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COMMD1 gene

Known as: Copper Metabolism (Murr1) Domain Containing 1 Gene, MGC27155, COPPER METABOLISM MURR1 DOMAIN-CONTAINING PROTEIN 1 
This gene is involved in the regulation of copper homeostasis, sodium uptake, and NF-kappa-B signaling.
National Institutes of Health

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COMMD1 wt Allele
Homo sapiensLigand BindingMolecular TransportSignal Transduction

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
p300-mediated acetylation of COMMD1 regulates its stability, and the ubiquitylation and nucleolar translocation of the RelA NF-κB subunit
ABSTRACT Nucleolar sequestration of the RelA subunit of nuclear factor (NF)-&kgr;B is an important mechanism for regulating NF… 
2014
2014
COMMD1/Murr1 Reinforces HIV-1 Latent Infection through IκB-α Stabilization
ABSTRACT The transcription factor NF-κB is important for HIV-1 transcription initiation in primary HIV-1 infection and… 
2008
2008
Tumor Suppressor ARF Promotes Non-classic Proteasome-independent Polyubiquitination of COMMD1*
Although the tumor suppressor ARF is generally accepted for its essential role in activating the p53 pathway, its p53-independent… 
2007
2007
Functional consequences of RNA interference targeting COMMD1 in a canine hepatic cell line in relation to copper toxicosis.
A deletion in the copper metabolism (Murr1) domain containing 1 (COMMD1) gene is associated with hepatic copper toxicosis in dogs… 
2007
2007
Expression and localization of cellular prion and COMMD1 proteins in human placenta throughout pregnancy.
Highly Cited
2006
Highly Cited
2006
Mutation analysis of 218 Chinese patients with Wilson disease revealed no correlation between the canine copper toxicosis gene MURR1 and Wilson disease
Wilson disease (WD) is the most common disorder resulting in hepatic copper overload. A similar form of copper-associated… 
2006
2006
Copper toxicosis gene MURR1 is not changed in Wilson disease patients with normal blood ceruloplasmin levels.
AIM To analyze our Wilson disease patient cohort (n=106) for alterations in the gene coding for MURR1. METHODS Patients with an… 
Highly Cited
2004
Highly Cited
2004
Analysis of the human homologue of the canine copper toxicosis gene MURR1 in Wilson disease patients
Wilson disease is a human disorder of copper metabolism resulting in toxic copper accumulation. Patients present with a high… 
Highly Cited
2003
Highly Cited
2003
The canine copper toxicosis gene MURR1 does not cause non-Wilsonian hepatic copper toxicosis.
2003
2003
Indirect molecular diagnosis of copper toxicosis in Bedlington terriers is complicated by haplotype diversity.
Positional cloning recently identified the mutation causing copper toxicosis (CT) in Bedlington terriers. Isolation of the MURR1… 
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