| D012150 |
Polymorphism, Restriction Fragment Length |
Variation occurring within a species in the presence or length of DNA fragment generated by a specific endonuclease at a specific site in the genome. Such variations are generated by mutations that create or abolish recognition sites for these enzymes or change the length of the fragment. |
RFLP,Restriction Fragment Length Polymorphism,RFLPs,Restriction Fragment Length Polymorphisms |
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| D002874 |
Chromosome Mapping |
Any method used for determining the location of and relative distances between genes on a chromosome. |
Gene Mapping,Linkage Mapping,Genome Mapping,Chromosome Mappings,Gene Mappings,Genome Mappings,Linkage Mappings,Mapping, Chromosome,Mapping, Gene,Mapping, Genome,Mapping, Linkage,Mappings, Chromosome,Mappings, Gene,Mappings, Genome,Mappings, Linkage |
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| D002895 |
Chromosomes, Human, Pair 5 |
One of the two pairs of human chromosomes in the group B class (CHROMOSOMES, HUMAN, 4-5). |
Chromosome 5 |
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| D004273 |
DNA, Neoplasm |
DNA present in neoplastic tissue. |
Neoplasm DNA |
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| D006579 |
Heterozygote |
An individual having different alleles at one or more loci regarding a specific character. |
Carriers, Genetic,Genetic Carriers,Carrier, Genetic,Genetic Carrier,Heterozygotes |
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| D006801 |
Humans |
Members of the species Homo sapiens. |
Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man |
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| D015179 |
Colorectal Neoplasms |
Tumors or cancer of the COLON or the RECTUM or both. Risk factors for colorectal cancer include chronic ULCERATIVE COLITIS; FAMILIAL POLYPOSIS COLI; exposure to ASBESTOS; and irradiation of the CERVIX UTERI. |
Colorectal Cancer,Colorectal Carcinoma,Colorectal Tumors,Neoplasms, Colorectal,Cancer, Colorectal,Cancers, Colorectal,Carcinoma, Colorectal,Carcinomas, Colorectal,Colorectal Cancers,Colorectal Carcinomas,Colorectal Neoplasm,Colorectal Tumor,Neoplasm, Colorectal,Tumor, Colorectal,Tumors, Colorectal |
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| D016153 |
Genes, Suppressor |
Genes that have a suppressor allele or suppressor mutation (SUPPRESSION, GENETIC) which cancels the effect of a previous mutation, enabling the wild-type phenotype to be maintained or partially restored. For example, amber suppressors cancel the effect of an AMBER NONSENSE MUTATION. |
Amber Suppressor Genes,Frameshift Suppressor Genes,Genes, Amber Suppressor,Genes, Frameshift Suppressor,Genes, Nonsense Mutation Suppressor,Genes, Ochre Suppressor,Genes, Second-Site Suppressor,Nonsense Mutation Suppressor Genes,Ochre Suppressor Genes,Second-Site Suppressor Genes,Genes, Opal Suppressor,Suppressor Genes,Amber Suppressor Gene,Frameshift Suppressor Gene,Gene, Amber Suppressor,Gene, Frameshift Suppressor,Gene, Ochre Suppressor,Gene, Opal Suppressor,Gene, Second-Site Suppressor,Gene, Suppressor,Genes, Second Site Suppressor,Ochre Suppressor Gene,Opal Suppressor Gene,Opal Suppressor Genes,Second Site Suppressor Genes,Second-Site Suppressor Gene,Suppressor Gene,Suppressor Gene, Amber,Suppressor Gene, Frameshift,Suppressor Gene, Ochre,Suppressor Gene, Opal,Suppressor Gene, Second-Site,Suppressor Genes, Amber,Suppressor Genes, Frameshift,Suppressor Genes, Ochre,Suppressor Genes, Opal,Suppressor Genes, Second-Site |
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