Similarities between Chromosome 22 and Karyotype
Chromosome 22 and Karyotype have 15 things in common (in Unionpedia): Autosome, Cell (biology), Centromere, Chromosomal translocation, Chromosome, Chromosome 21, Chronic myelogenous leukemia, DNA, Down syndrome, G banding, Gene, Human genome, Locus (genetics), Mitosis, Philadelphia chromosome.
Autosome
An autosome is a chromosome that is not an allosome (a sex chromosome).
Autosome and Chromosome 22 · Autosome and Karyotype ·
Cell (biology)
The cell (from Latin cella, meaning "small room") is the basic structural, functional, and biological unit of all known living organisms.
Cell (biology) and Chromosome 22 · Cell (biology) and Karyotype ·
Centromere
The centromere is the specialized DNA sequence of a chromosome that links a pair of sister chromatids (a dyad).
Centromere and Chromosome 22 · Centromere and Karyotype ·
Chromosomal translocation
In genetics, a chromosome translocation is a chromosome abnormality caused by rearrangement of parts between nonhomologous chromosomes.
Chromosomal translocation and Chromosome 22 · Chromosomal translocation and Karyotype ·
Chromosome
A chromosome (from Ancient Greek: χρωμόσωμα, chromosoma, chroma means colour, soma means body) is a DNA molecule with part or all of the genetic material (genome) of an organism.
Chromosome and Chromosome 22 · Chromosome and Karyotype ·
Chromosome 21
Chromosome 21 is one of the 23 pairs of chromosomes in humans.
Chromosome 21 and Chromosome 22 · Chromosome 21 and Karyotype ·
Chronic myelogenous leukemia
Chronic myelogenous leukemia (CML), also known as chronic myeloid leukemia, is a cancer of the white blood cells.
Chromosome 22 and Chronic myelogenous leukemia · Chronic myelogenous leukemia and Karyotype ·
DNA
Deoxyribonucleic acid (DNA) is a thread-like chain of nucleotides carrying the genetic instructions used in the growth, development, functioning and reproduction of all known living organisms and many viruses.
Chromosome 22 and DNA · DNA and Karyotype ·
Down syndrome
Down syndrome (DS or DNS), also known as trisomy 21, is a genetic disorder caused by the presence of all or part of a third copy of chromosome 21.
Chromosome 22 and Down syndrome · Down syndrome and Karyotype ·
G banding
G-banding, G banding, or Giemsa banding is a technique used in cytogenetics to produce a visible karyotype by staining condensed chromosomes.
Chromosome 22 and G banding · G banding and Karyotype ·
Gene
In biology, a gene is a sequence of DNA or RNA that codes for a molecule that has a function.
Chromosome 22 and Gene · Gene and Karyotype ·
Human genome
The human genome is the complete set of nucleic acid sequences for humans, encoded as DNA within the 23 chromosome pairs in cell nuclei and in a small DNA molecule found within individual mitochondria.
Chromosome 22 and Human genome · Human genome and Karyotype ·
Locus (genetics)
A locus (plural loci) in genetics is a fixed position on a chromosome, like the position of a gene or a marker (genetic marker).
Chromosome 22 and Locus (genetics) · Karyotype and Locus (genetics) ·
Mitosis
In cell biology, mitosis is a part of the cell cycle when replicated chromosomes are separated into two new nuclei.
Chromosome 22 and Mitosis · Karyotype and Mitosis ·
Philadelphia chromosome
The Philadelphia chromosome or Philadelphia translocation (Ph) is a specific genetic abnormality in chromosome 22 of leukemia cancer cells (particularly chronic myeloid leukemia (CML) cells).
Chromosome 22 and Philadelphia chromosome · Karyotype and Philadelphia chromosome ·
The list above answers the following questions
- What Chromosome 22 and Karyotype have in common
- What are the similarities between Chromosome 22 and Karyotype
Chromosome 22 and Karyotype Comparison
Chromosome 22 has 129 relations, while Karyotype has 190. As they have in common 15, the Jaccard index is 4.70% = 15 / (129 + 190).
References
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