Skip to search formSkip to main contentSkip to account menu

MTMR10 gene

Known as: FLJ20313, MTMR10, myotubularin related protein 10 
National Institutes of Health

Related topics

Related topics

1 relation
MTMR1 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Molecular, physiological and behavioral characterization of the heterozygous Df[h15q13]/+ mouse model associated with the human 15q13.3 microdeletion syndrome
2016
2016
15q13.3 homozygous knockout mouse model display epilepsy-, autism- and schizophrenia-related phenotypes
The 15q13.3 microdeletion syndrome is caused by a 1.5-MB hemizygous microdeletion located on 15q13.3 affecting seven genes: FAN1… 
2015
2015
Copy number variants in attention-deficit hyperactive disorder: identification of the 15q13 deletion and its functional role
Objectives Evidence has supported a role for rare copy number variants in the etiology of attention-deficit hyperactivity… 
Highly Cited
2011
Highly Cited
2011
Homozygous deletion of chromosome 15q13.3 including CHRNA7 causes severe mental retardation, seizures, muscular hypotonia, and the loss of KLF13 and TRPM1 potentially cause macrocytosis and…
Highly Cited
2008
Highly Cited
2008
Differential Gene Expression of TRPM1, the Potential Cause of Congenital Stationary Night Blindness and Coat Spotting Patterns (LP) in the Appaloosa Horse (Equus caballus)
The appaloosa coat spotting pattern in horses is caused by a single incomplete dominant gene (LP). Homozygosity for LP (LP/LP) is… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)