Table of Contents
7 relations: Chromosome 9, Finnish heritage disease, Gene, Lethal congenital contracture syndrome, Nucleoporin 155, Protein, Protein–protein interaction.
Chromosome 9
Chromosome 9 is one of the 23 pairs of chromosomes in humans. GLE1L and chromosome 9 are genes on human chromosome 9.
Finnish heritage disease
A Finnish heritage disease is any genetic disease or disorder that is significantly more common in people whose ancestors were ethnic Finns, natives of Finland and Northern Sweden (Meänmaa) and Northwest Russia (Karelia and Ingria).
See GLE1L and Finnish heritage disease
Gene
In biology, the word gene has two meanings.
See GLE1L and Gene
Lethal congenital contracture syndrome
Lethal congenital contracture syndrome 1 (LCCS1), also called Multiple contracture syndrome, Finnish type, is an autosomal recessive genetic disorder characterized by total immobility of a fetus, detectable at around the 13th week of pregnancy.
See GLE1L and Lethal congenital contracture syndrome
Nucleoporin 155
Nucleoporin 155 (Nup155) is a protein that in humans is encoded by the NUP155 gene.
Protein
Proteins are large biomolecules and macromolecules that comprise one or more long chains of amino acid residues.
Protein–protein interaction
Protein–protein interactions (PPIs) are physical contacts of high specificity established between two or more protein molecules as a result of biochemical events steered by interactions that include electrostatic forces, hydrogen bonding and the hydrophobic effect.
See GLE1L and Protein–protein interaction
References
Also known as GLE1 (gene).