+ allele
|
n
|
1
|
[ genetics ]
|
eng-30-05437785-n
|
(genetics) either of a pair (or series) of alternative forms of a gene that can occupy the same locus on a particular chromosome and that control the same character
|
+ allelic
|
a
|
1
|
[ genetics ]
|
eng-30-02612400-a
|
of or relating to alleles
|
+ allelomorph
|
n
|
1
|
[ genetics ]
|
eng-30-05437785-n
|
(genetics) either of a pair (or series) of alternative forms of a gene that can occupy the same locus on a particular chromosome and that control the same character
|
+ allelomorphic
|
a
|
1
|
[ genetics ]
|
eng-30-02612400-a
|
of or relating to alleles
|
+ ancestry
|
n
|
2
|
[ genetics ]
|
eng-30-04922787-n
|
inherited properties shared with others of your bloodline
|
+ bivalent
|
a
|
2
|
[ genetics ]
|
eng-30-01546826-a
|
used of homologous chromosomes associated in pairs in synapsis
|
+ blooded
|
a
|
1
|
[ genetics ]
|
eng-30-01903813-a
|
of unmixed ancestry
|
+ bloodline
|
n
|
2
|
[ genetics ]
|
eng-30-04923907-n
|
ancestry of a purebred animal
|
+ CFTR
|
n
|
1
|
[ genetics ]
|
eng-30-05439810-n
|
the gene that is mutated in cystic fibrosis
|
+ cistron
|
n
|
1
|
[ genetics ]
|
eng-30-05436752-n
|
(genetics) a segment of DNA that is involved in producing a polypeptide chain; it can include regions preceding and following the coding DNA as well as introns between the exons; it is considered a unit of heredity
|
+ cosmid
|
n
|
1
|
[ genetics ]
|
eng-30-01372199-n
|
(genetics) a large vector that is made from a bacteriophage and used to clone genes or gene fragments
|
+ cross
|
n
|
6
|
[ genetics ]
|
eng-30-00850425-n
|
(genetics) the act of mixing different species or varieties of animals or plants and thus to produce hybrids
|
+ crossbred
|
a
|
1
|
[ genetics ]
|
eng-30-01904156-a
|
bred from parents of different varieties or species
|
+ crossbreeding
|
n
|
1
|
[ genetics ]
|
eng-30-00850425-n
|
(genetics) the act of mixing different species or varieties of animals or plants and thus to produce hybrids
|
+ crossing
|
n
|
6
|
[ genetics ]
|
eng-30-00850425-n
|
(genetics) the act of mixing different species or varieties of animals or plants and thus to produce hybrids
|
+ cystic_fibrosis_transport_regulator
|
n
|
1
|
[ genetics ]
|
eng-30-05439810-n
|
the gene that is mutated in cystic fibrosis
|
+ cytogenetic
|
a
|
1
|
[ genetics ]
|
eng-30-02709441-a
|
of or relating to cytogenetics
|
+ cytogenetical
|
a
|
1
|
[ genetics ]
|
eng-30-02709441-a
|
of or relating to cytogenetics
|
+ cytogenetics
|
n
|
1
|
[ genetics ]
|
eng-30-06070738-n
|
the branch of biology that studies the cellular aspects of heredity (especially the chromosomes)
|
+ deletion
|
n
|
2
|
[ genetics ]
|
eng-30-07425577-n
|
(genetics) the loss or absence of one or more nucleotides from a chromosome
|
+ derivation
|
n
|
5
|
[ genetics ]
|
eng-30-04922787-n
|
inherited properties shared with others of your bloodline
|
+ descent
|
n
|
2
|
[ genetics ]
|
eng-30-04923743-n
|
properties attributable to your ancestry
|
+ dihybrid_cross
|
n
|
1
|
[ genetics ]
|
eng-30-00850873-n
|
hybridization using two traits with two alleles each
|
+ diploid
|
a
|
1
|
[ genetics ]
|
eng-30-01147622-a
|
of a cell or organism having two sets of chromosomes or twice the haploid number
|
+ dominance
|
n
|
3
|
[ genetics ]
|
eng-30-11413800-n
|
the organic phenomenon in which one of a pair of alleles present in a genotype is expressed in the phenotype and the other allele of the pair is not
|
+ dominant
|
a
|
2
|
[ genetics ]
|
eng-30-00793793-a
|
(of genes) producing the same phenotype whether its allele is identical or dissimilar
|
+ dominant
|
n
|
2
|
[ genetics ]
|
eng-30-05438130-n
|
an allele that produces the same phenotype whether its paired allele is identical or different
|
+ dominant_allele
|
n
|
1
|
[ genetics ]
|
eng-30-05438130-n
|
an allele that produces the same phenotype whether its paired allele is identical or different
|
+ dominant_gene
|
n
|
1
|
[ genetics ]
|
eng-30-05437600-n
|
gene that produces the same phenotype in the organism whether or not its allele identical
|
+ double
|
a
|
5
|
[ genetics ]
|
eng-30-01546826-a
|
used of homologous chromosomes associated in pairs in synapsis
|
+ endowed
|
a
|
1
|
[ genetics ]
|
eng-30-00671091-a
|
provided or supplied or equipped with (especially as by inheritance or nature)
|
+ extraction
|
n
|
2
|
[ genetics ]
|
eng-30-04923743-n
|
properties attributable to your ancestry
|
+ factor
|
n
|
7
|
[ genetics ]
|
eng-30-05436752-n
|
(genetics) a segment of DNA that is involved in producing a polypeptide chain; it can include regions preceding and following the coding DNA as well as introns between the exons; it is considered a unit of heredity
|
+ filial
|
a
|
1
|
[ genetics ]
|
eng-30-02884275-a
|
designating the generation or the sequence of generations following the parental generation
|
+ filiation
|
n
|
2
|
[ genetics ]
|
eng-30-04922787-n
|
inherited properties shared with others of your bloodline
|
+ full_blood
|
n
|
1
|
[ genetics ]
|
eng-30-04924003-n
|
descent from parents both of one pure breed
|
+ full-blood
|
a
|
1
|
[ genetics ]
|
eng-30-01903813-a
|
of unmixed ancestry
|
+ full-blooded
|
a
|
1
|
[ genetics ]
|
eng-30-01903813-a
|
of unmixed ancestry
|
+ functional_genomics
|
n
|
1
|
[ genetics ]
|
eng-30-06075218-n
|
the branch of genomics that determines the biological function of the genes and their products
|
+ gene
|
n
|
1
|
[ genetics ]
|
eng-30-05436752-n
|
(genetics) a segment of DNA that is involved in producing a polypeptide chain; it can include regions preceding and following the coding DNA as well as introns between the exons; it is considered a unit of heredity
|
+ gene_linkage
|
n
|
1
|
[ genetics ]
|
eng-30-04923024-n
|
(genetics) traits that tend to be inherited together as a consequence of an association between their genes; all of the genes of a given chromosome are linked (where one goes they all go)
|
+ gene_mutation
|
n
|
1
|
[ genetics ]
|
eng-30-07426406-n
|
(genetics) a mutation due to an intramolecular reorganization of a gene
|
+ genetic
|
a
|
4
|
[ genetics ]
|
eng-30-02734192-a
|
of or relating to the science of genetics
|
+ genetic
|
a
|
2
|
[ genetics ]
|
eng-30-02734544-a
|
of or relating to or produced by or being a gene
|
+ genetic_marker
|
n
|
1
|
[ genetics ]
|
eng-30-05438483-n
|
a specific gene that produces a recognizable trait and can be used in family or population studies
|
+ genetical
|
a
|
2
|
[ genetics ]
|
eng-30-02734192-a
|
of or relating to the science of genetics
|
+ genetical
|
a
|
1
|
[ genetics ]
|
eng-30-02734544-a
|
of or relating to or produced by or being a gene
|
+ genetically
|
r
|
1
|
[ genetics ]
|
eng-30-00123924-r
|
by genetic mechanisms
|
+ genic
|
a
|
1
|
[ genetics ]
|
eng-30-02734544-a
|
of or relating to or produced by or being a gene
|
+ genomics
|
n
|
1
|
[ genetics ]
|
eng-30-06077087-n
|
the branch of genetics that studies organisms in terms of their genomes (their full DNA sequences)
|
+ haploid
|
a
|
1
|
[ genetics ]
|
eng-30-01147433-a
|
of a cell or organism having a single set of chromosomes
|
+ haploidic
|
a
|
1
|
[ genetics ]
|
eng-30-01147433-a
|
of a cell or organism having a single set of chromosomes
|
+ haplotype
|
n
|
1
|
[ genetics ]
|
eng-30-05439582-n
|
(genetics) a combination of alleles (for different genes) that are located closely together on the same chromosome and that tend to be inherited together
|
+ hereditary_pattern
|
n
|
1
|
[ genetics ]
|
eng-30-04922338-n
|
(genetics) attributes acquired via biological heredity from the parents
|
+ heritable
|
a
|
1
|
[ genetics jurisprudence ]
|
eng-30-01313929-a
|
capable of being inherited
|
+ heterosis
|
n
|
1
|
[ genetics ]
|
eng-30-04922597-n
|
(genetics) the tendency of a crossbred organism to have qualities superior to those of either parent
|
+ heterozygote
|
n
|
1
|
[ genetics ]
|
eng-30-05432230-n
|
(genetics) an organism having two different alleles of a particular gene and so giving rise to varying offspring
|
+ heterozygous
|
a
|
1
|
[ genetics ]
|
eng-30-01200915-a
|
having dissimilar alleles at corresponding chromosomal loci
|
+ holandric_gene
|
n
|
1
|
[ genetics ]
|
eng-30-05442022-n
|
a gene located on a Y chromosome
|
+ homeobox
|
n
|
1
|
[ genetics ]
|
eng-30-05438778-n
|
one of various similar homeotic genes that are involved in bodily segmentation during embryonic development
|
+ homeobox_gene
|
n
|
1
|
[ genetics ]
|
eng-30-05438778-n
|
one of various similar homeotic genes that are involved in bodily segmentation during embryonic development
|
+ homeotic_gene
|
n
|
1
|
[ genetics ]
|
eng-30-05438642-n
|
one the genes that are involved in embryologic development
|
+ homozygote
|
n
|
1
|
[ genetics ]
|
eng-30-05432420-n
|
(genetics) an organism having two identical alleles of a particular gene and so breeding true for the particular characteristic
|
+ homozygous
|
a
|
1
|
[ genetics ]
|
eng-30-01200705-a
|
having identical alleles at corresponding chromosomal loci
|
+ hybrid_vigor
|
n
|
1
|
[ genetics ]
|
eng-30-04922597-n
|
(genetics) the tendency of a crossbred organism to have qualities superior to those of either parent
|
+ hybridisation
|
n
|
1
|
[ genetics ]
|
eng-30-00850425-n
|
(genetics) the act of mixing different species or varieties of animals or plants and thus to produce hybrids
|
+ hybridization
|
n
|
1
|
[ genetics ]
|
eng-30-00850425-n
|
(genetics) the act of mixing different species or varieties of animals or plants and thus to produce hybrids
|
+ hybridizing
|
n
|
1
|
[ genetics ]
|
eng-30-00850425-n
|
(genetics) the act of mixing different species or varieties of animals or plants and thus to produce hybrids
|
+ immungenetics
|
n
|
1
|
[ genetics ]
|
eng-30-80001110-n
|
the branch of medical research that explores the relationship between the immune system and genetics.
|
+ immunogenetic
|
a
|
1
|
[ genetics ]
|
eng-30-80000019-a
|
|
+ Immunogenetics
|
n
|
1
|
[ genetics ]
|
eng-30-80001110-n
|
the branch of medical research that explores the relationship between the immune system and genetics.
|
+ inherit
|
v
|
3
|
[ genetics ]
|
eng-30-02315759-v
|
receive by genetic transmission
|
+ inheritable
|
a
|
1
|
[ genetics jurisprudence ]
|
eng-30-01313929-a
|
capable of being inherited
|
+ inheritance
|
n
|
3
|
[ genetics ]
|
eng-30-04922338-n
|
(genetics) attributes acquired via biological heredity from the parents
|
+ insertional_mutagenesis
|
n
|
1
|
[ genetics ]
|
eng-30-07426241-n
|
(genetics) a mutation caused by the insertion of exogenous DNA into a genome
|
+ interbreeding
|
n
|
1
|
[ genetics ]
|
eng-30-00850425-n
|
(genetics) the act of mixing different species or varieties of animals or plants and thus to produce hybrids
|
+ inversion
|
n
|
4
|
[ genetics ]
|
eng-30-07425726-n
|
(genetics) a kind of mutation in which the order of the genes in a section of a chromosome is reversed
|
+ law_of_independent_assortment
|
n
|
1
|
[ genetics ]
|
eng-30-05884984-n
|
each member of a pair of homologous chromosomes separates independently of the members of other pairs so the results are random
|
+ law_of_segregation
|
n
|
1
|
[ genetics ]
|
eng-30-05884736-n
|
members of a pair of homologous chromosomes separate during the formation of gametes and are distributed to different gametes so that every gamete receives only one member of the pair
|
+ lethal_gene
|
n
|
1
|
[ genetics ]
|
eng-30-05438956-n
|
any gene that has an effect that causes the death of the organism at any stage of life
|
+ lineage
|
n
|
5
|
[ genetics ]
|
eng-30-04922787-n
|
inherited properties shared with others of your bloodline
|
+ linkage
|
n
|
2
|
[ genetics ]
|
eng-30-04923024-n
|
(genetics) traits that tend to be inherited together as a consequence of an association between their genes; all of the genes of a given chromosome are linked (where one goes they all go)
|
+ linkage_group
|
n
|
1
|
[ genetics ]
|
eng-30-05439100-n
|
any pair of genes that tend to be transmitted together
|
+ linked_genes
|
n
|
1
|
[ genetics ]
|
eng-30-05439100-n
|
any pair of genes that tend to be transmitted together
|
+ meiosis
|
n
|
1
|
[ genetics ]
|
eng-30-13512725-n
|
(genetics) cell division that produces reproductive cells in sexually reproducing organisms; the nucleus divides into four nuclei each containing half the chromosome number (leading to gametes in animals and spores in plants)
|
+ meiotic
|
a
|
1
|
[ genetics ]
|
eng-30-02763423-a
|
of or relating to meiosis
|
+ Mendel's_law
|
n
|
1
|
[ genetics ]
|
eng-30-05884433-n
|
(genetics) one of two principles of heredity formulated by Gregor Mendel on the basis of his experiments with plants; the principles were limited and modified by subsequent genetic research
|
+ miosis
|
n
|
1
|
[ genetics ]
|
eng-30-13512725-n
|
(genetics) cell division that produces reproductive cells in sexually reproducing organisms; the nucleus divides into four nuclei each containing half the chromosome number (leading to gametes in animals and spores in plants)
|
+ modifier
|
n
|
4
|
[ genetics ]
|
eng-30-05439286-n
|
a gene that modifies the effect produced by another gene
|
+ modifier_gene
|
n
|
1
|
[ genetics ]
|
eng-30-05439286-n
|
a gene that modifies the effect produced by another gene
|
+ molecular_genetics
|
n
|
1
|
[ genetics ]
|
eng-30-06077916-n
|
the branch of genetics concerned with the structure and activity of genetic material at the molecular level
|
+ monogenic
|
a
|
1
|
[ genetics ]
|
eng-30-01314863-a
|
of or relating to an inheritable character that is controlled by a single pair of genes
|
+ monohybrid_cross
|
n
|
1
|
[ genetics ]
|
eng-30-00850986-n
|
hybridization using a single trait with two alleles (as in Mendel's experiments with garden peas)
|
+ monoploid
|
a
|
1
|
[ genetics ]
|
eng-30-01147433-a
|
of a cell or organism having a single set of chromosomes
|
+ multivalent
|
a
|
1
|
[ genetics ]
|
eng-30-01547007-a
|
used of the association of three or more homologous chromosomes during the first division of meiosis
|
+ mutant_gene
|
n
|
1
|
[ genetics ]
|
eng-30-05439413-n
|
a gene that has changed so that the normal transmission and expression of a trait is affected
|
+ nonallele
|
n
|
1
|
[ genetics ]
|
eng-30-05439942-n
|
genes that are not competitors at the same locus
|
+ nondisjunction
|
n
|
1
|
[ genetics ]
|
eng-30-13522879-n
|
meiosis in which there is a failure of paired homologous chromosomes to separate; results in an abnormal number of chromosomes in the daughter cells
|
+ oncogene
|
n
|
1
|
[ genetics ]
|
eng-30-05440410-n
|
a gene that disposes normal cells to change into cancerous tumor cells
|
+ operator_gene
|
n
|
1
|
[ genetics ]
|
eng-30-05440046-n
|
a gene that activates the production of messenger RNA by adjacent structural genes
|
+ origin
|
n
|
2
|
[ genetics ]
|
eng-30-04923743-n
|
properties attributable to your ancestry
|
+ parental
|
a
|
1
|
[ genetics ]
|
eng-30-02884085-a
|
designating the generation of organisms from which hybrid offspring are produced
|
+ pedigree
|
n
|
3
|
[ genetics ]
|
eng-30-04923907-n
|
ancestry of a purebred animal
|
+ pharmacogenetics
|
n
|
1
|
[ genetics ]
|
eng-30-06079247-n
|
the branch of genetics that studies the genetically determined variations in responses to drugs in humans or laboratory organisms
|
+ point_mutation
|
n
|
1
|
[ genetics ]
|
eng-30-07426406-n
|
(genetics) a mutation due to an intramolecular reorganization of a gene
|
+ polygene
|
n
|
1
|
[ genetics ]
|
eng-30-05440555-n
|
a gene that by itself has little effect on the phenotype but which can act together with others to produce observable variations
|
+ polygenic
|
a
|
1
|
[ genetics ]
|
eng-30-01315025-a
|
of or relating to an inheritable character that is controlled by several genes at once; of or related to or determined by polygenes
|
+ polymorphism
|
n
|
1
|
[ genetics ]
|
eng-30-11493266-n
|
(genetics) the genetic variation within a population that natural selection can operate on
|
+ polyploid
|
a
|
1
|
[ genetics ]
|
eng-30-01147836-a
|
of a cell or organism having more than twice the haploid number of chromosomes
|
+ proteomics
|
n
|
1
|
[ genetics ]
|
eng-30-06077276-n
|
the branch of genetics that studies the full set of proteins encoded by a genome
|
+ proto-oncogene
|
n
|
1
|
[ genetics ]
|
eng-30-05440756-n
|
a normal gene that has the potential to become an oncogene
|
+ purebred
|
a
|
1
|
[ genetics ]
|
eng-30-01903617-a
|
bred for many generations from member of a recognized breed or strain
|
+ recessive
|
a
|
2
|
[ genetics ]
|
eng-30-00793988-a
|
(of genes) producing its characteristic phenotype only when its allele is identical
|
+ recessive
|
n
|
1
|
[ genetics ]
|
eng-30-05438315-n
|
an allele that produces its characteristic phenotype only when its paired allele is identical
|
+ recessive_allele
|
n
|
1
|
[ genetics ]
|
eng-30-05438315-n
|
an allele that produces its characteristic phenotype only when its paired allele is identical
|
+ recessive_gene
|
n
|
1
|
[ genetics ]
|
eng-30-05440875-n
|
gene that produces its characteristic phenotype only when its allele is identical
|
+ reciprocal
|
n
|
3
|
[ genetics ]
|
eng-30-00851146-n
|
hybridization involving a pair of crosses that reverse the sexes associated with each genotype
|
+ reciprocal_cross
|
n
|
1
|
[ genetics ]
|
eng-30-00851146-n
|
hybridization involving a pair of crosses that reverse the sexes associated with each genotype
|
+ recombination
|
n
|
2
|
[ genetics ]
|
eng-30-07374152-n
|
(genetics) a combining of genes or characters different from what they were in the parents
|
+ recombine
|
v
|
2
|
[ genetics ]
|
eng-30-00565858-v
|
cause genetic recombination
|
+ recombine
|
v
|
1
|
[ genetics ]
|
eng-30-00566024-v
|
undergo genetic recombination
|
+ reduction_division
|
n
|
1
|
[ genetics ]
|
eng-30-13512725-n
|
(genetics) cell division that produces reproductive cells in sexually reproducing organisms; the nucleus divides into four nuclei each containing half the chromosome number (leading to gametes in animals and spores in plants)
|
+ regulator_gene
|
n
|
1
|
[ genetics ]
|
eng-30-05441053-n
|
a gene that produces a repressor substance that inhibits an operator gene
|
+ regulatory_gene
|
n
|
1
|
[ genetics ]
|
eng-30-05441053-n
|
a gene that produces a repressor substance that inhibits an operator gene
|
+ repressor_gene
|
n
|
1
|
[ genetics ]
|
eng-30-05441224-n
|
gene that prevents a nonallele from being transcribed
|
+ reversion
|
n
|
2
|
[ genetics ]
|
eng-30-07426573-n
|
(genetics) a return to a normal phenotype (usually resulting from a second mutation)
|
+ saltation
|
n
|
2
|
[ genetics ]
|
eng-30-07426732-n
|
(genetics) a mutation that drastically changes the phenotype of an organism or species
|
+ sex_chromosome
|
n
|
1
|
[ genetics ]
|
eng-30-05443651-n
|
(genetics) a chromosome that determines the sex of an individual
|
+ single_nucleotide_polymorphism
|
n
|
1
|
[ genetics ]
|
eng-30-11493452-n
|
(genetics) genetic variation in a DNA sequence that occurs when a single nucleotide in a genome is altered; SNPs are usually considered to be point mutations that have been evolutionarily successful enough to recur in a significant proportion of the population of a species
|
+ SNP
|
n
|
1
|
[ genetics ]
|
eng-30-11493452-n
|
(genetics) genetic variation in a DNA sequence that occurs when a single nucleotide in a genome is altered; SNPs are usually considered to be point mutations that have been evolutionarily successful enough to recur in a significant proportion of the population of a species
|
+ structural_gene
|
n
|
1
|
[ genetics ]
|
eng-30-05441338-n
|
a gene that controls the production of a specific protein or peptide
|
+ structural_genomics
|
n
|
1
|
[ genetics ]
|
eng-30-06075378-n
|
the branch of genomics that determines the three-dimensional structures of proteins
|
+ suppresser
|
n
|
2
|
[ genetics ]
|
eng-30-05441468-n
|
a gene that suppresses the phenotypic expression of another gene (especially of a mutant gene)
|
+ suppresser_gene
|
n
|
1
|
[ genetics ]
|
eng-30-05441468-n
|
a gene that suppresses the phenotypic expression of another gene (especially of a mutant gene)
|
+ suppressor
|
n
|
2
|
[ genetics ]
|
eng-30-05441468-n
|
a gene that suppresses the phenotypic expression of another gene (especially of a mutant gene)
|
+ suppressor_gene
|
n
|
1
|
[ genetics ]
|
eng-30-05441468-n
|
a gene that suppresses the phenotypic expression of another gene (especially of a mutant gene)
|
+ test-cross
|
n
|
1
|
[ genetics ]
|
eng-30-00851316-n
|
a cross between an organism whose genotype for a certain trait is unknown and an organism that is homozygous recessive for that trait so the unknown genotype can be determined from that of the offspring
|
+ testcross
|
n
|
1
|
[ genetics ]
|
eng-30-00851316-n
|
a cross between an organism whose genotype for a certain trait is unknown and an organism that is homozygous recessive for that trait so the unknown genotype can be determined from that of the offspring
|
+ transform
|
v
|
6
|
[ genetics ]
|
eng-30-00382010-v
|
change (a bacterial cell) into a genetically distinct cell by the introduction of DNA from another cell of the same or closely related species
|
+ transformation
|
n
|
4
|
[ genetics ]
|
eng-30-00399030-n
|
(genetics) modification of a cell or bacterium by the uptake and incorporation of exogenous DNA
|
+ transforming_gene
|
n
|
1
|
[ genetics ]
|
eng-30-05440410-n
|
a gene that disposes normal cells to change into cancerous tumor cells
|
+ transgene
|
n
|
1
|
[ genetics ]
|
eng-30-05441686-n
|
an exogenous gene introduced into the genome of another organism
|
+ transposition
|
n
|
3
|
[ genetics ]
|
eng-30-07425903-n
|
(genetics) a kind of mutation in which a chromosomal segment is transfered to a new position on the same or another chromosome
|
+ triploid
|
a
|
1
|
[ genetics ]
|
eng-30-01148086-a
|
of a cell or organism having three complete sets of chromosomes
|
+ tumor_suppressor_gene
|
n
|
1
|
[ genetics ]
|
eng-30-05441806-n
|
a suppressor gene that blocks unscheduled cell division
|
+ underbred
|
a
|
2
|
[ genetics ]
|
eng-30-01904596-a
|
of inferior or mixed breed
|
+ unit_character
|
n
|
1
|
[ genetics ]
|
eng-30-04617106-n
|
(genetics) a character inherited on an all-or-none basis and dependent on the presence of a single gene
|
+ univalent
|
a
|
1
|
[ genetics ]
|
eng-30-01546593-a
|
used of a chromosome that is not paired or united with its homologous chromosome during synapsis
|
+ vector
|
n
|
4
|
[ genetics ]
|
eng-30-01372038-n
|
(genetics) a virus or other agent that is used to deliver DNA to a cell
|
+ X_chromosome
|
n
|
1
|
[ genetics ]
|
eng-30-05442594-n
|
the sex chromosome that is present in both sexes: singly in males and doubly in females
|
+ X-linked
|
a
|
1
|
[ genetics ]
|
eng-30-03145310-a
|
relating to genes or characteristics or conditions carried on the X chromosome
|
+ X-linked_dominant_inheritance
|
n
|
1
|
[ genetics ]
|
eng-30-04923299-n
|
hereditary pattern in which a dominant gene on the X chromosome causes a characteristic to be manifested in the offspring
|
+ X-linked_gene
|
n
|
1
|
[ genetics ]
|
eng-30-05441929-n
|
a gene located on an X chromosome
|
+ X-linked_recessive_inheritance
|
n
|
1
|
[ genetics ]
|
eng-30-04923496-n
|
hereditary pattern in which a recessive gene on the X chromosome results in the manifestation of characteristics in male offspring and a carrier state in female offspring
|
+ XX
|
n
|
2
|
[ genetics ]
|
eng-30-05442789-n
|
(genetics) normal complement of sex chromosomes in a female
|
+ XXX
|
n
|
2
|
[ genetics ]
|
eng-30-05442916-n
|
(genetics) abnormal complement of three X chromosomes in a female
|
+ XXY
|
n
|
1
|
[ genetics ]
|
eng-30-05443050-n
|
(genetics) abnormal complement of sex hormones in a male resulting in Klinefelter's syndrome
|
+ XY
|
n
|
1
|
[ genetics ]
|
eng-30-05443211-n
|
(genetics) normal complement of sex hormones in a male
|
+ XYY
|
n
|
1
|
[ genetics ]
|
eng-30-05443333-n
|
(genetics) abnormal complement of sex hormones in a male who has two Y chromosomes
|
+ Y_chromosome
|
n
|
1
|
[ genetics ]
|
eng-30-05443484-n
|
the sex chromosome that is carried by men
|
+ Y-linked_gene
|
n
|
1
|
[ genetics ]
|
eng-30-05442022-n
|
a gene located on a Y chromosome
|