10 12 13 14 20 21 22 23 Across Down 2. an allele whose effect is the absence either of normal gene product at the molecular level or of normal function at 1. The occurrence in a population of multiple forms of a trait or multiple alleles at a genetic locus the phenotypic level (two words) 3. the synthesis of RNA from a DNA template 4. the ribosome-mediated production of a polypeptide whose amino acid sequence is derived from the codon sequence of an 6. DNA sequence motif that influences the timing, cell, or tissue specificity, or level of expression of a gene (two words) 7. a mutation that alters a single base position in a DNA molecule by converting it to a different base or by the insertion/deletion of a single base in a DNA molecule (two words) MRNA molecule 5. the genotype or phenotype that is found in nature or in the standard laboratory stock for a given organism 9. the study of genes, and inheritance 11. One of the different forms of a gene that can exist at a single locus 12. a mutation that confers a mutant phenotype but still retains a low but detectable level of wild-type function 15. refers to specific pairing between nucleotides 8. a change to the sequence of a codon that does not change the encoded amino acid 10. an organism or cell containing a mutation 13. A section of RNA (three nucleotides in length) that encodes a single amino acid, also used to refer to the corresponding DNA sequence 14. The maleness gene, residing on the Y chromosome (acronym+word) 16. the fundamental physical and functional unit of heredity, a segment of DNA composed of a transcribed region and regulatory sequence that makes transcription possible 17. (verb) the process that produces a gene or wild type, (noun) a gene or chromosome that results from mutation 18. small regions at the ends of the X and Y chromosomes; they are homologous and undergo pairing and crossing over at meiosis (two words) 19. a polymorphism with only two forms (e.g. male and female) 20. An attribute of individual members of a species for which various heritable differences (traits) can be defined. 21. a cell having one chromosome set, or an organism composed of such cells 22. a nucleotide-pair difference at a given location in the genomes of two or more naturally occurring individuals 23. the cloning and molecular characterization of entire genomes (the analysis of genomes)
10 12 13 14 20 21 22 23 Across Down 2. an allele whose effect is the absence either of normal gene product at the molecular level or of normal function at 1. The occurrence in a population of multiple forms of a trait or multiple alleles at a genetic locus the phenotypic level (two words) 3. the synthesis of RNA from a DNA template 4. the ribosome-mediated production of a polypeptide whose amino acid sequence is derived from the codon sequence of an 6. DNA sequence motif that influences the timing, cell, or tissue specificity, or level of expression of a gene (two words) 7. a mutation that alters a single base position in a DNA molecule by converting it to a different base or by the insertion/deletion of a single base in a DNA molecule (two words) MRNA molecule 5. the genotype or phenotype that is found in nature or in the standard laboratory stock for a given organism 9. the study of genes, and inheritance 11. One of the different forms of a gene that can exist at a single locus 12. a mutation that confers a mutant phenotype but still retains a low but detectable level of wild-type function 15. refers to specific pairing between nucleotides 8. a change to the sequence of a codon that does not change the encoded amino acid 10. an organism or cell containing a mutation 13. A section of RNA (three nucleotides in length) that encodes a single amino acid, also used to refer to the corresponding DNA sequence 14. The maleness gene, residing on the Y chromosome (acronym+word) 16. the fundamental physical and functional unit of heredity, a segment of DNA composed of a transcribed region and regulatory sequence that makes transcription possible 17. (verb) the process that produces a gene or wild type, (noun) a gene or chromosome that results from mutation 18. small regions at the ends of the X and Y chromosomes; they are homologous and undergo pairing and crossing over at meiosis (two words) 19. a polymorphism with only two forms (e.g. male and female) 20. An attribute of individual members of a species for which various heritable differences (traits) can be defined. 21. a cell having one chromosome set, or an organism composed of such cells 22. a nucleotide-pair difference at a given location in the genomes of two or more naturally occurring individuals 23. the cloning and molecular characterization of entire genomes (the analysis of genomes)
Biology Today and Tomorrow without Physiology (MindTap Course List)
5th Edition
ISBN:9781305117396
Author:Cecie Starr, Christine Evers, Lisa Starr
Publisher:Cecie Starr, Christine Evers, Lisa Starr
Chapter7: Gene Expression And Control
Section: Chapter Questions
Problem 1DID
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Transcribed Image Text:10
12
13
14
20 21
22
23
Transcribed Image Text:Across
Down
2. an allele whose effect is the absence
either of normal gene product at the
molecular level or of normal function at
1. The occurrence in a population of
multiple forms of a trait or multiple
alleles at a genetic locus
the phenotypic level (two words)
3. the synthesis of RNA from a DNA
template
4. the ribosome-mediated production of a
polypeptide whose amino acid sequence
is derived from the codon sequence of an
6. DNA sequence motif that influences the
timing, cell, or tissue specificity, or level
of expression of a gene (two words)
7. a mutation that alters a single base
position in a DNA molecule by
converting it to a different base or by the
insertion/deletion of a single base in a
DNA molecule (two words)
MRNA molecule
5. the genotype or phenotype that is found
in nature or in the standard laboratory
stock for a given organism
9. the study of genes, and inheritance
11. One of the different forms of a gene that
can exist at a single locus
12. a mutation that confers a mutant
phenotype but still retains a low but
detectable level of wild-type function
15. refers to specific pairing between
nucleotides
8. a change to the sequence of a codon that
does not change the encoded amino acid
10. an organism or cell containing a mutation
13. A section of RNA (three nucleotides in
length) that encodes a single amino acid,
also used to refer to the corresponding
DNA sequence
14. The maleness gene, residing on the Y
chromosome (acronym+word)
16. the fundamental physical and functional
unit of heredity, a segment of DNA
composed of a transcribed region and
regulatory sequence that makes
transcription possible
17. (verb) the process that produces a gene or
wild type, (noun) a gene or chromosome
that results from mutation
18. small regions at the ends of the X and Y
chromosomes; they are homologous and
undergo pairing and crossing over at
meiosis (two words)
19. a polymorphism with only two forms
(e.g. male and female)
20. An attribute of individual members of a
species for which various heritable
differences (traits) can be defined.
21. a cell having one chromosome set, or an
organism composed of such cells
22. a nucleotide-pair difference at a given
location in the genomes of two or more
naturally occurring individuals
23. the cloning and molecular
characterization of entire genomes (the
analysis of genomes)
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