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Fact Sheets
A transcriptome is a collection of all the gene readouts present in a cell.
… A transcriptome is a collection of all the gene readouts present in a cell. … words, copied - into RNA ( ribonucleic acid ) . These gene readouts are called transcripts, and a transcriptome is a collection of all the gene readouts present in a cell. There are various kinds of …
News Release
The newly launched Impact of Genomic Variation on Function (IGVF) consortium to include 30 U.S. sites.
… The newly launched Impact of Genomic Variation on Function (IGVF) consortium to include 30 U.S. … $185 million over five years to the Impact of Genomic Variation on Function (IGVF) consortium, initiated and funded … investigators will work to understand how genomic variation alters human genome function, and how such …
Genetic Disorders
Fragile X syndrome is an inherited intellectual disability caused by a mutation in the FMR1 gene.
… intellectual disability caused by a mutation in the FMR1 gene. … are caused by an alteration (mutation) in the FMR1 gene where a DNA segment, known as the CGG triplet repeat, is … expanded CGG segment inactivates (silences) the FMR1 gene, which prevents the gene from producing a protein called …
Educational Resources
Codominance is a relationship between two versions of a gene.
… Codominance is a relationship between two versions of a gene. … of inheritance in which two versions (alleles) of the same gene are expressed separately to yield different traits in an … Codominance is a relationship between two versions of a gene. …
Educational Resources
Transcription is the process of making an RNA copy of a gene sequence.
… Transcription is the process of making an RNA copy of a gene sequence. … Cell, Cytoplasm, Deoxyribonucleic Acid (DNA), Gene, Gene Expression, Messenger RNA (mRNA), Nuclear Membrane, … to genomics, is the process of making an RNA copy of a gene’s DNA sequence. This copy, called messenger RNA (mRNA), …
Educational Resources
An oncogene is a mutated gene that contributes to the development of a cancer.
… An oncogene is a mutated gene that contributes to the development of a cancer. … Mutagen, Cancer, Cell, Mutation, Tumor Suppressor Gene … An oncogene is a mutated gene that has the potential to cause cancer. Before an … An oncogene is a mutated gene that contributes to the development of a cancer. …
Fact Sheets
Genetic mapping offers evidence that a disease transmitted from parent to child is linked to one or more genes and clues about where a gene lies on a chromosome.
… and provides clues about which chromosome contains the gene and precisely where the gene lies on that chromosome. … also provides clues about which chromosome contains the gene and precisely where the gene lies on that chromosome. Genetic maps have been used … as markers. DNA markers don't, by themselves, identify the gene responsible for the disease or trait; but they can tell …
Educational Resources
Sex linked is a trait in which a gene is located on a sex chromosome.
… Sex linked is a trait in which a gene is located on a sex chromosome. … Cell, Mutation, Gene, Sex Chromosome … Sex linked is a trait in which a gene is located on a sex chromosome. …
Educational Resources
An exon is the portion of a gene that codes for amino acids.
… An exon is the portion of a gene that codes for amino acids. … An exon is the portion of a gene that codes for amino acids. …
Educational Resources
An allele is one of two or more versions of a gene.
… An allele is one of two or more versions of a gene. … Allele, Gene, Homozygous, Autosomal, Mutation, Inherit, Heterozygous, … each parent, for any given genomic location where such variation exists. If the two alleles are the same, the … An allele is one of two or more versions of a gene. …