Similarities between 2p15-16.1 microdeletion syndrome and Chromosome 2
2p15-16.1 microdeletion syndrome and Chromosome 2 have 4 things in common (in Unionpedia): Base pair, Gene, Locus (genetics), Pseudogene.
Base pair
A base pair (bp) is a unit consisting of two nucleobases bound to each other by hydrogen bonds.
2p15-16.1 microdeletion syndrome and Base pair · Base pair and Chromosome 2 ·
Gene
In biology, a gene is a sequence of DNA or RNA that codes for a molecule that has a function.
2p15-16.1 microdeletion syndrome and Gene · Chromosome 2 and Gene ·
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).
2p15-16.1 microdeletion syndrome and Locus (genetics) · Chromosome 2 and Locus (genetics) ·
Pseudogene
Pseudogenes are segments of DNA that are related to real genes.
2p15-16.1 microdeletion syndrome and Pseudogene · Chromosome 2 and Pseudogene ·
The list above answers the following questions
- What 2p15-16.1 microdeletion syndrome and Chromosome 2 have in common
- What are the similarities between 2p15-16.1 microdeletion syndrome and Chromosome 2
2p15-16.1 microdeletion syndrome and Chromosome 2 Comparison
2p15-16.1 microdeletion syndrome has 32 relations, while Chromosome 2 has 191. As they have in common 4, the Jaccard index is 1.79% = 4 / (32 + 191).
References
This article shows the relationship between 2p15-16.1 microdeletion syndrome and Chromosome 2. To access each article from which the information was extracted, please visit: