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16q13-q21

A chromosome band present on 16q
National Institutes of Health

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3 relations
16qChromosomesMMP2 wt Allele

Papers overview

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2020
2020
An in silico analysis of deleterious single nucleotide polymorphisms and molecular dynamics simulation of disease linked mutations in genes responsible for neurodegenerative disorder
Abstract Mutation in two genes deglycase gene (DJ-1) and retromer complex component gene (VPS35) are linked with… 
2000
2000
Cloning and characterization of human VPS35 and mouse Vps35 and mapping of VPS35 to human chromosome 16q13-q21.
Maintenance of different organelles in eukaryotic cells depends on sorting proteins, which ensure the proper delivery of… 
1999
1999
Characterization of a novel C-kinesin (KIFC3) abundantly expressed in vertebrate retina and RPE.
Many forms of intracellular transport are mediated by microtubule-dependent motors of the kinesin superfamily (KIFs). To identify… 
1998
1998
Cloning of a novel C-terminal kinesin (KIFC3) that maps to human chromosome 16q13-q21 and thus is a candidate gene for Bardet-Biedl syndrome.
Kinesins are a large superfamily of microtubule motors that mediate specific motile processes. In a previous study, we identified… 
1994
1994
Chromosomal localization of human RNA polymerase II subunit genes.
The eukaryotic DNA-dependent RNA polymerase II (or B) is composed of 10 to 14 polypeptides ranging from 220 to 10 kDa. To gain… 
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