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CC2D1A gene

Known as: coiled-coil and C2 domain containing 1A, CC2D1A, mental retardation, nonsyndromic, autosomal recessive, 3 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Whole Blood Transcriptome Analysis for Lifelong Monitoring in Elite Sniffer Dogs Produced by Somatic Cell Nuclear Transfer.
Reproductive cloning by somatic cell nuclear transfer (SCNT) is a valuable method to propagate service dogs with desirable traits… 
2018
2018
Hypothalamic miR-219 regulates individual metabolic differences in response to diet-induced weight cycling
2016
2016
Computational Analysis and Polymorphism study of Tumor Suppressor Candidate Gene-3 for Non Syndromic Autosomal Recessive Mental Retardation
Computational Analysis and Polymorphism study of Tumor Suppressor Candidate Gene-3 for Non Syndromic Autosomal Recessive Mental… 
Review
2015
Review
2015
Syndromic craniosynostosis associated with microdeletion of chromosome 19p13.12–19p13.2
2015
2015
Whole-exome sequencing identified CC2D1A as the candidate gene for right isomerism
2013
2013
Phosphodiesterase activity is regulated by CC2D1A that is implicated in non-syndromic intellectual disability
Cyclic adenosine 3′,5′-monophosphate (cAMP) is a key regulator of many cellular processes, including in the neuronal system, and… 
2012
2012
INTERACTS WITH THE CHROMATIN REMODELING PROTEIN BRG1
The serotonin-1A (5-HT1A) receptor plays an important role in the regulation of the serotonin (5-HT) system as an autoreceptor on… 
2011
2011
Identification of Non-syndromic Intellectual Disability Genes and Their Overlap with Autism
Overlap between autism and NS-ID are significant in terms of genotype and phenotype. In this chapter, the focus is on determining… 
2010
2010
CC2D1A, a DM14 and C2 Domain Protein, Activates NF-κB through the Canonical Pathway*
CC2D1A is an evolutionarily conserved protein that contains four DM14 domains at the N terminus and a C2 domain at the C terminus… 
Review
2006
Review
2006
The genetics of mental retardation.
Genetic abnormalities frequently give rise to a mental retardation phenotype. Recent advances in resolution of comparative… 
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