ATP8B4 gene

Known as: ATP8B4, ATPase, CLASS I, TYPE 8B, MEMBER 4, ATPIM 
 
National Institutes of Health

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Genes

Papers overview

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2018
2018
Brief Report: Whole-Exome Sequencing to Identify Rare Variants and Gene Networks That Increase Susceptibility to Scleroderma in African Americans.
OBJECTIVE Whole-exome sequencing (WES) studies in systemic sclerosis (SSc) patients of European American (EA) ancestry have… (More)
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2016
2016
Identification of Rare Variants in ATP8B4 as a Risk Factor for Systemic Sclerosis by Whole-Exome Sequencing.
OBJECTIVE To determine the contribution of rare variants as genetic modifiers of the expressivity, penetrance, and severity of… (More)
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2014
2014
Microvilli as markers of disordered apical-membrane trafficking and assembly: bowel and liver.
M icrovillous inclusion disease (MVID), also known as microvillous atrophy, is a rare autosomal-recessive enteropathy due to… (More)
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2012
2012
Translocation t(11;14) (q13;q32) and genomic imbalances in multi-ethnic multiple myeloma patients: a Malaysian study
More than 50% of myeloma cases have normal karyotypes under conventional cytogenetic analysis due to low mitotic activity and… (More)
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2010
2010
Heteromeric interactions required for abundance and subcellular localization of human CDC50 proteins and class 1 P4-ATPases.
Members of the P(4) family of P-type ATPases (P(4)-ATPases) are believed to function as phospholipid flippases in complex with… (More)
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