Skip to search formSkip to main contentSkip to account menu

COMMD1 wt Allele

Known as: MURR1, Chromosome 2 Open Reading Frame 5 (MURR1) Gene, Copper Metabolism (Murr1) Domain Containing 1 wt Allele 
Human COMMD1 wild-type allele is located in the vicinity of 2p15 and is approximately 388 kb in length. This allele, which encodes COMM domain… 
National Institutes of Health

Related topics

Related topics

6 relations
2p15Homo sapiensLigand BindingMolecular Transport

Broader (1)

COMMD1 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
New insights into the biological role of COMMD 1 Bartuzi , Paulina
The transcription factor NF-κB plays a critical role in the inflammatory response and it has been implicated in various diseases… 
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… 
2009
2009
Xiaofeng Zheng COMMD 1 Promoting the Ubiquitination of RelA or B Activation by κ HSCARG Regulates
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… 
2005
2005
Quantitative PCR method to detect a 13-kb deletion in the MURR1 gene associated with copper toxicosis and HIV-1 replication
The recently discovered locus for copper toxicosis (CT) in Bedlington terriers (BT) has a 13-kb deletion enveloping the 187-bp… 
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… 
2004
2004
Evaluation of haplotypes associated with copper toxicosis in Bedlington Terriers in Australia.
OBJECTIVE To evaluate the haplotype distribution associated with the copper toxicosis gene and the segregation of the mutated… 
2004
2004
P0189 THE CANINE COPPER TOXICOSIS GENE MURR1 IS NOT IMPLICATED IN THE PATHOGENESIS OF WILSON DISEASE
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… 
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)