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)

Biochemistry
9th Edition
ISBN:9781319114671
Author:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.
Publisher:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.
Chapter1: Biochemistry: An Evolving Science
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10
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Transcribed Image Text: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)
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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