, a girl can have dmd (by several different means as, for example, if she has the dmd gene on both her x chromosomes and so is homozygous for dmd). (12 Dec 1998) |
| kidney, polycystic, autosomal recessive | Rare genetic disorder with autosomal recessive inheritance characterised by multiple cysts in both kidneys and associated hepatic lesions. Serious manifestations are usually present at birth and there is high perinatal mortality. (12 Dec 1998) |
| Bombay trait | A rare recessive trait at a locus that ordinarily manufactures H substance, the precursor from which the A and B phenotypes are elaborated; the mutant causes failure to produce H substance and no matter what the genotype at the ABO locus, the phenotype is O. The Bombay phenomenon is epistatic to the ABO locus. Origin: Bombay, India, where first reported (05 Mar 2000) |
| galtonian trait | A quantitative genetic trait due to contributions from many more of less equally important loci that resembles a continuous trait. (05 Mar 2000) |
| marker trait | A trait that may be of little importance in itself but which by association, linkage, or other means facilitates the detection, anticipation, or understanding of a disease or (for genetic diseases) the localization of the causative gene on the karyotype. (05 Mar 2000) |
| categorical trait | <genetics> A feature that can conveniently and effectively be analyzed by sorting into classes either because there is no satisfactory way of measuring it (as with blood groups) or because it falls into natural classes so that the variation among classes far exceeds that within classes (e.g., the phenotypic effects of many enzyme polymorphisms); existence of categories suggests but does not prove the operation of a major, simple, underlying cause. Synonym: qualitative trait. (05 Mar 2000) |
| penetrant trait | A trait that in the appropriate genotypes is phenotypically manifest; strictly, it is the trait that is penetrant, not the gene. See: penetrance. (05 Mar 2000) |
| recessive trait |
In genetics, the term "recessive gene" refers to an allele that causes a phenotype (visible or detectable characteristic) that is only seen in a homozygous genotype (an organism that has two copies of the same allele). Every person has two copies of every gene, one from mother and one from father. If a genetic trait is recessive, a person only needs to inherit two copies of the gene for the trait to be expressed. ...
출처: en.wikipedia.org/wiki/Recessive_trait
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| recessive trait |
A genetic disorder that appears only in patients who have two copies of a mutant allele, one from each parent. An individual who has one copy of the mutant allele is a carrier.
출처: www.cdc.gov/hemochromatosis/training/glossary.htm
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| recessive trait |
A trait that is expressed only when two copies of the gene responsible for the trait are present.
출처: www.nutrabio.com/Definitions/definitions_r.htm
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| recessive trait |
The quality of a gene or allele regarding its ability to express a phenotype. A recessive allele can only express its phenotype if both copies in a diploid organisms are identical. Often, a recessive allele is matched with a dominant allele, which overrides the activity of the recessive one. In this case, the effect of the gene cannot be seen, but it can still be inherited. ...
출처: www.whatislife.com/glossary.htm
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| recessive trait |
A characteristic determined by an allele that requires the presence of two identical alleles to be expressed.
출처: www.accessexcellence.org/RC/AB/WYW/wkbooks/PAP/glo...
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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