TKTL1: a variation present in this gene in modern humans seems to drive greater neuron growth than does an ancient hominin version present in Neanderthals and non-human primates.
Corresponding protein in UniProtKB/Swiss-Prot
TLR7: Gene involved in the fight against certain viral infections. Located on the X chromosome, this gene could explain in part the fact that males (who only have one copy of the X chromosome) have a greater risk of hospitalization and mortality than females when infected with SARS-CoV-2.
Corresponding protein in UniProtKB/Swiss-Prot
Boys are boys thanks to the precocious action of ‘male’ proteins such as SRY. In the absence of male proteins, the foetus becomes a girl. So are girls, girls by default? The concept dates from the 1950s and the question remains open…
Prolune - article: ♂ or ♀, that is the question
Bioinformatics expert: List of genes on chromosome X
Chromosomes XY: Male or female… all about an angle
NR0B1: This gene is essential in the development of female sexual characteristics.
Prolune - article: ♂ or ♀, that is the question
Corresponding protein in UniProtKB/Swiss-Prot
MAOA: Gene coding for a protein involved in the metabolism of neurotransmitters which each have their say in modulating our mood.
Protein Spotlight : approaching happiness
Corresponding protein in UniProtKB/Swiss-Prot
ACE2: This gene codes for a protein involved in the maturation of angiotensin, a hormone that regulates blood pressure. Protein ACE2 also happens to let the SARS-CoV-2 coronavirus into human cells.
Protein Spotlight : a way in
Protein Spotlight - comics: a way in
Corresponding protein in UniProtKB/Swiss-Prot
AR: This gene codes for an androgen receptor which is involved in the development of the male sexual characters. Certain variations in this gene are associated with the development of baldness in men.
Corresponding protein in UniProtKB/Swiss-Prot
DMD: Gene coding for a protein present in neuromuscular junctions. Certain variations are the cause of Duchenne disease, characterized by muscle paralysis.
Bioinformatics expert: Duchenne muscular dystrophy in the OMIM database
Corresponding protein in UniProtKB/Swiss-Prot
OPN1MW: OPN1MW: Gene whose certain variations cause red/green colour blindness. Colour blindness is generally found in boys because there is no backup copy of this gene on the Y chromosome.
MECP2: certain variations in this gene are the cause of Rett syndrome (mental retardation).
GABRA3: This gene is involved in nerve impulse transmission.
F8/F9: These genes are involved in blood coagulation and, if defective, are associated with haemophilia. The illness became infamous when Tsarevitch Alexis Nikolaïevitch of Russia suffered from it; it was transmitted to him from his great grand-mother, Queen Victoria of England.
ATP7A: This gene is involved in controlling the level of copper inside our cells.
Prolune - snapshot: Menkes protein
Protein Spotlight: Heavy metal
Corresponding protein (NLGN3) in UniProtKB/Swiss-Prot
NLGN3/NLGN4X: A group of genes encoding proteins involved in synaptic function. Variations in these genes are associated with autism spectrum disorders.
CYBB: This gene is involved in antibacterial activity thanks to the production of free radicals.