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ATP10A gene

Known as: ATPase phospholipid transporting 10A (putative), ATPase, CLASS V, TYPE 10C, KIAA0566 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
ATPase reaction cycle of P4‐ATPases affects their transport from the endoplasmic reticulum
P4‐ATPases belonging to the P‐type ATPase superfamily mediate active transport of phospholipids across cellular membranes. Most… 
2014
2014
Variable allelic expression of imprinted genes in human pluripotent stem cells during differentiation into specialized cell types in vitro.
Review
2012
Review
2012
Diet and Aging
Nutrition has important long-term consequences for health that are not only limited to the individual but can be passed on to the… 
2012
2012
Transient Silencing of a Type IV P-Type ATPase, Atp10c, Results in Decreased Glucose Uptake in C2C12 Myotubes
Atp10c is a strong candidate gene for diet-induced obesity and type 2 diabetes. To identify molecular and cellular targets of… 
2010
2010
Atp10a, a gene adjacent to the PWS/AS gene cluster, is not imprinted in mouse and is insensitive to the PWS-IC
Mutations affecting a cluster of coordinately regulated imprinted genes located at 15q11-q13 underlie both Prader–Willi syndrome… 
2008
2008
Association study of the 15q11‐q13 maternal expression domain in Japanese autistic patients
Chromosome 15q11‐q13 has been a focus of genetic studies of autism susceptibility, because cytogenetic abnormalities are… 
2004
2004
Physical Mapping of the Pink-Eyed Dilution Complex in Mouse Chromosome 7 shows that Atp10c is the only Transcript between Gabrb3 and Ube3a
Phenotypic analyses of a set of homozygous-lethal deletion mutants at the pink-eyed dilution (p) locus has resulted in the… 
Highly Cited
2003
Highly Cited
2003
Microarray analysis of gene/transcript expression in Prader-Willi syndrome: deletion versus UPD
Background: Prader-Willi syndrome (PWS), the most common genetic cause of marked obesity, is caused by genomic imprinting and… 
2003
2003
On the conflicting reports of imprinting status of mouse ATP10a in the adult brain: strain-background-dependent imprinting?
On the conflicting reports of imprinting status of mouse ATP10a in the adult brain: strain-background-dependent imprinting? 
2002
2002
Mutation screening and transmission disequilibrium study of ATP10C in autism.
Autism is a complex genetic disorder. Chromosome 15 is of particular interest in this disorder, because of previous reports of… 
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